3e6i:B (ILE474) to (ILE490) HUMAN CYTOCHROME P450 2E1 IN COMPLEX WITH THE INHIBITOR INDAZOLE | CYP2E1, P450 2E1, MONOOXYGENASE, ACETAMINOPHEN, OXIDOREDUCTASE, HEME, ENDOPLASMIC RETICULUM, IRON, MEMBRANE, METAL-BINDING, MICROSOME
3rl2:B (LYS6) to (PRO32) HIV NEF DERIVED PEPTIDE NEF73 COMPLEXED TO HLA-A*0301 | HLA-A*0301, CD8+ T CELL IMMUNITY, HIV DERIVED PEPTIDES, IMMUNE SYSTEM
2ahw:A (ALA379) to (CYS415) CRYSTAL STRUCTURE OF ACYL-COA TRANSFERASE FROM E. COLI O157:H7 (YDIF)- THIOESTER COMPLEX WITH COA- 2 | YDIF, COA TRANSFERASE, GLUTAMYL THIOESTER, STRUCTURAL GENOMICS, MONTREAL-KINGSTON BACTERIAL STRUCTURAL GENOMICS INITIATIVE, BSGI, TRANSFERASE
1n8o:E (GLY19) to (LEU55) CRYSTAL STRUCTURE OF A COMPLEX BETWEEN BOVINE CHYMOTRYPSIN AND ECOTIN | HYDROLASE
2obe:A (CYS132) to (VAL155) CRYSTAL STRUCTURE OF CHIMPANZEE ADENOVIRUS (TYPE 68/SIMIAN 25) MAJOR COAT PROTEIN HEXON | TRIMER, DOUBLE-BARREL SUBUNIT, VIRAL JELLYROLL, BASE, HYPERVARIABLE TOWER, VIRAL PROTEIN
2obe:A (PHE778) to (SER856) CRYSTAL STRUCTURE OF CHIMPANZEE ADENOVIRUS (TYPE 68/SIMIAN 25) MAJOR COAT PROTEIN HEXON | TRIMER, DOUBLE-BARREL SUBUNIT, VIRAL JELLYROLL, BASE, HYPERVARIABLE TOWER, VIRAL PROTEIN
2obe:B (PHE778) to (SER856) CRYSTAL STRUCTURE OF CHIMPANZEE ADENOVIRUS (TYPE 68/SIMIAN 25) MAJOR COAT PROTEIN HEXON | TRIMER, DOUBLE-BARREL SUBUNIT, VIRAL JELLYROLL, BASE, HYPERVARIABLE TOWER, VIRAL PROTEIN
2obe:C (CYS132) to (VAL155) CRYSTAL STRUCTURE OF CHIMPANZEE ADENOVIRUS (TYPE 68/SIMIAN 25) MAJOR COAT PROTEIN HEXON | TRIMER, DOUBLE-BARREL SUBUNIT, VIRAL JELLYROLL, BASE, HYPERVARIABLE TOWER, VIRAL PROTEIN
2obe:C (PHE778) to (SER856) CRYSTAL STRUCTURE OF CHIMPANZEE ADENOVIRUS (TYPE 68/SIMIAN 25) MAJOR COAT PROTEIN HEXON | TRIMER, DOUBLE-BARREL SUBUNIT, VIRAL JELLYROLL, BASE, HYPERVARIABLE TOWER, VIRAL PROTEIN
4wdi:A (HIS188) to (PRO210) WEAK TCR BINDING TO AN UNSTABLE INSULIN EPITOPE DRIVES TYPE 1 DIABETES | IMMUNOGLOBULIN, H-2KD, TYPE 1 DIABETES, IMMUNE SYSTEM
4wdi:D (HIS188) to (PRO210) WEAK TCR BINDING TO AN UNSTABLE INSULIN EPITOPE DRIVES TYPE 1 DIABETES | IMMUNOGLOBULIN, H-2KD, TYPE 1 DIABETES, IMMUNE SYSTEM
3ea1:B (ARG64) to (LEU91) CRYSTAL STRUCTURE OF THE Y247S/Y251S MUTANT OF PHOSPHATIDYLINOSITOL-SPECIFIC PHOSPHOLIPASE C FROM BACILLUS THURINGIENSIS | PHOSPHATIDYLINOSITOL-SPECIFIC PHOSPHOLIPASE C, PI-PLC, DIMER, INTERFACIALLY IMPAIRED, MEMBRANE BINDING, TIM BARREL, LIPID DEGRADATION, LYASE, SECRETED
1a5k:C (ASP431) to (SER493) K217E VARIANT OF KLEBSIELLA AEROGENES UREASE | HYDROLASE (UREA AMIDO), MUTANT, NICKEL METALLOENZYME, HYDROLASE
1a5l:C (ASP431) to (SER493) K217C VARIANT OF KLEBSIELLA AEROGENES UREASE | HYDROLASE (UREA AMIDO), MUTANT, NICKEL METALLOENZYME, HYDROLASE
2akj:A (GLY355) to (GLN377) STRUCTURE OF SPINACH NITRITE REDUCTASE | X-RAY CRYSTALLOGRAPHY; HEME; ELECTRON TRANSPORT, OXIDOREDUCTASE
1a5m:C (ASP431) to (SER493) K217A VARIANT OF KLEBSIELLA AEROGENES UREASE | HYDROLASE (UREA AMIDO), MUTANT, NICKEL METALLOENZYME, HYDROLASE
4wg2:B (GLU430) to (LYS452) P411BM3-CIS T438S I263F REGIOSELECTIVE C-H AMINATION CATALYST | P411BM3-CIS, ENGINEERING, CATALYSIS, OXIDOREDUCTASE
1a78:B (CYS17) to (LEU43) COMPLEX OF TOAD OVARY GALECTIN WITH THIO-DIGALACTOSE | S-LECTIN, CARBOHYDRATE BINDING, COMPLEX (LECTIN/SACCHARIDE)
4gwa:A (LEU34) to (SER60) CRYSTAL STRUCTURE OF A GH7 FAMILY CELLOBIOHYDROLASE FROM LIMNORIA QUADRIPUNCTATA | CELLOBIOHYDROLASE, GLYCOSYL HYDROLASE, HYDROLASE
4gwa:B (LEU34) to (SER60) CRYSTAL STRUCTURE OF A GH7 FAMILY CELLOBIOHYDROLASE FROM LIMNORIA QUADRIPUNCTATA | CELLOBIOHYDROLASE, GLYCOSYL HYDROLASE, HYDROLASE
1a8u:A (GLY6) to (GLY21) CHLOROPEROXIDASE T/BENZOATE COMPLEX | HALOPEROXIDASE, OXIDOREDUCTASE, BENZOATE COMPLEX
2oip:B (ASN250) to (ASP273) CRYSTAL STRUCTURE OF THE S290G ACTIVE SITE MUTANT OF TS- DHFR FROM CRYPTOSPORIDIUM HOMINIS | BIFUNCTIONAL ENZYME, TRANSFERASE, OXIDOREDUCTASE
3rqo:B (VAL312) to (ASN340) STRUCTURE OF THE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-((1S,2R/1R,2S)-2-(3-CLOROPHENYL) CYCLOPROPYLAMINO)ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2- AMINE | OXIDOREDUCTASE, ENZYME-INHIBITOR COMPLEX, OXIDOREDUCTASE-INHIBITOR COMPLEX
1ngw:B (SER121) to (PRO148) CHIMERIC AFFINITY MATURED FAB 7G12 COMPLEXED WITH MESOPORPHYRIN | ANTIBODY, IMMUNOGLOBULIN, ANTIGEN BINDING FRAGMENT, IMMUNE SYSTEM
2av7:D (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HTLV-1 TAX PEPTIDE BOUND TO HUMAN CLASS I MHC HLA-A2 WITH THE K66A MUTATION IN THE HEAVY CHAIN. | TAX PEPTIDE, MHC, MUTATED HLA-A2, K66A., IMMUNE SYSTEM
3egd:B (PHE766) to (PRO781) CRYSTAL STRUCTURE OF THE MAMMALIAN COPII-COAT PROTEIN SEC23A/24A COMPLEXED WITH THE SNARE PROTEIN SEC22 AND BOUND TO THE TRANSPORT SIGNAL SEQUENCE OF VESICULAR STOMATITIS VIRUS GLYCOPROTEIN | COPII COAT, TRANSPORT SIGNAL SEQUENCE, VESICLE, DISEASE MUTATION, ENDOPLASMIC RETICULUM, ER-GOLGI TRANSPORT, GOLGI APPARATUS, MEMBRANE, PROTEIN TRANSPORT, TRANSPORT, PHOSPHOPROTEIN, TRANSMEMBRANE
3egx:B (PHE766) to (PRO781) CRYSTAL STRUCTURE OF THE MAMMALIAN COPII-COAT PROTEIN SEC23A/24A COMPLEXED WITH THE SNARE PROTEIN SEC22B AND BOUND TO THE TRANSPORT SIGNAL SEQUENCE OF THE SNARE PROTEIN BET1 | COPII COAT PROTEIN, VESICLE TRANSPORT, TRANSPORT SIGNAL SEQUENCE, DISEASE MUTATION, ENDOPLASMIC RETICULUM, ER-GOLGI TRANSPORT, GOLGI APPARATUS, MEMBRANE, PROTEIN TRANSPORT, TRANSPORT, PHOSPHOPROTEIN, TRANSMEMBRANE
1ai7:B (SER1) to (PRO29) PENICILLIN ACYLASE COMPLEXED WITH PHENOL | ANTIBIOTIC RESISTANCE, LIGAND INDUCED CONFORMATIONAL CHANGE, HYDROLASE
1ajn:B (SER1) to (PRO29) PENICILLIN ACYLASE COMPLEXED WITH P-NITROPHENYLACETIC ACID | ANTIBIOTIC RESISTANCE, LIGAND INDUCED CONFORMATIONAL CHANGE, HYDROLASE
1ajp:B (SER1) to (PRO29) PENICILLIN ACYLASE COMPLEXED WITH 2,5-DIHYDROXYPHENYLACETIC ACID | ANTIBIOTIC RESISTANCE, LIGAND INDUCED CONFORMATIONAL CHANGE, HYDROLASE
3rwf:A (HIS188) to (PRO210) RHESUS MACAQUE MHC CLASS I MOLECULE MAMU-B*17-QW9 | ANTIGENIC PEPTIDES, T LYMPHOCYTES, IMMUNE RESPONSE, IMMUNE SYSTEM
3rwg:A (HIS188) to (PRO210) RHESUS MACAQUE MHC CLASS I MOLECULE MAMU-B*17-MW9 | ANTIGENIC PEPTIDES, T LYMPHOCYTES, IMMUNE RESPONSE, IMMUNE SYSTEM
4h1i:C (LYS278) to (HIS304) STRUCTURE OF HUMAN THYMIDYLATE SYNTHASE AT LOW SALT CONDITIONS | NUCLEOTIDE METABOLISM, CANCER CHEMOTHERAPY TARGET, METHYL TRANSFERASE, TRANSFERASE
4h24:D (GLU430) to (LYS452) CYTOCHROME P450BM3-CIS CYCLOPROPANATION CATALYST | CYTOCHROME P450, ENZYMATIC CYCLOPROPANATION, DIRECTED EVOLUTION, NON- NATURAL FUNCTION, OXIDOREDUCTASE
1ao7:A (HIS188) to (PRO210) COMPLEX BETWEEN HUMAN T-CELL RECEPTOR, VIRAL PEPTIDE (TAX), AND HLA-A 0201 | CLASS I MHC, T-CELL RECEPTOR, VIRAL PEPTIDE, COMPLEX (MHC-VIRAL PEPTIDE-RECEPTOR, COMPLEX (MHC-VIRAL PEPTIDE-RECEPTOR) COMPLEX
1aoe:B (ASP175) to (ARG191) CANDIDA ALBICANS DIHYDROFOLATE REDUCTASE COMPLEXED WITH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE (NADPH) AND 1,3-DIAMINO-7-(1-ETHYEPROPYE)-7H-PYRRALO-[3,2- F]QUINAZOLINE (GW345) | OXIDOREDUCTASE, ANTIFUNGAL TARGET, REDUCTASE
3eim:A (THR6) to (THR34) METAL EXCHANGE IN THERMOLYSIN | PROTEIN COPPER COMPLEX, HYDROLASE, METAL-BINDING, METALLOPROTEASE, PROTEASE, SECRETED, ZYMOGEN
4wqn:A (ALA476) to (LYS503) CRYSTAL STRUCTURE OF N6-METHYLADENOSINE RNA READER YTHDF2 | N6-METHYLADENOSINE RNA READER, RNA BINDING PROTEIN
3eiv:B (LEU83) to (ALA108) CRYSTAL STRUCTURE OF SINGLE-STRANDED DNA-BINDING PROTEIN FROM STREPTOMYCES COELICOLOR | SINGLE-STRANDED DNA-BINDING PROTEIN, STREPTOMYCES COELICOLOR, DNA DAMAGE, DNA REPAIR, DNA REPLICATION, DNA- BINDING, PHOSPHOPROTEIN, DNA BINDING PROTEIN
1aop:A (GLY347) to (LEU368) SULFITE REDUCTASE STRUCTURE AT 1.6 ANGSTROM RESOLUTION | OXIDOREDUCTASE, SIROHEME, [4FE-4S], SNIRR, SIX-ELECTRON REDUCTION, PHOSPHATE COMPLEX
2b3u:A (TYR52) to (ASP82) HUMAN SPERMINE SPERMIDINE ACETYLTRANSFERASE K26R MUTANT | ACYLTRANSFERASE, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC, TRANSFERASE
4h4k:A (THR264) to (GLU292) STRUCTURE OF THE CMR2-CMR3 SUBCOMPLEX OF THE CMR RNA-SILENCING COMPLEX | FERREDOXIN, PALM, RAMP, REPEAT ASSOCIATED MYSTERIOUS PROTEIN, POLYMERASE, NUCLEASE, RNA-INTERFERENCE, CMR PROTEINS CRISPR RNA, RNA BINDING PROTEIN
3ekb:A (GLU430) to (LYS452) CRYSTAL STRUCTURE OF THE A264C MUTANT HEME DOMAIN OF CYTOCHROME P450 BM3 | HEME LIGATION, P450, CYTOCHROME, CYTOPLASM, ELECTRON TRANSPORT, FAD, FLAVOPROTEIN, FMN, HEME, IRON, METAL- BINDING, MONOOXYGENASE, MULTIFUNCTIONAL ENZYME, NADP, OXIDOREDUCTASE, TRANSPORT
3ekc:A (LYS6) to (PRO32) STRUCTURE OF W60V BETA-2 MICROGLOBULIN MUTANT | BETA-2-MICROGLOBULIN, TRYPTOPHAN, GLYCINE, AMYLOIDOSIS, DRA, BETA FIBRILS, DISEASE MUTATION, GLYCATION, GLYCOPROTEIN, IMMUNE RESPONSE, IMMUNOGLOBULIN DOMAIN, MHC I, PYRROLIDONE CARBOXYLIC ACID, SECRETED, IMMUNE SYSTEM
3ekf:A (GLU430) to (LYS452) CRYSTAL STRUCTURE OF THE A264Q HEME DOMAIN OF CYTOCHROME P450 BM3 | HEME LIGATION, CYTOCHROME P450, CYTOPLASM, ELECTRON TRANSPORT, FAD, FLAVOPROTEIN, FMN, HEME, IRON, METAL- BINDING, MONOOXYGENASE, MULTIFUNCTIONAL ENZYME, NADP, OXIDOREDUCTASE, TRANSPORT
3ekf:B (GLU430) to (LYS452) CRYSTAL STRUCTURE OF THE A264Q HEME DOMAIN OF CYTOCHROME P450 BM3 | HEME LIGATION, CYTOCHROME P450, CYTOPLASM, ELECTRON TRANSPORT, FAD, FLAVOPROTEIN, FMN, HEME, IRON, METAL- BINDING, MONOOXYGENASE, MULTIFUNCTIONAL ENZYME, NADP, OXIDOREDUCTASE, TRANSPORT
4h73:D (ARG358) to (ASP371) THERMOSTABLE ALDEHYDE DEHYDROGENASE FROM PYROBACULUM SP. COMPLEXED WITH NADP+ | FOLD, PROTEIN, ALDEHYDE OXIDATION, NADP REDUCTION, INTRACELLULAR, CYTOPLASMIC, OXIDOREDUCTASE
1aw7:B (SER232) to (ASN265) Q136A MUTANT OF TOXIC SHOCK SYNDROME TOXIN-1 FROM S. AUREUS | TOXIN, SUPERANTIGEN
1aw7:D (SER632) to (ASN665) Q136A MUTANT OF TOXIC SHOCK SYNDROME TOXIN-1 FROM S. AUREUS | TOXIN, SUPERANTIGEN
3eoa:H (SER128) to (PRO155) CRYSTAL STRUCTURE THE FAB FRAGMENT OF EFALIZUMAB IN COMPLEX WITH LFA-1 I DOMAIN, FORM I | EFALIZUMAB, FAB, ANTIBODY, LFA-1, CD11A, I DOMAIN, ALTERNATIVE SPLICING, CALCIUM, GLYCOPROTEIN, INTEGRIN, MAGNESIUM, MEMBRANE, POLYMORPHISM, RECEPTOR, TRANSMEMBRANE, IMMUNE SYSTEM/CELL ADHESION COMPLEX
1nun:B (ARG165) to (GLY183) CRYSTAL STRUCTURE ANALYSIS OF THE FGF10-FGFR2B COMPLEX | BETA-TREFOIL FOLD, IMMUNOGLOBULIN-LIKE DOMAIN, HORMONE/GROWTH FACTOR/MEMBRANE PROTEIN COMPLEX
1axk:B (GLY212) to (ARG229) ENGINEERED BACILLUS BIFUNCTIONAL ENZYME GLUXYN-1 | GLUXYN-1, BIFUNCTIONAL, FUSION PROTEIN, 1,4-BETA-XYLANASE, 1,3-1,4-BETA-GLUCANASE, HYBRID ENZYME
1axs:H (SER120) to (PRO147) MATURE OXY-COPE CATALYTIC ANTIBODY WITH HAPTEN | OXY-COPE, CATALYTIC ANTIBODY, FAB FRAGMENT
3eqg:A (GLY75) to (LYS88) X-RAY STRUCTURE OF THE HUMAN MITOGEN-ACTIVATED PROTEIN KINASE KINASE 1 (MEK1) IN A TERNARY COMPLEX WITH PD, ADP AND MG2P | MEK1 KINASE, ATP-BINDING, DISEASE MUTATION, KINASE, NUCLEOTIDE- BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, TYROSINE-PROTEIN KINASE
2p20:A (LYS56) to (ASN76) ACETYL-COA SYNTHETASE, R584A MUTATION | ADENYLATE-FORMING ENZYMES, DOMAIN ALTERNATION, ACYL-COA LIGASE, LIGASE
4wv1:F (LEU163) to (ASN181) CRYSTAL STRUCTURE OF THE FGFR2 D2 DOMAIN IN COMPLEX WITH FAB 2B.1.3 | FGFR2, FAB, COMPLEX, ANTIBODY, TRANSFERASE-IMMUNE SYSTEM COMPLEX
2p2b:A (LYS56) to (ASN76) ACETYL-COA SYNTHETASE, V386A MUTATION | ADENYLATE-FORMING ENZYMES, DOMAIN ALTERNATION, ACYL-COA LIGASE, LIGASE
2p2b:B (LYS56) to (ASN76) ACETYL-COA SYNTHETASE, V386A MUTATION | ADENYLATE-FORMING ENZYMES, DOMAIN ALTERNATION, ACYL-COA LIGASE, LIGASE
2p2f:A (LYS56) to (ASN76) ACETYL-COA SYNTHETASE, WILD-TYPE WITH ACETATE, AMP, AND COA BOUND | ADENYLATE-FORMING ENZYMES, DOMAIN ALTERNATION, ACYL-COA LIGASE, LIGASE
2p2f:B (LYS56) to (ASN76) ACETYL-COA SYNTHETASE, WILD-TYPE WITH ACETATE, AMP, AND COA BOUND | ADENYLATE-FORMING ENZYMES, DOMAIN ALTERNATION, ACYL-COA LIGASE, LIGASE
2p2j:A (ASN57) to (ASN76) ACETYL-COA SYNTHETASE, K609A MUTATION | ADENYLATE-FORMING ENZYMES, DOMAIN ALTERNATION, ACYL-COA LIGASE, LIGASE
2p2m:A (LYS56) to (ASN76) ACETYL-COA SYNTHETASE, R194A MUTATION | ADENYLATE-FORMING ENZYMES, DOMAIN ALTERNATION, ACYL-COA LIGASE, LIGASE
2p2m:B (LYS56) to (ASN76) ACETYL-COA SYNTHETASE, R194A MUTATION | ADENYLATE-FORMING ENZYMES, DOMAIN ALTERNATION, ACYL-COA LIGASE, LIGASE
4wwn:A (SER400) to (SER417) CRYSTAL STRUCTURE OF HUMAN PI3K-GAMMA IN COMPLEX WITH (S)-N-(1-(7- FLUORO-2-(PYRIDIN-2-YL)QUINOLIN-3-YL)ETHYL)-9H-PURIN-6-AMINE AMG319 INHIBITOR | KINASE, PHOSPHOTRANSFER, PIP2
2be5:D (GLN717) to (SER752) CRYSTAL STRUCTURE OF THE T. THERMOPHILUS RNA POLYMERASE HOLOENZYME IN COMPLEX WITH INHIBITOR TAGETITOXIN | RNA POLYMERASE HOLOENZYME, TAGETITOXIN, ANTIBIOTIC, TRANSCRIPTION REGULATION, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, STRUCTURAL GENOMICS, TRANSFERASE
2p85:B (LYS476) to (LEU492) STRUCTURE OF HUMAN LUNG CYTOCHROME P450 2A13 WITH INDOLE BOUND IN TWO ALTERNATE CONFORMATIONS | CYP2A13, P450 2A13, P450, MONOOXYGENASE, NICOTINE OXIDASE, COUMARINE 7-HYDROXYLASE, NNK OXIDASE, 4-(METHYLNITROSAMINO)- 1-(3-PYRIDYL)-1-BUTANONE OXIDASE, OXIDOREDUCTASE, HEME
4hgg:A (GLU430) to (LYS452) CRYSTAL STRUCTURE OF P450 BM3 5F5R HEME DOMAIN VARIANT COMPLEXED WITH STYRENE | OXIDOREDUCTASE, P450 BM3, HEMOPROTEIN, STYRENE EPOXIDATION, INVERTED ENANTIOSELECTIVITY, HEME BINDING
4hgg:B (GLU430) to (LYS452) CRYSTAL STRUCTURE OF P450 BM3 5F5R HEME DOMAIN VARIANT COMPLEXED WITH STYRENE | OXIDOREDUCTASE, P450 BM3, HEMOPROTEIN, STYRENE EPOXIDATION, INVERTED ENANTIOSELECTIVITY, HEME BINDING
4hgj:A (GLU430) to (LYS452) CRYSTAL STRUCTURE OF P450 BM3 5F5 HEME DOMAIN VARIANT | OXIDOREDUCTASE, P450 BM3, HEMOPROTEIN, STYRENE EPOXIDATION, INVERTED ENANTIOSELECTIVITY, HEME BINDING
4hgj:B (GLU430) to (LYS452) CRYSTAL STRUCTURE OF P450 BM3 5F5 HEME DOMAIN VARIANT | OXIDOREDUCTASE, P450 BM3, HEMOPROTEIN, STYRENE EPOXIDATION, INVERTED ENANTIOSELECTIVITY, HEME BINDING
4x0k:A (PHE122) to (PRO149) ENGINEERED FAB FRAGMENT SPECIFIC FOR EYMPME (EE) PEPTIDE | ANTIBODY FRAGMENT, CRYSTALLIZATION CHAPERONE, FAB FRAGMENT, IMMUNE SYSTEM
4hi0:B (PRO32) to (ARG59) CRYSTAL STRUCTURE OF HELICOBACTER PYLORI UREASE ACCESSORY PROTEIN UREF/H/G COMPLEX | METALLOCHAPERONE, METAL BINDING PROTEIN, UREASE, CYTOSOL
4hi0:D (PRO32) to (ARG59) CRYSTAL STRUCTURE OF HELICOBACTER PYLORI UREASE ACCESSORY PROTEIN UREF/H/G COMPLEX | METALLOCHAPERONE, METAL BINDING PROTEIN, UREASE, CYTOSOL
2pc9:C (ASP253) to (LYS272) CRYSTAL STRUCTURE OF ATP-DEPENDENT PHOSPHOENOLPYRUVATE CARBOXYKINASE FROM THERMUS THERMOPHILUS HB8 | PHOSPHOENOLPYRUVATE CARBOXYKINASE, ADENOSINE TRIPHOSPHATE, THERMUS THERMOPHILUS HB8, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, LYASE
2pc9:D (ASP253) to (LYS272) CRYSTAL STRUCTURE OF ATP-DEPENDENT PHOSPHOENOLPYRUVATE CARBOXYKINASE FROM THERMUS THERMOPHILUS HB8 | PHOSPHOENOLPYRUVATE CARBOXYKINASE, ADENOSINE TRIPHOSPHATE, THERMUS THERMOPHILUS HB8, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, LYASE
4hl0:B (GLY22) to (PRO55) CRYSTAL STRUCTURE OF FULL-LENGTH TOXASCARIS LEONINA GALECTIN | CARBOHYDRATE RECOGNITION DOMAIN, GALECTIN, A REGULATORY MOLECULE, THE HOST IMMUNE SYSTEM, SUGAR BINDING PROTEIN
3f02:A (SER282) to (GLU300) CLEAVED HUMAN NEUROSERPIN | NEUROSERPIN, SERPIN, CLEAVED FORM, FENIB, HUMAN, DISEASE MUTATION, GLYCOPROTEIN, PROTEASE INHIBITOR, SECRETED, SERINE PROTEASE INHIBITOR, HYDROLASE INHIBITOR
3f02:B (SER282) to (GLU300) CLEAVED HUMAN NEUROSERPIN | NEUROSERPIN, SERPIN, CLEAVED FORM, FENIB, HUMAN, DISEASE MUTATION, GLYCOPROTEIN, PROTEASE INHIBITOR, SECRETED, SERINE PROTEASE INHIBITOR, HYDROLASE INHIBITOR
2bmh:A (GLU430) to (LYS452) MODELING PROTEIN-SUBSTRATE INTERACTIONS IN THE HEME DOMAIN OF CYTOCHROME P450BM-3 | OXIDOREDUCTASE(OXYGENASE)
2bmh:B (GLU430) to (LYS452) MODELING PROTEIN-SUBSTRATE INTERACTIONS IN THE HEME DOMAIN OF CYTOCHROME P450BM-3 | OXIDOREDUCTASE(OXYGENASE)
3f2p:A (THR6) to (THR34) THERMOLYSIN INHIBITION | PROTEIN FRAGMENT COMPLEX, CALCIUM, HYDROLASE, METAL-BINDING, METALLOPROTEASE, PROTEASE, SECRETED, ZINC, ZYMOGEN
4hnp:L (THR11) to (THR31) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH VINYLKETONE CARMAPHYCIN ANALOGUE VNK1 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4hnp:N (THR1) to (THR22) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH VINYLKETONE CARMAPHYCIN ANALOGUE VNK1 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4hnp:a (THR9) to (GLY31) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH VINYLKETONE CARMAPHYCIN ANALOGUE VNK1 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2bn7:A (GLU59) to (LEU83) MN SUBSTITUTED E. COLI AMINOPEPTIDASE P IN COMPLEX WITH PRODUCT AND ZN | HYDROLASE, PROLINE-SPECIFIC PEPTIDASE, PRODUCT COMPLEX, METALLOENZYME, PITA-BREAD FOLD, DINUCLEAR HYDROLASE
4x6z:I (THR1) to (GLN22) YEAST 20S PROTEASOME IN COMPLEX WITH PR-VI MODULATOR | 20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE
4x6z:J (ILE2) to (SER22) YEAST 20S PROTEASOME IN COMPLEX WITH PR-VI MODULATOR | 20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE
4x6z:X (ILE2) to (SER22) YEAST 20S PROTEASOME IN COMPLEX WITH PR-VI MODULATOR | 20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE
3f8r:D (ASN210) to (PRO252) CRYSTAL STRUCTURE OF SULFOLOBUS SOLFATARICUS THIOREDOXIN REDUCTASE B3 IN COMPLEX WITH TWO NADP MOLECULES | REDOX PROTEIN, NUCLEOTIDE BINDING, FAD, FLAVOPROTEIN, OXIDOREDUCTASE
4x83:C (SER221) to (PHE240) CRYSTAL STRUCTURE OF DSCAM1 ISOFORM 7.44, N-TERMINAL FOUR IG DOMAINS | IG FOLD, CELL ADHESION
4hpo:H (SER120) to (PRO147) CRYSTAL STRUCTURE OF RV144-ELICITED ANTIBODY CH58 IN COMPLEX WITH V2 PEPTIDE | IMMUNOGLOBULIN, IMMUNE SYSTEM-VIRAL PROTEIN COMPLEX
2bsr:A (HIS188) to (PRO210) CRYSTAL STRUCTURES AND KIR3DL1 RECOGNITION OF THREE IMMUNODOMINANT VIRAL PEPTIDES COMPLEXED TO HLA-B2705 | IMMUNE SYSTEM/PEPTIDE, MHC, HLA-B27, HUMAN EBV, HIV, GLYCOPROTEIN, MHC I, POLYMORPHISM, TRANSMEMBRANE, IMMUNOGLOBULIN DOMAIN, PYRROLIDONE CARBOXYLIC ACID, NUCLEAR PROTEIN, COMPLEX (ANTIGEN/PEPTIDE)
1oa2:C (ASP99) to (TYR124) COMPARISON OF FAMILY 12 GLYCOSIDE HYDROLASES AND RECRUITED SUBSTITUTIONS IMPORTANT FOR THERMAL STABILITY | HYDROLASE, CELLULASE, CELLULOSE DEGRADATION, ENDOGLUCANASE, GLYCOSYL HYDROLASE, GH FAMILY 12, TRICHODERMA REESEI CEL12A
1bu7:A (GLU430) to (LYS452) CRYOGENIC STRUCTURE OF CYTOCHROME P450BM-3 HEME DOMAIN | FATTY ACID MONOOXYGENASE, HEMOPROTEIN, P450, OXIDOREDUCTASE
1bu7:B (GLU430) to (LYS452) CRYOGENIC STRUCTURE OF CYTOCHROME P450BM-3 HEME DOMAIN | FATTY ACID MONOOXYGENASE, HEMOPROTEIN, P450, OXIDOREDUCTASE
1buq:B (ASP299) to (ALA325) SOLUTION STRUCTURE OF DELTA-5-3-KETOSTEROID ISOMERASE COMPLEXED WITH THE STEROID 19-NORTESTOSTERONE-HEMISUCCINATE | KETOSTEROID ISOMERASE-19NTHS, ENZYME-SUBSTRATE COMPLEX, ENZYMES
4hrc:V (THR1) to (GLN22) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE CARMAPHYCIN ANALOGUE 3 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4hrc:Z (THR11) to (THR31) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE CARMAPHYCIN ANALOGUE 3 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3fac:D (MET1) to (ARG42) CRYSTAL STRUCTURE OF RHODOBACTER SPHAEROIDES PROTEIN RSP_2168. NORTHEAST STRUCTURAL GENOMICS TARGET RHR83. | COMPLETE PROTEOME, RHODOBACTER SPHAEROIDES, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, UNKNOWN FUNCTION
1bvy:A (GLU430) to (LYS452) COMPLEX OF THE HEME AND FMN-BINDING DOMAINS OF THE CYTOCHROME P450(BM-3) | FATTY ACID MONOOXYGENASE, HEMOPROTEIN, FLAVOPROTEIN, ELECTRON TRANSFER, OXIDOREDUCTASE
1bvy:B (GLU430) to (LYS452) COMPLEX OF THE HEME AND FMN-BINDING DOMAINS OF THE CYTOCHROME P450(BM-3) | FATTY ACID MONOOXYGENASE, HEMOPROTEIN, FLAVOPROTEIN, ELECTRON TRANSFER, OXIDOREDUCTASE
4hrd:Z (THR11) to (THR31) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH THE NATURAL PRODUCT CARMAPHYCIN A | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4hrd:a (THR9) to (TYR30) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH THE NATURAL PRODUCT CARMAPHYCIN A | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3fb0:A (THR6) to (THR34) METAL EXCHANGE IN THERMOLYSIN | ZINC-FREE PROTEIN, CALCIUM, HYDROLASE, METAL-BINDING, METALLOPROTEASE, PROTEASE, SECRETED, ZINC, ZYMOGEN
3fbo:A (THR6) to (THR34) METAL EXCHANGE IN THERMOLYSIN | PROTEIN COPPER(II) COMPLEX, CALCIUM, HYDROLASE, METAL- BINDING, METALLOPROTEASE, PROTEASE, SECRETED, ZINC, ZYMOGEN
2pfr:A (ILE149) to (ASN172) HUMAN N-ACETYLTRANSFERASE 2 | ARYLAMINE N-ACETYLTRANSFERASE 2, ARYLAMIDE ACETYLASE 2, STRUCTURAL GENOMICS CONSORTIUM, SGC, TRANSFERASE
3fcq:A (THR6) to (THR34) THERMOLYSIN INHIBITION | PROTEIN FRAGMENT COMPLEX, CALCIUM, HYDROLASE, METAL-BINDING, METALLOPROTEASE, PROTEASE, SECRETED, ZINC, ZYMOGEN
4hx0:A (GLY81) to (GLU101) CRYSTAL STRUCTURE OF A PUTATIVE NUCLEOTIDYLTRANSFERASE (TM1012) FROM THERMOTOGA MARITIMA AT 1.87 A RESOLUTION | PUTATIVE NUCLEOTIDYLTRANSFERASE, TRANSFERASE
3sdi:Z (THR2) to (THR22) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 20 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3sdi:2 (THR1) to (THR22) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 20 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3ffc:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF CF34 TCR IN COMPLEX WITH HLA-B8/FLR | TCR-PEPTIDE-MHC, GLYCOPROTEIN, HOST-VIRUS INTERACTION, IMMUNE RESPONSE, MEMBRANE, MHC I, TRANSMEMBRANE, DISEASE MUTATION, GLYCATION, IMMUNOGLOBULIN DOMAIN, PYRROLIDONE CARBOXYLIC ACID, SECRETED, IMMUNE SYSTEM
3ffc:F (HIS188) to (PRO210) CRYSTAL STRUCTURE OF CF34 TCR IN COMPLEX WITH HLA-B8/FLR | TCR-PEPTIDE-MHC, GLYCOPROTEIN, HOST-VIRUS INTERACTION, IMMUNE RESPONSE, MEMBRANE, MHC I, TRANSMEMBRANE, DISEASE MUTATION, GLYCATION, IMMUNOGLOBULIN DOMAIN, PYRROLIDONE CARBOXYLIC ACID, SECRETED, IMMUNE SYSTEM
3sdk:L (THR2) to (THR22) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 34 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3sdk:2 (THR1) to (THR22) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 34 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1ofi:N (THR1) to (LEU22) ASYMMETRIC COMPLEX BETWEEN HSLV AND I-DOMAIN DELETED HSLU (H. INFLUENZAE) | CHAPERONE, HYDROLASE, ATP-BINDING
3fgd:A (THR6) to (THR34) DRUGSCORE FP: THERMOYLSIN IN COMPLEX WITH FRAGMENT. | DRUGSCORE FP, PROTEIN FRAGMENT COMPLEX, HYDROLASE, METAL-BINDING, METALLOPROTEASE, PROTEASE, SECRETED, ZYMOGEN
2pnt:A (GLN97) to (GLY120) CRYSTAL STRUCTURE OF THE PDZ DOMAIN OF HUMAN GRASP (GRP1) IN COMPLEX WITH THE C-TERMINAL PEPTIDE OF THE METABOTROPIC GLUTAMATE RECEPTOR TYPE 1 | SCAFFOLD PROTEIN, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, UNKNOWN FUNCTION
3sg9:A (ILE203) to (SER224) CRYSTAL STRUCTURE OF AMINOGLYCOSIDE-2''-PHOSPHOTRANSFERASE TYPE IVA KANAMYCIN A COMPLEX | ANTIBIOTIC RESISTANCE ENZYME, TRANSFERASE, AMINOGLYCOSIDE, PHOSPHOTRANSFERASE, TRANSFERASE-ANTIBIOTIC COMPLEX
3fjp:A (GLU189) to (LEU215) APO STRUCTURE OF BIOTIN PROTEIN LIGASE FROM AQUIFEX AEOLICUS | BPL, BIOTIN PROTEIN LIGASE, LIGASE
1cc3:A (VAL5) to (ASP23) PURPLE CUA CENTER | COPPER-A, ELECTRON TRANSPORT
1ce6:B (LYS6) to (PRO32) MHC CLASS I H-2DB COMPLEXED WITH A SENDAI VIRUS NUCLEOPROTEIN PEPTIDE | MHC CLASS I, ANTIGEN PRESENTATION, VIRAL PEPTIDE, COMPLEX
3sj8:A (ILE162) to (ARG176) CRYSTAL STRUCTURE OF THE 3C PROTEASE FROM COXSACKIEVIRUS A16 | CHYMOTRYPSIN-LIKE FOLD, PROTEASE, HYDROLASE
3sjv:B (LYS6) to (PRO32) CRYSTAL STRUCTURE OF THE RL42 TCR IN COMPLEX WITH HLA-B8-FLR | T CELL, IMMUNE SYSTEM
3flf:A (THR6) to (THR34) THERMOLYSIN INHIBITION | PROTEASE PHOSPHONAMIDATE INHIBITOR, HYDROLASE, METAL-BINDING, METALLOPROTEASE, PROTEASE, SECRETED, ZYMOGEN
1cg9:A (HIS188) to (PRO210) COMPLEX RECOGNITION OF THE SUPERTYPIC BW6-DETERMINANT ON HLA-B AND-C MOLECULES BY THE MONOCLONAL ANTIBODY SFR8-B6 | MHC CLASS I, HISTOCOMPATIBILITY COMPLEX, HLA B3501, COMPLEX (MHC CLASS I/ PEPTIDE), SFR8-B6 EPITOPE
3sm4:A (PRO104) to (CYS132) CRYSTAL STRUCTURE OF THE K131A MUTANT OF LAMBDA EXONUCLEASE IN COMPLEX WITH A 5'-PHOSPHORYLATED 14-MER/12-MER DUPLEX AND MAGNESIUM | HOMOLOGOUS RECOMBINATION, DNA REPAIR, RECOMBINEERING, SINGLE-STRAND ANNEALING, TYPE II RESTRICTION ENDONUCLEASE FOLD, 5'-3' DSDNA EXONUCLEASE, HYDROLASE-DNA COMPLEX
3sm4:C (PRO104) to (CYS132) CRYSTAL STRUCTURE OF THE K131A MUTANT OF LAMBDA EXONUCLEASE IN COMPLEX WITH A 5'-PHOSPHORYLATED 14-MER/12-MER DUPLEX AND MAGNESIUM | HOMOLOGOUS RECOMBINATION, DNA REPAIR, RECOMBINEERING, SINGLE-STRAND ANNEALING, TYPE II RESTRICTION ENDONUCLEASE FOLD, 5'-3' DSDNA EXONUCLEASE, HYDROLASE-DNA COMPLEX
3for:A (THR6) to (THR34) THERMOLYSIN COMPLEXED WITH BNPA (2-BENZYL-3-NITRO PROPANOIC ACID AMIDE) | HYDROLASE, CALCIUM, METAL-BINDING, METALLOPROTEASE, PROTEASE, SECRETED, ZINC, ZYMOGEN
3so3:C (SER120) to (PRO147) STRUCTURES OF FAB-PROTEASE COMPLEXES REVEAL A HIGHLY SPECIFIC NON- CANONICAL MECHANISM OF INHIBITION. | ANTIBODY-PROTEIN, PROTEIN-PROTEIN, PROTEASE INHIBITOR, DISEASE MUTATION, GLYCOPROTEIN, HYDROLASE, MEMBRANE, SERINE PROTEASE, SIGNAL-ANCHOR, TRANSMEMBRANE
3fpt:B (GLN69) to (VAL83) THE CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN EVASIN-1 AND CCL3 | NOVEL FOLD, GLYCOSYLATED PROTEIN, GLYCOPROTEIN, SECRETED, IMMUNE SYSTEM
3sot:B (THR268) to (PHE300) CRYSTAL STRUCTURE OF A MULTIDOMAIN PROTEIN INCLUDING DUF1735 (BACOVA_03322) FROM BACTEROIDES OVATUS AT 2.80 A RESOLUTION | STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-BIOLOGY, UNKNOWN FUNCTION
3sot:E (PRO269) to (PHE300) CRYSTAL STRUCTURE OF A MULTIDOMAIN PROTEIN INCLUDING DUF1735 (BACOVA_03322) FROM BACTEROIDES OVATUS AT 2.80 A RESOLUTION | STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-BIOLOGY, UNKNOWN FUNCTION
3sot:F (PRO269) to (PHE300) CRYSTAL STRUCTURE OF A MULTIDOMAIN PROTEIN INCLUDING DUF1735 (BACOVA_03322) FROM BACTEROIDES OVATUS AT 2.80 A RESOLUTION | STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-BIOLOGY, UNKNOWN FUNCTION
1os1:A (ASP269) to (LYS288) STRUCTURE OF PHOSPHOENOLPYRUVATE CARBOXYKINASE COMPLEXED WITH ATP,MG, CA AND PYRUVATE. | ENZYME MECHANISM, PHOSPHOTRANSFER,CALCIUM,ACTIVATION, LYASE
3fqx:A (HIS188) to (PRO210) PHOSPHORYLATION OF SELF-PEPTIDES ALTERS HUMAN LEUKOCYTE ANTIGEN CLASS I-RESTRICTED ANTIGEN PRESENTATION AND GENERATES TUMOR SPECIFIC EPITOPES | IMMUNE SYSTEM, PHOSPHORYLATION, GLYCOPROTEIN, IMMUNE RESPONSE, MEMBRANE, MHC I, PHOSPHOPROTEIN, TRANSMEMBRANE, DISEASE MUTATION, IMMUNOGLOBULIN DOMAIN, PYRROLIDONE CARBOXYLIC ACID, SECRETED, CANCER, TCR, SELF-EPITOPE
3fru:A (SER183) to (PRO207) NEONATAL FC RECEPTOR, PH 6.5 | COMPLEX (IMMUNOGLOBULIN-BINDING PROTEIN), COMPLEX (IMMUNOGLOBULIN- BINDING PROTEIN) COMPLEX
1cp9:B (ASN178) to (GLN200) CRYSTAL STRUCTURE OF PENICILLIN G ACYLASE FROM THE BRO1 MUTANT STRAIN OF PROVIDENCIA RETTGERI | ANTIBIOTIC RESISTANCE, AMIDOHYDROLASE, NTN-HYDROLASE FOLD, N-TERMINAL PYROGLUTAMATE, PENICILLIN BINDING PROTEIN, CALCIUM BINDING PROTEIN
1owi:A (SER87) to (SER104) SUBSTITUTED 2-NAPHTHAMIDINE INHIBITORS OF UROKINASE | PLASMINOGEN ACTIVATION, HYDROLASE, SERINE PROTEASE, GLYCOPROTEIN, KRINGLE, EGF-LIKE DOMAIN
3fu8:B (GLY151) to (TYR177) MELANOCARPUS ALBOMYCES LACCASE CRYSTAL SOAKED (10 SEC) WITH 2,6- DIMETHOXYPHENOL | LACCASE, MULTICOPPER OXIDASE, COMPLEX STRUCTURE, 2,6-DIMETHOXYPHENOL, OXIDATION OF PHENOLIC COMPOUNDS, GLYCOPROTEIN, LIGNIN DEGRADATION, METAL-BINDING, OXIDOREDUCTASE
3fu9:A (VAL149) to (TYR177) MELANOCARPUS ALBOMYCES LACCASE CRYSTAL SOAKED (20 MIN) WITH 2,6- DIMETHOXYPHENOL | LACCASE, MULTICOPPER OXIDASE, COMPLEX STRUCTURE, 2,6-DIMETHOXYPHENOL, OXIDATION OF PHENOLIC COMPOUNDS, GLYCOPROTEIN, LIGNIN DEGRADATION, METAL-BINDING, OXIDOREDUCTASE
2c7u:D (HIS188) to (PRO210) CONFLICTING SELECTIVE FORCES AFFECT CD8 T-CELL RECEPTOR CONTACT SITES IN AN HLA-A2 IMMUNODOMINANT HIV EPITOPE. | GLYCOPROTEIN-PEPTIDE COMPLEX, MHC, TCR, HLA-A2, HIV, GLYCOPROTEIN, IMMUNE RESPONSE, MHC I, TRANSMEMBRANE, IMMUNOGLOBULIN DOMAIN, PYRROLIDONE CARBOXYLIC ACID, GLYCOPROTEIN/PEPTIDE COMPLEX, AIDS
3fv4:A (THR6) to (THR34) THERMOLYSIN INHIBITION | PROTEASE PHOSPHONAMIDATE INHIBITOR, HYDROLASE, METAL-BINDING, METALLOPROTEASE, PROTEASE, SECRETED, ZYMOGEN
3fvq:A (GLU310) to (LEU340) CRYSTAL STRUCTURE OF THE NUCLEOTIDE BINDING DOMAIN FBPC COMPLEXED WITH ATP | NUCLEOTIDE BINDING DOMAIN, ABC MOTOR DOMAIN, FERRIC IRON TRANSPORT, ATP-BINDING, CELL INNER MEMBRANE, CELL MEMBRANE, HYDROLASE, ION TRANSPORT, IRON, IRON TRANSPORT, MEMBRANE, NUCLEOTIDE-BINDING, TRANSPORT
3ssb:A (THR6) to (THR34) STRUCTURE OF INSECT METALLOPROTEINASE INHIBITOR IN COMPLEX WITH THERMOLYSIN | THERMOLYSIN FOLD - FAMILY I8 FOLD, METALLOPROTEASE THERMOLYSIN INHIBITOR, ZN BINDING, SECRETED, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3ssb:B (THR6) to (THR34) STRUCTURE OF INSECT METALLOPROTEINASE INHIBITOR IN COMPLEX WITH THERMOLYSIN | THERMOLYSIN FOLD - FAMILY I8 FOLD, METALLOPROTEASE THERMOLYSIN INHIBITOR, ZN BINDING, SECRETED, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1cvs:C (LYS164) to (THR183) CRYSTAL STRUCTURE OF A DIMERIC FGF2-FGFR1 COMPLEX | FGF, FGFR, IMMUNOGLOBULIN-LIKE, SIGNAL TRANSDUCTION, DIMERIZATION, GROWTH FACTOR/GROWTH FACTOR RECEPTOR COMPLEX
1cvs:D (LYS164) to (THR183) CRYSTAL STRUCTURE OF A DIMERIC FGF2-FGFR1 COMPLEX | FGF, FGFR, IMMUNOGLOBULIN-LIKE, SIGNAL TRANSDUCTION, DIMERIZATION, GROWTH FACTOR/GROWTH FACTOR RECEPTOR COMPLEX
4xmk:H (SER120) to (PRO147) CRYSTAL STRUCTURE OF FAB OF HIV-1 GP120 V3-SPECIFIC HUMAN MONOCLONAL ANTIBODY 2424 IN COMPLEX WITH JR-FL V3 PEPTIDE | HIV-1 GP120, MONOCLONAL ANTIBODY, IMMUNE SYSTEM-VIRAL PROTEIN COMPLEX
4xmk:I (SER120) to (PRO147) CRYSTAL STRUCTURE OF FAB OF HIV-1 GP120 V3-SPECIFIC HUMAN MONOCLONAL ANTIBODY 2424 IN COMPLEX WITH JR-FL V3 PEPTIDE | HIV-1 GP120, MONOCLONAL ANTIBODY, IMMUNE SYSTEM-VIRAL PROTEIN COMPLEX
4xmk:J (SER120) to (PRO147) CRYSTAL STRUCTURE OF FAB OF HIV-1 GP120 V3-SPECIFIC HUMAN MONOCLONAL ANTIBODY 2424 IN COMPLEX WITH JR-FL V3 PEPTIDE | HIV-1 GP120, MONOCLONAL ANTIBODY, IMMUNE SYSTEM-VIRAL PROTEIN COMPLEX
4xml:H (SER120) to (PRO147) CRYSTAL STRUCTURE OF FAB OF HIV-1 GP120 V3-SPECIFIC HUMAN MONOCLONAL ANTIBODY 2424 | HIV-1 GP120, MONOCLONAL ANTIBODY, IMMUNE SYSTEM
3fxp:A (THR6) to (THR34) THERMOLYSIN INHIBITION | PROTEASE TRIAZOLIC INHIBITOR, CALCIUM, HYDROLASE, METAL- BINDING, METALLOPROTEASE, PROTEASE, SECRETED, ZINC, ZYMOGEN
3fxs:A (THR6) to (THR34) METAL EXCHANGE IN THERMOLYSIN | PROTEASE RUTHENIUM METAL EXCHANGE, CALCIUM, HYDROLASE, METAL-BINDING, METALLOPROTEASE, PROTEASE, SECRETED, ZINC, ZYMOGEN
1p0v:A (GLU430) to (LYS452) F393A MUTANT HEME DOMAIN OF FLAVOCYTOCHROME P450 BM3 | CYTOCHROME P450, FATTY ACID HYDROXYLASE, MONOOXYGENASE, OXIDOREDUCTASE
1p0x:A (GLU430) to (LYS452) F393Y MUTANT HEME DOMAIN OF FLAVOCYTOCHROME P450 BM3 | CYTOCHROME P450, FATTY ACID HYDROXYLASE, MONOOXYGENASE, OXIDOREDUCTASE
1p0x:B (GLU430) to (LYS452) F393Y MUTANT HEME DOMAIN OF FLAVOCYTOCHROME P450 BM3 | CYTOCHROME P450, FATTY ACID HYDROXYLASE, MONOOXYGENASE, OXIDOREDUCTASE
4igl:A (LYS1020) to (LEU1077) STRUCTURE OF THE RHS-REPEAT CONTAINING BC COMPONENT OF THE SECRETED ABC TOXIN COMPLEX FROM YERSINIA ENTOMOPHAGA | BETA-PROPELLER, RHS, TOXIN COMPLEX, TOXIN TRANSPORTER/CHAPERONE, SECRETED, TOXIN
4xnz:A (ASN392) to (GLN422) CRYSTAL STRUCTURE OF BROADLY AND POTENTLY NEUTRALIZING ANTIBODY VRC06B IN COMPLEX WITH HIV-1 CLADE A/E STRAIN 93TH057 GP120 | ANTIBODY, HIV-1, IMMUNE SYSTEM
2qaf:B (CYS177) to (ASN196) CRYSTAL STRUCTURE OF PLASMODIUM FALCIPARUM OROTIDINE 5'-PHOSPHATE DECARBOXYLASE COVALENTLY MODIFIED BY 6-IODO-UMP | CRYSTAL STRUCTURE,PLASMODIUM FALCIPARUM, OROTIDINE 5'-PHOSPHATE DECARBOXYLASE,COVALENTLY,6-IODO-UMP, LYASE
2qbx:A (THR66) to (GLY90) EPHB2/SNEW ANTAGONISTIC PEPTIDE COMPLEX | RECEPTOR TYROSINE KINASE, BI-DIRECTIONAL SIGNALING, TUMORIGENESIS, ANGIOGENESIS, SIGNALING PROTEIN, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, ACCELERATED TECHNOLOGIES CENTER FOR GENE TO 3D STRUCTURE, ATCG3D
3syy:A (GLY87) to (ILE113) CRYSTAL STRUCTURE OF AN ALKALINE EXONUCLEASE (LHK-EXO) FROM LARIBACTER HONGKONGENSIS | ALKALINE EXONUCLEASE, DIGEST DOUBLE STRANDED DNA, STRICT 5-3- POLARITY, HYDROLASE
1d7b:A (THR108) to (ASN128) CYTOCHROME DOMAIN OF CELLOBIOSE DEHYDROGENASE, PH 7.5 | B-TYPE CYTOCHROME, MET/HIS LIGATION, BETA SANDWICH, FE(II)- PROTOPORPHYRIN IX, OXIDOREDUCTASE
1d7c:A (THR108) to (ASN128) CYTOCHROME DOMAIN OF CELLOBIOSE DEHYDROGENASE, PH 4.6 | B-TYPE CYTOCHROME, MET/HIS LIGATION, BETA SANDWICH, FE(II)- PROTOPORPHYRIN IX, OXIDOREDUCTASE
1d7d:A (THR108) to (ASN128) CYTOCHROME DOMAIN OF CELLOBIOSE DEHYDROGENASE, HP3 FRAGMENT, PH 7.5 | B-TYPE CYTOCHROME, MET/HIS LIGATION, BETA SANDWICH, FE(II)- PROTOPORPHYRIN IX, OXIDOREDUCTASE
3g2y:A (ASP233) to (GLN254) CTX-M-9 CLASS A BETA-LACTAMASE COMPLEXED WITH COMPOUND 1 (GF4) | CTX-M, BETA-LACTAMASE, MOLECULAR DOCKING, FRAGMENT, INHIBITOR, ANTIBIOTIC RESISTANCE, HYDROLASE, PLASMID, HYDROLASE/HYDROLASE INHIBITOR COMPLEX
2qew:A (ASP311) to (VAL335) RAT CYTOSOLIC PEPCK, IN COMPLEX WITH MANGANESE ION. | PEPCK, PHOSPHOENOLPYRUVATE CARBOXYKINASE, GLUCONEOGENESIS, LYASE
3g3r:A (ASN360) to (ASP386) CRYSTAL STRUCTURE OF A EUKARYOTIC POLYPHOSPHATE POLYMERASE IN COMPLEX WITH APPNHP-MN2+ | POLYPHOSPHATE POLYMERASE, POLYPHOSPHATE KINASE, VTC COMPLEX, VACUOLAR TRANSPORTER CHAPERONE, TUNNEL ENZYME, MEMBRANE, PHOSPHOPROTEIN, TRANSMEMBRANE, VACUOLE, BIOSYNTHETIC PROTEIN
2qf2:A (ASP311) to (VAL335) RAT CYTOSOLIC PEPCK IN COMPLEX WITH OXALOACETIC ACID AND GDP. | PEPCK, PHOSPHOENOLPYRUVATE CARBOXYKINASE, KINASE, OAA, GDP, GLUCONEOGENESIS, LYASE
4xr7:G (LEU920) to (LEU939) STRUCTURE OF THE SACCHAROMYCES CEREVISIAE PAN2-PAN3 CORE COMPLEX | RNA DEGRADATION, DEADENYLATION, HYDROLASE, PSEUDOKINASE
4xr7:D (LEU920) to (LEU939) STRUCTURE OF THE SACCHAROMYCES CEREVISIAE PAN2-PAN3 CORE COMPLEX | RNA DEGRADATION, DEADENYLATION, HYDROLASE, PSEUDOKINASE
4xr7:A (LEU920) to (LEU939) STRUCTURE OF THE SACCHAROMYCES CEREVISIAE PAN2-PAN3 CORE COMPLEX | RNA DEGRADATION, DEADENYLATION, HYDROLASE, PSEUDOKINASE
2qil:A (GLY31) to (ASN65) TOXIC SHOCK SYNDROME TOXIN-1 AT 2.07 A RESOLUTION | STAPHYLOCOCCAL ENTEROTOXIN, SUPERANTIGEN, TOXIC SHOCK SYNDROME TOXIN
2qil:B (GLY31) to (ASN65) TOXIC SHOCK SYNDROME TOXIN-1 AT 2.07 A RESOLUTION | STAPHYLOCOCCAL ENTEROTOXIN, SUPERANTIGEN, TOXIC SHOCK SYNDROME TOXIN
4imk:B (SER136) to (PRO163) UNCROSSED FAB BINDING TO HUMAN ANGIOPOIETIN 2 | ANTIGEN-BINDING FRAGMENT (FAB), HUMAN ANGIOPOIETIN 2, IMMUNE SYSTEM
1pd0:A (PHE575) to (ARG590) CRYSTAL STRUCTURE OF THE COPII COAT SUBUNIT, SEC24, COMPLEXED WITH A PEPTIDE FROM THE SNARE PROTEIN SED5 (YEAST SYNTAXIN-5) | TRANSPORT PROTEIN
1pd1:A (PHE575) to (ARG590) CRYSTAL STRUCTURE OF THE COPII COAT SUBUNIT, SEC24, COMPLEXED WITH A PEPTIDE CONTAINING THE DXE CARGO SORTING SIGNAL OF YEAST SYS1 PROTEIN | TRANSPORT PROTEIN
4imx:A (VAL312) to (ASN340) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 3,5-BIS(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL) BENZONITRILE | OXIDOREDUCTASE NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4int:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH THE VINYL SULFONE LU122 | UPS, DRUG DISCOVERY, IRREVERSIBLE INHIBITION, NTN HYDROLASE, NON- LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4int:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH THE VINYL SULFONE LU122 | UPS, DRUG DISCOVERY, IRREVERSIBLE INHIBITION, NTN HYDROLASE, NON- LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4inr:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH THE VINYL SULFONE LU102 | UPS, DRUG DISCOVERY, IRREVERSIBLE INHIBITION, NTN HYDROLASE, NON- LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4inr:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH THE VINYL SULFONE LU102 | UPS, DRUG DISCOVERY, IRREVERSIBLE INHIBITION, NTN HYDROLASE, NON- LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4inu:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH THE VINYL SULFONE LU112 | UPS, DRUG DISCOVERY, IRREVERSIBLE INHIBITION, NTN HYDROLASE, NON- LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4inu:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH THE VINYL SULFONE LU112 | UPS, DRUG DISCOVERY, IRREVERSIBLE INHIBITION, NTN HYDROLASE, NON- LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1pg3:A (ASN57) to (ASN76) ACETYL COA SYNTHETASE, ACETYLATED ON LYS609 | AMP-FORMING; ADENYLATE-FORMING; THIOESTER-FORMING; LYSINE ACETYLATION, LIGASE
1pg3:B (ASN57) to (ASN76) ACETYL COA SYNTHETASE, ACETYLATED ON LYS609 | AMP-FORMING; ADENYLATE-FORMING; THIOESTER-FORMING; LYSINE ACETYLATION, LIGASE
1pg4:A (LYS56) to (ASN76) ACETYL COA SYNTHETASE, SALMONELLA ENTERICA | AMP-FORMING; ADENYLATE-FORMING; THIOESTER-FORMING, LIGASE
1pg4:B (LYS56) to (ASN76) ACETYL COA SYNTHETASE, SALMONELLA ENTERICA | AMP-FORMING; ADENYLATE-FORMING; THIOESTER-FORMING, LIGASE
3t2h:E (THR6) to (THR34) TETRAGONAL THERMOLYSIN IN THE PRESENCE OF TMAO | ALPHA/BETA, ZINC PROTEASE, HYDROLASE
3t2i:E (THR6) to (THR34) TETRAGONAL THERMOLYSIN IN THE PRESENCE OF SARCOSINE | ALPHA/BETA, ZINC PROTEASE, HYDROLASE
1dla:D (SER1) to (LEU16) NOVEL NADPH-BINDING DOMAIN REVEALED BY THE CRYSTAL STRUCTURE OF ALDOSE REDUCTASE | OXIDOREDUCTASE(NADP)
1pl3:A (THR108) to (ASN128) CYTOCHROME DOMAIN OF CELLOBIOSE DEHYDROGENASE, M65H MUTANT | B-TYPE CYTOCHROME, MUTANT, BIS-HIS LIGATION, BETA SANDWICH, FE(II)- PROTOPORPHYRIN IX, OXIDOREDUCTASE
3t51:A (LEU248) to (ILE267) CRYSTAL STRUCTURES OF THE PRE-EXTRUSION AND EXTRUSION STATES OF THE CUSBA ADAPTOR-TRANSPORTER COMPLEX | TRANSMEMBRANE HELIX, HEAVY METAL EFFLUX, TRANSPORT PROTEIN
1pma:Q (THR1) to (MET22) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
1pma:R (THR1) to (MET22) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
1pma:S (THR1) to (MET22) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
1pma:T (THR1) to (MET22) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
1pma:V (THR1) to (MET22) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
1pma:X (THR1) to (MET22) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
1pma:1 (THR1) to (MET22) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
1pma:2 (THR1) to (MET22) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
1dqg:A (LYS80) to (VAL122) CRYSTAL STRUCTURE OF THE CYSTEINE RICH DOMAIN OF MANNOSE RECEPTOR | BETA TREFOIL, MULTILECTIN RECEPTOR, PITUITARY HORMONES, SULFATED CARBOHYDRATE, SUGAR BINDING PROTEIN
2cwa:A (ARG199) to (ARG225) CRYSTAL STRUCTURE OF THE SINGLE-STRANDED DNA BINDING PROTEIN FROM THERMUS THERMOPHILUS HB8 | SSB, SINGLE-STRANDED DNA BINDING PROTEIN, THERMUS THERMOPHILUS HB8, STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, DNA BINDING PROTEIN
2qsf:A (GLY467) to (SER492) CRYSTAL STRUCTURE OF THE RAD4-RAD23 COMPLEX | ALPHA-BETA STRUCTURE, BETA HAIRPIN, TRANSGLUTAMINASE FOLD, DNA-DAMAGE RECOGNITION, DNA REPAIR, DNA BINDING PROTEIN, NUCLEOTIDE EXCISION REPAIR, XERODERMA PIGMENTOSUM
1dut:A (LYS24) to (LEU42) FIV DUTP PYROPHOSPHATASE | POLYPROTEIN, HYDROLASE, ASPARTYL PROTEASE, ENDONUCLEASE, RNA-DIRECTED DNA POLYMERASE, NUCLEOTIDE METABOLISM, ACID ANHYDRIDE HYDROLASE
1duz:D (HIS188) to (PRO210) HUMAN CLASS I HISTOCOMPATIBILITY ANTIGEN (HLA-A 0201) IN COMPLEX WITH A NONAMERIC PEPTIDE FROM HTLV-1 TAX PROTEIN | IMMUNOGLOBULIN FOLD, IMMUNE SYSTEM
3giv:A (HIS188) to (PRO210) ANTIGEN PROCESSING INFLUENCES HIV-SPECIFIC CYTOTOXIC T LYMPHOCYTE IMMUNODOMINANCE | HIV, MHC, ESCAPE, ANTIGEN, IMMUNE RECOGNITION, DISULFIDE BOND, GLYCOPROTEIN, HOST-VIRUS INTERACTION, IMMUNE RESPONSE, MEMBRANE, MHC I, PHOSPHOPROTEIN, TRANSMEMBRANE, DISEASE MUTATION, GLYCATION, IMMUNOGLOBULIN DOMAIN, PYRROLIDONE CARBOXYLIC ACID, SECRETED', IMMUNE SYSTEM
3t73:A (THR6) to (THR34) THERMOLYSIN IN COMPLEX WITH UBTLN22 | PROTEASE, METALLOPROTEASE, HYDROLYSIS OF PEPTIDE BONDS, PHOSPHORAMIDON, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3t74:A (THR6) to (THR34) THERMOLYSIN IN COMPLEX WITH UBTLN27 | PROTEASE, METALLOPROTEASE, HYDROLYSIS OF PEPTIDE BONDS, PHOSPHORAMIDON, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2qts:A (ASP184) to (LYS212) STRUCTURE OF AN ACID-SENSING ION CHANNEL 1 AT 1.9 A RESOLUTION AND LOW PH | ACID-SENSING, ION CHANNEL, TRIMER, MEMBRANE PROTEIN
2qts:B (ASP184) to (LYS212) STRUCTURE OF AN ACID-SENSING ION CHANNEL 1 AT 1.9 A RESOLUTION AND LOW PH | ACID-SENSING, ION CHANNEL, TRIMER, MEMBRANE PROTEIN
2qts:C (ASP184) to (LYS212) STRUCTURE OF AN ACID-SENSING ION CHANNEL 1 AT 1.9 A RESOLUTION AND LOW PH | ACID-SENSING, ION CHANNEL, TRIMER, MEMBRANE PROTEIN
2qts:E (ASP184) to (LYS212) STRUCTURE OF AN ACID-SENSING ION CHANNEL 1 AT 1.9 A RESOLUTION AND LOW PH | ACID-SENSING, ION CHANNEL, TRIMER, MEMBRANE PROTEIN
3gk7:B (LEU313) to (SER332) CRYSTAL STRUCTURE OF 4-HYDROXYBUTYRATE COA-TRANSFERASE FROM CLOSTRIDIUM AMINOBUTYRICUM | ALPHA/BETA PROTEIN, TRANSFERASE
3t8c:A (THR6) to (THR34) THERMOLYSIN IN COMPLEX WITH UBTLN30 | PROTEASE, METALLOPROTEASE, HYDROLYSIS OF PEPTIDE BONDS, PHOSPHORAMIDON, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3t8d:A (THR6) to (THR34) THERMOLYSIN IN COMPLEX WITH UBTLN31 | PROTEASE, METALLOPROTEASE, HYDROLYSIS OF PEPTIDE BONDS, PHOSPHORAMIDON, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3t8f:A (THR6) to (THR34) THERMOLYSIN IN COMPLEX WITH UBTLN34 | PROTEASE, METALLOPROTEASE, HYDROLYSIS OF PEPTIDE BONDS, PHOSPHORAMIDON, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3t8g:A (THR6) to (THR34) THERMOLYSIN IN COMPLEX WITH UBTLN26 | PROTEASE, METALLOPROTEASE, HYDROLYSIS OF PEPTIDE BONDS, PHOSPHORAMIDON, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3t8h:A (THR6) to (THR34) THERMOLYSIN IN COMPLEX WITH UBTLN29 | PROTEASE, METALLOPROTEASE, HYDROLYSIS OF PEPTIDE BONDS, PHOSPHORAMIDON, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2d0v:I (ASP417) to (ALA457) CRYSTAL STRUCTURE OF METHANOL DEHYDROGENASE FROM HYPHOMICROBIUM DENITRIFICANS | ELECTRON TRANSFER, OXIDOREDUCTASE, CALCIUM BINDING, METHANOL, PQQ
2d13:A (GLU207) to (TRP226) CRYSTAL STRUCTURE OF PH1257 FROM PYROCOCCUS HORIKOSHII OT3 | HYPOTHETICAL, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, UNKNOWN FUNCTION
4y12:A (ILE282) to (ILE300) CRYSTAL STRUCTURE OF THE S/T PROTEIN KINASE PKNG FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH AGS | S/T PROTEIN KINASE, PKNG, TRANSFERASE
1e0o:D (ARG165) to (GLY183) CRYSTAL STRUCTURE OF A TERNARY FGF1-FGFR2-HEPARIN COMPLEX | GROWTH FACTOR, RECEPTOR TYROSINE KINASE, HEPARIN, TERNARY COMPLEX, SIGNAL TRANSDUCTION
4y1y:A (LEU17) to (CSO42) COMPLEX OF HUMAN GALECTIN-1 AND (6OSO3)GALBETA1-3GLCNAC | COMPLEX, GALECTIN-1, SULFATED LACNAC, (6OSO3)GALBETA1-3GLCNAC, SUGAR BINDING PROTEIN
1pu5:B (PHE5) to (PRO32) GM2-ACTIVATOR PROTEIN CRYSTAL STRUCTURE | BETA CUP, LARGE LIPID BINDING POCKET, PROTEIN DYNAMICS, LIPID BINDING PROTEIN
1pu5:C (PHE5) to (PRO32) GM2-ACTIVATOR PROTEIN CRYSTAL STRUCTURE | BETA CUP, LARGE LIPID BINDING POCKET, PROTEIN DYNAMICS, LIPID BINDING PROTEIN
3gnc:A (LEU205) to (PRO232) CRYSTAL STRUCTURE OF GLUTARYL-COA DEHYDROGENASE FROM BURKHOLDERIA PSEUDOMALLEI WITH FRAGMENT 6421 | OXIDOREDUCTASE, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, SSGCID
1e28:A (HIS188) to (PRO210) NONSTANDARD PEPTIDE BINDING OF HLA-B*5101 COMPLEXED WITH HIV IMMUNODOMINANT EPITOPE KM2(TAFTIPSI) | HLA B51, HIV, MHC CLASS I, HISTOCOMPATIBILITY COMPLEX
3gpj:I (GLY-1) to (SER22) CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH SYRINGOLIN B | PROTEASOME, VIRULENCE, UBIQUITIN, CANCER THERAPY, IMMUNOLOGY, CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, THREONINE PROTEASE, ISOPEPTIDE BOND, UBL CONJUGATION, ZYMOGEN
3gpj:L (THR2) to (THR22) CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH SYRINGOLIN B | PROTEASOME, VIRULENCE, UBIQUITIN, CANCER THERAPY, IMMUNOLOGY, CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, THREONINE PROTEASE, ISOPEPTIDE BOND, UBL CONJUGATION, ZYMOGEN
3gpj:W (GLY-1) to (SER22) CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH SYRINGOLIN B | PROTEASOME, VIRULENCE, UBIQUITIN, CANCER THERAPY, IMMUNOLOGY, CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, THREONINE PROTEASE, ISOPEPTIDE BOND, UBL CONJUGATION, ZYMOGEN
3gpj:Z (THR2) to (THR22) CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH SYRINGOLIN B | PROTEASOME, VIRULENCE, UBIQUITIN, CANCER THERAPY, IMMUNOLOGY, CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, THREONINE PROTEASE, ISOPEPTIDE BOND, UBL CONJUGATION, ZYMOGEN
4y4y:A (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:B (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:C (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:D (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:E (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:F (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:G (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:H (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:I (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:J (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:K (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:L (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:M (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:N (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:O (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:P (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:Q (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:R (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:S (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:T (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:U (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:V (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:W (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:X (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:Y (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:Z (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:a (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:b (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:c (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y4y:d (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (C2 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
2d6m:A (GLY28) to (ALA58) CRYSTAL STRUCTURE OF MOUSE GALECTIN-9 N-TERMINAL CRD IN COMPLEX WITH LACTOSE | BETA SANDWICH, CARBOHYDRATE BINDING PROTEIN, GALECTIN, SUGAR BINDING PROTEIN
2d6m:B (GLY28) to (ALA58) CRYSTAL STRUCTURE OF MOUSE GALECTIN-9 N-TERMINAL CRD IN COMPLEX WITH LACTOSE | BETA SANDWICH, CARBOHYDRATE BINDING PROTEIN, GALECTIN, SUGAR BINDING PROTEIN
2d6o:X (GLY28) to (ALA58) CRYSTAL STRUCTURE OF MOUSE GALECTIN-9 N-TERMINAL CRD IN COMPLEX WITH N-ACETYLLACTOSAMINE DIMER | BETA SANDWICH, CARBOHYDRATE BINDING PROTEIN, GALECTIN, SUGAR BINDING PROTEIN
2d6p:A (GLN30) to (ALA58) CRYSTAL STRUCTURE OF MOUSE GALECTIN-9 N-TERMINAL CRD IN COMPLEX WITH T-ANTIGEN | BETA SANDWICH, CARBOHYDRATE BINDING PROTEIN, GALECTIN, SUGAR BINDING PROTEIN
3tbw:C (HIS188) to (PRO210) CRYSTAL STRUCTURE OF THE MURINE CLASS I MAJOR HISTOCOMPATIBILITY COMPLEX H-2DB IN COMPLEX WITH THE LCMV-DERIVED GP33 ALTERED PEPTIDE LIGAND (A2G, V3P, Y4S) | MURINE MHC, LCMV, RECEPTOR BINDING, BETA2-MICROGLOBULIN, IMMUNE SYSTEM, T CELL RECOGNITION, ANTIGEN PRESENTATION, ALTERED PEPTIDE LIGAND, AGONISM, ANTAGONISM, T CELL RECEPTOR, CD8, CELL SURFACE, IMMUNE SYSTEM-AGONIST COMPLEX
3tby:G (HIS188) to (PRO210) CRYSTAL STRUCTURE OF THE MURINE CLASS I MAJOR HISTOCOMPATIBILITY COMPLEX H-2DB IN COMPLEX WITH THE LCMV-DERIVED GP33 ALTERED PEPTIDE LIGAND (V3P, Y4F) | MURINE MHC, LCMV, RECEPTOR BINDING, BETA2-MICROGLOBULIN, IMMUNE SYSTEM, T CELL RECOGNITION, ANTIGEN PRESENTATION, ALTERED PEPTIDE LIGAND, AGONISM, ANTAGONISM, T CELL RECEPTOR, CD8, CELL SURFACE, IMMUNE SYSTEM-AGONIST COMPLEX
