3rki:A (GLY307) to (ARG336) STRUCTURAL BASIS FOR IMMUNIZATION WITH POST-FUSION RSV F TO ELICIT HIGH NEUTRALIZING ANTIBODY TITERS | FUSION PROTEIN, VIRAL PROTEIN
3rki:B (GLY307) to (ARG336) STRUCTURAL BASIS FOR IMMUNIZATION WITH POST-FUSION RSV F TO ELICIT HIGH NEUTRALIZING ANTIBODY TITERS | FUSION PROTEIN, VIRAL PROTEIN
1a4e:A (MET209) to (TYR228) CATALASE A FROM SACCHAROMYCES CEREVISIAE | OXIDOREDUCTASE, CATALASE, PEROXIDASE
1a4e:B (MET209) to (TYR228) CATALASE A FROM SACCHAROMYCES CEREVISIAE | OXIDOREDUCTASE, CATALASE, PEROXIDASE
1a4e:C (MET209) to (TYR228) CATALASE A FROM SACCHAROMYCES CEREVISIAE | OXIDOREDUCTASE, CATALASE, PEROXIDASE
1a4e:D (MET209) to (TYR228) CATALASE A FROM SACCHAROMYCES CEREVISIAE | OXIDOREDUCTASE, CATALASE, PEROXIDASE
3eaf:A (GLY385) to (ALA412) CRYSTAL STRUCTURE OF ABC TRANSPORTER, SUBSTRATE BINDING PROTEIN AEROPYRUM PERNIX | 11229A2, PSI2, NYSGXRC, ABC TRANSPORTER, SUBSTRATE BINDING PROTEIN, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, TRANSPORT PROTEIN
2anl:A (GLU67) to (GLY84) X-RAY CRYSTAL STRUCTURE OF THE ASPARTIC PROTEASE PLASMEPSIN 4 FROM THE MALARIAL PARASITE PLASMODIUM MALARIAE BOUND TO AN ALLOPHENYLNORSTATINE BASED INHIBITOR | PLASMODIUM PARASITE, PLASMEPSIN 4, ASPARTIC PROTEASE, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2anl:B (GLU67) to (GLY84) X-RAY CRYSTAL STRUCTURE OF THE ASPARTIC PROTEASE PLASMEPSIN 4 FROM THE MALARIAL PARASITE PLASMODIUM MALARIAE BOUND TO AN ALLOPHENYLNORSTATINE BASED INHIBITOR | PLASMODIUM PARASITE, PLASMEPSIN 4, ASPARTIC PROTEASE, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4gwq:G (ILE147) to (THR165) STRUCTURE OF THE MEDIATOR HEAD MODULE FROM S. CEREVISIAE IN COMPLEX WITH THE CARBOXY-TERMINAL DOMAIN (CTD) OF RNA POLYMERASE II RPB1 SUBUNIT | BINDING SITES, MEDIATOR COMPLEX, MODELS, MOLECULAR, PHOSPHORYLATION, PROTEIN STRUCTURE, TERTIARY, PROTEIN SUBUNITS, RNA POLYMERASE II, SACCHAROMYCES CEREVISIAE, STRUCTURE-ACTIVITY RELATIONSHIP, TRANSCRIPTION
3ebl:B (GLU111) to (SER130) CRYSTAL STRUCTURE OF RICE GID1 COMPLEXED WITH GA4 | ALPHA/BETA HYDROLASE, LIPASE, GIBBERELLIN SIGNALING PATHWAY, HYDROLASE, NUCLEUS, RECEPTOR, HYDROLASE RECEPTOR
3ebm:B (MET1) to (GLU32) CRYSTAL STRUCTURE OF HUMAN TRANSLATIONALLY CONTROLLED TUMOUR ASSOCIATED PROTEIN (HTCTP) MUTANT E12V | TCTP, E12V, CALCIUM, CYTOPLASM, PHOSPHOPROTEIN, CALCIUM- BINDING PROTEIN
