2oaj:A (ALA857) to (VAL887) CRYSTAL STRUCTURE OF SRO7 FROM S. CEREVISIAE | WD40 REPEAT, BETA PROPELLER, ENDOCYTOSIS/EXOCYTOSIS COMPLEX
1n8w:B (ASN213) to (GLU246) BIOCHEMICAL AND STRUCTURAL STUDIES OF MALATE SYNTHASE FROM MYCOBACTERIUM TUBERCULOSIS | MALATE SYNTHASE, GLYOXYLATE PATHWAY, MYCOBACTERIUM TUBERCULOSIS, MALATE, COENZYME A, GLCB, GLYOXYLATE, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, TB STRUCTURAL GENOMICS CONSORTIUM, TBSGC, LYASE
1a41:A (GLU141) to (HIS177) TYPE 1-TOPOISOMERASE CATALYTIC FRAGMENT FROM VACCINIA VIRUS | TYPE 1B TOPOISOMERASE, ISOMERASE
3rwr:B (LYS565) to (GLU614) CRYSTAL STRUCTURE OF THE HUMAN XRCC4-XLF COMPLEX | COMPLEX-FILAMENT, NON-HOMOLOGOUS END-JOINING, DNA AND PROTEIN BINDING, DNA BINDING PROTEIN-PROTEIN BINDING COMPLEX
1nqy:A (THR143) to (GLY179) THE STRUCTURE OF A COA PYROPHOSPHATASE FROM D. RADIODURANS | NUDIX, PYROPHOSPHATASE, DR1184, COA, HYDROLASE
3elz:C (PRO24) to (PHE63) CRYSTAL STRUCTURE OF ZEBRAFISH ILEAL BILE ACID-BINDIN PROTEIN COMPLEXED WITH CHOLIC ACID (CRYSTAL FORM A). | ILEAL BILE ACID-BINDING PROTEIN, ZEBRAFISH (DANIO RERIO), CHOLIC ACID, LIPID-BINDING, TRANSPORT, LIPID BINDING PROTEIN
2bj0:C (VAL158) to (LYS202) CRYSTAL STRUCTURE OF ACHBP FROM BULINUS TRUNCATUS REVALS THE CONSERVED STRUCTURAL SCAFFOLD AND SITES OF VARIATION IN NICOTINIC ACETYLCHOLINE RECEPTORS | 3D-STRUCTURE, GLYCOPROTEIN, GLYCPROTEIN, IGG FOLD, IMMUNOGLOBULIN DOMAIN, PENTAMER, SIGNAL
4hnp:E (PHE19) to (LYS60) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH VINYLKETONE CARMAPHYCIN ANALOGUE VNK1 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4hnp:S (PHE19) to (LYS60) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH VINYLKETONE CARMAPHYCIN ANALOGUE VNK1 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4x6z:T (PHE20) to (LYS61) YEAST 20S PROTEASOME IN COMPLEX WITH PR-VI MODULATOR | 20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE
3s9i:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 2-4-DIOXO-4-PHENYLBUTANOIC ACID INHIBITOR | INHIBITOR COMPLEX, STRUCTURAL GENOMICS, MYCOBACTERIUM TUBERCULOSIS STRUCTURAL PROTEOMICS PROJECT, XMTB, MALATE SYNTHASE, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX
4hrc:E (PHE19) to (LYS60) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE CARMAPHYCIN ANALOGUE 3 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4hrc:S (PHE19) to (LYS60) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE CARMAPHYCIN ANALOGUE 3 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4hrd:E (PHE19) to (LYS60) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH THE NATURAL PRODUCT CARMAPHYCIN A | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4hrd:S (PHE19) to (LYS60) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH THE NATURAL PRODUCT CARMAPHYCIN A | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3faw:A (SER1056) to (ALA1100) CRYSTAL STRUCTURE OF THE GROUP B STREPTOCOCCUS PULLULANASE SAP | TIM BARREL, BETA BARREL, HYDROLASE, CELL WALL, PEPTIDOGLYCAN-ANCHOR, SECRETED
3s9z:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 4-(2-BROMOPHENYL)-2,4-DIOXOBUTANOIC ACID INHIBITOR | INHIBITOR COMPLEX, STRUCTURAL GENOMICS, MYCOBACTERIUM TUBERCULOSIS STRUCTURAL PROTEOMICS PROJECT, XMTB, MALATE SYNTHASE, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX
3fax:A (SER1056) to (ASN1099) THE CRYSTAL STRUCTURE OF GBS PULLULANASE SAP IN COMPLEX WITH MALTOTETRAOSE | TIM BARREL, ALPHA AMYLASE DOMAIN, PULLULANASE DOMAIN, HYDROLASE, CELL WALL, PEPTIDOGLYCAN-ANCHOR, SECRETED
3sad:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 4-(2-MEHTYLPHENYL)-2,4-DIOXOBUTANOIC ACID INHIBITOR | INHIBITOR COMPLEX, STRUCTURAL GENOMICS, MYCOBACTERIUM TUBERCULOSIS STRUCTURAL PROTEOMICS PROJECT, XMTB, MALATE SYNTHASE, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX
3saz:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 4-(3-BROMOPHENYL)-2,4-DIOXOBUTANOIC ACID INHIBITOR | INHIBITOR COMPLEX, STRUCTURAL GENOMICS, MYCOBACTERIUM TUBERCULOSIS STRUCTURAL PROTEOMICS PROJECT, XMTB, MALATE SYNTHASE, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX
3sb0:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 4-(2-CHLORO-6-FLUORO-3-METHYLPHENYL)-2,4-DIOXOBUTANOIC ACID INHIBITOR | INHIBITOR COMPLEX, STRUCTURAL GENOMICS, MYCOBACTERIUM TUBERCULOSIS STRUCTURAL PROTEOMICS PROJECT, XMTB, MALATE SYNTHASE, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX
4hu4:A (ARG541) to (PRO590) CRYSTAL STRUCTURE OF EAL DOMAIN OF THE E. COLI DOSP - DIMERIC FORM | EAL DOMAIN; CYCLIC DI-GMP PHOSPHODIESTERASE; TIM-BARREL; ECDOS; DIRECT OXYGEN SENSOR, SIGNALING PROTEIN,HYDROLASE
2phb:A (GLY25) to (THR54) AN ORALLY EFFICACIOUS FACTOR XA INHIBITOR | FXA COAGULATION FACTOR INHIBITOR, BLOOD CLOTTING
3sdi:E (PHE22) to (LYS65) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 20 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3sdk:S (PHE22) to (LYS65) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 34 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4i3c:B (PRO27) to (PHE69) CRYSTAL STRUCTURE OF FLUORESCENT PROTEIN UNAG N57Q MUTANT | FLUORESCENT PROTEIN, BILIRUBIN BINDING PROTEIN, LIPOCALIN, BETA BARREL, CYTOSOL
3shj:E (GLN23) to (LYS65) PROTEASOME IN COMPLEX WITH HYDROXYUREA DERIVATIVE HU10 | UBIQUITIN, DRUG DEVELOPMENT, CANCER, IMMUNOLOGY, PROTEIN DEGRADATION, UNFOLDED PROTEIN SUBSTRATES, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3shj:S (GLN23) to (LYS65) PROTEASOME IN COMPLEX WITH HYDROXYUREA DERIVATIVE HU10 | UBIQUITIN, DRUG DEVELOPMENT, CANCER, IMMUNOLOGY, PROTEIN DEGRADATION, UNFOLDED PROTEIN SUBSTRATES, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1opb:A (PHE27) to (PHE64) THE CRYSTAL STRUCTURES OF HOLO-AND APO-CELLULAR RETINOL BINDING PROTEIN II | RETINOL TRANSPORT
1opb:B (PHE27) to (ASP63) THE CRYSTAL STRUCTURES OF HOLO-AND APO-CELLULAR RETINOL BINDING PROTEIN II | RETINOL TRANSPORT
1opb:C (PHE27) to (ASP63) THE CRYSTAL STRUCTURES OF HOLO-AND APO-CELLULAR RETINOL BINDING PROTEIN II | RETINOL TRANSPORT
1p69:A (ASN520) to (TRP563) STRUCTURAL BASIS FOR VARIATION IN ADENOVIRUS AFFINITY FOR THE CELLULAR RECEPTOR CAR (P417S MUTANT) | VIRUS, VIRAL PROTEIN, VIRAL PROTEIN/RECEPTOR COMPLEX
1d8c:A (THR212) to (ASP243) MALATE SYNTHASE G COMPLEXED WITH MAGNESIUM AND GLYOXYLATE | ALPHA-BETA BARREL, TIM BARREL, GLYOXYLATE CYCLE, ENOLIZATION, CONDENSATION, CONCERTED ACID-BASE CATALYSIS, LYASE
1p8d:A (ILE309) to (SER336) X-RAY CRYSTAL STRUCTURE OF LXR LIGAND BINDING DOMAIN WITH 24(S),25- EPOXYCHOLESTEROL | LXR, EPOXYCHOLESTEROL, NUCLEAR RECEPTOR, STEROID RECEPTOR, LIVER X RECEPTOR, TRANSCRIPTION, MEMBRANE PROTEIN-PROTEIN BINDING COMPLEX
1p9k:A (LYS40) to (ALA79) THE SOLUTION STRUCTURE OF YBCJ FROM E. COLI REVEALS A RECENTLY DISCOVERED ALFAL MOTIF INVOLVED IN RNA-BINDING | ALFAL MOTIF, RNA-BINDING PROTEIN, E.COLI, MONTREAL-KINGSTON BACTERIAL STRUCTURAL GENOMICS INITIATIVE, BSGI, STRUCTURAL GENOMICS, RNA BINDING PROTEIN
4inr:E (PHE19) to (LYS60) 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:S (PHE19) to (LYS60) 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
3gj4:C (HIS30) to (THR66) CRYSTAL STRUCTURE OF HUMAN RANGDP-NUP153ZNF3 COMPLEX | G PROTEIN, GDP, RAN, NUP153, NUCLEAR PORE, ZINC FINGER, ACETYLATION, CYTOPLASM, GTP-BINDING, HOST-VIRUS INTERACTION, ISOPEPTIDE BOND, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, PROTEIN TRANSPORT, TRANSPORT, UBL CONJUGATION, DNA-BINDING, METAL-BINDING, MRNA TRANSPORT, NUCLEAR PORE COMPLEX, TRANSLOCATION, ZINC, ZINC- FINGER, TRANSPORT PROTEIN