3tby:J (HIS188) to (PRO210) CRYSTAL STRUCTURE OF THE MURINE CLASS I MAJOR HISTOCOMPATIBILITY COMPLEX H-2DB IN COMPLEX WITH THE LCMV-DERIVED GP33 ALTERED PEPTIDE LIGAND (V3P, Y4F) | MURINE MHC, LCMV, RECEPTOR BINDING, BETA2-MICROGLOBULIN, IMMUNE SYSTEM, T CELL RECOGNITION, ANTIGEN PRESENTATION, ALTERED PEPTIDE LIGAND, AGONISM, ANTAGONISM, T CELL RECEPTOR, CD8, CELL SURFACE, IMMUNE SYSTEM-AGONIST COMPLEX
2d8t:A (VAL26) to (SER46) SOLUTION STRUCTURE OF THE RING DOMAIN OF THE HUMAN RING FINGER PROTEIN 146 | RING FINGER PROTEIN 146, DACTYLIDIN, RNF146, RING DOMAIN, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, METAL BINDING PROTEIN
3gqt:B (GLY204) to (PRO232) CRYSTAL STRUCTURE OF GLUTARYL-COA DEHYDROGENASE FROM BURKHOLDERIA PSEUDOMALLEI WITH FRAGMENT (1,4-DIMETHYL-1,2,3,4- TETRAHYDROQUINOXALIN-6-YL)METHYLAMINE | SSGCID, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, GLUTARYL-COA DEHYDROGENASE, BUPSA.00027.A, FRAGMENT CRYSTALLOGRAPHY, FRAGMENTS OF LIFE, OXIDOREDUCTASE
4y5z:A (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:B (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:C (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:D (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:E (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:F (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:G (VAL233) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:H (VAL233) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:I (PRO229) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:J (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:K (PRO229) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:L (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:M (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:N (VAL233) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:O (VAL233) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:P (PRO229) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:R (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:S (VAL233) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:U (PRO229) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:V (VAL233) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:W (PRO229) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:X (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:Y (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:Z (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:a (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:c (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:e (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:g (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:i (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:k (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:m (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:o (PRO229) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:q (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:r (VAL233) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:s (PRO229) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:t (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:u (PRO229) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:w (PRO229) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:x (PRO229) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:y (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:z (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:0 (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:1 (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:2 (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:3 (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:4 (VAL233) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:6 (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:b (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:d (PRO229) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:f (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:j (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:l (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:n (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y5z:p (VAL233) to (GLU260) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
4y69:L (GLY10) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4y69:Z (GLY10) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2dck:A (ASN64) to (ASP89) A TETRAGONAL-LATTICE STRUCTURE OF ALKALIPHILIC XYNJ FROM BACILLUS SP. 41M-1 | FAMILY 11, XYLAN BINDING DOMAIN (XBM), BETA-JELLY ROLL, ALKALIPHILIC XYLANASE, HYDROLASE
3grw:A (LYS162) to (ASN181) FGFR3 IN COMPLEX WITH A FAB | FGFR3, FAB, PROTEIN-PROTEIN COMPLEX, RECEPTOR TYROSINE KINASE, ATP- BINDING, IMMUNOGLOBULIN DOMAIN, KINASE, MEMBRANE, NUCLEOTIDE- BINDING, RECEPTOR, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE, TRANSFERASE-IMMUNE SYSTEM COMPLEX
4y6a:L (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-PAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4y6a:Z (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-PAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4y6v:L (GLY10) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4y6v:Z (GLY10) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4y6z:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y6z:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y70:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAV-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y70:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAV-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y74:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y74:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
2dew:X (MET589) to (PRO604) CRYSTAL STRUCTURE OF HUMAN PEPTIDYLARGININE DEIMINASE 4 IN COMPLEX WITH HISTONE H3 N-TERMINAL TAIL INCLUDING ARG8 | HISTONE MODIFICATION ENZYME, HYDROLASE
2dey:X (MET589) to (PRO604) CRYSTAL STRUCTURE OF HUMAN PEPTIDYLARGININE DEIMINASE 4 IN COMPLEX WITH HISTONE H4 N-TERMINAL TAIL INCLUDING ARG3 | HISTONE MODIFICATION ENZYME, HYDROLASE
4y77:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAF-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y77:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAF-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y78:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y78:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4j70:L (GLY10) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH THE BELACTOSIN DERIVATIVE 3E | PROTEASOME, DRUG DISCOVERY, IRREVERSIBLE INHIBITION, BETA-LACTONE, NTN HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4j70:N (THR1) to (THR22) YEAST 20S PROTEASOME IN COMPLEX WITH THE BELACTOSIN DERIVATIVE 3E | PROTEASOME, DRUG DISCOVERY, IRREVERSIBLE INHIBITION, BETA-LACTONE, NTN HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4j70:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH THE BELACTOSIN DERIVATIVE 3E | PROTEASOME, DRUG DISCOVERY, IRREVERSIBLE INHIBITION, BETA-LACTONE, NTN HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3tgr:A (ASN392) to (GLN422) CRYSTAL STRUCTURE OF UNLIGANDED HIV-1 CLADE C STRAIN C1086 GP120 CORE | HIV-1 GP120, UNLIGANDED, CLADE C1086, VIRAL PROTEIN
3tgr:B (ASN392) to (GLN422) CRYSTAL STRUCTURE OF UNLIGANDED HIV-1 CLADE C STRAIN C1086 GP120 CORE | HIV-1 GP120, UNLIGANDED, CLADE C1086, VIRAL PROTEIN
1e8r:A (ASN22) to (GLU45) SOLUTION STRUCTURE OF TYPE X CBD | HYDROLASE, BETA STRANDS, ANTIPARALLEL SHEETS
4y7w:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y7w:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y7x:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAA-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y7x:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAA-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y7y:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAA-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y7y:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAA-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y80:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAI-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y80:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAI-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y81:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAY-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y81:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAY-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y82:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAY-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y82:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAY-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y84:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH N3-A(4,4-F2P)NLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y84:W (ILE10) to (SER30) YEAST 20S PROTEASOME IN COMPLEX WITH N3-A(4,4-F2P)NLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y84:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH N3-A(4,4-F2P)NLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8g:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APNLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8g:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APNLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8h:I (ILE10) to (SER30) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8h:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8h:W (ILE10) to (SER30) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8h:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8j:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8j:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8l:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-APLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8l:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-APLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8m:L (GLY10) to (THR31) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8m:N (THR1) to (THR22) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8m:Z (GLY10) to (THR31) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8m:b (THR1) to (THR22) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8n:L (GLY10) to (THR31) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAE- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8n:Z (GLY10) to (THR31) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAE- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
3tid:B (LYS6) to (PRO32) CRYSTAL STRUCTURE OF THE LCMV DERIVED PEPTIDE GP34 IN COMPLEX WITH THE MURINE MHC CLASS I H-2 KB | ANTIGEN PRESENTATION, PEPTIDE BINDING, IGG, MHC, IMMUNE SYSTEM
4y8o:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAF- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8o:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAF- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8q:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAY- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8q:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAY- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4jbw:A (GLN253) to (ARG286) CRYSTAL STRUCTURE OF E. COLI MALTOSE TRANSPORTER MALFGK2 IN COMPLEX WITH ITS REGULATORY PROTEIN EIIAGLC | ABC TRANSPORTER ATPASE INDUCER EXCLUSION CARBON CATABOLITE REPRESSION, TRANSPORT PROTEIN
4jbw:B (GLN253) to (ARG286) CRYSTAL STRUCTURE OF E. COLI MALTOSE TRANSPORTER MALFGK2 IN COMPLEX WITH ITS REGULATORY PROTEIN EIIAGLC | ABC TRANSPORTER ATPASE INDUCER EXCLUSION CARBON CATABOLITE REPRESSION, TRANSPORT PROTEIN
3tj9:D (LEU63) to (GLU79) CRYSTAL STRUCTURE OF HELICOBACTER PYLORI UREE BOUND TO ZN2+ | METAL BINDING PROTEIN, UREASE ACCESSORY PROTEIN
4y8s:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8s:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8t:L (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8t:Z (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8u:L (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-PAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8u:Z (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-PAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y9y:L (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H116E MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4y9y:N (THR1) to (THR22) YEAST 20S PROTEASOME BETA2-H116E MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4y9y:Z (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H116E MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4y9y:b (THR1) to (THR22) YEAST 20S PROTEASOME BETA2-H116E MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3tli:A (THR6) to (THR34) THERMOLYSIN (10% ISOPROPANOL SOAKED CRYSTALS) | HYDROLASE, METALLOPROTEINASE, ORGANIC SOLVENT
4y9z:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA2-H116E MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y9z:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA2-H116E MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya0:L (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H116E MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya0:Z (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H116E MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
1eey:A (HIS188) to (PRO210) CRYSTAL STRUCTURE DETERMINATION OF HLA A2 COMPLEXED TO PEPTIDE GP2 WITH THE SUBSTITUTION (I2L/V5L/L9V) | MAJOR HISTICOMPATIBILITY COMPLEX, PEPTIDE BINDING, CRYSTALLOGRAPHY, IMMUNE SYSTEM
1eez:D (HIS188) to (PRO210) CRYSTAL STRUCTURE DETERMINATION OF HLA-A2.1 COMPLEXED TO GP2 PEPTIDE VARIANT(I2L/V5L) | MAJOR HISTOCOMPATIBILITY COMPLEX, PEPTIDE BINDING, CRYSTALLOGRAPHY, IMMUNE SYSTEM
4ya1:L (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H116N MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ya1:N (THR1) to (THR22) YEAST 20S PROTEASOME BETA2-H116N MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ya1:Z (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H116N MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ya1:b (THR1) to (THR22) YEAST 20S PROTEASOME BETA2-H116N MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ya2:L (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H116N MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya2:Z (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H116N MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya3:L (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H116N MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya3:Z (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H116N MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya4:L (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H114D MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ya4:N (THR1) to (THR22) YEAST 20S PROTEASOME BETA2-H114D MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ya4:Z (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H114D MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ya4:b (THR1) to (THR22) YEAST 20S PROTEASOME BETA2-H114D MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3tmn:E (THR6) to (THR34) THE BINDING OF L-VALYL-L-TRYPTOPHAN TO CRYSTALLINE THERMOLYSIN ILLUSTRATES THE MODE OF INTERACTION OF A PRODUCT OF PEPTIDE HYDROLYSIS | HYDROLASE, METALLOPROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ya7:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya7:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya9:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-LAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya9:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-LAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
2dtm:L (GLY84) to (PRO113) THERMODYNAMIC AND STRUCTURAL ANALYSES OF HYDROLYTIC MECHANISM BY CATALYTIC ANTIBODIES | CATALYTIC ANTIBODY, ESTER HYDROLYSIS, ESTEROLYTIC, FAB, IMMUNOGLOBULIN, IMMUNE SYSTEM
2dud:B (ASP99) to (ILE122) CRYSTAL STRUCTURE OF HUMAN MITOCHONDRIAL SINGLE-STRANDED DNA-BINDING PROTEIN(HMTSSB) | MITOCHONDRIA, SSB, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, DNA BINDING PROTEIN
1qdm:B (ILE283) to (ALA300) CRYSTAL STRUCTURE OF PROPHYTEPSIN, A ZYMOGEN OF A BARLEY VACUOLAR ASPARTIC PROTEINASE. | ASPARTIC PROTEINASES, PHYTEPSIN, SAPOSIN-LIKE DOMAIN, ZYMOGEN STRUCTURE, HYDROLASE
1ejr:C (ASP1431) to (SER1493) CRYSTAL STRUCTURE OF THE D221A VARIANT OF KLEBSIELLA AEROGENES UREASE | ALPHA-BETA BARREL, NICKEL METALLOENZYME, HYDROLASE
1ejt:C (ASP1431) to (SER1493) CRYSTAL STRUCTURE OF THE H219Q VARIANT OF KLEBSIELLA AEROGENES UREASE | ALPHA-BETA BARREL, NICKEL METALLOENZYME, HYDROLASE
1eju:C (ASP1431) to (SER1493) CRYSTAL STRUCTURE OF THE H320N VARIANT OF KLEBSIELLA AEROGENES UREASE | ALPHA-BETA BARREL, NICKEL METALLOENZYME, HYDROLASE
1ejv:C (ASP1431) to (SER1493) CRYSTAL STRUCTURE OF THE H320Q VARIANT OF KLEBSIELLA AEROGENES UREASE | ALPHA-BETA BARREL, NICKEL METALLOENZYME, HYDROLASE
2dw5:A (MET589) to (PRO604) CRYSTAL STRUCTURE OF HUMAN PEPTIDYLARGININE DEIMINASE 4 IN COMPLEX WITH N-ALPHA-BENZOYL-N5-(2-FLUORO-1-IMINOETHYL)-L-ORNITHINE AMIDE | PROTEIN-INHIBITOR COMPLEX, HYDROLASE
4ydj:A (SER120) to (PRO147) CRYSTAL STRUCTURE OF BROADLY AND POTENTLY NEUTRALIZING ANTIBODY 44- VRC13.01 IN COMPLEX WITH HIV-1 CLADE AE STRAIN 93TH057 GP120 | ANTIBODY, HIV-1, IMMUNE SYSTEM
3h09:B (GLY876) to (SER901) THE STRUCTURE OF HAEMOPHILUS INFLUENZAE IGA1 PROTEASE | SERINE PROTEASE, IMMUNOGLOBULIN A1, BETA HELIX, HYDROLASE, MEMBRANE, PROTEASE, SECRETED, TRANSMEMBRANE, VIRULENCE, ZYMOGEN
2dyy:E (GLN19) to (PRO34) CRYSTAL STRUCTURE OF PUTATIVE TRANSLATION INITIATION INHIBITOR PH0854 FROM PYROCOCCUS HORIKOSHII | PUTATIVE TRANSLATION INITIATION INHIBITOR, PYROCOCCUS HORIKOSHII, TRIMER, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, UNKNOWN FUNCTION
1ep4:B (THR58) to (ASP110) CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH S- 1153 | HIV-1 REVERSE TRANSCRIPTASE, AIDS, NON-NUCLEOSIDE INHIBITOR, S-1153, DRUG DESIGN, TRANSFERASE
1qil:B (SER32) to (ASN65) INACTIVE MUTANT TOXIC SHOCK SYNDROME TOXIN-1 AT 2.5 A | TOXIN, SUPERANTIGEN, STAPHYLOCOCCAL ENTEROTOXIN
1qil:C (SER32) to (ASN65) INACTIVE MUTANT TOXIC SHOCK SYNDROME TOXIN-1 AT 2.5 A | TOXIN, SUPERANTIGEN, STAPHYLOCOCCAL ENTEROTOXIN
1evt:C (LYS164) to (THR183) CRYSTAL STRUCTURE OF FGF1 IN COMPLEX WITH THE EXTRACELLULAR LIGAND BINDING DOMAIN OF FGF RECEPTOR 1 (FGFR1) | IMMUNOGLOBULIN (IG) LIKE DOMAINS BELONGING TO THE I-SET SUBGROUP WITHIN IG-LIKE DOMAINS, B-TREFOIL FOLD, GROWTH FACTOR/GROWTH FACTOR RECEPTOR COMPLEX
1evt:D (LYS164) to (THR183) CRYSTAL STRUCTURE OF FGF1 IN COMPLEX WITH THE EXTRACELLULAR LIGAND BINDING DOMAIN OF FGF RECEPTOR 1 (FGFR1) | IMMUNOGLOBULIN (IG) LIKE DOMAINS BELONGING TO THE I-SET SUBGROUP WITHIN IG-LIKE DOMAINS, B-TREFOIL FOLD, GROWTH FACTOR/GROWTH FACTOR RECEPTOR COMPLEX
3h32:E (GLY420) to (ARG455) CRYSTAL STRUCTURE OF D-DIMER FROM HUMAN FIBRIN COMPLEXED WITH GLY-HIS- ARG-PRO-TYR-AMIDE | FIBRINOGEN, FIBRIN CLOTS, BLOOD CLOTTING, AMYLOID, AMYLOIDOSIS, BLOOD COAGULATION, DISEASE MUTATION, DISULFIDE BOND, GLYCOPROTEIN, ISOPEPTIDE BOND, PHOSPHOPROTEIN, SECRETED, PYRROLIDONE CARBOXYLIC ACID, SULFATION, CDNA FLJ75335, TRANSCRIPT VARIANT GAMMA-A, MRNA, ISOFORM CRA_M
2tli:A (THR6) to (THR34) THERMOLYSIN (5% ISOPROPANOL SOAKED CRYSTALS) | HYDROLASE, METALLOPROTEINASE, ORGANIC SOLVENT
2tmn:E (THR6) to (THR34) CRYSTALLOGRAPHIC STRUCTURAL ANALYSIS OF PHOSPHORAMIDATES AS INHIBITORS AND TRANSITION-STATE ANALOGS OF THERMOLYSIN | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, METALLOPROTEINASE
2tss:A (SER32) to (ASN65) TOXIC SHOCK SYNDROME TOXIN-1 FROM STAPHYLOCOCCUS AUREUS: ORTHORHOMBICC222(1) CRYSTAL FORM | TOXIN, SUPERANTIGEN, SIGNAL
2tss:B (SER32) to (ASN65) TOXIC SHOCK SYNDROME TOXIN-1 FROM STAPHYLOCOCCUS AUREUS: ORTHORHOMBICC222(1) CRYSTAL FORM | TOXIN, SUPERANTIGEN, SIGNAL
2tss:C (SER32) to (ASN65) TOXIC SHOCK SYNDROME TOXIN-1 FROM STAPHYLOCOCCUS AUREUS: ORTHORHOMBICC222(1) CRYSTAL FORM | TOXIN, SUPERANTIGEN, SIGNAL
4yiz:E (GLN101) to (GLY121) CRYSTAL STRUCTURE OF ENGINEERED TGAMA1 LACKING THE DII LOOP IN COMPLEX WITH AN EIMERIA TENELLA RON2D3 PEPTIDE | APICOMPLEXA, INVASION, MOVING JUNCTION, PARASITE, PROTEIN ENGINEERING, PAN DOMAIN, IMMUNE SYSTEM
2uut:A (ARG25) to (GLY47) THE 2.4 ANGSTROM RESOLUTION STRUCTURE OF THE D346G MUTANT OF THE SAPPORO VIRUS RDRP POLYMERASE | NUCLEOTIDE-BINDING, NUCLEOTIDYLTRANSFERASE, COVALENT PROTEIN-RNA LINKAGE, POLYMERASE, RNA ELONGATION, TRANSFERASE ACTIVITY, MUTANT, CAPSID PROTEIN, RNA REPLICATION, STRUCTURAL PROTEIN, PROTEASE, HELICASE, HYDROLASE, TRANSFERASE, RNA-DIRECTED RNA POLYMERASE, POLYPROTEIN, ATP-BINDING, THIOL PROTEASE
3h6f:N (THR302) to (GLN322) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR HT1171 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6i:J (THR302) to (GLN322) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6i:L (THR302) to (GLN322) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6i:N (THR302) to (GLN322) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6i:P (THR302) to (GLN322) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6i:R (THR302) to (GLN322) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6i:T (THR302) to (GLN322) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6i:Z (THR302) to (GLN322) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
4jsq:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH THE DIMERIZED LINEAR MIMETIC OF TMC-95A - YCP:4E | UPS, PROTEASOME, DRUG DISCOVERY, NON-COVALENT REVERSIBLE INHIBITION, BIVALENCE, TMC-95A DERIVATIVES, NTN HYDROLASE, NON-LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4jsq:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH THE DIMERIZED LINEAR MIMETIC OF TMC-95A - YCP:4E | UPS, PROTEASOME, DRUG DISCOVERY, NON-COVALENT REVERSIBLE INHIBITION, BIVALENCE, TMC-95A DERIVATIVES, NTN HYDROLASE, NON-LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4jsu:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH THE DIMERIZED LINEAR MIMETIC OF TMC-95A - YCP:3A | UPS, PROTEASOME, DRUG DISCOVERY, NON-COVALENT REVERSIBLE INHIBITION, BIVALENCE, TMC-95A DERIVATIVES, NTN HYDROLASE, NON-LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4jsu:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH THE DIMERIZED LINEAR MIMETIC OF TMC-95A - YCP:3A | UPS, PROTEASOME, DRUG DISCOVERY, NON-COVALENT REVERSIBLE INHIBITION, BIVALENCE, TMC-95A DERIVATIVES, NTN HYDROLASE, NON-LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2e86:A (LEU12) to (VAL31) AZIDE BOUND TO COPPER CONTAINING NITRITE REDUCTASE FROM A. FAECALIS S- 6 | NITRITE REDUCTASE, AZIDE, INHIBITOR, KINETIC STUDIES, OXIDOREDUCTASE
4jt0:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH THE DIMERIZED LINEAR MIMETIC OF TMC-95A - YCP:4A | UPS, PROTEASOME, DRUG DISCOVERY, NON-COVALENT REVERSIBLE INHIBITION, BIVALENCE, TMC-95A DERIVATIVES, NTN HYDROLASE, NON-LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4jt0:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH THE DIMERIZED LINEAR MIMETIC OF TMC-95A - YCP:4A | UPS, PROTEASOME, DRUG DISCOVERY, NON-COVALENT REVERSIBLE INHIBITION, BIVALENCE, TMC-95A DERIVATIVES, NTN HYDROLASE, NON-LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3h9k:C (LYS278) to (HIS304) STRUCTURES OF THYMIDYLATE SYNTHASE R163K WITH SUBSTRATES AND INHIBITORS SHOW SUBUNIT ASYMMETRY | TRANSFERASE, METHYLTRANSFERASE, NUCLEOTIDE BIOSYNTHESIS
2eak:B (LEU29) to (ALA59) CRYSTAL STRUCTURE OF HUMAN GALECTIN-9 N-TERMINAL CRD IN COMPLEX WITH LACTOSE | BETA SANDWICH, CARBOHYDRATE BINDING PROTEIN, GALECTIN, SUGAR BINDING PROTEIN
2eak:C (LEU29) to (ALA59) CRYSTAL STRUCTURE OF HUMAN GALECTIN-9 N-TERMINAL CRD IN COMPLEX WITH LACTOSE | BETA SANDWICH, CARBOHYDRATE BINDING PROTEIN, GALECTIN, SUGAR BINDING PROTEIN
2eal:A (LEU29) to (ALA59) CRYSTAL STRUCTURE OF HUMAN GALECTIN-9 N-TERMINAL CRD IN COMPLEX WITH FORSSMAN PENTASACCHARIDE | BETA SANDWICH, CARBOHYDRATE BINDING PROTEIN, GALECTIN, SUGAR BINDING PROTEIN
3hav:C (MET198) to (GLY217) STRUCTURE OF THE STREPTOMYCIN-ATP-APH(2")-IIA TERNARY COMPLEX | AMINOGLYCOSIDE, STREPTOMYCIN, ANTIBIOTIC RESISTANCE, TRANSFERASE
1f7d:A (LYS24) to (LEU42) CRYSTAL STRUCTURES OF FELINE IMMUNODEFICIENCY VIRUS DUTP PYROPHOSPHATASE AND ITS NUCLEOTIDE COMPLEXES IN THREE CRYSTAL FORMS | EIGHT STRANDED BETA-BARREL, VIRAL PROTEIN, HYDROLASE
1f7d:B (LYS224) to (LEU242) CRYSTAL STRUCTURES OF FELINE IMMUNODEFICIENCY VIRUS DUTP PYROPHOSPHATASE AND ITS NUCLEOTIDE COMPLEXES IN THREE CRYSTAL FORMS | EIGHT STRANDED BETA-BARREL, VIRAL PROTEIN, HYDROLASE
1f7n:A (GLU25) to (LEU42) CRYSTAL STRUCTURES OF FELINE IMMUNODEFICIENCY VIRUS DUTP PYROPHOSPHATASE AND ITS NUCLEOTIDE COMPLEXES IN THREE CRYSTAL FORMS. | EIGHT STRANDED BETA BARREL PROTEIN, VIRAL PROTEIN, HYDROLASE
1f7o:A (GLU25) to (MET43) CRYSTAL STRUCTURES OF FELINE IMMUNODEFICIENCY VIRUS DUTP PYROPHOSPHATASE AND ITS NUCLEOTIDE COMPLEXES IN THREE CRYSTAL FORMS. | EIGHT STRANDED BETA BARREL PROTEIN, VIRAL PROTEIN, HYDROLASE
1f7o:B (GLU225) to (MET243) CRYSTAL STRUCTURES OF FELINE IMMUNODEFICIENCY VIRUS DUTP PYROPHOSPHATASE AND ITS NUCLEOTIDE COMPLEXES IN THREE CRYSTAL FORMS. | EIGHT STRANDED BETA BARREL PROTEIN, VIRAL PROTEIN, HYDROLASE
1f7o:C (GLU425) to (MET443) CRYSTAL STRUCTURES OF FELINE IMMUNODEFICIENCY VIRUS DUTP PYROPHOSPHATASE AND ITS NUCLEOTIDE COMPLEXES IN THREE CRYSTAL FORMS. | EIGHT STRANDED BETA BARREL PROTEIN, VIRAL PROTEIN, HYDROLASE
1f7q:A (GLU25) to (MET43) CRYSTAL STRUCTURES OF FELINE IMMUNODEFICIENCY VIRUS DUTP PYROPHOSPHATASE AND ITS NUCLEOTIDE COMPLEXES IN THREE CRYSTAL FORMS. | EIGHT STRANDED BETA BARREL PROTEIN, VIRAL PROTEIN, HYDROLASE
1f7q:C (GLU425) to (MET443) CRYSTAL STRUCTURES OF FELINE IMMUNODEFICIENCY VIRUS DUTP PYROPHOSPHATASE AND ITS NUCLEOTIDE COMPLEXES IN THREE CRYSTAL FORMS. | EIGHT STRANDED BETA BARREL PROTEIN, VIRAL PROTEIN, HYDROLASE
1fah:B (GLU430) to (LYS452) STRUCTURE OF CYTOCHROME P450 | MONOOXYGENASE, ELECTRON TRANSPORT, HEME
2uwh:C (GLU430) to (LYS452) CYTOCHROME P450 BM3 MUTANT IN COMPLEX WITH PALMITIC ACID | FATTY-ACID BINDING, MULTIFUNCTIONAL ENZYME, METAL-BINDING, OXIDOREDUCTASE, ELECTRON TRANSPORT, TRANSPORT, HYDROXYLASE, FLAVOPROTEIN, MONOOXYGENASE, FMN, FAD, NADP, IRON, HEME, REDOX, MEMBRANE, CYTOCHROME P450 BM3 MUTANT
2uwh:D (GLU430) to (LYS449) CYTOCHROME P450 BM3 MUTANT IN COMPLEX WITH PALMITIC ACID | FATTY-ACID BINDING, MULTIFUNCTIONAL ENZYME, METAL-BINDING, OXIDOREDUCTASE, ELECTRON TRANSPORT, TRANSPORT, HYDROXYLASE, FLAVOPROTEIN, MONOOXYGENASE, FMN, FAD, NADP, IRON, HEME, REDOX, MEMBRANE, CYTOCHROME P450 BM3 MUTANT
2uwh:F (GLU430) to (LYS452) CYTOCHROME P450 BM3 MUTANT IN COMPLEX WITH PALMITIC ACID | FATTY-ACID BINDING, MULTIFUNCTIONAL ENZYME, METAL-BINDING, OXIDOREDUCTASE, ELECTRON TRANSPORT, TRANSPORT, HYDROXYLASE, FLAVOPROTEIN, MONOOXYGENASE, FMN, FAD, NADP, IRON, HEME, REDOX, MEMBRANE, CYTOCHROME P450 BM3 MUTANT
4jy4:B (SER118) to (PRO145) CRYSTAL STRUCTURE OF HUMAN FAB PGT121, A BROADLY REACTIVE AND POTENT HIV-1 NEUTRALIZING ANTIBODY | BROADLY NEUTRALIZING ANTIBODY AGAINST HIV-1, HIV-1 ENV GP120 SUBUNIT, IMMUNE SYSTEM
3u7w:H (THR195) to (ASP221) CRYSTAL STRUCTURE OF NIH45-46 FAB | IG FOLD, ANTIBODY, HIV GP120, IMMUNE SYSTEM
3u7v:A (MSE36) to (ASN63) THE STRUCTURE OF A PUTATIVE BETA-GALACTOSIDASE FROM CAULOBACTER CRESCENTUS CB15. | STRUCTURAL GENOMICS, PSI-BIOLOGY, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, TIM BARREL, GLYCO_HYDRO_42, CARBOHYDRATE TRANSPORT AND METABOLISM, HYDROLASE
3u83:A (ASP37) to (PRO58) CRYSTAL STRUCTURE OF NECTIN-1 | NECTIN-1, HINGE REGION PLASITICITY, CELL ADHESION
3hf2:A (GLU430) to (LYS452) CRYSTAL STRUCTURE OF THE I401P MUTANT OF CYTOCHROME P450 BM3 | P450 FAMILY PROTEIN FOLD, OXIDOREDUCTASE, ELECTRON TRANSPORT, FAD, FLAVOPROTEIN, FMN, HEME, IRON, METAL-BINDING, MONOOXYGENASE, MULTIFUNCTIONAL ENZYME, NADP, TRANSPORT
3hf2:B (GLU430) to (LYS452) CRYSTAL STRUCTURE OF THE I401P MUTANT OF CYTOCHROME P450 BM3 | P450 FAMILY PROTEIN FOLD, OXIDOREDUCTASE, ELECTRON TRANSPORT, FAD, FLAVOPROTEIN, FMN, HEME, IRON, METAL-BINDING, MONOOXYGENASE, MULTIFUNCTIONAL ENZYME, NADP, TRANSPORT
3hf9:x (THR302) to (GLN322) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME OPEN-GATE MUTANT MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, OPEN GATE, MUTANT, HYDROLASE, PROTEASOME
3hf9:4 (THR302) to (GLN322) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME OPEN-GATE MUTANT MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, OPEN GATE, MUTANT, HYDROLASE, PROTEASOME
1r56:B (LYS127) to (SER154) UNCOMPLEXED URATE OXIDASE FROM ASPERGILLUS FLAVUS | OXIDOREDUCTASE, URIC ACID DEGRADATION, DIMERIC BARREL, TUNNEL-SHAPED PROTEIN
1r56:G (ARG128) to (SER154) UNCOMPLEXED URATE OXIDASE FROM ASPERGILLUS FLAVUS | OXIDOREDUCTASE, URIC ACID DEGRADATION, DIMERIC BARREL, TUNNEL-SHAPED PROTEIN
3uaa:A (GLY55) to (GLN81) MULTICOPPER OXIDASE CUEO MUTANT C500SE506Q (DATA1) | MULTICOPPER OXIDASE, METAL BINDING PROTEIN
3uab:A (GLY55) to (GLN81) MULTICOPPER OXIDASE CUEO MUTANT C500SE506Q (DATA2) | MULTICOPPER OXIDASE, METAL BINDING PROTEIN
3uac:A (GLY55) to (GLN81) MULTICOPPER OXIDASE CUEO MUTANT C500SE506Q (DATA4) | MULTICOPPER OXIDASE, METAL BINDING PROTEIN
3uad:A (GLY55) to (GLN81) MULTICOPPER OXIDASE CUEO MUTANT C500SE506Q (DATA5) | MULTICOPPER OXIDASE, METAL BINDING PROTEIN
3uae:A (GLY55) to (GLN81) MULTICOPPER OXIDASE CUEO MUTANT C500SE506Q (DATA6) | MULTICOPPER OXIDASE, METAL BINDING PROTEIN
1fj3:A (THR6) to (THR34) THERMOLYSIN (50% ACETONE SOAKED) | HYDROLASE, METALLOPROTEINASE, ORGANIC SOLVENT
2v3m:F (LYS144) to (LEU172) STRUCTURE OF THE GAR1 DOMAIN OF NAF1 | RIBOSOMAL PROTEIN, NAF1, GAR1, SNORNP, PHOSPHORYLATION, HYPOTHETICAL PROTEIN
1fjo:A (THR6) to (THR34) THERMOLYSIN (60% ACETONE SOAKED CRYSTALS) | METALLOPROTEINASE, ORGANIC SOLVENT, HYDROLASE
1fjt:A (THR6) to (THR34) THERMOLYSIN (50% ACETONITRILE SOAKED CRYSTALS) | METALLOPROTEINASE, ORGANIC SOLVENT, HYDROLASE
1fju:A (THR6) to (THR34) THERMOLYSIN (80% ACETONITRILE SOAKED CRYSTALS) | METALLOPROTEINASE, ORGANIC SOLVENT, HYDROLASE
1fjv:A (THR6) to (THR34) THERMOLYSIN (60% ACETONITRILE SOAKED CRYSTALS) | METALLOPROTEINASE, ORGANIC SOLVENT, HYDROLASE
1fjw:A (THR6) to (THR34) THERMOLYSIN (50 MM PHENOL SOAKED) | METALLOPROTEINASE, ORGANIC SOLVENT, HYDROLASE
1fl6:H (SER120) to (PRO147) THE HAPTEN COMPLEXED GERMLINE PRECURSOR TO SULFIDE OXIDASE CATALYTIC ANTIBODY 28B4 | CATALYTIC ANTIBODY, GERMLINE ANTIBODY, SULFIDE OXIDASE, IMMUNE SYSTEM
1fl6:B (SER120) to (PRO147) THE HAPTEN COMPLEXED GERMLINE PRECURSOR TO SULFIDE OXIDASE CATALYTIC ANTIBODY 28B4 | CATALYTIC ANTIBODY, GERMLINE ANTIBODY, SULFIDE OXIDASE, IMMUNE SYSTEM
3hj3:A (ASN250) to (ASP273) CRYSTAL STRUCTURE OF THE CHTS-DHFR F207A NON-ACTIVE SITE MUTANT | TS, DHFR, ENZYME, CROSSOVER, NON-ACTIVE SITE, OXIDOREDUCTASE
3hj3:C (ASN250) to (ASP273) CRYSTAL STRUCTURE OF THE CHTS-DHFR F207A NON-ACTIVE SITE MUTANT | TS, DHFR, ENZYME, CROSSOVER, NON-ACTIVE SITE, OXIDOREDUCTASE
4k3y:C (PHE121) to (GLY139) CRYSTAL STRUCTURE OF A SUBTYPE N11 NEURAMINIDASE-LIKE PROTEIN OF A/FLAT-FACED BAT/PERU/033/2010 (H18N11) | INFLUENZA VIRUS, NEURAMINIDASE-LIKE, N11, BETA PROPELLER, VIRAL PROTEIN
1fnt:K (ILE2) to (ARG22) CRYSTAL STRUCTURE OF THE 20S PROTEASOME FROM YEAST IN COMPLEX WITH THE PROTEASOME ACTIVATOR PA26 FROM TRYPANOSOME BRUCEI AT 3.2 ANGSTROMS RESOLUTION | MULTICATALYTIC PROTEINASE, 20S PROTEASOME, PROTEIN DEGRADATION, ANTIGEN PROCESSING, PROTEASE, PROTEASOME ACTIVATOR, CELL ADHESION, INTERFERON INDUCTION, HYDROLASE/HYDROLASE ACTIVATOR COMPLEX
1fnt:Y (ILE2) to (ARG22) CRYSTAL STRUCTURE OF THE 20S PROTEASOME FROM YEAST IN COMPLEX WITH THE PROTEASOME ACTIVATOR PA26 FROM TRYPANOSOME BRUCEI AT 3.2 ANGSTROMS RESOLUTION | MULTICATALYTIC PROTEINASE, 20S PROTEASOME, PROTEIN DEGRADATION, ANTIGEN PROCESSING, PROTEASE, PROTEASOME ACTIVATOR, CELL ADHESION, INTERFERON INDUCTION, HYDROLASE/HYDROLASE ACTIVATOR COMPLEX
3hkb:C (PHE52) to (LEU70) TUBULIN: RB3 STATHMIN-LIKE DOMAIN COMPLEX | ALPHA-TUBULIN, BETA-TUBULIN, GTPASE, MICROTUBULE, STATHMIN, TUBULIN, CELL CYCLE
2v5c:A (LEU162) to (VAL179) FAMILY 84 GLYCOSIDE HYDROLASE FROM CLOSTRIDIUM PERFRINGENS, 2.1 ANGSTROM STRUCTURE | GLYCOSIDASE, CLOSTRIDIUM PERFRINGENS, GH84, GH84C, HYDROLASE, COILED COIL, FAMILY 84 GLYCOSIDE HYDROLASE, CARBOHYDRATE BINDING MODULE
3hkd:A (PHE52) to (LEU70) TUBULIN-TN16 : RB3 STATHMIN-LIKE DOMAIN COMPLEX | ALPHA-TUBULIN, BETA-TUBULIN, COLCHICINE DOMAIN, GTPASE, MICROTUBULE, STATHMIN, TUBULIN, CELL CYCLE
3hkd:C (PHE52) to (LEU70) TUBULIN-TN16 : RB3 STATHMIN-LIKE DOMAIN COMPLEX | ALPHA-TUBULIN, BETA-TUBULIN, COLCHICINE DOMAIN, GTPASE, MICROTUBULE, STATHMIN, TUBULIN, CELL CYCLE
3hke:C (PHE52) to (LEU70) TUBULIN-T138067: RB3 STATHMIN-LIKE DOMAIN COMPLEX | ALPHA-TUBULIN, BETA-TUBULIN, COLCHICINE DOMAIN, COVALENT BINDING, GTPASE, MICROTUBULE, STATHMIN, TUBULIN, CELL CYCLE
2ewr:A (GLY81) to (GLU101) CRYSTAL STRUCTURE OF A PUTATIVE NUCLEOTIDYLTRANSFERASE (TM1012) FROM THERMOTOGA MARITIMA AT 1.60 A RESOLUTION | PUTATIVE NUCLEOTIDYLTRANSFERASE, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, TRANSFERASE
2v5s:B (LYS220) to (PHE239) STRUCTURAL BASIS FOR DSCAM ISOFORM SPECIFICITY | DOWN SYNDROME, IMMUNOGLOBULIN DOMAIN, CELL ADHESION, MEMBRANE, DEVELOPMENTAL PROTEIN
2exe:A (GLU295) to (GLY322) CRYSTAL STRUCTURE OF THE PHOSPHORYLATED CLK3 | DUAL-SPECIFICITY KINASE, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, TRANSFERASE
1fq9:C (LYS164) to (THR183) CRYSTAL STRUCTURE OF A TERNARY FGF2-FGFR1-HEPARIN COMPLEX | I-SET SUBGROUP WITHIN THE IMMUNOGLOBULIN SUPERFAMILY, B-TREFOIL FOLD, GROWTH FACTOR-GROWTH FACTOR RECEPTOR COMPLEX
1fq9:D (LYS164) to (THR183) CRYSTAL STRUCTURE OF A TERNARY FGF2-FGFR1-HEPARIN COMPLEX | I-SET SUBGROUP WITHIN THE IMMUNOGLOBULIN SUPERFAMILY, B-TREFOIL FOLD, GROWTH FACTOR-GROWTH FACTOR RECEPTOR COMPLEX
2f16:L (THR2) to (THR22) CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH BORTEZOMIB | BETA-SANDWICH FLANKED BY HELICES, COMPLEX STRUCTURE COVALENTLY BOUND TO THE SYNTHETIC INIHIBTOR BORTEZOMIB, HYDROLASE
2f16:Z (THR2) to (THR22) CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH BORTEZOMIB | BETA-SANDWICH FLANKED BY HELICES, COMPLEX STRUCTURE COVALENTLY BOUND TO THE SYNTHETIC INIHIBTOR BORTEZOMIB, HYDROLASE
2v9c:A (THR119) to (ILE142) X-RAY CRYSTALLOGRAPHIC STRUCTURE OF A PSEUDOMONAS AERUGINOSA AZOREDUCTASE IN COMPLEX WITH METHYL RED. | FMN, NAD, FLAVODOXIN, FLAVOPROTEIN, OXIDOREDUCTASE, NADPH-DEPENDENT, FLAVIN MONONUCLEOTIDE
1rhh:B (SER120) to (PRO147) CRYSTAL STRUCTURE OF THE BROADLY HIV-1 NEUTRALIZING FAB X5 AT 1.90 ANGSTROM RESOLUTION | FAB, ANTIBODY, X5, HIV-1, BROADLY NEUTRALIZING, IMMUNE SYSTEM
2vag:A (ASP300) to (GLY327) CRYSTAL STRUCTURE OF DI-PHOSPHORYLATED HUMAN CLK1 IN COMPLEX WITH A NOVEL SUBSTITUTED INDOLE INHIBITOR | SERINE/THREONINE-PROTEIN KINASE, TYROSINE-PROTEIN KINASE, NUCLEUS, TRANSFERASE
4yw8:A (ASP311) to (VAL335) STRUCTURE OF RAT CYTOSOLIC PEPCK IN COMPLEX WITH 3-MERCAPTOPICOLINIC ACID | KINASE, GLUCONEOGENESIS, LYASE, TRANSFERASE
4yw9:A (ASP311) to (VAL335) STRUCTURE OF RAT CYTOSOLIC PEPCK IN COMPLEX WITH 3-MERCAPTOPICOLINIC ACID AND GTP | KINASE, GLUCONEOGENESIS, LYASE, TRANSFERASE
4ywg:I (SER120) to (PRO147) CRYSTAL STRUCTURE OF 830A IN COMPLEX WITH V1V2 | HIV-1 GP120, THE V1V2 REGION, ANTIBODY, COMPLEX STRUCTURE, VIRAL PROTEIN-IMMUNE SYSTEM COMPLEX
1fwa:C (ASP431) to (SER493) KLEBSIELLA AEROGENES UREASE, C319A VARIANT AT PH 7.5 | HYDROLASE(UREA AMIDO), MUTANT, NICKEL METALLOENZYME, HYDROLASE
1fwb:C (ASP431) to (SER493) KLEBSIELLA AEROGENES UREASE, C319A VARIANT AT PH 6.5 | HYDROLASE(UREA AMIDO), MUTANT, NICKEL METALLOENZYME, HYDROLASE
1fwd:C (ASP431) to (SER493) KLEBSIELLA AEROGENES UREASE, C319A VARIANT AT PH 9.4 | HYDROLASE(UREA AMIDO), MUTANT, NICKEL METALLOENZYME, HYDROLASE
1fwc:C (ASP431) to (SER493) KLEBSIELLA AEROGENES UREASE, C319A VARIANT AT PH 8.5 | HYDROLASE(UREA AMIDO), MUTANT, NICKEL METALLOENZYME, HYDROLASE
1fwe:C (ASP431) to (SER493) KLEBSIELLA AEROGENES UREASE, C319A VARIANT WITH ACETOHYDROXAMIC ACID (AHA) BOUND | HYDROLASE(UREA AMIDO), MUTANT, INHIBITOR-BOUND, NICKEL METALLOENZYME, HYDROLASE
1fwf:C (ASP431) to (SER493) KLEBSIELLA AEROGENES UREASE, C319D VARIANT | HYDROLASE(UREA AMIDO), MUTANT, NICKEL METALLOENZYME, HYDROLASE
1fwg:C (ASP431) to (SER493) KLEBSIELLA AEROGENES UREASE, C319S VARIANT | HYDROLASE(UREA AMIDO), MUTANT, NICKEL METALLOENZYME, HYDROLASE
1fwh:C (ASP431) to (SER493) KLEBSIELLA AEROGENES UREASE, C319Y VARIANT | HYDROLASE(UREA AMIDO), MUTANT, NICKEL METALLOENZYME, HYDROLASE
1fwi:C (ASP431) to (SER493) KLEBSIELLA AEROGENES UREASE, H134A VARIANT | HYDROLASE(UREA AMIDO), MUTANT, NICKEL METALLOENZYME, HYDROLASE
1fwj:C (ASP431) to (SER493) KLEBSIELLA AEROGENES UREASE, NATIVE | HYDROLASE(UREA AMIDO), NICKEL METALLOENZYME, HYDROLASE
4kaq:H (SER128) to (PRO155) STRUCTURE OF RITUXIMAB FAB | MONOCLONAL ANTIBODY, IMMUNE SYSTEM
2f5k:A (LYS32) to (LYS64) CRYSTAL STRUCTURE OF THE CHROMO DOMAIN OF HUMAN MRG15 | BETA BARREL, GENE REGULATION
2f5k:B (LYS32) to (LYS64) CRYSTAL STRUCTURE OF THE CHROMO DOMAIN OF HUMAN MRG15 | BETA BARREL, GENE REGULATION
2f5k:E (LYS32) to (LYS64) CRYSTAL STRUCTURE OF THE CHROMO DOMAIN OF HUMAN MRG15 | BETA BARREL, GENE REGULATION
3um8:A (ASN338) to (ASP361) WILD-TYPE PLASMODIUM FALCIPARUM DHFR-TS COMPLEXED WITH CYCLOGUANIL AND NADPH | MALARIAL DHFR-TS, CYCLOGUANIL, ANTIFOLATE, NADPH, OXIDOREDUCTASE, TRANSFERASE-INHIBITOR COMPLEX
1fxh:B (ASN178) to (GLN200) MUTANT OF PENICILLIN ACYLASE IMPAIRED IN CATALYSIS WITH PHENYLACETIC ACID IN THE ACTIVE SITE | NTN-HYDROLASE FOLD
1fxv:B (SER1) to (PRO29) PENICILLIN ACYLASE MUTANT IMPAIRED IN CATALYSIS WITH PENICILLIN G IN THE ACTIVE SITE | NTN-HYDROLASE FOLD
2f74:A (THR190) to (PRO210) MURINE MHC CLASS I H-2DB IN COMPLEX WITH HUMAN B2-MICROGLOBULIN AND LCMV-DERIVED IMMUNODMINANT PEPTIDE GP33 | MURINE MHC, LCMV, RECEPTOR BINDING, BETA2-MICROGLOBULIN, IMMUNE SYSTEM
3un4:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH PR-957 (MORPHOLINE) | PROTEASOME, ANTIGEN PRESENTATION, DRUG DEVELOPMENT, PROTEIN DEGRADATION, HYDROLASE -HYDROLASE-INHIBITOR COMPLEX, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3un4:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH PR-957 (MORPHOLINE) | PROTEASOME, ANTIGEN PRESENTATION, DRUG DEVELOPMENT, PROTEIN DEGRADATION, HYDROLASE -HYDROLASE-INHIBITOR COMPLEX, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3un8:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH PR-957 (EPOXIDE) | PROTEASOME, ANTIGEN PRESENTATION, DRUG DEVELOPMENT, PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBTIOR COMPLEX
3un8:M (THR9) to (GLY31) YEAST 20S PROTEASOME IN COMPLEX WITH PR-957 (EPOXIDE) | PROTEASOME, ANTIGEN PRESENTATION, DRUG DEVELOPMENT, PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBTIOR COMPLEX
3un8:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH PR-957 (EPOXIDE) | PROTEASOME, ANTIGEN PRESENTATION, DRUG DEVELOPMENT, PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBTIOR COMPLEX
1fza:C (GLY352) to (PRO388) CRYSTAL STRUCTURE OF FIBRINOGEN FRAGMENT D | BLOOD COAGULATION, PLASMA, PLATELET, FIBRINOGEN, FIBRIN
1fza:F (GLY352) to (PRO388) CRYSTAL STRUCTURE OF FIBRINOGEN FRAGMENT D | BLOOD COAGULATION, PLASMA, PLATELET, FIBRINOGEN, FIBRIN
1fzd:A (GLY806) to (PRO843) STRUCTURE OF RECOMBINANT ALPHAEC DOMAIN FROM HUMAN FIBRINOGEN-420 | BLOOD COAGULATION, FIBRINOGEN-420, ALPHAEC DOMAIN, FIBRINOGEN RELATED DOMAIN, GLYCOSYLATED PROTEIN
1g0u:L (THR2) to (THR22) A GATED CHANNEL INTO THE PROTEASOME CORE PARTICLE | PROTEASOME, UBIQUITIN, DEGRADATION, PROTEASE, NTN-HYDROLASE
1g0u:Z (THR2) to (THR22) A GATED CHANNEL INTO THE PROTEASOME CORE PARTICLE | PROTEASOME, UBIQUITIN, DEGRADATION, PROTEASE, NTN-HYDROLASE
1g0u:2 (THR1) to (THR22) A GATED CHANNEL INTO THE PROTEASOME CORE PARTICLE | PROTEASOME, UBIQUITIN, DEGRADATION, PROTEASE, NTN-HYDROLASE
2f9z:C (GLY8) to (SER26) COMPLEX BETWEEN THE CHEMOTAXIS DEAMIDASE CHED AND THE CHEMOTAXIS PHOSPHATASE CHEC FROM THERMOTOGA MARITIMA | BACTERIAL CHEMOTAXIS, SIGNAL TRANSDUCTION, RECEPTOR DEAMIDASE, ASPARTYL PHOSPHATASE, PROTEIN COMPLEX, RECIPROCAL REGULATION, SIGNALING PROTEIN
1g13:B (PHE3) to (PRO30) HUMAN GM2 ACTIVATOR STRUCTURE | BETA CUP, LIGAND BINDING PROTEIN
1g13:C (PHE3) to (PRO30) HUMAN GM2 ACTIVATOR STRUCTURE | BETA CUP, LIGAND BINDING PROTEIN
4kf0:A (GLU430) to (LYS452) STRUCTURE OF THE A82F P450 BM3 HEME DOMAIN | P450, MONOOXYGENASE, OXIDOREDUCTASE
4kf0:B (GLU430) to (LYS452) STRUCTURE OF THE A82F P450 BM3 HEME DOMAIN | P450, MONOOXYGENASE, OXIDOREDUCTASE
2fak:I (GLY-1) to (SER22) CRYSTAL STRUCTURE OF SALINOSPORAMIDE A IN COMPLEX WITH THE YEAST 20S PROTEASOME | PROTEASOME, UBIQUITIN, DRUG DESIGN, INHIBITOR, PROTEASE, HYDROLASE
2fak:L (THR2) to (THR22) CRYSTAL STRUCTURE OF SALINOSPORAMIDE A IN COMPLEX WITH THE YEAST 20S PROTEASOME | PROTEASOME, UBIQUITIN, DRUG DESIGN, INHIBITOR, PROTEASE, HYDROLASE
2fak:N (THR1) to (THR22) CRYSTAL STRUCTURE OF SALINOSPORAMIDE A IN COMPLEX WITH THE YEAST 20S PROTEASOME | PROTEASOME, UBIQUITIN, DRUG DESIGN, INHIBITOR, PROTEASE, HYDROLASE
2fak:W (GLY-1) to (SER22) CRYSTAL STRUCTURE OF SALINOSPORAMIDE A IN COMPLEX WITH THE YEAST 20S PROTEASOME | PROTEASOME, UBIQUITIN, DRUG DESIGN, INHIBITOR, PROTEASE, HYDROLASE
2fak:Z (THR2) to (THR22) CRYSTAL STRUCTURE OF SALINOSPORAMIDE A IN COMPLEX WITH THE YEAST 20S PROTEASOME | PROTEASOME, UBIQUITIN, DRUG DESIGN, INHIBITOR, PROTEASE, HYDROLASE
2fak:2 (THR1) to (THR22) CRYSTAL STRUCTURE OF SALINOSPORAMIDE A IN COMPLEX WITH THE YEAST 20S PROTEASOME | PROTEASOME, UBIQUITIN, DRUG DESIGN, INHIBITOR, PROTEASE, HYDROLASE
3une:p (THR1) to (THR22) MOUSE CONSTITUTIVE 20S PROTEASOME | 20S PROTEASOME COMPRISES 28 SUBUNITS, PROTEASE, CYTOSOL, HYDROLASE
3une:2 (THR11) to (GLU31) MOUSE CONSTITUTIVE 20S PROTEASOME | 20S PROTEASOME COMPRISES 28 SUBUNITS, PROTEASE, CYTOSOL, HYDROLASE
4kf2:A (GLU430) to (LYS452) STRUCTURE OF THE P4509 BM3 A82F F87V HEME DOMAIN | P450, MONOOXYGENASE, OXIDOREDUCTASE
4kf2:B (GLU430) to (LYS452) STRUCTURE OF THE P4509 BM3 A82F F87V HEME DOMAIN | P450, MONOOXYGENASE, OXIDOREDUCTASE
3unf:N (THR1) to (ALA22) MOUSE 20S IMMUNOPROTEASOME IN COMPLEX WITH PR-957 | PROTEASOME, ANTIGEN PRESENTATION, DRUG DEVELOPMENT, PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3unf:b (THR1) to (ALA22) MOUSE 20S IMMUNOPROTEASOME IN COMPLEX WITH PR-957 | PROTEASOME, ANTIGEN PRESENTATION, DRUG DEVELOPMENT, PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4z1l:N (THR1) to (THR22) YEAST 20S PROTEASOME IN COMPLEX WITH BELACTOSIN C DERIVATIVE 3 | HYDROLASE, PROTEASOME, INHIBITOR, BINDING ANALYSIS, LEAD STRUCTURE MOTIF, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4z1l:b (THR1) to (THR22) YEAST 20S PROTEASOME IN COMPLEX WITH BELACTOSIN C DERIVATIVE 3 | HYDROLASE, PROTEASOME, INHIBITOR, BINDING ANALYSIS, LEAD STRUCTURE MOTIF, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1rts:A (CYS37) to (ARG62) THYMIDYLATE SYNTHASE FROM RAT IN TERNARY COMPLEX WITH DUMP AND TOMUDEX | THYMIDYLATE SYNTHASE, METHYLTRANSFERASE, DUMP, TOMUDEX, ANTIFOLATE
1rts:B (CYS37) to (ARG62) THYMIDYLATE SYNTHASE FROM RAT IN TERNARY COMPLEX WITH DUMP AND TOMUDEX | THYMIDYLATE SYNTHASE, METHYLTRANSFERASE, DUMP, TOMUDEX, ANTIFOLATE
3unh:W (GLY8) to (ILE29) MOUSE 20S IMMUNOPROTEASOME | 20S PROTEASOME COMPRISES 28 SUBUNITS, PROTEASE, CYTOSOL, HYDROLASE
1g3i:G (THR1) to (LEU22) CRYSTAL STRUCTURE OF THE HSLUV PROTEASE-CHAPERONE COMPLEX | CHAPERONE/HYDROLASE
1g3i:H (THR1) to (LEU22) CRYSTAL STRUCTURE OF THE HSLUV PROTEASE-CHAPERONE COMPLEX | CHAPERONE/HYDROLASE
1g3i:I (THR1) to (LEU22) CRYSTAL STRUCTURE OF THE HSLUV PROTEASE-CHAPERONE COMPLEX | CHAPERONE/HYDROLASE
1g3i:J (THR1) to (LEU22) CRYSTAL STRUCTURE OF THE HSLUV PROTEASE-CHAPERONE COMPLEX | CHAPERONE/HYDROLASE
1g3i:K (THR1) to (LEU22) CRYSTAL STRUCTURE OF THE HSLUV PROTEASE-CHAPERONE COMPLEX | CHAPERONE/HYDROLASE
1g3i:L (THR1) to (LEU22) CRYSTAL STRUCTURE OF THE HSLUV PROTEASE-CHAPERONE COMPLEX | CHAPERONE/HYDROLASE
1g3i:M (ILE3) to (LEU22) CRYSTAL STRUCTURE OF THE HSLUV PROTEASE-CHAPERONE COMPLEX | CHAPERONE/HYDROLASE
1g3i:N (THR1) to (LEU22) CRYSTAL STRUCTURE OF THE HSLUV PROTEASE-CHAPERONE COMPLEX | CHAPERONE/HYDROLASE
1g3i:O (ILE3) to (LEU22) CRYSTAL STRUCTURE OF THE HSLUV PROTEASE-CHAPERONE COMPLEX | CHAPERONE/HYDROLASE
1g3i:P (THR1) to (LEU22) CRYSTAL STRUCTURE OF THE HSLUV PROTEASE-CHAPERONE COMPLEX | CHAPERONE/HYDROLASE
1g3i:Q (THR1) to (LEU22) CRYSTAL STRUCTURE OF THE HSLUV PROTEASE-CHAPERONE COMPLEX | CHAPERONE/HYDROLASE
1g3i:R (THR1) to (LEU22) CRYSTAL STRUCTURE OF THE HSLUV PROTEASE-CHAPERONE COMPLEX | CHAPERONE/HYDROLASE
1g65:L (THR2) to (THR22) CRYSTAL STRUCTURE OF EPOXOMICIN:20S PROTEASOME REVEALS A MOLECULAR BASIS FOR SELECTIVITY OF ALPHA,BETA-EPOXYKETONE PROTEASOME INHIBITORS | PROTEASOME, EPOXOMICIN, UBIQUITIN, NTN-HYDOLASE, PROTEASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
1g65:Z (THR2) to (THR22) CRYSTAL STRUCTURE OF EPOXOMICIN:20S PROTEASOME REVEALS A MOLECULAR BASIS FOR SELECTIVITY OF ALPHA,BETA-EPOXYKETONE PROTEASOME INHIBITORS | PROTEASOME, EPOXOMICIN, UBIQUITIN, NTN-HYDOLASE, PROTEASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
1g72:A (ASP410) to (ASP450) CATALYTIC MECHANISM OF QUINOPROTEIN METHANOL DEHYDROGENASE: A THEORETICAL AND X-RAY CRYSTALLOGRAPHIC INVESTIGATION | QUINOPROTEIN, OXIDOREDUCTASE
1g72:C (ASP410) to (ASP450) CATALYTIC MECHANISM OF QUINOPROTEIN METHANOL DEHYDROGENASE: A THEORETICAL AND X-RAY CRYSTALLOGRAPHIC INVESTIGATION | QUINOPROTEIN, OXIDOREDUCTASE
1ryp:M (GLY1) to (THR22) CRYSTAL STRUCTURE OF THE 20S PROTEASOME FROM YEAST AT 2.4 ANGSTROMS RESOLUTION | MULTICATALYTIC PROTEINASE, 20S PROTEASOME, PROTEIN DEGRADATION, ANTIGEN PROCESSING, HYDROLASE, PROTEASE
1ryp:1 (GLY1) to (THR22) CRYSTAL STRUCTURE OF THE 20S PROTEASOME FROM YEAST AT 2.4 ANGSTROMS RESOLUTION | MULTICATALYTIC PROTEINASE, 20S PROTEASOME, PROTEIN DEGRADATION, ANTIGEN PROCESSING, HYDROLASE, PROTEASE
4z4q:B (GLU1243) to (PRO1260) QUINAZOLINEDIONE(PD 0305970)-DNA CLEAVAGE COMPLEX OF TOPOISOMERASE IV FROM S. PNEUMONIAE | TOPOISOMERASE IV, CLEAVAGE COMPLEX, DNA, QUINOLONE, ISOMERASE
2vhi:A (THR292) to (PRO323) CRYSTAL STRUCTURE OF A PYRIMIDINE DEGRADING ENZYME FROM DROSOPHILA MELANOGASTER | HYDROLASE
2vhh:B (GLY291) to (PRO323) CRYSTAL STRUCTURE OF A PYRIMIDINE DEGRADING ENZYME FROM DROSOPHILA MELANOGASTER | HYDROLASE
2vhh:C (GLY291) to (PRO323) CRYSTAL STRUCTURE OF A PYRIMIDINE DEGRADING ENZYME FROM DROSOPHILA MELANOGASTER | HYDROLASE
2vhh:D (GLY291) to (PRO323) CRYSTAL STRUCTURE OF A PYRIMIDINE DEGRADING ENZYME FROM DROSOPHILA MELANOGASTER | HYDROLASE
3hpj:A (HIS188) to (PRO210) HUMAN CLASS I MHC HLA-A2 IN COMPLEX WITH THE WT-1 (126-134) PEPTIDE | WT-1, WT1, WT126 PEPTIDE, NONAPEPTIDE, MHC CLASS I, HLA-A2, CANCER VACCINE, DISULFIDE BOND, GLYCOPROTEIN, HOST-VIRUS INTERACTION, IMMUNE RESPONSE, MEMBRANE, MHC I, PHOSPHOPROTEIN, TRANSMEMBRANE, DISEASE MUTATION, GLYCATION, IMMUNOGLOBULIN DOMAIN, PYRROLIDONE CARBOXYLIC ACID, SECRETED, IMMUNE SYSTEM
4z5r:K (SER120) to (PRO147) RONTALIZUMAB FAB BOUND TO INTERFERON-A2 | ANTIBODY, INTERFERON, CYTOKINE-IMMUNE SYSTEM COMPLEX
2fib:A (GLY352) to (PRO388) RECOMBINANT HUMAN GAMMA-FIBRINOGEN CARBOXYL TERMINAL FRAGMENT (RESIDUES 143-411) COMPLEXED TO THE PEPTIDE GLY- PRO-ARG-PRO AT PH 6.0 | FIBRINOGEN, BLOOD COAGULATION, FIBRIN POLYMERIZATION, COMPLEX (BLOOD COAGULATION/PEPTIDE)
2fjh:H (SER128) to (PRO155) STRUCTURE OF THE B20-4 FAB, A PHAGE DERIVED FAB FRAGMENT, IN COMPLEX WITH VEGF | VEGF, FAB, PROTEIN FAB COMPLEX, CYSTINE KNOT, HORMONE-GROWTH FACTOR- IMMUNE SYSTEM COMPLEX
1gan:A (HIS16) to (LEU43) COMPLEX OF TOAD OVARY GALECTIN WITH N-ACETYLGALACTOSE | S-LECTIN, CARBOHYDRATE BINDING, LECTIN