3ebm:D (MET1) to (GLU32) CRYSTAL STRUCTURE OF HUMAN TRANSLATIONALLY CONTROLLED TUMOUR ASSOCIATED PROTEIN (HTCTP) MUTANT E12V | TCTP, E12V, CALCIUM, CYTOPLASM, PHOSPHOPROTEIN, CALCIUM- BINDING PROTEIN
2aqx:B (GLY806) to (ASP822) CRYSTAL STRUCTURE OF THE CATALYTIC AND CAM-BINDING DOMAINS OF INOSITOL 1,4,5-TRISPHOSPHATE 3-KINASE B | IP3K, ITPKB, IP3-3K, IP3-3KB, INOSITOL, KINASE, IP3, CALMODULIN BINDING, TRANSFERASE
3edq:C (PHE114) to (ASP135) CRYSTAL STRUCTURE OF CASPASE-3 WITH INHIBITOR AC-LDESD-CHO | ENZYME CATALYSIS, CYSTEINE PROTEASE, APOPTOSIS, S-NITROSYLATION, THIOL PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3edr:A (CYS136) to (PRO158) THE CRYSTAL STRUCTURE OF CASPASE-7 IN COMPLEX WITH ACETYL-LDESD-CHO | CASPASE, PEPTIDE INHIBITOR, APOPTOSIS, THIOL PROTEASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3edy:A (ASP451) to (TRP470) CRYSTAL STRUCTURE OF THE PRECURSOR FORM OF HUMAN TRIPEPTIDYL-PEPTIDASE 1 | PROTEASE, TPP1, SEDOLISIN, BATTEN DISEASE, LINCL, ZYMOGEN, PRODOMAIN, EXOPEPTIDASE, ENDOPEPTIDASE, S53 FAMILY, CLN2, CATALYTIC TRIAD, OXYANION HOLE, DISEASE MUTATION, EPILEPSY, GLYCOPROTEIN, HYDROLASE, LYSOSOME, NEURONAL CEROID LIPOFUSCINOSIS, SERINE PROTEASE
4wjv:H (ASN251) to (LEU272) CRYSTAL STRUCTURE OF RSA4 IN COMPLEX WITH THE NSA2 BINDING PEPTIDE | RIBOSOME BIOGENESIS RIBOSOME ASSEMBLY, PROTEIN BINDING
1af6:A (GLY245) to (ASN264) MALTOPORIN SUCROSE COMPLEX | MEMBRANE PROTEIN, SPECIFIC PORIN, BETA BARREL, SUGAR TRANSPORT, SUCROSE
1af6:B (GLY245) to (ASN264) MALTOPORIN SUCROSE COMPLEX | MEMBRANE PROTEIN, SPECIFIC PORIN, BETA BARREL, SUGAR TRANSPORT, SUCROSE
1af6:C (GLY245) to (ASN264) MALTOPORIN SUCROSE COMPLEX | MEMBRANE PROTEIN, SPECIFIC PORIN, BETA BARREL, SUGAR TRANSPORT, SUCROSE
2awn:A (SER3) to (VAL18) CRYSTAL STRUCTURE OF THE ADP-MG-BOUND E. COLI MALK (CRYSTALLIZED WITH ATP-MG) | ATP-BINDING CASSETTE, TRANSPORT PROTEIN
3rux:A (GLN231) to (SER258) CRYSTAL STRUCTURE OF BIOTIN-PROTEIN LIGASE BIRA FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH AN ACYLSULFAMIDE BISUBSTRATE INHIBITOR | BIOTIN-PROTEIN LIGASE, LIGASE-LIGASE INHIBITOR COMPLEX
3rux:B (GLN231) to (SER258) CRYSTAL STRUCTURE OF BIOTIN-PROTEIN LIGASE BIRA FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH AN ACYLSULFAMIDE BISUBSTRATE INHIBITOR | BIOTIN-PROTEIN LIGASE, LIGASE-LIGASE INHIBITOR COMPLEX