3gj5:A (HIS30) to (THR66) CRYSTAL STRUCTURE OF HUMAN RANGDP-NUP153ZNF4 COMPLEX | G PROTEIN, GDP, RAN, NUP153, NUCLEAR PORE, ZINC FINGER, ACETYLATION, CYTOPLASM, GTP-BINDING, HOST-VIRUS INTERACTION, ISOPEPTIDE BOND, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, PROTEIN TRANSPORT, TRANSPORT, UBL CONJUGATION, DNA-BINDING, METAL-BINDING, MRNA TRANSPORT, NUCLEAR PORE COMPLEX, TRANSLOCATION, ZINC, ZINC- FINGER, TRANSPORT PROTEIN
3gj5:C (HIS30) to (THR66) CRYSTAL STRUCTURE OF HUMAN RANGDP-NUP153ZNF4 COMPLEX | G PROTEIN, GDP, RAN, NUP153, NUCLEAR PORE, ZINC FINGER, ACETYLATION, CYTOPLASM, GTP-BINDING, HOST-VIRUS INTERACTION, ISOPEPTIDE BOND, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, PROTEIN TRANSPORT, TRANSPORT, UBL CONJUGATION, DNA-BINDING, METAL-BINDING, MRNA TRANSPORT, NUCLEAR PORE COMPLEX, TRANSLOCATION, ZINC, ZINC- FINGER, TRANSPORT PROTEIN
3gj8:A (HIS30) to (THR66) CRYSTAL STRUCTURE OF HUMAN RANGDP-NUP153ZNF34 COMPLEX | G PROTEIN, GDP, RAN, NUP153, NUCLEAR PORE, ZINC FINGER, ACETYLATION, CYTOPLASM, GTP-BINDING, HOST-VIRUS INTERACTION, ISOPEPTIDE BOND, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, PROTEIN TRANSPORT, TRANSPORT, UBL CONJUGATION, DNA-BINDING, METAL-BINDING, MRNA TRANSPORT, NUCLEAR PORE COMPLEX, TRANSLOCATION, ZINC, ZINC- FINGER, TRANSPORT PROTEIN
3gj8:C (HIS30) to (THR66) CRYSTAL STRUCTURE OF HUMAN RANGDP-NUP153ZNF34 COMPLEX | G PROTEIN, GDP, RAN, NUP153, NUCLEAR PORE, ZINC FINGER, ACETYLATION, CYTOPLASM, GTP-BINDING, HOST-VIRUS INTERACTION, ISOPEPTIDE BOND, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, PROTEIN TRANSPORT, TRANSPORT, UBL CONJUGATION, DNA-BINDING, METAL-BINDING, MRNA TRANSPORT, NUCLEAR PORE COMPLEX, TRANSLOCATION, ZINC, ZINC- FINGER, TRANSPORT PROTEIN
3gpj:E (GLN23) to (LYS65) 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:S (GLN23) to (LYS65) 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
3gpw:E (PHE22) to (LYS65) CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH SALINOSPORAMIDE DERIVATIVES: IRREVERSIBLE INHIBITOR LIGAND | PROTEASOME, UBIQUITIN, CANCER THERAPY, IMMUNOLOGY, TIME- DEPENDENT ELIMINATION OF A DEFINED LEAVING GROUP, CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, THREONINE PROTEASE, ISOPEPTIDE BOND, UBL CONJUGATION, ZYMOGEN
3gpw:S (PHE22) to (LYS65) CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH SALINOSPORAMIDE DERIVATIVES: IRREVERSIBLE INHIBITOR LIGAND | PROTEASOME, UBIQUITIN, CANCER THERAPY, IMMUNOLOGY, TIME- DEPENDENT ELIMINATION OF A DEFINED LEAVING GROUP, CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, THREONINE PROTEASE, ISOPEPTIDE BOND, UBL CONJUGATION, ZYMOGEN
3tcq:A (SER107) to (LEU158) CRYSTAL STRUCTURE OF MATRIX PROTEIN VP40 FROM EBOLA VIRUS SUDAN | SEATTLE STRUCTURAL GENOMICS CENTERS FOR INFECTIOUS DISEASE, SSGCID, EBOLA, SEBOV, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, MATRIX PROTEIN, VIRAL PROTEIN
4y69:E (PHE19) to (LYS60) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4y69:S (PHE19) to (LYS60) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4y6a:E (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-PAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4y6a:S (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-PAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4y6v:E (PHE19) to (LYS60) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4j5x:B (ALA279) to (ALA312) CRYSTAL STRUCTURE OF THE SR12813-BOUND PXR/RXRALPHA LBD HETEROTETRAMER COMPLEX | PREGNANE X RECEPTOR, RETINOID X RECEPTOR ALPHA, LIGAND BINDING DOMAIN, NUCLEAR RECEPTOR, SR12813, ALPHA HELICAL SANDWICH, UNIQUE INTERMOLECULAR BETA-SHEET DIMERIZATION, XENOBIOTIC SENSING, UPREGULATION OF DRUG METABOLISM ENZYMES, RETINOIC ACID-BINDING PROTEIN
4j70:E (PHE19) to (LYS60) YEAST 20S PROTEASOME IN COMPLEX WITH THE BELACTOSIN DERIVATIVE 3E | PROTEASOME, DRUG DISCOVERY, IRREVERSIBLE INHIBITION, BETA-LACTONE, NTN HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4j70:S (PHE19) to (LYS60) YEAST 20S PROTEASOME IN COMPLEX WITH THE BELACTOSIN DERIVATIVE 3E | PROTEASOME, DRUG DISCOVERY, IRREVERSIBLE INHIBITION, BETA-LACTONE, NTN HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4y84:E (GLN20) to (LYS60) YEAST 20S PROTEASOME IN COMPLEX WITH N3-A(4,4-F2P)NLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y84:S (GLN20) to (LYS60) YEAST 20S PROTEASOME IN COMPLEX WITH N3-A(4,4-F2P)NLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8g:E (GLN20) to (LYS60) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APNLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8g:S (GLN20) to (LYS60) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APNLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8h:E (GLN20) to (LYS60) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8h:S (GLN20) to (LYS60) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8n:E (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAE- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8s:E (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8s:S (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8t:E (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8t:S (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya0:E (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA2-H116E MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya0:S (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA2-H116E MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya1:E (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA2-H116N MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ya1:S (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA2-H116N MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ya4:E (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA2-H114D MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ya4:S (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA2-H114D MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4jf5:A (SER192) to (LEU230) STRUCTURE OF OXA-23 AT PH 4.1 | BETA-LACTAMASE, HYDROLASE
1qfg:A (GLY636) to (ASN693) E. COLI FERRIC HYDROXAMATE RECEPTOR (FHUA) | TONB-DEPENDENT RECEPTOR, INTEGRAL OUTER MEMBRANE PROTEIN, FERRICHROME-IRON RECEPTOR, ACTIVE TRANSPORT, IRON TRANSPORT PROTEIN, LIPOPOLYSACCHARIDE, METAL TRANSPORT
1f2t:A (GLY35) to (LYS101) CRYSTAL STRUCTURE OF ATP-FREE RAD50 ABC-ATPASE | DNA DOUBLE-STRAND BREAK REPAIR, ABC ATPASE, REPLICATION
1f2u:A (GLY35) to (GLY105) CRYSTAL STRUCTURE OF RAD50 ABC-ATPASE | DNA DOUBLE-STRAND BREAK REPAIR, ABC-ATPASE, REPLICATION
1f2u:C (GLY35) to (LYS101) CRYSTAL STRUCTURE OF RAD50 ABC-ATPASE | DNA DOUBLE-STRAND BREAK REPAIR, ABC-ATPASE, REPLICATION
4jsq:E (PHE19) to (LYS60) 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:S (PHE19) to (LYS60) 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:E (GLN20) to (LYS60) 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:S (GLN20) to (LYS60) 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
2e8y:B (SER623) to (ALA663) CRYSTAL STRUCTURE OF PULLULANASE TYPE I FROM BACILLUS SUBTILIS STR. 168 | MULTIPLE DOMAIN, BETA-ALPHA-BARREL, ALPHA-AMYLASE-FAMILY, HYDROLASE