1gan:B (CYS17) to (LEU43) COMPLEX OF TOAD OVARY GALECTIN WITH N-ACETYLGALACTOSE | S-LECTIN, CARBOHYDRATE BINDING, LECTIN
3utz:B (SER126) to (PRO153) ENDOGENOUS-LIKE INHIBITORY ANTIBODIES TARGETING ACTIVATED METALLOPROTEINASE MOTIFS SHOW THERAPEUTIC POTENTIAL | STRUCTURAL GENOMICS, ISRAEL STRUCTURAL PROTEOMICS CENTER, ISPC, FAB DOMAIN, IMMUNE SYSTEM
3utz:F (SER126) to (PRO153) ENDOGENOUS-LIKE INHIBITORY ANTIBODIES TARGETING ACTIVATED METALLOPROTEINASE MOTIFS SHOW THERAPEUTIC POTENTIAL | STRUCTURAL GENOMICS, ISRAEL STRUCTURAL PROTEOMICS CENTER, ISPC, FAB DOMAIN, IMMUNE SYSTEM
4z76:D (HIS188) to (PRO210) WEAK TCR BINDING TO AN UNSTABLE INSULIN EPITOPE DRIVES TYPE 1 DIABETES | IMMUNOGLOBULIN, H-2KD, TYPE 1 DIABETES, IMMUNE SYSTEM
3hr5:L (ALA89) to (PRO118) M1PRIME PEPTIDE FROM IGE BOUND BY HUMANIZED ANTIBODY 47H4 FAB | FAB-PEPTIDE COMPLEX, IMMUNE SYSTEM
3hr5:J (SER124) to (PRO151) M1PRIME PEPTIDE FROM IGE BOUND BY HUMANIZED ANTIBODY 47H4 FAB | FAB-PEPTIDE COMPLEX, IMMUNE SYSTEM
1s3o:B (ILE98) to (PHE123) HUMAN MITOCHONDRIAL SINGLE STRAND DNA BINDING PROTEIN (HMSSB) | OB FOLD, DNA BINDING PROTEIN
3uzr:A (MSE198) to (GLY217) CRYSTAL STRUCTURE OF AMINOGLYCOSIDE PHOSPHOTRANSFERASE APH(2'')-IB, APO FORM | STRUCTURAL GENOMICS, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID, EUKARYOTIC PROTEIN KINASE-LIKE FOLD, AMINOGLYCOSIDE PHOSPHOTRANSFERASE, TRANSFERASE, ANTIBIOTIC RESISTANCE, CYTOPLASMIC, INTRACELLULAR
3hvd:B (SER402) to (ALA423) THE PROTECTIVE ANTIGEN COMPONENT OF ANTHRAX TOXIN FORMS FUNCTIONAL OCTAMERIC COMPLEXES | BACILLUS ANTHRACIS, ANTHRAX PROTECTIVE ANTIGEN, OCTAMER, XRAY-CRYSTALLOGRAPHY, TRANSPORT PROTEIN, TOXIN
3hvd:D (SER402) to (ALA423) THE PROTECTIVE ANTIGEN COMPONENT OF ANTHRAX TOXIN FORMS FUNCTIONAL OCTAMERIC COMPLEXES | BACILLUS ANTHRACIS, ANTHRAX PROTECTIVE ANTIGEN, OCTAMER, XRAY-CRYSTALLOGRAPHY, TRANSPORT PROTEIN, TOXIN
3hvd:F (SER402) to (ALA423) THE PROTECTIVE ANTIGEN COMPONENT OF ANTHRAX TOXIN FORMS FUNCTIONAL OCTAMERIC COMPLEXES | BACILLUS ANTHRACIS, ANTHRAX PROTECTIVE ANTIGEN, OCTAMER, XRAY-CRYSTALLOGRAPHY, TRANSPORT PROTEIN, TOXIN
3hvd:H (SER402) to (ALA423) THE PROTECTIVE ANTIGEN COMPONENT OF ANTHRAX TOXIN FORMS FUNCTIONAL OCTAMERIC COMPLEXES | BACILLUS ANTHRACIS, ANTHRAX PROTECTIVE ANTIGEN, OCTAMER, XRAY-CRYSTALLOGRAPHY, TRANSPORT PROTEIN, TOXIN
1s7u:D (HIS188) to (PRO210) CRYSTAL STRUCTURES OF THE MURINE CLASS I MAJOR HISTOCOMPATIBILITY COMPLEX H-2DB IN COMPLEX WITH LCMV-DERIVED GP33 INDEX PEPTIDE AND THREE OF ITS ESCAPE VARIANTS | LCMV, MHC CLASS I, IMMUNE ESCAPE, IMMUNE SYSTEM
1s7u:G (LYS186) to (PRO210) CRYSTAL STRUCTURES OF THE MURINE CLASS I MAJOR HISTOCOMPATIBILITY COMPLEX H-2DB IN COMPLEX WITH LCMV-DERIVED GP33 INDEX PEPTIDE AND THREE OF ITS ESCAPE VARIANTS | LCMV, MHC CLASS I, IMMUNE ESCAPE, IMMUNE SYSTEM
1s7u:J (LYS186) to (PRO210) CRYSTAL STRUCTURES OF THE MURINE CLASS I MAJOR HISTOCOMPATIBILITY COMPLEX H-2DB IN COMPLEX WITH LCMV-DERIVED GP33 INDEX PEPTIDE AND THREE OF ITS ESCAPE VARIANTS | LCMV, MHC CLASS I, IMMUNE ESCAPE, IMMUNE SYSTEM
1s7w:G (HIS188) to (PRO210) CRYSTAL STRUCTURES OF THE MURINE CLASS I MAJOR HISTOCOMPATIBILITY COMPLEX H-2DB IN COMPLEX WITH LCMV-DERIVED GP33 INDEX PEPTIDE AND THREE OF ITS ESCAPE VARIANTS | LCMV, MHC CLASS I, IMMUNE ESCAPE, IMMUNE SYSTEM
1s7x:A (HIS188) to (PRO210) CRYSTAL STRUCTURES OF THE MURINE CLASS I MAJOR HISTOCOMPATIBILITY COMPLEX H-2DB IN COMPLEX WITH LCMV- DERIVED GP33 INDEX PEPTIDE AND THREE OF ITS ESCAPE VARIANTS | LCMV, MHC CLASS I, IMMUNE ESCAPE, IMMUNE SYSTEM
1s7x:J (HIS188) to (PRO210) CRYSTAL STRUCTURES OF THE MURINE CLASS I MAJOR HISTOCOMPATIBILITY COMPLEX H-2DB IN COMPLEX WITH LCMV- DERIVED GP33 INDEX PEPTIDE AND THREE OF ITS ESCAPE VARIANTS | LCMV, MHC CLASS I, IMMUNE ESCAPE, IMMUNE SYSTEM
4knz:B (GLU14) to (ASN37) THYMIDYLATE SYNTHASE TERNARY COMPLEX WITH DUMP AND CB3717 | ALPHA/BETA PROTEIN, METHYLTRANSFERASE, METHYLENETETRAHYDROFOLATE, ANTIFOLATE, TRANSFERASE
4ko7:C (VAL5) to (ASP23) INVESTIGATING THE FUNCTIONAL SIGNIFICANCE OF THE INTERLOCKED PAIR STRUCTURAL DETERMINANTS IN PSEUDOMONAS AERUGINOSA AZURIN (V31I/W48F/V95I) | CUPREDOXIN FOLD, COMPUTATIONAL PROTEIN DESIGN, COPPER BINDING, ELECTRON TRANSPORT
3hye:Z (GLY1) to (THR22) CRYSTAL STRUCTURE OF 20S PROTEASOME IN COMPLEX WITH HYDROXYLATED SALINOSPORAMIDE | CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, PROTEASOME, THREONINE PROTEASE, ISOPEPTIDE BOND, UBL CONJUGATION, ZYMOGEN
2vq0:B (LEU232) to (GLU260) CAPSID STRUCTURE OF SESBANIA MOSAIC VIRUS COAT PROTEIN DELETION MUTANT RCP(DELTA 48 TO 59) | CAPSID PROTEIN, SESBANIA MOSAIC VIRUS, VIRION, BETA-ANNULUS, COAT PROTEIN, VIRUS ASSEMBLY, VIRAL PROTEIN
2vq0:C (PRO229) to (GLU260) CAPSID STRUCTURE OF SESBANIA MOSAIC VIRUS COAT PROTEIN DELETION MUTANT RCP(DELTA 48 TO 59) | CAPSID PROTEIN, SESBANIA MOSAIC VIRUS, VIRION, BETA-ANNULUS, COAT PROTEIN, VIRUS ASSEMBLY, VIRAL PROTEIN
1slv:A (GLY19) to (LEU55) RAT ANIONIC N143H, E151H TRYPSIN COMPLEXED TO A86H ECOTIN; COPPER- BOUND | SERINE PROTEASE, INHIBITOR, COMPLEX, METAL BINDING SITES, PROTEIN ENGINEERING, PROTEASE-SUBSTRATE INTERACTIONS, METALLOPROTEINS, COMPLEX (SERINE PROTEASE-INHIBITOR) COMPLEX
1slw:A (GLY19) to (LEU55) RAT ANIONIC N143H, E151H TRYPSIN COMPLEXED TO A86H ECOTIN; NICKEL- BOUND | SERINE PROTEASE, INHIBITOR, COMPLEX, METAL BINDING SITES, PROTEIN ENGINEERING, PROTEASE-SUBSTRATE INTERACTIONS, METALLOPROTEINS, COMPLEX (SERINE PROTEASE-INHIBITOR) COMPLEX
1smi:A (GLU430) to (LYS452) A SINGLE MUTATION OF P450 BM3 INDUCES THE CONFORMATIONAL REARRANGEMENT SEEN UPON SUBSTRATE-BINDING IN WILD-TYPE ENZYME | MONOOXYGENASE; FATTY ACID OXYGENASE; CYTOCHROME P450; SUBSTRATE BINDING, OXIDOREDUCTASE
1smi:B (GLU430) to (LYS452) A SINGLE MUTATION OF P450 BM3 INDUCES THE CONFORMATIONAL REARRANGEMENT SEEN UPON SUBSTRATE-BINDING IN WILD-TYPE ENZYME | MONOOXYGENASE; FATTY ACID OXYGENASE; CYTOCHROME P450; SUBSTRATE BINDING, OXIDOREDUCTASE
1smv:A (PRO221) to (GLU252) PRIMARY STRUCTURE OF SESBANIA MOSAIC VIRUS COAT PROTEIN: ITS IMPLICATIONS TO THE ASSEMBLY AND ARCHITECTURE OF THE VIRUS | COAT PROTEIN (VIRAL), ICOSAHEDRAL VIRUS
3vcl:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA-B7 WITH THE HCMV PP65 PEPTIDE RPHERNGFTVL | CLASS I HISTOCOMPATIBILITY ANTIGEN, ANTIGEN PRESENTATION, T-CELL RECEPTOR, MEMBRANE, IMMUNE SYSTEM
2g8d:A (GLU16) to (ASP39) LACTOBACILLUS CASEI THYMIDYLATE SYNTHASE Y261W-DUMP COMPLEX | BETA SHEET, ALPHA/BETA PROTEIN, METHYLTRANSFERASE, DUMP COMPLEX, ACTIVE SITE MUTATION, TRANSFERASE
1gvm:A (PHE199) to (LYS222) CHOLINE BINDING DOMAIN OF THE MAJOR AUTOLYSIN (C-LYTA) FROM STREPTOCOCCUS PNEUMONIAE | CHOLINE-BINDING DOMAIN, CELL WALL ATTACHMENT
1gvm:C (LYS198) to (LYS222) CHOLINE BINDING DOMAIN OF THE MAJOR AUTOLYSIN (C-LYTA) FROM STREPTOCOCCUS PNEUMONIAE | CHOLINE-BINDING DOMAIN, CELL WALL ATTACHMENT
2vw9:A (LEU1079) to (PHE1104) SINGLE STRANDED DNA BINDING PROTEIN COMPLEX FROM HELICOBACTER PYLORI | DNA REPLICATION, SINGLE-STRANDED DNA, SINGLE-STRANDED DNA BINDING PROTEIN, OLIGONUCLEOTIDE/OLIGOSACCHARIDE BINDING FOLD, HELICOBACTER PYLORI, OB-FOLD, DNA DAMAGE, DNA REPAIR, DNA-BINDING PROTEIN
2vw9:B (LEU2079) to (MET2105) SINGLE STRANDED DNA BINDING PROTEIN COMPLEX FROM HELICOBACTER PYLORI | DNA REPLICATION, SINGLE-STRANDED DNA, SINGLE-STRANDED DNA BINDING PROTEIN, OLIGONUCLEOTIDE/OLIGOSACCHARIDE BINDING FOLD, HELICOBACTER PYLORI, OB-FOLD, DNA DAMAGE, DNA REPAIR, DNA-BINDING PROTEIN
2vwe:C (THR85) to (PRO112) CRYSTAL STRUCTURE OF VASCULAR ENDOTHELIAL GROWTH FACTOR-B IN COMPLEX WITH A NEUTRALIZING ANTIBODY FAB FRAGMENT | IMMUNE SYSTEM, GLYCOPROTEIN, CYSTEINE-KNOT, GROWTH FACTOR, VEGF-B, MITOGEN, SECRETED, ANGIOGENESIS, NEUTRALIZING ANTIBODY, HEPARIN-BINDING, ALTERNATIVE SPLICING
3i7u:A (GLY63) to (GLU89) CRYSTAL STRUCTURE OF AP4A HYDROLASE (AQ_158) FROM AQUIFEX AEOLICUS VF5 | NUDIX PROTEIN, DIADENOSINE POLYPHOSPHATE, AP4A, HYDROLASE, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI
4ky4:B (PRO572) to (HIS601) CRYSTAL STRUCTURE OF NON-CLASSICAL TS INHIBITOR 2 IN COMPLEX WITH TOXOPLASMA GONDII TS-DHFR | SYNTHASE, BIFUNCTIONAL, OXIDOREDUCTASE, TRANSFERASE
4ky4:D (PRO572) to (GLY602) CRYSTAL STRUCTURE OF NON-CLASSICAL TS INHIBITOR 2 IN COMPLEX WITH TOXOPLASMA GONDII TS-DHFR | SYNTHASE, BIFUNCTIONAL, OXIDOREDUCTASE, TRANSFERASE
4ky4:E (ILE573) to (GLY602) CRYSTAL STRUCTURE OF NON-CLASSICAL TS INHIBITOR 2 IN COMPLEX WITH TOXOPLASMA GONDII TS-DHFR | SYNTHASE, BIFUNCTIONAL, OXIDOREDUCTASE, TRANSFERASE
4ky4:F (ILE573) to (HIS601) CRYSTAL STRUCTURE OF NON-CLASSICAL TS INHIBITOR 2 IN COMPLEX WITH TOXOPLASMA GONDII TS-DHFR | SYNTHASE, BIFUNCTIONAL, OXIDOREDUCTASE, TRANSFERASE
4ky4:G (ILE573) to (GLY602) CRYSTAL STRUCTURE OF NON-CLASSICAL TS INHIBITOR 2 IN COMPLEX WITH TOXOPLASMA GONDII TS-DHFR | SYNTHASE, BIFUNCTIONAL, OXIDOREDUCTASE, TRANSFERASE
1gxw:A (THR6) to (THR34) THE 2.2 A RESOLUTION STRUCTURE OF THERMOLYSIN CRYSTALLIZED IN PRESENCE OF POTASSIUM THIOCYANATE | HYDROLASE, THERMOLYSIN, METALLOENDOPEPTIDASE, THIOCYANATE, SALTING-IN, METALLOPROTEASE
2vyu:A (GLY4) to (ILE29) CRYSTAL STRUCTURE OF CHOLINE BINDING PROTEIN F FROM STREPTOCOCCUS PNEUMONIAE IN THE PRESENCE OF A PEPTIDOGLYCAN ANALOGUE (TETRASACCHARIDE-PENTAPEPTIDE) | CHOLINE-BINDING PROTEIN, CBPF, PEPTIDOGLYCAN, CHOLINE-BINDING-PROTEIN, LIPID-BINDING PROTEIN
1h0h:K (LYS920) to (LYS976) TUNGSTEN CONTAINING FORMATE DEHYDROGENASE FROM DESULFOVIBRIO GIGAS | ELECTRON TRANSPORT, TUNGSTEN SELENIUM FORMATE DEHYDROGENASE, SELENOCYSTEINE, MOLYBDOPTERIN, MGD, IRON-SULPHUR CLUSTER, PERIPLASMIC
3vfs:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA B*3508LPEP-P5ALA , PEPTIDE MUTANT P5-ALA | HLA B*3508, EPSTEIN BARR VIRUS, TCR, T CELL, IMMUNE SYSTEM, ANTIGEN- PRESENTING MOLECULE
3vi2:B (CYS177) to (THR195) CRYSTAL STRUCTURE ANALYSIS OF PLASMODIUM FALCIPARUM OMP DECARBOXYLASE IN COMPLEX WITH INHIBITOR HMOA | OROTIDINE 5 F-MONOPHOSPHATE DECARBOXYLASE, LYASE-LYASE INHIBITOR COMPLEX
1h2g:B (ASN178) to (GLN200) ALTERED SUBSTRATE SPECIFICITY MUTANT OF PENICILLIN ACYLASE | AMIDOHYDROLASE, ANTIBIOTIC RESISTANCE, ALTERED SPECIFICITY, ZYMOGEN, HYDROLASE
3ib4:A (LYS6) to (PRO32) THE DOUBLE MUTANT OF BETA-2 MICROGLOBULIN K58P-W60G | AMYLOIDOSIS, BETA-SANDWICH, GLYCINE, PROLINE, MUTATION, DIALYSIS RELATED AMYLOIDOSIS, DE LOOP, DISEASE MUTATION, DISULFIDE BOND, GLYCATION, GLYCOPROTEIN, IMMUNE RESPONSE, IMMUNOGLOBULIN DOMAIN, MHC I, PYRROLIDONE CARBOXYLIC ACID, SECRETED, IMMUNE SYSTEM
2vzo:A (ARG335) to (ASP366) CRYSTAL STRUCTURE OF AMYCOLATOPSIS ORIENTALIS EXO- CHITOSANASE CSXA | GH2, CSXA, PNP-GLUCOSAMINE, GLYCOSIDE HYDROLASE, EXO-BETA-D-GLUCOSAMINIDASE, HYDROLASE
2vzo:B (ARG335) to (PRO365) CRYSTAL STRUCTURE OF AMYCOLATOPSIS ORIENTALIS EXO- CHITOSANASE CSXA | GH2, CSXA, PNP-GLUCOSAMINE, GLYCOSIDE HYDROLASE, EXO-BETA-D-GLUCOSAMINIDASE, HYDROLASE
1h4h:C (CYS83) to (GLY102) OLIGOSACCHARIDE-BINDING TO FAMILY 11 XYLANASES: BOTH COVALENT INTERMEDIATE AND MUTANT-PRODUCT COMPLEXES DISPLAY 2,5B CONFORMATIONS AT THE ACTIVE-CENTRE | GLYCOSIDE HYDROLASE, XYLANASE, OLIGOSACCHARIDE, TRANSITION-STATE, INTERMEDIATE, MUTANT, BOAT CONFORMATION
2gpl:L (THR2) to (THR22) TMC-95 BASED BIPHENYL-ETHER MACROCYCLES: SPECIFIC PROTEASOME INHIBITORS | PROTEASOMAL SUBUNIT FOLD REPRESENTS AN ANTIPARALLEL BETA- SHEET FLANKED BY HELICES; NTN-HYDROLASE
2gpl:Z (THR2) to (THR22) TMC-95 BASED BIPHENYL-ETHER MACROCYCLES: SPECIFIC PROTEASOME INHIBITORS | PROTEASOMAL SUBUNIT FOLD REPRESENTS AN ANTIPARALLEL BETA- SHEET FLANKED BY HELICES; NTN-HYDROLASE
1h6f:A (GLY120) to (CYS140) HUMAN TBX3, A TRANSCRIPTION FACTOR RESPONSIBLE FOR ULNAR-MAMMARY SYNDROME , BOUND TO A PALINDROMIC DNA SITE | TRANSCRIPTION FACTOR, TBX3, T-BOX TRANSCRIPTION FACTOR, ULNAR-MAMMARY SYNDROME, HOLT-ORAM-SYNDROME, IG-FOLD, DNA-BINDING, REPRESSOR, NUCLEAR PROTEIN, DEVELOPMENTAL PROTEIN
1t7v:A (SER188) to (PRO212) ZN-ALPHA-2-GLYCOPROTEIN; BACULO-ZAG PEG 200 | MHC CLASS I HOMOLOG, PEG, LIPID BINDING PROTEIN
1t7w:A (SER188) to (PRO212) ZN-ALPHA-2-GLYCOPROTEIN; CHO-ZAG PEG 400 | MHC CLASS I HOMOLOG, LIPID BINDING PROTEIN
1t7y:A (SER188) to (PRO212) ZN-ALPHA-2-GLYCOPROTEIN; BACULO-ZAG PEG 200, NO GLYCEROL | MHC CLASS I HOMOLOG, LIPID BINDING PROTEIN
3ijh:C (TYR87) to (PRO112) STRUCTURE OF S67-27 IN COMPLEX WITH KO | ANTIBODY, KDO, CHLAMYDIA, LPS, FAB, CARBOHYDRATE, IMMUNE SYSTEM
3ijs:C (TYR87) to (PRO112) STRUCTURE OF S67-27 IN COMPLEX WITH TSBP | ANTIBODY, KDO, CHLAMYDIA, LPS, FAB, CARBOHYDRATE, IMMUNE SYSTEM
3ikc:C (TYR87) to (PRO112) STRUCTURE OF S67-27 IN COMPLEX WITH KDO(2.8)-7-O-METHYL-KDO | ANTIBODY, KDO, CHLAMYDIA, LPS, FAB, CARBOHYDRATE, IMMUNE SYSTEM
4lcc:C (LYS296) to (PRO320) CRYSTAL STRUCTURE OF A HUMAN MAIT TCR IN COMPLEX WITH A BACTERIAL ANTIGEN BOUND TO HUMANIZED BOVINE MR1 | IMMUNOGLOBULIN DOMAIN, MHC-CLASS I-LIKE, ANTIGEN PRESENTATION, ANTIGEN RECOGNITION, B VITAMINS METABOLITES, CELL MEMBRANE, IMMUNE SYSTEM
4zs7:H (SER129) to (PRO156) STRUCTURAL MIMICRY OF RECEPTOR INTERACTION BY ANTAGONISTIC IL-6 ANTIBODIES | INTERLEUKINE 6 COMPLEX, FAB FRAGMENT, DROMEDERY, IMMUNE SYSTEM
4ldg:A (ILE231) to (CYS253) CRYSTAL STRUCTURE OF CPSET8 FROM CRYPTOSPORIDIUM, CGD4_370 | SET DOMAIN, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, UNKNOWN FUNCTION
1tdb:A (THR281) to (TYR307) STRUCTURES OF THYMIDYLATE SYNTHASE WITH A C-TERMINAL DELETION: ROLE OF THE C-TERMINUS IN ALIGNMENT OF D/UMP AND CH2H4FOLATE | TRANSFERASE (METHYLTRANSFERASE)
3in0:D (VAL5) to (ASP23) CRYSTAL STRUCTURE OF THE F114P/M121Q VARIANT OF PSEUDOMONAS AERUGINOSA AZURIN IN THE CU(II) STATE | CUPREDOXIN, AZURIN, GREEK KEY, BETA BARREL, ELECTRON TRANSFER, COPPER, DISULFIDE BOND, ELECTRON TRANSPORT, METAL-BINDING, PERIPLASM, TRANSPORT
4len:A (ASP233) to (GLN254) CTX-M-9 IN COMPLEX WITH THE BROAD SPECTRUM INHIBITOR 3-(2- CARBOXYVINYL)BENZO(B)THIOPHENE-2-BORONIC ACID | BINDING SITES, STRUCTURE BASE DRUG DESIGN, DRUG DISCOVERY, MOLECULAR, ENZYME INHIBITORS, BETA LACTAMASES, BORONIC ACIDS, BROAD SPECTRUM, BACTERIAL RESISTANCE, DOUBLE PERTURBATION CYCLE ANALYSIS, THERMODYNAMICS, STRUCTURE ACTIVITY RELATIONSHIP, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3inu:H (SER120) to (PRO149) CRYSTAL STRUCTURE OF AN UNBOUND KZ52 NEUTRALIZING ANTI-EBOLAVIRUS ANTIBODY. | ANTIBODY FRAGMENT (FAB), IMMUNOGLOBULIN FOLD, IMMUNE SYSTEM
3inu:M (SER120) to (PRO149) CRYSTAL STRUCTURE OF AN UNBOUND KZ52 NEUTRALIZING ANTI-EBOLAVIRUS ANTIBODY. | ANTIBODY FRAGMENT (FAB), IMMUNOGLOBULIN FOLD, IMMUNE SYSTEM
1tg7:A (TYR45) to (GLU66) NATIVE STRUCTURE OF BETA-GALACTOSIDASE FROM PENICILLIUM SP. | TIM BARREL DOMAIN, GLYCOSIDE HYDROLASE, FAMILY GH35, GLYCOPROTEIN, PENICILLIUM, HYDROLASE
4zuv:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF EQUINE MHC I(EQCA-N*00602) IN COMPLEXED WITH EQUINE INFECTIOUS ANAEMIA VIRUS (EIAV) DERIVED PEPTIDE ENV-RW12 | LENTIVIRUS VACCINE, IMMUNE SYSTEM
4zv3:B (THR301) to (PRO318) CRYSTAL STRUCTURE OF THE N- AND C-TERMINAL DOMAINS OF MOUSE ACYL-COA THIOESTERASE 7 | THIOESTERASE, DOUBLE HOTDOG, INFLAMMATION, HYDROLASE
1tjj:B (PHE5) to (PRO32) HUMAN GM2 ACTIVATOR PROTEIN PAF COMPLEX | PLATELET ACTIVATING FACTOR, LIPID BINDING POCKET, BETA-CUP TOPOLOGY, PROTEIN DYNAMICS, SIGNALING PROTEIN
1hhj:A (HIS188) to (PRO210) THE ANTIGENIC IDENTITY OF PEPTIDE(SLASH)MHC COMPLEXES: A COMPARISON OF THE CONFORMATION OF FIVE PEPTIDES PRESENTED BY HLA-A2 | HISTOCOMPATIBILITY ANTIGEN
1hhj:D (HIS188) to (PRO210) THE ANTIGENIC IDENTITY OF PEPTIDE(SLASH)MHC COMPLEXES: A COMPARISON OF THE CONFORMATION OF FIVE PEPTIDES PRESENTED BY HLA-A2 | HISTOCOMPATIBILITY ANTIGEN
3irn:D (ASN252) to (SER273) TRYPANOSOMA CRUZI DIHYDROFOLATE REDUCTASE-THYMIDYLATE SYNTHASE COMPLEXED WITH NADPH AND CYCLOGUANIL | TRYPANOSOMA CRUZI,DHFR-TS ANTIFOLATE COMPLEX, METHYLTRANSFERASE, MULTIFUNCTIONAL ENZYME, NADP, NUCLEOTIDE BIOSYNTHESIS, ONE-CARBON METABOLISM, OXIDOREDUCTASE, TRANSFERASE
3iro:B (ASN252) to (SER273) TRYPANOSOMA CRUZI DIHYDROFOLATE REDUCTASE-THYMIDYLATE SYNTHASE COMPLEXED WITH NADPH AND Q-8 ANTIFOLATE | TRYPANOSOMA CRUZI, DHFR-TS ANTIFOLATE COMPLEX, METHYLTRANSFERASE, MULTIFUNCTIONAL ENZYME, NADP, NUCLEOTIDE BIOSYNTHESIS, ONE-CARBON METABOLISM, OXIDOREDUCTASE, TRANSFERASE
1tli:A (THR6) to (THR34) THERMOLYSIN (2% ISOPROPANOL SOAKED CRYSTALS) | HYDROLASE, METALLOPROTEINASE, ORGANIC SOLVENT
1tlp:E (THR6) to (THR34) CRYSTALLOGRAPHIC STRUCTURAL ANALYSIS OF PHOSPHORAMIDATES AS INHIBITORS AND TRANSITION-STATE ANALOGS OF THERMOLYSIN | METALLOPROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1tlx:A (THR6) to (THR34) THERMOLYSIN (NATIVE) | HYDROLASE, METALLOPROTEINASE, ORGANIC SOLVENT
1hlc:A (SER16) to (ASN43) X-RAY CRYSTAL STRUCTURE OF THE HUMAN DIMERIC S-LAC LECTIN, L-14-II, IN COMPLEX WITH LACTOSE AT 2.9 ANGSTROMS RESOLUTION | LECTIN
3vlb:A (MET349) to (GLY365) CRYSTAL STRUCTURE OF XEG-EDGP | CELL-WALL, PLANT PROTEIN-HYDROLASE COMPLEX
3vlb:C (MET349) to (GLY365) CRYSTAL STRUCTURE OF XEG-EDGP | CELL-WALL, PLANT PROTEIN-HYDROLASE COMPLEX
3vly:A (GLY355) to (GLN377) ASSIMILATORY NITRITE REDUCTASE (NII3) - N226K MUTANT - SO3 PARTIAL COMPLEX FROM TOBACCO LEAF | NII3 N226K MUTANT, SO3 PARTIAL COMPLEX, 3 ALPHA/BETA DOMAINS, REDUCTASE, OXIDOREDUCTASE
3vlz:A (GLY355) to (GLN377) ASSIMILATORY NITRITE REDUCTASE (NII3) - N226K MUTANT - SO3 FULL COMPLEX FROM TOBACCO LEAF | NII3 N226K MUTANT, SO3 FULL COMPLEX, 3 ALPHA/BETA DOMAINS, REDUCTASE, OXIDOREDUCTASE
1ts2:A (SER32) to (ASN65) T128A MUTANT OF TOXIC SHOCK SYNDROME TOXIN-1 FROM S. AUREUS | TOXIN, SUPERANTIGEN
1ts2:B (SER232) to (ASN265) T128A MUTANT OF TOXIC SHOCK SYNDROME TOXIN-1 FROM S. AUREUS | TOXIN, SUPERANTIGEN
1ts2:C (SER432) to (ASN465) T128A MUTANT OF TOXIC SHOCK SYNDROME TOXIN-1 FROM S. AUREUS | TOXIN, SUPERANTIGEN
1ts3:A (SER32) to (ASN65) H135A MUTANT OF TOXIC SHOCK SYNDROME TOXIN-1 FROM S. AUREUS | TOXIN, SUPERANTIGEN
1ts3:B (SER232) to (ASN265) H135A MUTANT OF TOXIC SHOCK SYNDROME TOXIN-1 FROM S. AUREUS | TOXIN, SUPERANTIGEN
1tsx:A (GLU16) to (ASP39) THYMIDYLATE SYNTHASE R179E MUTANT | TRANSFERASE, METHYLTRANSFERASE, NUCLEOTIDE BIOSYNTHESIS
4llf:A (GLY229) to (GLU256) CRYSTAL STRUCTURE OF CUCUMBER NECROSIS VIRUS | BETA BARREL, VIRUS, TOMBUSVIRUS, VIRAL BETA BARREL, VIRUS CAPSID, EXTRACELLULAR
4llf:A (ILE345) to (GLY360) CRYSTAL STRUCTURE OF CUCUMBER NECROSIS VIRUS | BETA BARREL, VIRUS, TOMBUSVIRUS, VIRAL BETA BARREL, VIRUS CAPSID, EXTRACELLULAR
4llf:B (GLY229) to (GLU256) CRYSTAL STRUCTURE OF CUCUMBER NECROSIS VIRUS | BETA BARREL, VIRUS, TOMBUSVIRUS, VIRAL BETA BARREL, VIRUS CAPSID, EXTRACELLULAR
4llf:E (GLY229) to (GLU256) CRYSTAL STRUCTURE OF CUCUMBER NECROSIS VIRUS | BETA BARREL, VIRUS, TOMBUSVIRUS, VIRAL BETA BARREL, VIRUS CAPSID, EXTRACELLULAR
4llf:F (GLY229) to (GLU256) CRYSTAL STRUCTURE OF CUCUMBER NECROSIS VIRUS | BETA BARREL, VIRUS, TOMBUSVIRUS, VIRAL BETA BARREL, VIRUS CAPSID, EXTRACELLULAR
4llf:H (GLY229) to (GLU256) CRYSTAL STRUCTURE OF CUCUMBER NECROSIS VIRUS | BETA BARREL, VIRUS, TOMBUSVIRUS, VIRAL BETA BARREL, VIRUS CAPSID, EXTRACELLULAR
4llf:K (GLY229) to (GLU256) CRYSTAL STRUCTURE OF CUCUMBER NECROSIS VIRUS | BETA BARREL, VIRUS, TOMBUSVIRUS, VIRAL BETA BARREL, VIRUS CAPSID, EXTRACELLULAR
4llf:K (ILE345) to (GLY360) CRYSTAL STRUCTURE OF CUCUMBER NECROSIS VIRUS | BETA BARREL, VIRUS, TOMBUSVIRUS, VIRAL BETA BARREL, VIRUS CAPSID, EXTRACELLULAR
4llf:L (GLY229) to (GLU256) CRYSTAL STRUCTURE OF CUCUMBER NECROSIS VIRUS | BETA BARREL, VIRUS, TOMBUSVIRUS, VIRAL BETA BARREL, VIRUS CAPSID, EXTRACELLULAR
4llf:N (GLY229) to (GLU256) CRYSTAL STRUCTURE OF CUCUMBER NECROSIS VIRUS | BETA BARREL, VIRUS, TOMBUSVIRUS, VIRAL BETA BARREL, VIRUS CAPSID, EXTRACELLULAR
4llf:N (ILE345) to (GLY360) CRYSTAL STRUCTURE OF CUCUMBER NECROSIS VIRUS | BETA BARREL, VIRUS, TOMBUSVIRUS, VIRAL BETA BARREL, VIRUS CAPSID, EXTRACELLULAR
4llf:O (GLY229) to (GLU256) CRYSTAL STRUCTURE OF CUCUMBER NECROSIS VIRUS | BETA BARREL, VIRUS, TOMBUSVIRUS, VIRAL BETA BARREL, VIRUS CAPSID, EXTRACELLULAR
4zzg:I (THR1) to (GLN22) YEAST 20S PROTEASOME IN COMPLEX WITH BLM-PEP ACTIVATOR | 20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE
4zzg:W (THR1) to (GLN22) YEAST 20S PROTEASOME IN COMPLEX WITH BLM-PEP ACTIVATOR | 20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE
3vr2:A (ILE40) to (SER66) CRYSTAL STRUCTURE OF NUCLEOTIDE-FREE A3B3 COMPLEX FROM ENTEROCOCCUS HIRAE V-ATPASE [EA3B3] | V-ATPASE, ENTEROCOCCUS HIRAE, ROTARY MOTOR, P-LOOP, HYDROLASE, NA(+)- ATPASE, ATP BINDING
3vr5:A (ILE40) to (SER66) CRYSTAL STRUCTURE OF NUCLEOTIDE-FREE ENTEROCOCCUS HIRAE V1-ATPASE [EV1(L)] | V-ATPASE, ENTEROCOCCUS HIRAE, ROTARY MOTOR, P-LOOP, HYDROLASE, NA(+)- ATPASE, ATP BINDING
4lly:A (SER126) to (PRO153) CRYSTAL STRUCTURE OF PERTUZUMAB CLAMBDA FAB WITH VARIABLE AND CONSTANT DOMAIN REDESIGNS (VRD2 AND CRD2) AT 1.6A | FAB, IMMUNE SYSTEM
4lly:C (SER126) to (PRO153) CRYSTAL STRUCTURE OF PERTUZUMAB CLAMBDA FAB WITH VARIABLE AND CONSTANT DOMAIN REDESIGNS (VRD2 AND CRD2) AT 1.6A | FAB, IMMUNE SYSTEM
2whz:A (THR6) to (THR34) DIPEPTIDE INHIBITORS OF THERMOLYSIN | HYDROLASE-INHIBITOR COMPLEX, DIPEPTIDE INHIBITORS, HYDROLASE
2wi0:A (THR6) to (THR34) DIPEPTIDE INHIBITORS OF THERMOLYSIN | HYDROLASE, METAL-BINDING
3vri:A (HIS188) to (PRO210) HLA-B*57:01-RVAQLENVYI IN COMPLEX WITH ABACAVIR | HUMAN LEUKOCYTE ANTIGEN, ANTIGEN PRESENTATION, IMMUNE SYSTEM, T-CELL RECEPTOR
3vrj:A (HIS188) to (PRO210) HLA-B*57:01-LTTKLTNTNI IN COMPLEX WITH ABACAVIR | HUMAN LEUKOCYTE ANTIGEN, ANTIGEN PRESENTATION, IMMUNE SYSTEM, T-CELL RECEPTOR
2wim:A (PRO123) to (SER141) CRYSTAL STRUCTURE OF NCAM2 IG1-3 | CELL MEMBRANE, CELL ADHESION, TRANSMEMBRANE, IMMUNOGLOBULIN DOMAIN
1twg:H (LEU111) to (ARG146) RNA POLYMERASE II COMPLEXED WITH CTP | TRANSCRIPTION, MRNA, MULTIPROTEIN COMPLEX, MOLECULAR MACHINE, ZINC MOTIFS
2wj7:D (LEU26) to (ASP46) HUMAN ALPHAB CRYSTALLIN | DESMIN-RELATED MYOPATHY, PHOSPHOPROTEIN, DISEASE MUTATION, EYE LENS PROTEIN, METHYLATION, POLYMORPHISM, GLYCOPROTEIN, CATARACT, OXIDATION, CHAPERONE, ACETYLATION
1tyv:A (GLY351) to (ASN378) STRUCTURE OF TAILSPIKE-PROTEIN | COMPLEX, VIRAL ADHESION PROTEIN, RECEPTOR, ENDOGLYCOSIDASE CARBOHYDRATE, CELL RECEPTOR, RECOGNITION, BINDING PROTEIN LIPOPOLYSACCHARIDE
1hxy:A (VAL89) to (PRO114) CRYSTAL STRUCTURE OF STAPHYLOCOCCAL ENTEROTOXIN H IN COMPLEX WITH HUMAN MHC CLASS II | COMPLEX, IMMUNE SYSTEM/TOXIN COMPLEX
2hpd:B (GLU430) to (LYS452) CRYSTAL STRUCTURE OF HEMOPROTEIN DOMAIN OF P450BM-3, A PROTOTYPE FOR MICROSOMAL P450'S | OXIDOREDUCTASE(OXYGENASE)
1hyt:A (THR6) to (THR34) RE-DETERMINATION AND REFINEMENT OF THE COMPLEX OF BENZYLSUCCINIC ACID WITH THERMOLYSIN AND ITS RELATION TO THE COMPLEX WITH CARBOXYPEPTIDASE A | HYDROLASE(METALLOPROTEINASE)
4lqi:I (GLY-1) to (SER22) YEAST 20S PROTEASOME IN COMPLEX WITH VIBRALACTONE | BETA-LACTONE, INHIBITOR, NATURAL PRODUCT, TARGET IDENTIFICATION, NTN- PROTEASE, CELLULAR PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4lqi:L (GLY0) to (THR21) YEAST 20S PROTEASOME IN COMPLEX WITH VIBRALACTONE | BETA-LACTONE, INHIBITOR, NATURAL PRODUCT, TARGET IDENTIFICATION, NTN- PROTEASE, CELLULAR PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4lqi:Z (GLY0) to (THR21) YEAST 20S PROTEASOME IN COMPLEX WITH VIBRALACTONE | BETA-LACTONE, INHIBITOR, NATURAL PRODUCT, TARGET IDENTIFICATION, NTN- PROTEASE, CELLULAR PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3vx7:A (SER118) to (ILE150) CRYSTAL STRUCTURE OF KLUYVEROMYCES MARXIANUS ATG7NTD-ATG10 COMPLEX | UBIQUITIN CONJUGATION, E1-E2 COMPLEX, LIGASE
3vx8:D (PHE137) to (ILE168) CRYSTAL STRUCTURE OF ARABIDOPSIS THALIANA ATG7NTD-ATG3 COMPLEX | E1-E2 COMPLEX, LIGASE
2wob:C (ALA102) to (GLY120) 3B' CARBOHYDRATE-BINDING MODULE FROM THE CEL9V GLYCOSIDE HYDROLASE FROM CLOSTRIDIUM THERMOCELLUM. ORTHORHOMBIC STRUCTURE | CELLULOSE DEGRADATION, HYDROLASE, GLYCOSIDE HYDROLASE
2wob:E (GLY103) to (GLY120) 3B' CARBOHYDRATE-BINDING MODULE FROM THE CEL9V GLYCOSIDE HYDROLASE FROM CLOSTRIDIUM THERMOCELLUM. ORTHORHOMBIC STRUCTURE | CELLULOSE DEGRADATION, HYDROLASE, GLYCOSIDE HYDROLASE
3vzh:A (GLN65) to (LEU96) CRYSTAL STRUCTURE OF CRISPR-ASSOCIATED PROTEIN | RRM, RIBONUCLEASE, NUCLEIC ACID, DNA BINDING PROTEIN
1i3r:H (THR124) to (PRO150) CRYSTAL STRUCTURE OF A MUTANT IEK CLASS II MHC MOLECULE | MHC CLASSII, IMMUNE SYSTEM
4ltc:L (THR11) to (THR31) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH ENONE CARMAPHYCIN ANALOGUE 6 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ltc:Z (THR11) to (THR31) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH ENONE CARMAPHYCIN ANALOGUE 6 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1i50:B (ILE912) to (ILE948) RNA POLYMERASE II CRYSTAL FORM II AT 2.8 A RESOLUTION | TRANSCRIPTION, MRNA, MULTIPROTEIN COMPLEX, MOLECULAR MACHINE, ZINC MOTIFS
3w2v:B (THR264) to (GLU292) CRYSTAL STRUCTURE OF THE CMR2DHD-CMR3 SUBCOMPLEX BOUND TO 3'-AMP | FERREDOXIN-LIKE FOLD, IMMUNE SYSTEM
3w2w:B (THR264) to (GLU292) CRYSTAL STRUCTURE OF THE CMR2DHD-CMR3 SUBCOMPLEX BOUND TO ATP | FERREDOXIN-LIKE FOLD, IMMUNE SYSTEM
5a3l:A (PHE89) to (VAL124) STRUCTURE OF CEA1A IN COMPLEX WITH N-ACETYLGLUCOSAMINE | CELL ADHESION, FUNGAL ADHESION, CHITIN ADHESION, PA14-DOMAIN, FLOCCULIN-RELATED
5a3m:A (PHE89) to (VAL124) STRUCTURE OF CEA1A IN COMPLEX WITH CHITOBIOSE | ADHESION PROTEIN, FUNGAL ADHESION, CHITIN ADHESION, PA14-DOMAIN, FLOCCULIN-RELATED
5a3y:A (THR6) to (THR34) SAD STRUCTURE OF THERMOLYSIN OBTAINED BY MULTI CRYSTAL DATA COLLECTION | HYDROLASE, MULTI CRYSTAL DATA COLLECTION, SYNCHROTRON SERIAL CRYSTALLOGRAPHY, SSX, SAD
1i7r:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF CLASS I MHC A2 IN COMPLEX WITH PEPTIDE P1058 | MHC FOLD, IMMUNE SYSTEM
1i7t:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF CLASS I MHC A2 IN COMPLEX WITH PEPTIDE P1049-5V | MHC FOLD, IMMUNE SYSTEM
1i7t:D (HIS188) to (PRO210) CRYSTAL STRUCTURE OF CLASS I MHC A2 IN COMPLEX WITH PEPTIDE P1049-5V | MHC FOLD, IMMUNE SYSTEM
2hyk:A (LEU60) to (TYR87) THE CRYSTAL STRUCTURE OF AN ENDO-BETA-1,3-GLUCANASE FROM ALKALIPHILIC NOCARDIOPSIS SP.STRAIN F96 | FAMILY 16, BETA-JELLY ROLL, BACTERIAL ENDO-BETA-1,3-GLUCANASE, HYDROLASE
5a53:C (LYS205) to (ILE234) CRYSTAL STRUCTURE OF THE RPF2-RRS1 COMPLEX | TRANSCRIPTION, 5S RNP, RIBOSOME ASSEMBLY, RRS1, RPF2, BRIX DOMAIN
1ia2:B (ASP175) to (ARG191) CANDIDA ALBICANS DIHYDROFOLATE REDUCTASE COMPLEXED WITH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE (NADPH) AND 5-[(4-METHYLPHENYL)SULFANYL]-2,4- QUINAZOLINEDIAMINE (GW578) | OXIDOREDUCTASE, ANTIFUNGAL TARGET, REDUCTASE
2wsv:A (THR560) to (ALA591) GALECTIN DOMAIN OF PORCINE ADENOVIRUS TYPE 4 NADC-1 ISOLATE FIBRE COMPLEXED WITH LACTOSE | TANDEM-REPEAT-TYPE, VIRAL PROTEIN, CARBOHYDRATE RECOGNITION DOMAIN
2wt1:A (THR560) to (ALA591) GALECTIN DOMAIN OF PORCINE ADENOVIRUS TYPE 4 NADC-1 ISOLATE FIBRE COMPLEXED WITH LACTO-N-NEO-TETRAOSE | VIRAL PROTEIN
1ibq:B (SER177) to (GLY200) ASPERGILLOPEPSIN FROM ASPERGILLUS PHOENICIS | ASPERGILLOPEPSIN, ASPARTIC PROTEINASE, HYDROLASE
1ue1:B (LYS84) to (PRO108) CRYSTAL STRUCTURE OF THE SINGLE-STRANDED DNA-BINDING PROTEIN FROM MYCOBACTERIUM TUBERCULOSIS | OLIGONUCLEOTIDE BINDING FOLD, DNA-BINDING PROTEIN, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, TB STRUCTURAL GENOMICS CONSORTIUM, TBSGC, DNA BINDING PROTEIN
1uf3:A (THR100) to (ASP119) CRYSTAL STRUCTURE OF TT1561 OF THERMUS THERMOPHILUS HB8 | METALLO-DEPENDENT PHOSPHATASES, THERMUS THERMOPHILUS, STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, UNKNOWN FUNCTION
1uf3:B (THR100) to (ASP119) CRYSTAL STRUCTURE OF TT1561 OF THERMUS THERMOPHILUS HB8 | METALLO-DEPENDENT PHOSPHATASES, THERMUS THERMOPHILUS, STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, UNKNOWN FUNCTION
1uf3:C (THR100) to (ASP119) CRYSTAL STRUCTURE OF TT1561 OF THERMUS THERMOPHILUS HB8 | METALLO-DEPENDENT PHOSPHATASES, THERMUS THERMOPHILUS, STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, UNKNOWN FUNCTION
1uf3:D (THR100) to (ASP119) CRYSTAL STRUCTURE OF TT1561 OF THERMUS THERMOPHILUS HB8 | METALLO-DEPENDENT PHOSPHATASES, THERMUS THERMOPHILUS, STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, UNKNOWN FUNCTION
1uf3:E (THR100) to (ASP119) CRYSTAL STRUCTURE OF TT1561 OF THERMUS THERMOPHILUS HB8 | METALLO-DEPENDENT PHOSPHATASES, THERMUS THERMOPHILUS, STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, UNKNOWN FUNCTION
1uf3:F (THR100) to (ASP119) CRYSTAL STRUCTURE OF TT1561 OF THERMUS THERMOPHILUS HB8 | METALLO-DEPENDENT PHOSPHATASES, THERMUS THERMOPHILUS, STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, UNKNOWN FUNCTION
1uf3:G (THR100) to (ASP119) CRYSTAL STRUCTURE OF TT1561 OF THERMUS THERMOPHILUS HB8 | METALLO-DEPENDENT PHOSPHATASES, THERMUS THERMOPHILUS, STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, UNKNOWN FUNCTION
1uf3:H (THR100) to (ASP119) CRYSTAL STRUCTURE OF TT1561 OF THERMUS THERMOPHILUS HB8 | METALLO-DEPENDENT PHOSPHATASES, THERMUS THERMOPHILUS, STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, UNKNOWN FUNCTION
1ifg:A (GLY19) to (LEU55) CRYSTAL STRUCTURE OF A MONOMERIC FORM OF GENERAL PROTEASE INHIBITOR, ECOTIN IN ABSENCE OF A PROTEASE | MONOMERIC ECOTIN, SERINE PROTEASE INHIBITOR, HYDROLASE INHIBITOR
1ui7:A (LEU352) to (GLY380) SITE-DIRECTED MUTAGENESIS OF HIS433 INVOLVED IN BINDING OF COPPER ION IN ARTHROBACTER GLOBIFORMIS AMINE OXIDASE | OXIDOREDUCTASE, COPPER, AMINE OXIDASE, QUINONE COFACTOR, TPQ, HISTIDINE, METAL COORDINATION
2wvm:A (ASN7) to (GLU25) H309A MUTANT OF MANNOSYL-3-PHOSPHOGLYCERATE SYNTHASE FROM THERMUS THERMOPHILUS HB27 IN COMPLEX WITH GDP-ALPHA-D-MANNOSE AND MG(II) | GT-A FOLD, TRANSFERASE, GLYCOSYLTRANSFERASE, RETAINING MECHANISM, GLUCOSYL TRANSFERASE
2wvm:B (ASN7) to (GLU25) H309A MUTANT OF MANNOSYL-3-PHOSPHOGLYCERATE SYNTHASE FROM THERMUS THERMOPHILUS HB27 IN COMPLEX WITH GDP-ALPHA-D-MANNOSE AND MG(II) | GT-A FOLD, TRANSFERASE, GLYCOSYLTRANSFERASE, RETAINING MECHANISM, GLUCOSYL TRANSFERASE
1ii2:A (ASP242) to (LYS261) CRYSTAL STRUCTURE OF PHOSPHOENOLPYRUVATE CARBOXYKINASE (PEPCK) FROM TRYPANOSOMA CRUZI | PHOSPHATE BINDING LOOP, LYASE
3w83:A (SER44) to (PHE61) STRUCTURE OF TRYPANOSOMA CRUZI DIHYDROOROTATE DEHYDROGENASE IN COMPLEX WITH MII-6-097 | ROSSMANN FOLD, OXIDOREDUCTASE, DIHYDROOROTATE/OROTATE AND FUMARATE/SUCCINATE BINDING, CYTOSOL, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
1ilu:F (CYS3) to (ASP23) X-RAY CRYSTAL STRUCTURE THE TWO SITE-SPECIFIC MUTANTS ILE7SER AND PHE110SER OF AZURIN FROM PSEUDOMONAS AERUGINOSA | ELECTRON TRANSFER PROTEIN, METALLOPROTEIN
3w9a:A (GLY220) to (GLY243) CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF THE GLYCOSIDE HYDROLASE FAMILY 131 PROTEIN FROM COPRINOPSIS CINEREA | GH131, BETA-JELLY ROLL, HYDROLASE
1uly:A (ARG67) to (ASN89) CRYSTAL STRUCTURE ANALYSIS OF THE ARSR HOMOLOGUE DNA-BINDING PROTEIN FROM P. HORIKOSHII OT3 | HELIX-TURN-HELIX, STRUCTURAL GENOMICS, DNA BINDING PROTEIN
1um4:H (SER126) to (PRO153) CATALYTIC ANTIBODY 21H3 WITH HAPTEN | CATALYTIC ANTIBODY LIGAND TRANSESTERIFICATION, IMMUNE SYSTEM
2ww5:A (GLU98) to (LEU124) 3D-STRUCTURE OF THE MODULAR AUTOLYSIN LYTC FROM STREPTOCOCCUS PNEUMONIAE AT 1.6 A RESOLUTION | HYDROLASE, GLYCOSIDASE, CHOLINE-BINDING PROTEIN
2wwc:A (GLU98) to (LEU124) 3D-STRUCTURE OF THE MODULAR AUTOLYSIN LYTC FROM STREPTOCOCCUS PNEUMONIAE IN COMPLEX WITH SYNTHETIC PEPTIDOGLYCAN LIGAND | HYDROLASE, GLYCOSIDASE, CHOLINE-BINDING PROTEIN
2wwc:A (TRP160) to (LYS185) 3D-STRUCTURE OF THE MODULAR AUTOLYSIN LYTC FROM STREPTOCOCCUS PNEUMONIAE IN COMPLEX WITH SYNTHETIC PEPTIDOGLYCAN LIGAND | HYDROLASE, GLYCOSIDASE, CHOLINE-BINDING PROTEIN
2wxf:A (ILE899) to (LEU916) THE CRYSTAL STRUCTURE OF THE MURINE CLASS IA PI 3-KINASE P110DELTA IN COMPLEX WITH PIK-39. | TRANSFERASE, PHOSPHOPROTEIN, ISOFORM-SPECIFIC INHIBITORS, CANCER
4m5z:H (SER120) to (PRO147) CRYSTAL STRUCTURE OF BROADLY NEUTRALIZING ANTIBODY 5J8 BOUND TO 2009 PANDEMIC INFLUENZA HEMAGGLUTININ, HA1 SUBUNIT | HEMAGGLUTININ, IMMUNOGLOBULIN FOLD, VIRAL PROTEIN-IMMUNE SYSTEM COMPLEX
2wxl:A (ILE899) to (LEU916) THE CRYSTAL STRUCTURE OF THE MURINE CLASS IA PI 3-KINASE P110DELTA IN COMPLEX WITH ZSTK474. | TRANSFERASE, PHOSPHOPROTEIN, ISOFORM-SPECIFIC INHIBITORS, CANCER
4m65:A (THR6) to (THR34) IN SITU THERMOLYSIN CRYSTALLIZED ON A MITEGEN MICROMESH WITH ASPARAGINE LIGAND | ASPARAGINE, HYDROLASE
2wxq:A (ILE899) to (LEU916) THE CRYSTAL STRUCTURE OF THE MURINE CLASS IA PI 3-KINASE P110DELTA IN COMPLEX WITH AS15. | TRANSFERASE, PHOSPHOPROTEIN, ISOFORM-SPECIFIC INHIBITORS, CANCER
4m75:L (VAL20) to (ASP47) CRYSTAL STRUCTURE OF LSM1-7 COMPLEX | SM LIKE PROTEIN, RNA SPLICING, STRUCTURAL PROTEIN, RNA BINDING PROTEIN
4m77:I (VAL15) to (ASN42) CRYSTAL STRUCTURE OF LSM2-8 COMPLEX, SPACE GROUP I212121 | SM LIKE PROTEIN, RNA SPLICING, STRUCTURAL PROTEIN
4mb8:C (THR136) to (THR165) EVOLUTIONARY HISTORY AND METABOLIC INSIGHTS OF ANCIENT MAMMALIAN URICASES | URIC ACID OXIDASE, LYSOZOME, OXIDOREDUCTASE
1usx:B (PHE447) to (ARG480) CRYSTAL STRUCTURE OF THE NEWCASTLE DISEASE VIRUS HEMAGGLUTININ-NEURAMINIDASE COMPLEXED WITH THIOSIALOSIDE | HYDROLASE, NEURAMINIDASE, HEMAGGLUTININ, SIALIDASE
1uu5:A (ASP103) to (TYR128) X-RAY CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMICOLA GRISEA CEL12A SOAKED WITH CELLOTETRAOSE | HYDROLASE, CELLULASE, CELLULOSE DEGRADATION, ENDOGLUCANASE, GLYCOSYL HYDROLASE, GH FAMILY 12, HUMICOLA GRISEA CEL12A, LIGAND COMPLEX
2x09:B (ARG335) to (PRO365) INHIBITION OF THE EXO-BETA-D-GLUCOSAMINIDASE CSXA BY A GLUCOSAMINE-CONFIGURED CASTANOSPERMINE AND AN AMINO- AUSTRALINE ANALOGUE | EXO-BETA-D-GLUCOSAMINIDASE, GLYCOSIDE HYDROLASE, GH2, CSXA, HYDROLASE, GLYCOSIDASE
2ihf:A (GLU83) to (GLU108) CRYSTAL STRUCTURE OF DELETION MUTANT DELTA 228-252 R190A OF THE SINGLE-STRANDED DNA BINDING PROTEIN FROM THERMUS AQUATICUS | SINGLE-STRANDED DNA BINDING PROTEIN (SSB), THERMOPHILE ORGANISM, PROTEIN-DNA INTERACTION, PROTEIN-PROTEIN INTERACTION, DNA BINDING PROTEIN
5adj:A (LEU313) to (ASN340) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-(2-(METHYLAMINO)ETHYL) PHENOXY)METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
1iw7:N (GLN717) to (SER752) CRYSTAL STRUCTURE OF THE RNA POLYMERASE HOLOENZYME FROM THERMUS THERMOPHILUS AT 2.6A RESOLUTION | RNA POLYMERASE HOLOENZYME, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, STRUCTURAL GENOMICS, TRANSFERASE
2ij2:A (GLU430) to (LYS452) ATOMIC STRUCTURE OF THE HEME DOMAIN OF FLAVOCYTOCHROME P450- BM3 | CYTOCHROME P450, P450BM3, MONOXYGENASE, HEME BINDING PROTEIN, ATOMIC RESOLUTION, OXIDOREDUCTASE
2ij2:B (GLU430) to (LYS452) ATOMIC STRUCTURE OF THE HEME DOMAIN OF FLAVOCYTOCHROME P450- BM3 | CYTOCHROME P450, P450BM3, MONOXYGENASE, HEME BINDING PROTEIN, ATOMIC RESOLUTION, OXIDOREDUCTASE
2ij3:A (GLU430) to (LYS452) STRUCTURE OF THE A264H MUTANT OF CYTOCHROME P450 BM3 | HEME LIGATION, HISTIDINE LIGATION, CYTOCHROME P450, P450 BM3, OXIDOREDUCTASE
2ij3:B (GLU430) to (LYS452) STRUCTURE OF THE A264H MUTANT OF CYTOCHROME P450 BM3 | HEME LIGATION, HISTIDINE LIGATION, CYTOCHROME P450, P450 BM3, OXIDOREDUCTASE
5agv:A (GLU350) to (SER388) THE SLIDING CLAMP OF MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH A NATURAL PRODUCT. | TRANSFERASE-ANTIBIOTIC COMPLEX, TRANSFERASE, DNAN, NATURAL PRODUCT, SLIDING CLAMP
2x2z:D (GLN101) to (GLY121) CRYSTAL STRUCTURE AMA1 FROM TOXOPLASMA GONDII | MEMBRANE PROTEIN, INVASION, MOVING JUNCTION
2x2z:E (GLN101) to (GLY121) CRYSTAL STRUCTURE AMA1 FROM TOXOPLASMA GONDII | MEMBRANE PROTEIN, INVASION, MOVING JUNCTION
2iou:H (ALA437) to (ALA453) MAJOR TROPISM DETERMINANT P1 (MTD-P1) VARIANT COMPLEXED WITH BORDETELLA BROCHISEPTICA VIRULENCE FACTOR PERTACTIN EXTRACELLULAR DOMAIN (PRN-E). | MTD; PRN; PERTACTIN, VIRAL PROTEIN-MEMBRANE PROTEIN COMPLEX
2iou:H (GLY456) to (GLY479) MAJOR TROPISM DETERMINANT P1 (MTD-P1) VARIANT COMPLEXED WITH BORDETELLA BROCHISEPTICA VIRULENCE FACTOR PERTACTIN EXTRACELLULAR DOMAIN (PRN-E). | MTD; PRN; PERTACTIN, VIRAL PROTEIN-MEMBRANE PROTEIN COMPLEX
5ahj:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH MACYRANONE A | HYDROLASE, PROTEASOME, NATURAL PRODUCT, TARGET IDENTIFICATION, INHIBITION, BINDING ANALYSIS
5ahj:N (THR1) to (THR22) YEAST 20S PROTEASOME IN COMPLEX WITH MACYRANONE A | HYDROLASE, PROTEASOME, NATURAL PRODUCT, TARGET IDENTIFICATION, INHIBITION, BINDING ANALYSIS
5ahj:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH MACYRANONE A | HYDROLASE, PROTEASOME, NATURAL PRODUCT, TARGET IDENTIFICATION, INHIBITION, BINDING ANALYSIS
5ahj:b (THR1) to (THR22) YEAST 20S PROTEASOME IN COMPLEX WITH MACYRANONE A | HYDROLASE, PROTEASOME, NATURAL PRODUCT, TARGET IDENTIFICATION, INHIBITION, BINDING ANALYSIS
3win:D (GLY48) to (TYR74) CLOSTRIDIUM BOTULINUM HEMAGGLUTININ | BACTERIAL PATHOGENESIS, BACTERIAL TOXINS, CARBOHYDRATE-BINDING PROTEIN, E-CADHERIN, EPITHELIAL CELL, PROTEIN COMPLEXES, BOTULINUM TOXIN, HEMAGGLUTININ, BETA-TREFOIL, TOXIN
2x4s:D (HIS188) to (PRO210) CRYSTAL STRUCTURE OF MHC CLASS I HLA-A2.1 BOUND TO A PEPTIDE REPRESENTING THE EPITOPE OF THE H5N1 (AVIAN FLU) NUCLEOPROTEIN | PHOTOCLEAVABLE PEPTIDE, GLYCOPROTEIN, IMMUNE SYSTEM, IMMUNOGLOBULIN DOMAIN, MATRIX (M1)
5air:A (MET26) to (GLN46) STRUCTURAL ANALYSIS OF MOUSE GSK3BETA FUSED WITH LRP6 PEPTIDE. | TRANSFERASE, LRP6, GSK3 BETA
1j36:A (SER339) to (VAL357) CRYSTAL STRUCTURE OF DROSOPHILA ANCE | ANGIOTENSIN, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1j36:B (SER339) to (VAL357) CRYSTAL STRUCTURE OF DROSOPHILA ANCE | ANGIOTENSIN, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1j3i:D (THR573) to (HIS599) WILD-TYPE PLASMODIUM FALCIPARUM DIHYDROFOLATE REDUCTASE- THYMIDYLATE SYNTHASE (PFDHFR-TS) COMPLEXED WITH WR99210, NADPH, AND DUMP | BIFUNCTIONAL, OXIDOREDUCTASE, TRANSFERASE
2x6f:B (LEU811) to (LEU828) THE CRYSTAL STRUCTURE OF THE DROSOPHILA CLASS III PI3-KINASE VPS34 IN COMPLEX WITH 3-METHYLADENINE | TRANSFERASE
2x6h:B (LEU811) to (LEU828) THE CRYSTAL STRUCTURE OF THE DROSOPHILA CLASS III PI3-KINASE VPS34 | TRANSFERASE
2x6u:A (GLY71) to (VAL91) CRYSTAL STRUCTURE OF HUMAN TBX5 IN THE DNA-FREE FORM | DEVELOPMENTAL PROTEIN, DNA-BINDING, HOLT-ORAM-SYNDROME, IG-FOLD, NUCLEAR PROTEIN, REPRESSOR, TBX3, TRANSCRIPTION, TRANSCRIPTION REGULATION
2x6v:B (THR72) to (VAL91) CRYSTAL STRUCTURE OF HUMAN TBX5 IN THE DNA-BOUND AND DNA- FREE FORM | TRANSCRIPTION-DNA COMPLEX, HOLT-ORAM-SYNDROME, DEVELOPMENTAL PROTEIN, TRANSCRIPTION REGULATION, REPRESSOR, DNA-BINDING, TRANSCRIPTION, NUCLEAR PROTEIN
1j7h:A (ALA21) to (ASN37) SOLUTION STRUCTURE OF HI0719, A HYPOTHETICAL PROTEIN FROM HAEMOPHILUS INFLUENZAE | ALPHA/BETA FOLD, HOMOTRIMER, STRUCTURE 2 FUNCTION PROJECT, S2F, STRUCTURAL GENOMICS, UNKNOWN FUNCTION
1j7h:B (ALA21) to (ASN37) SOLUTION STRUCTURE OF HI0719, A HYPOTHETICAL PROTEIN FROM HAEMOPHILUS INFLUENZAE | ALPHA/BETA FOLD, HOMOTRIMER, STRUCTURE 2 FUNCTION PROJECT, S2F, STRUCTURAL GENOMICS, UNKNOWN FUNCTION
1j7h:C (ALA21) to (ASN37) SOLUTION STRUCTURE OF HI0719, A HYPOTHETICAL PROTEIN FROM HAEMOPHILUS INFLUENZAE | ALPHA/BETA FOLD, HOMOTRIMER, STRUCTURE 2 FUNCTION PROJECT, S2F, STRUCTURAL GENOMICS, UNKNOWN FUNCTION
2x7y:A (GLU430) to (LYS452) P450 BM3 F87A IN COMPLEX WITH DMSO | ELECTRON TRANSPORT, OXIDOREDUCTASE, DMSO-INHIBITION, METAL-BINDING
2x80:A (GLU430) to (LYS452) P450 BM3 F87A IN COMPLEX WITH DMSO | ELECTRON TRANSPORT, OXIDOREDUCTASE, DMSO-INHIBITION, METAL-BINDING
2x80:B (GLU430) to (LYS452) P450 BM3 F87A IN COMPLEX WITH DMSO | ELECTRON TRANSPORT, OXIDOREDUCTASE, DMSO-INHIBITION, METAL-BINDING
4mji:F (HIS188) to (PRO210) T CELL RESPONSE TO A HIV REVERSE TRANSCRIPTASE EPITOPE PRESENTED BY THE PROTECTIVE ALLELE HLA-B*51:01 | HIV, PEPTIDE-MAJOR HISTOCOMPATIBILITY COMPLEX, PMHC, SURFACE PLASMON RESONANCE, SPR, T-CELL, T-CELL RECEPTOR, TCR, IMMUNOGLOBULIN, CLASS I MHC, ANTIGEN PRESENTATION, IMMUNE SYSTEM
1j86:A (THR148) to (ARG174) HUMAN HIGH AFFINITY FC RECEPTOR FC(EPSILON)RI(ALPHA), MONOCLINIC CRYSTAL FORM 2 | IMMUNE SYSTEM, FC RECEPTOR, IGE RECEPTOR, GLYCOPROTEIN
3wlv:D (TYR147) to (VAL179) THERMOSTABLE URATE OXIDASE FROM BACILLUS SP. TB-90 | TUNNEL FOLD MOTIF, OXIDASE, OXIDOREDUCTASE
4mk0:A (ARG587) to (ARG625) CRYSTAL STRUCTURE OF G PROTEIN-COUPLED RECEPTOR KINASE 2 IN COMPLEX WITH A A RATIONALLY DESIGNED PAROXETINE DERIVATIVE | INHIBITOR COMPLEX, PROTEIN KINASE, HYDROLASE, ATP BINDING, PHOSPHORYLATION, PERIPHERAL MEMBRANE PROTEIN, SIGNALING PROTEIN- INHIBITOR COMPLEX
2x8o:A (THR164) to (VAL197) CRYSTAL STRUCTURE OF CBPF IN COMPLEX WITH ATROPINE BY SOAKING | CHOLINE-BINDING PROTEIN, LIPID-BINDING-PROTEIN
2x8p:A (GLY4) to (ILE29) CRYSTAL STRUCTURE OF CBPF IN COMPLEX WITH ATROPINE BY CO- CRYSTALLIZATION | CHOLINE-BINDING PROTEIN, LIPID-BINDING-PROTEIN
2x8z:A (SER339) to (VAL357) CRYSTAL STRUCTURE OF ANCE-CAPTOPRIL COMPLEX | HYDROLASE, ACE INHIBITOR, ZINC METALLOPEPTIDASE
2x8y:A (SER339) to (VAL357) CRYSTAL STRUCTURE OF ANCE | HYDROLASE, ACE INHIBITOR, ZINC METALLOPEPTIDASE
2x91:A (SER339) to (VAL357) CRYSTAL STRUCTURE OF ANCE-LISINOPRIL COMPLEX | HYDROLASE, ACE INHIBITOR, ZINC METALLOPEPTIDASE
2x92:A (SER339) to (VAL357) CRYSTAL STRUCTURE OF ANCE-RAMIPRILAT COMPLEX | METALLOPROTEASE, CARBOXYPEPTIDASE, ACE INHIBITOR, HYDROLASE, GLYCOPROTEIN
2x94:A (SER339) to (VAL357) CRYSTAL STRUCTURE OF ANCE-PERINDOPRILAT COMPLEX | METALLOPROTEASE, CARBOXYPEPTIDASE, ACE INHIBITOR, HYDROLASE, GLYCOPROTEIN
2x95:A (SER339) to (VAL357) CRYSTAL STRUCTURE OF ANCE-LISINOPRIL-TRYPTOPHAN ANALOGUE, LISW-S COMPLEX | METALLOPROTEASE, CARBOXYPEPTIDASE, ACE INHIBITOR, HYDROLASE, GLYCOPROTEIN
3wo3:F (PRO26) to (SER44) CRYSTAL STRUCTURE OF IL-18 IN COMPLEX WITH IL-18 RECEPTOR ALPHA | BINARY COMPLEX, BETA TREFOIL FOLD (LIGAND), THREE IMMUNOGLOBULIN-LIKE DOMAINS (RECEPTOR), IMMUNITY, INFLAMMATION, AUTOIMMUNITY, ALLERGY, INTERLEUKIN-18 RECEPTOR BETA, GLYCOSYLATION, SERUM, MEMBRANE, IMMUNE SYSTEM
1vb2:A (LEU232) to (GLU260) T=1 CAPSID STRUCTURE OF SESBANIA MOSAIC VIRUS COAT PROTEIN DELETION MUTANT CP-N(DELTA)65-D146N-D149N | T=1 CAPSIDS, CALCIUM MUTANT, ICOSAHEDRAL VIRUS
5an9:F (HIS95) to (ARG139) MECHANISM OF EIF6 RELEASE FROM THE NASCENT 60S RIBOSOMAL SUBUNIT | TRANSLATION, RIBOSOMOPATHY, EFL1, GTPASE, RIBOSOME BIOGENESIS
1jge:A (HIS188) to (PRO210) HLA-B*2705 BOUND TO NONA-PEPTIDE M9 | MHC (MAJOR HISTOCOMPATIBILITY COMPLEX), HLA (HUMAN LEUKOCYTE ANTIGEN), IMMUNE SYSTEM
2j0g:A (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO N-ACETYL-MANNOSAMINE | LECTIN, GLYCOPROTEIN, INNATE IMMUNITY, FIBRINOGEN-LIKE DOMAIN, COLLAGEN, IMMUNOLOGY, LECTIN-LIKE, PATTERN- RECOGNITION-PROTEIN
2j0g:B (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO N-ACETYL-MANNOSAMINE | LECTIN, GLYCOPROTEIN, INNATE IMMUNITY, FIBRINOGEN-LIKE DOMAIN, COLLAGEN, IMMUNOLOGY, LECTIN-LIKE, PATTERN- RECOGNITION-PROTEIN
2j0g:C (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO N-ACETYL-MANNOSAMINE | LECTIN, GLYCOPROTEIN, INNATE IMMUNITY, FIBRINOGEN-LIKE DOMAIN, COLLAGEN, IMMUNOLOGY, LECTIN-LIKE, PATTERN- RECOGNITION-PROTEIN
2j0g:E (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO N-ACETYL-MANNOSAMINE | LECTIN, GLYCOPROTEIN, INNATE IMMUNITY, FIBRINOGEN-LIKE DOMAIN, COLLAGEN, IMMUNOLOGY, LECTIN-LIKE, PATTERN- RECOGNITION-PROTEIN
2j0g:F (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO N-ACETYL-MANNOSAMINE | LECTIN, GLYCOPROTEIN, INNATE IMMUNITY, FIBRINOGEN-LIKE DOMAIN, COLLAGEN, IMMUNOLOGY, LECTIN-LIKE, PATTERN- RECOGNITION-PROTEIN
2j0h:A (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO ACETYL-CHOLINE | GLYCOPROTEIN, FICRINOGEN-LIKE, INNATE IMMUNITY, PATTERN RECOGNITION PROTEIN, LECTIN, COLLAGEN, IMMUNOLOGY, LECTIN- LIKE
2j0h:B (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO ACETYL-CHOLINE | GLYCOPROTEIN, FICRINOGEN-LIKE, INNATE IMMUNITY, PATTERN RECOGNITION PROTEIN, LECTIN, COLLAGEN, IMMUNOLOGY, LECTIN- LIKE
2j0h:D (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO ACETYL-CHOLINE | GLYCOPROTEIN, FICRINOGEN-LIKE, INNATE IMMUNITY, PATTERN RECOGNITION PROTEIN, LECTIN, COLLAGEN, IMMUNOLOGY, LECTIN- LIKE
2j0h:E (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO ACETYL-CHOLINE | GLYCOPROTEIN, FICRINOGEN-LIKE, INNATE IMMUNITY, PATTERN RECOGNITION PROTEIN, LECTIN, COLLAGEN, IMMUNOLOGY, LECTIN- LIKE
2j0h:F (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO ACETYL-CHOLINE | GLYCOPROTEIN, FICRINOGEN-LIKE, INNATE IMMUNITY, PATTERN RECOGNITION PROTEIN, LECTIN, COLLAGEN, IMMUNOLOGY, LECTIN- LIKE
2j0y:B (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO B-1,3-D-GLUCAN | GLYCOPROTEIN, FICRINOGEN-LIKE, INNATE IMMUNITY, PATTERN RECOGNITION PROTEIN, LECTIN, COLLAGEN, IMMUNOLOGY, LECTIN- LIKE
2j0y:E (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO B-1,3-D-GLUCAN | GLYCOPROTEIN, FICRINOGEN-LIKE, INNATE IMMUNITY, PATTERN RECOGNITION PROTEIN, LECTIN, COLLAGEN, IMMUNOLOGY, LECTIN- LIKE
2j0y:F (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO B-1,3-D-GLUCAN | GLYCOPROTEIN, FICRINOGEN-LIKE, INNATE IMMUNITY, PATTERN RECOGNITION PROTEIN, LECTIN, COLLAGEN, IMMUNOLOGY, LECTIN- LIKE
2j1g:A (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO N-ACETYL-CYSTEIN | GLYCOPROTEIN, FICRINOGEN-LIKE, INNATE IMMUNITY, PATTERN RECOGNITION PROTEIN, LECTIN, COLLAGEN, IMMUNOLOGY, LECTIN- LIKE, SUGAR BINDING PROTEIN
2j1g:C (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO N-ACETYL-CYSTEIN | GLYCOPROTEIN, FICRINOGEN-LIKE, INNATE IMMUNITY, PATTERN RECOGNITION PROTEIN, LECTIN, COLLAGEN, IMMUNOLOGY, LECTIN- LIKE, SUGAR BINDING PROTEIN
2j1m:A (GLU430) to (LYS452) P450 BM3 HEME DOMAIN IN COMPLEX WITH DMSO | OXIDOREDUCTASE, DMSO-INHIBITION, P450, IRON, HEME, ORGANIC SOLVENT, FLAVOPROTEIN, MONOOXYGENASE, METAL-BINDING, MEMBRANE
2j1m:B (GLU430) to (LYS452) P450 BM3 HEME DOMAIN IN COMPLEX WITH DMSO | OXIDOREDUCTASE, DMSO-INHIBITION, P450, IRON, HEME, ORGANIC SOLVENT, FLAVOPROTEIN, MONOOXYGENASE, METAL-BINDING, MEMBRANE
2j2p:A (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO N-ACETYL-CYSTEIN (150MM) | GLYCOPROTEIN, FICRINOGEN-LIKE, INNATE IMMUNITY, PATTERN RECOGNITION PROTEIN, LECTIN, COLLAGEN, IMMUNOLOGY, LECTIN- LIKE
2j2p:C (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO N-ACETYL-CYSTEIN (150MM) | GLYCOPROTEIN, FICRINOGEN-LIKE, INNATE IMMUNITY, PATTERN RECOGNITION PROTEIN, LECTIN, COLLAGEN, IMMUNOLOGY, LECTIN- LIKE
2j2p:F (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO N-ACETYL-CYSTEIN (150MM) | GLYCOPROTEIN, FICRINOGEN-LIKE, INNATE IMMUNITY, PATTERN RECOGNITION PROTEIN, LECTIN, COLLAGEN, IMMUNOLOGY, LECTIN- LIKE
2j3f:B (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO N-ACETYL-D-GALACTOSAMINE | SUGAR BINDING PROTEIN, COLLAGEN, IMMUNOLOGY, GLYCOPROTEIN
2j3f:D (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO N-ACETYL-D-GALACTOSAMINE | SUGAR BINDING PROTEIN, COLLAGEN, IMMUNOLOGY, GLYCOPROTEIN
2j3f:F (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO N-ACETYL-D-GALACTOSAMINE | SUGAR BINDING PROTEIN, COLLAGEN, IMMUNOLOGY, GLYCOPROTEIN
2j3g:B (GLY257) to (PRO287) L-FICOLIN | LECTIN, GLYCOPROTEIN, INNATE IMMUNITY, FIBRINOGEN-LIKE DOMAIN, COLLAGEN, IMMUNOLOGY, LECTIN-LIKE, PATTERN- RECOGNITION-PROTEIN
2j3g:C (GLY257) to (PRO287) L-FICOLIN | LECTIN, GLYCOPROTEIN, INNATE IMMUNITY, FIBRINOGEN-LIKE DOMAIN, COLLAGEN, IMMUNOLOGY, LECTIN-LIKE, PATTERN- RECOGNITION-PROTEIN
2j3g:D (GLY257) to (PRO287) L-FICOLIN | LECTIN, GLYCOPROTEIN, INNATE IMMUNITY, FIBRINOGEN-LIKE DOMAIN, COLLAGEN, IMMUNOLOGY, LECTIN-LIKE, PATTERN- RECOGNITION-PROTEIN
2j3g:E (GLY257) to (PRO287) L-FICOLIN | LECTIN, GLYCOPROTEIN, INNATE IMMUNITY, FIBRINOGEN-LIKE DOMAIN, COLLAGEN, IMMUNOLOGY, LECTIN-LIKE, PATTERN- RECOGNITION-PROTEIN
2j3g:F (GLY257) to (PRO287) L-FICOLIN | LECTIN, GLYCOPROTEIN, INNATE IMMUNITY, FIBRINOGEN-LIKE DOMAIN, COLLAGEN, IMMUNOLOGY, LECTIN-LIKE, PATTERN- RECOGNITION-PROTEIN
1vfx:A (GLU143) to (GLU170) CRYSTAL STRUCTURE OF THE KIF1A MOTOR DOMAIN COMPLEXED WITH ADP-MG-ALFX | KINESIN, MICROTUBULE, MOTOR, TRANSPORT PROTEIN
2j3o:B (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO N-ACETYL-D-GLUCOSAMINE | SUGAR BINDING PROTEIN, LECTIN, COLLAGEN, IMMUNOLOGY, GLYCOPROTEIN
2j3o:D (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO N-ACETYL-D-GLUCOSAMINE | SUGAR BINDING PROTEIN, LECTIN, COLLAGEN, IMMUNOLOGY, GLYCOPROTEIN
2j3o:E (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO N-ACETYL-D-GLUCOSAMINE | SUGAR BINDING PROTEIN, LECTIN, COLLAGEN, IMMUNOLOGY, GLYCOPROTEIN
2j3o:F (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO N-ACETYL-D-GLUCOSAMINE | SUGAR BINDING PROTEIN, LECTIN, COLLAGEN, IMMUNOLOGY, GLYCOPROTEIN
2j3u:B (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO GALACTOSE | LECTIN, COLLAGEN, IMMUNOLOGY, GLYCOPROTEIN, SUGAR BINDING PROTEIN
2j3u:C (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO GALACTOSE | LECTIN, COLLAGEN, IMMUNOLOGY, GLYCOPROTEIN, SUGAR BINDING PROTEIN
2j3u:E (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO GALACTOSE | LECTIN, COLLAGEN, IMMUNOLOGY, GLYCOPROTEIN, SUGAR BINDING PROTEIN
2j3u:F (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO GALACTOSE | LECTIN, COLLAGEN, IMMUNOLOGY, GLYCOPROTEIN, SUGAR BINDING PROTEIN
1jlf:B (PRO59) to (ASP110) CRYSTAL STRUCTURE OF Y188C MUTANT HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH NEVIRAPINE | HIV-1 REVERSE TRANSCRIPTASE, AIDS, NON-NUCLEOSIDE INHIBITOR, NEVIRAPINE, DRUG RESISTANCE MUTATIONS, DRUG DESIGN, TRANSFERASE
2j4s:A (GLU430) to (LYS452) P450 BM3 HEME DOMAIN IN COMPLEX WITH DMSO | FLAVOPROTEIN, MONOOXYGENASE, METAL-BINDING, P450, IRON, HEME, OXIDOREDUCTASE, DMSO-INHIBITION, ORGANIC SOLVENT
2j4s:B (GLU430) to (LYS452) P450 BM3 HEME DOMAIN IN COMPLEX WITH DMSO | FLAVOPROTEIN, MONOOXYGENASE, METAL-BINDING, P450, IRON, HEME, OXIDOREDUCTASE, DMSO-INHIBITION, ORGANIC SOLVENT
5aun:B (LYS72) to (THR93) CRYSTAL STRUCTURE OF THE HYPAB-NI COMPLEX | PROTEIN COMPLEX, METALLOCHAPERONE
3ws3:C (HIS212) to (PRO234) CRYSTAL STRUCTURE OF H-2D IN COMPLEX WITH AN INSULIN DERIVED PEPTIDE | CLASS I MHC, MAJOR HISTOCOMPATIBILITY COMPLEX, INSULIN, H-2D, STRUCTURAL GENOMICS, PSI-BIOLOGY, NEW YORK STRUCTURAL GENOMICS RESEARCH CONSORTIUM, NYSGRC, IMMUNE SYSTEM
4mru:A (PHE303) to (TRP347) CRYSTAL STRUCTURE OF A SUSD HOMOLOG (BT1281) FROM BACTEROIDES THETAIOTAOMICRON VPI-5482 AT 1.90 A RESOLUTION | TPR- LIKE PROTEIN, MUCIN O-GLYCAN BINDING, PF12741 FAMILY, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-BIOLOGY, SUGAR BINDING PROTEIN
3wsp:A (GLU430) to (LYS452) CRYSTAL STRUCTURE OF P450BM3 WITH N-PERFLUORONONANOYL-L-TRYPTOPHAN | CYTOCHROME P450, OXIDOREDUCTASE
3wsp:B (GLU430) to (LYS452) CRYSTAL STRUCTURE OF P450BM3 WITH N-PERFLUORONONANOYL-L-TRYPTOPHAN | CYTOCHROME P450, OXIDOREDUCTASE
2j61:A (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO N-ACETYLGLUCOSAMINE (FORME C) | GLYCOPROTEIN, FICRINOGEN-LIKE, INNATE IMMUNITY, PATTERN RECOGNITION PROTEIN, LECTIN, COLLAGEN, IMMUNOLOGY, LECTIN- LIKE
2xhm:A (SER339) to (VAL357) CRYSTAL STRUCTURE OF ANCE-K26 COMPLEX | HYDROLASE, ACE INHIBITOR, ZINC METALLOPEPTIDASE
1jps:H (SER124) to (PRO151) CRYSTAL STRUCTURE OF TISSUE FACTOR IN COMPLEX WITH HUMANIZED FAB D3H44 | ANTIGEN-ANTIBODY RECOGNITION, HUMANIZED ANTIBODY, BLOOD COAGULATION, INTERFACE WATER MOLECULES, CRYSTAL STRUCTURE, IMMUNE SYSTEM
3j6e:A (PHE52) to (LEU70) ENERGY MINIMIZED AVERAGE STRUCTURE OF MICROTUBULES STABILIZED BY GMPCPP | MICROTUBULE, GMPCPP, STRUCTURAL PROTEIN
3j6e:C (PHE52) to (LEU70) ENERGY MINIMIZED AVERAGE STRUCTURE OF MICROTUBULES STABILIZED BY GMPCPP | MICROTUBULE, GMPCPP, STRUCTURAL PROTEIN
3j6e:E (PHE52) to (LEU70) ENERGY MINIMIZED AVERAGE STRUCTURE OF MICROTUBULES STABILIZED BY GMPCPP | MICROTUBULE, GMPCPP, STRUCTURAL PROTEIN
3j6e:G (PHE52) to (LEU70) ENERGY MINIMIZED AVERAGE STRUCTURE OF MICROTUBULES STABILIZED BY GMPCPP | MICROTUBULE, GMPCPP, STRUCTURAL PROTEIN
3j6e:I (PHE52) to (LEU70) ENERGY MINIMIZED AVERAGE STRUCTURE OF MICROTUBULES STABILIZED BY GMPCPP | MICROTUBULE, GMPCPP, STRUCTURAL PROTEIN
3j6e:K (PHE52) to (LEU70) ENERGY MINIMIZED AVERAGE STRUCTURE OF MICROTUBULES STABILIZED BY GMPCPP | MICROTUBULE, GMPCPP, STRUCTURAL PROTEIN
3j6e:M (PHE52) to (LEU70) ENERGY MINIMIZED AVERAGE STRUCTURE OF MICROTUBULES STABILIZED BY GMPCPP | MICROTUBULE, GMPCPP, STRUCTURAL PROTEIN
3j6e:O (PHE52) to (LEU70) ENERGY MINIMIZED AVERAGE STRUCTURE OF MICROTUBULES STABILIZED BY GMPCPP | MICROTUBULE, GMPCPP, STRUCTURAL PROTEIN
3j6e:Q (PHE52) to (LEU70) ENERGY MINIMIZED AVERAGE STRUCTURE OF MICROTUBULES STABILIZED BY GMPCPP | MICROTUBULE, GMPCPP, STRUCTURAL PROTEIN
4mtw:E (THR6) to (THR34) THERMOLYSIN IN COMPLEX WITH UBTLN36 | PROTEASE, METALLOPROTEASE,HYDROLYSIS OF PEPTIDE BONDS, 2- PHOSPHORAMIDON, METALLOPROTEASE, HYDROLYSIS OF PEPTIDE BONDS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1jqb:B (ASP2074) to (ASN2127) ALCOHOL DEHYDROGENASE FROM CLOSTRIDIUM BEIJERINCKII: CRYSTAL STRUCTURE OF MUTANT WITH ENHANCED THERMAL STABILITY | TETRAMER OF 222 SYMMETRY, WATER-MEDIATED INTERSUBUNIT SALT BRIDGES, ROSSMANN FOLD, OXIDOREDUCTASE
3wtx:F (GLU61) to (ARG80) CRYSTAL STRUCTURE OF THE COMPLEX COMPRISED OF ETS1(Y329A), RUNX1, CBFBETA, AND THE TCRALPHA GENE ENHANCER DNA | PROTEIN-DNA COMPLEX, DNA-BINDING, METHYLATION, NUCLEUS, PHOSPHOPROTEIN, TRANSCRIPTION REGULATION, ISOPEPTIDE BOND, PROTO- ONCOGENE, TRANSCRIPTION-DNA COMPLEX
3j6p:B (TYR52) to (LEU70) PSEUDO-ATOMIC MODEL OF DYNEIN MICROTUBULE BINDING DOMAIN-TUBULIN COMPLEX BASED ON A CRYOEM MAP | MOTOR PROTEIN-CYTOSKELETON COMPLEX, MOTOR PROTEIN-STRUCTURAL PROTEIN COMPLEX
3wuc:A (GLY17) to (ILE45) X-RAY CRYSTAL STRUCTURE OF XENOPUS LAEVIS GALECTIN-VA | BETA-SANDWICH, LECTIN, CARBOHYDRATE/SUGAR BINDING, SUGAR BINDING PROTEIN
3wud:A (HIS16) to (VAL43) X-RAY CRYSTAL STRUCTURE OF XENOPUS LAEVIS GALECTIN-IB | BETA-SANDWICH, LECTIN, CARBOHYDRATE/SUGAR BINDING, SUGAR BINDING PROTEIN
3wv6:A (LEU29) to (ALA59) CRYSTAL STRUCTURE OF A PROTEASE-RESISTANT MUTANT FORM OF HUMAN GALECTIN-9 | BETA SANDWICH, CARBOHYDRATE-BINDING, OLIGOSACCHARIDE, SUGAR BINDING PROTEIN
3wv6:B (LEU29) to (ALA59) CRYSTAL STRUCTURE OF A PROTEASE-RESISTANT MUTANT FORM OF HUMAN GALECTIN-9 | BETA SANDWICH, CARBOHYDRATE-BINDING, OLIGOSACCHARIDE, SUGAR BINDING PROTEIN
4mwf:H (SER120) to (PRO147) STRUCTURE OF HEPATITIS C VIRUS ENVELOPE GLYCOPROTEIN E2 CORE BOUND TO BROADLY NEUTRALIZING ANTIBODY AR3C | IMMUNOGLOBULIN FOLD, HCV E2, IMMUNE SYSTEM
4mwp:E (THR6) to (THR34) THERMOLYSIN IN COMPLEX WITH UBTLN46 | PROTEASE, METALLOPROTEASE, HYDROLYSIS OF PEPTIDE BONDS, 2- PHOSPHORAMIDON, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4mxj:E (THR6) to (THR34) THERMOLYSIN IN COMPLEX WITH UBTLN35 | PROTEASE,METALLOPROTEASE,HYDROLYSIS OF PEPTIDE BONDS, 2- PHOSPHORAMIDON, PROTEASE, METALLOPROTEASE, HYDROLYSIS OF PEPTIDE BONDS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3wxr:H (THR1) to (THR22) YEAST 20S PROTEASOME WITH A MUTATION OF ALPHA7 SUBUNIT | UPS, 20S PROTEASOME, HYDROLASE, PROTEASE, 19S REGULATORY PARTICLE, MULTICATALYTIC PROTEASE
3wxr:X (ILE2) to (SER22) YEAST 20S PROTEASOME WITH A MUTATION OF ALPHA7 SUBUNIT | UPS, 20S PROTEASOME, HYDROLASE, PROTEASE, 19S REGULATORY PARTICLE, MULTICATALYTIC PROTEASE
4mzn:E (THR6) to (THR34) THERMOLYSIN IN COMPLEX WITH UBTLN59 | PROTEASE, METALLOPROTEASE, HYDROLYSIS OF PEPTIDE BONDS, 2- PHOSPHORAMIDON, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3x0y:F (ARG144) to (PHE161) CRYSTAL STRUCTURE OF FMN-BOUND DSZC FROM RHODOCOCCUS ERYTHROPOLIS D-1 | DBT MONOOXYGENASE, DESULFURIZATION, ACYL-COA DEHYDROGENASE DOMAIN, FMN-DEPENDENT, OXIDOREDUCTASE
3x13:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA-B*0801.N80I | IMMUNOGLOBULIN FOLD, IMMUNITY, ANTIGEN PRESENTATION, IMMUNE RECEPTORS, LILR, TCR, KIR, PLASMA MEMBRANE, IMMUNE SYSTEM
3x14:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA-B*0801.N80I.R82L.G83R | IMMUNOGLOBULIN FOLD, IMMUNITY, ANTIGEN PRESENTATION, IMMUNE RECEPTORS, LILR, TCR, KIR, PLASMA MEMBRANE, IMMUNE SYSTEM
2xrb:A (SER271) to (ALA290) STRUCTURE OF THE N-TERMINAL FOUR DOMAINS OF THE COMPLEMENT REGULATOR RAT CRRY | IMMUNE SYSTEM, IMMUNOLOGY
4n4e:E (THR6) to (THR34) THERMOLYSIN IN COMPLEX WITH UBTLN58 | PROTEASE, METALLOPROTEASE, HYDROLYSIS OF PEPTIDE BONDS, 2- PHOSPHORAMIDON, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4n5p:E (THR6) to (THR34) THERMOLYSIN IN COMPLEX WITH UBTLN20 | PROTEASE, METALLOPROTEASE, HYDROLYSIS OF PEPTIDE BONDS, 2- PHOSPHORAMIDON, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5b7m:B (GLY55) to (GLN81) STRUCTURE OF PERDEUTERATED CUEO - THE SIGNAL PEPTIDE WAS TRUNCATED BY HRV3C PROTEASE | MULTICOPPER OXIDASE, PERDEUTERATED, OXIDOREDUCTASE
4n66:E (THR6) to (THR34) THERMOLYSIN IN COMPLEX WITH UBTLN37 | PROTEASE, METALLOPROTEASE, HYDROLYSIS OF PEPTIDE BONDS, 2- PHOSPHORAMIDON, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3jao:A (PHE52) to (LEU70) CILIARY MICROTUBULE DOUBLET | TUBULIN, MICROTUBULE DOUBLET, CILIA, STRUCTURAL PROTEIN
1w72:I (SER120) to (PRO149) CRYSTAL STRUCTURE OF HLA-A1:MAGE-A1 IN COMPLEX WITH FAB- HYB3 | IMMUNE SYSTEM, HLA/FAB FRAGMENT, HUMAN LEUCOCYTE ANTIGEN, PEPTIDE-SPECIFIC FAB, TCR-LIKE BINDING, MHC-I
2jhm:F (GLY266) to (PRO296) STRUCTURE OF GLOBULAR HEADS OF M-FICOLIN AT NEUTRAL PH | LECTIN, COLLAGEN, ACIDIC PH, COMPLEMENT, GLYCOPROTEIN, POLYMORPHISM, INNATE IMMUNITY, SUGAR-BINDING PROTEIN
5bqd:B (THR72) to (VAL91) CRYSTAL STRUCTURE OF TBX5 (1-239) DIMER | CARDIAC, TRANSCRIPTION FACTOR, CHD, NKX, TBX, DNA BINDING, TRANSCRIPTION
5bqe:B (ALA105) to (CYS128) CRYSTAL STRUCTURE OF NORRIN IN COMPLEX WITH THE CYSTEINE-RICH DOMAIN OF FRIZZLED 4 -METHYLATED FORM | WNT SIGNALLING PATHWAY, NORRIE DISEASE PROTEIN, GLYCOPROTEIN, G PROTEIN COUPLED RECEPTOR, SIGNALING PROTEIN
4n9s:A (ARG128) to (SER154) HIGH RESOLUTION X-RAY STRUCTURE OF URATE OXIDASE IN COMPLEX WITH 8- HYDROXYXANTHINE | URATE OXIDASE, URICASE, OXIDOREDUCTASE
4nbd:B (THR214) to (PHE239) CARBAZOLE-BOUND OXYGENASE WITH PHE275 REPLACED BY TRP AND FERREDOXIN COMPLEX OF CARBAZOLE 1,9A-DIOXYGENASE (FORM2) | RIESKE NON-HEME IRON OXYGENASE, CARBAZOLE 1,9A-DIOXYGENASE, OXIDOREDUCTASE
4nc2:A (GLY14) to (GLU39) CRYSTAL STRUCTURE OF TCDB-B1 BOUND TO B39 VHH | ANTIBODY-ANTIGEN COMPLEX, IMMUNE SYSTEM
1wc7:H (SER120) to (PRO147) FAB FRAGMENT OF PLP-DEPENDENT CATALYTIC ANTIBODY 15A9 IN COMPLEX WITH PHOSPHOPYRIDOXYL-L-ALANINE | ANTIBODY, CATALYTIC ANTIBODY, TRANSAMINATION, PYRIDOXAL-PHOSPHATE, PHOSPHOPYRIDOXYL-L-ALANINE
3zi6:A (THR6) to (THR34) STRUCTURE OF THERMOLYSIN SOLVED BY SAD FROM DATA COLLECTED BY DIRECT DATA COLLECTION (DDC) USING THE GROB ROBOT GONIOMETER | HYDROLASE
5bv7:H (SER133) to (PRO160) CRYSTAL STRUCTURE OF HUMAN LCAT (L4F, N5D) IN COMPLEX WITH FAB OF AN AGONISTIC ANTIBODY | A/B HYDROLASE, IMMUNE SYSTEM, HYDROLASE-IMMUNE SYSTEM COMPLEX
5by6:B (HIS36) to (CYS59) CRYSTAL STRUCTURE OF TRICHINELLA SPIRALIS THYMIDYLATE SYNTHASE COMPLEXED WITH DUMP | TRICHINELLA SPIRALIS, PARASITIC NEMATODE, PROTEIN-LIGAND COMPLEX, METHYLTRANSFERASE, TRANSFERASE
5by6:C (HIS36) to (CYS59) CRYSTAL STRUCTURE OF TRICHINELLA SPIRALIS THYMIDYLATE SYNTHASE COMPLEXED WITH DUMP | TRICHINELLA SPIRALIS, PARASITIC NEMATODE, PROTEIN-LIGAND COMPLEX, METHYLTRANSFERASE, TRANSFERASE
2kea:A (ILE253) to (SER281) NMR SOLUTION STRUCTURE OF THE HACS1 SH3 DOMAIN | SH3 DOMAIN, ALTERNATIVE SPLICING, PHOSPHOPROTEIN, POLYMORPHISM, PROTEIN BINDING
2l3s:A (THR268) to (ASP296) STRUCTURE OF THE AUTOINHIBITED CRK | ADAPTER PROTEIN, STRUCTURAL PROTEIN
4nmj:F (ARG358) to (ASP371) THERMOSTABLE ALDEHYDE DEHYDROGENASE FROM PYROBACULUM SP. COMPLEXED WITH NADP+ AT 2 A RESOLUTION | ALDEHYDE OXIDATION, NADP REDUCTION, INTRACELLULAR, OXIDOREDUCTASE
4nmj:H (ARG358) to (ASP371) THERMOSTABLE ALDEHYDE DEHYDROGENASE FROM PYROBACULUM SP. COMPLEXED WITH NADP+ AT 2 A RESOLUTION | ALDEHYDE OXIDATION, NADP REDUCTION, INTRACELLULAR, OXIDOREDUCTASE
2y8s:D (GLN101) to (GLY121) CO-STRUCTURE OF AN AMA1 MUTANT (Y230A) WITH A SURFACE EXPOSED REGION OF RON2 FROM TOXOPLASMA GONDII | MEMBRANE PROTEIN, MOVING JUNCTION, INVASION
4nnn:L (THR11) to (THR31) YCP IN COMPLEX WITH MG132 | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, ALDEHYDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4nnn:Z (THR11) to (THR31) YCP IN COMPLEX WITH MG132 | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, ALDEHYDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4nnw:I (ILE10) to (SER30) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-KETOALDEHYDE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, KETOALDEHYDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4nnw:W (ILE10) to (SER30) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-KETOALDEHYDE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, KETOALDEHYDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4nnx:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF PKD2 PHOSPHOPEPTIDE BOUND TO HLA-A2 | PHOSPHOSERINE, PHOSPHOPEPTIDE, MHC, POST TRANSLATIONAL MODIFICATION, TUMOR IMMUNOLOGY, TUMOR ANTIGENS, NEOEPITOPE, IMMUNE SYSTEM-ANTIGEN COMPLEX
4no1:L (THR11) to (THR31) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-B(OH)2 | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, BORONIC ACID, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no1:Z (THR11) to (THR31) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-B(OH)2 | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, BORONIC ACID, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no2:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF RQA_V PHOSPHOPEPTIDE BOUND TO HLA-A2 | PHOSPHOSERINE, PHOSPHOPEPTIDE, PEPTIDE-MHC COMPLEX, MHC, TUMOR IMMUNOLOGY, PEPTIDE CONFORMATION, POST TRANSLATIONAL MODIFICATION, TUMOR ANTIGEN, NEOEPITOPE, IMMUNE SYSTEM-ANTIGEN COMPLEX
4no4:B (CYS17) to (CYS43) CRYSTAL STRUCTURE OF GALECTIN-1 L11A MUTANT | BETA BARREL, LACTOSE BINDING PROTEIN, LACTOSE, APOPTOSIS
4no4:D (CYS17) to (CYS43) CRYSTAL STRUCTURE OF GALECTIN-1 L11A MUTANT | BETA BARREL, LACTOSE BINDING PROTEIN, LACTOSE, APOPTOSIS
4no5:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF NON-PHOSPHORYLATED FORM OF AMPD2 PHOSPHOPEPTIDE BOUND TO HLA-A2 | NONPHOSPHORYLATED PEPTIDE, PEPTIDE-MHC COMPLEX, MHC, PEPTIDE CONFORMATION, TUMOR IMMUNOLOGY, POST TRANSLATIONAL MODIFICATION, TUMOR ANTIGENS, IMMUNE SYSTEM-ANTIGEN COMPLEX
3zqz:A (SER339) to (VAL357) CRYSTAL STRUCTURE OF ANCE IN COMPLEX WITH A SELENIUM ANALOGUE OF CAPTOPRIL | HYDROLASE, INHIBITOR DESIGN
4no6:I (ILE10) to (SER30) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-VINYLSULFONE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, VINYLSULFONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no6:W (ILE10) to (SER30) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-VINYLSULFONE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, VINYLSULFONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no8:I (GLY8) to (SER30) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-KETOAMIDE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, KETOAMIDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no8:L (THR11) to (THR31) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-KETOAMIDE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, KETOAMIDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no8:W (GLY8) to (SER30) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-KETOAMIDE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, KETOAMIDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no8:Z (THR11) to (THR31) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-KETOAMIDE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, KETOAMIDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4nqv:G (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA A*0101 IN COMPLEX WITH NP44, AN 9-MER INFLUENZA EPITOPE | IMMUNE SYSTEM, HLA PRESENTING H7N9 VIRAL EPITOPE, T CELL RECEPTOR, IMMUNE SYSTEM-VIRAL PROTEIN COMPLEX
1knx:C (ALA179) to (ILE203) HPR KINASE/PHOSPHATASE FROM MYCOPLASMA PNEUMONIAE | HPR KINASE, HPR KINASE/PHOSPHATASE, HPRK/P, KINASE, PHOSPHATASE, P-LOOP, WALKER A BOX, CATABOLITE REPRESSION, TRANSFERASE/HYDROLASE COMPLEX
1knx:F (ALA179) to (ILE203) HPR KINASE/PHOSPHATASE FROM MYCOPLASMA PNEUMONIAE | HPR KINASE, HPR KINASE/PHOSPHATASE, HPRK/P, KINASE, PHOSPHATASE, P-LOOP, WALKER A BOX, CATABOLITE REPRESSION, TRANSFERASE/HYDROLASE COMPLEX
3zuf:D (LYS198) to (GLU218) PADRON OFF (NON-FLUORESCENT) BTRANS | GFP VARIANTS, FLUORESCENT PROTEIN, POSITIVE PHOTOSWITCHING, FPS, RSFPS, CRYO-PROBE, INTERMEDIATE STATE, ISOMERIZATION
4nrx:H (SER120) to (PRO147) CRYSTAL STRUCTURE OF HIV-1 NEUTRALIZING ANTIBODY M66 IN COMPLEX WITH GP41 MPER PEPTIDE | IMMUNOGLOBULIN, NEUTRALIZING ANTIBODY, HIV-1 GP41, MEMBRANE PROXIMAL EXTERNAL REGION, MPER, IMMUNE SYSTEM
4nrx:A (SER120) to (PRO147) CRYSTAL STRUCTURE OF HIV-1 NEUTRALIZING ANTIBODY M66 IN COMPLEX WITH GP41 MPER PEPTIDE | IMMUNOGLOBULIN, NEUTRALIZING ANTIBODY, HIV-1 GP41, MEMBRANE PROXIMAL EXTERNAL REGION, MPER, IMMUNE SYSTEM
4nrx:D (SER137) to (PRO164) CRYSTAL STRUCTURE OF HIV-1 NEUTRALIZING ANTIBODY M66 IN COMPLEX WITH GP41 MPER PEPTIDE | IMMUNOGLOBULIN, NEUTRALIZING ANTIBODY, HIV-1 GP41, MEMBRANE PROXIMAL EXTERNAL REGION, MPER, IMMUNE SYSTEM
1x35:A (LEU232) to (GLU260) RECOMBINANT T=3 CAPSID OF A SITE SPECIFIC MUTANT OF SEMV CP | T=3 CAPSIDS, BETA-ANNULUS, ICOSAHEDRAL VIRUS
1x35:B (LEU232) to (GLU260) RECOMBINANT T=3 CAPSID OF A SITE SPECIFIC MUTANT OF SEMV CP | T=3 CAPSIDS, BETA-ANNULUS, ICOSAHEDRAL VIRUS
1kpr:C (HIS188) to (PRO210) THE HUMAN NON-CLASSICAL MAJOR HISTOCOMPATIBILITY COMPLEX MOLECULE HLA-E | HLA-E, MHC, NON-CLASSICAL MHC, HLA, BETA 2 MICROGLOBULIN, IMMUNE SYSTEM
1kqf:A (LYS958) to (LYS1014) FORMATE DEHYDROGENASE N FROM E. COLI | OXIDOREDUCTASE, SELENIUM, SELENOCYSTEINE, SECYS, MOLYBDENUM, MOLYBDOPTERIN, MPT, MOLYBDOPTERIN GUANINE DINUCLEOTIDE, MGD, IRON SULFUR CLUSTER, FE4S4, FORMATE, DEHYDROGENASE, ANAEROBIC, INTEGRAL MEMBRANE PROTEIN
1kqg:A (LYS958) to (LYS1014) FORMATE DEHYDROGENASE N FROM E. COLI | OXIDOREDUCTASE, SELENIUM, SELENOCYSTEINE, SECYS, MOLYBDENUM, MOLYBDOPTERIN, MPT, MOLYBDOPTERIN GUANINE DINUCLEOTIDE, MGD, IRON SULFUR CLUSTER, FE4S4, FORMATE, DEHYDROGENASE, ANAEROBIC, INTEGRAL MEMBRANE PROTEIN
1krb:C (ASP431) to (SER493) CRYSTAL STRUCTURE OF KLEBSIELLA AEROGENES UREASE, ITS APOENZYME AND TWO ACTIVE SITE MUTANTS | ACTIVE SITE MUTANT, NICKEL METALLOENZYME, HYDROLASE (UREA AMIDO), HYDROLASE
1kra:C (ASP431) to (SER493) CRYSTAL STRUCTURE OF KLEBSIELLA AEROGENES UREASE, ITS APOENZYME AND TWO ACTIVE SITE MUTANTS | APOENZYME, NICKEL METALLOENZYME, HYDROLASE (UREA AMIDO)
1krc:C (ASP431) to (SER493) CRYSTAL STRUCTURE OF KLEBSIELLA AEROGENES UREASE, ITS APOENZYME AND TWO ACTIVE SITE MUTANTS | ACTIVE SITE MUTANT, NICKEL METALLOENZYME, HYDROLASE (UREA AMIDO)
2mpo:A (SER12) to (ASP33) STRUCTURAL BASIS OF TOXOPLASMA GONDII MIC2-ASSOCIATED PROTEIN INTERACTION WITH MIC2 | TOXOPLASMA GONDII, PLASMODIUM, MICRONEME, MIC2, M2AP, CELL ADHESION
1ktl:C (HIS188) to (PRO210) THE HUMAN NON-CLASSICAL MAJOR HISTOCOMPATIBILITY COMPLEX MOLECULE HLA-E | HLA-E, MHC, NON-CLASSICAL MHC, HLA, BETA 2 MICROGLOBULIN, IMMUNE SYSTEM
5c71:D (LEU269) to (GLY294) THE STRUCTURE OF ASPERGILLUS ORYZAE A-GLUCURONIDASE COMPLEXED WITH GLYCYRRHETINIC ACID MONOGLUCURONIDE | BETA-GLUCURONIDASE; GLYCYRRHETINIC ACID MONOGLUCURONIDE, HYDROLASE
1kv7:A (GLY55) to (GLN81) CRYSTAL STRUCTURE OF CUEO, A MULTI-COPPER OXIDASE FROM E. COLI INVOLVED IN COPPER HOMEOSTASIS | MULTI-COPPER OXIDASE, T1 (BLUE) COPPER, OXIDOREDUCTASE
4nyt:B (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO PHOSPHOCHOLINE | SOLUBLE INNATE IMMUNE RECOGNITION, EXTRACELLULAR, IMMUNE SYSTEM
1kyi:G (THR1) to (LEU22) HSLUV (H. INFLUENZAE)-NLVS VINYL SULFONE INHIBITOR COMPLEX | PROKARYOTIC PROTEASOME, PROTEASE, AAA-PROTEIN, ATP-DEPENDENT CHAPERONE; CLP/HSP100, VINYL SULFONE INHIBITOR, CHAPERONE-HYDROLASE COMPLEX
1kyi:H (THR1) to (LEU22) HSLUV (H. INFLUENZAE)-NLVS VINYL SULFONE INHIBITOR COMPLEX | PROKARYOTIC PROTEASOME, PROTEASE, AAA-PROTEIN, ATP-DEPENDENT CHAPERONE; CLP/HSP100, VINYL SULFONE INHIBITOR, CHAPERONE-HYDROLASE COMPLEX
1kyi:I (THR1) to (LEU22) HSLUV (H. INFLUENZAE)-NLVS VINYL SULFONE INHIBITOR COMPLEX | PROKARYOTIC PROTEASOME, PROTEASE, AAA-PROTEIN, ATP-DEPENDENT CHAPERONE; CLP/HSP100, VINYL SULFONE INHIBITOR, CHAPERONE-HYDROLASE COMPLEX
1kyi:K (THR1) to (LEU22) HSLUV (H. INFLUENZAE)-NLVS VINYL SULFONE INHIBITOR COMPLEX | PROKARYOTIC PROTEASOME, PROTEASE, AAA-PROTEIN, ATP-DEPENDENT CHAPERONE; CLP/HSP100, VINYL SULFONE INHIBITOR, CHAPERONE-HYDROLASE COMPLEX
1kyi:L (ILE3) to (LEU22) HSLUV (H. INFLUENZAE)-NLVS VINYL SULFONE INHIBITOR COMPLEX | PROKARYOTIC PROTEASOME, PROTEASE, AAA-PROTEIN, ATP-DEPENDENT CHAPERONE; CLP/HSP100, VINYL SULFONE INHIBITOR, CHAPERONE-HYDROLASE COMPLEX
2nnb:A (GLU430) to (LYS452) THE Q403K MUTNAT HEME DOMAIN OF FLAVOCYTOCHROME P450 BM3 | FLAVOCYTOCHROME P450, HEME DOMAIN, FATTY-ACID HYDROXYLASE, OXIDOREDUCTASE
2nnb:B (GLU430) to (LYS452) THE Q403K MUTNAT HEME DOMAIN OF FLAVOCYTOCHROME P450 BM3 | FLAVOCYTOCHROME P450, HEME DOMAIN, FATTY-ACID HYDROXYLASE, OXIDOREDUCTASE
41bi:A (PHE99) to (SER152) INTERLEUKIN-1 BETA (IL-1 BETA) (MUTANT WITH CYS 8 REPLACED BY ALA (C8A) | CYTOKINE
4a09:A (ALA692) to (PRO716) STRUCTURE OF HSDDB1-DRDDB2 BOUND TO A 15 BP CPD-DUPLEX (PURINE AT D-1 POSITION) AT 3.1 A RESOLUTION (CPD 2) | DNA-BINDING PROTEIN-DNA COMPLEX, DNA DAMAGE REPAIR, DDB
4o2e:D (HIS188) to (PRO210) A PEPTIDE COMPLEXED WITH HLA-B*3901 | IG-LIKE, IMMUNE SYSTEM
4o2f:A (HIS188) to (PRO210) A PEPTIDE COMPLEXED WITH HLA-B*3901 | IG-LIKE, IMMUNE SYSTEM
1l3f:E (THR6) to (THR34) THERMOLYSIN IN THE ABSENCE OF SUBSTRATE HAS AN OPEN CONFORMATION | HYDROLASE, THERMOLYSIN, MATRIX METALLOPROTEASE, ZINC METALLOPROTEASE, HINGE-BENDING
5cck:H (SER120) to (PRO147) CRYSTAL STRUCTURE OF HUMAN ANTI-HIV-1 BROADLY NEUTRALIZING ANTIBODY 3BC315 FAB | HIV-1, ENV, BNAB, ANTIBODY, IMMUNE SYSTEM
3jse:H (THR1) to (MET22) CRYSTAL STRUCTURE OF ARCHAEAL 20S PROTEASOME IN COMPLEX WITH MUTATED P26 ACTIVATOR | 20S PROTEASOME, PA26, PROTEASOME ACTIVATION, CYTOPLASM, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE, HYDROLASE/HYDROLASE ACTIVATOR COMPLEX
3jse:I (THR1) to (MET22) CRYSTAL STRUCTURE OF ARCHAEAL 20S PROTEASOME IN COMPLEX WITH MUTATED P26 ACTIVATOR | 20S PROTEASOME, PA26, PROTEASOME ACTIVATION, CYTOPLASM, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE, HYDROLASE/HYDROLASE ACTIVATOR COMPLEX
3jse:J (THR1) to (MET22) CRYSTAL STRUCTURE OF ARCHAEAL 20S PROTEASOME IN COMPLEX WITH MUTATED P26 ACTIVATOR | 20S PROTEASOME, PA26, PROTEASOME ACTIVATION, CYTOPLASM, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE, HYDROLASE/HYDROLASE ACTIVATOR COMPLEX
3jse:K (THR1) to (MET22) CRYSTAL STRUCTURE OF ARCHAEAL 20S PROTEASOME IN COMPLEX WITH MUTATED P26 ACTIVATOR | 20S PROTEASOME, PA26, PROTEASOME ACTIVATION, CYTOPLASM, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE, HYDROLASE/HYDROLASE ACTIVATOR COMPLEX
3jse:L (THR1) to (MET22) CRYSTAL STRUCTURE OF ARCHAEAL 20S PROTEASOME IN COMPLEX WITH MUTATED P26 ACTIVATOR | 20S PROTEASOME, PA26, PROTEASOME ACTIVATION, CYTOPLASM, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE, HYDROLASE/HYDROLASE ACTIVATOR COMPLEX
3jse:M (THR1) to (MET22) CRYSTAL STRUCTURE OF ARCHAEAL 20S PROTEASOME IN COMPLEX WITH MUTATED P26 ACTIVATOR | 20S PROTEASOME, PA26, PROTEASOME ACTIVATION, CYTOPLASM, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE, HYDROLASE/HYDROLASE ACTIVATOR COMPLEX
3jse:N (THR1) to (MET22) CRYSTAL STRUCTURE OF ARCHAEAL 20S PROTEASOME IN COMPLEX WITH MUTATED P26 ACTIVATOR | 20S PROTEASOME, PA26, PROTEASOME ACTIVATION, CYTOPLASM, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE, HYDROLASE/HYDROLASE ACTIVATOR COMPLEX
1l5g:B (GLY73) to (ARG91) CRYSTAL STRUCTURE OF THE EXTRACELLULAR SEGMENT OF INTEGRIN AVB3 IN COMPLEX WITH AN ARG-GLY-ASP LIGAND | GENU, HYBRID DOMAIN, BETA-TAIL DOMAIN, PSI DOMAIN, EGF DOMAIN, MIDAS, ADMIDAS, LIMBS, CAGE MOTIF, PROPELLER, A-DOMAIN, THIGH DOMAIN, CALF DOMAIN, RGD LIGAND, CELL ADHESION
4o4p:A (GLU430) to (LYS452) STRUCTURE OF P450 BM3 A82F F87V IN COMPLEX WITH S-OMEPRAZOL | P450, MONOXYGENASE, OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4o4p:B (GLU430) to (LYS452) STRUCTURE OF P450 BM3 A82F F87V IN COMPLEX WITH S-OMEPRAZOL | P450, MONOXYGENASE, OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3jsu:A (ASN338) to (ASP361) QUADRUPLE MUTANT(N51I+C59R+S108N+I164L) PLASMODIUM FALCIPARUM DIHYDROFOLATE REDUCTASE-THYMIDYLATE SYNTHASE(PFDHFR-TS) COMPLEXED WITH QN254, NADPH, AND DUMP | ROSSMANN FOLD, OXIDOREDUCTASE, TRANSFERASE
3jsu:B (THR573) to (HIS599) QUADRUPLE MUTANT(N51I+C59R+S108N+I164L) PLASMODIUM FALCIPARUM DIHYDROFOLATE REDUCTASE-THYMIDYLATE SYNTHASE(PFDHFR-TS) COMPLEXED WITH QN254, NADPH, AND DUMP | ROSSMANN FOLD, OXIDOREDUCTASE, TRANSFERASE
5cd2:A (GLU172) to (SER202) THE CRYSTAL STRUCTURE OF ENDO-1,4-D-GLUCANASE FROM VIBRIO FISCHERI ES114 | STRUCTURAL GENOMICS, PSI-BIOLOGY, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, HYDROLASE
3jtl:H (THR1) to (MET22) CRYSTAL STRUCTURE OF ARCHAEAL 20S PROTEASOME IN COMPLEX WITH MUTATED P26 ACTIVATOR | 20S PROTEASOME, PA26, CYTOPLASM, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3jtl:I (THR1) to (MET22) CRYSTAL STRUCTURE OF ARCHAEAL 20S PROTEASOME IN COMPLEX WITH MUTATED P26 ACTIVATOR | 20S PROTEASOME, PA26, CYTOPLASM, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3jtl:M (THR1) to (MET22) CRYSTAL STRUCTURE OF ARCHAEAL 20S PROTEASOME IN COMPLEX WITH MUTATED P26 ACTIVATOR | 20S PROTEASOME, PA26, CYTOPLASM, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3jtl:N (THR1) to (MET22) CRYSTAL STRUCTURE OF ARCHAEAL 20S PROTEASOME IN COMPLEX WITH MUTATED P26 ACTIVATOR | 20S PROTEASOME, PA26, CYTOPLASM, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
4o5l:H (SER120) to (PRO147) CRYSTAL STRUCTURE OF BROADLY NEUTRALIZING ANTIBODY F045-092 | FAB, FRAGMENT ANTIGEN BINDING, IMMUNOGLOBULIN FOLD, IMMUNE SYSTEM
2nup:B (PHE766) to (PRO781) CRYSTAL STRUCTURE OF THE HUMAN SEC23A/24A HETERODIMER, COMPLEXED WITH THE SNARE PROTEIN SEC22B | HUMAN COPII SEC23/24 COMPLEXED WITH SEC22, PROTEIN TRANSPORT
2nut:B (PHE766) to (PRO781) CRYSTAL STRUCTURE OF THE HUMAN SEC23A/24A HETERODIMER, COMPLEXED WITH THE SNARE PROTEIN SEC22B | HUMAN COPII SEC23/24 COMPLEXED WITH SEC22, PROTEIN TRANSPORT
4a11:B (LEU73) to (GLY91) STRUCTURE OF THE HSDDB1-HSCSA COMPLEX | DNA BINDING PROTEIN, DNA DAMAGE REPAIR
2ypl:A (HIS188) to (PRO210) STRUCTURAL FEATURES UNDERLYING T-CELL RECEPTOR SENSITIVITY TO CONCEALED MHC CLASS I MICROPOLYMORPHISMS | IMMUNE SYSTEM-VIRAL PROTEIN COMPLEX, MICROPOLYMORPHISM
5cex:B (SER118) to (PRO145) CRYSTAL STRUCTURE OF FAB 32H+109L, A PUTATIVE PRECURSOR OF THE PGT121 FAMILY OF POTENT HIV-1 ANTIBODIES | HIV-1, IMMUNE SYSTEM, ANTIBODY
5cex:D (SER118) to (PRO145) CRYSTAL STRUCTURE OF FAB 32H+109L, A PUTATIVE PRECURSOR OF THE PGT121 FAMILY OF POTENT HIV-1 ANTIBODIES | HIV-1, IMMUNE SYSTEM, ANTIBODY
5cey:B (SER118) to (PRO145) CRYSTAL STRUCTURE OF FAB 9H+3L, A PUTATIVE PRECURSOR OF THE PGT121 FAMILY OF POTENT HIV-1 ANTIBODIES | HIV-1, ANTIBODY, IMMUNE SYSTEM
5cey:D (SER118) to (PRO145) CRYSTAL STRUCTURE OF FAB 9H+3L, A PUTATIVE PRECURSOR OF THE PGT121 FAMILY OF POTENT HIV-1 ANTIBODIES | HIV-1, ANTIBODY, IMMUNE SYSTEM
1l9q:A (LEU12) to (VAL31) CRYSTAL STRUCTURE OF THE I257L VARIANT OF THE COPPER- CONTAINING NITRITE REDUCTASE FROM ALCALIGENES FAECALIS S-6 | CUPREDOXIN FOLD, OXIDOREDUCTASE
1l9u:B (ARG175) to (SER204) THERMUS AQUATICUS RNA POLYMERASE HOLOENZYME AT 4 A RESOLUTION | HELIX-TURN-HELIX, COILED-COIL, TRANSCRIPTION
1l9u:K (ARG175) to (SER204) THERMUS AQUATICUS RNA POLYMERASE HOLOENZYME AT 4 A RESOLUTION | HELIX-TURN-HELIX, COILED-COIL, TRANSCRIPTION
5cgg:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ALPHA- CHLOROACETAMIDE 1 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cgg:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ALPHA- CHLOROACETAMIDE 1 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cgh:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ALPHA- CHLOROACETAMIDE 5 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cgh:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ALPHA- CHLOROACETAMIDE 5 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cgi:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ONX 0914 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cgi:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ONX 0914 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
3k0i:A (LEU248) to (ILE267) CRYSTAL STRUCTURE OF CU(I)CUSA | TRANSMEMBRANE HELIX, CELL INNER MEMBRANE, CELL MEMBRANE, COPPER TRANSPORT, ION TRANSPORT, MEMBRANE, TRANSMEMBRANE, TRANSPORT, TRANSPORT PROTEIN
1ldp:H (ALA187) to (PRO210) CRYSTAL STRUCTURE OF MURINE MHC CLASS I H-2LD WITH A MIXTURE OF BOUND PEPTIDES | COMPLEX (MHC I/PEPTIDE), MAJOR HISTOCOMPATIBILITY COMPLEX, IMMUNOLOGY, CELLULAR IMMUNITY, PEPTIDE ANTIGEN, CELL SURFACE RECEPTOR, ANTIGEN RECEPTOR, ANTIGEN PRESENTATION
2yxw:A (GLY55) to (GLN81) THE DELETION MUTANT OF MULTICOPPER OXIDASE CUEO | MULTICOPPER OXIDASE, OXIDOREDUCTASE
2yxw:B (GLY55) to (GLN81) THE DELETION MUTANT OF MULTICOPPER OXIDASE CUEO | MULTICOPPER OXIDASE, OXIDOREDUCTASE
2yxw:B (THR347) to (ASN418) THE DELETION MUTANT OF MULTICOPPER OXIDASE CUEO | MULTICOPPER OXIDASE, OXIDOREDUCTASE
2yy1:A (LEU36) to (ALA66) CRYSTAL STURCTURE OF N-TERMINAL DOMAIN OF HUMAN GALECTIN-9 CONTAINING L-ACETYLLACTOSAMINE | SUGER BINDING, GALECTIN, HUMAN, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, SUGAR BINDING PROTEIN
2ny7:H (SER120) to (PRO149) HIV-1 GP120 ENVELOPE GLYCOPROTEIN COMPLEXED WITH THE BROADLY NEUTRALIZING CD4-BINDING-SITE ANTIBODY B12 | HIV, GP120, BROADLY NEUTRALIZING ANTIBODY, B12, VIRAL PROTEIN-IMMUNE SYSTEM COMPLEX
3k2h:A (CYS395) to (ASP416) CO-CRYSTAL STRUCTURE OF DIHYDROFOLATE REDUCTASE/THYMIDYLATE SYNTHASE FROM BABESIA BOVIS WITH DUMP, PEMETREXED AND NADP | NIAID, SSGCID, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, ALIMTA, FOLIC ACID ANALOG, THYA, FOLATE ANTIMETABOLITES, TIC-BORNE PARASITIC PROTOZOAN, BABESIOSIS, MALARIA-LIKE DISEASE, METHYLTRANSFERASE, TRANSFERASE
3k2h:B (HIS241) to (ASP264) CO-CRYSTAL STRUCTURE OF DIHYDROFOLATE REDUCTASE/THYMIDYLATE SYNTHASE FROM BABESIA BOVIS WITH DUMP, PEMETREXED AND NADP | NIAID, SSGCID, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, ALIMTA, FOLIC ACID ANALOG, THYA, FOLATE ANTIMETABOLITES, TIC-BORNE PARASITIC PROTOZOAN, BABESIOSIS, MALARIA-LIKE DISEASE, METHYLTRANSFERASE, TRANSFERASE
4ohj:A (SER72) to (ASN105) CRYSTAL STRUCTURE OF TOXIC SHOCK SYNDROME TOXIN-1 (TSST-1) FROM STAPHYLOCOCCUS AUREUS | STRUCTURAL GENOMICS, NIAID, NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID, TOXIN
4ohj:B (GLY71) to (ASN105) CRYSTAL STRUCTURE OF TOXIC SHOCK SYNDROME TOXIN-1 (TSST-1) FROM STAPHYLOCOCCUS AUREUS | STRUCTURAL GENOMICS, NIAID, NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID, TOXIN
2z4q:A (GLY89) to (PRO118) CRYSTAL STRUCTURE OF A MURINE ANTIBODY FAB 528 | IMMUNE SYSTEM
4oi1:A (THR391) to (ASP418) CLP1 BOUND TO SSRNA DINUCLEOTIDE GC, ADP, ALF4-, AND MG2+(TRANSITION STATE, DATA SET II) | POLYNUCLEOTIDE KINASE, RNA BINDING PROTEIN-RNA COMPLEX
4oi5:E (THR6) to (THR34) GLYCEROL-FREE STRUCTURE OF THERMOLYSIN IN COMPLEX WITH UBTLN58 | PROTEASE, METALLOPROTEASE, HYDROLYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1lnd:E (THR6) to (THR34) A STRUCTURAL ANALYSIS OF METAL SUBSTITUTIONS IN THERMOLYSIN | HYDROLASE (METALLOPROTEASE)
2o2p:A (VAL409) to (GLY427) CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF RAT 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE | ALDEHYDE DEHYDROGENASE, FDH, OXIDOREDUCTASE
2o2p:B (VAL409) to (GLY427) CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF RAT 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE | ALDEHYDE DEHYDROGENASE, FDH, OXIDOREDUCTASE
2o2p:C (VAL409) to (GLY427) CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF RAT 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE | ALDEHYDE DEHYDROGENASE, FDH, OXIDOREDUCTASE
2o2p:D (VAL409) to (GLY427) CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF RAT 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE | ALDEHYDE DEHYDROGENASE, FDH, OXIDOREDUCTASE
4a57:D (ARG257) to (GLY280) CRYSTAL STRUCTURE OF TOXOPLASMA GONDII NUCLEOSIDE TRIPHOSPHATE DIPHOSPHOHYDROLASE 3 (NTPDASE3) | HYDROLASE, NTPDASE
4a5b:A (ALA83) to (ARG104) CRYSTAL STRUCTURE OF THE C258S/C268S VARIANT OF TOXOPLASMA GONDII NUCLEOSIDE TRIPHOSPHATE DIPHOSPHOHYDROLASE 1 (NTPDASE1) | HYDROLASE, NTPDASE
2za3:A (CYS177) to (ASN196) CRYSTAL STRUCTURE OF OROTIDINE 5'-MONOPHOSPHATE DECARBOXYLASE COMPLEXED WITH URIDINE 5'-MONOPHOSPHATE FROM P.FALCIPARUM | OROTIDINE 5'-MONOPHOSPHATE DECARBOXYLASE, PLASMODIUM FALCIPARUM, URIDINE 5'-MONOPHOSPHATE, LYASE, PYRIMIDINE BIOSYNTHESIS
3k70:C (GLN939) to (ARG968) CRYSTAL STRUCTURE OF THE COMPLETE INITIATION COMPLEX OF RECBCD | RECOMBINATION, HELICASE, NUCLEASE, HYDROLASE, DNA REPAIR, ATP-BINDING, DNA DAMAGE, ENDONUCLEASE, EXONUCLEASE, NUCLEOTIDE-BINDING, HYDROLASE/DNA COMPLEX
2zba:C (MSE384) to (GLU414) CRYSTAL SRUCTURE OF F. SPOROTRICHIOIDES TRI101 COMPLEXED WITH COENZYME A AND T-2 | ACETYLTRANSFERASE, BAHD SUPERFAMILY, TRICHOTHECENE, DEOXYNIVALENOL, T-2, ACETYL COA, FUSARIUM, TRI101, TRANSFERASE
1lwh:A (ILE136) to (ASP160) CRYSTAL STRUCTURE OF T. MARITIMA 4-ALPHA-GLUCANOTRANSFERASE | 4-ALPHA-GLUCANOTRANSFERASE, ALPHA-AMYLASE FAMILY, THERMOTOGA MARITIMA, ACARBOSE
4ojl:B (GLU631) to (GLY647) CRYSTAL STRUCTURE OF PUTATIVE TAILSPIKE PROTEIN (TSP1, ORF210) FROM ESCHERICHIA COLI O157:H7 BACTERIOHAGE CBA120 IN COMPLEX WITH GLUCOSE | PARALLEL BETA HELIX, PUTATIVE ENDO-GLYCOSIDASE, BACTERIAL POLYSACCHARIDE, PHAGE BASEPLATE, PHAGE TAIL, VIRAL PROTEIN
2zcg:B (CYS177) to (ASN196) STRUCTURE AND INHIBITION OF OROTIDINE 5'-PHOSPHATE DECARBOXYLASE FROM PLASMODIUM FALCIPARUM | TIM BARREL, DECARBOXYLASE, LYASE, PYRIMIDINE BIOSYNTHESIS
1xnk:B (ASN58) to (ASN83) BETA-1,4-XYLANASE FROM CHAETOMIUM THERMOPHILUM COMPLEXED WITH METHYL THIOXYLOPENTOSIDE | XYLANASE, GLYCOSIDE HYDROLASE, FAMILY 11, GLYCOSIDASE, THIOINHIBITOR, SULPHUR CONTAINING INHIBITOR, HYDROLASE
2zcy:W (GLY-1) to (SER22) YEAST 20S PROTEASOME:SYRINGOLIN A-COMPLEX | ALPHA/BETA SANDWICH, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, PROTEASOME, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN
2zdz:A (ILE345) to (GLY396) X-RAY STRUCTURE OF BACE-1 IN COMPLEX WITH COMPOUND 3.B.10 | BACE, ASPARTYL PROTEASE, ACYLGUANIDINE INHIBITOR, ALTERNATIVE SPLICING, GLYCOPROTEIN, HYDROLASE, MEMBRANE, TRANSMEMBRANE, ZYMOGEN
4olu:H (SER120) to (PRO147) CRYSTAL STRUCTURE OF ANTIBODY VRC07 IN COMPLEX WITH CLADE A/E 93TH057 HIV-1 GP120 CORE | VRC07 ANTIBODY, PASSIVE TRANSFER, NEUTRALIZATION, IN VIVO PROTECTION, AUTOREACTIVITY, LENTIVIRAL INFECTION, ENHANCED POTENCY, HIV-1 GP120, VIRAL PROTEIN-IMMUNE SYSTEM COMPLEX
4om1:H (SER120) to (PRO147) CRYSTAL STRUCTURE OF ANTIBODY VRC07-I30Q, G54W, S58N IN COMPLEX WITH CLADE A/E 93TH057 HIV-1 GP120 CORE | VRC07 ANTIBODY, PASSIVE TRANSFER, NEUTRALIZATION, IN VIVO PROTECTION, AUTOREACTIVITY, LENTIVIRAL INFECTION, ENHANCED POTENCY, HIV-1 GP120, VRC07-I30Q, VIRAL PROTEIN-IMMUNE SYSTEM COMPLEX
2zhk:A (LEU29) to (ALA59) CRYSTAL STRUCTURE OF HUMAN GALECTIN-9 N-TERMINAL CRD IN COMPLEX WITH N-ACETYLLACTOSAMINE DIMER (CRYSTAL 1) | BETA SANDWICH, CARBOHYDRATE BINDING PROTEIN, GALECTIN, SECRETED, SUGAR BINDING PROTEIN
2zhk:B (LEU29) to (ALA59) CRYSTAL STRUCTURE OF HUMAN GALECTIN-9 N-TERMINAL CRD IN COMPLEX WITH N-ACETYLLACTOSAMINE DIMER (CRYSTAL 1) | BETA SANDWICH, CARBOHYDRATE BINDING PROTEIN, GALECTIN, SECRETED, SUGAR BINDING PROTEIN
2zhl:A (LEU29) to (ALA59) CRYSTAL STRUCTURE OF HUMAN GALECTIN-9 N-TERMINAL CRD IN COMPLEX WITH N-ACETYLLACTOSAMINE DIMER (CRYSTAL 2) | BETA SANDWICH, CARBOHYDRATE BINDING PROTEIN, GALECTIN, SUGAR BINDING PROTEIN
2zhl:B (LEU29) to (ALA59) CRYSTAL STRUCTURE OF HUMAN GALECTIN-9 N-TERMINAL CRD IN COMPLEX WITH N-ACETYLLACTOSAMINE DIMER (CRYSTAL 2) | BETA SANDWICH, CARBOHYDRATE BINDING PROTEIN, GALECTIN, SUGAR BINDING PROTEIN
2zhl:C (LEU29) to (ALA59) CRYSTAL STRUCTURE OF HUMAN GALECTIN-9 N-TERMINAL CRD IN COMPLEX WITH N-ACETYLLACTOSAMINE DIMER (CRYSTAL 2) | BETA SANDWICH, CARBOHYDRATE BINDING PROTEIN, GALECTIN, SUGAR BINDING PROTEIN
2zhl:D (LEU29) to (ALA59) CRYSTAL STRUCTURE OF HUMAN GALECTIN-9 N-TERMINAL CRD IN COMPLEX WITH N-ACETYLLACTOSAMINE DIMER (CRYSTAL 2) | BETA SANDWICH, CARBOHYDRATE BINDING PROTEIN, GALECTIN, SUGAR BINDING PROTEIN
2zhm:A (LEU29) to (ALA59) CRYSTAL STRUCTURE OF HUMAN GALECTIN-9 N-TERMINAL CRD IN COMPLEX WITH N-ACETYLLACTOSAMINE TRIMER (CRYSTAL 1) | BETA SANDWICH, CARBOHYDRATE BINDING PROTEIN, GALECTIN, SUGAR BINDING PROTEIN
2zhm:B (LEU29) to (ALA59) CRYSTAL STRUCTURE OF HUMAN GALECTIN-9 N-TERMINAL CRD IN COMPLEX WITH N-ACETYLLACTOSAMINE TRIMER (CRYSTAL 1) | BETA SANDWICH, CARBOHYDRATE BINDING PROTEIN, GALECTIN, SUGAR BINDING PROTEIN
2zhm:C (LEU29) to (ALA59) CRYSTAL STRUCTURE OF HUMAN GALECTIN-9 N-TERMINAL CRD IN COMPLEX WITH N-ACETYLLACTOSAMINE TRIMER (CRYSTAL 1) | BETA SANDWICH, CARBOHYDRATE BINDING PROTEIN, GALECTIN, SUGAR BINDING PROTEIN
2zhm:D (LEU29) to (ALA59) CRYSTAL STRUCTURE OF HUMAN GALECTIN-9 N-TERMINAL CRD IN COMPLEX WITH N-ACETYLLACTOSAMINE TRIMER (CRYSTAL 1) | BETA SANDWICH, CARBOHYDRATE BINDING PROTEIN, GALECTIN, SUGAR BINDING PROTEIN
3kd4:A (GLY474) to (THR501) CRYSTAL STRUCTURE OF A PUTATIVE PROTEASE (BDI_1141) FROM PARABACTEROIDES DISTASONIS ATCC 8503 AT 2.00 A RESOLUTION | PUTATIVE PROTEASE, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, HYDROLASE
3kd4:B (GLY474) to (THR501) CRYSTAL STRUCTURE OF A PUTATIVE PROTEASE (BDI_1141) FROM PARABACTEROIDES DISTASONIS ATCC 8503 AT 2.00 A RESOLUTION | PUTATIVE PROTEASE, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, HYDROLASE
1m4z:B (GLN72) to (ARG92) CRYSTAL STRUCTURE OF THE N-TERMINAL BAH DOMAIN OF ORC1P | DNA REPLICATION, TRANSCRIPTIONAL SILENCING, CHROMATIN, BAH DOMAIN, GENE REGULATION
2zjh:A (ILE283) to (GLY334) CRYSTAL STRUCTURE OF THE HUMAN BACE1 CATALYTIC DOMAIN IN COMPLEX WITH N-(1-BENZYL-PIPERIDIN-4-YL)-4-MERCAPTO-BUTYRAMIDE | BACE1, SMALL-MOLECULE INHIBITOR, ASPARTYL PROTEASE, GLYCOPROTEIN, HYDROLASE, MEMBRANE, PROTEASE, TRANSMEMBRANE, ZYMOGEN
2zjl:A (ILE283) to (GLY334) CRYSTAL STRUCTURE OF THE HUMAN BACE1 CATALYTIC DOMAIN IN COMPLEX WITH N-[1-(5-BROMO-2,3-DIMETHOXY-BENZYL)-PIPERIDIN- 4-YL]-4-MERCAPTO-BUTYRAMIDE | BACE1, SMALL-MOLECULE INHIBITOR, TETHERING, ALTERNATIVE SPLICING, ASPARTYL PROTEASE, GLYCOPROTEIN, HYDROLASE, MEMBRANE, PROTEASE, TRANSMEMBRANE, ZYMOGEN
5cuy:A (LEU319) to (SER337) CRYSTAL STRUCTURE OF TRYPANOSOMA BRUCEI VACUOLAR SOLUBLE PYROPHOSPHATASES IN APO FORM | SUBSTRATE BINDING, ACIDOCALCISOMAL PYROPHOSPHATASE, METAL BINDING PROTEIN
4aa1:A (SER339) to (VAL357) CRYSTAL STRUCTURE OF ANCE IN COMPLEX WITH ANGIOTENSIN-II | HYDROLASE-HORMONE COMPLEX, HYDROLASE, SUBSTRATE BINDING
4aa2:A (SER339) to (VAL357) CRYSTAL STRUCTURE OF ANCE IN COMPLEX WITH BRADYKININ POTENTIATING PEPTIDE B | HYDROLASE-PEPTIDE COMPLEX, HYDROLASE, SUBSTRATE BINDING, INHIBITOR
1m79:B (ASP175) to (ARG191) CANDIDA ALBICANS DIHYDROFOLATE REDUCTASE COMPLEXED WITH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE (NADPH) AND 5-(4-METHOXYPHENOXY)-2,4-QUINAZOLINEDIAMINE (GW1466) | OXIDOREDUCTASE, ANTIFUNGAL TARGET, REDUCTASE
1xxf:C (GLY19) to (LEU55) CRYSTAL STRUCTURE OF THE FXIA CATALYTIC DOMAIN IN COMPLEX WITH ECOTIN MUTANT (ECOTINP) | FXIA; CATALYTIC DOMAIN; SERINE PROTEASE; ECOTIN; SUBSTRATE- LIKE INTERACTION, BLOOD CLOTTING/HYDROLASE INHIBITOR COMPLEX
5cz6:L (GLY10) to (THR31) YEAST 20S PROTEASOME BETA5-T1A MUTANT IN COMPLEX WITH SYRINGOLIN A, PROPEPTIDE EXPRESSED IN TRANS | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cz6:Z (GLY10) to (THR31) YEAST 20S PROTEASOME BETA5-T1A MUTANT IN COMPLEX WITH SYRINGOLIN A, PROPEPTIDE EXPRESSED IN TRANS | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cz5:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA1-T1A MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cz5:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA1-T1A MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
1xxj:D (ARG128) to (SER154) URATE OXIDASE FROM ASPERGILLUS FLAVUS COMPLEXED WITH 5- AMINO 6-NITRO URACIL | OXIDOREDUCTASE, URIC ACID DEGRADATION, DIMERIC BARREL, TUNNEL-SHAPED PROTEIN
5cza:L (GLY10) to (THR31) YEAST 20S PROTEASOME BETA5-D166N MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5cza:N (THR1) to (THR22) YEAST 20S PROTEASOME BETA5-D166N MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5cza:Z (GLY10) to (THR31) YEAST 20S PROTEASOME BETA5-D166N MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5cza:b (THR1) to (THR22) YEAST 20S PROTEASOME BETA5-D166N MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
1y0l:H (SER120) to (PRO149) CATALYTIC ELIMINATION ANTIBODY 34E4 IN COMPLEX WITH HAPTEN | IMMUNOGLOBULIN, CATALYTIC ANTIBODY, CHIMERIC FAB, HAPTEN COMPLEX, IMMUNE SYSTEM
1y0l:F (SER120) to (PRO149) CATALYTIC ELIMINATION ANTIBODY 34E4 IN COMPLEX WITH HAPTEN | IMMUNOGLOBULIN, CATALYTIC ANTIBODY, CHIMERIC FAB, HAPTEN COMPLEX, IMMUNE SYSTEM
4ovm:H (ASP87) to (PRO107) CRYSTAL STRUCTURE OF SGCJ PROTEIN FROM STREPTOMYCES CARZINOSTATICUS | NEOCARZINOSTATIN BIOSYNTHESIS, UNKNOWN FUNCITON, PSI-BIOLOGY, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, ENZYME DISCOVERY FOR NATURAL PRODUCT BIOSYNTHESIS, NATPRO, STRUCTURAL GENOMICS, UNKNOWN FUNCTION
4acj:A (LEU691) to (THR719) CRYSTAL STRUCTURE OF THE TLDC DOMAIN OF OXIDATION RESISTANCE PROTEIN 2 FROM ZEBRAFISH | IMMUNE SYSTEM
2ztn:A (ALA565) to (PRO603) HEPATITIS E VIRUS ORF2 (GENOTYPE 3) | HEV, VIRUS
4ow3:A (THR6) to (THR34) THERMOLYSIN STRUCTURE DETERMINED BY FREE-ELECTRON LASER | THERMOLYSIN, PROTEASE
5d0s:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-D166N MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0s:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-D166N MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0t:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-D166N MUTANT IN COMPLEX WITH MG132 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0t:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-D166N MUTANT IN COMPLEX WITH MG132 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0v:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-T1C MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0v:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-T1C MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0w:L (GLY10) to (THR31) YEAST 20S PROTEASOME BETA5-T1S MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5d0w:N (THR1) to (THR22) YEAST 20S PROTEASOME BETA5-T1S MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5d0w:Z (GLY10) to (THR31) YEAST 20S PROTEASOME BETA5-T1S MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5d0w:b (THR1) to (THR22) YEAST 20S PROTEASOME BETA5-T1S MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5d0x:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-T1S MUTANT IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0x:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-T1S MUTANT IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0z:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-T1S MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0z:N (THR1) to (THR22) YEAST 20S PROTEASOME BETA5-T1S MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0z:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-T1S MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d2l:B (LYS6) to (PRO32) CRYSTAL STRUCTURE OF TCR C7 IN COMPLEX WITH HCMV NLV EPITOPE PRESENTED BY HLA-A2 | TCR, HCMV, HLA-A2, COMPLEX, IMMUNE SYSTEM
5d2l:D (LYS6) to (PRO32) CRYSTAL STRUCTURE OF TCR C7 IN COMPLEX WITH HCMV NLV EPITOPE PRESENTED BY HLA-A2 | TCR, HCMV, HLA-A2, COMPLEX, IMMUNE SYSTEM
3km5:A (LEU1188) to (ASN1218) CRYSTAL STRUCTURE ANALYSIS OF THE K2 CLEAVED ADHESIN DOMAIN OF LYS- GINGIPAIN (KGP) | BETA JELLY ROLL BARREL, CLEAVED ADHESIN FAMILY, LYS-GINGIPAIN, HEMAGGLUTINATION DOMAIN, CELL INVASION
4p24:C (ILE107) to (LEU157) PORE FORMING TOXIN | PORE FORMING TOXIN
4p24:F (ILE107) to (LEU157) PORE FORMING TOXIN | PORE FORMING TOXIN
4p24:G (ILE107) to (LEU157) PORE FORMING TOXIN | PORE FORMING TOXIN
3koh:B (ILE474) to (ILE490) CYTOCHROME P450 2E1 WITH OMEGA-IMIDAZOLYL OCTANOIC ACID | CYP2E1, P450 2E1, MONOOXYGENASE, HEME, FATTY ACID, MICROSOME, MEMBRANE, OXIDOREDUCTASE, ENDOPLASMIC RETICULUM, IRON, METAL-BINDING
1y7w:A (ASN77) to (ALA95) CRYSTAL STRUCTURE OF A HALOTOLERANT CARBONIC ANHYDRASE FROM DUNALIELLA SALINA | ALPHA-TYPE CARBONIC ANHYDRASE, HALTOLERANT PROTEIN, ALGAL CARBONIC ANHYDRASE, SALT TOLERANT PROTEIN, ZINC ENZYME, ANION TOLERANCE, DUNALIELLA SALINA CARBONIC ANHYDRASE, DCA II, ISRAEL STRUCTURAL PROTEOMICS CENTER, ISPC, STRUCTURAL GENOMICS, LYASE
1y7w:B (ASN77) to (ALA95) CRYSTAL STRUCTURE OF A HALOTOLERANT CARBONIC ANHYDRASE FROM DUNALIELLA SALINA | ALPHA-TYPE CARBONIC ANHYDRASE, HALTOLERANT PROTEIN, ALGAL CARBONIC ANHYDRASE, SALT TOLERANT PROTEIN, ZINC ENZYME, ANION TOLERANCE, DUNALIELLA SALINA CARBONIC ANHYDRASE, DCA II, ISRAEL STRUCTURAL PROTEOMICS CENTER, ISPC, STRUCTURAL GENOMICS, LYASE
1y8e:B (SER225) to (ARG244) VCP:SURAMIN COMPLEX | BETA BARREL, VIRAL PROTEIN
1y96:A (VAL20) to (PHE49) CRYSTAL STRUCTURE OF THE GEMIN6/GEMIN7 HETERODIMER FROM THE HUMAN SMN COMPLEX | SM FOLD, PROTEIN COMPLEX, RNA BINDING PROTEIN
1y96:C (VAL20) to (PHE49) CRYSTAL STRUCTURE OF THE GEMIN6/GEMIN7 HETERODIMER FROM THE HUMAN SMN COMPLEX | SM FOLD, PROTEIN COMPLEX, RNA BINDING PROTEIN
1ya7:H (THR1) to (MET22) IMPLICATIONS FOR INTERACTIONS OF PROTEASOME WITH PAN AND PA700 FROM THE 1.9 A STRUCTURE OF A PROTEASOME-11S ACTIVATOR COMPLEX | ARCHAEAL PROTEASOME, PA26, COPMLEX, OPEN GATE, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
1ya7:I (THR1) to (MET22) IMPLICATIONS FOR INTERACTIONS OF PROTEASOME WITH PAN AND PA700 FROM THE 1.9 A STRUCTURE OF A PROTEASOME-11S ACTIVATOR COMPLEX | ARCHAEAL PROTEASOME, PA26, COPMLEX, OPEN GATE, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
1ya7:J (THR1) to (MET22) IMPLICATIONS FOR INTERACTIONS OF PROTEASOME WITH PAN AND PA700 FROM THE 1.9 A STRUCTURE OF A PROTEASOME-11S ACTIVATOR COMPLEX | ARCHAEAL PROTEASOME, PA26, COPMLEX, OPEN GATE, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
1ya7:K (THR1) to (MET22) IMPLICATIONS FOR INTERACTIONS OF PROTEASOME WITH PAN AND PA700 FROM THE 1.9 A STRUCTURE OF A PROTEASOME-11S ACTIVATOR COMPLEX | ARCHAEAL PROTEASOME, PA26, COPMLEX, OPEN GATE, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
1ya7:L (THR1) to (MET22) IMPLICATIONS FOR INTERACTIONS OF PROTEASOME WITH PAN AND PA700 FROM THE 1.9 A STRUCTURE OF A PROTEASOME-11S ACTIVATOR COMPLEX | ARCHAEAL PROTEASOME, PA26, COPMLEX, OPEN GATE, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
1ya7:M (THR1) to (MET22) IMPLICATIONS FOR INTERACTIONS OF PROTEASOME WITH PAN AND PA700 FROM THE 1.9 A STRUCTURE OF A PROTEASOME-11S ACTIVATOR COMPLEX | ARCHAEAL PROTEASOME, PA26, COPMLEX, OPEN GATE, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
1ya7:N (THR1) to (MET22) IMPLICATIONS FOR INTERACTIONS OF PROTEASOME WITH PAN AND PA700 FROM THE 1.9 A STRUCTURE OF A PROTEASOME-11S ACTIVATOR COMPLEX | ARCHAEAL PROTEASOME, PA26, COPMLEX, OPEN GATE, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