2e8z:B (SER623) to (ALA663) CRYSTAL STRUCTURE OF PULLULANASE TYPE I FROM BACILLUS SUBTILIS STR. 168 COMPLEXED WITH ALPHA-CYCLODEXTRIN | MULTIPLE DOMAIN, BETA-ALPHA-BARREL, ALPHA-AMYLASE-FAMILY, ALPHA- CYCLODEXTRIN, HYDROLASE
4jt0:E (GLN20) to (LYS60) 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:S (GLN20) to (LYS60) 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
2ei6:A (GLY25) to (THR54) FACTOR XA IN COMPLEX WITH THE INHIBITOR (-)-CIS-N1-[(5- CHLOROINDOL-2-YL)CARBONYL]-N2-[(5-METHYL-4,5,6,7- TETRAHYDROTHIAZOLO[5,4-C]PYRIDIN-2-YL)CARBONYL]-1,2- CYCLOHEXANEDIAMINE | GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM- BINDING
2ei7:A (GLY25) to (THR54) FACTOR XA IN COMPLEX WITH THE INHIBITOR TRANS-N1-[(5- CHLOROINDOL-2-YL)CARBONYL]-N2-[(5-METHYL-4,5,6,7- TETRAHYDROTHIAZOLO[5,4-C]PYRIDIN-2-YL)CARBONYL]-1,2- CYCLOHEXANEDIAMINE | GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM- BINDING
2ei8:A (GLY25) to (THR54) FACTOR XA IN COMPLEX WITH THE INHIBITOR (1S,2R,4S)-N1-[(5- CHLOROINDOL-2-YL)CARBONYL]-4-(N,N-DIMETHYLCARBAMOYL)-N2- [(5-METHYL-4,5,6,7-TETRAHYDROTHIAZOLO[5,4-C]PYRIDIN-2-YL) CARBONYL]-1,2-CYCLOHEXANEDIAMINE | GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM- BINDING
1fi1:A (GLY636) to (ASN693) FHUA IN COMPLEX WITH LIPOPOLYSACCHARIDE AND RIFAMYCIN CGP4832 | OUTER MEMBRANE PROTEIN; TONB-DEPENDENT RECEPTOR; FHUA; SIDEROPHORE RECEPTOR; INTEGRAL MEMBRANE PROTEIN; LIPOPOLYSACCHARIDE; RIFAMYCIN CGP 4832; BETA-BARREL; ANTIBIOTIC, METAL TRANSPORT
2exn:A (CYS42) to (PRO70) SOLUTION STRUCTURE FOR THE PROTEIN CODED BY GENE LOCUS BB0938 OF BORDETELLA BRONCHISEPTICA. NORTHEAST STRUCTURAL GENOMICS TARGET BOR11. | BETA BARREL CONTAINING FOLD; AUTOSTRUCTURE; AUTOASSIGN; NMR STRUCTURE; BOR11, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, UNKNOWN FUNCTION
2f16:E (PHE22) to (LYS65) 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:S (PHE22) to (LYS65) 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
4yw4:A (PRO139) to (SER172) STREPTOCOCCUS PNEUMONIAE SIALIDASE NANC | SIALIDASE, NEURAMINIDASE, NANC, CBM40, HYDROLASE
4yw4:B (PRO139) to (SER172) STREPTOCOCCUS PNEUMONIAE SIALIDASE NANC | SIALIDASE, NEURAMINIDASE, NANC, CBM40, HYDROLASE
4yx7:E (PRO33) to (LEU69) COMPLEX OF SPAO(SPOA1,2) AND ORGB(APAR)::T4LYSOZYME FUSION PROTEIN | TYPE III SECRETION SYSTEM, PROTEIN TRANSPORT
3un4:E (GLN20) to (LYS60) 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:S (GLN20) to (LYS60) 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:E (GLN20) to (LYS60) YEAST 20S PROTEASOME IN COMPLEX WITH PR-957 (EPOXIDE) | PROTEASOME, ANTIGEN PRESENTATION, DRUG DEVELOPMENT, PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBTIOR COMPLEX
1g5w:A (PHE27) to (SER63) SOLUTION STRUCTURE OF HUMAN HEART-TYPE FATTY ACID BINDING PROTEIN | NMR SPECTROSCOPY, PROTEIN-LIGAND INTERACTIONS, SELECTED-FIT BINDING, LIPID BINDING PROTEIN
1g65:S (GLN23) to (LYS65) 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
1ryp:F (GLN21) to (LYS61) CRYSTAL STRUCTURE OF THE 20S PROTEASOME FROM YEAST AT 2.4 ANGSTROMS RESOLUTION | MULTICATALYTIC PROTEINASE, 20S PROTEASOME, PROTEIN DEGRADATION, ANTIGEN PROCESSING, HYDROLASE, PROTEASE
1ryp:T (GLN21) to (LYS61) CRYSTAL STRUCTURE OF THE 20S PROTEASOME FROM YEAST AT 2.4 ANGSTROMS RESOLUTION | MULTICATALYTIC PROTEINASE, 20S PROTEASOME, PROTEIN DEGRADATION, ANTIGEN PROCESSING, HYDROLASE, PROTEASE
2fgz:A (ASP966) to (ILE1013) CRYSTAL STRUCTURE ANALYSIS OF APO PULLULANASE FROM KLEBSIELLA PNEUMONIAE | MULTIPLE DOMAIN, BETA-ALPHA-BARREL, ALPHA-AMYLASE-FAMILY, HYDROLASE
2fh6:A (ASP966) to (ILE1013) CRYSTAL STRUCTURE ANALYSIS OF KLEBSIELLA PNEUMONIAE PULLULANASE COMPLEXED WITH GLUCOSE | MULTIPLE DOMAIN, BETA-ALPHA-BARREL, ALPHA-AMYLASE-FAMILY, COMPLEX WITH GLUCOSE, HYDROLASE
2fh8:A (ASP966) to (ILE1013) CRYSTAL STRUCTURE ANALYSIS OF KLEBSIELLA PNEUMONIAE PULLULANASE COMPLEXED WITH ISOMALTOSE | MULTIPLE DOMAIN, BETA-ALPHA-BARREL, ALPHA-AMYLASE-FAMILY, COMPLEX WITH ISOMALTOSE, HYDROLASE
2fhc:A (ASP966) to (ILE1013) CRYSTAL STRUCTURE ANALYSIS OF KLEBSIELLA PNEUMONIAE PULLULANASE COMPLEXED WITH MALTOTRIOSE | MULTIPLE DOMAIN, BETA-ALPHA-BARREL, ALPHA-AMYLASE-FAMILY, COMPLEX WITH MALTOTRIOSE, HYDROLASE
2fhf:A (ASP966) to (ILE1013) CRYSTAL STRUCTURE ANALYSIS OF KLEBSIELLA PNEUMONIAE PULLULANASE COMPLEXED WITH MALTOTETRAOSE | MULTIPLE DOMAIN, BETA-ALPHA-BARREL, ALPHA-AMYLASE-FAMILY, COMPLEX WITH MALTOTETRAOSE, HYDROLASE
2ftb:A (ASN29) to (PHE62) CRYSTAL STRUCTURE OF AXOLOTL (AMBYSTOMA MEXICANUM) LIVER BILE ACID-BINDING PROTEIN BOUND TO OLEIC ACID | LIVER BILE ACID-BINDING PROTEIN, LIVER BASIC FATTY ACID- BINDING PROTEIN, AXOLOTL, OLEIC ACID, BABP, LB-FABP, LIPID BINDING PROTEIN
4koo:B (LYS169) to (PRO210) CRYSTAL STRUCTURE OF WHY1 FROM ARABIDOPSIS THALIANA | PLANT, WHIRLY, SINGLE-STRANDED DNA BINDING PROTEIN, DNA BINDING PROTEIN
4koo:C (LYS169) to (PRO210) CRYSTAL STRUCTURE OF WHY1 FROM ARABIDOPSIS THALIANA | PLANT, WHIRLY, SINGLE-STRANDED DNA BINDING PROTEIN, DNA BINDING PROTEIN
4koo:D (LYS169) to (PRO210) CRYSTAL STRUCTURE OF WHY1 FROM ARABIDOPSIS THALIANA | PLANT, WHIRLY, SINGLE-STRANDED DNA BINDING PROTEIN, DNA BINDING PROTEIN
4koq:A (LYS173) to (PRO214) CRYSTAL STRUCTURE OF WHY3 FROM ARABIDOPSIS THALIANA | PLANT, WHIRLY, SINGLE-STRANDED DNA BINDING PROTEIN, DNA BINDING PROTEIN
3hye:E (PHE22) to (LYS65) CRYSTAL STRUCTURE OF 20S PROTEASOME IN COMPLEX WITH HYDROXYLATED SALINOSPORAMIDE | CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, PROTEASOME, THREONINE PROTEASE, ISOPEPTIDE BOND, UBL CONJUGATION, ZYMOGEN
3hye:S (PHE22) to (LYS65) CRYSTAL STRUCTURE OF 20S PROTEASOME IN COMPLEX WITH HYDROXYLATED SALINOSPORAMIDE | CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, PROTEASOME, THREONINE PROTEASE, ISOPEPTIDE BOND, UBL CONJUGATION, ZYMOGEN
3i2m:X (LYS27) to (ASN64) THE CRYSTAL STRUCTURE OF PF-8, THE DNA POLYMERASE ACCESSORY SUBUNIT FROM KAPOSI S SARCOMA-ASSOCIATED HERPESVIRUS | PROCESSIVITY, REPLICATION
1smp:A (SER413) to (ILE459) CRYSTAL STRUCTURE OF A COMPLEX BETWEEN SERRATIA MARCESCENS METALLO-PROTEASE AND AN INHIBITOR FROM ERWINIA CHRYSANTHEMI | COMPLEX (METALLOPROTEASE/INHIBITOR)
4ktr:A (ALA26) to (THR60) CRYSTAL STRUCTURE OF 2-O-ALPHA-GLUCOSYLGLYCEROL PHOSPHORYLASE IN COMPLEX WITH ISOFAGOMINE AND GLYCEROL | (ALPHA/ALPHA)6 BARREL, PHOSPHORYLASE, TRANSFERASE
3vcf:B (LEU219) to (PHE249) SSV1 INTEGRASE C-TERMINAL CATALYTIC DOMAIN (174-335AA) | CATALYZES SITE-SPECIFIC INTEGRATION, RECOMBINATION
2g7b:A (VAL26) to (PHE65) CRYSTAL STRUCTURE OF THE R132K:R111L:L121E MUTANT OF CELLULAR RETINOIC ACID BINDING PROTEIN TYPE II IN COMPLEX WITH ALL-TRANS-RETINAL AT 1.18 ANGSTROMS RESOLUTION | CRABPII, RETINOIC ACID, RETINOIDS, BETA BARREL, CRYSTALLOGRAPHY, X-RAY, HIGH RESOLUTION, SCHIFF BASE, PROTONATED SCHIFF BASE, RETINAL, TRANSPORT PROTEIN
1h2c:A (SER107) to (LEU158) EBOLA VIRUS MATRIX PROTEIN VP40 N-TERMINAL DOMAIN IN COMPLEX WITH RNA (HIGH-RESOLUTION VP40[55-194] VARIANT). | VIRUS/VIRAL PROTEIN, FILOVIRUS, EBOLA VIRUS, MATRIX PROTEIN VP40, ASSEMBLY, BUDDING
1h2d:B (SER107) to (LEU158) EBOLA VIRUS MATRIX PROTEIN VP40 N-TERMINAL DOMAIN IN COMPLEX WITH RNA (LOW-RESOLUTION VP40[31-212] VARIANT). | VIRUS/VIRAL PROTEIN, FILOVIRUS, EBOLA VIRUS, MATRIX PROTEIN VP40, ASSEMBLY, BUDDING