1mrc:L (PHE87) to (PRO113) PREPARATION, CHARACTERIZATION AND CRYSTALLIZATION OF AN ANTIBODY FAB FRAGMENT THAT RECOGNIZES RNA. CRYSTAL STRUCTURES OF NATIVE FAB AND THREE FAB-MONONUCLEOTIDE COMPLEXES | IMMUNOGLOBULIN
3kpm:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA B*4402 IN COMPLEX WITH EEYLKAWTF, A MIMOTOPE | HLA B*4402, ALLORECOGNITION, TCR RECOGNITION, MIMOTOPE PEPTIDE, DISULFIDE BOND, GLYCOPROTEIN, HOST-VIRUS INTERACTION, IMMUNE RESPONSE, MEMBRANE, MHC I, TRANSMEMBRANE, IMMUNE SYSTEM
1yau:H (THR1) to (MET22) STRUCTURE OF ARCHEABACTERIAL 20S PROTEASOME- PA26 COMPLEX | PROTEASOME 20S, PA26 PROTEASOME ACTIVATOR 11S, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
1yau:I (THR1) to (MET22) STRUCTURE OF ARCHEABACTERIAL 20S PROTEASOME- PA26 COMPLEX | PROTEASOME 20S, PA26 PROTEASOME ACTIVATOR 11S, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
1yau:J (THR1) to (MET22) STRUCTURE OF ARCHEABACTERIAL 20S PROTEASOME- PA26 COMPLEX | PROTEASOME 20S, PA26 PROTEASOME ACTIVATOR 11S, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
1yau:K (THR1) to (MET22) STRUCTURE OF ARCHEABACTERIAL 20S PROTEASOME- PA26 COMPLEX | PROTEASOME 20S, PA26 PROTEASOME ACTIVATOR 11S, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
1yau:L (THR1) to (MET22) STRUCTURE OF ARCHEABACTERIAL 20S PROTEASOME- PA26 COMPLEX | PROTEASOME 20S, PA26 PROTEASOME ACTIVATOR 11S, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
1yau:M (THR1) to (MET22) STRUCTURE OF ARCHEABACTERIAL 20S PROTEASOME- PA26 COMPLEX | PROTEASOME 20S, PA26 PROTEASOME ACTIVATOR 11S, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
1yau:N (THR1) to (MET22) STRUCTURE OF ARCHEABACTERIAL 20S PROTEASOME- PA26 COMPLEX | PROTEASOME 20S, PA26 PROTEASOME ACTIVATOR 11S, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
4ai6:A (HIS2461) to (GLU2488) DYNEIN MOTOR DOMAIN - ADP COMPLEX | MOTOR PROTEIN, AAA+ PROTEIN, ASCE PROTEIN, P-LOOP NTPASE, CYTOSKELETAL MOTOR, ATPASE
3kr3:H (SER129) to (PRO156) CRYSTAL STRUCTURE OF IGF-II ANTIBODY COMPLEX | ANTIBODY-TARGET COMPLEX, CARBOHYDRATE METABOLISM, GLUCOSE METABOLISM, GLYCOPROTEIN, GROWTH FACTOR, HORMONE, MITOGEN, OSTEOGENESIS, SECRETED, IMMUNE SYSTEM
5d7l:B (LYS6) to (PRO32) STRUCTURE OF HUMAN MR1-5-OP-RU IN COMPLEX WITH HUMAN MAV36 TCR | RECEPTOR, ANTIGEN, IMMUNE SYSTEM
4pel:B (ASN178) to (GLN200) S1C MUTANT OF PENICILLIN G ACYLASE FROM KLUYVERA CITROPHILA | NTN HYDROLASE, PGA, SLOW PROCESSING, HYDROLASE
4pel:F (ASN178) to (GLN200) S1C MUTANT OF PENICILLIN G ACYLASE FROM KLUYVERA CITROPHILA | NTN HYDROLASE, PGA, SLOW PROCESSING, HYDROLASE
4pel:H (ASN178) to (GLN200) S1C MUTANT OF PENICILLIN G ACYLASE FROM KLUYVERA CITROPHILA | NTN HYDROLASE, PGA, SLOW PROCESSING, HYDROLASE
3kx4:B (GLU430) to (LYS452) CRYSTAL STRUCTURE OF BACILLUS MEGATERIUM BM3 HEME DOMAIN MUTANT I401E | CYTOCHROME P450, I401E MUTANT, HEME DOMAIN, CYTOPLASM, ELECTRON TRANSPORT, FAD, FLAVOPROTEIN, FMN, HEME, IRON, METAL-BINDING, MONOOXYGENASE, MULTIFUNCTIONAL ENZYME, NADP, OXIDOREDUCTASE, TRANSPORT
1yms:A (ASP233) to (GLN254) X-RAY CRYSTALLOGRAPHIC STRUCTURE OF CTX-M-9 BETA-LACTAMASE COMPLEXED WITH NAFCININ-LIKE BORONIC ACID INHIBITOR | CTX-M, BETA-LACTAMASE, TRANSITION STATE, ACYLATION, HYDROLASE
4akg:A (HIS2461) to (GLU2488) DYNEIN MOTOR DOMAIN - ATP COMPLEX | MOTOR PROTEIN, AAA+ PROTEIN, ASCE PROTEIN, P-LOOP NTPASE, CYTOSKELETAL MOTOR, ATPASE
5ddy:A (SER463) to (LEU479) BINARY COMPLEX OF HUMAN POLYMERASE LAMBDA WITH DCTP | POLYMERASE LAMBDA, TRANSFERASE
5ddy:G (SER463) to (PRO480) BINARY COMPLEX OF HUMAN POLYMERASE LAMBDA WITH DCTP | POLYMERASE LAMBDA, TRANSFERASE
5de2:B (ILE95) to (LEU119) STRUCTURAL MECHANISM OF NEK7 ACTIVATION BY NEK9-INDUCED DIMERISATION | PROTEIN KINASE, MITOSIS, PROTEIN-PROTEIN INTERACTION, TRANSFERASE
5dg1:A (THR20) to (ASN46) SUGAR BINDING PROTEIN - HUMAN GALECTIN-2 | GALECTIN-2, SUGAR BINDING PROTEIN
1yqo:A (GLU430) to (LYS452) T268A MUTANT HEME DOMAIN OF FLAVOCYTOCHROME P450 BM3 | CYTOCHROME P450, FATTY ACID HYDROXYLASE, OXIDOREDUCTASE
1yqo:B (GLU430) to (LYS452) T268A MUTANT HEME DOMAIN OF FLAVOCYTOCHROME P450 BM3 | CYTOCHROME P450, FATTY ACID HYDROXYLASE, OXIDOREDUCTASE
1yqp:A (GLU430) to (LYS452) T268N MUTANT CYTOCHROME DOMAIN OF FLAVOCYTOCHROME P450 BM3 | CYTOCHROME P450, FATTY ACID HYDROXYLASE, OXIDOREDUCTASE
3l3d:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA-B*4402 IN COMPLEX WITH THE F3A MUTANT OF A SELF-PEPTIDE DERIVED FROM DPA*0201 | IMMUNOGLOBULIN DOMAIN, IMMUNE RESPONSE, MAJOR HISTOCOMPATIBILITY COMPLEX CLASS I, MHC-I PEPTIDE COMPLEX, ALTERED PEPTIDE LIGAND, IMMUNE SYSTEM
3l7f:H (SER128) to (PRO155) STRUCTURE OF IL-13 ANTIBODY H2L6, A HUMANIZED VARIANT OF C836 | IMMUNOGLOBULIN FOLD, MONOCLONAL ANTIBODY, IMMUNE SYSTEM
3l7f:B (SER128) to (PRO155) STRUCTURE OF IL-13 ANTIBODY H2L6, A HUMANIZED VARIANT OF C836 | IMMUNOGLOBULIN FOLD, MONOCLONAL ANTIBODY, IMMUNE SYSTEM
3l7q:B (GLN18) to (PRO33) CRYSTAL STRUCTURE OF ALDR FROM STREPTOCOCCUS MUTANS | ALDR, STREPTOCOCCUS MUTANS, TRANSLATION INITIATION INHIBITOR, REGULATOR-LIKE, TRANSLATION
5dof:D (SER33) to (PRO48) CRYSTAL STRUCTURE OF TETRAHYMENA P19 | TELOMERASE, OB FOLD, TETRAHYMENA, DNA BINDING PROTEIN
4ps3:A (SER400) to (SER417) STRUCTURE OF PI3K GAMMA IN COMPLEX WITH 1-[6-(5-METHOXYPYRIDIN-3-YL)- 1,3-BENZOTHIAZOL-2-YL]-3-[2-(1-PROPYL-1H-IMIDAZOL-4-YL)ETHYL]UREA | SERINE/THREONINE PROTEIN KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
3ldk:A (ARG487) to (SER503) CRYSTAL STRUCTURE OF A. JAPONICUS CB05 | FIVE-BLADED BETA-PROPELLER FOLD, HYDROLASE
3ajz:A (MET13) to (ALA40) CRYSTAL STRUCTURE OF ANCESTRAL CONGERIN CON-ANC | ANCESTRAL PROTEIN, GALECTIN, LECTIN, SUGAR BINDING PROTEIN
4ps8:A (SER400) to (SER417) STRUCTURE OF PI3K GAMMA IN COMPLEX WITH N-[6-(5,6-DIMETHOXYPYRIDIN-3- YL)-1,3-BENZOTHIAZOL-2-YL]ACETAMIDE | SERINE/THREONINE PROTEIN KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
3lcy:D (LYS15) to (GLY33) TITIN IG TANDEM DOMAINS A164-A165 | TITIN, A-BAND, IG TANDEM DOMAINS, ATP-BINDING, CALMODULIN-BINDING, CARDIOMYOPATHY, DISEASE MUTATION, DISULFIDE BOND, IMMUNOGLOBULIN DOMAIN, ISOPEPTIDE BOND, KELCH REPEAT, KINASE, LIMB-GIRDLE MUSCULAR DYSTROPHY, MAGNESIUM, METAL-BINDING, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TPR REPEAT, TRANSFERASE, WD REPEAT
3lem:A (ASP486) to (SER503) CRYSTAL STRUCTURE OF FRUCTOSYLTRANSFERASE (D191A) FROM A. JAPONICUS IN COMPLEX WITH NYSTOSE | PROTEIN-OLIGOSACCHARIDE COMPLEX, FIVE BLADED BETA-PROPELLER FOLD, HYDROLASE
1z7q:M (THR11) to (THR31) CRYSTAL STRUCTURE OF THE 20S PROTEASOME FROM YEAST IN COMPLEX WITH THE PROTEASOME ACTIVATOR PA26 FROM TRYPANOSOME BRUCEI AT 3.2 ANGSTROMS RESOLUTION | 20S, PROTEASOME, PA26, ACTIVATOR, MULTI-CATALYTIC PROTEASE, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
1z7q:a (THR11) to (THR31) CRYSTAL STRUCTURE OF THE 20S PROTEASOME FROM YEAST IN COMPLEX WITH THE PROTEASOME ACTIVATOR PA26 FROM TRYPANOSOME BRUCEI AT 3.2 ANGSTROMS RESOLUTION | 20S, PROTEASOME, PA26, ACTIVATOR, MULTI-CATALYTIC PROTEASE, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
3lfi:A (ASP486) to (SER503) CRYSTAL STRUCTURE OF FRUCTOSYLTRANSFERASE (WILD-TYPE) FROM A. JAPONICUS IN COMPLEX WITH GLUCOSE | PROTEIN-OLIGOSACCHARIDE COMPLEX, FIVE BLADED BETA-PROPELLER FOLD, HYDROLASE
5dpe:E (THR6) to (THR34) THERMOLYSIN IN COMPLEX WITH INHIBITOR. | HYDROLASE, METALLOPROTEASE, HYDROLASE INHIBITOR COMPLEX
5dpf:E (THR6) to (THR34) THERMOLYSIN IN COMPLEX WITH INHIBITOR. | PROTEASE, METALLOPROTEASE, HYDROLASE, HYDROLASE INHIBITOR COMPLEX
3alp:B (ASN36) to (PRO58) CELL ADHESION PROTEIN | IMMUNOGLOBULIN-LIKE DOMAIN, V-SET, C2-SET, CELL ADHESION
3alq:U (LEU118) to (GLU133) CRYSTAL STRUCTURE OF TNF-TNFR2 COMPLEX | LIGAND-RECEPTOR COMPLEX, CYTOKINE, CYTOKINE-CYTOKINE RECEPTOR COMPLEX
1z9g:E (THR6) to (THR34) CRYSTAL STRUCTURE ANALYSIS OF THERMOLYSIN COMPLEXED WITH THE INHIBITOR (R)-RETRO-THIORPHAN | ENZYME-INHIBITOR COMPLEX; ZINC ENDOPEPTIDASE; GAMMA TURN; THERMOSTABLE, HYDROLASE
5drz:B (SER120) to (PRO147) CRYSTAL STRUCTURE OF ANTI-HIV-1 ANTIBODY F240 FAB IN COMPLEX WITH GP41 PEPTIDE | IGG, VIRAL PROTEIN, HIV GP41 ENVELOPE PROTEIN, IMMUNE SYSTEM
3lig:A (ARG487) to (SER503) CRYSTAL STRUCTURE OF FRUCTOSYLTRANSFERASE (D191A) FROM A. JAPONICUS | FIVE BLADED BETA-PROPELLER FOLD, HYDROLASE
1zhb:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF THE MURINE CLASS I MAJOR HISTOCOMPATIBILITY COMPLEX OF H-2DB, B2-MICROGLOBULIN, AND A 9-RESIDUE PEPTIDE DERIVED FROM RAT DOPAMINE BETA- MONOOXIGENASE | MHC, TCR-CROSSREACTIVITY, SELF-LIGAND, AUTOIMMUNITY, IMMUNE SYSTEM
1zhb:D (HIS188) to (PRO210) CRYSTAL STRUCTURE OF THE MURINE CLASS I MAJOR HISTOCOMPATIBILITY COMPLEX OF H-2DB, B2-MICROGLOBULIN, AND A 9-RESIDUE PEPTIDE DERIVED FROM RAT DOPAMINE BETA- MONOOXIGENASE | MHC, TCR-CROSSREACTIVITY, SELF-LIGAND, AUTOIMMUNITY, IMMUNE SYSTEM
1zhb:G (HIS188) to (PRO210) CRYSTAL STRUCTURE OF THE MURINE CLASS I MAJOR HISTOCOMPATIBILITY COMPLEX OF H-2DB, B2-MICROGLOBULIN, AND A 9-RESIDUE PEPTIDE DERIVED FROM RAT DOPAMINE BETA- MONOOXIGENASE | MHC, TCR-CROSSREACTIVITY, SELF-LIGAND, AUTOIMMUNITY, IMMUNE SYSTEM
1zhb:J (HIS188) to (PRO210) CRYSTAL STRUCTURE OF THE MURINE CLASS I MAJOR HISTOCOMPATIBILITY COMPLEX OF H-2DB, B2-MICROGLOBULIN, AND A 9-RESIDUE PEPTIDE DERIVED FROM RAT DOPAMINE BETA- MONOOXIGENASE | MHC, TCR-CROSSREACTIVITY, SELF-LIGAND, AUTOIMMUNITY, IMMUNE SYSTEM
3lkl:A (ALA2) to (PHE23) CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF ANTI-SIGMA FACTOR ANTAGONIST STAS FROM RHODOBACTER SPHAEROIDES | MCSG, PSI, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, TRANSPORT PROTEIN
1zhi:A (LEU74) to (ARG92) COMPLEX OF THE S. CEREVISIAE ORC1 AND SIR1 INTERACTING DOMAINS | PROTEIN COMPLEX, BAH DOMAIN, OIR DOMAIN, TRANSCRIPTION-REPLICATION COMPLEX
5dur:B (SER128) to (PRO155) INFLUENZA A VIRUS H5 HEMAGGLUTININ GLOBULAR HEAD IN COMPLEX WITH ANTIBODY 100F4 | INFLUENZA VIRUS, ANTIBODY, COMPLEX, NEUTRALIZE, IMMUNE SYSTEM
3lmj:H (SER132) to (PRO159) STRUCTURE OF HUMAN ANTI HIV 21C FAB | IMMUNOGLOBULIN, IMMUNE SYSTEM
4arx:A (PRO556) to (THR580) LEPIDOPTERA-SPECIFIC TOXIN CRY1AC FROM BACILLUS THURINGIENSIS SSP. KURSTAKI HD-73 | TOXIN, MEMBRANE PORE-FORMING TOXIN, INSECTICIDAL PROTEIN LEPIDOPTERAN SPECIFICITY, RECEPTOR BINDING SITE
4arx:B (PRO556) to (THR580) LEPIDOPTERA-SPECIFIC TOXIN CRY1AC FROM BACILLUS THURINGIENSIS SSP. KURSTAKI HD-73 | TOXIN, MEMBRANE PORE-FORMING TOXIN, INSECTICIDAL PROTEIN LEPIDOPTERAN SPECIFICITY, RECEPTOR BINDING SITE
3ln5:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA-B*4104 IN COMPLEX WITH A 11MER SELF-PEPTIDE DERIVED FROM S-METHYL-5-THIOADENOSINE PHOSPHORYLASE | IMMUNOGLOBULIN DOMAIN, IMMUNE RESPONSE, MAJOR HISTOCOMPATIBILITY COMPLEX CLASS I, MHC-I PEPTIDE COMPLEX, PEPTIDE-BINDING MOTIFS, DISULFIDE BOND, IMMUNE SYSTEM
4q1r:A (LEU17) to (CYS42) GALECTIN-1 IN COMPLEX WITH LIGAND AN027 | RATIONAL DRUG DESIGN, SUGAR BINDING PROTEIN
4q1s:N (THR1) to (THR22) YEAST 20S PROTEASOME IN COMPLEX WITH KENDOMYCIN | PROTEASOME, NATURAL PRODUCT, QUINONE METHIDE, COVALENT BINDING, EXOSITE, HYDROLASE-TOXIN COMPLEX
4q1s:b (THR1) to (THR22) YEAST 20S PROTEASOME IN COMPLEX WITH KENDOMYCIN | PROTEASOME, NATURAL PRODUCT, QUINONE METHIDE, COVALENT BINDING, EXOSITE, HYDROLASE-TOXIN COMPLEX
4q26:A (LEU17) to (CYS42) CRYSTAL STRUCTURE OF GALECTIN-1 IN COMPLEX WITH N-ACETYLLACTOSAMINE | SUGAR BINDING PROTEIN
4q26:B (LEU17) to (CYS42) CRYSTAL STRUCTURE OF GALECTIN-1 IN COMPLEX WITH N-ACETYLLACTOSAMINE | SUGAR BINDING PROTEIN
4q26:H (LEU17) to (CYS42) CRYSTAL STRUCTURE OF GALECTIN-1 IN COMPLEX WITH N-ACETYLLACTOSAMINE | SUGAR BINDING PROTEIN
4q27:A (LEU17) to (CYS42) GALECTIN-1 IN COMPLEX WITH A CLICK-ACTIVATED N-ACETYLLACTOSAMINE | SUGAR BINDING PROTEIN
4q2b:A (THR152) to (ASN179) THE CRYSTAL STRUCTURE OF AN ENDO-1,4-D-GLUCANASE FROM PSEUDOMONAS PUTIDA KT2440 | STRUCTURAL GENOMICS, PSI-BIOLOGY, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, HYDROLASE
4q2b:B (THR152) to (ASN179) THE CRYSTAL STRUCTURE OF AN ENDO-1,4-D-GLUCANASE FROM PSEUDOMONAS PUTIDA KT2440 | STRUCTURAL GENOMICS, PSI-BIOLOGY, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, HYDROLASE
4q2b:C (THR152) to (ASN179) THE CRYSTAL STRUCTURE OF AN ENDO-1,4-D-GLUCANASE FROM PSEUDOMONAS PUTIDA KT2440 | STRUCTURAL GENOMICS, PSI-BIOLOGY, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, HYDROLASE
4q2b:D (THR152) to (ASN179) THE CRYSTAL STRUCTURE OF AN ENDO-1,4-D-GLUCANASE FROM PSEUDOMONAS PUTIDA KT2440 | STRUCTURAL GENOMICS, PSI-BIOLOGY, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, HYDROLASE
4q2b:E (THR152) to (ASN179) THE CRYSTAL STRUCTURE OF AN ENDO-1,4-D-GLUCANASE FROM PSEUDOMONAS PUTIDA KT2440 | STRUCTURAL GENOMICS, PSI-BIOLOGY, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, HYDROLASE
4q2b:F (THR152) to (ASN179) THE CRYSTAL STRUCTURE OF AN ENDO-1,4-D-GLUCANASE FROM PSEUDOMONAS PUTIDA KT2440 | STRUCTURAL GENOMICS, PSI-BIOLOGY, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, HYDROLASE
4asu:H (SER81) to (LEU100) F1-ATPASE IN WHICH ALL THREE CATALYTIC SITES CONTAIN BOUND NUCLEOTIDE, WITH MAGNESIUM ION RELEASED IN THE EMPTY SITE | HYDROLASE
4asr:A (SER339) to (VAL357) CRYSTAL STRUCTURE OF ANCE IN COMPLEX WITH THR6-BRADYKININ | HYDROLASE, ZINC METALLOPROTEASE, SUBSTRATE RECOGNITION
4q2f:A (LEU17) to (CYS42) GALECTIN-1 IN COMPLEX WITH LIGAND AN020 | SUGAR BINDING PROTEIN
1zo4:A (GLU430) to (LYS452) CRYSTAL STRUCTURE OF A328S MUTANT OF THE HEME DOMAIN OF P450BM-3 | CYTOCHROME P-450, HEMEPROTEIN A328S, OXIDOREDUCTASE
1zo4:B (GLU430) to (LYS452) CRYSTAL STRUCTURE OF A328S MUTANT OF THE HEME DOMAIN OF P450BM-3 | CYTOCHROME P-450, HEMEPROTEIN A328S, OXIDOREDUCTASE
3lrs:E (SER120) to (PRO147) STRUCTURE OF PG16, AN ANTIBODY WITH BROAD AND POTENT NEUTRALIZATION OF HIV-1 | NEUTRALIZING ANTIBODIES, LONG CDRH3, HIV-1, IMMUNE SYSTEM
3ls7:A (THR6) to (THR34) CRYSTAL STRUCTURE OF THERMOLYSIN IN COMPLEX WITH XENON | PROTEIN-XE COMPLEX, PROTEASE, HYDROLASE, METALLOPROTEASE, METAL- BINDING, SECRETED, ZYMOGEN
3lsd:A (LEU29) to (ALA59) N-DOMAIN OF HUMAN ADHESION/GROWTH-REGULATORY GALECTIN-9 | MANINLY BETA, ALTERNATIVE SPLICING, CYTOPLASM, LECTIN, POLYMORPHISM, SECRETED, SUGAR BINDING PROTEIN
3lse:A (LEU29) to (ALA59) N-DOMAIN OF HUMAN ADHESION/GROWTH-REGULATORY GALECTIN-9 IN COMPLEX WITH LACTOSE | MAINLY BETA, ALTERNATIVE SPLICING, CYTOPLASM, LECTIN, POLYMORPHISM, SECRETED, SUGAR BINDING PROTEIN
3aqp:A (ARG203) to (GLY231) CRYSTAL STRUCTURE OF SECDF, A TRANSLOCON-ASSOCIATED MEMBRANE PROTEIN, FROM THERMUS THRMOPHILUS | MEMBRANE PROTEIN, SECDF, SEC, TRANSLOCON, CELL MEMBRANE, MEMBRANE, PROTEIN TRANSPORT, TRANSLOCATION, TRANSMEMBRANE, TRANSPORT
3aqp:B (ARG203) to (GLY231) CRYSTAL STRUCTURE OF SECDF, A TRANSLOCON-ASSOCIATED MEMBRANE PROTEIN, FROM THERMUS THRMOPHILUS | MEMBRANE PROTEIN, SECDF, SEC, TRANSLOCON, CELL MEMBRANE, MEMBRANE, PROTEIN TRANSPORT, TRANSLOCATION, TRANSMEMBRANE, TRANSPORT
4awd:B (GLY131) to (GLU158) CRYSTAL STRUCTURE OF THE BETA-PORPHYRANASE BPGH16B (BACPLE_01689) FROM THE HUMAN GUT BACTERIUM BACTEROIDES PLEBEIUS | HYDROLASE
5e78:B (GLU430) to (LYS452) CRYSTAL STRUCTURE OF P450 BM3 HEME DOMAIN VARIANT COMPLEXED WITH CO(III)SEP | BM3, P450, MEDIATED ELECTRON TRANSPORT, CO(III)SEP, OXIDOREDUCTASE
4b09:C (PHE221) to (VAL240) STRUCTURE OF UNPHOSPHORYLATED BAER DIMER | TRANSCRIPTION, RESPONSE REGULATOR, DNA BINDING
5e7t:B (ASN162) to (SER194) STRUCTURE OF THE TRIPOD (BPPUCT-A-L) FROM THE BASEPLATE OF BACTERIOPHAGE TUC2009 | BACTERIOPHAGES, LACTOCOCCUS LACTIS, SIPHOVIRIDAE, NANOBODY, RECEPTOR BINDING PROTEIN, VIRAL PROTEIN
2a1k:A (LEU33) to (PRO49) RB69 SINGLE-STRANDED DNA BINDING PROTEIN CORE DOMAIN | ZN2+ BINDING SUBDOMAIN, 5-STRANDED BETA-SHEET, OB FOLD, SINGLE-STRANDED DNA BINDING, DNA BINDING PROTEIN
5e9z:A (GLU430) to (LYS452) CYTOCHROME P450 BM3 MUTANT M11 | METABOLISM, MOLECULAR DYNAMICS, FREE ENERGY CALCULATIONS, THERMODYNAMIC INTEGRATION, OXIDOREDUCTASE
5e9z:B (GLU430) to (LYS452) CYTOCHROME P450 BM3 MUTANT M11 | METABOLISM, MOLECULAR DYNAMICS, FREE ENERGY CALCULATIONS, THERMODYNAMIC INTEGRATION, OXIDOREDUCTASE
5e9z:C (GLU430) to (LYS452) CYTOCHROME P450 BM3 MUTANT M11 | METABOLISM, MOLECULAR DYNAMICS, FREE ENERGY CALCULATIONS, THERMODYNAMIC INTEGRATION, OXIDOREDUCTASE
5e9z:D (GLU430) to (LYS452) CYTOCHROME P450 BM3 MUTANT M11 | METABOLISM, MOLECULAR DYNAMICS, FREE ENERGY CALCULATIONS, THERMODYNAMIC INTEGRATION, OXIDOREDUCTASE
4qes:A (GLY6) to (GLY21) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS, QUADRUPLE MUTANT, I222 FORM | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, OXIDOREDUCTASE, VIRAL PROTEIN
4qes:B (GLY6) to (GLY21) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS, QUADRUPLE MUTANT, I222 FORM | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, OXIDOREDUCTASE, VIRAL PROTEIN
4qes:C (GLY6) to (GLY21) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS, QUADRUPLE MUTANT, I222 FORM | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, OXIDOREDUCTASE, VIRAL PROTEIN
4b52:B (ALA1) to (THR30) CRYSTAL STRUCTURE OF GENTLYASE, THE NEUTRAL METALLOPROTEASE OF PAENIBACILLUS POLYMYXA | HYDROLASE, THERMOLYSIN LIKE PROTEASE
3m4v:A (GLU430) to (LYS452) CRYSTAL STRUCTURE OF THE A330P MUTANT OF CYTOCHROME P450 BM3 | CYTOCHROME P450 FOLD, ELECTRON TRANSPORT, FAD, FLAVOPROTEIN, FMN, HEME, IRON, METAL-BINDING, MONOOXYGENASE, MULTIFUNCTIONAL ENZYME, NADP, OXIDOREDUCTASE
3m4v:B (GLU430) to (LYS452) CRYSTAL STRUCTURE OF THE A330P MUTANT OF CYTOCHROME P450 BM3 | CYTOCHROME P450 FOLD, ELECTRON TRANSPORT, FAD, FLAVOPROTEIN, FMN, HEME, IRON, METAL-BINDING, MONOOXYGENASE, MULTIFUNCTIONAL ENZYME, NADP, OXIDOREDUCTASE
2a6e:N (GLN717) to (SER752) CRYSTAL STRUCTURE OF THE T. THERMOPHILUS RNA POLYMERASE HOLOENZYME | RNA POLYMERASE HOLOENZYME, BRIDGE HELIX, TRANSCRIPTION REGULATION, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, STRUCTURAL GENOMICS, TRANSFERASE
3b0g:A (GLY355) to (GLN377) ASSIMILATORY NITRITE REDUCTASE (NII3) FROM TOBBACO LEAF | SIROHEME, FE4S4 BINDING PROTEIN, OXIDOREDUCTASE
3b0h:B (GLY355) to (GLN377) ASSIMILATORY NITRITE REDUCTASE (NII4) FROM TOBBACO ROOT | SIROHEME, FE4S4 BINDING PROTEIN, OXIDOREDUCTASE
3b0m:A (GLY355) to (GLN377) M175K MUTANT OF ASSIMILATORY NITRITE REDUCTASE (NII3) FROM TOBBACO LEAF | SIROHEME, FE4S4 BINDING PROTEIN, OXIDOREDUCTASE
5eeb:A (ARG358) to (ASP371) APO FORM OF THERMOSTABLE ALDEHYDE DEHYDROGENASE FROM PYROBACULUM SP. 1860 | THERMOSTABLE ALDEHYDE DEHYDROGENASE, OXIDOREDUCTASE
5eeb:C (ARG358) to (ASP371) APO FORM OF THERMOSTABLE ALDEHYDE DEHYDROGENASE FROM PYROBACULUM SP. 1860 | THERMOSTABLE ALDEHYDE DEHYDROGENASE, OXIDOREDUCTASE
5eeb:H (ARG358) to (ASP371) APO FORM OF THERMOSTABLE ALDEHYDE DEHYDROGENASE FROM PYROBACULUM SP. 1860 | THERMOSTABLE ALDEHYDE DEHYDROGENASE, OXIDOREDUCTASE
3b1t:A (MET589) to (PRO604) CRYSTAL STRUCTURE OF HUMAN PEPTIDYLARGININE DEIMINASE 4 IN COMPLEX WITH O-CL-AMIDINE | NUCLEI, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2a7g:E (THR6) to (THR34) ON THE ROUTINE USE OF SOFT X-RAYS IN MACROMOLECULAR CRYSTALLOGRAPHY, PART III- THE OPTIMAL DATA COLLECTION WAVELENGTH | TRANSFERASE
4qhk:K (SER120) to (PRO147) UCA (UNBOUND) FROM CH103 LINEAGE | FAB FRAGMENT, HIV-1, ANTIBODY, IMMUNE SYSTEM
2a83:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA-B*2705 COMPLEXED WITH THE GLUCAGON RECEPTOR (GR) PEPTIDE (RESIDUES 412-420) | IMMUNE SYSTEM, MHC (MAJOR HISTOCOMPATIBILITY COMPLEX),HLA-B*2705
4qhu:B (SER122) to (PRO149) CRYSTAL STRUCTURE OF IL-17A/FAB6785 COMPLEX | ANTIBODY-ANTIGEN INTERACTION, RECEPTOR DIFFERENTIATION, MOLECULAR ASYMMETRY, CYSTINE KNOT, CYTOKINE IL-17, IL-17RA, IL-17RC, IMMUNE SYSTEM
3b43:A (HIS10) to (GLY27) I-BAND FRAGMENT I65-I70 FROM TITIN | I-SET IG FOLD, EXTENDED POLY-IG FILAMENT, TITIN, ELASTIC FILAMENT, STRUCTURAL PROTEIN
2aaz:A (LYS279) to (GLY309) CRYPTOCOCCUS NEOFORMANS THYMIDYLATE SYNTHASE COMPLEXED WITH SUBSTRATE AND AN ANTIFOLATE | METHYL TRANSFERASE, NUCLEOTIDE BIOSYNTHESIS, TRANSFERASE
3maw:A (ILE274) to (SER307) STRUCTURE OF THE NEWCASTLE DISEASE VIRUS F PROTEIN IN THE POST-FUSION CONFORMATION | FUSION PROTEIN, CLASS I, PARAMYXOVIRUS, GLYCOPROTEIN, VIRAL PROTEIN
3maw:B (ILE274) to (SER307) STRUCTURE OF THE NEWCASTLE DISEASE VIRUS F PROTEIN IN THE POST-FUSION CONFORMATION | FUSION PROTEIN, CLASS I, PARAMYXOVIRUS, GLYCOPROTEIN, VIRAL PROTEIN
2ad7:A (ASP410) to (ASP450) CRYSTAL STRUCTURE OF METHANOL DEHYDROGENASE FROM M. W3A1 (FORM C) IN THE PRESENCE OF METHANOL | METHANOL DEHYDROGENASE, PQQ CONFIGURATION, METHANOL, OXIDOREDUCTASE
2ad7:C (ASP410) to (ASP450) CRYSTAL STRUCTURE OF METHANOL DEHYDROGENASE FROM M. W3A1 (FORM C) IN THE PRESENCE OF METHANOL | METHANOL DEHYDROGENASE, PQQ CONFIGURATION, METHANOL, OXIDOREDUCTASE
2ad8:A (ASP410) to (ASP450) CRYSTAL STRUCTURE OF METHANOL DEHYDROGENASE FROM M. W3A1 (FORM C) IN THE PRESENCE OF ETHANOL | METHANOL DEHYDROGENASE, PQQ CONFIGURATION, ETHANOL, OXIDOREDUCTASE
2ad8:C (ASP410) to (ASP450) CRYSTAL STRUCTURE OF METHANOL DEHYDROGENASE FROM M. W3A1 (FORM C) IN THE PRESENCE OF ETHANOL | METHANOL DEHYDROGENASE, PQQ CONFIGURATION, ETHANOL, OXIDOREDUCTASE
4qls:I (ILE10) to (SER30) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 11 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qls:L (THR11) to (THR31) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 11 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qls:N (THR1) to (THR22) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 11 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qls:W (ILE10) to (SER30) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 11 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qls:Z (THR11) to (THR31) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 11 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qls:b (THR1) to (THR22) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 11 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4bbr:B (ILE912) to (ILE948) STRUCTURE OF RNA POLYMERASE II-TFIIB COMPLEX | TRANSCRIPTION, RNA POLYMERASE, TFIIB
4qlq:I (ILE10) to (SER30) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 8 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlq:L (THR11) to (THR31) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 8 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlq:W (ILE10) to (SER30) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 8 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlq:Z (THR11) to (THR31) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 8 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlt:I (ILE10) to (SER30) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 2 (PR924) | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlt:L (THR11) to (THR31) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 2 (PR924) | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlt:N (THR1) to (THR22) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 2 (PR924) | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlt:W (ILE10) to (SER30) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 2 (PR924) | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlt:Z (THR11) to (THR31) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 2 (PR924) | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlt:b (THR1) to (THR22) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 2 (PR924) | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlu:L (THR11) to (THR31) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 9 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlu:N (THR1) to (THR22) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 9 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlu:Z (THR11) to (THR31) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 9 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlu:b (THR1) to (THR22) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 9 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2ag2:B (PHE5) to (PRO32) CRYSTAL STRUCTURE ANALYSIS OF GM2-ACTIVATOR PROTEIN COMPLEXED WITH PHOSPHATIDYLCHOLINE | PHOSPHOLIPID-PROTEIN COMPLEX, LIPID ACYL CHAIN STACKING, PACKAGING, LIPID BINDING PROTEIN
3b90:B (GLY174) to (GLU190) CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF PECTATE LYASE PELI FROM ERWINIA CHRYSANTHEMI | PECTATE LYASE, PECTIN, GALACTURONIC ACID, ERWINIA CHRYSANTHEMI, RIGHT-HANDED PARALLEL BETA HELIX FOLD, CATALYTIC DOMAIN, LYASE
3mg0:L (THR2) to (THR22) STRUCTURE OF YEAST 20S PROTEASOME WITH BORTEZOMIB | 20S PROTEASOME, HYDROLASE
3mg0:W (ILE2) to (SER22) STRUCTURE OF YEAST 20S PROTEASOME WITH BORTEZOMIB | 20S PROTEASOME, HYDROLASE
3mg4:M (THR1) to (TYR22) STRUCTURE OF YEAST 20S PROTEASOME WITH COMPOUND 1 | 20S PROTEASOME, HYDROLASE
3mg4:1 (THR1) to (TYR22) STRUCTURE OF YEAST 20S PROTEASOME WITH COMPOUND 1 | 20S PROTEASOME, HYDROLASE
3mg4:2 (THR1) to (THR22) STRUCTURE OF YEAST 20S PROTEASOME WITH COMPOUND 1 | 20S PROTEASOME, HYDROLASE
3mg6:I (ILE2) to (SER22) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 6 | 20S PROTEASOME, HYDROLASE
3mg6:W (ILE2) to (SER22) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 6 | 20S PROTEASOME, HYDROLASE
5ek6:F (ARG358) to (ASP371) THERMOSTABLE ALDEHYDE DEHYDROGENASE FROM PYROBACULUM SP. 1860 COMPLEXED WITH NADP AND ISOBUTYRALDEHYDE | THERMOSTABLE ALDEHYDE DEHYDROGENASE, OXIDOREDUCTASE
5ek6:H (ARG358) to (ASP371) THERMOSTABLE ALDEHYDE DEHYDROGENASE FROM PYROBACULUM SP. 1860 COMPLEXED WITH NADP AND ISOBUTYRALDEHYDE | THERMOSTABLE ALDEHYDE DEHYDROGENASE, OXIDOREDUCTASE
3mg7:L (THR2) to (THR22) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 8 | 20S PROTEASOME, HYDROLASE
3mg7:W (GLY1) to (SER22) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 8 | 20S PROTEASOME, HYDROLASE
3mg8:L (THR2) to (THR22) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 16 | 20S PROTEASOME, HYDROLASE
3mg8:2 (THR1) to (THR22) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 16 | 20S PROTEASOME, HYDROLASE
3mi6:D (GLU280) to (SER302) CRYSTAL STRUCTURE OF THE ALPHA-GALACTOSIDASE FROM LACTOBACILLUS BREVIS, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET LBR11. | NESG, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, HYDROLASE
3mjk:A (VAL152) to (CYS179) STRUCTURE OF A GROWTH FACTOR PRECURSOR | CYSTINE-KNOT, GROWTH FACTOR, HORMONE
3bdu:A (SER2) to (THR33) CRYSTAL STRUCTURE OF PROTEIN Q6D8G1 AT THE RESOLUTION 1.9 A. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET EWR22A. | X_RAY, NESG, Q6D8G1, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, LIPOPROTEIN
3bdu:C (TYR5) to (THR33) CRYSTAL STRUCTURE OF PROTEIN Q6D8G1 AT THE RESOLUTION 1.9 A. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET EWR22A. | X_RAY, NESG, Q6D8G1, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, LIPOPROTEIN
3bdu:F (SER3) to (THR33) CRYSTAL STRUCTURE OF PROTEIN Q6D8G1 AT THE RESOLUTION 1.9 A. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET EWR22A. | X_RAY, NESG, Q6D8G1, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, LIPOPROTEIN
3bdu:G (SER3) to (THR33) CRYSTAL STRUCTURE OF PROTEIN Q6D8G1 AT THE RESOLUTION 1.9 A. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET EWR22A. | X_RAY, NESG, Q6D8G1, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, LIPOPROTEIN
3ben:A (GLU430) to (LYS452) STRUCTURE OF N-(12-IMIDAZOLYL-DODECANOYL)-L-LEUCINE INHIBITOR BOUND TO THE HEME DOMAIN OF CYTOCHROME P450-BM3 | PROTEIN-SUBSTRATE COMPLEX, HEMEPROTEIN, ELECTRON TRANSPORT, FAD, FLAVOPROTEIN, FMN, IRON, MEMBRANE, METAL-BINDING, MONOOXYGENASE, MULTIFUNCTIONAL ENZYME, NADP, OXIDOREDUCTASE, TRANSPORT
3ben:B (GLU430) to (LYS452) STRUCTURE OF N-(12-IMIDAZOLYL-DODECANOYL)-L-LEUCINE INHIBITOR BOUND TO THE HEME DOMAIN OF CYTOCHROME P450-BM3 | PROTEIN-SUBSTRATE COMPLEX, HEMEPROTEIN, ELECTRON TRANSPORT, FAD, FLAVOPROTEIN, FMN, IRON, MEMBRANE, METAL-BINDING, MONOOXYGENASE, MULTIFUNCTIONAL ENZYME, NADP, OXIDOREDUCTASE, TRANSPORT
4qrp:F (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA B*0801 IN COMPLEX WITH HSKKKCDEL AND DD31 TCR | HLA B*0801, HUAMN HEPATITIS C VIRUS, TCR, T CELL, IMMUNE SYSTEM
4qrs:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA B*0801 IN COMPLEX WITH ELK_IYM, ELKRKMIYM | HLA B*0801, CMV, TCR, T CELL, IMMUNE SYSTEM
4qru:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA B*0801 IN COMPLEX WITH ELR_MYM, ELRRKMMYM | HLA B*0801, CMV, TCR, T CELL, IMMUNE SYSTEM
3mme:C (SER120) to (PRO147) STRUCTURE AND FUNCTIONAL DISSECTION OF PG16, AN ANTIBODY WITH BROAD AND POTENT NEUTRALIZATION OF HIV-1 | NEUTRALIZING ANTIBODIES, LONG CDRH3, HIV-1, IMMUNE SYSTEM
3mnv:D (SER120) to (PRO149) CRYSTAL STRUCTURE OF THE NON-NEUTRALIZING HIV ANTIBODY 13H11 FAB FRAGMENT | HIV-1, HIV, GP41, MPER, 13H11, 2F5, Z13, 4E10, FAB ANTIBODY, IMMUNE SYSTEM
3mof:A (ASP311) to (VAL335) THE STRUCTURE OF RAT CYTOSOLIC PEPCK MUTANT A467G IN COMPLEX WITH OXALATE AND GTP | KINASE, GLUCONEOGENESIS, LYASE
4qtp:D (THR8) to (ASP27) CRYSTAL STRUCTURE OF AN ANTI-SIGMA FACTOR ANTAGONIST FROM MYCOBACTERIUM PARATUBERCULOSIS | STRUCTURAL GENOMICS, NIAID, NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, SSGCID, STAS DOMAIN, ANTI-SIGMA FACTOR ANTAGONIST, PROTEIN BINDING
3mre:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF MHC CLASS I HLA-A2 MOLECULE COMPLEXED WITH EBV BMLF1-280-288 NONAPEPTIDE | MHC CLASS I, HLA, IMMUNE SYSTEM, IMMUNE RESPONSE, NONAPEPTIDE, VIRAL PEPTIDE, EPSTEIN-BARR VIRUS, BMLF1 PROTEIN, EB2 PROTEIN
4qux:L (GLY10) to (THR31) YCP BETA5-A49T-MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qux:N (THR1) to (THR22) YCP BETA5-A49T-MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qux:Z (GLY10) to (THR31) YCP BETA5-A49T-MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qux:b (THR1) to (THR22) YCP BETA5-A49T-MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv1:L (THR11) to (THR31) YCP BETA5-M45A MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qv1:N (THR1) to (THR22) YCP BETA5-M45A MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qv1:Z (THR11) to (THR31) YCP BETA5-M45A MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qv1:b (THR1) to (THR22) YCP BETA5-M45A MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4quy:L (GLY10) to (THR31) YCP BETA5-A49S-MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4quy:N (THR1) to (THR22) YCP BETA5-A49S-MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4quy:Z (GLY10) to (THR31) YCP BETA5-A49S-MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4quy:b (THR1) to (THR22) YCP BETA5-A49S-MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv0:L (THR11) to (THR31) YCP BETA5-A49T-A50V-DOUBLE MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv0:N (THR1) to (THR22) YCP BETA5-A49T-A50V-DOUBLE MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv0:Z (THR11) to (THR31) YCP BETA5-A49T-A50V-DOUBLE MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv0:b (THR1) to (THR22) YCP BETA5-A49T-A50V-DOUBLE MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
3ms3:A (THR6) to (THR34) CRYSTAL STRUCTURE OF THERMOLYSIN IN COMPLEX WITH ANILINE | PROTEASE, HYDROLASE, ANILINE, FRAGEMENT SOAKING, FRAGMENT BASED LEAD DISCOVERY, METALLOPROTEASE, METAL-BINDING, SECRETED, ZYMOGEN
4qv3:L (THR11) to (THR31) YCP BETA5-M45V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv3:Z (THR11) to (THR31) YCP BETA5-M45V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
3msa:A (THR6) to (THR34) CRYSTAL STRUCTURE OF THERMOLYSIN IN COMPLEX WITH 3-BROMOPHENOL | PROTEASE, HYDROLASE, FRAGMENT SOAKING, METALLOPROTEASE, METAL- BINDING, SECRETED, ZYMOGEN, 3-BROMOPHENOL, FRAGMENT BASED LEAD DISCOVERY
4qv4:L (GLY10) to (THR31) YCP BETA5-M45T MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv4:N (THR1) to (THR22) YCP BETA5-M45T MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv4:Z (GLY10) to (THR31) YCP BETA5-M45T MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv4:b (THR1) to (THR22) YCP BETA5-M45T MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
3msf:A (THR6) to (THR34) CRYSTAL STRUCTURE OF THERMOLYSIN IN COMPLEX WITH UREA | PROTEASE, HYDROLASE, FRAGMENT SOAKING, METALLOPROTEASE, METAL- BINDING, SECRETED, ZYMOGEN, UREA, FRAGMENT BASED LEAD DISCOVERY
3bjp:A (LYS127) to (SER154) URATE OXIDASE CYANIDE URIC ACID TERNARY COMPLEX | URIC ACID, CYANIDE, INHIBITION, DEGRADATION MECHANISM, ACETYLATION, OXIDOREDUCTASE, PEROXISOME, PURINE METABOLISM
4qv5:L (GLY10) to (THR31) YCP BETA5-M45I MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv5:N (THR1) to (THR22) YCP BETA5-M45I MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv5:Z (GLY10) to (THR31) YCP BETA5-M45I MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv5:b (THR1) to (THR22) YCP BETA5-M45I MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
3msn:A (THR6) to (THR34) CRYSTAL STRUCTURE OF THERMOLYSIN IN COMPLEX WITH N-METHYLUREA | PROTEASE, HYDROLASE, FRAGMENT SOAKING, METALLOPROTEASE, METAL- BINDING, SECRETED, ZYMOGEN, N-METHYLUREA, FRAGMENT BASED LEAD DISCOVERY
4qv6:L (THR11) to (THR31) YCP BETA5-A49V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv6:Z (THR11) to (THR31) YCP BETA5-A49V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv7:L (GLY10) to (THR31) YCP BETA5-A50V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv7:N (THR1) to (THR22) YCP BETA5-A50V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv7:Z (GLY10) to (THR31) YCP BETA5-A50V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv7:b (THR1) to (THR22) YCP BETA5-A50V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv8:L (GLY10) to (THR31) YCP BETA5-C52F MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv8:N (THR1) to (THR22) YCP BETA5-C52F MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv8:Z (GLY10) to (THR31) YCP BETA5-C52F MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv8:b (THR1) to (THR22) YCP BETA5-C52F MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv9:L (GLY10) to (THR31) YCP BETA5-C63F MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv9:Z (GLY10) to (THR31) YCP BETA5-C63F MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qvl:L (THR11) to (THR31) YCP IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvl:Z (THR11) to (THR31) YCP IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvm:L (THR11) to (THR31) YCP BETA5-M45A MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvm:Z (THR11) to (THR31) YCP BETA5-M45A MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvn:L (THR11) to (THR31) YCP BETA5-M45V MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvn:Z (THR11) to (THR31) YCP BETA5-M45V MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvp:L (THR11) to (THR31) YCP BETA5-M45T MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvp:Z (THR11) to (THR31) YCP BETA5-M45T MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvq:L (THR11) to (THR31) YCP BETA5-M45I MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4qvq:Z (THR11) to (THR31) YCP BETA5-M45I MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4qvw:L (THR11) to (THR31) YCP BETA5-A49S-MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4qvw:Z (THR11) to (THR31) YCP BETA5-A49S-MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4qvy:L (THR11) to (THR31) YCP BETA5-A49T-MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvy:Z (THR11) to (THR31) YCP BETA5-A49T-MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw0:L (THR11) to (THR31) YCP BETA5-A49T-A50V-DOUBLE MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw0:Z (THR11) to (THR31) YCP BETA5-A49T-A50V-DOUBLE MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw1:L (THR11) to (THR31) YCP BETA5-A50V MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw1:Z (THR11) to (THR31) YCP BETA5-A50V MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw5:L (THR11) to (THR31) YCP BETA5-M45A MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw5:Z (THR11) to (THR31) YCP BETA5-M45A MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw4:L (THR11) to (THR31) YCP IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw4:Z (THR11) to (THR31) YCP IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw6:L (THR11) to (THR31) YCP BETA5-M45V MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw6:Z (THR11) to (THR31) YCP BETA5-M45V MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwj:L (THR11) to (THR31) YCP BETA5-A49T-MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwj:Z (THR11) to (THR31) YCP BETA5-A49T-MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwf:I (ILE10) to (SER30) YCP BETA5-M45I MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwf:L (THR11) to (THR31) YCP BETA5-M45I MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwf:W (ILE10) to (SER30) YCP BETA5-M45I MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwf:Z (THR11) to (THR31) YCP BETA5-M45I MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwk:L (THR11) to (THR31) YCP BETA5-A49T-A50V-DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwk:Z (THR11) to (THR31) YCP BETA5-A49T-A50V-DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwl:L (THR11) to (THR31) YCP BETA5-A50V MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwl:Z (THR11) to (THR31) YCP BETA5-A50V MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3bpw:A (CYS177) to (ASN196) CRYSTAL STRUCTURE OF P. FALCIPARUM OROTIDINE 5'-MONOPHOSPHATE DECARBOXYLASE COMPLEXED WITH XMP | P. FALCIPARUM, OROTIDINE 5'-MONOPHOSPHATE DECARBOXYLASE, XMP, LYASE, PYRIMIDINE BIOSYNTHESIS
4qwr:L (THR11) to (THR31) YCP BETA5-C52F MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwr:Z (THR11) to (THR31) YCP BETA5-C52F MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qws:L (THR11) to (THR31) YCP BETA5-C63F MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qws:Z (THR11) to (THR31) YCP BETA5-C63F MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5f1i:G (ARG189) to (PRO211) MHC WITH 9-MER PEPTIDE | MHC, IMMUNE SYSTEM
5f1i:J (ARG189) to (PRO211) MHC WITH 9-MER PEPTIDE | MHC, IMMUNE SYSTEM
4qwu:L (THR11) to (THR31) YCP BETA5-C52F MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwx:I (ILE10) to (SER30) YCP IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwx:L (THR11) to (THR31) YCP IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwx:N (THR1) to (THR22) YCP IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwx:W (ILE10) to (SER30) YCP IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwx:Z (THR11) to (THR31) YCP IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwx:b (THR1) to (THR22) YCP IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qxj:L (THR11) to (THR31) YCP BETA5-M45A MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qxj:Z (THR11) to (THR31) YCP BETA5-M45A MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3mwa:A (CYS177) to (ASN196) CRYSTAL STRUCTURE OF PLASMODIUM FALCIPARUM OROTIDINE 5'-MONOPHOSPHATE DECARBOXYLASE COVALENTLY MODIFIED BY 2-PRIME-FLUORO-6-IODO-UMP | CRYSTAL STRUCTURE,PLASMODIUM FALCIPARUM, OROTIDINE 5'-MONOPHOSPHATE DECARBOXYLASE, COVALENTLY, 2-PRIME-FLUORO-6-IODO-UMP, LYASE
5f4l:A (ASN392) to (GLN422) HIV-1 GP120 COMPLEX WITH JP-III-048 | CRYSTAL STRUCTURE OF HIV-1 GP120 COMPLEX WITH JP-III-048, VIRAL PROTEIN
5f4u:B (ASN392) to (GLN422) HIV-1 GP120 COMPLEX WITH BNM-IV-197 | GP120, VIRAL PROTEIN
4qyz:I (SER195) to (ASN231) CRYSTAL STRUCTURE OF A CRISPR RNA-GUIDED SURVEILLANCE COMPLEX, CASCADE, BOUND TO A SSDNA TARGET | CRISPR-ASSOCIATED, BACTERIAL IMMUNITY, CAS3, IMMUNE SYSTEM-DNA-RNA COMPLEX
5f6h:K (SER124) to (PRO151) CRYSTAL STRUCTURE OF TIER 2 NEUTRALIZING ANTIBODY DH427 FROM A RHESUS MACAQUE | FAB FRAGMENT, HIV-1, ANTIBODY, IMMUNE SYSTEM
5f6h:I (SER124) to (PRO151) CRYSTAL STRUCTURE OF TIER 2 NEUTRALIZING ANTIBODY DH427 FROM A RHESUS MACAQUE | FAB FRAGMENT, HIV-1, ANTIBODY, IMMUNE SYSTEM
5f6h:M (SER124) to (PRO151) CRYSTAL STRUCTURE OF TIER 2 NEUTRALIZING ANTIBODY DH427 FROM A RHESUS MACAQUE | FAB FRAGMENT, HIV-1, ANTIBODY, IMMUNE SYSTEM
5f6h:O (SER124) to (PRO151) CRYSTAL STRUCTURE OF TIER 2 NEUTRALIZING ANTIBODY DH427 FROM A RHESUS MACAQUE | FAB FRAGMENT, HIV-1, ANTIBODY, IMMUNE SYSTEM
4qz0:L (THR11) to (THR31) YCP BETA5-M45V MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz0:N (THR1) to (THR22) YCP BETA5-M45V MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz0:Z (THR11) to (THR31) YCP BETA5-M45V MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz0:b (THR1) to (THR22) YCP BETA5-M45V MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3mxw:H (SER120) to (PRO147) CRYSTAL STRUCTURE SONIC HEDGEHOG BOUND TO THE 5E1 FAB FRAGMENT | ANTIBODY COMPLEX, FAB FRAGMENT, METALLOPROTEASE, CALCIUM BINDING, ZINC HYDROLASE, DEVELOPMENT, MORPHOGEN, SIGNALING PROTEIN
4qz2:L (THR11) to (THR31) YCP BETA5-M45I MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz2:N (THR1) to (THR22) YCP BETA5-M45I MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz2:Z (THR11) to (THR31) YCP BETA5-M45I MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz2:b (THR1) to (THR22) YCP BETA5-M45I MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz3:L (THR11) to (THR31) YCP BETA5-A49V MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz3:Z (THR11) to (THR31) YCP BETA5-A49V MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3myj:D (HIS188) to (PRO210) HUMAN CLASS I MHC HLA-A2 IN COMPLEX WITH THE WT-1 (126-134) (R1Y) PEPTIDE VARIANT. | WT-1 PEPTIDE, R1Y MUTATION, NONAPEPTIDE, MHC CLASS I, HLA-A2, CANCER VACCINE, DISULFIDE BOND, GLYCOPROTEIN, HOST-VIRUS INTERACTION, IMMUNE RESPONSE, MEMBRANE, MHC I, PHOSPHOPROTEIN, TRANSMEMBRANE, DISEASE MUTATION, GLYCATION, IMMUNOGLOBULIN DOMAIN, PYRROLIDONE CARBOXYLIC ACID, SECRETED, IMMUNE SYSTEM
4qz4:L (THR11) to (THR31) YCP BETA5-A49S MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz4:Z (THR11) to (THR31) YCP BETA5-A49S MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz5:L (THR11) to (THR31) YCP BETA5-A49T-MUTANT IN COMPLEX WITH ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz5:Z (THR11) to (THR31) YCP BETA5-A49T-MUTANT IN COMPLEX WITH ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz6:L (THR11) to (THR31) YCP BETA5-A49T-A50V DOUBLE MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz6:Z (THR11) to (THR31) YCP BETA5-A49T-A50V DOUBLE MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qzw:L (THR11) to (THR31) YCP BETA5-C52F MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qzw:Z (THR11) to (THR31) YCP BETA5-C52F MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qzx:L (THR11) to (THR31) YCP BETA5-C63F MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qzx:Z (THR11) to (THR31) YCP BETA5-C63F MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r00:L (THR11) to (THR31) YCP BETA5-C52F MUTANT IN COMPLEX WITH OMURALIDE | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r00:N (THR1) to (THR22) YCP BETA5-C52F MUTANT IN COMPLEX WITH OMURALIDE | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r00:Z (THR11) to (THR31) YCP BETA5-C52F MUTANT IN COMPLEX WITH OMURALIDE | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r00:b (THR1) to (THR22) YCP BETA5-C52F MUTANT IN COMPLEX WITH OMURALIDE | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qzz:L (THR11) to (THR31) YCP IN COMPLEX WITH OMURALIDE | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qzz:N (THR1) to (THR22) YCP IN COMPLEX WITH OMURALIDE | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qzz:Z (THR11) to (THR31) YCP IN COMPLEX WITH OMURALIDE | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qzz:b (THR1) to (THR22) YCP IN COMPLEX WITH OMURALIDE | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3n21:A (THR6) to (THR34) CRYSTAL STRUCTURE OF THERMOLYSIN IN COMPLEX WITH S-1,2-PROPANDIOL | PROTEASE, HYDROLASE, FRAGMENT SOAKING, METALLOPROTEASE, METAL- BINDING, SECRETED, ZYMOGEN, S-1,2-PROPANDIOL, FRAGMENT BASED LEAD DISCOVERY
3n2g:A (PHE52) to (LEU70) TUBULIN-NSC 613863: RB3 STATHMIN-LIKE DOMAIN COMPLEX | ALPHA-TUBULIN, BETA-TUBULIN, COLCHICINE DOMAIN, MICROTUBULE, STATHMIN, TUBULIN, CELL CYCLE
3n2g:C (PHE52) to (LEU70) TUBULIN-NSC 613863: RB3 STATHMIN-LIKE DOMAIN COMPLEX | ALPHA-TUBULIN, BETA-TUBULIN, COLCHICINE DOMAIN, MICROTUBULE, STATHMIN, TUBULIN, CELL CYCLE
3bze:A (HIS188) to (PRO210) THE HUMAN NON-CLASSICAL MAJOR HISTOCOMPATIBILITY COMPLEX MOLECULE HLA- E | MHC FOLD, TRANSMEMBRANE, DISEASE MUTATION, GLYCATION, GLYCOPROTEIN, IMMUNE RESPONSE, IMMUNOGLOBULIN DOMAIN, MHC I, PYRROLIDONE CARBOXYLIC ACID, SECRETED, IMMUNE SYSTEM
3bze:E (HIS188) to (PRO210) THE HUMAN NON-CLASSICAL MAJOR HISTOCOMPATIBILITY COMPLEX MOLECULE HLA- E | MHC FOLD, TRANSMEMBRANE, DISEASE MUTATION, GLYCATION, GLYCOPROTEIN, IMMUNE RESPONSE, IMMUNOGLOBULIN DOMAIN, MHC I, PYRROLIDONE CARBOXYLIC ACID, SECRETED, IMMUNE SYSTEM
3c06:A (THR281) to (TYR307) LACTOBACILLUS CASEI THYMIDYLATE SYNTHASE TERNARY COMPLEX WITH DUMP AND THE PHTALIMIDIC DERIVATIVE 14C IN MULTIPLE BINDING MODES-MODE 1 | METHYLTRANSFERASE, STRUCTURE-BASED DRUG DESIGN, NUCLEOTIDE BIOSYNTHESIS, TRANSFERASE
4r12:A (ASN534) to (LEU567) CRYSTAL STRUCTURE OF THE GAMMA-SECRETASE COMPONENT NICASTRIN | ALPHA/BETA, NICASTRIN, PUTATIVE SUBSTRATE-RECRUITING COMPONENT, GAMMA-SECRETASE COMPLEX, PROTEIN BINDING
3n34:A (CYS177) to (ASN196) CRYSTAL STRUCTURE OF PLASMODIUM FALCIPARUM OROTIDINE 5'-MONOPHOSPHATE DECARBOXYLASE COMPLEXED WITH 5-FLUORO-6-AMINO-UMP, PRODUCED FROM 5- FLUORO-6-AZIDO-UMP | P. FALCIPARUM, OROTIDINE 5'-MONOPHOSPHATE DECARBOXYLASE, 5-FLUORO-6- AMINO-UMP, 5-FLUORO-6-AZIDO-UMP, LYASE
4r17:L (GLY10) to (THR31) LIGAND-INDUCED AZIRIDINE-FORMATION AT SUBUNIT BETA5 OF THE YEAST 20S PROTEASOME | PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, UMPOLUNG, CROSSLINK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r17:Z (GLY10) to (THR31) LIGAND-INDUCED AZIRIDINE-FORMATION AT SUBUNIT BETA5 OF THE YEAST 20S PROTEASOME | PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, UMPOLUNG, CROSSLINK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r18:L (GLY10) to (THR31) LIGAND-INDUCED LYS33-THR1 CROSSLINKING AT SUBUNIT BETA5 OF THE YEAST 20S PROTEASOME | PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, UMPOLUNG, CROSSLINK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r18:Z (GLY10) to (THR31) LIGAND-INDUCED LYS33-THR1 CROSSLINKING AT SUBUNIT BETA5 OF THE YEAST 20S PROTEASOME | PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, UMPOLUNG, CROSSLINK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4bvl:B (THR5) to (GLY20) STRUCTURE OF 202-208 DELETION MUTANT OF PHAZ7 PHB DEPOLYMERASE | HYDROLASE, CATALYTIC TRIAD, BIOPOLYMER BINDING
4r4b:D (SER120) to (PRO147) CRYSTAL STRUCTURE OF THE ANTI-HIV-1 ANTIBODY 2.2C | IGG, FAB, HIV, IMMUNOGLOBULIN DOMAIN, IMMUNE SYSTEM
5fgd:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-H(-2)L-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgd:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-H(-2)L-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fg7:L (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-T1A MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5fg7:N (THR1) to (THR22) YEAST 20S PROTEASOME BETA2-T1A MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5fg7:Z (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-T1A MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5fg7:b (THR1) to (THR22) YEAST 20S PROTEASOME BETA2-T1A MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5fg9:L (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-T(-2)V MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5fg9:Z (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-T(-2)V MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5fge:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-H(-2)T-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fge:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-H(-2)T-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgf:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-H(-2)A-T1A-K81R TRIPLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgf:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-H(-2)A-T1A-K81R TRIPLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
3c5e:A (ARG447) to (SER468) CRYSTAL STRUCTURE OF HUMAN ACYL-COA SYNTHETASE MEDIUM-CHAIN FAMILY MEMBER 2A (L64P MUTATION) IN COMPLEX WITH ATP | MIDDLE-CHAIN ACYL-COA SYNTHETASE, XENOBIOTIC/MEDIUM-CHAIN FATTY ACID- COA LIGASE, STRUCTURAL GENOMICS CONSORTIUM, SGC, ATP-BINDING, FATTY ACID METABOLISM, LIPID METABOLISM, MAGNESIUM, METAL-BINDING, MITOCHONDRION, NUCLEOTIDE-BINDING POLYMORPHISM, TRANSIT PEPTIDE, LIGASE
5fhs:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fhs:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
3ca9:B (GLU32) to (ARG51) EVOLUTION OF CHLORELLA VIRUS DUTPASE | DUTPASE CHLORELLA VIRUS, HYDROLASE
3cbd:B (GLU430) to (LYS452) DIRECTED EVOLUTION OF CYTOCHROME P450 BM3, TO OCTANE MONOXYGENASE 139-3 | CYTOCHROME P450, HEMEPROTEIN 139-3, ELECTRON TRANSPORT, FAD, FLAVOPROTEIN, FMN, IRON, MEMBRANE, METAL-BINDING, MONOOXYGENASE, MULTIFUNCTIONAL ENZYME, NADP, OXIDOREDUCTASE, TRANSPORT
4r96:D (SER126) to (PRO153) STRUCTURE OF A LLAMA GLAMA FAB 48A2 AGAINST HUMAN CMET | IMMUNOGLOBULIN DOMAINS, IMMUNE SYSTEM, CMET
4r9j:G (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO GLUCOSAMINE-6-SULFATE | FIBRINOGEN-LIKE DOMAIN, INNATE IMMUNITY, PATTERN RECOGNITION PROTEIN, LECTIN, IMMUNOLOGY, LECTIN-LIKE, SUGAR BINDING PROTEIN, PLASMA, EXTRACELLULAR
4r9j:A (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO GLUCOSAMINE-6-SULFATE | FIBRINOGEN-LIKE DOMAIN, INNATE IMMUNITY, PATTERN RECOGNITION PROTEIN, LECTIN, IMMUNOLOGY, LECTIN-LIKE, SUGAR BINDING PROTEIN, PLASMA, EXTRACELLULAR
4r9t:B (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO SULPHATES | FIBRINOGEN-LIKE DOMAIN, INNATE IMMUNITY, PATTERN RECOGNITION PROTEIN, LECTIN, IMMUNOLOGY, LECTIN-LIKE, SUGAR BINDING PROTEIN, PLASMA, EXTRACELLULAR
4r9t:A (GLY257) to (PRO287) L-FICOLIN COMPLEXED TO SULPHATES | FIBRINOGEN-LIKE DOMAIN, INNATE IMMUNITY, PATTERN RECOGNITION PROTEIN, LECTIN, IMMUNOLOGY, LECTIN-LIKE, SUGAR BINDING PROTEIN, PLASMA, EXTRACELLULAR
4c0s:A (SER300) to (ASP328) MAMMALIAN TRANSLATION ELONGATION FACTOR EEF1A2 | TRANSLATION
4rdn:B (ALA476) to (LYS503) STRUCTURE OF YTH-YTHDF2 IN COMPLEX WITH M6A | M6A METHYLATED RNA BINDING, ATYPICAL BETA-PROPELLER, RNA BINDING, M6A METHYLATED RNA, RNA BINDING PROTEIN
4rdo:B (ALA476) to (LYS503) STRUCTURE OF YTH-YTHDF2 IN THE FREE STATE | RNA BINDING, ATYPICAL BETA-PROPELLER, M6A METHYLATED RNA, RNA BINDING PROTEIN
4rdo:F (ALA476) to (LYS503) STRUCTURE OF YTH-YTHDF2 IN THE FREE STATE | RNA BINDING, ATYPICAL BETA-PROPELLER, M6A METHYLATED RNA, RNA BINDING PROTEIN
3cfk:H (SER120) to (PRO149) CRYSTAL STRUCTURE OF CATALYTIC ELIMINATION ANTIBODY 34E4, TRICLINIC CRYSTAL FORM | IMMUNOGLOBULIN, CATALYTIC ANTIBODY, CHIMERIC FAB, APO FORM, PROTON TRANSFER, CONFORMATIONAL CHANGE, IMMUNE SYSTEM, CHIMERA, IMMUNOGLOBULIN DOMAIN, IMMUNOGLOBULIN V REGION
3cfk:D (SER120) to (PRO149) CRYSTAL STRUCTURE OF CATALYTIC ELIMINATION ANTIBODY 34E4, TRICLINIC CRYSTAL FORM | IMMUNOGLOBULIN, CATALYTIC ANTIBODY, CHIMERIC FAB, APO FORM, PROTON TRANSFER, CONFORMATIONAL CHANGE, IMMUNE SYSTEM, CHIMERA, IMMUNOGLOBULIN DOMAIN, IMMUNOGLOBULIN V REGION
3cfk:I (SER120) to (PRO149) CRYSTAL STRUCTURE OF CATALYTIC ELIMINATION ANTIBODY 34E4, TRICLINIC CRYSTAL FORM | IMMUNOGLOBULIN, CATALYTIC ANTIBODY, CHIMERIC FAB, APO FORM, PROTON TRANSFER, CONFORMATIONAL CHANGE, IMMUNE SYSTEM, CHIMERA, IMMUNOGLOBULIN DOMAIN, IMMUNOGLOBULIN V REGION
3cfk:K (SER120) to (PRO149) CRYSTAL STRUCTURE OF CATALYTIC ELIMINATION ANTIBODY 34E4, TRICLINIC CRYSTAL FORM | IMMUNOGLOBULIN, CATALYTIC ANTIBODY, CHIMERIC FAB, APO FORM, PROTON TRANSFER, CONFORMATIONAL CHANGE, IMMUNE SYSTEM, CHIMERA, IMMUNOGLOBULIN DOMAIN, IMMUNOGLOBULIN V REGION
3cgh:A (PHE316) to (TRP359) CRYSTAL STRUCTURE OF A SUSD HOMOLOG (BT_3984) FROM BACTEROIDES THETAIOTAOMICRON VPI-5482 AT 1.70 A RESOLUTION | STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, METAL BINDING PROTEIN
3nh7:H (SER127) to (PRO154) CRYSTAL STRUCTURE OF THE NEUTRALIZING FAB FRAGMENT ABD1556 BOUND TO THE BMP TYPE I RECEPTOR IA | ANTIBODY-ANTIGEN COMPLEX, BMP RECEPTOR EXTRACELLULAR DOMAIN, BONE MORPHOGENETIC PROTEIN, IMMUNE SYSTEM
3nic:F (VAL48) to (GLN87) DNA BINDING AND CLEAVAGE BY THE GIY-YIG ENDONUCLEASE R.ECO29KI INACTIVE VARIANT Y49F | TYPE II RESTRICTION ENDONUCLEASE, GIY-YIG ENDONUCLEASE, DNA-BOUND, HYDROLASE-DNA COMPLEX
4c56:K (LYS98) to (PRO124) X-RAY STRUCTURE OF THE COMPLEX BETWEEN STAPHYLOCOCCAL ENTEROTOXIN B, T CELL RECEPTOR AND MAJOR HISTOCOMPATIBILITY COMPLEX CLASS II | IMMUNE SYSTEM-TOXIN COMPLEX
3njv:A (ASP139) to (ARG156) RHAMNOGALACTURONAN LYASE FROM ASPERGILLUS ACULEATUS K150A SUBSTRATE COMPLEX | CARBOHYDRATE ACTIVE ENZYME, LYASE, PECTIN DEGRADATION, POLYSACCHARIDE LYASE FAMILY 4
3nl1:A (GLU118) to (GLY134) CRYSTAL STRUCTURE OF SALICYLATE 1,2-DIOXYGENASE FROM PSEUDOAMINOBACTER SALICYLATOXIDANS ADDUCTS WITH GENTISATE | BETA-SANDWICH, OXIDOREDUCTASE
3nli:B (VAL312) to (ASN340) STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE N368D MUTANT HEME DOMAIN COMPLEXED WITH 6-{{(3'R,4'R)-3'-[2"-(3'''- FLUOROPHENETHYLAMINO)ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN- 2-AMINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
4rht:D (GLY101) to (GLY115) CRYSTAL STRUCTURES OF MYCOBACTERIUM TUBERCULOSIS 6-OXOPURINE PHOSPHORIBOSYLTRANSFERASE WHICH IS A POTENTIAL TARGET FOR DRUG DEVELOPMENT AGAINST THIS DISEASE | 6-OXOPURINE PHOSPHORIBOSYLTRANSFERASES, GMP, TRANSFERASE
3nn7:A (THR6) to (THR34) CRYSTAL STRUCTURE OF THERMOLYSIN IN COMPLEX WITH 2-BROMOACETATE | PROTEASE, HYDROLASE, FRAGMENT SOAKING, METALLOPROTEASE, METAL- BINDING, SECRETED, ZYMOGEN, 2-BROMOACETATE, FRAGMENT-BASED LEAD DISCOVERY
4ca7:A (SER339) to (VAL357) DROSOPHILA ANGIOTENSIN CONVERTING ENZYME (ANCE) IN COMPLEX WITH A PHOSPHINIC TRIPEPTIDE FI | HYDROLASE, ZINC METALLOPEPTIDASE, INHIBITOR BINDING
4ca8:A (SER339) to (VAL357) DROSOPHILA ANGIOTENSIN CONVERTING ENZYME (ANCE) IN COMPLEX WITH A PHOSPHINIC TRIPEPTIDE FII | HYDROLASE, ZINC METALLOPEPTIDASE, INHIBITOR BINDING
5fsj:A (THR6) to (THR34) STRUCTURE OF THERMOLYSIN PREPARED BY THE 'SOAK-AND-FREEZE' METHOD UNDER 45 BAR OF OXYGEN PRESSURE | HYDROLASE, METALLOPROTEINASE, THERMOLYSINE, DIOXYGEN, PRESSURE, FLASH FREEZING
5fsp:A (THR6) to (THR34) STRUCTURE OF THERMOLYSIN PREPARED BY THE 'SOAK-AND-FREEZE' METHOD UNDER 100 BAR OF KRYPTON PRESSURE | HYDROLASE, METALLOPROTEINASE, THERMOLYSINE, KRYPTON, PRESSURE, FLASH FREEZING
5fss:A (THR6) to (THR34) STRUCTURE OF THERMOLYSIN PREPARED BY THE 'SOAK-AND-FREEZE' METHOD UNDER 40 BAR OF KRYPTON PRESSURE | HYDROLASE, METALLOPROTEINASE, THERMOLYSINE, KRYPTON, PRESSURE, FLASH FREEZING
3nrr:B (HIS241) to (ASP264) CO-CRYSTAL STRUCTURE OF DIHYDROFOLATE REDUCTASE-THYMIDYLATE SYNTHASE FROM BABESIA BOVIS WITH DUMP, RALTITREXED AND NADP | STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, SSGCID, NIAID, DIHYDROFOLATE REDUCTASE, THYMIDYLATE SYNTHASE, DHFR, TS, THYA, OXIDOREDUCTASE, METHYLTRANSFERASE, BABESIOSIS, DUMP, NADP, RALTITREXED, TOMUDEX, TRANSFERASE
3nsc:A (GLY55) to (GLN81) C500S MUTANT OF CUEO BOUND TO CU(II) | MULTICOPPER OXIDASE, T1 DEPLETED C500S MUTATION, OXIDOREDUCTASE
4rnr:A (SER120) to (PRO147) CRYSTAL STRUCTURE OF BROADLY NEUTRALIZING ANTI-HIV ANTIBODY PGT130 | PGT130, PGT 130, IMMUNOGLOBULIN FOLD, BROADLY NEUTRALIZING ANTIBODY, HIV-1 GP120 BINDING, N-LINKED GLYCAN, IMMUNE SYSTEM
4rnr:C (SER120) to (PRO147) CRYSTAL STRUCTURE OF BROADLY NEUTRALIZING ANTI-HIV ANTIBODY PGT130 | PGT130, PGT 130, IMMUNOGLOBULIN FOLD, BROADLY NEUTRALIZING ANTIBODY, HIV-1 GP120 BINDING, N-LINKED GLYCAN, IMMUNE SYSTEM
5fv9:A (LYS521) to (LEU540) CRYSTAL STRUCTURE OF GALNAC-T2 IN COMPLEX WITH COMPOUND 16D | TRANSFERASE
3csl:A (GLY205) to (PRO239) STRUCTURE OF THE SERRATIA MARCESCENS HEMOPHORE RECEPTOR HASR IN COMPLEX WITH ITS HEMOPHORE HASA AND HEME | OUTER MEMBRANE PROTEIN, BETA-BARREL, HEMOPHORE RECEPTOR, TONB BOX, HEME, IRON, METAL-BINDING, SECRETED, MEMBRANE PROTEIN-HEME BINDING PROTEIN COMPLEX
4rsn:A (GLU430) to (LYS452) CRYSTAL STRUCTURE OF THE E267V MUTANT OF CYTOCHROME P450 BM3 | BIFUNCTIONAL P-450/NADPH-P450 REDUCTASE, HEME DOMAIN, OXIDOREDUCTASE
4rsn:B (GLU430) to (LYS452) CRYSTAL STRUCTURE OF THE E267V MUTANT OF CYTOCHROME P450 BM3 | BIFUNCTIONAL P-450/NADPH-P450 REDUCTASE, HEME DOMAIN, OXIDOREDUCTASE
3cu1:C (ARG165) to (ASN184) CRYSTAL STRUCTURE OF 2:2:2 FGFR2D2:FGF1:SOS COMPLEX | FIBROBLAST GROWTH FACTOR 1, FIBROBLAST GROWTH FACTOR RECEPTOR 2, D2 DOMAIN, SUCROSE OCTA SULFATE, ALTERNATIVE SPLICING, ATP-BINDING, DISEASE MUTATION, ECTODERMAL DYSPLASIA, GLYCOPROTEIN, HEPARIN-BINDING, IMMUNOGLOBULIN DOMAIN, KINASE, LACRIMO-AURICULO-DENTO-DIGITAL SYNDROME, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SECRETED, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE, ACETYLATION, ANGIOGENESIS, DEVELOPMENTAL PROTEIN, DIFFERENTIATION, MITOGEN, TRANSFERASE/HORMONE COMPLEX
4rtd:A (HIS1590) to (GLU1606) ESCHERICHIA COLI ALPHA-2-MACROGLOBULIN ACTIVATED BY PORCINE ELASTASE | THIOESTER DOMAIN, MACROGLOBULIN, LIPID BINDING PROTEIN
3nzj:L (THR2) to (THR22) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH LIGAND 2A | UBIQUITIN, PROTEIN DEGRADATION, N-TERMINAL NUCLEOPHILIC HYDROLASE, 19S REGULATORY PARTICLE, UBIQUITIN-TAGGED SUBSTRATES, CYTOSOL, NUCLEUS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3nzj:Z (THR2) to (THR22) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH LIGAND 2A | UBIQUITIN, PROTEIN DEGRADATION, N-TERMINAL NUCLEOPHILIC HYDROLASE, 19S REGULATORY PARTICLE, UBIQUITIN-TAGGED SUBSTRATES, CYTOSOL, NUCLEUS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3nzw:L (THR2) to (THR22) CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH 2B | UBIQUITIN, PROTEIN DEGRADATION, N-TERMINAL NUCLEOPHILIC HYDROLASE, 19S REGULATORY PARTICLE, UBIQUITIN-TAGGED SUBSTRATES, CYTOSOL, NUCLEUS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3nzw:Z (THR2) to (THR22) CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH 2B | UBIQUITIN, PROTEIN DEGRADATION, N-TERMINAL NUCLEOPHILIC HYDROLASE, 19S REGULATORY PARTICLE, UBIQUITIN-TAGGED SUBSTRATES, CYTOSOL, NUCLEUS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3o11:L (ALA83) to (PRO111) ANTI-BETA-AMYLOID ANTIBODY C706 FAB IN SPACE GROUP C2 | IMMUNOGLOBULIN FOLD, IMMUNE SYSTEM
5fxn:A (THR6) to (THR34) STRUCTURE OF THERMOLYSIN SOLVED BY SAD FROM DATA COLLECTED BY DIRECT DATA COLLECTION (DDC) USING THE ESRF ROBODIFF GONIOMETER | HYDROLASE
4cmr:A (ILE18) to (ARG43) THE CRYSTAL STRUCTURE OF NOVEL EXO-TYPE MALTOSE-FORMING AMYLASE(PY04_0872) FROM PYROCOCCUS SP. ST04 | HYDROLASE, GLYCOSIDE HYDROLASE FAMILY 57, EXO-TYPE HYDROLASE
4s0h:A (THR72) to (GLY93) TBX5 DB, NKX2.5 HD, ANF DNA COMPLEX | TRANSCRIPTION FACTOR, TRANSCRIPTION-DNA COMPLEX
3d18:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA-B*2709 COMPLEXED WITH A VARIANT OF THE LATENT MEMBRANE PROTEIN 2 PEPTIDE (LMP2(L)) OF EPSTEIN-BARR VIRUS | IMMUNE SYSTEM-COMPLEX, GLYCOPROTEIN, HOST-VIRUS INTERACTION, IMMUNE RESPONSE, MEMBRANE, MHC I, TRANSMEMBRANE, DISEASE MUTATION, GLYCATION, IMMUNOGLOBULIN DOMAIN, PYRROLIDONE CARBOXYLIC ACID, SECRETED, PHOSPHOPROTEIN, IMMUNE SYSTEM
3d29:L (THR2) to (THR22) PROTEASOME INHIBITION BY FELLUTAMIDE B | ANTI-PARALLEL BETA-SHEET STRUCTURE FLANKED BY ALPHA-HELICES, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, PROTEASOME, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN
3d29:N (THR1) to (THR22) PROTEASOME INHIBITION BY FELLUTAMIDE B | ANTI-PARALLEL BETA-SHEET STRUCTURE FLANKED BY ALPHA-HELICES, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, PROTEASOME, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN
3d29:Z (THR2) to (THR22) PROTEASOME INHIBITION BY FELLUTAMIDE B | ANTI-PARALLEL BETA-SHEET STRUCTURE FLANKED BY ALPHA-HELICES, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, PROTEASOME, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN
3d29:2 (THR1) to (THR22) PROTEASOME INHIBITION BY FELLUTAMIDE B | ANTI-PARALLEL BETA-SHEET STRUCTURE FLANKED BY ALPHA-HELICES, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, PROTEASOME, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN
4cr4:2 (THR1) to (GLN22) DEEP CLASSIFICATION OF A LARGE CRYO-EM DATASET DEFINES THE CONFORMATIONAL LANDSCAPE OF THE 26S PROTEASOME | HYDROLASE, AAA-ATPASE, ATP-ANALOG, CLASSIFICATION
4tli:A (THR6) to (THR34) THERMOLYSIN (25% ISOPROPANOL SOAKED CRYSTALS) | HYDROLASE, METALLOPROTEINASE, ORGANIC SOLVENT
3ob8:A (THR698) to (VAL728) STRUCTURE OF THE BETA-GALACTOSIDASE FROM KLUYVEROMYCES LACTIS IN COMPLEX WITH GALACTOSE | TIM BARREL, TETRAMER, GH2, BETA-GALACTOSIDASE, GALACTOSE, GLYCOSIDASE, HYDROLASE
3ob8:B (THR698) to (VAL728) STRUCTURE OF THE BETA-GALACTOSIDASE FROM KLUYVEROMYCES LACTIS IN COMPLEX WITH GALACTOSE | TIM BARREL, TETRAMER, GH2, BETA-GALACTOSIDASE, GALACTOSE, GLYCOSIDASE, HYDROLASE
3ob8:D (THR698) to (VAL728) STRUCTURE OF THE BETA-GALACTOSIDASE FROM KLUYVEROMYCES LACTIS IN COMPLEX WITH GALACTOSE | TIM BARREL, TETRAMER, GH2, BETA-GALACTOSIDASE, GALACTOSE, GLYCOSIDASE, HYDROLASE
3ob8:C (THR698) to (VAL728) STRUCTURE OF THE BETA-GALACTOSIDASE FROM KLUYVEROMYCES LACTIS IN COMPLEX WITH GALACTOSE | TIM BARREL, TETRAMER, GH2, BETA-GALACTOSIDASE, GALACTOSE, GLYCOSIDASE, HYDROLASE
4tln:A (THR6) to (THR34) BINDING OF HYDROXAMIC ACID INHIBITORS TO CRYSTALLINE THERMOLYSIN SUGGESTS A PENTACOORDINATE ZINC INTERMEDIATE IN CATALYSIS | HYDROLASE (METALLOPROTEINASE)
3oba:A (THR698) to (VAL728) STRUCTURE OF THE BETA-GALACTOSIDASE FROM KLUYVEROMYCES LACTIS | TIM BARREL, TETRAMER, GH2, GLYCOSIDASE, HYDROLASE
3oba:C (THR698) to (VAL728) STRUCTURE OF THE BETA-GALACTOSIDASE FROM KLUYVEROMYCES LACTIS | TIM BARREL, TETRAMER, GH2, GLYCOSIDASE, HYDROLASE
3oba:D (THR698) to (VAL728) STRUCTURE OF THE BETA-GALACTOSIDASE FROM KLUYVEROMYCES LACTIS | TIM BARREL, TETRAMER, GH2, GLYCOSIDASE, HYDROLASE
3oba:B (THR698) to (VAL728) STRUCTURE OF THE BETA-GALACTOSIDASE FROM KLUYVEROMYCES LACTIS | TIM BARREL, TETRAMER, GH2, GLYCOSIDASE, HYDROLASE
4cun:A (VAL312) to (ASN340) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (9AS)-2-AMINO-9A-METHYL-8,9,9A,10- TETRAHYDROBENZO[G]PTERIDINE-4,6(3H,7H)-DIONE | OXIDOREDUCTASE, COFACTOR ANALOG COMPLEX
3day:A (ARG447) to (SER468) CRYSTAL STRUCTURE OF HUMAN ACYL-COA SYNTHETASE MEDIUM-CHAIN FAMILY MEMBER 2A (L64P MUTATION) IN COMPLEX WITH AMP-CPP | MIDDLE-CHAIN ACYL-COA SYNTHETASE, XENOBIOTIC/MEDIUM-CHAIN FATTY ACID- COA LIGASE, STRUCTURAL GENOMICS CONSORTIUM, SGC, ATP-BINDING, FATTY ACID METABOLISM, LIPID METABOLISM, MAGNESIUM, METAL-BINDING, MITOCHONDRION, NUCLEOTIDE-BINDING POLYMORPHISM, TRANSIT PEPTIDE, LIGASE
4tnl:A (THR6) to (THR34) 1.8 A RESOLUTION ROOM TEMPERATURE STRUCTURE OF THERMOLYSIN RECORDED USING AN XFEL | ZN PROTEASE, X-RAY FREE ELECTRON LASER, HYDROLASE
4cwu:C (GLN798) to (SER875) CRYSTAL STRUCTURE DERIVED MODELS OF ADENOVIRUS CEMENT PROTEINS AT 3.8A | VIRUS, ADENOVIRUS, CEMENT PROTEINS, PROTEIN VI
4cwu:D (HIS898) to (ARG929) CRYSTAL STRUCTURE DERIVED MODELS OF ADENOVIRUS CEMENT PROTEINS AT 3.8A | VIRUS, ADENOVIRUS, CEMENT PROTEINS, PROTEIN VI
4cwu:I (GLN798) to (PRO873) CRYSTAL STRUCTURE DERIVED MODELS OF ADENOVIRUS CEMENT PROTEINS AT 3.8A | VIRUS, ADENOVIRUS, CEMENT PROTEINS, PROTEIN VI
4cwu:K (GLN798) to (ILE872) CRYSTAL STRUCTURE DERIVED MODELS OF ADENOVIRUS CEMENT PROTEINS AT 3.8A | VIRUS, ADENOVIRUS, CEMENT PROTEINS, PROTEIN VI
3oeu:L (THR2) to (THR22) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 24 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3oeu:N (THR1) to (THR22) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 24 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3oeu:Z (THR2) to (THR22) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 24 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3oev:N (THR1) to (THR22) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 25 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3oev:W (GLY-1) to (SER22) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 25 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3oev:2 (THR1) to (THR22) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 25 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4tqo:B (ASP444) to (ALA478) THE CRYSTAL STRUCTURE OF METHANOL DEHYDROGENASE FROM METHYLOCOCCUS CAPSULATUS (BATH) | DIMER, 8-FOLD CORE PROPELLER FOLD, OXIDOREDUCTASE
4tqo:A (ASP444) to (ALA478) THE CRYSTAL STRUCTURE OF METHANOL DEHYDROGENASE FROM METHYLOCOCCUS CAPSULATUS (BATH) | DIMER, 8-FOLD CORE PROPELLER FOLD, OXIDOREDUCTASE
4tqo:D (ASP444) to (ALA478) THE CRYSTAL STRUCTURE OF METHANOL DEHYDROGENASE FROM METHYLOCOCCUS CAPSULATUS (BATH) | DIMER, 8-FOLD CORE PROPELLER FOLD, OXIDOREDUCTASE
4tqo:F (ASP444) to (ALA478) THE CRYSTAL STRUCTURE OF METHANOL DEHYDROGENASE FROM METHYLOCOCCUS CAPSULATUS (BATH) | DIMER, 8-FOLD CORE PROPELLER FOLD, OXIDOREDUCTASE
4tqo:G (ASP444) to (LYS477) THE CRYSTAL STRUCTURE OF METHANOL DEHYDROGENASE FROM METHYLOCOCCUS CAPSULATUS (BATH) | DIMER, 8-FOLD CORE PROPELLER FOLD, OXIDOREDUCTASE
4tqo:H (ASP444) to (ALA478) THE CRYSTAL STRUCTURE OF METHANOL DEHYDROGENASE FROM METHYLOCOCCUS CAPSULATUS (BATH) | DIMER, 8-FOLD CORE PROPELLER FOLD, OXIDOREDUCTASE
3og2:A (VAL46) to (GLU66) NATIVE CRYSTAL STRUCTURE OF TRICHODERMA REESEI BETA-GALACTOSIDASE | TIM BARREL DOMAIN, GLYCOSIDE HYDROLASE, FAMILY 35, GLYCOPROTEIN, HYDROLASE
5ggq:H (VAL121) to (PRO147) CRYSTAL STRUCTURE OF NIVOLUMAB FAB FRAGMENT | THERAPEUTIC ANTIBODY, IMMUNE SYSTEM
3dg8:C (ASN340) to (ASP361) QUADRUPLE MUTANT (N51I+C59R+S108N+I164L) PLASMODIUM FALCIPARUM DIHYDROFOLATE REDUCTASE-THYMIDYLATE SYNTHASE (PFDHFR-TS) COMPLEXED WITH RJF670, NADPH, AND DUMP | ALPHA-BETA, METHYLTRANSFERASE, OXIDOREDUCTASE, TRANSFERASE
3dgi:A (GLU430) to (LYS452) CRYSTAL STRUCTURE OF F87A/T268A MUTANT OF CYP BM3 | CYTOCHROME P450, BM3, DMSO, CYTOPLASM, ELECTRON TRANSPORT, FAD, FLAVOPROTEIN, FMN, HEME, IRON, METAL-BINDING, MONOOXYGENASE, MULTIFUNCTIONAL ENZYME, NADP, OXIDOREDUCTASE, TRANSPORT
3dgi:B (GLU430) to (LYS452) CRYSTAL STRUCTURE OF F87A/T268A MUTANT OF CYP BM3 | CYTOCHROME P450, BM3, DMSO, CYTOPLASM, ELECTRON TRANSPORT, FAD, FLAVOPROTEIN, FMN, HEME, IRON, METAL-BINDING, MONOOXYGENASE, MULTIFUNCTIONAL ENZYME, NADP, OXIDOREDUCTASE, TRANSPORT
3ogr:A (VAL46) to (GLU66) COMPLEX STRUCTURE OF BETA-GALACTOSIDASE FROM TRICHODERMA REESEI WITH GALACTOSE | TIM BARREL DOMAIN, GLYCOSIDE HYDROLASE, FAMILY 35, GLYCOPROTEIN, HYDROLASE
3ogs:A (VAL46) to (GLU66) COMPLEX STRUCTURE OF BETA-GALACTOSIDASE FROM TRICHODERMA REESEI WITH IPTG | TIM BARREL DOMAIN, GLYCOSIDE HYDROLASE, FAMILY 35, GLYCOPROTEIN, HYDROLASE
4d1j:D (ALA36) to (ASN66) THE STRUCTURE OF THE GH35 BETA-GALACTOSIDASE BGL35A FROM CELLVIBRIO JAPONICAS IN COMPLEX WITH 1- DEOXYGALACTONOJIRIMYCIN | HYDROLASE, ENZYME-CARBOHYDRATE INTERACTION, GLYCOSIDASE INHIBITION
4d1j:F (GLU41) to (ASN66) THE STRUCTURE OF THE GH35 BETA-GALACTOSIDASE BGL35A FROM CELLVIBRIO JAPONICAS IN COMPLEX WITH 1- DEOXYGALACTONOJIRIMYCIN | HYDROLASE, ENZYME-CARBOHYDRATE INTERACTION, GLYCOSIDASE INHIBITION
4d1j:G (GLU41) to (ASN66) THE STRUCTURE OF THE GH35 BETA-GALACTOSIDASE BGL35A FROM CELLVIBRIO JAPONICAS IN COMPLEX WITH 1- DEOXYGALACTONOJIRIMYCIN | HYDROLASE, ENZYME-CARBOHYDRATE INTERACTION, GLYCOSIDASE INHIBITION
4d1j:H (GLU41) to (ASN66) THE STRUCTURE OF THE GH35 BETA-GALACTOSIDASE BGL35A FROM CELLVIBRIO JAPONICAS IN COMPLEX WITH 1- DEOXYGALACTONOJIRIMYCIN | HYDROLASE, ENZYME-CARBOHYDRATE INTERACTION, GLYCOSIDASE INHIBITION
5glz:A (GLY22) to (PRO55) TL-GAL WITH GLUCOSE | CARBOHYDRATES, TL-GALECTIN, ANTI-INFLAMMATION, SUGAR BINDING PROTEIN
5glz:B (GLY22) to (PRO55) TL-GAL WITH GLUCOSE | CARBOHYDRATES, TL-GALECTIN, ANTI-INFLAMMATION, SUGAR BINDING PROTEIN
3dl5:A (VAL404) to (ASP426) CRYSTAL STRUCTURE OF THE A287F ACTIVE SITE MUTANT OF TS- DHFR FROM CRYPTOSPORIDIUM HOMINIS | ENZYME ACTIVE SITE MUTANT, ENZYME-LIGAND COMPLEX, , OXIDOREDUCTASE
3dl5:C (ASN250) to (ASP273) CRYSTAL STRUCTURE OF THE A287F ACTIVE SITE MUTANT OF TS- DHFR FROM CRYPTOSPORIDIUM HOMINIS | ENZYME ACTIVE SITE MUTANT, ENZYME-LIGAND COMPLEX, , OXIDOREDUCTASE
3dl5:E (ASN250) to (ARG275) CRYSTAL STRUCTURE OF THE A287F ACTIVE SITE MUTANT OF TS- DHFR FROM CRYPTOSPORIDIUM HOMINIS | ENZYME ACTIVE SITE MUTANT, ENZYME-LIGAND COMPLEX, , OXIDOREDUCTASE
3dl5:E (LEU405) to (ASP426) CRYSTAL STRUCTURE OF THE A287F ACTIVE SITE MUTANT OF TS- DHFR FROM CRYPTOSPORIDIUM HOMINIS | ENZYME ACTIVE SITE MUTANT, ENZYME-LIGAND COMPLEX, , OXIDOREDUCTASE
3okx:A (ASP119) to (PRO144) CRYSTAL STRUCTURE OF YAEB-LIKE PROTEIN FROM RHODOPSEUDOMONAS PALUSTRIS | PSI-2, MIDWEST CENTER FOR STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, MCSG, UNKNOWN FUNCTION, STRUCTURAL GENOMICS
4tvz:B (ASP212) to (TRP239) CRYSTAL STRUCTURE OF SCARB2 IN NEURAL CONDITION (PH7.5) | LIPID BINDING TUNNEL, PROTEIN BINDING
3dmk:A (ASP221) to (GLY239) CRYSTAL STRUCTURE OF DOWN SYNDROME CELL ADHESION MOLECULE (DSCAM) ISOFORM 1.30.30, N-TERMINAL EIGHT IG DOMAINS | IG DOMAINS, IMMUNOGLOBULIN DOMAIN, CELL ADHESION
3dmk:B (ASP221) to (GLY239) CRYSTAL STRUCTURE OF DOWN SYNDROME CELL ADHESION MOLECULE (DSCAM) ISOFORM 1.30.30, N-TERMINAL EIGHT IG DOMAINS | IG DOMAINS, IMMUNOGLOBULIN DOMAIN, CELL ADHESION
3dmk:C (ASP221) to (GLY239) CRYSTAL STRUCTURE OF DOWN SYNDROME CELL ADHESION MOLECULE (DSCAM) ISOFORM 1.30.30, N-TERMINAL EIGHT IG DOMAINS | IG DOMAINS, IMMUNOGLOBULIN DOMAIN, CELL ADHESION
3do0:A (THR6) to (THR34) THERMOLYSIN BY CLASSICAL HANGING DROP METHOD AFTER HIGH X- RAY DOSE ON ESRF ID14-2 BEAMLINE | HYDROLASE, METALLOPROTEINASE, CALCIUM, METAL-BINDING, METALLOPROTEASE, PROTEASE, SECRETED, ZINC, ZYMOGEN
3do1:A (THR6) to (THR34) THERMOLYSIN BY CLASSICAL HANGING DROP METHOD BEFORE HIGH X- RAY DOSE ON ESRF ID14-2 BEAMLINE | HYDROLASE, METALLOPROTEINASE, CALCIUM, METAL-BINDING, METALLOPROTEASE, PROTEASE, SECRETED, ZINC, ZYMOGEN
3do2:A (THR6) to (THR34) THERMOLYSIN BY LB NANOTEMPLATE METHOD AFTER HIGH X-RAY DOSE ON ESRF ID14-2 BEAMLINE | HYDROLASE, METALLOPROTEINASE, CALCIUM, METAL-BINDING, METALLOPROTEASE, PROTEASE, SECRETED, ZINC, ZYMOGEN
5h8j:B (ASN222) to (PRO245) CRYSTAL STRUCTURE OF MEDICAGO TRUNCATULA N-CARBAMOYLPUTRESCINE AMIDOHYDROLASE (MTCPA) IN COMPLEX WITH CADAVERINE | AMIDASE, HELICAL OCTAMER, ALPHA-BETA-BETA-ALPHA SANDWICH FOLD, PUTRESCINE BIOSYNTHESIS, HYDROLASE
5h8j:J (GLY221) to (PRO245) CRYSTAL STRUCTURE OF MEDICAGO TRUNCATULA N-CARBAMOYLPUTRESCINE AMIDOHYDROLASE (MTCPA) IN COMPLEX WITH CADAVERINE | AMIDASE, HELICAL OCTAMER, ALPHA-BETA-BETA-ALPHA SANDWICH FOLD, PUTRESCINE BIOSYNTHESIS, HYDROLASE
5h8l:B (GLY221) to (PRO245) CRYSTAL STRUCTURE OF MEDICAGO TRUNCATULA N-CARBAMOYLPUTRESCINE AMIDOHYDROLASE (MTCPA) C158S MUTANT IN COMPLEX WITH PUTRESCINE | AMIDASE, HELICAL OCTAMER, ALPHA-BETA-BETA-ALPHA SANDWICH FOLD, HYDROLASE
5h8l:J (GLY221) to (PRO245) CRYSTAL STRUCTURE OF MEDICAGO TRUNCATULA N-CARBAMOYLPUTRESCINE AMIDOHYDROLASE (MTCPA) C158S MUTANT IN COMPLEX WITH PUTRESCINE | AMIDASE, HELICAL OCTAMER, ALPHA-BETA-BETA-ALPHA SANDWICH FOLD, HYDROLASE
4d91:A (THR6) to (THR34) THERMOLYSIN IN COMPLEX WITH DMSO AND ACETATE | PROTEASE, METALLOPROTEASE, HYDROLYSIS OF PEPTIDE BONDS, PHOSPHORAMIDON, HYDROLASE
4u1k:A (HIS188) to (PRO210) HLA CLASS I MICROPOLYMORPHISMS DETERMINE PEPTIDE-HLA LANDSCAPE AND DICTATE DIFFERENTIAL HIV-1 ESCAPE THROUGH IDENTICAL EPITOPES | IMMUNOGLOBULIN, HLA, HIV, IMMUNE SYSTEM
4u1l:A (HIS188) to (PRO210) HLA CLASS I MICROPOLYMORPHISMS DETERMINE PEPTIDE-HLA LANDSCAPE AND DICTATE DIFFERENTIAL HIV-1 ESCAPE THROUGH IDENTICAL EPITOPES | IMMUNOGLOBULIN, HLA, HIV, IMMUNE SYSTEM
5h8v:A (GLY409) to (GLY430) CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN MAIZE SULFITE REDUCTASE AND FERREDOXIN IN THE FORM-1 CRYSTAL | FERREDOXIN, SULFITE REDUCTASE, OXIDOREDUCTASE
5h8v:B (GLY409) to (GLY430) CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN MAIZE SULFITE REDUCTASE AND FERREDOXIN IN THE FORM-1 CRYSTAL | FERREDOXIN, SULFITE REDUCTASE, OXIDOREDUCTASE
5h92:A (GLY104) to (PRO133) CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN MAIZE SULFITE REDUCTASE AND FERREDOXIN IN THE FORM-3 CRYSTAL | FERREDOXIN, SULFITE REDUCTASE, OXIDOREDUCTASE-ELECTRON TRANSPORT COMPLEX
5h92:A (GLY409) to (GLY430) CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN MAIZE SULFITE REDUCTASE AND FERREDOXIN IN THE FORM-3 CRYSTAL | FERREDOXIN, SULFITE REDUCTASE, OXIDOREDUCTASE-ELECTRON TRANSPORT COMPLEX
5h92:B (GLY104) to (PRO133) CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN MAIZE SULFITE REDUCTASE AND FERREDOXIN IN THE FORM-3 CRYSTAL | FERREDOXIN, SULFITE REDUCTASE, OXIDOREDUCTASE-ELECTRON TRANSPORT COMPLEX
5h92:B (GLY409) to (GLY431) CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN MAIZE SULFITE REDUCTASE AND FERREDOXIN IN THE FORM-3 CRYSTAL | FERREDOXIN, SULFITE REDUCTASE, OXIDOREDUCTASE-ELECTRON TRANSPORT COMPLEX
3dt4:A (ASP311) to (VAL335) THE STRUCTURE OF RAT CYTOSOLIC PEPCK IN COMPLEX WITH OXALATE AND GTP | KINASE, GLUCONEOGENESIS, LYASE, DECARBOXYLASE, GTP-BINDING, NUCLEOTIDE-BINDING
3dt4:C (ASP311) to (VAL335) THE STRUCTURE OF RAT CYTOSOLIC PEPCK IN COMPLEX WITH OXALATE AND GTP | KINASE, GLUCONEOGENESIS, LYASE, DECARBOXYLASE, GTP-BINDING, NUCLEOTIDE-BINDING
3dt7:A (ASP311) to (VAL335) THE STRUCTURE OF RAT CYTOSOLIC PEPCK IN COMPLEX WITH BETA- SULFOPYRUVATE AND GTP | KINASE, GLUCONEOGENESIS, LYASE, DECARBOXYLASE, GTP-BINDING, NUCLEOTIDE-BINDING
4d9j:A (VAL5) to (GLY21) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, DE NOVO PROTEIN
4d9j:C (VAL5) to (GLY21) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, DE NOVO PROTEIN
4d9j:F (VAL5) to (GLY21) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, DE NOVO PROTEIN
4d9j:I (VAL5) to (GLY21) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, DE NOVO PROTEIN
4d9j:K (VAL5) to (GLY21) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, DE NOVO PROTEIN
4d9j:L (VAL5) to (GLY21) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, DE NOVO PROTEIN
4d9w:A (THR6) to (THR34) THERMOLYSIN IN COMPLEX WITH UBTLN32 | PROTEASE, METALLOPROTEASE, HYDROLYSIS OF PEPTIDE BONDS, PHOSPHORAMIDON, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3dwn:B (GLN204) to (GLY259) CRYSTAL STRUCTURE OF THE LONG-CHAIN FATTY ACID TRANSPORTER FADL MUTANT A77E/S100R | BETA BARREL, OUTER MEMBRANE PROTEIN, LIPID TRANSPORT, MEMBRANE, OUTER MEMBRANE, PHAGE RECOGNITION, TRANSMEMBRANE, TRANSPORT
4de1:A (ASP233) to (GLN254) CTX-M-9 CLASS A BETA-LACTAMASE COMPLEXED WITH COMPOUND 18 | CTX-M, BETA-LACTAMASE, MOLECULAR DOCKING, FRAGMENT, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3dy3:L (THR2) to (THR22) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH THE EPIMER FORM OF SPIROLACTACYSTIN | PROTEASOME, INHIBITOR, PROTEIN DEGRADATION, UBIQUITIN- PROTEASOME-PATHWAY, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN
3dy3:Z (THR2) to (THR22) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH THE EPIMER FORM OF SPIROLACTACYSTIN | PROTEASOME, INHIBITOR, PROTEIN DEGRADATION, UBIQUITIN- PROTEASOME-PATHWAY, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN
5hgb:J (HIS188) to (PRO210) HLA*A2402 COMPLEXED WITH HIV NEF138 8MER EPITOPE | HLA, ANTIGEN PRESENTATION, HIV, IMMUNE SYSTEM
4u6y:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA-A*0201 IN COMPLEX WITH FLNDK, A 15 MER SELF- PEPTIDE | HLA A*0201, LIGANDOME, TCR, T CELL, IMMUNE SYSTEM
3p7p:E (THR6) to (THR34) RADIATION DAMAGE STUDY OF THERMOLYSIN - 100K STRUCTURE A (0.1 MGY) | ALPHA/BETA PROTEIN, HYDROLASE
3p7q:E (THR6) to (THR34) RADIATION DAMAGE STUDY OF THERMOLYSIN - 100K STRUCTURE B (2.5 MGY) | ALPHA/BETA PROTEIN, HYDROLASE
3p7r:E (THR6) to (THR34) RADIATION DAMAGE STUDY OF THERMOLYSIN - 100K STRUCTURE C (4.9 MGY) | ALPHA/BETA PROTEIN, HYDROLASE
3p7s:E (THR6) to (THR34) RADIATION DAMAGE STUDY OF THERMOLYSIN - 100K STRUCTURE D (7.2 MGY) | ALPHA/BETA PROTEIN, HYDROLASE
3p7t:E (THR6) to (THR34) RADIATION DAMAGE STUDY OF THERMOLYSIN - 160K STRUCTURE A (0.1 MGY) | ALPHA/BETA PROTEIN, HYDROLASE
3p7u:E (THR6) to (THR34) RADIATION DAMAGE STUDY OF THERMOLYSIN - 160K STRUCTURE B (2.4 MGY) | ALPHA/BETA PROTEIN, HYDROLASE
3p7v:E (THR6) to (THR34) RADIATION DAMAGE STUDY OF THERMOLYSIN - 160K STRUCTURE C (4.8 MGY) | ALPHA/BETA PROTEIN, HYDROLASE
3p7w:E (THR6) to (THR34) RADIATION DAMAGE STUDY OF THERMOLYSIN - 160K STRUCTURE D (7.1 MGY) | ALPHA/BETA PROTEIN, HYDROLASE
4doi:B (ARG1047) to (LEU1065) CRYSTAL STRUCTURE OF ARABIDOPSIS THALIANA CHALCONE ISOMERASE AT3G55120 (ATCHI) | CHALCONE-FLAVANONE ISOMERASE, ISOMERASE
5hp8:A (GLN81) to (GLY96) CRYSTAL STRUCTURES OF RIDA IN COMPLEX WITH PYRUVATE | RIDA, ENAMINE/IMINE, DEAMINATION, HYDROLASE
5hp8:B (GLN81) to (GLY96) CRYSTAL STRUCTURES OF RIDA IN COMPLEX WITH PYRUVATE | RIDA, ENAMINE/IMINE, DEAMINATION, HYDROLASE
5hp8:C (GLN81) to (GLY96) CRYSTAL STRUCTURES OF RIDA IN COMPLEX WITH PYRUVATE | RIDA, ENAMINE/IMINE, DEAMINATION, HYDROLASE
5hqd:A (THR6) to (THR34) ACOUSTIC INJECTORS FOR DROP-ON-DEMAND SERIAL FEMTOSECOND CRYSTALLOGRAPHY | HYDROLASE, METALLOPROTEINASE, XFEL
4dpd:B (THR573) to (HIS599) WILD TYPE PLASMODIUM FALCIPARUM DIHYDROFOLATE REDUCTASE-THYMIDYLATE SYNTHASE (PFDHFR-TS), DHF COMPLEX, NADP+, DUMP | DHFR, ROSSMANN FOLD, REDUCTASE, NADPH BINDING, OXIDOREDUCTASE, TRANSFERASE
3e38:B (GLN29) to (VAL48) CRYSTAL STRUCTURE OF A TWO-DOMAIN PROTEIN CONTAINING PREDICTED PHP- LIKE METAL-DEPENDENT PHOSPHOESTERASE (BVU_3505) FROM BACTEROIDES VULGATUS ATCC 8482 AT 2.20 A RESOLUTION | STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, HYDROLASE
5hs3:C (LYS278) to (PRO305) HUMAN THYMIDYLATE SYNTHASE COMPLEXED WITH DUMP AND 3-AMINO-2-BENZOYL- 4-METHYLTHIENO[2,3-B]PYRIDIN-6-OL | NHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4dq1:A (MET204) to (ASP224) THYMIDYLATE SYNTHASE FROM STAPHYLOCOCCUS AUREUS. | STRUCTURAL GENOMICS, PSI-BIOLOGY, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, STRUCTURES OF MTB PROTEINS CONFERRING SUSCEPTIBILITY TO KNOWN MTB INHIBITORS, MTBI, THYMIDYLATE SYNTHASE, TRANSFERASE
5ht6:A (GLU113) to (LYS135) CRYSTAL STRUCTURE OF THE SET DOMAIN OF THE HUMAN MLL5 METHYLTRANSFERASE | SET DOMAIN, TRANSFERASE
3pb1:E (SER95) to (SER110) CRYSTAL STRUCTURE OF A MICHAELIS COMPLEX BETWEEN PLASMINOGEN ACTIVATOR INHIBITOR-1 AND UROKINASE-TYPE PLASMINOGEN ACTIVATOR | PAI-1, UPA, MICHAELIS COMPLEX, STRUCTURAL GENOMICS, STRUCTURE 2 FUNCTION PROJECT, S2F, HYDROLASE INHIBITOR-HYDROLASE COMPLEX
3e47:J (ILE3) to (GLY23) CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH HOMOBELACTOSIN C | PROTEASOME, UBIQUITIN, PROTEIN DEGRADATION, INHIBITOR, IMMUNOLOGY, CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, THREONINE PROTEASE, UBL CONJUGATION, ZYMOGEN
3e47:L (THR2) to (THR22) CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH HOMOBELACTOSIN C | PROTEASOME, UBIQUITIN, PROTEIN DEGRADATION, INHIBITOR, IMMUNOLOGY, CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, THREONINE PROTEASE, UBL CONJUGATION, ZYMOGEN
3e47:Z (THR2) to (THR22) CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH HOMOBELACTOSIN C | PROTEASOME, UBIQUITIN, PROTEIN DEGRADATION, INHIBITOR, IMMUNOLOGY, CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, THREONINE PROTEASE, UBL CONJUGATION, ZYMOGEN
4dt8:B (ILE203) to (SER224) CRYSTAL STRUCTURE OF AMINOGLYCOSIDE-2''-PHOSPHOTRANSFERASE TYPE IVA IN COMPLEX WITH ADENOSINE | AMINOGLYCOSIDE KINASE, TRANSFERASE
4dt9:A (ILE203) to (SER224) CRYSTAL STRUCTURE OF AMINOGLYCOSIDE-2''-PHOSPHOTRANSFERASE TYPE IVA IN COMPLEX WITH GUANOSINE | AMINOGLYCOSIDE KINASE, TRANSFERASE
5hxv:A (GLY84) to (ASN102) THE CRYSTAL STRUCTURE OF THERMOSTABLE XYLANASE MUTANT | GLYCOSIDE HYDROLASE FAMILY 11 ENDO-XYLANASE, HYDROLASE
5hxv:D (GLY84) to (ASN102) THE CRYSTAL STRUCTURE OF THERMOSTABLE XYLANASE MUTANT | GLYCOSIDE HYDROLASE FAMILY 11 ENDO-XYLANASE, HYDROLASE
5hxv:I (GLY84) to (ASN102) THE CRYSTAL STRUCTURE OF THERMOSTABLE XYLANASE MUTANT | GLYCOSIDE HYDROLASE FAMILY 11 ENDO-XYLANASE, HYDROLASE
4dtw:B (GLU430) to (LYS452) CYTOCHROME P450 BM3H-8C8 MRI SENSOR BOUND TO SEROTONIN | CYTOCHROME P450, MRI CONTRAST SENSOR, DIRECTED EVOLUTION, OXIDOREDUCTASE
4dty:B (GLU430) to (LYS452) CYTOCHROME P450 BM3H-8C8 MRI SENSOR, NO LIGAND | CYTOCHROME P450, MRI CONTRAST SENSOR, DIRECTED EVOLUTION, OXIDOREDUCTASE
4dty:A (GLU430) to (LYS452) CYTOCHROME P450 BM3H-8C8 MRI SENSOR, NO LIGAND | CYTOCHROME P450, MRI CONTRAST SENSOR, DIRECTED EVOLUTION, OXIDOREDUCTASE
4dtz:A (GLU430) to (LYS452) CYTOCHROME P450 BM3H-8C8 MRI SENSOR BOUND TO DOPAMINE | CYTOCHROME P450, MRI CONTRAST SENSOR, DIRECTED EVOLUTION, OXIDOREDUCTASE
4dtz:B (GLU430) to (LYS452) CYTOCHROME P450 BM3H-8C8 MRI SENSOR BOUND TO DOPAMINE | CYTOCHROME P450, MRI CONTRAST SENSOR, DIRECTED EVOLUTION, OXIDOREDUCTASE
4du2:B (GLU430) to (LYS452) CYTOCHROME P450 BM3H-B7 MRI SENSOR BOUND TO DOPAMINE | CYTOCHROME P450, MRI CONTRAST SENSOR, DIRECTED EVOLUTION, OXIDOREDUCTASE
4du2:A (GLU430) to (LYS452) CYTOCHROME P450 BM3H-B7 MRI SENSOR BOUND TO DOPAMINE | CYTOCHROME P450, MRI CONTRAST SENSOR, DIRECTED EVOLUTION, OXIDOREDUCTASE
4duf:A (GLU430) to (LYS452) CYTOCHROME P450 BM3H-2G9 MRI SENSOR BOUND TO SEROTONIN | CYTOCHROME P450, MRI CONTRAST SENSOR, DIRECTED EVOLUTION, OXIDOREDUCTASE
4duf:B (GLU430) to (LYS452) CYTOCHROME P450 BM3H-2G9 MRI SENSOR BOUND TO SEROTONIN | CYTOCHROME P450, MRI CONTRAST SENSOR, DIRECTED EVOLUTION, OXIDOREDUCTASE
4duf:D (GLU430) to (LYS452) CYTOCHROME P450 BM3H-2G9 MRI SENSOR BOUND TO SEROTONIN | CYTOCHROME P450, MRI CONTRAST SENSOR, DIRECTED EVOLUTION, OXIDOREDUCTASE
4dua:A (GLU430) to (LYS452) CYTOCHROME P450 BM3H-9D7 MRI SENSOR, NO LIGAND | CYTOCHROME P450, MRI CONTRAST SENSOR, DIRECTED EVOLUTION, OXIDOREDUCTASE
4dua:B (GLU430) to (LYS452) CYTOCHROME P450 BM3H-9D7 MRI SENSOR, NO LIGAND | CYTOCHROME P450, MRI CONTRAST SENSOR, DIRECTED EVOLUTION, OXIDOREDUCTASE
4dud:A (GLU430) to (LYS452) CYTOCHROME P450 BM3H-2G9C6 MRI SENSOR, NO LIGAND | CYTOCHROME P450, MRI CONTRAST SENSOR, DIRECTED EVOLUTION, OXIDOREDUCTASE
4dud:B (GLU430) to (LYS452) CYTOCHROME P450 BM3H-2G9C6 MRI SENSOR, NO LIGAND | CYTOCHROME P450, MRI CONTRAST SENSOR, DIRECTED EVOLUTION, OXIDOREDUCTASE
5i15:H (SER126) to (PRO153) CRYSTAL STRUCTURE OF HUMAN GERMLINE ANTIBODY IGHV1-69/IGKV1-39 | MONOCLONAL ANTIBODY, IMMUNE SYSTEM
3pgf:H (SER120) to (PRO147) CRYSTAL STRUCTURE OF MALTOSE BOUND MBP WITH A CONFORMATIONALLY SPECIFIC SYNTHETIC ANTIGEN BINDER (SAB) | MALTODEXTRIN BINDING PROTEIN, FAB, ANTIBODY FRAGMENT, ENGINEERED BINDING PROTEIN, MALTODEXTRIN BINDING PROTEIN-DE NOVO PROTEIN COMPLEX
5i5k:A (TYR322) to (LEU356) STRUCTURE OF COMPLEMENT C5 IN COMPLEX WITH ECULIZUMAB | COMPLEMENT, FAB, IMMUNE SYSTEM
3pnh:B (VAL312) to (ASN340) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-((2-FLUORO-2-(3-FLUOROPHENYL) ETHYL) AMINO)ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | HEME ENZYME, INHIBITOR, OXIDOREDUCTASE-INHIBITOR COMPLEX
3pnw:N (SER136) to (PRO163) CRYSTAL STRUCTURE OF THE TUDOR DOMAIN OF HUMAN TDRD3 IN COMPLEX WITH AN ANTI-TDRD3 FAB | FAB, STRUCTURAL GENOMICS CONSORTIUM, ANTIBODY, SGC, PROTEIN BINDING- IMMUNE SYSTEM COMPLEX
3pnw:T (SER136) to (PRO163) CRYSTAL STRUCTURE OF THE TUDOR DOMAIN OF HUMAN TDRD3 IN COMPLEX WITH AN ANTI-TDRD3 FAB | FAB, STRUCTURAL GENOMICS CONSORTIUM, ANTIBODY, SGC, PROTEIN BINDING- IMMUNE SYSTEM COMPLEX
5i8h:I (SER118) to (PRO145) CRYSTAL STRUCTURE OF HIV-1 BG505 SOSIP.664 PREFUSION ENV TRIMER IN COMPLEX WITH V3 LOOP-TARGETING ANTIBODY PGT122 FAB AND FUSION PEPTIDE-TARGETING ANTIBODY VRC34.01 FAB | HIV-1, ENVELOPE, TRIMER, FUSION PEPTIDE, ANTIBODY, NEUTRALIZING, IMMUNE SYSTEM
5i8k:H (SER123) to (PRO150) HHH1 FAB FRAGMENT | ANTIBODY, GLYCAN BINDING, FAB, ALLERGY, IMMUNE SYSTEM
4upt:A (VAL312) to (ASN340) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N'-[4-[[(2S,4R)-4-[3-[(C-THIOPHEN-2- YLCARBONIMIDOYL)AMINO]PHENOXY]PYRROLIDIN-2- YL]METHOXY]PHENYL]THIOPHENE-2-CARBOXIMIDAMIDE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4uq2:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA-A1101 IN COMPLEX WITH AN AZOBENZENE-CONTAINING PEPTIDE | AZOBENZENE, HLA-A, SYNTHETIC PEPTIDE, IMMUNE SYSTEM
4uq2:C (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA-A1101 IN COMPLEX WITH AN AZOBENZENE-CONTAINING PEPTIDE | AZOBENZENE, HLA-A, SYNTHETIC PEPTIDE, IMMUNE SYSTEM
3pps:A (THR153) to (TYR178) CRYSTAL STRUCTURE OF AN ASCOMYCETE FUNGAL LACCASE FROM THIELAVIA ARENARIA | BETA BARREL, CUPREDOXIN FOLD, OXIDOREDUCTASE, COPPER BINDING
3pps:D (THR153) to (TYR178) CRYSTAL STRUCTURE OF AN ASCOMYCETE FUNGAL LACCASE FROM THIELAVIA ARENARIA | BETA BARREL, CUPREDOXIN FOLD, OXIDOREDUCTASE, COPPER BINDING
5icz:D (SER126) to (PRO153) CETUXIMAB FAB IN COMPLEX WITH GQFDLSTRRLKG PEPTIDE | ANTIBODY, ANTI-EGFR, IMMUNE SYSTEM
5ifi:C (VAL84) to (ASN103) CRYSTAL STRUCTURE OF ACETYL-COA SYNTHETASE IN COMPLEX WITH ADENOSINE- 5'-PROPYLPHOSPHATE FROM CRYPTOCOCCUS NEOFORMANS H99 | SSGCID, NIH, NIAID, SBRI, UW, BERYLLIUM, SYNTHETASE, ACS1, PRX, PROPYL-AMP, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, LIGASE
3pqu:A (GLN414) to (GLU431) THE CRYSTAL STRUCTURES OF PORCINE PATHOGEN ASH57_TBPB | LIPOPROTEIN, TRANSFERRIN RECEPTOR, IRON ACQUISITION, VACCINE CANDIDATE, BETA-BARREL, TRANSFERRIN BINDING, TRANSFERRIN, OUTERMEMBRANE, LIPID BINDING PROTEIN
4uv4:H (SER120) to (PRO147) CRYSTAL STRUCTURE OF ANTI-FPR FPRO0165 FAB FRAGMENT | IMMUNE SYSTEM, ANTIBODY ENGINEERING, PHAGE DISPLAY, LONG CDR, FORMYL PEPTIDE RECEPTOR-1
3prx:A (LYS321) to (LEU356) STRUCTURE OF COMPLEMENT C5 IN COMPLEX WITH CVF AND SSL7 | IMMUNE SYSTEM, COMPLEMENT, STAPHYLOCOCCUS AUREUS, IMMUNE SYSTEM-TOXIN COMPLEX
3prx:C (LYS321) to (LEU356) STRUCTURE OF COMPLEMENT C5 IN COMPLEX WITH CVF AND SSL7 | IMMUNE SYSTEM, COMPLEMENT, STAPHYLOCOCCUS AUREUS, IMMUNE SYSTEM-TOXIN COMPLEX
4eb4:D (CYS37) to (ARG62) CRYSTAL STRUCTURE OF MOUSE THYMIDYLATE SYNTHASE IN TERNARY COMPLEX WITH DUMP AND TOMUDEX | TERNARY COMPLEX, METHYLTRANSFERASE, NUCLEOTIDE BIOSYNTHESIS, TRANSFERASE
3psx:A (GLU430) to (LYS452) CRYSTAL STRUCTURE OF THE KT2 MUTANT OF CYTOCHROME P450 BM3 | CYTOCHROME P450 FOLD, OXIDOREDUCTASE
3psx:B (GLU430) to (LYS452) CRYSTAL STRUCTURE OF THE KT2 MUTANT OF CYTOCHROME P450 BM3 | CYTOCHROME P450 FOLD, OXIDOREDUCTASE
3puk:B (ALA510) to (ILE537) RE-REFINEMENT OF THE CRYSTAL STRUCTURE OF MUNC18-3 AND SYNTAXIN4 N- PEPTIDE COMPLEX | MEMBRANE TRAFFICKING, SM PROTEIN, SYNTAXIN, SNARE PROTEINS, SYNTAXIN BINDING PROTEIN, ENDOCYTOSIS-EXOCYTOSIS COMPLEX
4ef3:A (GLY55) to (GLN81) MULTICOPPER OXIDASE CUEO (CITRATE BUFFER) | MULTICOPPER OXIDASE, METAL BINDING PROTEIN
5ik7:A (THR2938) to (GLY2955) LAMININ A2LG45 I-FORM, APO. | EXTRACELLULAR MATRIX, LIGAND BINDING, LG DOMAIN, STRUCTURAL PROTEIN
3pvm:A (LEU323) to (LEU356) STRUCTURE OF COMPLEMENT C5 IN COMPLEX WITH CVF | IMMUNE SYSTEM, COMPLEMENT
5im7:C (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA-B5801, A PROTECTIVE HLA ALLELE FOR HIV-1 INFECTION | HLA, HIV, QW9, IMMUNE SYSTEM
3pwj:D (HIS188) to (PRO210) HUMAN CLASS I MHC HLA-A2 IN COMPLEX WITH THE HUD (G2L,I9V) PEPTIDE VARIANT | HUD ANTIGEN, TAX PEPTIDE, NONAPEPTIDE, MHC CLASS I, HLA-A2, TCR A6, CROSS-REACTIVITY, PROTEIN BINDING
3pwp:A (HIS188) to (PRO210) THE COMPLEX BETWEEN TCR A6 AND HUMAN CLASS I MHC HLA-A2 WITH THE BOUND HUD PEPTIDE | TAX PEPTIDE, HUD EPITOPE, NONAPEPTIDE, MHC CLASS I, HLA-A2, TCR A6, CROSS-REACTIVITY, PROTEIN BINDING
5inc:C (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA-B5801, A PROTECTIVE HLA ALLELE FOR HIV-1 INFECTION | HLA, HIV, QW9_S3T, IMMUNE SYSTEM
3q07:A (LYS234) to (GLN252) CTX-M-9 S70G IN COMPLEX WITH PIPERACILLIN | BETA-LACTAMASE, ESBL, CTX-M, CTX-M-9, BETA-LACTAM, PIPERACILLIN, MICHAELIS, ANTIBIOTIC RESISTANCE, HYDROLASE, ALPHA BETA FOLD, HYDROLASE-ANTIBIOTIC COMPLEX
3q07:B (LYS234) to (GLN252) CTX-M-9 S70G IN COMPLEX WITH PIPERACILLIN | BETA-LACTAMASE, ESBL, CTX-M, CTX-M-9, BETA-LACTAM, PIPERACILLIN, MICHAELIS, ANTIBIOTIC RESISTANCE, HYDROLASE, ALPHA BETA FOLD, HYDROLASE-ANTIBIOTIC COMPLEX
5iro:K (LYS6) to (PRO32) CRYSTAL STRUCTURE OF A COMPLEX BETWEEN THE HUMAN ADENOVIRUS TYPE 4 E3- 19K PROTEIN AND MHC CLASS MOLECULE HLA-A2/TAX | AD4 E3-19K-HLA-A2 COMPLEX, IMMUNE EVASION FUNCTION, MHC CLASS I MOLECULE, IMMUNE SYSTEM-TRANSCRIPTION COMPLEX
4ep8:C (ASP1431) to (SER1493) INITIAL UREASE STRUCTURE FOR RADIATION DAMAGE EXPERIMENT AT 100 K | ALPHA-BETA BARREL, NICKEL METALLOENZYME, HYDROLASE, RADIATION DAMAGE
4epb:C (ASP1431) to (SER1493) FINAL UREASE STRUCTURE FOR RADIATION DAMAGE EXPERIMENT AT 100 K | ALPHA-BETA BARREL, NICKEL METALLOENZYME, HYDROLASE, RADIATION DAMAGE
4epe:C (ASP1431) to (SER1493) FINAL UREASE STRUCTURE FOR RADIATION DAMAGE EXPERIMENT AT 300 K | ALPHA-BETA BARREL, NICKEL METALLOENZYME, HYDROLASE, RADIATION DAMAGE
4eu2:N (THR1) to (GLY23) CRYSTAL STRUCTURE OF 20S PROTEASOME WITH NOVEL INHIBITOR K-7174 | PROTEASOME INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3qda:A (LYS6) to (PRO32) CRYSTAL STRUCTURE OF W95L BETA-2 MICROGLOBULIN | TRYPTOPHAN, IMMUNOGLOBIN, BETA-SANDWICH, HYDROPHOBIC POCKET, AMYLOIDOSIS, DRA, MHC CLASS I, IMMUNE SYSTEM
3qdq:A (LEU313) to (SER332) COMPLEX BETWEEN 4-HYDROXYBUTYRATE COA-TRANSFERASE FROM CLOSTRIDIUM AMINOBUTYRICUM AND COA | COA TRANSFERASE FAMILY I; SINGLE SUBUNIT COA TRANSFERASE, COA, TRANSFERASE
3qfj:A (LYS186) to (PRO210) THE COMPLEX BETWEEN TCR A6 AND HUMAN CLASS I MHC HLA-A2 WITH THE MODIFIED TAX (Y5F) PEPTIDE | TAX PEPTIDE, NONAPEPTIDE, MHC CLASS I, HLA-A2, TCR A6, CROSS- REACTIVITY, Y5F MUTATION, IMMUNE SYSTEM
4f3d:A (ASN316) to (GLY333) STRUCTURE OF RPE65: P65 CRYSTAL FORM GROWN IN FOS-CHOLINE-10 | MONOTOPIC MEMBRANE PROTEIN, METALLOPROTEIN, NON-HEME IRON PROTEIN, BETA-PROPELLER, SMOOTH ER MEMBRANE, ISOMERASE, HYDROLASE
4f3d:B (ASN316) to (GLY333) STRUCTURE OF RPE65: P65 CRYSTAL FORM GROWN IN FOS-CHOLINE-10 | MONOTOPIC MEMBRANE PROTEIN, METALLOPROTEIN, NON-HEME IRON PROTEIN, BETA-PROPELLER, SMOOTH ER MEMBRANE, ISOMERASE, HYDROLASE
3qga:C (ASP432) to (PHE492) 3.0 A MODEL OF IRON CONTAINING UREASE UREA2B2 FROM HELICOBACTER MUSTELAE | IRON METALLOENZYME, ALPHA-BETA BARREL, UREASE, HYDROLASE
3qga:F (ASP432) to (PHE492) 3.0 A MODEL OF IRON CONTAINING UREASE UREA2B2 FROM HELICOBACTER MUSTELAE | IRON METALLOENZYME, ALPHA-BETA BARREL, UREASE, HYDROLASE
3qga:I (ASP432) to (PHE492) 3.0 A MODEL OF IRON CONTAINING UREASE UREA2B2 FROM HELICOBACTER MUSTELAE | IRON METALLOENZYME, ALPHA-BETA BARREL, UREASE, HYDROLASE
3qga:L (ASP432) to (PHE492) 3.0 A MODEL OF IRON CONTAINING UREASE UREA2B2 FROM HELICOBACTER MUSTELAE | IRON METALLOENZYME, ALPHA-BETA BARREL, UREASE, HYDROLASE
3qga:O (ASP432) to (PHE492) 3.0 A MODEL OF IRON CONTAINING UREASE UREA2B2 FROM HELICOBACTER MUSTELAE | IRON METALLOENZYME, ALPHA-BETA BARREL, UREASE, HYDROLASE
3qga:R (ASP432) to (PHE492) 3.0 A MODEL OF IRON CONTAINING UREASE UREA2B2 FROM HELICOBACTER MUSTELAE | IRON METALLOENZYME, ALPHA-BETA BARREL, UREASE, HYDROLASE
5j1w:B (ASP300) to (GLY327) CRYSTAL STRUCTURE OF HUMAN CLK1 IN COMPLEX WITH PYRIDO[3,4- G]QUINAZOLINE DERIVATIVE ZW31 (COMPOUND 14) | TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, TYROSINE-PROTEIN KINASE, NUCLEUS, INHIBITOR, STRUCTURAL GENOMICS CONSORTIUM, SGC
3qgk:C (ASP432) to (PHE492) 3.0 A MODEL OF IRON CONTAINING UREASE UREA2B2 FROM HELICOBACTER MUSTELAE (REFINED W/ NO ORDERED SOLVENT) | IRON METALLOENZYME, ALPHA-BETA BARREL, UREASE, HYDROLASE
3qgk:F (ASP432) to (PHE492) 3.0 A MODEL OF IRON CONTAINING UREASE UREA2B2 FROM HELICOBACTER MUSTELAE (REFINED W/ NO ORDERED SOLVENT) | IRON METALLOENZYME, ALPHA-BETA BARREL, UREASE, HYDROLASE
3qgk:I (ASP432) to (PHE492) 3.0 A MODEL OF IRON CONTAINING UREASE UREA2B2 FROM HELICOBACTER MUSTELAE (REFINED W/ NO ORDERED SOLVENT) | IRON METALLOENZYME, ALPHA-BETA BARREL, UREASE, HYDROLASE
3qgk:L (ASP432) to (PHE492) 3.0 A MODEL OF IRON CONTAINING UREASE UREA2B2 FROM HELICOBACTER MUSTELAE (REFINED W/ NO ORDERED SOLVENT) | IRON METALLOENZYME, ALPHA-BETA BARREL, UREASE, HYDROLASE
3qgk:O (ASP432) to (PHE492) 3.0 A MODEL OF IRON CONTAINING UREASE UREA2B2 FROM HELICOBACTER MUSTELAE (REFINED W/ NO ORDERED SOLVENT) | IRON METALLOENZYME, ALPHA-BETA BARREL, UREASE, HYDROLASE
3qgk:R (ASP432) to (PHE492) 3.0 A MODEL OF IRON CONTAINING UREASE UREA2B2 FROM HELICOBACTER MUSTELAE (REFINED W/ NO ORDERED SOLVENT) | IRON METALLOENZYME, ALPHA-BETA BARREL, UREASE, HYDROLASE
3qh1:A (THR6) to (THR34) STRUCTURE OF THERMOLYSIN IN COMPLEX WITH N-BENZYLOXYCARBONYL-L- ASPARTIC ACID | HYDROLASE, METALLOPROTEINASE, N-BENZYLOXYCARBONYL-L-ASPARTIC ACID, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3qh5:A (THR6) to (THR34) STRUCTURE OF THERMOLYSIN IN COMPLEX WITH N-CARBOBENZYLOXY-L-ASPARTIC ACID AND L-PHENYLALANINE METHYL ESTER | HYDROLASE, METALLOPROTEINASE, L-PHENYLALANINE METHYL ESTER, N- CARBOBENZYLOXY-L-ASPARIC ACID, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3qj7:B (THR16) to (ASP37) CRYSTAL STRUCTURE OF THE MYCOBACTERIUM TUBERCULOSIS THYMIDYLATE SYNTHASE (THYA) BOUND TO DUMP | THYMIDILATE SYNTHASE, STRUCTURAL GENOMICS, TB STRUCTURAL GENOMICS CONSORTIUM, TBSGC, TRANSFERASE
3qk0:A (SER400) to (SER417) CRYSTAL STRUCTURE OF PI3K-GAMMA IN COMPLEX WITH BENZOTHIAZOLE 82 | P110, TRANSFERASE, KINASE, INHIBITOR, ATP-BINDING, P84, P101, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
3qm4:A (HIS477) to (VAL495) HUMAN CYTOCHROME P450 (CYP) 2D6 - PRINOMASTAT COMPLEX | CYP2D6, P450 2D6, P450, MONOOXYGENASE, PRINOMASTAT, HEME, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4uy9:B (ILE274) to (ALA298) STRUCTURE OF MLK1 KINASE DOMAIN WITH LEUCINE ZIPPER 1 | MLK FAMILY, MLK1 AND MLK3 SUBTYPE, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, SH3 DOMAIN, TRANSFERASE
4uyl:B (PRO496) to (HIS519) CRYSTAL STRUCTURE OF STEROL 14-ALPHA DEMETHYLASE (CYP51B) FROM A PATHOGENIC FILAMENTOUS FUNGUS ASPERGILLUS FUMIGATUS IN COMPLEX WITH VNI | CYTOCHROME P450, OXIDOREDUCTASE, MONOOXYGENASE, STEROL BIOSYNTHESIS, EUKARYOTIC MEMBRANES, CYTOCHROME P450 FOLD, ENDOPLASMIC RETICULUM MEMBRANE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3qo1:B (SER126) to (PRO153) MONOCLINIC FORM OF IGG1 FAB FRAGMENT (APO FORM) SHARING SAME FV AS IGA | IMMUNOGLOBULIN FOLD, ANTIBODY, SERUM, IMMUNE SYSTEM
3qpx:H (SER126) to (PRO153) CRYSTAL STRUCTURE OF FAB C2507 | IMMUNOGLOBULIN, IMMUNE SYSTEM, MOUSE IL-17A
3qq3:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF SWINE MAJOR HISTOCOMPATIBILITY COMPLEX CLASS I SLA-1 0401 AND IDENTIFICATION OF 2009 PANDEMIC SWINE-ORIGIN INFLUENZA A H1N1 VIRUS CYTOTOXIC T LYMPHOCYTE EPITOPE PEPTIDES | SWINE MHC CLASS 1, SLA-1*0401, EPITOPE OF INFLUENZA VIRUS, IMMUNE SYSTEM
3qq3:B (LYS8) to (PRO34) CRYSTAL STRUCTURE OF SWINE MAJOR HISTOCOMPATIBILITY COMPLEX CLASS I SLA-1 0401 AND IDENTIFICATION OF 2009 PANDEMIC SWINE-ORIGIN INFLUENZA A H1N1 VIRUS CYTOTOXIC T LYMPHOCYTE EPITOPE PEPTIDES | SWINE MHC CLASS 1, SLA-1*0401, EPITOPE OF INFLUENZA VIRUS, IMMUNE SYSTEM
4fff:B (ARG380) to (GLY392) CRYSTAL STRUCTURE OF LEVAN FRUCTOTRANSFERASE FROM ARTHROBACTER UREAFACIENS | GLYCOSIDE HYDROLASE, HYDROLASE
4fff:D (ARG380) to (GLY392) CRYSTAL STRUCTURE OF LEVAN FRUCTOTRANSFERASE FROM ARTHROBACTER UREAFACIENS | GLYCOSIDE HYDROLASE, HYDROLASE