3iez:B (GLN1499) to (ILE1537) CRYSTAL STRUCTURE OF THE RASGAP C-TERMINAL (RGC) DOMAIN OF IQGAP2 | GAP, STRUCTURAL GENOMICS CONSORTIUM, SGC, ALTERNATIVE SPLICING, CALMODULIN-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SIGNALING PROTEIN
2gpl:E (PHE22) to (LYS65) TMC-95 BASED BIPHENYL-ETHER MACROCYCLES: SPECIFIC PROTEASOME INHIBITORS | PROTEASOMAL SUBUNIT FOLD REPRESENTS AN ANTIPARALLEL BETA- SHEET FLANKED BY HELICES; NTN-HYDROLASE
2gpl:S (PHE22) to (LYS65) TMC-95 BASED BIPHENYL-ETHER MACROCYCLES: SPECIFIC PROTEASOME INHIBITORS | PROTEASOMAL SUBUNIT FOLD REPRESENTS AN ANTIPARALLEL BETA- SHEET FLANKED BY HELICES; NTN-HYDROLASE
2gq3:B (ASN213) to (GLU246) MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH MAGNESIUM, MALATE, AND COENZYME A | TIM BARREL, COENZYME A, TRANSFERASE
2grx:A (GLY636) to (ASN693) CRYSTAL STRUCTURE OF TONB IN COMPLEX WITH FHUA, E. COLI OUTER MEMBRANE RECEPTOR FOR FERRICHROME | BETA BARREL, OUTER MEMBRANE, HETEROCOMPLEX, INTER-PROTEIN BETA SHEET, PROTEIN-PROTEIN, METAL TRANSPORT
2grx:B (GLY636) to (ASN693) CRYSTAL STRUCTURE OF TONB IN COMPLEX WITH FHUA, E. COLI OUTER MEMBRANE RECEPTOR FOR FERRICHROME | BETA BARREL, OUTER MEMBRANE, HETEROCOMPLEX, INTER-PROTEIN BETA SHEET, PROTEIN-PROTEIN, METAL TRANSPORT
4ld8:A (SER107) to (LEU158) CRYSTAL STRUCTURE OF DIMERIC SUDAN VIRUS VP40 | VIRAL MATRIX PROTEIN, MATRIX ASSEMBLY, VIRAL BUDDING, VIRAL TRANSCRIPTION REGULATION, VIRAL PROTEIN
4ldb:A (SER107) to (LEU158) CRYSTAL STRUCTURE OF EBOLA VIRUS VP40 DIMER | VIRAL MATRIX PROTEIN, VIRAL BUDDING, ASSEMBLY, VIRAL TRANSCRIPTION REGULATION, VIRAL PROTEIN
4ldb:B (SER107) to (LEU158) CRYSTAL STRUCTURE OF EBOLA VIRUS VP40 DIMER | VIRAL MATRIX PROTEIN, VIRAL BUDDING, ASSEMBLY, VIRAL TRANSCRIPTION REGULATION, VIRAL PROTEIN
4ldb:C (SER107) to (LEU158) CRYSTAL STRUCTURE OF EBOLA VIRUS VP40 DIMER | VIRAL MATRIX PROTEIN, VIRAL BUDDING, ASSEMBLY, VIRAL TRANSCRIPTION REGULATION, VIRAL PROTEIN
4ldb:D (SER107) to (LEU158) CRYSTAL STRUCTURE OF EBOLA VIRUS VP40 DIMER | VIRAL MATRIX PROTEIN, VIRAL BUDDING, ASSEMBLY, VIRAL TRANSCRIPTION REGULATION, VIRAL PROTEIN
4ldd:B (SER107) to (LEU158) CRYSTAL STRUCTURE OF EBOLA VIRUS VP40 HEXAMER | EBOLAVIRUS MATRIX ASSEMBLY, VIRAL PROTEIN
4ldd:C (SER107) to (LEU158) CRYSTAL STRUCTURE OF EBOLA VIRUS VP40 HEXAMER | EBOLAVIRUS MATRIX ASSEMBLY, VIRAL PROTEIN
4ldd:A (SER107) to (LEU158) CRYSTAL STRUCTURE OF EBOLA VIRUS VP40 HEXAMER | EBOLAVIRUS MATRIX ASSEMBLY, VIRAL PROTEIN
4ldm:A (SER107) to (LEU158) CRYSTAL STRUCTURE OF AN RNA-FREE VP40 OCTAMERIC RING | EBOLAVIRUS MATRIX PROTEIN, RNA BINDING RING, VIRAL TRANSCRIPTION REGULATION, VIRAL PROTEIN
2gys:B (THR3) to (ASN42) 2.7 A STRUCTURE OF THE EXTRACELLULAR DOMAINS OF THE HUMAN BETA COMMON RECEPTOR INVOLVED IN IL-3, IL-5, AND GM-CSF SIGNALLING | DIMER OF INTERLOCKING CHAINS OF FIBRONECTIN-III DOMAINS, FOUR FIBRONECTIN-III DOMAINS PER CHAIN, SIGNALING PROTEIN, CYTOKINE
3vnf:A (PRO13) to (ASN50) STRUCTURE OF THE EBOLAVIRUS PROTEIN VP24 FROM SUDAN | EBOLAVIRUS, INTERFERON ANTAGONIST, VP24, STAT1, ZAIRE, SUDAN, RESTON, VP35, KARYOPHERIN ALPHA, IFN RESPONSE PATHWAY, VIRAL PROTEIN
4zzg:F (GLN21) to (LYS61) YEAST 20S PROTEASOME IN COMPLEX WITH BLM-PEP ACTIVATOR | 20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE
4zzg:T (GLN21) to (LYS61) YEAST 20S PROTEASOME IN COMPLEX WITH BLM-PEP ACTIVATOR | 20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE
3vst:C (ALA165) to (ASN200) THE COMPLEX STRUCTURE OF XYLC WITH TRIS | GLYCOSIDE HYDROLASE, BETA-XYLOSIDASE, PRODUCT INHIBITION, HYDROLASE
4lp7:C (PRO45) to (ASN91) CRYSTAL STRUCTURE OF THE HUMAN METAPNEUMOVIRUS MATRIX PROTEIN | TWISTED BETA SANDWICH, VIRAL MATRIX, LIPID BINDING, CALCIUM BINDING PROTEIN
4lqi:E (PHE22) to (LYS65) YEAST 20S PROTEASOME IN COMPLEX WITH VIBRALACTONE | BETA-LACTONE, INHIBITOR, NATURAL PRODUCT, TARGET IDENTIFICATION, NTN- PROTEASE, CELLULAR PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4lqi:S (PHE22) to (LYS65) YEAST 20S PROTEASOME IN COMPLEX WITH VIBRALACTONE | BETA-LACTONE, INHIBITOR, NATURAL PRODUCT, TARGET IDENTIFICATION, NTN- PROTEASE, CELLULAR PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ltc:E (PHE19) to (LYS60) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH ENONE CARMAPHYCIN ANALOGUE 6 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ltc:S (PHE19) to (LYS60) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH ENONE CARMAPHYCIN ANALOGUE 6 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1u5i:A (ASN117) to (ASP155) CRYSTAL STRUCTURE ANALYSIS OF RAT M-CALPAIN MUTANT LYS10 THR | CALPAIN, SULFHYDRYL PROTEASE, CRYSTAL STRUCTURE, HYDROLASE
1uqw:B (GLY152) to (LYS180) CRYSTAL STRUCTURE OF YLIB PROTEIN FROM ESCHERICHIA COI | ZN BINDING PROTEIN, TRANSPORT, LIPOPROTEIN, BACTERIAL TARGETS AT IGS-CNRS, FRANCE, BIGS, STRUCTURAL GENOMICS
1iv8:A (ASP135) to (PRO162) CRYSTAL STRUCTURE OF MALTOOLIGOSYL TREHALOSE SYNTHASE | TREHALOSE SYNTHASE, BETA ALPHA BARREL, INTRAMOLECULAR TRANSGLUCOSYLATION, ISOMERASE
1v7v:A (ASN166) to (PHE204) CRYSTAL STRUCTURE OF VIBRIO PROTEOLYTICUS CHITOBIOSE PHOSPHORYLASE | BETA-SANDWICH, (ALPHA/ALPHA)6 BARREL, TRANSFERASE
1v7w:A (ASN166) to (PHE204) CRYSTAL STRUCTURE OF VIBRIO PROTEOLYTICUS CHITOBIOSE PHOSPHORYLASE IN COMPLEX WITH GLCNAC | BETA-SANDWICH, (ALPHA/ALPHA)6 BARREL, TRANSFERASE
1v7x:A (ASN166) to (PHE204) CRYSTAL STRUCTURE OF VIBRIO PROTEOLYTICUS CHITOBIOSE PHOSPHORYLASE IN COMPLEX WITH GLCNAC AND SULFATE | BETA-SANDWICH, (ALPHA/ALPHA)6 BARREL, TRANSFERASE
1jd2:E (PHE22) to (LYS65) CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME:TMC-95A COMPLEX: A NON- COVALENT PROTEASOME INHIBITOR | BETA-SANDWICH, PROTEASOME:INHIBITOR COMPLEX, HYDROLASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3wtf:A (THR73) to (PRO113) STRUCTURE OF PAXX | DNA REPAIR, SCAFFOLD, IMMUNE SYSTEM
2j94:A (GLY25) to (THR54) CRYSTAL STRUCTURE OF A HUMAN FACTOR XA INHIBITOR COMPLEX | GAMMA- CARBOXYGLUTAMIC ACID, SERINE PROTEASE, EGF-LIKE DOMAIN, BLOOD COAGULATION, POLYMORPHISM, GLYCOPROTEIN, HYDROXYLATION, GAMMA-CARBOXYGLUTAMIC ACID, CALCIUM, ZYMOGEN, COMPLEX, PROTEASE, HYDROLASE
5az4:B (GLU667) to (PHE717) CRYSTAL STRUCTURE OF A 79KDA FRAGMENT OF FLGE, THE HOOK PROTEIN FROM CAMPYLOBACTER JEJUNI | FLAGELLUM, HOOK, UNIVERSAL JOINT, MOTOR PROTEIN
1w1w:A (SER40) to (ILE121) SC SMC1HD:SCC1-C COMPLEX, ATPGS | COHESIN, CHROMOSOME SEGREGATION, CELL ADHESION, KLEISIN, MITOSIS, CELL CYCLE
1w1w:D (GLY38) to (ILE121) SC SMC1HD:SCC1-C COMPLEX, ATPGS | COHESIN, CHROMOSOME SEGREGATION, CELL ADHESION, KLEISIN, MITOSIS, CELL CYCLE
1kac:A (ASN520) to (TRP563) KNOB DOMAIN FROM ADENOVIRUS SEROTYPE 12 IN COMPLEX WITH DOMAIN 1 OF ITS CELLULAR RECEPTOR CAR | ADHESION PROTEIN RECEPTOR COMPLEX, VIRAL PROTEIN/RECEPTOR COMPLEX
2k62:A (ILE28) to (THR63) NMR SOLUTION STRUCTURE OF THE SUPRAMOLECULAR ADDUCT BETWEEN A LIVER CYTOSOLIC BILE ACID BINDING PROTEIN AND A BILE ACID-BASED GD(III)-CHELATE | HEPATOSPECIFIC CONTRAST AGENT, HADDOCK, GD(III) BILE ACID ADDUCT, ACETYLATION, CYTOPLASM, LIPID-BINDING, TRANSPORT, LIPID BINDING PROTEIN
1wu1:A (GLY25) to (THR54) FACTOR XA IN COMPLEX WITH THE INHIBITOR 4-[(5-CHLOROINDOL-2-YL) SULFONYL]-2-(2-METHYLPROPYL)-1-[[5-(PYRIDIN-4-YL) PYRIMIDIN-2- YL]CARBONYL]PIPERAZINE | GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM-BINDING
1kgl:A (VAL27) to (PHE64) SOLUTION STRUCTURE OF CELLULAR RETINOL BINDING PROTEIN TYPE- I IN COMPLEX WITH ALL-TRANS-RETINOL | BETA BARREL, RETINOID CARRIER, HOLO FORM, NMR SPECTROSCOPY, 15N ISOTOPE ENRICHMENT, LIPID BINDING PROTEIN
5c7v:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 1H-PYRROLE-2-CARBOXYLIC ACID | FRAGMENT, COMPLEX, INHIBITOR, TRANSFERASE
5c9u:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 2-(2-(2,4-DICHLOROPHENYL)HYDRAZINYL)-2-OXOACETIC ACID | FRAGMENT, COMPLEX, ACETYL-TRANSFERASE, TRANSFERASE
5c9w:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH (Z)-N-(2-BROMOPHENYL)-2-(HYDROXYIMINO)ACETAMIDE | FRAGMENT, COMPLEX, OXIDOREDUCTASE
5cak:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 2-HYDROXY-3-(1H-INDOL-3-YL)PROPANOIC ACID | FRAGMENT, COMPLEX, ACETYLTRANSFERASE, TRANSFERASE
5cbb:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 5-(3H-INDOL-3-YLIDENE)-2,5-DIHYDRO-1H-PYRAZOLE-3- CARBOXYLATE | FRAGMENT, COMPLEX, ACETYLTRANSFERASE, TRANSFERASE
5cbi:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 5-CHLORO-2-HYDROXYBENZONITRILE | FRAGMENT, COMPLEX, ACETYLTRANSFERASE, TRANSFERASE
5cbj:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 3-(PHENYLTHIO)ACRYLIC ACID | COMPLEX, FRAGMENT, TRANSFERASE
5cc3:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 6-BROMO-1H-INDOLE-2-CARBOXYLIC ACID | COMPLEX, FRAGMENT, TRANSFERASE
5cc5:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 1H-INDOLE-3-CARBOXYLIC ACID | COMPLEX, FRAGMENT, TRANSFERASE
5cc7:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 1H-INDOLE-6-CARBOXYLIC ACID | COMPLEX, FRAGMENT, TRANSFERASE
5ccz:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 3-(4-FLUOROPHENYL)-4-METHYL-1H-PYRAZOL-5-AMINE | FRAGMENT, COMPLEX, ACETYLTRANSFERASE, TRANSFERASE
2nub:A (LYS120) to (PRO165) STRUCTURE OF AQUIFEX AEOLICUS ARGONUATE | RNASEH, ARGONAUTE, RIBONUCLEASE, RNAI, RISC, SIGNALING PROTEIN
2yoc:A (ASP954) to (ILE1001) CRYSTAL STRUCTURE OF PULA FROM KLEBSIELLA OXYTOCA | HYDROLASE, GLYCOSYL HYDROLASE, TYPE 2 SECRETION SYSTEMS
2yoc:B (ASP954) to (ILE1001) CRYSTAL STRUCTURE OF PULA FROM KLEBSIELLA OXYTOCA | HYDROLASE, GLYCOSYL HYDROLASE, TYPE 2 SECRETION SYSTEMS
5cew:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 2-(PYRIDIN-4-YL)THIAZOLIDINE-4-CARBOXYLIC ACID | COMPLEX, FRAGMENT, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
5cjm:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 4H-THIENO[3,2-B]PYRROLE-5-CARBOXYLIC ACID | FRAGMENT, COMPLEX, ACETYLTRANSFERASE, TRANSFERASE
2z0l:A (GLY103) to (PRO147) CRYSTAL STRUCTURE OF EBV-DNA POLYMERASE ACCESSORY PROTEIN BMRF1 | ALPHA/BETA PROTEIN, ACTIVATOR, DNA-BINDING, EARLY PROTEIN, NUCLEUS, TRANSCRIPTION, TRANSCRIPTION REGULATION, REPLICATION, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI
2zcy:E (GLN23) to (LYS65) YEAST 20S PROTEASOME:SYRINGOLIN A-COMPLEX | ALPHA/BETA SANDWICH, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, PROTEASOME, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN
2zcy:S (GLN23) to (LYS65) YEAST 20S PROTEASOME:SYRINGOLIN A-COMPLEX | ALPHA/BETA SANDWICH, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, PROTEASOME, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN
1m4z:A (THR4) to (GLY51) CRYSTAL STRUCTURE OF THE N-TERMINAL BAH DOMAIN OF ORC1P | DNA REPLICATION, TRANSCRIPTIONAL SILENCING, CHROMATIN, BAH DOMAIN, GENE REGULATION
4aby:A (GLU62) to (ARG124) CRYSTAL STRUCTURE OF DEINOCOCCUS RADIODURANS RECN HEAD DOMAIN | HYDROLASE, DNA REPAIR, DOUBLE STRAND BREAK REPAIR, ATPASE, NUCLEOTIDE BINDING DOMAIN
4aby:C (GLU62) to (ARG124) CRYSTAL STRUCTURE OF DEINOCOCCUS RADIODURANS RECN HEAD DOMAIN | HYDROLASE, DNA REPAIR, DOUBLE STRAND BREAK REPAIR, ATPASE, NUCLEOTIDE BINDING DOMAIN
4aby:D (GLU62) to (ALA123) CRYSTAL STRUCTURE OF DEINOCOCCUS RADIODURANS RECN HEAD DOMAIN | HYDROLASE, DNA REPAIR, DOUBLE STRAND BREAK REPAIR, ATPASE, NUCLEOTIDE BINDING DOMAIN
1mdw:B (GLU118) to (ASP155) CRYSTAL STRUCTURE OF CALCIUM-BOUND PROTEASE CORE OF CALPAIN II REVEALS THE BASIS FOR INTRINSIC INACTIVATION | CALPAIN CYSTEINE PROTEASE FOLD, TWO COOPERATIVE CALCIUM SITES, HELIX INSTABILITY, TRYPTOPHAN-BASED ACTIVE SITE BLOCKAGE, HYDROLASE
4ad8:A (GLU62) to (SER126) CRYSTAL STRUCTURE OF A DELETION MUTANT OF DEINOCOCCUS RADIODURANS RECN | DNA BINDING PROTEIN, DNA REPAIR, ATPASE DOMAIN
5d0t:E (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA5-D166N MUTANT IN COMPLEX WITH MG132 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0t:S (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA5-D166N MUTANT IN COMPLEX WITH MG132 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0w:E (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA5-T1S MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5d0w:S (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA5-T1S MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5d0x:E (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA5-T1S MUTANT IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0x:S (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA5-T1S MUTANT IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
1mx8:A (ASN26) to (GLY67) TWO HOMOLOGOUS RAT CELLULAR RETINOL-BINDING PROTEINS DIFFER IN LOCAL STRUCTURE AND FLEXIBILITY | BETA-BARREL, HELIX-TURN-HELIX, VITAMIN A, RETONOL BINDING, TRANSPORT, LIPID BINDING PROTEIN
5dac:A (THR41) to (THR113) ATP-GAMMA-S BOUND RAD50 FROM CHAETOMIUM THERMOPHILUM IN COMPLEX WITH DNA | ATPASE, ATPYS BOUND, HYDROLASE
5dac:B (THR41) to (THR113) ATP-GAMMA-S BOUND RAD50 FROM CHAETOMIUM THERMOPHILUM IN COMPLEX WITH DNA | ATPASE, ATPYS BOUND, HYDROLASE
3kzt:A (GLY112) to (PRO148) CRYSTAL STRUCTURE OF PROTEIN OF UNKNOWN FUNCTION (NP_812423.1) FROM BACTEROIDES THETAIOTAOMICRON VPI-5482 AT 2.10 A RESOLUTION | PROTEIN OF UNKNOWN FUNCTION, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, UNKNOWN FUNCTION
5dki:E (PHE19) to (LYS60) YEAST 20S PROTEASOME IN COMPLEX WITH ALKYNE-PI | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, TARGET DELIVERY, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5dki:S (PHE19) to (LYS60) YEAST 20S PROTEASOME IN COMPLEX WITH ALKYNE-PI | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, TARGET DELIVERY, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5dkj:E (PHE19) to (LYS60) YEAST 20S PROTEASOME IN COMPLEX WITH OCTREOTIDE-PI | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, TARGET DELIVERY, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5dkj:S (PHE19) to (LYS60) YEAST 20S PROTEASOME IN COMPLEX WITH OCTREOTIDE-PI | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, TARGET DELIVERY, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5drc:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 2-HYDROXY-4-(1H-INDOL-3-YL)-4-OXOBUT-2-ENOIC ACID | ACETYLTRANSFERASE, TRANSFERASE
5dri:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 2-HYDROXY-4-(1H-INDOL-5-YL)-4-OXOBUT-2-ENOIC ACID INHIBITOR | ACETYLTRANSFERASE, TRANSFERASE
5dx7:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 5-(5-CHLOROTHIOPHEN-2-YL)ISOXAZOLE-3-CARBOXYLIC ACID | ACETYLTRANSFERASE, TRANSFERASE
4q1s:E (PHE19) to (LYS60) YEAST 20S PROTEASOME IN COMPLEX WITH KENDOMYCIN | PROTEASOME, NATURAL PRODUCT, QUINONE METHIDE, COVALENT BINDING, EXOSITE, HYDROLASE-TOXIN COMPLEX
4q1s:S (PHE19) to (LYS60) YEAST 20S PROTEASOME IN COMPLEX WITH KENDOMYCIN | PROTEASOME, NATURAL PRODUCT, QUINONE METHIDE, COVALENT BINDING, EXOSITE, HYDROLASE-TOXIN COMPLEX