4ffg:C (ARG380) to (GLY392) CRYSTAL STRUCTURE OF LEVAN FRUCTOTRANSFERASE FROM ARTHROBACTER UREAFACIENS IN COMPLEX WITH DFA-IV | GLYCOSIDE HYDROLASE, TRANSFERASE
4ffg:D (ARG380) to (GLY392) CRYSTAL STRUCTURE OF LEVAN FRUCTOTRANSFERASE FROM ARTHROBACTER UREAFACIENS IN COMPLEX WITH DFA-IV | GLYCOSIDE HYDROLASE, TRANSFERASE
4ffi:B (ARG380) to (GLY392) CRYSTAL STRUCTURE OF LEVAN FRUCTOTRANSFERASE D54N MUTANT FROM ARTHROBACTER UREAFACIENS IN COMPLEX WITH LEVANBIOSE | GLYCOSIDE HYDROLASE, TRANSFERASE
4ffi:D (ARG380) to (GLY392) CRYSTAL STRUCTURE OF LEVAN FRUCTOTRANSFERASE D54N MUTANT FROM ARTHROBACTER UREAFACIENS IN COMPLEX WITH LEVANBIOSE | GLYCOSIDE HYDROLASE, TRANSFERASE
5jb1:C (THR337) to (THR385) PSEUDO-ATOMIC STRUCTURE OF HUMAN PAPILLOMAVIRUS TYPE 59 L1 VIRUS-LIKE PARTICLE | CAPSID, T=7 ICOSAHEDRAL, VIRUS-LIKE PARTICLE, VIRUS
3r7r:A (SER400) to (SER417) STRUCTURE-BASED DESIGN OF THIENOBENZOXEPIN INHIBITORS OF PI3-KINASE | KINASE P110, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4fog:C (THR14) to (ASP37) CRYSTAL STRUCTURE OF MTB THYA IN COMPLEX WITH 5-FLUORO-DUMP AND 5- METHYLTETRAHYDROFOLIC ACID | STRUCTURAL GENOMICS, TB STRUCTURAL GENOMICS CONSORTIUM, TBSGC, TRANSFERASE, THYMIDYLATE SYNTHASE
4fog:D (THR14) to (ASP37) CRYSTAL STRUCTURE OF MTB THYA IN COMPLEX WITH 5-FLUORO-DUMP AND 5- METHYLTETRAHYDROFOLIC ACID | STRUCTURAL GENOMICS, TB STRUCTURAL GENOMICS CONSORTIUM, TBSGC, TRANSFERASE, THYMIDYLATE SYNTHASE
5jhr:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH THE PEPTIDIC EPOXYKETONE INHIBITOR 27 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5jhr:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH THE PEPTIDIC EPOXYKETONE INHIBITOR 27 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5jhs:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH THE PEPTIDIC EPOXYKETONE INHIBITOR 15 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5jhs:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH THE PEPTIDIC EPOXYKETONE INHIBITOR 15 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5jk7:B (LEU691) to (TYR718) THE X-RAY STRUCTURE OF THE DDB1-DCAF1-VPR-UNG2 COMPLEX | CULLIN4-RING E3 UBIQUITIN LIGASE HIV-1 VPR UNG2, DNA BINDING PROTEIN- HYDROLASE COMPLEX, VIRAL PROTEIN-DNA BINDING PROTEIN COMPLEX
4fq1:H (SER120) to (PRO147) CRYSTAL STRUCTURE OF PGT121 FAB | IG FOLD, ANTI HIV, ANTIBODY, IMMUNE SYSTEM
4fqs:A (THR14) to (ASP37) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS THYA IN COMPLEX WITH UMP AND PEMETREXED | TRANSFERASE, FOLATE BINDING, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
3rhj:B (VAL409) to (GLY427) CRYSTAL STRUCTURE OF THE E673A MUTANT OF THE C-TERMINAL DOMAIN OF RAT 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH CO-PURIFIED NADP | FDH, OXIDOREDUCTASE
3rhr:B (VAL409) to (VAL458) CRYSTAL STRUCTURE OF THE C707A MUTANT OF THE C-TERMINAL DOMAIN OF 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH NADPH | FDH, OXIDOREDUCTASE
3rhr:C (VAL409) to (VAL458) CRYSTAL STRUCTURE OF THE C707A MUTANT OF THE C-TERMINAL DOMAIN OF 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH NADPH | FDH, OXIDOREDUCTASE
3rhr:D (VAL409) to (VAL458) CRYSTAL STRUCTURE OF THE C707A MUTANT OF THE C-TERMINAL DOMAIN OF 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH NADPH | FDH, OXIDOREDUCTASE
3rhl:B (VAL409) to (GLY427) CRYSTAL STRUCTURE OF THE E673A/C707A DOUBLE MUTANT OF THE C-TERMINAL DOMAIN OF RAT 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH CO-PURIFIED NADP | FDH, OXIDOREDUCTASE
3rhl:C (VAL409) to (VAL458) CRYSTAL STRUCTURE OF THE E673A/C707A DOUBLE MUTANT OF THE C-TERMINAL DOMAIN OF RAT 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH CO-PURIFIED NADP | FDH, OXIDOREDUCTASE
3rhm:B (VAL409) to (GLY427) CRYSTAL STRUCTURE OF THE E673Q MUTANT OF C-TERMINAL DOMAIN OF 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE | FDH, OXIDOREDUCTASE
3rho:B (VAL409) to (GLY427) CRYSTAL STRUCTURE OF THE E673Q MUTANT OF C-TERMINAL DOMAIN OF 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH NADP | FDH, OXIDOREDUCTASE
3rho:C (VAL409) to (GLY427) CRYSTAL STRUCTURE OF THE E673Q MUTANT OF C-TERMINAL DOMAIN OF 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH NADP | FDH, OXIDOREDUCTASE
3rho:D (VAL409) to (GLY427) CRYSTAL STRUCTURE OF THE E673Q MUTANT OF C-TERMINAL DOMAIN OF 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH NADP | FDH, OXIDOREDUCTASE
3rhq:B (VAL409) to (VAL458) CRYSTAL STRUCTURE OF THE C707A MUTANT OF C-TERMINAL DOMAIN OF 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH NADP | FDH, OXIDOREDUCTASE
3rhq:C (VAL409) to (VAL458) CRYSTAL STRUCTURE OF THE C707A MUTANT OF C-TERMINAL DOMAIN OF 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH NADP | FDH, OXIDOREDUCTASE
3rhq:D (VAL409) to (VAL458) CRYSTAL STRUCTURE OF THE C707A MUTANT OF C-TERMINAL DOMAIN OF 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH NADP | FDH, OXIDOREDUCTASE
4fxl:A (LYS6) to (PRO32) CRYSTAL STRUCTURE OF THE D76N BETA-2 MICROGLOBULIN MUTANT | IMMUNOGLOBIN, BETA-SANDWITCH, AMYLOIDOSIS, PATHOLOGIC MUTATION, GENETIC DISEASE, MHC CLASS I, IMMUNE SYSTEM
5jtd:A (GLU430) to (LYS452) CRYSTAL STRUCTURE OF THE RU(BPY)2PHENA FUNCTIONALIZED P450 BM3 L407C HEME DOMAIN MUTANT IN COMPLEX WITH DMSO. | HYBRID P450 BM3 ENZYMES, ELECTRON TRANSFER, PHOTOSENSITIZER, PHOTOCATALYTIC ACTIVITY, OXIDOREDUCTASE
5jtd:B (GLU430) to (LYS452) CRYSTAL STRUCTURE OF THE RU(BPY)2PHENA FUNCTIONALIZED P450 BM3 L407C HEME DOMAIN MUTANT IN COMPLEX WITH DMSO. | HYBRID P450 BM3 ENZYMES, ELECTRON TRANSFER, PHOTOSENSITIZER, PHOTOCATALYTIC ACTIVITY, OXIDOREDUCTASE
4fzc:L (THR11) to (THR31) 20S YEAST PROTEASOME IN COMPLEX WITH CEPAFUNGIN I | UBIQUITIN, PROTEASOME, DRUG DEVELOPMENT, INHIBITOR, NATURAL PRODUCT, N-TERMINAL NUCLEOPHILIC HYDROLASE, PROTEIN DEGRADATION, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4fzc:Z (THR11) to (THR31) 20S YEAST PROTEASOME IN COMPLEX WITH CEPAFUNGIN I | UBIQUITIN, PROTEASOME, DRUG DEVELOPMENT, INHIBITOR, NATURAL PRODUCT, N-TERMINAL NUCLEOPHILIC HYDROLASE, PROTEIN DEGRADATION, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4fze:H (SER120) to (PRO147) CRYSTAL STRUCTURE OF N26_I1 FAB, AN ADCC MEDIATING ANTI-HIV-1 ANTIBODY. | ADCC, ANTI-HIV-1 ENV ANTIBODY N26_I1, VIRAL GLYCOPROTEIN GP120, HIV-1 ENV, IMMUNE SYSTEM, CD4I ANTIBODY, FAB
5jvd:A (PHE52) to (LEU70) TUBULIN-TUB092 COMPLEX | CELL CYCLE, TUBULIN FOLD, CYTOSKELETON, MICROTUBULE
4g4s:J (ILE11) to (SER31) STRUCTURE OF PROTEASOME-PBA1-PBA2 COMPLEX | ALPHA BETA, NTN-HYDROLASE, PEPTIDE BINDING, HYDROLASE-CHAPERONE COMPLEX
4g4s:M (THR1) to (THR21) STRUCTURE OF PROTEASOME-PBA1-PBA2 COMPLEX | ALPHA BETA, NTN-HYDROLASE, PEPTIDE BINDING, HYDROLASE-CHAPERONE COMPLEX
4g4s:P (LEU70) to (SER91) STRUCTURE OF PROTEASOME-PBA1-PBA2 COMPLEX | ALPHA BETA, NTN-HYDROLASE, PEPTIDE BINDING, HYDROLASE-CHAPERONE COMPLEX
4g6a:H (SER120) to (PRO147) STRUCTURE OF THE HEPATITIS C VIRUS ENVELOPE GLYCOPROTEIN E2 ANTIGENIC REGION 412-423 BOUND TO THE BROADLY NEUTRALIZING ANTIBODY AP33 | IMMUNOGLOBULIN FOLD, IMMUNE SYSTEM
5k6x:A (ARG14) to (GLY32) SIDEKICK-2 IMMUNOGLOBULIN DOMAINS 1-4, CRYSTAL FORM 1 | CELL ADHESION, IMMUNOGLOBULIN
5k6y:A (ARG14) to (GLY32) SIDEKICK-2 IMMUNOGLOBULIN DOMAINS 1-4, CRYSTAL FORM 2 | CELL ADHESION, IMMUNOGLOBULIN
5k70:B (ARG14) to (GLY32) SIDEKICK-2 IMMUNOGLOBULIN DOMAINS 1-4 H18R/N22S MUTANT | CELL ADHESION, IMMUNOGLOBULIN
4g9d:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA B2705-KK10 | TCR, T CELL, HLA B*2705, KK10, KK10-L6M, HIV, IMMUNE ESCAPE, IMMUNE SYSTEM
5kan:H (SER135) to (PRO162) CRYSTAL STRUCTURE OF MULTIDONOR HV1-18-CLASS BROADLY NEUTRALIZING INFLUENZA A ANTIBODY 16.G.07 IN COMPLEX WITH A/HONG KONG/1-4-MA21- 1/1968 (H3N2) HEMAGGLUTININ | INFLUENZA, MULTIDONOR, H5, UNIVERSAL INFLUENZA VACCINE, IMMUNE SYSTEM
4ger:A (ALA1) to (THR30) CRYSTAL STRUCTURE OF GENTLYASE, THE NEUTRAL METALLOPROTEASE OF PAENIBACILLUS POLYMYXA | PROTEASE, METALLOPROTEINASE, TISSUE DISAGGREGATION, THERMOLYSIN-LIKE PROTEASE, HYDROLASE
4ger:B (ALA1) to (THR30) CRYSTAL STRUCTURE OF GENTLYASE, THE NEUTRAL METALLOPROTEASE OF PAENIBACILLUS POLYMYXA | PROTEASE, METALLOPROTEINASE, TISSUE DISAGGREGATION, THERMOLYSIN-LIKE PROTEASE, HYDROLASE
5ken:N (CYS92) to (THR110) EBOV GP IN COMPLEX WITH VARIABLE FAB DOMAINS OF IGGS C4G7 AND C13C6 | EBOLA VIRUS SURFACE GLYCOPROTEIN, THERAPEUTIC ANTIBODY COCKTAIL, ZMAPP, VIRAL PROTEIN-IMMUNE SYSTEM COMPLEX
5kiz:A (GLU320) to (LYS349) SOLUTION STRUCTURE OF A REPACKED VERSION OF HIF-2 ALPHA PAS-B | CAVITY, REPACKING, ROSETTA, TRANSCRIPTION
4gks:A (HIS188) to (PRO210) A2-MHC COMPLEX CARRYING FLTGIGIITV | MAJOR HISTOCOMPATIBILITY COMPLEX, T-CELL RECEPTOR, IMMUNO, IMMUNOGLOBULIN, RECOGNITION, MHC, TCR, IMMUNE SYSTEM
4glr:J (SER120) to (PRO147) STRUCTURE OF THE ANTI-PTAU FAB (PT231/PS235_1) IN COMPLEX WITH PHOSPHOEPITOPE PT231/PS235 | IGG1 FAB, ANTI-PTAU ANTIBODY, PHOSPHORYLATED TAU PEPTIDE, PHOSPHORYLATION, IMMUNE SYSTEM
4gnz:C (VAL409) to (VAL458) CRYSTAL STRUCTURE OF THE C707S MUTANT OF C-TERMINAL DOMAIN OF 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH NADP | ALDEHYDE DEHYDROGENASE, FDH, OXIDOREDUCTASE
4gnz:D (VAL409) to (VAL458) CRYSTAL STRUCTURE OF THE C707S MUTANT OF C-TERMINAL DOMAIN OF 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH NADP | ALDEHYDE DEHYDROGENASE, FDH, OXIDOREDUCTASE
4go0:B (VAL409) to (GLY427) CRYSTAL STRUCTURE OF THE C707S MUTANT OF C-TERMINAL DOMAIN OF 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH NADPH | ALDEHYDE DEHYDROGENASE, FDH, OXIDOREDUCTASE
4go0:C (VAL409) to (GLY427) CRYSTAL STRUCTURE OF THE C707S MUTANT OF C-TERMINAL DOMAIN OF 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH NADPH | ALDEHYDE DEHYDROGENASE, FDH, OXIDOREDUCTASE
4goa:A (ASP704) to (SER766) CRYSTAL STRUCTURE OF JACK BEAN UREASE INHIBITED WITH FLUORIDE | JACK BEAN UREASE, FLUORIDE-INHIBITION, HYDROLYSIS, CME, KCX, HYDROLASE
5l52:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 14 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l52:N (THR1) to (THR22) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 14 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l52:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 14 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l52:b (THR1) to (THR22) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 14 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l54:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 16 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l54:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 16 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l55:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 18 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l55:N (THR1) to (THR22) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 18 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l55:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 18 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l55:b (THR1) to (THR22) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 18 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l5a:L (GLY10) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; R57T) | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5l5a:Z (GLY10) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; R57T) | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5l5b:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5l5b:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5l5d:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH ONX 0914 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5d:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH ONX 0914 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5h:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5h:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5i:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 9 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5i:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 9 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5o:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 16 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5o:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 16 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5p:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 17 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5p:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 17 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5q:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE 18 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5q:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE 18 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5s:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; V31M) AND HUMAN BETA6 (97-111; 118-133) IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5s:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; V31M) AND HUMAN BETA6 (97-111; 118-133) IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5u:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; V31M) AND HUMAN BETA6 (97-111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 17 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5u:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; V31M) AND HUMAN BETA6 (97-111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 17 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5v:L (THR11) to (THR31) 'YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; V31M) AND HUMAN BETA6 (97-111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 18 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5v:Z (THR11) to (THR31) 'YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; V31M) AND HUMAN BETA6 (97-111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 18 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5w:J (ILE3) to (ARG23) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5l5w:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5l5w:X (ILE3) to (ARG23) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5l5w:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5l5x:K (THR1) to (ALA22) 'YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH ONX 0914 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5x:Y (THR1) to (ALA22) 'YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH ONX 0914 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5y:J (ILE3) to (ARG23) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5y:X (ILE3) to (ARG23) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5z:J (ILE3) to (ARG23) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5z:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5z:X (ILE3) to (ARG23) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5z:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l60:J (ILE3) to (ARG23) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l60:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l60:X (ILE3) to (ARG23) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l60:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l61:J (ILE3) to (ARG23) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (99- 132) IN COMPLEX WITH EPOXYKETONE INHIBITOR 14 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l61:K (THR1) to (ALA22) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (99- 132) IN COMPLEX WITH EPOXYKETONE INHIBITOR 14 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l61:X (ILE3) to (ARG23) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (99- 132) IN COMPLEX WITH EPOXYKETONE INHIBITOR 14 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l61:Y (THR1) to (ALA22) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (99- 132) IN COMPLEX WITH EPOXYKETONE INHIBITOR 14 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l62:J (ILE3) to (ARG23) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 16 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l62:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 16 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l62:X (ILE3) to (ARG23) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 16 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l62:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 16 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l64:J (ILE3) to (ARG23) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 18 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l64:X (ILE3) to (ARG23) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 18 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l65:K (THR1) to (ALA22) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l65:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l65:Y (THR1) to (ALA22) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l65:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l66:K (THR1) to (ALA22) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l66:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l66:Y (THR1) to (ALA22) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l66:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l67:K (THR1) to (ALA22) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l67:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l67:Y (THR1) to (ALA22) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l67:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l68:K (THR1) to (ALA22) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 14 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l68:Y (THR1) to (ALA22) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 14 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l69:K (THR1) to (ALA22) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 16 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l69:Y (THR1) to (ALA22) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 16 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l6a:K (THR1) to (ALA22) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 17 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l6a:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 17 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l6a:Y (THR1) to (ALA22) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 17 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l6a:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 17 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l6b:K (THR1) to (ALA22) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH ONX 0914 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l6b:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH ONX 0914 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l6b:Y (THR1) to (ALA22) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH ONX 0914 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l6b:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH ONX 0914 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l6c:K (THR1) to (ALA22) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 18 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l6c:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 18 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l6c:Y (THR1) to (ALA22) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 18 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l6c:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 18 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5le5:W (GLY7) to (ILE29) NATIVE HUMAN 20S PROTEASOME AT 1.8 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5ley:M (THR9) to (TYR30) HUMAN 20S PROTEASOME COMPLEX WITH OPROZOMIB AT 1.9 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lez:H (THR1) to (GLU22) HUMAN 20S PROTEASOME COMPLEX WITH OPROZOMIB IN MG-ACETATE AT 2.2 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lez:I (GLY7) to (ILE29) HUMAN 20S PROTEASOME COMPLEX WITH OPROZOMIB IN MG-ACETATE AT 2.2 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf0:W (GLY7) to (ILE29) HUMAN 20S PROTEASOME COMPLEX WITH EPOXOMICIN AT 2.4 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf3:I (GLY7) to (ILE29) HUMAN 20S PROTEASOME COMPLEX WITH BORTEZOMIB AT 2.1 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf3:W (GLY7) to (ILE29) HUMAN 20S PROTEASOME COMPLEX WITH BORTEZOMIB AT 2.1 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf4:W (GLY7) to (ILE29) HUMAN 20S PROTEASOME COMPLEX WITH DELANZOMIB AT 2.0 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5ltt:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; R57T)IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5ltt:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; R57T)IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5swz:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF NP1-B17 TCR-H2DB-NP COMPLEX | H2DB, INFLUENZA, NP366, REVERSED DOCKING, NAIVE T CELL, NP1-B17 TCR, TCR, T CELL, IMMUNE SYSTEM
5t0h:N (THR2) to (GLY23) STRUCTURAL BASIS FOR DYNAMIC REGULATION OF THE HUMAN 26S PROTEASOME | UBIQUITIN-PROTEASOME SYSTEM, AAA-ATPASE, HYDROLASE
5t0i:O (THR1) to (GLY23) STRUCTURAL BASIS FOR DYNAMIC REGULATION OF THE HUMAN 26S PROTEASOME | UBIQUITIN-PROTEASOME SYSTEM, AAA-ATPASE, HYDROLASE
5t0i:S (THR11) to (GLU31) STRUCTURAL BASIS FOR DYNAMIC REGULATION OF THE HUMAN 26S PROTEASOME | UBIQUITIN-PROTEASOME SYSTEM, AAA-ATPASE, HYDROLASE
5t0j:N (THR2) to (THR22) STRUCTURAL BASIS FOR DYNAMIC REGULATION OF THE HUMAN 26S PROTEASOME | UBIQUITIN-PROTEASOME SYSTEM, AAA-ATPASE, HYDROLASE
5t3b:B (PHE79) to (ALA105) CRYSTAL STRUCTURE OF BPGH50 | (ALPHA/ALPHA)6 BARREL, GLYCOSIDE HYDROLASE, HYDROLASE
6tli:A (THR6) to (THR34) THERMOLYSIN (60% ISOPROPANOL SOAKED CRYSTALS) | HYDROLASE, METALLOPROTEINASE, ORGANIC SOLVENT
7tli:A (THR6) to (THR34) THERMOLYSIN (90% ISOPROPANOL SOAKED CRYSTALS) | HYDROLASE, METALLOPROTEINASE, ORGANIC SOLVENT
7tln:A (THR6) to (THR34) STRUCTURAL ANALYSIS OF THE INHIBITION OF THERMOLYSIN BY AN ACTIVE- SITE-DIRECTED IRREVERSIBLE INHIBITOR | HYDROLASE (METALLOPROTEINASE)
8tli:A (THR6) to (THR34) THERMOLYSIN (100% ISOPROPANOL SOAKED CRYSTALS) | HYDROLASE, METALLOPROTEINASE, ORGANIC SOLVENT
1a1m:A (HIS188) to (PRO210) MHC CLASS I MOLECULE B*5301 COMPLEXED WITH PEPTIDE TPYDINQML FROM GAG PROTEIN OF HIV2 | MAJOR HISTOCOMPATIBILITY ANTIGEN, MHC, HLA, HLA-B53, HIV, COMPLEX (ANTIGEN/PEPTIDE)
2ak4:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF SB27 TCR IN COMPLEX WITH HLA-B*3508- 13MER PEPTIDE | T CELL RECEPTOR, BULGED EPITOPES, PMHC/TCR COMPLEX, IMMUNE SYSTEM
2ak4:F (HIS188) to (PRO210) CRYSTAL STRUCTURE OF SB27 TCR IN COMPLEX WITH HLA-B*3508- 13MER PEPTIDE | T CELL RECEPTOR, BULGED EPITOPES, PMHC/TCR COMPLEX, IMMUNE SYSTEM
2ak4:K (HIS188) to (PRO210) CRYSTAL STRUCTURE OF SB27 TCR IN COMPLEX WITH HLA-B*3508- 13MER PEPTIDE | T CELL RECEPTOR, BULGED EPITOPES, PMHC/TCR COMPLEX, IMMUNE SYSTEM
2ak4:L (LYS6) to (PRO32) CRYSTAL STRUCTURE OF SB27 TCR IN COMPLEX WITH HLA-B*3508- 13MER PEPTIDE | T CELL RECEPTOR, BULGED EPITOPES, PMHC/TCR COMPLEX, IMMUNE SYSTEM
2ak4:Q (HIS188) to (PRO210) CRYSTAL STRUCTURE OF SB27 TCR IN COMPLEX WITH HLA-B*3508- 13MER PEPTIDE | T CELL RECEPTOR, BULGED EPITOPES, PMHC/TCR COMPLEX, IMMUNE SYSTEM
1aj7:H (SER120) to (PRO147) IMMUNOGLOBULIN 48G7 GERMLINE FAB ANTIBODY COMPLEXED WITH HAPTEN 5-(PARA-NITROPHENYL PHOSPHONATE)-PENTANOIC ACID. AFFINITY MATURATION OF AN ESTEROLYTIC ANTIBODY | GERMLINE ANTIBODY, FAB, CATALYTIC ANTIBODY, AFFINITY MATURATION, IMMUNOGLOBULIN
2aza:A (ALA5) to (ASP23) STRUCTURE OF AZURIN FROM ALCALIGENES DENITRIFICANS. REFINEMENT AT 1.8 ANGSTROMS RESOLUTION AND COMPARISON OF THE TWO CRYSTALLOGRAPHICALLY INDEPENDENT MOLECULES | ELECTRON TRANSPORT PROTEIN(CUPROPROTEIN)
1ajk:A (PHE9) to (GLY29) CIRCULARLY PERMUTED (1-3,1-4)-BETA-D-GLUCAN 4- GLUCANOHYDROLASE CPA16M-84 | HYDROLASE, GLUCANASE, CIRCULAR PERMUTATION
1ajk:B (PHE9) to (GLY29) CIRCULARLY PERMUTED (1-3,1-4)-BETA-D-GLUCAN 4- GLUCANOHYDROLASE CPA16M-84 | HYDROLASE, GLUCANASE, CIRCULAR PERMUTATION
1azb:A (ALA5) to (ASP23) STRUCTURE OF APO-AZURIN FROM ALCALIGENES DENITRIFICANS AT 1.8 ANGSTROMS RESOLUTION | ELECTRON TRANSPORT(COPPER)
1azc:A (ALA5) to (ASP23) STRUCTURE OF APO-AZURIN FROM ALCALIGENES DENITRIFICANS AT 1.8 ANGSTROMS RESOLUTION | ELECTRON TRANSPORT(COPPER)
4hgf:A (GLU430) to (LYS452) CRYSTAL STRUCTURE OF P450 BM3 5F5K HEME DOMAIN VARIANT COMPLEXED WITH STYRENE | OXIDOREDUCTASE, P450 BM3, HEMOPROTEIN, STYRENE EPOXIDATION, INVERTED ENANTIOSELECTIVITY, HEME BINDING
4hgf:B (GLU430) to (LYS452) CRYSTAL STRUCTURE OF P450 BM3 5F5K HEME DOMAIN VARIANT COMPLEXED WITH STYRENE | OXIDOREDUCTASE, P450 BM3, HEMOPROTEIN, STYRENE EPOXIDATION, INVERTED ENANTIOSELECTIVITY, HEME BINDING
4hgh:A (GLU430) to (LYS452) CRYSTAL STRUCTURE OF P450 BM3 5F5 HEME DOMAIN VARIANT COMPLEXED WITH STYRENE (DATASET I) | OXIDOREDUCTASE, P450 BM3, HEMOPROTEIN, STYRENE EPOXIDATION, INVERTED ENANTIOSELECTIVITY, HEME BINDING
4hgh:B (GLU430) to (LYS452) CRYSTAL STRUCTURE OF P450 BM3 5F5 HEME DOMAIN VARIANT COMPLEXED WITH STYRENE (DATASET I) | OXIDOREDUCTASE, P450 BM3, HEMOPROTEIN, STYRENE EPOXIDATION, INVERTED ENANTIOSELECTIVITY, HEME BINDING
4hgi:A (GLU430) to (LYS452) CRYSTAL STRUCTURE OF P450 BM3 5F5 HEME DOMAIN VARIANT COMPLEXED WITH STYRENE (DATASET II) | OXIDOREDUCTASE, P450 BM3, HEMOPROTEIN, STYRENE EPOXIDATION, INVERTED ENANTIOSELECTIVITY, HEME BINDING
4hgi:B (GLU430) to (LYS452) CRYSTAL STRUCTURE OF P450 BM3 5F5 HEME DOMAIN VARIANT COMPLEXED WITH STYRENE (DATASET II) | OXIDOREDUCTASE, P450 BM3, HEMOPROTEIN, STYRENE EPOXIDATION, INVERTED ENANTIOSELECTIVITY, HEME BINDING
3eyv:H (SER126) to (PRO153) ANTI-LEWIS Y FAB FRAGMENT WITH LEWIS Y ANTIGEN IN THE PRESENCE OF ZINC IONS | IMMUNOGLOBULIN FOLD, BETA BARREL, HUMANIZED ANTIBODY, ANTIGEN BINDING FRAGMENT, IMMUNE SYSTEM
3eyv:B (SER126) to (PRO153) ANTI-LEWIS Y FAB FRAGMENT WITH LEWIS Y ANTIGEN IN THE PRESENCE OF ZINC IONS | IMMUNOGLOBULIN FOLD, BETA BARREL, HUMANIZED ANTIBODY, ANTIGEN BINDING FRAGMENT, IMMUNE SYSTEM
2bml:A (PHE199) to (LYS222) OFLOXACIN-LIKE ANTIBIOTICS INHIBIT PNEUMOCOCCAL CELL WALL DEGRADING VIRULENCE FACTORS | CHOLINE-BINDING DOMAIN, CELL WALL ATTACHMENT, OFLOXACIN- LIKE ANTIBIOTICS
3f8d:D (ASN210) to (PRO252) STRUCTURE OF SULFOLOBUS SOLFATARICUS THIOREDOXIN REDUCTASE MUTANT C147A | REDOX PROTEIN, NUCLEOTIDE BINDING, FAD, FLAVOPROTEIN, OXIDOREDUCTASE
4x8j:B (PHE87) to (PRO113) CRYSTAL STRUCTURE OF MURINE 12F4 FAB MONOCLONAL ANTIBODY AGAINST ADAMTS5 | MONOCLONAL, IMMUNE SYSTEM
4x93:A (ILE61) to (VAL82) CRYSTAL STRUCTURE OF LYSOSOMAL PHOSPHOLIPASE A2 CRYSTALLIZED IN THE PRESENCE OF METHYL ARACHIDONYL FLUOROPHOSPHONATE (TETRAGONAL FORM) | HYDROLASE, PHOSPHOLIPASE, ESTERASE, ACYLTRANSFERASE, TRANSFERASE
4x94:A (ILE61) to (VAL82) CRYSTAL STRUCTURE OF LYSOSOMAL PHOSPHOLIPASE A2 CRYSTALLIZED IN THE PRESENCE OF METHYL ARACHIDONYL FLUOROPHOSPHONATE (HEXAGONAL FORM) | HYDROLASE, PHOSPHOLIPASE, ESTERASE, ACYLTRANSFERASE, TRANSFERASE
1bwd:B (LEU318) to (ARG338) INOSAMINE-PHOSPHATE AMIDINOTRANSFERASE STRB1 FROM STREPTOMYCES GRISEUS | AMIDINOTRANSFERASE, STREPTOMYCIN
1ofh:G (THR1) to (LEU22) ASYMMETRIC COMPLEX BETWEEN HSLV AND I-DOMAIN DELETED HSLU (H. INFLUENZAE) | CHAPERONE, HYDROLASE, ATP-BINDING
1ofh:I (THR1) to (LEU22) ASYMMETRIC COMPLEX BETWEEN HSLV AND I-DOMAIN DELETED HSLU (H. INFLUENZAE) | CHAPERONE, HYDROLASE, ATP-BINDING
1ofh:N (ILE3) to (LEU22) ASYMMETRIC COMPLEX BETWEEN HSLV AND I-DOMAIN DELETED HSLU (H. INFLUENZAE) | CHAPERONE, HYDROLASE, ATP-BINDING
1c5d:B (SER124) to (PRO151) THE CRYSTAL STRUCTURE OF THE FAB FRAGMENT OF A RAT MONOCLONAL ANTIBODY AGAINST THE MAIN IMMUNOGENIC REGION OF THE HUMAN MUSCLE ACETYLCHOLINE RECEPTOR | IMMUNOGLOBULIN, IMMUNE SYSTEM
3skm:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF THE HLA-B8FLRGRAYVL, MUTANT G8V OF THE FLR PEPTIDE | T CELL RECEPTOR, IMMUNE SYSTEM
3skm:B (LYS6) to (PRO32) CRYSTAL STRUCTURE OF THE HLA-B8FLRGRAYVL, MUTANT G8V OF THE FLR PEPTIDE | T CELL RECEPTOR, IMMUNE SYSTEM
3fmc:A (ILE343) to (GLU366) CRYSTAL STRUCTURE OF A PUTATIVE SUCCINYLGLUTAMATE DESUCCINYLASE / ASPARTOACYLASE FAMILY PROTEIN (SAMA_0604) FROM SHEWANELLA AMAZONENSIS SB2B AT 1.80 A RESOLUTION | PUTATIVE SUCCINYLGLUTAMATE DESUCCINYLASE / ASPARTOACYLASE, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, HYDROLASE
2pyh:A (ARG140) to (ASN159) AZOTOBACTER VINELANDII MANNURONAN C-5 EPIMERASE ALGE4 A-MODULE COMPLEXED WITH MANNURONAN TRISACCHARIDE | BETA-HELIX, EPIMERASE, MANNURONIC ACID, ISOMERASE
2pzi:A (ILE282) to (ILE300) CRYSTAL STRUCTURE OF PROTEIN KINASE PKNG FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH TETRAHYDROBENZOTHIOPHENE AX20017 | SERINE/THREONINE-PROTEIN KINASE, ATP-RECOGNITION, KINASE-INHIBITOR COMPLEX, RUBREDOXIN FOLD, TPR DOMAIN, TRANSFERASE
3spv:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF A PEPTIDE-HLA COMPLEX | IMMUNOLOGY, RECEPTOR, HLA, HLA-B*0801, EBV, MHC, TCR, T CELL, IMMUNE SYSTEM
1cnf:A (HIS118) to (CYS143) STRUCTURAL STUDIES ON CORN NITRATE REDUCTASE: REFINED STRUCTURE OF THE CYTOCHROME B REDUCTASE FRAGMENT AT 2.5 ANGSTROMS, ITS ADP COMPLEX AND AN ACTIVE SITE MUTANT AND MODELING OF THE CYTOCHROME B DOMAIN | OXIDOREDUCTASE, NITROGENOUS ACCEPTOR, NITRATE ASSIMILATING ENZYME
3fvp:A (THR6) to (THR34) THERMOLYSIN INHIBITION | PROTEASE PHOSPHONAMIDATE INHIBITOR, HYDROLASE, METAL-BINDING, METALLOPROTEASE, PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1p3h:C (LYS2) to (GLY40) CRYSTAL STRUCTURE OF THE MYCOBACTERIUM TUBERCULOSIS CHAPERONIN 10 TETRADECAMER | BETA BARREL, ACIDIC CLUSTER, FLEXIBLE LOOP, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, TB STRUCTURAL GENOMICS CONSORTIUM, TBSGC, CHAPERONE
1p3h:L (LYS2) to (GLY40) CRYSTAL STRUCTURE OF THE MYCOBACTERIUM TUBERCULOSIS CHAPERONIN 10 TETRADECAMER | BETA BARREL, ACIDIC CLUSTER, FLEXIBLE LOOP, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, TB STRUCTURAL GENOMICS CONSORTIUM, TBSGC, CHAPERONE
3t2j:E (THR6) to (THR34) TETRAGONAL THERMOLYSIN IN THE PRESENCE OF BETAINE | ALPHA/BETA, ZINC PROTEASE, HYDROLASE
1dlm:A (ARG180) to (CYS202) STRUCTURE OF CATECHOL 1,2-DIOXYGENASE FROM ACINETOBACTER CALCOACETICUS NATIVE DATA | METALLOPROTEIN, DIOXYGENASE, AROMATIC COMPOUND DEGRADATION, MIXED ALPHA HELIX/ BETA STRAND, OXIDOREDUCTASE
3t2t:A (LEU17) to (CYS42) CRYSTAL STRUCTURE OF HUMAN GALECTIN-1 IN COMPLEX WITH METHYL 2-O- ACETYL-3-O-TOLUOYL-BETA-D-TALOPYRANOSIDE | BETA SANDWICH, LECTIN, SUGAR BINDING PROTEIN-INHIBITOR COMPLEX
2cul:A (GLY126) to (ASP148) CRYSTAL STRUCTURE OF THE GIDA-RELATED PROTEIN FROM THERMUS THERMOPHILUS HB8 | ROSSMANN FOLD, PROTEIN-FAD COMPLEX, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, STRUCTURAL GENOMICS, OXIDOREDUCTASE
4itv:E (VAL5) to (GLY21) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS, TRIPLE MUTANT, P212121 FORM | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRIC OLIGOMERIC DOMAINS, BIOMATERIALS, OXIDOREDUCTASE
4itv:I (GLY6) to (GLY21) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS, TRIPLE MUTANT, P212121 FORM | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRIC OLIGOMERIC DOMAINS, BIOMATERIALS, OXIDOREDUCTASE
4itv:L (GLY6) to (GLY21) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS, TRIPLE MUTANT, P212121 FORM | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRIC OLIGOMERIC DOMAINS, BIOMATERIALS, OXIDOREDUCTASE
4y0x:A (ILE282) to (ILE300) CRYSTAL STRUCTURE OF THE S/T PROTEIN KINASE PKNG FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH ADP | S/T PROTEIN KINASE, PKNG, TRANSFERASE
4y1u:A (LEU17) to (CSO42) COMPLEX OF HUMAN GALECTIN-1 AND GALBETA1-4GLCNAC | COMPLEX, GALECTIN-1, LECTIN, TYPE 2 LACNAC, SUGAR BINDING PROTEIN
3gpt:L (THR2) to (THR22) CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH SALINOSPORAMIDE DERIVATIVES: SLOW SUBSTRATE LIGAND | PROTEASOME, UBIQUITIN, CANCER THERAPY, INHIBITOR, IMMUNOLOGY, TIME DEPENDENT LEAVING GROUP ELIMINATION, CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, THREONINE PROTEASE, ISOPEPTIDE BOND, UBL CONJUGATION, ZYMOGEN
3gpt:Z (THR2) to (THR22) CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH SALINOSPORAMIDE DERIVATIVES: SLOW SUBSTRATE LIGAND | PROTEASOME, UBIQUITIN, CANCER THERAPY, INHIBITOR, IMMUNOLOGY, TIME DEPENDENT LEAVING GROUP ELIMINATION, CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, THREONINE PROTEASE, ISOPEPTIDE BOND, UBL CONJUGATION, ZYMOGEN
2d6n:A (GLY28) to (ALA58) CRYSTAL STRUCTURE OF MOUSE GALECTIN-9 N-TERMINAL CRD IN COMPLEX WITH N-ACETYLLACTOSAMINE | BETA SANDWICH, CARBOHYDRATE BINDING PROTEIN, GALECTIN, SUGAR BINDING PROTEIN
2d6n:B (GLY28) to (ALA58) CRYSTAL STRUCTURE OF MOUSE GALECTIN-9 N-TERMINAL CRD IN COMPLEX WITH N-ACETYLLACTOSAMINE | BETA SANDWICH, CARBOHYDRATE BINDING PROTEIN, GALECTIN, SUGAR BINDING PROTEIN
1pyy:A (ARG76) to (ALA98) DOUBLE MUTANT PBP2X T338A/M339F FROM STREPTOCOCCUS PNEUMONIAE STRAIN R6 AT 2.4 A RESOLUTION | PENICILLIN-BINDING PROTEIN, ANTIBIOTIC RESISTANCE, PEPTIDOGLYCAN SYNTHESIS, CELL WALL, TRANSMEMBRANE, TRANSPEPTIDASE
4y75:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAF-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y75:W (GLY8) to (SER30) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAF-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y75:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAF-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y75:b (THR1) to (THR22) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAF-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
2r6g:A (GLN253) to (ARG286) THE CRYSTAL STRUCTURE OF THE E. COLI MALTOSE TRANSPORTER | ABC TRANSPORTER, CATALYTIC INTERMEDIATE, E. COLI MALTOSE TRANSPORTER, MBP, MALTODEXTRIN BINDING PROTEIN, MALK, ATP BINDING CASSETTE, ATP- BINDING, HYDROLASE, INNER MEMBRANE, MEMBRANE, NUCLEOTIDE-BINDING, SUGAR TRANSPORT, TRANSMEMBRANE, HYDROLASE-TRANSPORT PROTEIN COMPLEX
3gtl:B (ILE912) to (ILE948) BACKTRACKED RNA POLYMERASE II COMPLEX WITH 13MER WITH G<>U MISMATCH | TRANSCRIPTION, TRANSFERASE, DNA-RNA HYBRID, BACKTRACK, DNA-DIRECTED RNA POLYMERASE, DNA BINDING, ISOPEPTIDE BOND, MAGNESIUM, METAL BINDING, NUCLEOTIDYLTRANSFERASE, NUCLEUS, PHOSPHOPROTEIN, ZINC- FINGER, DNA DAMAGE, DNA REPAIR, TRANSFERASE-DNA-RNA HYBRID COMPLEX
4y8i:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8i:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8k:L (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH H-APLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8k:Z (THR11) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH H-APLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8p:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAL- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8p:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAL- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8r:L (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H116D MUTANT | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS
4y8r:N (THR1) to (THR22) YEAST 20S PROTEASOME BETA2-H116D MUTANT | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS
4y8r:Z (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H116D MUTANT | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS
4y8r:b (THR1) to (THR22) YEAST 20S PROTEASOME BETA2-H116D MUTANT | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS
4y8w:C (LEU462) to (PRO483) CRYSTAL STRUCTURE OF HUMAN CYTOCHROME P450 21A2 PROGESTERONE COMPLEX | STEROID HYDROXYLATION, MONOOXYGENASES, ADRENAL STEROIDOGENESIS, CONGENITAL ADRENAL HYPERPLASIA, ADDISON'S DISEASE, KINETIC ISOTOPE EFFECTS, OXIDOREDUCTASE
4ya5:L (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya5:Z (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
3to3:A (TYR68) to (GLN88) CRYSTAL STRUCTURE OF PETROBACTIN BIOSYNTHESIS PROTEIN ASBB FROM BACILLUS ANTHRACIS STR. STERNE | STRUCTURAL GENOMICS, PSI-BIOLOGY, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, ALPHA-BETA STRUCTURE, ADENYLATION, CYTOSOL, BIOSYNTHETIC PROTEIN
1ejs:C (ASP1431) to (SER1493) CRYSTAL STRUCTURE OF THE H219N VARIANT OF KLEBSIELLA AEROGENES UREASE | ALPHA-BETA BARREL, NICKEL METALLOENZYME, HYDROLASE
2dyp:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF LILRB2(LIR2/ILT4/CD85D) COMPLEXED WITH HLA-G | IMMUNOGLOBULIN-LIKE, IMMUNE SYSTEM
4jrx:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF CA5 TCR-HLA B*3505-LPEP COMPLEX | TCR, T CELL, HLA B*3508, LPEP, EBV, ALLOREACTIVITY, IMMUNE SYSTEM
1f7k:A (LYS24) to (LEU42) CRYSTAL STRUCTURES OF FELINE IMMUNODEFICIENCY VIRUS DUTP PYROPHOSPHATASE AND ITS NUCLEOTIDE COMPLEXES IN THREE CRYSTAL FORMS. | EIGHT STRANDED BETA BARREL PROTEIN, VIRAL PROTEIN, HYDROLASE
1f7p:A (GLU25) to (MET43) CRYSTAL STRUCTURES OF FELINE IMMUNODEFICIENCY VIRUS DUTP PYROPHOSPHATASE AND ITS NUCLEOTIDE COMPLEXES IN THREE CRYSTAL FORMS. | EIGHT STRANDED BETA BARREL PROTEIN, VIRAL PROTEIN, HYDROLASE
1f7p:C (GLU425) to (MET443) CRYSTAL STRUCTURES OF FELINE IMMUNODEFICIENCY VIRUS DUTP PYROPHOSPHATASE AND ITS NUCLEOTIDE COMPLEXES IN THREE CRYSTAL FORMS. | EIGHT STRANDED BETA BARREL PROTEIN, VIRAL PROTEIN, HYDROLASE
1fg2:D (HIS188) to (PRO210) CRYSTAL STRUCTURE OF THE LCMV PEPTIDIC EPITOPE GP33 IN COMPLEX WITH THE MURINE CLASS I MHC MOLECULE H-2DB | IG FOLD, IMMUNE SYSTEM
1fg2:G (HIS188) to (PRO210) CRYSTAL STRUCTURE OF THE LCMV PEPTIDIC EPITOPE GP33 IN COMPLEX WITH THE MURINE CLASS I MHC MOLECULE H-2DB | IG FOLD, IMMUNE SYSTEM
1fg2:J (HIS188) to (PRO210) CRYSTAL STRUCTURE OF THE LCMV PEPTIDIC EPITOPE GP33 IN COMPLEX WITH THE MURINE CLASS I MHC MOLECULE H-2DB | IG FOLD, IMMUNE SYSTEM
1fjq:A (THR6) to (THR34) THERMOLYSIN (70% ACETONE SOAKED CRYSTALS) | METALLOPROTEINASE, ORGANIC SOLVENT, HYDROLASE
4yse:C (LEU12) to (VAL31) HIGH RESOLUTION SYNCHROTRON STRUCTURE OF COPPER NITRITE REDUCTASE FROM ALCALIGENES FAECALIS | NITRITE, COPPER, REDUCTASE, OXIDOREDUCTASE
3unb:N (THR1) to (THR22) MOUSE CONSTITUTIVE 20S PROTEASOME IN COMPLEX WITH PR-957 | 20S PROTEASOME COMPRISES 28 SUBUNITS; EACH SUBUNIT ADOPTS THE FOLD OF AN ANTIPARALLEL BETA-SHEET FLANKED BY HELICES, PROTEASE, REGULATORY COMPLEXES, COVALENT BINDING OF PR-957 TO ALL ACTIVE SITES, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3unb:W (GLY8) to (ILE29) MOUSE CONSTITUTIVE 20S PROTEASOME IN COMPLEX WITH PR-957 | 20S PROTEASOME COMPRISES 28 SUBUNITS; EACH SUBUNIT ADOPTS THE FOLD OF AN ANTIPARALLEL BETA-SHEET FLANKED BY HELICES, PROTEASE, REGULATORY COMPLEXES, COVALENT BINDING OF PR-957 TO ALL ACTIVE SITES, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3unb:X (MET1) to (SER23) MOUSE CONSTITUTIVE 20S PROTEASOME IN COMPLEX WITH PR-957 | 20S PROTEASOME COMPRISES 28 SUBUNITS; EACH SUBUNIT ADOPTS THE FOLD OF AN ANTIPARALLEL BETA-SHEET FLANKED BY HELICES, PROTEASE, REGULATORY COMPLEXES, COVALENT BINDING OF PR-957 TO ALL ACTIVE SITES, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3unb:b (THR1) to (THR22) MOUSE CONSTITUTIVE 20S PROTEASOME IN COMPLEX WITH PR-957 | 20S PROTEASOME COMPRISES 28 SUBUNITS; EACH SUBUNIT ADOPTS THE FOLD OF AN ANTIPARALLEL BETA-SHEET FLANKED BY HELICES, PROTEASE, REGULATORY COMPLEXES, COVALENT BINDING OF PR-957 TO ALL ACTIVE SITES, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3unb:k (GLY8) to (ILE29) MOUSE CONSTITUTIVE 20S PROTEASOME IN COMPLEX WITH PR-957 | 20S PROTEASOME COMPRISES 28 SUBUNITS; EACH SUBUNIT ADOPTS THE FOLD OF AN ANTIPARALLEL BETA-SHEET FLANKED BY HELICES, PROTEASE, REGULATORY COMPLEXES, COVALENT BINDING OF PR-957 TO ALL ACTIVE SITES, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3unb:1 (THR1) to (ALA22) MOUSE CONSTITUTIVE 20S PROTEASOME IN COMPLEX WITH PR-957 | 20S PROTEASOME COMPRISES 28 SUBUNITS; EACH SUBUNIT ADOPTS THE FOLD OF AN ANTIPARALLEL BETA-SHEET FLANKED BY HELICES, PROTEASE, REGULATORY COMPLEXES, COVALENT BINDING OF PR-957 TO ALL ACTIVE SITES, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3unb:4 (THR1) to (THR22) MOUSE CONSTITUTIVE 20S PROTEASOME IN COMPLEX WITH PR-957 | 20S PROTEASOME COMPRISES 28 SUBUNITS; EACH SUBUNIT ADOPTS THE FOLD OF AN ANTIPARALLEL BETA-SHEET FLANKED BY HELICES, PROTEASE, REGULATORY COMPLEXES, COVALENT BINDING OF PR-957 TO ALL ACTIVE SITES, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4z3g:B (SER87) to (PHE112) CRYSTAL STRUCTURE OF THE LECTIN DOMAIN OF PAPG FROM E. COLI BI47 IN COMPLEX WITH 4-METHOXYPHENYL BETA-D-GALABIOSE IN SPACE GROUP P212121 | UPEC, URINARY TRACT INFECTION, FIMBRIAL ADHESIN, ADHESIN, TYPE I PILI, PAPG, CARBOHYDRATE BINDING, SUGAR BINDING PROTEIN
3upr:C (HIS188) to (PRO210) HLA-B*57:01 COMPLEXED TO PEP-V AND ABACAVIR | HLA-B*57:01, MHC, ANTIGEN PRESENTING CELL, T-CELL RECEPTOR, HUMAN LEUKOCYTE ANTIGEN, DRUG HYPERSENSITIVITY, ABACAVIR HYPERSENSITIVITY, REPERTOIRE-ALTERING SMALL MOLECULE, IMMUNE RESPONSE, IMMUNOGLOBULIN- LIKE BETA-SANDWICH, IMMUNE SYSTEM
2fgq:X (GLY40) to (ASP64) HIGH RESOLUTION X-RAY STRUCTURE OF OMP32 IN COMPLEX WITH MALATE | PORIN, MALATE, OUTER MEMBRANE PROTEIN, MEMBRANE PROTEIN
3hur:A (VAL347) to (GLY375) CRYSTAL STRUCTURE OF ALANINE RACEMASE FROM OENOCOCCUS OENI | STRUCTURAL GENOMICS, ISOMERASE, PYRIDOXAL PHOSPHATE, PSI-2, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC
1gk9:B (SER1) to (PRO29) CRYSTAL STRUCTURES OF PENICILLIN ACYLASE ENZYME-SUBSTRATE COMPLEXES: STRUCTURAL INSIGHTS INTO THE CATALYTIC MECHANISM | ANTIBIOTIC RESISTANCE, AMIDASE, NTN-HYDROLASE,
4kpb:A (GLU430) to (LYS452) CRYSTAL STRUCTURE OF CYTOCHROME P450 BM-3 R47E MUTANT | HEME-DEPENDENT STEREOSPECIFIC OXIDATION OF SUBSTRATES, OXIDOREDUCTASE
4kpb:B (GLU430) to (LYS452) CRYSTAL STRUCTURE OF CYTOCHROME P450 BM-3 R47E MUTANT | HEME-DEPENDENT STEREOSPECIFIC OXIDATION OF SUBSTRATES, OXIDOREDUCTASE
3v5h:A (HIS188) to (PRO210) HLA-A2.1 KVAEIVHFL | PEPTIDE-BINDING GROOVE, T CELL RECEPTOR, IMMUNE SYSTEM
3v5h:D (HIS188) to (PRO210) HLA-A2.1 KVAEIVHFL | PEPTIDE-BINDING GROOVE, T CELL RECEPTOR, IMMUNE SYSTEM
4kr7:A (ASP144) to (TYR166) CRYSTAL STRUCTURE OF A 4-THIOURIDINE SYNTHETASE - RNA COMPLEX WITH BOUND ATP | TRNA MODIFICATION, THIOURIDINE, SULFURTRANSFERASE, ADENYLATION, THUMP DOMAIN, PP-LOOP MOTIF, 4-THIOURIDINE SYNTHESIS, TRANSFERASE-RNA COMPLEX
4kr7:B (ASP144) to (TYR166) CRYSTAL STRUCTURE OF A 4-THIOURIDINE SYNTHETASE - RNA COMPLEX WITH BOUND ATP | TRNA MODIFICATION, THIOURIDINE, SULFURTRANSFERASE, ADENYLATION, THUMP DOMAIN, PP-LOOP MOTIF, 4-THIOURIDINE SYNTHESIS, TRANSFERASE-RNA COMPLEX
1smj:B (GLU430) to (LYS452) STRUCTURE OF THE A264E MUTANT OF CYTOCHROME P450 BM3 COMPLEXED WITH PALMITOLEATE | MONOOXYGENASE; FATTY ACID OXYGENASE; CYTOCHROME P450; SUBSTRATE BINDING; PALMITOLEATE, OXIDOREDUCTASE
2g4z:A (THR6) to (THR34) ANOMALOUS SUBSTRUCTURE OF THERMOLYSIN | ANOMALOUS SUBSTRUCTURE OF THERMOLYSIN, HYDROLASE
1snr:A (LEU12) to (VAL31) NITRIC OXIDE BOUND TO CU NITRITE REDUCTASE | NITRIC OXIDE, NITRITE REDUCTASE, OXIDOREDUCTASE
3vdx:A (GLY6) to (GLY21) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, DE NOVO PROTEIN
3vdx:B (GLY6) to (GLY21) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, DE NOVO PROTEIN
3vdx:C (GLY6) to (GLY21) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, DE NOVO PROTEIN
1h1a:B (ASN58) to (ASN83) THERMOPHILIC B-1,4-XYLANASE FROM CHAETOMIUM THERMOPHILUM | HYDROLASE, XYLANASE, GLYCOSYL HYDROLASE, FAMILY 11, THERMOSTABILITY GLYCOSIDASE
4l29:K (HIS188) to (PRO210) STRUCTURE OF WTMHC CLASS I WITH NY-ESO1 DOUBLE MUTANT | MHC, BETA-2 MICROGLOBULIN, HLA_A0201, NY-ESO1, D76N VARIANT, IMMUNGLOBULIN, BETA SANDWITCH, IMMUNE SYSTEM
4l29:O (HIS188) to (PRO210) STRUCTURE OF WTMHC CLASS I WITH NY-ESO1 DOUBLE MUTANT | MHC, BETA-2 MICROGLOBULIN, HLA_A0201, NY-ESO1, D76N VARIANT, IMMUNGLOBULIN, BETA SANDWITCH, IMMUNE SYSTEM
4l3c:K (HIS188) to (PRO210) STRUCTURE OF HLA-A2 IN COMPLEX WITH D76N B2M MUTANT AND NY-ESO1 DOUBLE MUTANT | MHC, BETA-2 MICROGLOBULIN, HLA_A0201, NY-ESO1, D76N VARIANT, IMMUNGLOBULIN, BETA SANDWITCH, IMMUNE SYSTEM, AMYLOID AGGREGATION
2vzu:B (ARG335) to (PRO365) COMPLEX OF AMYCOLATOPSIS ORIENTALIS EXO-CHITOSANASE CSXA D469A WITH PNP-BETA-D-GLUCOSAMINE | GH2, CSXA, PNP-GLUCOSAMINE, GLYCOSIDE HYDROLASE, EXO-BETA-D-GLUCOSAMINIDASE, HYDROLASE
3ij4:A (ASP184) to (LYS212) CESIUM SITES IN THE CRYSTAL STRUCTURE OF A FUNCTIONAL ACID SENSING ION CHANNEL IN THE DESENSITIZED STATE | ACID-SENSING, FUNCTIONAL, ION CHANNEL, TRIMER, MEMBRANE PROTEIN, SODIUM CHANNEL, CELL MEMBRANE, GLYCOPROTEIN, ION TRANSPORT, IONIC CHANNEL, MEMBRANE, SODIUM, SODIUM TRANSPORT, TRANSMEMBRANE, TRANSPORT, TRANSPORT PROTEIN, CESIUM, ANOMALOUS
1hcx:B (LYS198) to (LYS222) CHOLINE BINDING DOMAIN OF THE MAJOR AUTOLYSIN (C-LYTA) FROM STREPTOCOCCUS PNEUMONIAE | CHOLINE-BINDING DOMAIN, CELL WALL ATTACHMENT
3vkq:A (GLY355) to (GLN377) ASSIMILATORY NITRITE REDUCTASE (NII3) - NO2 COMPLEX FROM TOBBACO LEAF ANALYSED WITH MIDDLE X-RAY DOSE | MIDDLE X-RAY DOSE, 3 ALPHA/BETA DOMAINS, REDUCTASE, SIROHEME, FE4S4, NITRITE, OXIDOREDUCTASE
3vkr:A (GLY355) to (GLN377) ASSIMILATORY NITRITE REDUCTASE (NII3) - NO2 COMPLEX FROM TOBBACO LEAF ANALYSED WITH HIGH X-RAY DOSE | HIGH X-RAY DOSE, 3 ALPHA/BETA DOMAINS, REDUCTASE, SIROHEME, FE4S4, NITRITE, OXIDOREDUCTASE
1hsa:A (HIS188) to (PRO210) THE THREE-DIMENSIONAL STRUCTURE OF HLA-B27 AT 2.1 ANGSTROMS RESOLUTION SUGGESTS A GENERAL MECHANISM FOR TIGHT PEPTIDE BINDING TO MHC | HISTOCOMPATIBILITY ANTIGEN
1hsa:D (HIS188) to (PRO210) THE THREE-DIMENSIONAL STRUCTURE OF HLA-B27 AT 2.1 ANGSTROMS RESOLUTION SUGGESTS A GENERAL MECHANISM FOR TIGHT PEPTIDE BINDING TO MHC | HISTOCOMPATIBILITY ANTIGEN
5a0q:H (THR2) to (THR22) CRYO-EM REVEALS THE CONFORMATION OF A SUBSTRATE ANALOGUE IN THE HUMAN 20S PROTEASOME CORE | HYDROLASE, PROTEASOME, 20S, ADAAHX3L3VS, LIGAND, INHIBITOR, DRUG DESIGN
5a0q:V (THR2) to (THR22) CRYO-EM REVEALS THE CONFORMATION OF A SUBSTRATE ANALOGUE IN THE HUMAN 20S PROTEASOME CORE | HYDROLASE, PROTEASOME, 20S, ADAAHX3L3VS, LIGAND, INHIBITOR, DRUG DESIGN
1i1f:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HUMAN CLASS I MHC (HLA-A2.1) COMPLEXED WITH BETA 2-MICROGLOBULIN AND HIV-RT VARIANT PEPTIDE I1Y | HUMAN CLASS I MHC, HIV, IMMUNE SYSTEM
1i1f:D (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HUMAN CLASS I MHC (HLA-A2.1) COMPLEXED WITH BETA 2-MICROGLOBULIN AND HIV-RT VARIANT PEPTIDE I1Y | HUMAN CLASS I MHC, HIV, IMMUNE SYSTEM
2wo4:A (ALA102) to (GLY120) 3B' CARBOHYDRATE-BINDING MODULE FROM THE CEL9V GLYCOSIDE HYDROLASE FROM CLOSTRIDIUM THERMOCELLUM, IN-HOUSE DATA | CELLULOSE DEGRADATION, HYDROLASE, GLYCOSIDE HYDROLASE
2hzs:F (TYR34) to (PRO163) STRUCTURE OF THE MEDIATOR HEAD SUBMODULE MED8C/18/20 | BETA BARREL, CHANNEL, HELIX, TRANSCRIPTION
2wvk:A (ASN7) to (GLU25) MANNOSYL-3-PHOSPHOGLYCERATE SYNTHASE FROM THERMUS THERMOPHILUS HB27 APOPROTEIN | GT-A FOLD, TRANSFERASE
2iaa:C (VAL5) to (ASP23) CRYSTAL STRUCTURE OF AN ELECTRON TRANSFER COMPLEX BETWEEN AROMATIC AMINE DEPHYDROGENASE AND AZURIN FROM ALCALIGENES FAECALIS (FORM 2) | QUINOPROTEIN, TRYPTOPHAN TRYPTOPHYLQUINONE, CUPREDOXIN, ELECTRON TRANSFER, OXIDOREDUCTASE/ELECTRON TRANSPORT COMPLEX
4m5y:H (SER120) to (PRO147) CRYSTAL STRUCTURE OF BROADLY NEUTRALIZING FAB 5J8 | IMMUNOGLOBULIN FOLD, FRAGMENT ANTIGEN BINDING, INFLUENZA HEMAGGLUTININ RECEPTOR BINDING SITE, IMMUNE SYSTEM
4m7h:A (GLY426) to (PRO456) CRYSTAL STRUCTURE OF TETRAMERIC FIBRINOGEN-LIKE RECOGNITION DOMAIN OF FIBCD1 | FIBRINOGEN-LIKE DOMAIN, N-ACETYL-BINDING PROTEIN, PUTATIVE CHITIN RECEPTOR, CARBOHYDRATE/SUGAR BINDING, SUGAR BINDING PROTEIN
4m7h:B (GLY426) to (PRO456) CRYSTAL STRUCTURE OF TETRAMERIC FIBRINOGEN-LIKE RECOGNITION DOMAIN OF FIBCD1 | FIBRINOGEN-LIKE DOMAIN, N-ACETYL-BINDING PROTEIN, PUTATIVE CHITIN RECEPTOR, CARBOHYDRATE/SUGAR BINDING, SUGAR BINDING PROTEIN