4q46:A (SER444) to (ASN484) THE SECOND STRUCTURE OF INFLUENZA B PB2 CAP-BINDING DOMAIN COMPLEX WITH GDP | CAP BINDING, VIRAL PROTEIN
4q6u:A (HIS0) to (LYS26) CRYSTAL STRUCTURE OF A PUTATIVE UNCHARACTERIZED PROTEIN FROM MYCOBACTERIUM TUBERCULOSIS | SEATTLE STRUCTURAL GENOICS FOR INFECTIOUS DISEASE, MYCOBACTERIUM TUBERCULOSIS, STRUCTURAL GENOMICS, SSGCID, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, UNKNOWN FUNCTION
3auy:A (SER39) to (LYS99) CRYSTAL STRUCTURE OF RAD50 BOUND TO ADP | DNA REPAIR, ABC TRANSPORTER ATPASE DOMAIN-LIKE, P-LOOP CONTAINING NUCLEOSIDE TRIPHOSPHATE HYDROLASES, MRE11, RECOMBINATION
3auy:B (SER39) to (LYS99) CRYSTAL STRUCTURE OF RAD50 BOUND TO ADP | DNA REPAIR, ABC TRANSPORTER ATPASE DOMAIN-LIKE, P-LOOP CONTAINING NUCLEOSIDE TRIPHOSPHATE HYDROLASES, MRE11, RECOMBINATION
5ecv:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 2-HYDROXY-4-(4-METHYL-1H-INDOL-5-YL)-4-OXOBUT-2-ENOIC ACID | TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4qgw:B (VAL26) to (ASN64) CRYSTAL STURCTURE OF THE R132K:R111L:L121D MUTANT OF CELLULAR RETINOIC ACID BINDING PROTEINII COMPLEXED WITH A SYNTHETIC LIGAND (MEROCYANINE) AT 1.77 ANGSTROM RESOLUTION | PROTEIN ENGINEERING, PROTEIN FLUORESCENCE, MEROCYANINE DYES FOR FLUORESCENT PROTEIN LABELING, FLUORESCENT PROTEIN TAG, MEROCYANINE PROTONATED SCHIFF BASE IMINIUM, PROTEIN BINDING
4qls:E (GLN20) to (LYS60) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 11 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qls:S (GLN20) to (LYS60) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 11 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlu:E (PHE19) to (LYS60) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 9 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlu:S (PHE19) to (LYS60) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 9 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3mg4:E (PHE22) to (LYS65) STRUCTURE OF YEAST 20S PROTEASOME WITH COMPOUND 1 | 20S PROTEASOME, HYDROLASE
3mg4:S (PHE22) to (LYS65) STRUCTURE OF YEAST 20S PROTEASOME WITH COMPOUND 1 | 20S PROTEASOME, HYDROLASE
3mg6:S (GLN23) to (LYS65) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 6 | 20S PROTEASOME, HYDROLASE
3mg8:S (GLN23) to (LYS65) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 16 | 20S PROTEASOME, HYDROLASE
4be7:B (LEU129) to (LYS168) MUTANT (K220R) OF THE HSDR SUBUNIT OF THE ECOR124I RESTRICTION ENZYME IN COMPLEX WITH ATP | HYDROLASE, DNA RESTRICTION, DNA MODIFICATION
4qux:E (PHE19) to (LYS60) YCP BETA5-A49T-MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qux:S (PHE19) to (LYS60) YCP BETA5-A49T-MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4quy:E (PHE19) to (LYS60) YCP BETA5-A49S-MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4quy:S (PHE19) to (LYS60) YCP BETA5-A49S-MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv6:E (GLN20) to (LYS60) YCP BETA5-A49V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv6:S (GLN20) to (LYS60) YCP BETA5-A49V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv9:E (GLN20) to (LYS60) YCP BETA5-C63F MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv9:S (GLN20) to (LYS60) YCP BETA5-C63F MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qvl:E (PHE19) to (LYS60) YCP IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvl:S (PHE19) to (LYS60) YCP IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvm:E (PHE19) to (LYS60) YCP BETA5-M45A MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvm:S (PHE19) to (LYS60) YCP BETA5-M45A MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvw:E (PHE19) to (LYS60) YCP BETA5-A49S-MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4qvw:S (PHE19) to (LYS60) YCP BETA5-A49S-MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4qw0:E (PHE19) to (LYS60) YCP BETA5-A49T-A50V-DOUBLE MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw0:S (PHE19) to (LYS60) YCP BETA5-A49T-A50V-DOUBLE MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r02:E (PHE19) to (LYS60) YCP IN COMPLEX WITH BSC4999 (ALPHA-KETO PHENYLAMIDE) | CANCER, PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, REVERSIBLE COVALENT LIGAND, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3n1k:A (SER145) to (PRO186) CRYSTAL STRUCTURE OF A STWHY2-CERE32 COMPLEX | SINGLE-STRANDED DNA BINDING PROTEIN, PLANT, WHIRLY, PROTEIN-DNA COMPLEX, DNA BINDING PROTEIN-DNA COMPLEX
3n1l:A (SER145) to (PRO186) CRYSTAL STRUCTURE OF A STWHY2-RCERE32 COMPLEX | SINGLE-STRANDED DNA BINDING PROTEIN, PLANT, WHIRLY, PROTEIN-DNA COMPLEX, DNA BINDING PROTEIN-DNA COMPLEX
5f9t:B (PRO139) to (SER172) CRYSTAL STRUCTURE OF STREPTOCOCCUS PNEUMONIAE NANC, COVALENT COMPLEX WITH A FLUORINATED NEU5AC DERIVATIVE | SIALIDASE, NEURAMINIDASE, COVALENT INTERMEDIATE, CBM40, HYDROLASE
4r17:E (GLN20) to (LYS60) LIGAND-INDUCED AZIRIDINE-FORMATION AT SUBUNIT BETA5 OF THE YEAST 20S PROTEASOME | PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, UMPOLUNG, CROSSLINK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r17:S (GLN20) to (LYS60) LIGAND-INDUCED AZIRIDINE-FORMATION AT SUBUNIT BETA5 OF THE YEAST 20S PROTEASOME | PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, UMPOLUNG, CROSSLINK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r18:E (GLN20) to (LYS60) 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:S (GLN20) to (LYS60) LIGAND-INDUCED LYS33-THR1 CROSSLINKING AT SUBUNIT BETA5 OF THE YEAST 20S PROTEASOME | PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, UMPOLUNG, CROSSLINK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4c21:A (GLU418) to (LEU462) L-FUCOSE ISOMERASE IN COMPLEX WITH FUCITOL | FUCOSE PROCESSING, ISOMERASE
4c47:B (LYS28) to (SER118) SALMONELLA ENTERICA TRIMERIC LIPOPROTEIN SADB | CELL ADHESION, BACTERIAL ADHESION, MEMBRANE TRAFFICKING, MEMBRANE INSERTION, AUTOTRANSPORT, POLAR CORE RESIDUES
3nzj:E (PHE22) to (LYS65) 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:S (PHE22) to (LYS65) 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:E (PHE22) to (LYS65) 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:S (PHE22) to (LYS65) 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
3d29:E (GLN23) to (LYS65) 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:S (GLN23) to (LYS65) 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
4cvw:A (THR775) to (VAL827) STRUCTURE OF THE BARLEY LIMIT DEXTRINASE-LIMIT DEXTRINASE INHIBITOR COMPLEX | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, STARCH DEBRANCHING ENZYME, GLYCOSIDE HYDROLASE FAMILY 13, PULLULANASE, CEREAL-TYPE INHIBITOR, CM-PROTEIN, ENDOGENOUS INHIBITOR
4cvw:B (THR775) to (VAL827) STRUCTURE OF THE BARLEY LIMIT DEXTRINASE-LIMIT DEXTRINASE INHIBITOR COMPLEX | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, STARCH DEBRANCHING ENZYME, GLYCOSIDE HYDROLASE FAMILY 13, PULLULANASE, CEREAL-TYPE INHIBITOR, CM-PROTEIN, ENDOGENOUS INHIBITOR
3oeu:S (PHE22) to (LYS65) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 24 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3oev:S (PHE22) to (LYS65) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 25 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4cyv:C (SER187) to (LEU236) STRUCTURE OF THE A_MALLARD_SWEDEN_51_2002 H10 AVIAN HAEMMAGLUTININ | VIRAL PROTEIN