1uri:A (ALA5) to (ASP23) AZURIN MUTANT WITH MET 121 REPLACED BY GLN | ELECTRON TRANSPORT, COPPER, PERIPLASMIC, SIGNAL
2x05:A (ARG335) to (ASP366) INHIBITION OF THE EXO-BETA-D-GLUCOSAMINIDASE CSXA BY A GLUCOSAMINE-CONFIGURED CASTANOSPERMINE AND AN AMINO- AUSTRALINE ANALOGUE | EXO-BETA-D-GLUCOSAMINIDASE, GLYCOSIDE HYDROLASE, GH2, CSXA, HYDROLASE, GLYCOSIDASE
2ih8:A (GLY151) to (TYR177) A LOW-DOSE CRYSTAL STRUCTURE OF A RECOMBINANT MELANOCARPUS ALBOMYCES LACCASE | LACCASE, MULTICOPPER OXIDASE, REDOX-ENZYME, OXIDOREDUCTASE
2ij4:A (GLU430) to (LYS452) STRUCTURE OF THE A264K MUTANT OF CYTOCHROME P450 BM3 | LYSINE HEME LIGATION, CYTOCHROME P450, P450 BM3, OXIDOREDUCTASE
2ij4:B (GLU430) to (LYS452) STRUCTURE OF THE A264K MUTANT OF CYTOCHROME P450 BM3 | LYSINE HEME LIGATION, CYTOCHROME P450, P450 BM3, OXIDOREDUCTASE
1uwe:H (SER120) to (PRO147) MOLECULAR MECHANISM OF ENANTIOSELECTIVE PROTON TRANSFER TO CARBON IN CATALYTIC ANTIBODY 14D9 | ANTIBODY
1uwe:V (SER120) to (PRO147) MOLECULAR MECHANISM OF ENANTIOSELECTIVE PROTON TRANSFER TO CARBON IN CATALYTIC ANTIBODY 14D9 | ANTIBODY
1uwe:Y (SER120) to (PRO147) MOLECULAR MECHANISM OF ENANTIOSELECTIVE PROTON TRANSFER TO CARBON IN CATALYTIC ANTIBODY 14D9 | ANTIBODY
1j38:A (SER339) to (VAL357) CRYSTAL STRUCTURE OF DROSOPHILA ANCE | ANGIOTENSIN, HYDROLASE
1j38:B (SER339) to (VAL357) CRYSTAL STRUCTURE OF DROSOPHILA ANCE | ANGIOTENSIN, HYDROLASE
2x6i:B (LEU811) to (LEU828) THE CRYSTAL STRUCTURE OF THE DROSOPHILA CLASS III PI3-KINASE VPS34 IN COMPLEX WITH PIK-90 | TRANSFERASE
2x90:A (SER339) to (VAL357) CRYSTAL STRUCTURE OF ANCE-ENALAPRILAT COMPLEX | HYDROLASE, ACE INHIBITOR, ZINC METALLOPEPTIDASE
2x93:A (SER339) to (VAL357) CRYSTAL STRUCTURE OF ANCE-TRANDOLAPRILAT COMPLEX | METALLOPROTEASE, CARBOXYPEPTIDASE, ACE INHIBITOR, HYDROLASE, GLYCOPROTEIN
2x96:A (HIS337) to (VAL357) CRYSTAL STRUCTURE OF ANCE-RXPA380 COMPLEX | HYDROLASE, ACE INHIBITOR, ZINC METALLOPEPTIDASE
2x97:A (SER339) to (VAL357) CRYSTAL STRUCTURE OF ANCE-RXP407 COMPLEX | HYDROLASE, ACE INHIBITOR, ZINC METALLOPEPTIDASE
1jc9:A (GLY231) to (PRO261) TACHYLECTIN 5A FROM TACHYPLEUS TRIDENTATUS (JAPANESE HORSESHOE CRAB) | LECTIN, FIBRINOGEN RELATED, SUGAR BINDING PROTEIN
3woe:D (ALA90) to (ASP109) CRYSTAL STRUCTURE OF P23-45 GP39 (6-109) BOUND TO THERMUS THERMOPHILUS RNA POLYMERASE BETA-FLAP DOMAIN | TRANSCRIPTION, RNA POLYMERASE, TRANSFERASE-TRANSCRIPTION COMPLEX
1jme:A (GLU430) to (LYS452) CRYSTAL STRUCTURE OF PHE393HIS CYTOCHROME P450 BM3 | CYTOCHROME P450, FATTY ACID HYDROXYLASE, MONOOXYGENASE, OXIDOREDUCTASE
2xfx:A (HIS188) to (PRO210) CATTLE MHC CLASS I N01301 PRESENTING AN 11MER FROM THEILERIA PARVA | IMMUNE SYSTEM, MAJOR HISTOCOMPATIBILITY, EAST COAST FEVER, THEILERIOSIS
2j62:B (LEU162) to (VAL179) STRUCTURE OF A BACTERIAL O-GLCNACASE IN COMPLEX WITH GLCNACSTATIN | HYDROLASE
5aww:Y (ALA246) to (LEU266) PRECISE RESTING STATE OF THERMUS THERMOPHILUS SECYEG | TRANSLOCON, MEMBRANE PROTEIN, PROTEIN TRANSPORT-IMMUNE SYSTEM COMPLEX
3x1l:B (PRO263) to (GLU292) CRYSTAL STRUCTURE OF THE CRISPR-CAS RNA SILENCING CMR COMPLEX BOUND TO A TARGET ANALOG | RNA-RECOGNITION MOTIF, RNA SILENCING, RNA BINDING, RNA BINDING PROTEIN-RNA-DNA COMPLEX
3x1l:C (THR259) to (SER299) CRYSTAL STRUCTURE OF THE CRISPR-CAS RNA SILENCING CMR COMPLEX BOUND TO A TARGET ANALOG | RNA-RECOGNITION MOTIF, RNA SILENCING, RNA BINDING, RNA BINDING PROTEIN-RNA-DNA COMPLEX
3x1l:D (THR259) to (SER299) CRYSTAL STRUCTURE OF THE CRISPR-CAS RNA SILENCING CMR COMPLEX BOUND TO A TARGET ANALOG | RNA-RECOGNITION MOTIF, RNA SILENCING, RNA BINDING, RNA BINDING PROTEIN-RNA-DNA COMPLEX
5bou:L (GLY10) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH A BETA1 / BETA2 SPECIFIC NON- PEPTIDIC SULFONAMIDE LIGAND | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, NON-COVALENT LIGAND, BINDING ANALYSIS
5bou:Z (GLY10) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH A BETA1 / BETA2 SPECIFIC NON- PEPTIDIC SULFONAMIDE LIGAND | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, NON-COVALENT LIGAND, BINDING ANALYSIS
4nc0:A (GLY13) to (ASP39) CRYSTAL STRUCTURE OF TCDA-A2 BOUND TO A26.8 VHH | ANTIBODY-ANTIGEN COMPLEX, IMMUNE SYSTEM
4nfm:A (GLY95) to (ARG112) HUMAN TAU TUBULIN KINASE 1 (TTBK1) | PROTEIN KINASE, PHOSPHOTRANSFERASE, TRANSFERASE
2y22:E (LEU89) to (ASP109) HUMAN ALPHAB-CRYSTALLIN DOMAIN (RESIDUES 67-157) | SMALL HEAT SHOCK PROTEIN, CHAPERONE, STRESS PROTEIN, EYE LENS PROTEIN, CATARACT
2y22:F (LEU89) to (ASP109) HUMAN ALPHAB-CRYSTALLIN DOMAIN (RESIDUES 67-157) | SMALL HEAT SHOCK PROTEIN, CHAPERONE, STRESS PROTEIN, EYE LENS PROTEIN, CATARACT
5bxl:L (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-G170A MUTANT | HYDROLASE, IMMUNODEFICIENCY, PROTEASOME, MUTANT, ASSEMBLY DEFECT
5bxl:Z (GLY10) to (THR31) YEAST 20S PROTEASOME BETA2-G170A MUTANT | HYDROLASE, IMMUNODEFICIENCY, PROTEASOME, MUTANT, ASSEMBLY DEFECT
5bxn:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA2-G170A MUTANT IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, IMMUNODEFICIENCY, PROTEASOME, MUTANT, ASSEMBLY DEFECT
5bxn:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA2-G170A MUTANT IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, IMMUNODEFICIENCY, PROTEASOME, MUTANT, ASSEMBLY DEFECT
2kau:C (ASP431) to (SER493) THE CRYSTAL STRUCTURE OF UREASE FROM KLEBSIELLA AEROGENES AT 2.2 ANGSTROMS RESOLUTION | NICKEL METALLOENZYME, HYDROLASE (UREA AMIDO), HYDROLASE
1wnr:A (MET1) to (LYS38) CRYSTAL STRUCTURE OF THE CPN10 FROM THERMUS THERMOPHILUS HB8 | CO-CHAPERONIN, PROTEIN CPN10, GROES, THERMUS THERMOPHILUS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, STRUCTURAL GENOMICS, CHAPERONE
1wnr:B (MET1) to (LYS38) CRYSTAL STRUCTURE OF THE CPN10 FROM THERMUS THERMOPHILUS HB8 | CO-CHAPERONIN, PROTEIN CPN10, GROES, THERMUS THERMOPHILUS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, STRUCTURAL GENOMICS, CHAPERONE
1wnr:D (MET1) to (LYS38) CRYSTAL STRUCTURE OF THE CPN10 FROM THERMUS THERMOPHILUS HB8 | CO-CHAPERONIN, PROTEIN CPN10, GROES, THERMUS THERMOPHILUS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, STRUCTURAL GENOMICS, CHAPERONE
1wnr:E (MET1) to (LYS38) CRYSTAL STRUCTURE OF THE CPN10 FROM THERMUS THERMOPHILUS HB8 | CO-CHAPERONIN, PROTEIN CPN10, GROES, THERMUS THERMOPHILUS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, STRUCTURAL GENOMICS, CHAPERONE
1wnr:F (MET1) to (LYS38) CRYSTAL STRUCTURE OF THE CPN10 FROM THERMUS THERMOPHILUS HB8 | CO-CHAPERONIN, PROTEIN CPN10, GROES, THERMUS THERMOPHILUS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, STRUCTURAL GENOMICS, CHAPERONE
3zo9:B (THR494) to (GLN516) THE STRUCTURE OF TREHALOSE SYNTHASE (TRES) OF MYCOBACTERIUM SMEGMATIS | HYDROLASE, GLYCOHYDROLASE, DRUG DESIGN, TUBERCULOSIS
4nmk:B (ARG358) to (ASP371) THERMOSTABLE ALDEHYDE DEHYDROGENASE FROM PYROBACULUM SP. CRYSTALLIZED IN MICROGRAVITY (COMPLEX WITH NADP+) | ALDEHYDE OXIDATION, NADP REDUCTION, INTRACELLULAR, OXIDOREDUCTASE
4nmk:H (ARG358) to (ASP371) THERMOSTABLE ALDEHYDE DEHYDROGENASE FROM PYROBACULUM SP. CRYSTALLIZED IN MICROGRAVITY (COMPLEX WITH NADP+) | ALDEHYDE OXIDATION, NADP REDUCTION, INTRACELLULAR, OXIDOREDUCTASE
4nny:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF NON-PHOSPHORYLATED FORM OF PKD2 PHOSPHOPEPTIDE BOUND TO HLA-A2 | NONPHOSPHORYLATED EPITOPE, PEPTIDE-MHC COMPLEX, MHC, POST TRANSLATIONAL MODIFICATION, PEPTIDE CONFORMATION, TUMOR IMMUNOLOGY, TUMOR ANTIGEN, IMMUNE SYSTEM-ANTIGEN COMPLEX
4no3:A (LYS186) to (PRO210) CRYSTAL STRUCTURE OF AMPD2 PHOSPHOPEPTIDE BOUND TO HLA-A2 | PHOSPHOSERINE, PHOSPHOPEPTIDE, PEPTIDE-MHC COMPLEX, MHC, TUMOR IMMUNOLOGY, PEPTIDE CONFORMATION, POST TRANSLATIONAL MODIFICATION, TUMOR ANTIGEN, NEOEPITOPE, IMMUNE SYSTEM-ANTIGEN COMPLEX
4no9:I (ILE10) to (SER30) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-EPOXYKETONE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, EPOXYKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no9:L (GLY10) to (THR31) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-EPOXYKETONE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, EPOXYKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no9:W (ILE10) to (SER30) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-EPOXYKETONE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, EPOXYKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no9:Z (GLY10) to (THR31) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-EPOXYKETONE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, EPOXYKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1x33:A (LEU232) to (GLU260) T=3 RECOMBINANT CAPSID OF SEMV CP | T=3 CAPSIDS, RECOMBINANT CP, ICOSAHEDRAL VIRUS
1x33:B (LEU232) to (GLU260) T=3 RECOMBINANT CAPSID OF SEMV CP | T=3 CAPSIDS, RECOMBINANT CP, ICOSAHEDRAL VIRUS
1x33:C (LEU232) to (GLU260) T=3 RECOMBINANT CAPSID OF SEMV CP | T=3 CAPSIDS, RECOMBINANT CP, ICOSAHEDRAL VIRUS
2mpa:L (GLY89) to (PRO118) BACTERICIDAL ANTIBODY AGAINST NEISSERIA MENINGITIDIS | MURINE IMMUNOGLOBULIN IGG2A KAPPA, BACTERICIDAL ANTIBODY, EPITOPE P1.16 OF PORA FROM NEISSERIA MENINGITIDIS, COMPLEX (IMMUNOGLOBULIN- PEPTIDE), IMMUNE SYSTEM
3jrm:H (THR1) to (MET22) CRYSTAL STRUCTURE OF ARCHAEAL 20S PROTEASOME IN COMPLEX WITH MUTATED P26 ACTIVATOR | 20S PROTEASOME, PA26, CYTOPLASM, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE, HYDROLASE/HYDROLASE ACTIVATOR COMPLEX
3jrm:I (THR1) to (MET22) CRYSTAL STRUCTURE OF ARCHAEAL 20S PROTEASOME IN COMPLEX WITH MUTATED P26 ACTIVATOR | 20S PROTEASOME, PA26, CYTOPLASM, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE, HYDROLASE/HYDROLASE ACTIVATOR COMPLEX
3jrm:J (THR1) to (MET22) CRYSTAL STRUCTURE OF ARCHAEAL 20S PROTEASOME IN COMPLEX WITH MUTATED P26 ACTIVATOR | 20S PROTEASOME, PA26, CYTOPLASM, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE, HYDROLASE/HYDROLASE ACTIVATOR COMPLEX
3jrm:K (THR1) to (MET22) CRYSTAL STRUCTURE OF ARCHAEAL 20S PROTEASOME IN COMPLEX WITH MUTATED P26 ACTIVATOR | 20S PROTEASOME, PA26, CYTOPLASM, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE, HYDROLASE/HYDROLASE ACTIVATOR COMPLEX
3jrm:L (THR1) to (MET22) CRYSTAL STRUCTURE OF ARCHAEAL 20S PROTEASOME IN COMPLEX WITH MUTATED P26 ACTIVATOR | 20S PROTEASOME, PA26, CYTOPLASM, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE, HYDROLASE/HYDROLASE ACTIVATOR COMPLEX
3jrm:M (THR1) to (MET22) CRYSTAL STRUCTURE OF ARCHAEAL 20S PROTEASOME IN COMPLEX WITH MUTATED P26 ACTIVATOR | 20S PROTEASOME, PA26, CYTOPLASM, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE, HYDROLASE/HYDROLASE ACTIVATOR COMPLEX
3jrm:N (THR1) to (MET22) CRYSTAL STRUCTURE OF ARCHAEAL 20S PROTEASOME IN COMPLEX WITH MUTATED P26 ACTIVATOR | 20S PROTEASOME, PA26, CYTOPLASM, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE, HYDROLASE/HYDROLASE ACTIVATOR COMPLEX
4o5i:W (SER120) to (PRO147) CRYSTAL STRUCTURE OF BROADLY NEUTRALIZING ANTIBODY F045-092 IN COMPLEX WITH A/VICTORIA/361/2011 (H3N2) INFLUENZA HEMAGGLUTININ | IMMUNOGLOBULIN, VIRUS ATTACHMENT AND ENTRY, IMMUNE RECOGNITION, VIRAL PROTEIN-IMMUNE SYSTEM COMPLEX
3jyn:A (ARG78) to (LEU101) CRYSTAL STRUCTURES OF PSEUDOMONAS SYRINGAE PV. TOMATO DC3000 QUINONE OXIDOREDUCTASE COMPLEXED WITH NADPH | ROSSMANN FOLD, PROTEIN-NADPH COMPLEX, OXIDOREDUCTASE
5cgf:L (GLY10) to (THR31) YEAST 20S PROTEASOME BETA5-G48C MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5cgf:Z (GLY10) to (THR31) YEAST 20S PROTEASOME BETA5-G48C MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2yxf:A (LYS6) to (PRO32) THE HIGH RESOLUTION CRYSTAL STRUCTURE OF BETA2- MICROGLOBULIN UNDER PHYSIOLOGICAL CONDITIONS | IMMUNE SYSTEM
5cjs:H (SER120) to (PRO149) CRYSTAL STRUCTURE OF A MONOMERIC INFLUENZA HEMAGGLUTININ STEM IN COMPLEX WITH AN BROADLY NEUTRALIZING ANTIBODY CR9114 | HEMAGGLUTININ, TRIMER, INFLUENZA, IMMUNOGEN, MONOCLONAL, ANTIBODY, NEUTRALIZING, INFLUENZA VACCINE, GLYCOPROTEIN, VIRAL PROTEIN-IMMUNE SYSTEM COMPLEX
2o2q:B (VAL409) to (GLY427) CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF RAT 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH NADP | ALDEHYDE DEHYDROGENASE, FDH, OXIDOREDUCTASE
2o2q:C (VAL409) to (VAL458) CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF RAT 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH NADP | ALDEHYDE DEHYDROGENASE, FDH, OXIDOREDUCTASE
2o2q:D (VAL409) to (VAL458) CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF RAT 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH NADP | ALDEHYDE DEHYDROGENASE, FDH, OXIDOREDUCTASE
4oly:H (SER120) to (PRO147) CRYSTAL STRUCTURE OF ANTIBODY VRC07-G54R IN COMPLEX WITH CLADE A/E 93TH057 HIV-1 GP120 CORE | VRC07 ANTIBODY, PASSIVE TRANSFER, NEUTRALIZATION, IN VIVO PROTECTION, AUTOREACTIVITY, LENTIVIRAL INFECTION, ENHANCED POTENCY, HIV-1 GP120, VRC07-G54R, VIRAL PROTEIN-IMMUNE SYSTEM COMPLEX
5cz4:L (GLY10) to (THR31) YEAST 20S PROTEASOME AT 2.3 A RESOLUTION | HYDROLASE-HYDROLASE COMPLEX, UBIQUITIN-DEGRADATION SYSTEM, PROTEASOME, NTN-HYDROLASE, THR-PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5cz4:Z (GLY10) to (THR31) YEAST 20S PROTEASOME AT 2.3 A RESOLUTION | HYDROLASE-HYDROLASE COMPLEX, UBIQUITIN-DEGRADATION SYSTEM, PROTEASOME, NTN-HYDROLASE, THR-PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5cz4:b (THR1) to (THR22) YEAST 20S PROTEASOME AT 2.3 A RESOLUTION | HYDROLASE-HYDROLASE COMPLEX, UBIQUITIN-DEGRADATION SYSTEM, PROTEASOME, NTN-HYDROLASE, THR-PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5cz7:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-T1A BETA5-K81R DOUBLE MUTANT IN COMPLEX WITH BORTEZOMIB, PROPEPTIDE EXPRESSED IN CIS | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cz7:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-T1A BETA5-K81R DOUBLE MUTANT IN COMPLEX WITH BORTEZOMIB, PROPEPTIDE EXPRESSED IN CIS | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cz8:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-L(-49)S-K33A MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cz8:N (THR1) to (THR22) YEAST 20S PROTEASOME BETA5-L(-49)S-K33A MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cz8:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-L(-49)S-K33A MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cz8:b (THR1) to (THR22) YEAST 20S PROTEASOME BETA5-L(-49)S-K33A MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cz9:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-D17N MUTANT IN COMPLEX WITH CARFILZOMIB; PROPEPTIDE EXPRESSED IN TRANS | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cz9:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-D17N MUTANT IN COMPLEX WITH CARFILZOMIB; PROPEPTIDE EXPRESSED IN TRANS | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
1y18:H (SER120) to (PRO149) FAB FRAGMENT OF CATALYTIC ELIMINATION ANTIBODY 34E4 E(H50)D MUTANT IN COMPLEX WITH HAPTEN | IMMUNOGLOBULIN, CATALYTIC ANTIBODY, CHIMERIC FAB, HAPTEN COMPLEX, IMMUNE SYSTEM
1y18:B (SER120) to (PRO149) FAB FRAGMENT OF CATALYTIC ELIMINATION ANTIBODY 34E4 E(H50)D MUTANT IN COMPLEX WITH HAPTEN | IMMUNOGLOBULIN, CATALYTIC ANTIBODY, CHIMERIC FAB, HAPTEN COMPLEX, IMMUNE SYSTEM
1mhe:A (HIS188) to (PRO210) THE HUMAN NON-CLASSICAL MAJOR HISTOCOMPATIBILITY COMPLEX MOLECULE HLA-E | HLA-E, HLA E, MAJOR HISTOCOMPATIBILITY COMPLEX, MHC, HLA, BETA 2 MICROGLOBULIN, PEPTIDE, LEADER PEPTIDE, NON- CLASSICAL MHC, CLASS IB MHC
1mhe:C (HIS188) to (PRO210) THE HUMAN NON-CLASSICAL MAJOR HISTOCOMPATIBILITY COMPLEX MOLECULE HLA-E | HLA-E, HLA E, MAJOR HISTOCOMPATIBILITY COMPLEX, MHC, HLA, BETA 2 MICROGLOBULIN, PEPTIDE, LEADER PEPTIDE, NON- CLASSICAL MHC, CLASS IB MHC
3kpl:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA B*4402 IN COMPLEX WITH EEYLQAFTY A SELF PEPTIDE FROM THE ABCD3 PROTEIN | HLA B*4402, ALLORECOGNITION, TCR RECOGNITION, SELF PEPTIDE, DISULFIDE BOND, GLYCOPROTEIN, HOST-VIRUS INTERACTION, IMMUNE RESPONSE, MEMBRANE, MHC I, IMMUNE SYSTEM
3kpp:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA B*4405 IN COMPLEX WITH EEYLQAFTY A SELF PEPTIDE FROM THE ABCD3 PROTEIN | HLA B*4405, ALLORECOGNITION, TCR RECOGNITION, SELF PEPTIDE, DISULFIDE BOND, GLYCOPROTEIN, HOST-VIRUS INTERACTION, IMMUNE RESPONSE, MEMBRANE, MHC I, TRANSMEMBRANE, IMMUNE SYSTEM
1yar:H (THR1) to (MET22) STRUCTURE OF ARCHEABACTERIAL 20S PROTEASOME MUTANT D9S- PA26 COMPLEX | PROTEASOME 20S, PA26 PROTEASOME ACTIVATOR 11S, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
1yar:I (THR1) to (MET22) STRUCTURE OF ARCHEABACTERIAL 20S PROTEASOME MUTANT D9S- PA26 COMPLEX | PROTEASOME 20S, PA26 PROTEASOME ACTIVATOR 11S, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
1yar:J (THR1) to (MET22) STRUCTURE OF ARCHEABACTERIAL 20S PROTEASOME MUTANT D9S- PA26 COMPLEX | PROTEASOME 20S, PA26 PROTEASOME ACTIVATOR 11S, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
1yar:K (THR1) to (MET22) STRUCTURE OF ARCHEABACTERIAL 20S PROTEASOME MUTANT D9S- PA26 COMPLEX | PROTEASOME 20S, PA26 PROTEASOME ACTIVATOR 11S, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
1yar:L (THR1) to (MET22) STRUCTURE OF ARCHEABACTERIAL 20S PROTEASOME MUTANT D9S- PA26 COMPLEX | PROTEASOME 20S, PA26 PROTEASOME ACTIVATOR 11S, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
1yar:M (THR1) to (MET22) STRUCTURE OF ARCHEABACTERIAL 20S PROTEASOME MUTANT D9S- PA26 COMPLEX | PROTEASOME 20S, PA26 PROTEASOME ACTIVATOR 11S, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
1yar:N (THR1) to (MET22) STRUCTURE OF ARCHEABACTERIAL 20S PROTEASOME MUTANT D9S- PA26 COMPLEX | PROTEASOME 20S, PA26 PROTEASOME ACTIVATOR 11S, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
1yif:A (GLU396) to (ASN410) CRYSTAL STRUCTURE OF BETA-1,4-XYLOSIDASE FROM BACILLUS SUBTILIS, NEW YORK STRUCTURAL GENOMICS CONSORTIUM | GLYCOSIDASE, XYLAN, XYLOSIDASE, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC, HYDROLASE
1yif:B (GLU396) to (ASN410) CRYSTAL STRUCTURE OF BETA-1,4-XYLOSIDASE FROM BACILLUS SUBTILIS, NEW YORK STRUCTURAL GENOMICS CONSORTIUM | GLYCOSIDASE, XYLAN, XYLOSIDASE, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC, HYDROLASE
1yif:D (GLU396) to (ASN410) CRYSTAL STRUCTURE OF BETA-1,4-XYLOSIDASE FROM BACILLUS SUBTILIS, NEW YORK STRUCTURAL GENOMICS CONSORTIUM | GLYCOSIDASE, XYLAN, XYLOSIDASE, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC, HYDROLASE
4pem:B (GLY264) to (PRO292) CRYSTAL STRUCTURE OF S1G MUTANT OF PENICILLIN G ACYLASE FROM KLUYVERA CITROPHILA | NTN HYDROLASE, PGA, SLOW PROCESSING MUTANT, HYDROLASE
4pem:D (ASN441) to (GLN463) CRYSTAL STRUCTURE OF S1G MUTANT OF PENICILLIN G ACYLASE FROM KLUYVERA CITROPHILA | NTN HYDROLASE, PGA, SLOW PROCESSING MUTANT, HYDROLASE
4pem:F (ASN441) to (GLN463) CRYSTAL STRUCTURE OF S1G MUTANT OF PENICILLIN G ACYLASE FROM KLUYVERA CITROPHILA | NTN HYDROLASE, PGA, SLOW PROCESSING MUTANT, HYDROLASE
4pem:H (ASN441) to (GLN463) CRYSTAL STRUCTURE OF S1G MUTANT OF PENICILLIN G ACYLASE FROM KLUYVERA CITROPHILA | NTN HYDROLASE, PGA, SLOW PROCESSING MUTANT, HYDROLASE
3kx5:A (GLU430) to (LYS452) CRYSTAL STRUCTURE OF BACILLUS MEGATERIUM BM3 HEME DOMAIN MUTANT F261E | CYTOCHROME P450, F261E MUTANT, HEME DOMAIN, CYTOPLASM, ELECTRON TRANSPORT, FAD, FLAVOPROTEIN, FMN, HEME, IRON, METAL-BINDING, MONOOXYGENASE, MULTIFUNCTIONAL ENZYME, NADP, OXIDOREDUCTASE, TRANSPORT
3kx5:B (GLU430) to (LYS452) CRYSTAL STRUCTURE OF BACILLUS MEGATERIUM BM3 HEME DOMAIN MUTANT F261E | CYTOCHROME P450, F261E MUTANT, HEME DOMAIN, CYTOPLASM, ELECTRON TRANSPORT, FAD, FLAVOPROTEIN, FMN, HEME, IRON, METAL-BINDING, MONOOXYGENASE, MULTIFUNCTIONAL ENZYME, NADP, OXIDOREDUCTASE, TRANSPORT
5def:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF B*27:04 COMPLEX BOUND TO THE PVIPR PEPTIDE | IMMUNE SYSTEM-COMPLEX, IMMUNE SYSTEM, MHC MAJOR HISTOCOMPATIBILITY COMPLEX), HLA- B*2704
1n5a:G (HIS188) to (PRO210) CRYSTAL STRUCTURE OF THE MURINE CLASS I MAJOR HISTOCOMPATIBILITY COMPLEX OF H-2DB, B2-MICROGLOBULIN, AND A 9-RESIDUE IMMUNODOMINANT PEPTIDE EPITOPE GP33 DERIVED FROM LCMV | MURINE MHC, VIRAL ESCAPE, LCMV, IMMUNODOMINANT EPITOPE, IMMUNE SYSTEM
4q1p:A (LEU17) to (CYS42) GALECTIN-1 IN COMPLEX WITH LIGAND NB169 | RATIONAL DRUG DESIGN, SUGAR BINDING PROTEIN
4asq:A (SER339) to (VAL357) CRYSTAL STRUCTURE OF ANCE IN COMPLEX WITH BRADYKININ | HYDROLASE, ZINC METALLOPROTEASE, SUBSTRATE RECOGNITION
5dyp:A (GLU430) to (LYS452) CRYSTAL STRUCTURE OF ASP251GLY/GLN307HIS MUTANT OF CYTOCHROME P450 BM3 | CYTOCHROME P450, RANDOM MUTAGENESIS, DRUG METABOLISM, OXIDOREDUCTASE
5dyp:C (GLU430) to (LYS451) CRYSTAL STRUCTURE OF ASP251GLY/GLN307HIS MUTANT OF CYTOCHROME P450 BM3 | CYTOCHROME P450, RANDOM MUTAGENESIS, DRUG METABOLISM, OXIDOREDUCTASE
5dyz:A (GLU430) to (LYS452) CRYSTAL STRUCTURE OF ASP251GLY/GLN307HIS MUTANT OF CYTOCHROME P450 BM3 IN COMPLEX WITH N-PALMITOYLGLYCINE | CYTOCHROME P450, RANDOM MUTAGENESIS, DRUG METABOLISM, SUBSTRATE, OXIDOREDUCTASE
5e2u:H (SER120) to (PRO147) STRUCTURE OF ANTI-TAU AT8 FAB IN THE PRESENCE OF PHOSPHOPEPTIDE | IMMUNE SYSTEM
1zv2:A (LEU44) to (VAL63) CU-CONTAINING NITRITE REDUCTASE | COPPER PROTEIN, NITRITE REDUCTION, DENITRIFICATION, OXIDOREDUCTASE
3lyb:A (ALA16) to (PRO31) STRUCTURE OF PUTATIVE ENDORIBONUCLEASE(KP1_3112) FROM KLEBSIELLA PNEUMONIAE | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC, HYDROLASE
3lyb:B (ALA16) to (PRO31) STRUCTURE OF PUTATIVE ENDORIBONUCLEASE(KP1_3112) FROM KLEBSIELLA PNEUMONIAE | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC, HYDROLASE
3lyb:C (ALA16) to (PRO31) STRUCTURE OF PUTATIVE ENDORIBONUCLEASE(KP1_3112) FROM KLEBSIELLA PNEUMONIAE | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC, HYDROLASE
3lyb:D (ALA16) to (PRO31) STRUCTURE OF PUTATIVE ENDORIBONUCLEASE(KP1_3112) FROM KLEBSIELLA PNEUMONIAE | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC, HYDROLASE
4qff:B (GLY6) to (GLY21) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS, QUADRUPLE MUTANT, P212121 FORM | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, OXIDOREDUCTASE, VIRAL PROTEIN
4qff:H (GLY6) to (GLY21) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS, QUADRUPLE MUTANT, P212121 FORM | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, OXIDOREDUCTASE, VIRAL PROTEIN
4qff:L (GLY6) to (GLY21) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS, QUADRUPLE MUTANT, P212121 FORM | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, OXIDOREDUCTASE, VIRAL PROTEIN
2ad6:A (ASP410) to (ASP450) CRYSTAL STRUCTURE OF METHANOL DEHYDROGENASE FROM M. W3A1 (FORM C) | METHANOL DEHYDROGENASE, PQQ CONFIGURATION, NATIVE, OXIDOREDUCTASE
2ad6:C (ASP410) to (ASP450) CRYSTAL STRUCTURE OF METHANOL DEHYDROGENASE FROM M. W3A1 (FORM C) | METHANOL DEHYDROGENASE, PQQ CONFIGURATION, NATIVE, OXIDOREDUCTASE
4qlv:L (THR11) to (THR31) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 17 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlv:Z (THR11) to (THR31) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 17 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3bdm:L (THR2) to (THR22) YEAST 20S PROTEASOME:GLIDOBACTIN A-COMPLEX | PROTEASOME, UBIQUITIN, PROTEOLYSIS, PATHOGEN, VIRULENCE FACTOR, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN
3bdm:Z (THR2) to (THR22) YEAST 20S PROTEASOME:GLIDOBACTIN A-COMPLEX | PROTEASOME, UBIQUITIN, PROTEOLYSIS, PATHOGEN, VIRULENCE FACTOR, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN
5eqn:A (VAL198) to (HIS222) STRUCTURE OF PHOSPHONATE HYDROXYLASE | PHOSPHONATE HYDROXYLASE, DIOXYGENASES, HYDROLASE
3mlx:H (SER120) to (PRO147) CRYSTAL STRUCTURE OF ANTI-HIV-1 V3 FAB 3074 IN COMPLEX WITH AN MN V3 PEPTIDE | HUMAN MONOCLONAL ANTIBODY, FAB, HIV-1, GP120, THIRD VARIABLE LOOP, ANTIBODY-ANTIGEN INTERACTION, IMMUNE SYSTEM
3mrc:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF MHC CLASS I HLA-A2 MOLECULE COMPLEXED WITH HCMV PP65-495-503 NONAPEPTIDE V6C VARIANT | MHC CLASS I, HLA, IMMUNE SYSTEM, IMMUNE RESPONSE, NONAPEPTIDE, VIRAL PEPTIDE, CYTOMEGALOVIRUS, PP65 PROTEIN
3mro:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF MHC CLASS I HLA-A2 MOLECULE COMPLEXED WITH MELAN- A MART1 DECAPEPTIDE VARIANT | MHC CLASS I, HLA, IMMUNE SYSTEM, IMMUNE RESPONSE, DECAPEPTIDE, TUMORAL PEPTIDE, MELAN-A, MART1
4qw7:L (THR11) to (THR31) YCP BETA5-M45T MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw7:Z (THR11) to (THR31) YCP BETA5-M45T MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwi:L (THR11) to (THR31) YCP BETA5-A49S-MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwi:Z (THR11) to (THR31) YCP BETA5-A49S-MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5f3b:A (SER123) to (PRO150) STRUCTURE OF MYOSTATIN IN COMPLEX WITH CHIMERIC RK35 ANTIBODY | MYOSTATIN, ANTIBODY, COMPLEX, SIGNALING PROTEIN-IMMUNE SYSTEM COMPLEX
5f3b:E (SER123) to (PRO150) STRUCTURE OF MYOSTATIN IN COMPLEX WITH CHIMERIC RK35 ANTIBODY | MYOSTATIN, ANTIBODY, COMPLEX, SIGNALING PROTEIN-IMMUNE SYSTEM COMPLEX
5f4p:D (ASN392) to (GLN422) HIV-1 GP120 COMPLEX WITH BNM-III-170 | VIRAL PROTEIN
4qz1:I (ILE10) to (SER30) YCP BETA5-M45T MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz1:W (ILE10) to (SER30) YCP BETA5-M45T MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3n05:B (HIS126) to (LEU151) CRYSTAL STRUCTURE OF NH3-DEPENDENT NAD+ SYNTHETASE FROM STREPTOMYCES AVERMITILIS | LIGASE, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, PSI, NYSGRC, NEW YORK STRUCTURAL GENOMICS RESEARCH CONSORTIUM, NYSGXRC, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS
4btk:A (GLY119) to (ARG136) TTBK1 IN COMPLEX WITH INHIBITOR | TRANSFERASE, STRUCTURE-KINETICS RELATIONSHIP
3n2k:C (PHE52) to (LEU70) TUBULIN-NSC 613862: RB3 STATHMIN-LIKE DOMAIN COMPLEX | ALPHA-TUBULIN, BETA-TUBULIN, COLCHICINE DOMAIN, COVALENT BINDING, MICROTUBULE, STATHMIN, TUBULIN, CELL CYCLE
5fb8:B (SER148) to (PRO175) STRUCTURE OF INTERLEUKIN-16 BOUND TO THE 14.1 ANTIBODY | CYTOKINE, INTERLEUKIN, ANTIBODY, COMPLEX, IMMUNE SYSTEM
4r2g:Q (SER138) to (PRO165) CRYSTAL STRUCTURE OF PGT124 FAB BOUND TO HIV-1 JRCSF GP120 CORE AND TO CD4 | PROTEIN-PROTEIN COMPLEX, IGG, ANTI-HIV ANTIBODIES, GP120, IMMUNE SYSTEM
3n5p:A (LEU313) to (ASN340) STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 4-(2-(6-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL)PYRIDIN-2-YL) ETHYL)-6-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n6d:B (PRO316) to (ASN340) STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE H373S SINGLE MUTANT HEME DOMAIN COMPLEXED WITH 6,6'-(2,2'-(5-AMINO-1,3-PHENYLENE) BIS(ETHANE-2,1-DIYL))BIS(4-METHYLPYRIDIN-2-AMINE) | NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
5fga:L (GLY10) to (THR31) YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5fga:Z (GLY10) to (THR31) YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5fgg:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-L(-49S)_D17N DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgg:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA5-L(-49S)_D17N DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgi:L (THR11) to (THR31) YEAST 20S PROTEASOME BETA1-T1A BETA2-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgi:Z (THR11) to (THR31) YEAST 20S PROTEASOME BETA1-T1A BETA2-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4r67:H (THR1) to (THR22) HUMAN CONSTITUTIVE 20S PROTEASOME IN COMPLEX WITH CARFILZOMIB | HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r67:V (THR1) to (THR22) HUMAN CONSTITUTIVE 20S PROTEASOME IN COMPLEX WITH CARFILZOMIB | HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r67:j (THR1) to (THR22) HUMAN CONSTITUTIVE 20S PROTEASOME IN COMPLEX WITH CARFILZOMIB | HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r67:x (THR1) to (THR22) HUMAN CONSTITUTIVE 20S PROTEASOME IN COMPLEX WITH CARFILZOMIB | HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3c91:J (THR1) to (MET22) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:K (THR1) to (MET22) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:L (THR1) to (MET22) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:M (THR1) to (MET22) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:N (THR1) to (MET22) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:X (THR1) to (MET22) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:Y (THR1) to (MET22) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:Z (THR1) to (MET22) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:1 (THR1) to (MET22) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:2 (THR1) to (MET22) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:J (THR1) to (MET22) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:K (THR1) to (MET22) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:L (THR1) to (MET22) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:M (THR1) to (MET22) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:N (THR1) to (MET22) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:X (THR1) to (MET22) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:Y (THR1) to (MET22) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:Z (THR1) to (MET22) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:1 (THR1) to (MET22) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:2 (THR1) to (MET22) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
4rax:A (GLY2400) to (PRO2455) A REGULATORY DOMAIN OF AN ION CHANNEL | SANDWICH FOLD, NOVEL STRUCTURE, EXTRA-CELLULAR, REGULATORY DOMAIN, REGULATORY, STRUCTURAL PROTEIN
5fjw:D (VAL458) to (ASN476) YEAST DELTA-COP-I MU-HOMOLOGY DOMAIN COMPLEXED WITH DSL1 WXWX(MSE) PEPTIDE | PROTEIN TRANSPORT, COP-I, VESICLE COAT PROTEIN
3ch1:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF H-2DB IN COMPLEX WITH CHIMERIC GP100 | MHC, H-2DB, GLYCOPROTEIN, IMMUNE RESPONSE, MEMBRANE, MHC I, TRANSMEMBRANE, IMMUNOGLOBULIN DOMAIN, SECRETED, DISEASE MUTATION, MELANIN BIOSYNTHESIS, IMMUNE SYSTEM
3ch1:J (HIS188) to (PRO210) CRYSTAL STRUCTURE OF H-2DB IN COMPLEX WITH CHIMERIC GP100 | MHC, H-2DB, GLYCOPROTEIN, IMMUNE RESPONSE, MEMBRANE, MHC I, TRANSMEMBRANE, IMMUNOGLOBULIN DOMAIN, SECRETED, DISEASE MUTATION, MELANIN BIOSYNTHESIS, IMMUNE SYSTEM
5fmg:K (THR3) to (SER24) STRUCTURE AND FUNCTION BASED DESIGN OF PLASMODIUM-SELECTIVE PROTEASOME INHIBITORS | HYDROLASE, PROTEASOME, 20S, PLASMODIUM, MALARIA, INHIBITOR, DRUG DESIGN, CRYO-EM
5fmg:M (THR39) to (LEU59) STRUCTURE AND FUNCTION BASED DESIGN OF PLASMODIUM-SELECTIVE PROTEASOME INHIBITORS | HYDROLASE, PROTEASOME, 20S, PLASMODIUM, MALARIA, INHIBITOR, DRUG DESIGN, CRYO-EM
5fmg:Y (THR3) to (SER24) STRUCTURE AND FUNCTION BASED DESIGN OF PLASMODIUM-SELECTIVE PROTEASOME INHIBITORS | HYDROLASE, PROTEASOME, 20S, PLASMODIUM, MALARIA, INHIBITOR, DRUG DESIGN, CRYO-EM
5fmg:a (THR39) to (LEU59) STRUCTURE AND FUNCTION BASED DESIGN OF PLASMODIUM-SELECTIVE PROTEASOME INHIBITORS | HYDROLASE, PROTEASOME, 20S, PLASMODIUM, MALARIA, INHIBITOR, DRUG DESIGN, CRYO-EM
3nkt:A (GLU118) to (GLY134) CRYSTAL STRUCTURE OF SALICYLATE 1,2-DIOXYGENASE FROM PSEUDOAMINOBACTER SALICYLATOXIDANS ADDUCTS WITH NAPHTHOATE | BETA-SANDWICH, OXIDOREDUCTASE
3npl:A (GLU430) to (LYS449) STRUCTURE OF RU(BPY)2(A-PHEN)(K97C) P450 BM3 HEME DOMAIN, A RUTHENIUM MODIFIED P450 BM3 MUTANT | P450 BM3 HEME DOMAIN, MUTANT PROTEINS, ELECTRON TRANSFER, OXIDOREDUCTASE
3npl:B (GLU430) to (LYS449) STRUCTURE OF RU(BPY)2(A-PHEN)(K97C) P450 BM3 HEME DOMAIN, A RUTHENIUM MODIFIED P450 BM3 MUTANT | P450 BM3 HEME DOMAIN, MUTANT PROTEINS, ELECTRON TRANSFER, OXIDOREDUCTASE
3nru:C (ILE68) to (ASN94) LIGAND BINDING DOMAIN OF EPHA7 | KINASE, TRANSFERASE
3nru:H (ILE68) to (ASN94) LIGAND BINDING DOMAIN OF EPHA7 | KINASE, TRANSFERASE
4rsc:A (ASN316) to (GLY333) CRYSTAL STRUCTURE OF RPE65 IN COMPLEX WITH EMIXUSTAT AND PALMITATE | 7-BLADED BETA PROPELLER, MONOTOPIC MEMBRANE PROTEIN, NON-HEME IRON ENZYME, RETINOID ISOMERASE, SMOOTH ENDOPLASMIC RETICULUM, ISOMERASE
4rur:L (GLY10) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH THE ALKALOID INDOLO-PHAKELLIN (4) | PROTEASOME, ALKALOID, REVERSIBLE INHIBITION, DRUG DISCOVERY, HALOGEN BONDING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4rur:Z (GLY10) to (THR31) YEAST 20S PROTEASOME IN COMPLEX WITH THE ALKALOID INDOLO-PHAKELLIN (4) | PROTEASOME, ALKALOID, REVERSIBLE INHIBITION, DRUG DISCOVERY, HALOGEN BONDING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3d2u:E (VAL192) to (PRO216) STRUCTURE OF UL18, A PEPTIDE-BINDING VIRAL MHC MIMIC, BOUND TO A HOST INHIBITORY RECEPTOR | MHC CLASS I HOMOLOG, DISEASE MUTATION, GLYCATION, GLYCOPROTEIN, IMMUNE RESPONSE, IMMUNOGLOBULIN DOMAIN, MHC I, PYRROLIDONE CARBOXYLIC ACID, SECRETED, MEMBRANE, PHOSPHOPROTEIN, RECEPTOR, TRANSMEMBRANE, IMMUNE SYSTEM
3d39:B (LYS6) to (PRO32) THE COMPLEX BETWEEN TCR A6 AND HUMAN CLASS I MHC HLA-A2 WITH THE MODIFIED HTLV-1 TAX (Y5(4-FLUOROPHENYLALANINE)) PEPTIDE | HTLV-1 TAX PEPTIDE, 4-FLUOROPHENYLALANINE, MHC CLASS I, HLA-A2, T- CELL RECEPTOR A6, GLYCOPROTEIN, HOST-VIRUS INTERACTION, IMMUNE RESPONSE, MEMBRANE, MHC I, PHOSPHOPROTEIN, TRANSMEMBRANE, DISEASE MUTATION, GLYCATION, IMMUNOGLOBULIN DOMAIN, PYRROLIDONE CARBOXYLIC ACID, SECRETED, IMMUNE SYSTEM
4tr7:A (GLU351) to (ASP391) CRYSTAL STRUCTURE OF DNA POLYMERASE SLIDING CLAMP FROM MYCOBATERIUM TUBERCULOSIS | SLIDING CLAMP, PROCESSIVITY, DNA BINDING PROTEIN
5gjq:q (GLY9) to (ILE30) STRUCTURE OF THE HUMAN 26S PROTEASOME BOUND TO USP14-UBAL | PROTEIN COMPLEX, HUMAN PROTEASOME, HYDROLASE
3dhj:A (LYS6) to (PRO32) BETA 2 MICROGLOBULIN MUTANT W60C | BETA-2-MICROGLOBULIN, TRYPTOPHAN, GLYCINE, AMYLOIDOSIS, DRA, BETA FIBRILS, DISEASE MUTATION, GLYCATION, GLYCOPROTEIN, IMMUNE RESPONSE, IMMUNOGLOBULIN DOMAIN, MHC I, PYRROLIDONE CARBOXYLIC ACID, SECRETED, IMMUNE SYSTEM
3dhn:A (ARG174) to (SER193) CRYSTAL STRUCTURE OF THE PUTATIVE EPIMERASE Q89Z24_BACTN FROM BACTEROIDES THETAIOTAOMICRON. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET BTR310. | EPIMERASE, REDUCTASE, DEHYDRATASE, PF01370, Q89Z24_BACTN, NESG, BTR310, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, ISOMERASE, LYASE
4d1i:A (GLU41) to (ASN66) THE STRUCTURE OF THE GH35 BETA-GALACTOSIDASE BGL35A FROM CELLVIBRIO JAPONICUS | HYDROLASE, ENZYME-CARBOHYDRATE INTERACTION, GLYCOSIDASE INHIBITION
4d1i:B (GLU41) to (ASN66) THE STRUCTURE OF THE GH35 BETA-GALACTOSIDASE BGL35A FROM CELLVIBRIO JAPONICUS | HYDROLASE, ENZYME-CARBOHYDRATE INTERACTION, GLYCOSIDASE INHIBITION
4d1i:E (GLU41) to (ASN66) THE STRUCTURE OF THE GH35 BETA-GALACTOSIDASE BGL35A FROM CELLVIBRIO JAPONICUS | HYDROLASE, ENZYME-CARBOHYDRATE INTERACTION, GLYCOSIDASE INHIBITION
4d1i:F (GLU41) to (ASN66) THE STRUCTURE OF THE GH35 BETA-GALACTOSIDASE BGL35A FROM CELLVIBRIO JAPONICUS | HYDROLASE, ENZYME-CARBOHYDRATE INTERACTION, GLYCOSIDASE INHIBITION
4d1i:G (GLU41) to (ASN66) THE STRUCTURE OF THE GH35 BETA-GALACTOSIDASE BGL35A FROM CELLVIBRIO JAPONICUS | HYDROLASE, ENZYME-CARBOHYDRATE INTERACTION, GLYCOSIDASE INHIBITION
4d1i:H (GLU41) to (ASN66) THE STRUCTURE OF THE GH35 BETA-GALACTOSIDASE BGL35A FROM CELLVIBRIO JAPONICUS | HYDROLASE, ENZYME-CARBOHYDRATE INTERACTION, GLYCOSIDASE INHIBITION
3dnz:A (THR6) to (THR34) THERMOLYSIN BY LB NANOTEMPLATE METHOD BEFORE HIGH X-RAY DOSE ON ESRF ID14-2 BEAMLINE | HYDROLASE, METALLOPROTEINASE, CALCIUM, METAL-BINDING, METALLOPROTEASE, PROTEASE, SECRETED, ZINC, ZYMOGEN
5h8i:B (ASN222) to (PRO245) CRYSTAL STRUCTURE OF MEDICAGO TRUNCATULA N-CARBAMOYLPUTRESCINE AMIDOHYDROLASE (MTCPA) IN COMPLEX WITH N-(DIHYDROXYMETHYL)PUTRESCINE | AMIDASE, HELICAL OCTAMER, ALPHA-BETA-BETA-ALPHA SANDWICH FOLD, INTERMEDIATE, HYDROLASE
5h8k:F (GLY221) to (PRO245) CRYSTAL STRUCTURE OF MEDICAGO TRUNCATULA N-CARBAMOYLPUTRESCINE AMIDOHYDROLASE (MTCPA) C158S MUTANT | AMIDASE, HELICAL OCTAMER, ALPHA-BETA-BETA-ALPHA SANDWICH FOLD, HYDROLASE
5h8y:A (GLY104) to (PRO133) CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN MAIZE SULFITE REDUCTASE AND FERREDOXIN IN THE FORM-2 CRYSTAL | FERREDOXIN, SULFITE REDUCTASE, OXIDOREDUCTASE-ELECTRON TRANSPORT COMPLEX
5h8y:C (GLY104) to (PRO133) CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN MAIZE SULFITE REDUCTASE AND FERREDOXIN IN THE FORM-2 CRYSTAL | FERREDOXIN, SULFITE REDUCTASE, OXIDOREDUCTASE-ELECTRON TRANSPORT COMPLEX
3oq3:B (ARG195) to (ARG228) STRUCTURAL BASIS OF TYPE-I INTERFERON SEQUESTRATION BY A POXVIRUS DECOY RECEPTOR | ECTROMELIA, MOUSEPOX VIRUS, MOSCOW STRAIN, CYTOKINE DECOY RECEPTOR, VIRUS/VIRAL PROTEIN, TYPE-1 INTERFERON, SOLUBLE A/B-IFNR, VIRAL IMMUNE EVASION, IMMUNOGLOBULIN DOMAIN, STRUCTURAL GENOMICS, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID, IMMUNOGLOBULIN-LIKE, IFN-ALPHA/BETA BINDING PROTEIN, IFN-ALPHA, EXTRACELLULAR, SECRETED, CYTOKINE-VIRAL PROTEIN COMPLEX
3dtb:A (ASP311) to (VAL335) THE STRUCTURE OF RAT CYTOSOLIC PEPCK IN COMPLEX WITH PHOSPHOGLYCOLATE AND GDP | KINASE, GLUCONEOGENESIS, LYASE, DECARBOXYLASE, GTP-BINDING, NUCLEOTIDE-BINDING
3dx7:A (HIS188) to (PRO210) CRYSTAL STRUCTURE OF HLA-B*4403 PRESENTING 10MER EBV ANTIGEN | MHC, GLYCOPROTEIN, GLYCATION, HOST-VIRUS INTERACTION, IMMUNE RESPONSE, MEMBRANE, MHC I, TRANSMEMBRANE, PYRROLIDONE CARBOXYLIC ACID, DISEASE MUTATION, IMMUNE SYSTEM
3owe:L (GLY85) to (ASN116) CRYSTAL STRUCTURE OF STAPHYLOCOCCAL ENTEROTOXIN G (SEG) IN COMPLEX WITH A HIGH AFFINITY MUTANT MOUSE T-CELL RECEPTOR CHAIN | T-CELL RECEPTOR V BETA DOMAIN, COMPLEX STRUCTURE, IGG DOMAINS, B GRASP, VIRULENCE FACTORS, IMMUNE SYSTEM
4de0:A (ASP233) to (GLN254) CTX-M-9 CLASS A BETA-LACTAMASE COMPLEXED WITH COMPOUND 16 | CTX-M, HYDROLASE/HYDROLASE INHIBITOR, MOLECULAR DOCKING, FRAGMENT, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3dy4:W (GLY-1) to (SER22) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH SPIROLACTACYSTIN | PROTEASOME, INHIBITOR, PROTEIN DEGRADATION, UBIQUITIN-PROTEASOME- PATHWAY, HYDROLASE, NUCLEUS, PROTEASE, THREONINE PROTEASE, PHOSPHOPROTEIN, ZYMOGEN
4dtb:A (ILE203) to (SER224) CRYSTAL STRUCTURE OF F95Y AMINOGLYCOSIDE-2''-PHOSPHOTRANSFERASE TYPE IVA IN COMPLEX WITH GUANOSINE | AMINOGLYCOSIDE KINASE, TRANSFERASE
5hys:H (SER128) to (PRO155) STRUCTURE OF IGE COMPLEXED WITH OMALIZUMAB | IMMUNE SYSTEM
5hys:A (SER128) to (PRO155) STRUCTURE OF IGE COMPLEXED WITH OMALIZUMAB | IMMUNE SYSTEM
4duc:A (GLU430) to (LYS452) CYTOCHROME P450 BM3H-2G9 MRI SENSOR, NO LIGAND | CYTOCHROME P450, MRI CONTRAST SENSOR, DIRECTED EVOLUTION, OXIDOREDUCTASE
4duc:B (GLU430) to (LYS452) CYTOCHROME P450 BM3H-2G9 MRI SENSOR, NO LIGAND | CYTOCHROME P450, MRI CONTRAST SENSOR, DIRECTED EVOLUTION, OXIDOREDUCTASE
5ik4:A (THR2938) to (GLY2955) LAMININ A2LG45 C-FORM, APO. | EXTRACELLULAR MATRIX, LIGAND BINDING, LG DOMAIN, STRUCTURAL PROTEIN
5ik8:A (THR2938) to (GLY2955) LAMININ A2LG45 I-FORM, G6/7 BOUND. | EXTRACELLULAR MATRIX, LIGAND BINDING, LG DOMAIN, STRUCTURAL PROTEIN
5ik8:B (THR2938) to (GLY2955) LAMININ A2LG45 I-FORM, G6/7 BOUND. | EXTRACELLULAR MATRIX, LIGAND BINDING, LG DOMAIN, STRUCTURAL PROTEIN
4epd:C (ASP1431) to (SER1493) INITIAL UREASE STRUCTURE FOR RADIATION DAMAGE EXPERIMENT AT 300 K | ALPHA-BETA BARREL, NICKEL METALLOENZYME, HYDROLASE, RADIATION DAMAGE
5izl:B (ASP229) to (SER247) THE CRYSTAL STRUCTURE OF HUMAN EEFSEC IN COMPLEX WITH GDPCP | ELONGATION FACTOR, SELENOCYSTEINE, SELENOCYSTEINE TRNA, TRANSLATION, GTPASE, GDPCP, GTP
3qgo:A (THR6) to (THR34) STRUCTURE OF THERMOLYSIN IN COMPLEX WITH L-PHENYLALANINE METHYLESTER | HYDROLASE, METALLOPROTEINASE, L-PHENYLALANINE METHYL ESTER
4f7b:A (GLY207) to (TRP239) STRUCTURE OF THE LYSOSOMAL DOMAIN OF LIMP-2 | STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, SCAVENGER RECEPTOR, LIPID TRANSPORT, ENDOCYTOSIS, ATHEROSCLEROSIS, LIPOPROTEIN, CELL ADHESION
4f7b:B (GLY211) to (TRP239) STRUCTURE OF THE LYSOSOMAL DOMAIN OF LIMP-2 | STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, SCAVENGER RECEPTOR, LIPID TRANSPORT, ENDOCYTOSIS, ATHEROSCLEROSIS, LIPOPROTEIN, CELL ADHESION
4f7b:C (GLY207) to (TRP239) STRUCTURE OF THE LYSOSOMAL DOMAIN OF LIMP-2 | STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, SCAVENGER RECEPTOR, LIPID TRANSPORT, ENDOCYTOSIS, ATHEROSCLEROSIS, LIPOPROTEIN, CELL ADHESION
4f7b:D (GLY211) to (TRP239) STRUCTURE OF THE LYSOSOMAL DOMAIN OF LIMP-2 | STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, SCAVENGER RECEPTOR, LIPID TRANSPORT, ENDOCYTOSIS, ATHEROSCLEROSIS, LIPOPROTEIN, CELL ADHESION
4f7b:E (GLY211) to (TRP239) STRUCTURE OF THE LYSOSOMAL DOMAIN OF LIMP-2 | STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, SCAVENGER RECEPTOR, LIPID TRANSPORT, ENDOCYTOSIS, ATHEROSCLEROSIS, LIPOPROTEIN, CELL ADHESION
4f7b:F (GLY207) to (TRP239) STRUCTURE OF THE LYSOSOMAL DOMAIN OF LIMP-2 | STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, SCAVENGER RECEPTOR, LIPID TRANSPORT, ENDOCYTOSIS, ATHEROSCLEROSIS, LIPOPROTEIN, CELL ADHESION
4fq2:H (SER120) to (PRO147) CRYSTAL STRUCTURE OF 10-1074 FAB | IG FOLD, ANTI HIV, ANTIBODY, IMMUNE SYSTEM
5jlh:F (GLY249) to (VAL272) CRYO-EM STRUCTURE OF A HUMAN CYTOPLASMIC ACTOMYOSIN COMPLEX AT NEAR- ATOMIC RESOLUTION | CONTRACTILE FILAMENT, MUSCLE, THIN FILAMENT, CYTOSKELETON, STRUCTURAL PROTEIN, HYDROLASE COMPLEX, F-ACTIN, TROPOMYOSIN, FILAMENT, MYOSIN, PROTEIN POLYMERS, CRYO EM, CONTRACTILE PROTEIN
5jlh:G (GLY249) to (VAL272) CRYO-EM STRUCTURE OF A HUMAN CYTOPLASMIC ACTOMYOSIN COMPLEX AT NEAR- ATOMIC RESOLUTION | CONTRACTILE FILAMENT, MUSCLE, THIN FILAMENT, CYTOSKELETON, STRUCTURAL PROTEIN, HYDROLASE COMPLEX, F-ACTIN, TROPOMYOSIN, FILAMENT, MYOSIN, PROTEIN POLYMERS, CRYO EM, CONTRACTILE PROTEIN
3rhp:A (VAL409) to (GLY427) CRYSTAL STRUCTURE OF THE C707A MUTANT OF THE C-TERMINAL DOMAIN OF 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE | FDH, OXIDOREDUCTASE
3rhp:B (VAL409) to (GLY427) CRYSTAL STRUCTURE OF THE C707A MUTANT OF THE C-TERMINAL DOMAIN OF 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE | FDH, OXIDOREDUCTASE
3rhp:C (VAL409) to (GLY427) CRYSTAL STRUCTURE OF THE C707A MUTANT OF THE C-TERMINAL DOMAIN OF 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE | FDH, OXIDOREDUCTASE
4fzg:L (THR11) to (THR31) 20S YEAST PROTEASOME IN COMPLEX WITH GLIDOBACTIN | UBIQUITIN, PROTEASOME, DRUG DEVELOPMENT, INHIBITOR, NATURAL PRODUCT, N-TERMINAL NUCLEOPHILIC HYDROLASE, PROTEIN DEGRADATION, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4fzg:N (THR1) to (THR22) 20S YEAST PROTEASOME IN COMPLEX WITH GLIDOBACTIN | UBIQUITIN, PROTEASOME, DRUG DEVELOPMENT, INHIBITOR, NATURAL PRODUCT, N-TERMINAL NUCLEOPHILIC HYDROLASE, PROTEIN DEGRADATION, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4fzg:Z (THR11) to (THR31) 20S YEAST PROTEASOME IN COMPLEX WITH GLIDOBACTIN | UBIQUITIN, PROTEASOME, DRUG DEVELOPMENT, INHIBITOR, NATURAL PRODUCT, N-TERMINAL NUCLEOPHILIC HYDROLASE, PROTEIN DEGRADATION, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4fzg:b (THR1) to (THR22) 20S YEAST PROTEASOME IN COMPLEX WITH GLIDOBACTIN | UBIQUITIN, PROTEASOME, DRUG DEVELOPMENT, INHIBITOR, NATURAL PRODUCT, N-TERMINAL NUCLEOPHILIC HYDROLASE, PROTEIN DEGRADATION, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4g4e:A (ILE3) to (LEU22) CRYSTAL STRUCTURE OF THE L88A MUTANT OF HSLV FROM ESCHERICHIA COLI | ATP-DEPENDENT PROTEASE, HSLU ATPASE, HSLV PROTEASE, HSLVU, PORE MOTIF, HYDROLASE
4g4e:B (ILE3) to (LEU22) CRYSTAL STRUCTURE OF THE L88A MUTANT OF HSLV FROM ESCHERICHIA COLI | ATP-DEPENDENT PROTEASE, HSLU ATPASE, HSLV PROTEASE, HSLVU, PORE MOTIF, HYDROLASE
4g4e:C (THR2) to (LEU22) CRYSTAL STRUCTURE OF THE L88A MUTANT OF HSLV FROM ESCHERICHIA COLI | ATP-DEPENDENT PROTEASE, HSLU ATPASE, HSLV PROTEASE, HSLVU, PORE MOTIF, HYDROLASE
4g4e:D (THR2) to (LEU22) CRYSTAL STRUCTURE OF THE L88A MUTANT OF HSLV FROM ESCHERICHIA COLI | ATP-DEPENDENT PROTEASE, HSLU ATPASE, HSLV PROTEASE, HSLVU, PORE MOTIF, HYDROLASE
4g4e:E (ILE3) to (LEU22) CRYSTAL STRUCTURE OF THE L88A MUTANT OF HSLV FROM ESCHERICHIA COLI | ATP-DEPENDENT PROTEASE, HSLU ATPASE, HSLV PROTEASE, HSLVU, PORE MOTIF, HYDROLASE
4g4e:F (ILE3) to (LEU22) CRYSTAL STRUCTURE OF THE L88A MUTANT OF HSLV FROM ESCHERICHIA COLI | ATP-DEPENDENT PROTEASE, HSLU ATPASE, HSLV PROTEASE, HSLVU, PORE MOTIF, HYDROLASE
4g4e:G (ILE3) to (LEU22) CRYSTAL STRUCTURE OF THE L88A MUTANT OF HSLV FROM ESCHERICHIA COLI | ATP-DEPENDENT PROTEASE, HSLU ATPASE, HSLV PROTEASE, HSLVU, PORE MOTIF, HYDROLASE
4g4e:H (ILE3) to (LEU22) CRYSTAL STRUCTURE OF THE L88A MUTANT OF HSLV FROM ESCHERICHIA COLI | ATP-DEPENDENT PROTEASE, HSLU ATPASE, HSLV PROTEASE, HSLVU, PORE MOTIF, HYDROLASE
4g4e:I (ILE3) to (LEU22) CRYSTAL STRUCTURE OF THE L88A MUTANT OF HSLV FROM ESCHERICHIA COLI | ATP-DEPENDENT PROTEASE, HSLU ATPASE, HSLV PROTEASE, HSLVU, PORE MOTIF, HYDROLASE
4g4e:J (THR1) to (LEU22) CRYSTAL STRUCTURE OF THE L88A MUTANT OF HSLV FROM ESCHERICHIA COLI | ATP-DEPENDENT PROTEASE, HSLU ATPASE, HSLV PROTEASE, HSLVU, PORE MOTIF, HYDROLASE
4g4e:K (ILE3) to (LEU22) CRYSTAL STRUCTURE OF THE L88A MUTANT OF HSLV FROM ESCHERICHIA COLI | ATP-DEPENDENT PROTEASE, HSLU ATPASE, HSLV PROTEASE, HSLVU, PORE MOTIF, HYDROLASE
4g4e:L (THR2) to (LEU22) CRYSTAL STRUCTURE OF THE L88A MUTANT OF HSLV FROM ESCHERICHIA COLI | ATP-DEPENDENT PROTEASE, HSLU ATPASE, HSLV PROTEASE, HSLVU, PORE MOTIF, HYDROLASE
4g6f:B (SER120) to (PRO147) CRYSTAL STRUCTURE OF 10E8 FAB IN COMPLEX WITH AN HIV-1 GP41 PEPTIDE | IMMUNOGLOBULIN, MPER, ANTIBODY, IMMUNE SYSTEM
4ga9:A (LEU18) to (CYS43) CRYSTAL STRUCTURE OF RAT GALECTIN-1 IN COMPLEX WITH LACTOSE | JELLYROLL LIKE/BETA BARREL, CARBOHYDRATE-BINDING PROTEIN
4gk7:L (THR1) to (THR21) YEAST 20S PROTEASOME IN COMPLEX WITH THE SYRINGOLIN-GLIDOBACTIN CHIMERA | PROTEASOME, CANCER, PROTEIN DEGRADATION, INHIBITION, NATURAL PRODUCT DERIVATIVE, NTN-HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, 12-MEMBERED DIPEPTIDE-MACROLACTAM
4gk7:Z (THR1) to (THR21) YEAST 20S PROTEASOME IN COMPLEX WITH THE SYRINGOLIN-GLIDOBACTIN CHIMERA | PROTEASOME, CANCER, PROTEIN DEGRADATION, INHIBITION, NATURAL PRODUCT DERIVATIVE, NTN-HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, 12-MEMBERED DIPEPTIDE-MACROLACTAM
4gqs:A (THR469) to (HIS492) STRUCTURE OF HUMAN MICROSOMAL CYTOCHROME P450 (CYP) 2C19 | MONOOXYGENASE, DRUG METABOLIZING ENZYME, OXIDOREDUCTASE, HEME PROTEIN
5l5e:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l5e:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l5f:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5f:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5r:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138;V31M) AND HUMAN BETA6 (97-111; 118-133) | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5l5r:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138;V31M) AND HUMAN BETA6 (97-111; 118-133) | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5l5t:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; V31M) AND HUMAN BETA6 (97-111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 16 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5t:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; V31M) AND HUMAN BETA6 (97-111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 16 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l63:J (ILE3) to (ARG23) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 17 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l63:L (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 17 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l63:X (ILE3) to (ARG23) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 17 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l63:Z (THR11) to (THR31) YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 17 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5t0g:S (THR11) to (GLU31) STRUCTURAL BASIS FOR DYNAMIC REGULATION OF THE HUMAN 26S PROTEASOME | UBIQUITIN-PROTEASOME SYSTEM, AAA-ATPASE, HYDROLASE