4cyz:A (SER187) to (LEU236) STRUCTURE OF THE A_MALLARD_SWEDEN_51_2002 H10 AVIAN HAEMMAGLUTININ IN COMPLEX WITH AVIAN RECEPTOR ANALOG LSTA | VIRAL PROTEIN
4cyz:E (THR188) to (LEU236) STRUCTURE OF THE A_MALLARD_SWEDEN_51_2002 H10 AVIAN HAEMMAGLUTININ IN COMPLEX WITH AVIAN RECEPTOR ANALOG LSTA | VIRAL PROTEIN
4d00:A (SER180) to (LEU229) HAEMAGGLUTININ OF H10N8 INFLUENZA VIRUS ISOLATED FROM HUMANS IN COMPLEX WITH HUMAN RECEPTOR ANALOGUE 6'SLN | VIRAL PROTEIN, H10N8, INFLUENZA, SIALIC ACID, GLYCOPROTEIN, VIRUS RECEPTOR, AVIAN FLU, SIALYLLACTOSAMINE, LSTA
4d00:C (SER180) to (LEU229) HAEMAGGLUTININ OF H10N8 INFLUENZA VIRUS ISOLATED FROM HUMANS IN COMPLEX WITH HUMAN RECEPTOR ANALOGUE 6'SLN | VIRAL PROTEIN, H10N8, INFLUENZA, SIALIC ACID, GLYCOPROTEIN, VIRUS RECEPTOR, AVIAN FLU, SIALYLLACTOSAMINE, LSTA
4d00:E (SER180) to (LEU229) HAEMAGGLUTININ OF H10N8 INFLUENZA VIRUS ISOLATED FROM HUMANS IN COMPLEX WITH HUMAN RECEPTOR ANALOGUE 6'SLN | VIRAL PROTEIN, H10N8, INFLUENZA, SIALIC ACID, GLYCOPROTEIN, VIRUS RECEPTOR, AVIAN FLU, SIALYLLACTOSAMINE, LSTA
3dgv:C (TYR29) to (GLY67) CRYSTAL STRUCTURE OF THROMBIN ACTIVATABLE FIBRINOLYSIS INHIBITOR (TAFI) | BLOOD COAGULATION, FIBRINOLYSIS, CARBOXYPEPTIDASE, PROTEIN STABILITY, GLYCOPROTEIN, HYDROLASE, METAL-BINDING, METALLOPROTEASE, PROTEASE, SECRETED, ZYMOGEN
4d4t:A (PRO44) to (CYS91) RSV MATRIX PROTEIN | VIRAL PROTEIN
5gxh:A (PRO76) to (ALA106) THE STRUCTURE OF THE GEMIN5 WD40 DOMAIN WITH AAUUUUUG | SNRNP ASSEMBLY, SNRNA, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, RNA BINDING PROTEIN-RNA COMPLEX
5gxi:A (PRO76) to (ALA106) STRUCUTRE OF THE GEMIN5 WD40 DOMAIN IN COMPLEX WITH AAUUUUUGAG | SNRNP ASSEMBLY, SNRNA, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, RNA BINDING PROTEIN-RNA COMPLEX
5h1k:B (PRO76) to (ALA106) CRYSTAL STRUCTURE OF WD40 REPEAT DOMAINS OF GEMIN5 IN COMPLEX WITH 13- NT U4 SNRNA FRAGMENT | WD REPEAT, GEMIN5, SMN, RNA BINDING, U4 SNRNA, SPLICING-RNA COMPLEX
5h1l:A (PRO76) to (ALA106) CRYSTAL STRUCTURE OF WD40 REPEAT DOMAINS OF GEMIN5 IN COMPLEX WITH 7- NT U4 SNRNA FRAGMENT | WD REPEAT, GEMIN5, SMN, U4 SNRNA, RNA BINDING, SPLICING-RNA COMPLEX
5h8m:A (ASN213) to (PRO245) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE C619A, G459A MUTANT IN COMPLEX WITH PRODUCT MALATE | TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
5h8p:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN APO FORM | FRAGMENT, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
5h8u:B (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS WILD-TYPE MALATE SYNTHASE IN COMPLEX WITH PRODUCT MALATE | TRANSFERASE
3dy3:E (GLN23) to (LYS65) 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:S (GLN23) to (LYS65) 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
3e2e:A (ALA691) to (LYS741) CRYSTAL STRUCTURE OF AN INTERMEDIATE COMPLEX OF T7 RNAP AND 7NT OF RNA | T7 RNA POLYMERASE, DNA-DIRECTED RNA POLYMERASE, TRANSCRIPTION, NUCLEOTIDYLTRANSFERASE, TRANSFERASE, TRANSFERASE-RNA-DNA COMPLEX
3e3j:C (VAL693) to (LYS741) CRYSTAL STRUCTURE OF AN INTERMEDIATE COMPLEX OF T7 RNAP AND 8NT OF RNA | T7 RNA POLYMERASE, DNA-DIRECTED RNA POLYMERASE, TRANSCRIPTION, NUCLEOTIDYLTRANSFERASE, TRANSFERASE, TRANSFERASE/RNA/DNA COMPLEX
3pjt:B (ASP409) to (ALA461) STRUCTURE OF PSEUDOMONAS FLUORESCENCE LAPD EAL DOMAIN COMPLEXED WITH C-DI-GMP, C2221 | TIM BARREL, C-DI-GMP RECEPTOR, LYASE
4eu2:F (PHE20) to (LYS61) CRYSTAL STRUCTURE OF 20S PROTEASOME WITH NOVEL INHIBITOR K-7174 | PROTEASOME INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4eu2:T (PHE20) to (LYS61) CRYSTAL STRUCTURE OF 20S PROTEASOME WITH NOVEL INHIBITOR K-7174 | PROTEASOME INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3qc5:X (ASN567) to (ASP593) GSPB | CARBOHYDRATE/SUGAR BINDING, SUGAR BINDING PROTEIN
4eza:A (GLN24) to (ASN61) CRYSTAL STRUCTURE OF THE ATYPICAL PHOSPHOINOSITIDE (API) BINDING DOMAIN OF IQGAP2 | GAP, STRUCTURAL GENOMICS CONSORTIUM, SGC, SIGNALING PROTEIN
4eza:B (GLN24) to (ILE62) CRYSTAL STRUCTURE OF THE ATYPICAL PHOSPHOINOSITIDE (API) BINDING DOMAIN OF IQGAP2 | GAP, STRUCTURAL GENOMICS CONSORTIUM, SGC, SIGNALING PROTEIN
3qks:A (GLY35) to (LYS101) MRE11 RAD50 BINDING DOMAIN BOUND TO RAD50 | RECA-LIKE FOLD, COILED-COILS, ATPASE, EXONUCLEASE, ENDONUCLEASE, ATP BINDING, DNA BINDING, REPLICATION
3qkt:B (GLY35) to (GLY105) RAD50 ABC-ATPASE WITH ADJACENT COILED-COIL REGION IN COMPLEX WITH AMP- PNP | RECA-LIKE FOLD, COILED-COILS, ATPASE, ATP BINDING, DNA BINDING, MRE11, REPLICATION
3qku:A (GLY35) to (LYS101) MRE11 RAD50 BINDING DOMAIN IN COMPLEX WITH RAD50 AND AMP-PNP | RECA-LIKE FOLD, COILED-COILS, ATPASE, EXONUCLEASE, ENDONUCLEASE, ATP BINDING, DNA BINDING, REPLICATION
3qku:B (GLY35) to (GLY105) MRE11 RAD50 BINDING DOMAIN IN COMPLEX WITH RAD50 AND AMP-PNP | RECA-LIKE FOLD, COILED-COILS, ATPASE, EXONUCLEASE, ENDONUCLEASE, ATP BINDING, DNA BINDING, REPLICATION
3r1x:B (ALA84) to (GLY118) CRYSTAL STRUCTURE OF 2-OXO-3-DEOXYGALACTONATE KINASE FROM KLEBSIELLA PNEUMONIAE | STRUCTURAL GENOMICS, PSI-BIOLOGY, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, 2-OXO-3-DEOXYGALACTONATE KINASE, 2-DEHYDRO-3- DEOXYGALACTONOKINASE, 2-KETO-3-DEOXYGALACTONATE KINASE, DELEY- DOUDOROFF PATHWAY, TRANSFERASE
3r9y:A (SER145) to (THR188) CRYSTAL STRUCTURE OF STWHY2 K67A (FORM I) | STWHY2, SINGLE-STRANDED DNA BINDING PROTEIN, PLANT, POTATO, WHIRLY, MITOCHONDRIA, DNA BINDING PROTEIN
4fpg:A (ALA95) to (SER128) CRYSTAL STRUCTURE OF THE NANB SIALIDASE FROM STREPTOCOCCUS PNEUMONIAE IN COMPLEX WITH 2-[(3-HYDROXYBENZYL)AMMONIO]ETHANESULFONATE | HYDROLASE, INTRAMOLECULAR TRANS-SIALIDASE, GLYCOSIDASE, DRUG DESIGN, NEURAMINIDASE, HYDROLASE-INHIBITOR COMPLEX
4g1m:B (CYS435) to (PRO464) RE-REFINEMENT OF ALPHA V BETA 3 STRUCTURE | PROTEIN BINDING
5l5b:E (PHE19) to (LYS60) 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:S (PHE19) to (LYS60) 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:E (PHE19) to (LYS60) 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:S (PHE19) to (LYS60) 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:E (PHE19) to (LYS60) 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:S (PHE19) to (LYS60) 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:E (PHE19) to (LYS60) 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:S (PHE19) to (LYS60) 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
5l61:E (PHE19) to (LYS60) 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:S (PHE19) to (LYS60) 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:E (PHE19) to (LYS60) 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:S (PHE19) to (LYS60) 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
5l65:E (PHE19) to (LYS60) 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
5l69:E (PHE19) to (LYS60) 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:S (PHE19) to (LYS60) 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
5l6c:E (PHE19) to (LYS60) 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:S (PHE19) to (LYS60) 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
5l8o:B (SER25) to (PHE64) CRYSTAL STRUCTURE OF HUMAN FABP6 IN COMPLEX WITH CHOLATE | FABP6, FATTY ACID BINDING PROTEIN 6, ILEAL BILE ACID BINDING PROTEIN, I-BABP, ILEAL, GASTROTROPIN, FRAGMENTS, CHOLATE, LIPID BINDING PROTEIN
5t8g:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 2-OXO-4-((THIOPHENE-2-CARBONYL)OXY)BUTANOIC ACID | TRANSFERASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
5tee:A (PRO76) to (LEU107) CRYSTAL STRUCTURE OF GEMIN5 WD40 REPEATS IN APO FORM | STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, SPLICING
5tef:A (PRO76) to (ALA106) CRYSTAL STRUCTURE OF GEMIN5 WD40 REPEATS IN COMPLEX WITH M7GPPPG | STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, SPLICING
1n8i:A (ASN213) to (ASP244) BIOCHEMICAL AND STRUCTURAL STUDIES OF MALATE SYNTHASE FROM MYCOBACTERIUM TUBERCULOSIS | MALATE SYNTHASE, GLYOXYLATE PATHWAY, MYCOBACTERIUM TUBERCULOSIS, ACETYL COENZYME A, ISOCITRATE LYASE, PERSISTENCE, GLCB, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, TB STRUCTURAL GENOMICS CONSORTIUM, TBSGC
2p95:A (GLY25) to (THR54) FACTOR XA IN COMPLEX WITH THE INHIBITOR 5-CHLORO-N-((1R,2S)- 2-(4-(2-OXOPYRIDIN-1(2H)-YL)BENZAMIDO) CYCLOPENTYL) THIOPHENE-2-CARBOXAMIDE | GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM- BINDING
2qre:C (ARG491) to (ASP540) CRYSTAL STRUCTURE OF THE ADENYLATE SENSOR FROM AMP-ACTIVATED PROTEIN KINASE IN COMPLEX WITH 5-AMINOIMIDAZOLE-4-CARBOXAMIDE 1-BETA-D- RIBOFURANOTIDE (ZMP) | AMPK, 5-AMINOIMIDAZOLE-4-CARBOXAMIDE 1-BETA-D-RIBOFURANOTIDE, ZMP, AICAR PHOSPHATE, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, CBS DOMAIN
3gpt:E (GLN23) to (LYS65) 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:S (GLN23) to (LYS65) 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
3tdd:E (PHE22) to (LYS65) CRYSTAL STRUCTURE OF YEAST CP IN COMPLEX WITH BELACTOSIN C | UBIQUITIN, INHIBITOR, PROTEASOME, DRUG DEVELOPMENT, PRIMED SUBSTRATE BINDING CHANNEL, BETA-SANDWICH FLANKED BY ALPHA-HELICES, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3tdd:S (PHE22) to (LYS65) CRYSTAL STRUCTURE OF YEAST CP IN COMPLEX WITH BELACTOSIN C | UBIQUITIN, INHIBITOR, PROTEASOME, DRUG DEVELOPMENT, PRIMED SUBSTRATE BINDING CHANNEL, BETA-SANDWICH FLANKED BY ALPHA-HELICES, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ya5:E (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4yw2:B (PRO139) to (SER172) CRYSTAL STRUCTURE OF STREPTOCOCCUS PNEUMONIAE NANC, COMPLEX 6'SL | SIALIDASE, NEURAMINIDASE, 6'SL, CBM40, HYDROLASE
2fcp:A (GLY634) to (ASN691) FERRIC HYDROXAMATE UPTAKE RECEPTOR (FHUA) FROM E.COLI | TONB-DEPENDENT RECEPTOR, INTEGRAL OUTER MEMBRANE PROTEIN, FERRICHROME-IRON RECEPTOR, ACTIVE TRANSPORT, IRON TRANSPORT PROTEIN, MEMBRANE PROTEIN
2fhb:A (ASP966) to (ILE1013) CRYSTAL STRUCTURE ANALYSIS OF KLEBSIELLA PNEUMONIAE PULLULANASE COMPLEXED WITH MALTOSE | MULTIPLE DOMAIN, BETA-ALPHA-BARREL, ALPHA-AMYLASE-FAMILY, COMPLEX WITH MALTOSE, HYDROLASE
2vqp:A (PRO44) to (CYS91) STRUCTURE OF THE MATRIX PROTEIN FROM HUMAN RESPIRATORY SYNCYTIAL VIRUS | VIRAL PROTEIN, VIRAL MATRIX PROTEIN, PERIPHERAL MEMBRANE PROTEIN, RSV, VIRION, MATRIX PROTEIN, ENVELOPE PROTEIN
2vqp:A (THR182) to (ASP225) STRUCTURE OF THE MATRIX PROTEIN FROM HUMAN RESPIRATORY SYNCYTIAL VIRUS | VIRAL PROTEIN, VIRAL MATRIX PROTEIN, PERIPHERAL MEMBRANE PROTEIN, RSV, VIRION, MATRIX PROTEIN, ENVELOPE PROTEIN
3v9x:A (GLY9) to (HIS61) CRYSTAL STRUCTURE OF RNASE T IN COMPLEX WITH A PREFERRED SSDNA (AAA) WITH TWO MG IN THE ACTIVE SITE | DEDD NUCLEASES FAMILY, EXO-NUCLEASE, HYDROLASE-DNA COMPLEX
2gcj:C (GLN278) to (GLN321) CRYSTAL STRUCTURE OF THE POB3 MIDDLE DOMAIN | CHROMATIN, FACT, DOUBLE PH DOMAIN, REPLICATION
1ik9:A (LYS63) to (ARG107) CRYSTAL STRUCTURE OF A XRCC4-DNA LIGASE IV COMPLEX | DNA END JOINING, DOUBLE-STRAND BREAK REPAIR, V(D)J RECOMBINATION, PROTEIN-PROTEIN COMPLEX, COILED COIL, GENE REGULATION/LIGASE COMPLEX
5b0v:B (PRO95) to (ILE146) CRYSTAL STRUCTURE OF MARBURG VIRUS VP40 DIMER | MARBURG VIRUS, VIRUS ASSEMBLY PROTEIN, IMMUNOSUPPRESSION, FILOVIRUS, VIRAL PROTEIN
3zgx:A (ASN39) to (LEU113) CRYSTAL STRUCTURE OF THE KLEISIN-N SMC INTERFACE IN PROKARYOTIC CONDENSIN | CELL CYCLE
5bxl:E (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA2-G170A MUTANT | HYDROLASE, IMMUNODEFICIENCY, PROTEASOME, MUTANT, ASSEMBLY DEFECT
5bxl:S (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA2-G170A MUTANT | HYDROLASE, IMMUNODEFICIENCY, PROTEASOME, MUTANT, ASSEMBLY DEFECT
2lba:A (PRO24) to (ASP66) SOLUTION STRUCTURE OF CHICKEN ILEAL BABP IN COMPLEX WITH GLYCOCHENODEOXYCHOLIC ACID | ILEAL BILE ACID BINDING PROTEIN, LIPID BINDING PROTEIN
1x3l:A (PRO23) to (GLU46) CRYSTAL STRUCTURE OF THE PH0495 PROTEIN FROM PYROCOCCCUS HORIKOSHII OT3 | STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, TRANSFERASE
5c9x:A (ASN213) to (GLU246) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 2,4-DICHLORO-5-FLUOROBENZOIC ACID | FRAGMENT, COMPLEX, TRANSFERASE
5cj0:A (LYS63) to (ARG107) CRYSTAL STRUCTURE OF AMINO ACIDS 1631-1692 OF MYH7 | MYOSIN, COILED-COIL, MOTOR PROTEIN
3bdm:E (GLN23) to (LYS65) YEAST 20S PROTEASOME:GLIDOBACTIN A-COMPLEX | PROTEASOME, UBIQUITIN, PROTEOLYSIS, PATHOGEN, VIRULENCE FACTOR, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN
3bdm:S (GLN23) to (LYS65) YEAST 20S PROTEASOME:GLIDOBACTIN A-COMPLEX | PROTEASOME, UBIQUITIN, PROTEOLYSIS, PATHOGEN, VIRULENCE FACTOR, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN
4qw3:E (PHE19) to (LYS60) YCP BETA5-C63F MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw3:S (PHE19) to (LYS60) YCP BETA5-C63F MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3n1h:A (SER145) to (PRO186) CRYSTAL STRUCTURE OF STWHY2 | STWHY2, SINGLE-STRANDED DNA BINDING PROTEIN, PLANT, POTATO, WHIRLY, DNA BINDING PROTEIN
5fgh:E (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) IN COMPLEX WITH MG132 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgh:S (PHE19) to (LYS60) YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) IN COMPLEX WITH MG132 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
3nzx:E (PHE22) to (LYS65) CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH LIGAND 2C | UBIQUITIN, PROTEIN DEGRADATION, N-TERMINAL NUCLEOPHILIC HYDROLASE, 19S REGULATORY PARTICLE, UBIQUITIN-TAGGED SUBSTRATES, CYTOSOL, NUCLEUS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3nzx:S (PHE22) to (LYS65) CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH LIGAND 2C | UBIQUITIN, PROTEIN DEGRADATION, N-TERMINAL NUCLEOPHILIC HYDROLASE, 19S REGULATORY PARTICLE, UBIQUITIN-TAGGED SUBSTRATES, CYTOSOL, NUCLEUS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4fpe:A (ALA95) to (SER128) CRYSTAL STRUCTURE OF THE NANB SIALIDASE FROM STREPTOCOCCUS PNEUMONIAE IN COMPLEX WITH 2-[(4-METHOXYBENZYL)AMMONIO]ETHANESULFONATE | HYDROLASE, INTRAMOLECULAR TRANS-SIALIDASE, GLYCOSIDASE, DRUG DESIGN, NEURAMINIDASE, HYDROLASE-INHIBITOR COMPLEX
4fzg:E (PHE19) to (LYS60) 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:S (PHE19) to (LYS60) 20S YEAST PROTEASOME IN COMPLEX WITH GLIDOBACTIN | UBIQUITIN, PROTEASOME, DRUG DEVELOPMENT, INHIBITOR, NATURAL PRODUCT, N-TERMINAL NUCLEOPHILIC HYDROLASE, PROTEIN DEGRADATION, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4gk7:E (PHE22) to (LYS63) 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:S (PHE22) to (LYS63) 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
5l5r:E (PHE19) to (LYS60) 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:S (GLN20) to (LYS60) 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
5l63:E (PHE19) to (LYS60) 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:S (PHE19) to (LYS60) 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