3eht:A (ASN-108) to (LEU-87) CRYSTAL STRUCTURE OF THE EXTRACELLULAR DOMAIN OF HUMAN CORTICOTROPIN RELEASING FACTOR RECEPTOR TYPE 1 (CRFR1) IN COMPLEX WITH CRF | G PROTEIN-COUPLED RECEPTOR, CORTICOTROPIN RELEASING FACTOR, SCR FOLD, MBP FUSION, EXTRACELLULAR DOMAIN, SUGAR TRANSPORT, TRANSPORT, CELL MEMBRANE, GLYCOPROTEIN, MEMBRANE, PHOSPHOPROTEIN, RECEPTOR, TRANSDUCER, TRANSMEMBRANE, AMIDATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, HORMONE, SECRETED, MEMBRANE PROTEIN
1am5:A (VAL265) to (SER284) THE CRYSTAL STRUCTURE AND PROPOSED AMINO ACID SEQUENCE OF A PEPSIN FROM ATLANTIC COD (GADUS MORHUA) | ASPARTYL PROTEASE, ACID PROTEINASE, HYDROLASE
1anf:A (ASN241) to (ILE266) MALTODEXTRIN BINDING PROTEIN WITH BOUND MALTOSE | PERIPLASMIC BINDING PROTEIN, SUGAR TRANSPORT
4h4p:A (VAL74) to (GLY103) CRYSTAL STRUCTURE OF FERREDOXIN REDUCTASE, BPHA4 E175Q/Q177K MUTANT (OXIDIZED FORM) | FLAVOPROTEIN, OXIDOREDUCTASE
4h4r:A (VAL74) to (GLY103) CRYSTAL STRUCTURE OF FERREDOXIN REDUCTASE, BPHA4 E175C/Q177G MUTANT (OXIDIZED FORM) | FLAVOPROTEIN, OXIDOREDUCTASE
4h4t:A (VAL74) to (GLY103) CRYSTAL STRUCTURE OF FERREDOXIN REDUCTASE, BPHA4 T176R MUTANT (OXIDIZED FORM) | FLAVOPROTEIN, OXIDOREDUCTASE
4h4x:A (VAL74) to (GLY103) CRYSTAL STRUCTURE OF FERREDOXIN REDUCTASE, BPHA4 E175A/T176R/Q177G MUTANT (OXIDIZED FORM) | FLAVOPROTEIN, OXIDOREDUCTASE
4h7m:A (ASP121) to (ILE137) THE X-RAY CRYSTAL STRUCTURE OF THE TRICHODERMA HARZIANUM ENDOGLUCANASE 3 FROM FAMILY GH12 | HYDROLASE, ENDOGLUCANASE, GH12
1nud:A (ASP621) to (ASP644) ROLE OF CALCIUM IONS IN THE ACTIVATION AND ACTIVITY OF THE TRANSGLUTAMINASE 3 ENZYME (3 CALCIUMS, ACTIVE FORM) | TRANSGLUTAMINASE 3, X-RAY CRYSTALLOGRAPHY, METALLOENZYME, CALCIUM ION, TRANSFERASE
1nuf:A (ASP621) to (ASP644) ROLE OF CALCIUM IONS IN THE ACTIVATION AND ACTIVITY OF THE TRANSGLUTAMINASE 3 ENZYME | TRANSGLUTAMINASE 3, X-RAY CRYSTALLOGRAPHY, METALLOENZYME, CALCIUM ION, TRANSFERASE
1nug:B (ASP621) to (ASP644) ROLE OF CALCIUM IONS IN THE ACTIVATION AND ACTIVITY OF THE TRANSGLUTAMINASE 3 ENZYME (2 CALCIUMS, 1 MG, INACTIVE FORM) | TRANSGLUTAMINASE 3, X-RAY CRYSTALLOGRAPHY, METALLOENZYME, CALCIUM ION, TRANSFERASE
1axk:A (ALA321) to (GLY342) ENGINEERED BACILLUS BIFUNCTIONAL ENZYME GLUXYN-1 | GLUXYN-1, BIFUNCTIONAL, FUSION PROTEIN, 1,4-BETA-XYLANASE, 1,3-1,4-BETA-GLUCANASE, HYBRID ENZYME
2b8w:A (GLY9) to (ALA23) CRYSTAL-STRUCTURE OF THE N-TERMINAL LARGE GTPASE DOMAIN OF HUMAN GUANYLATE BINDING PROTEIN 1 (HGBP1) IN COMPLEX WITH GMP/ALF4 | PROTEIN- GUANINE NUCLEOTIDE COMPLEX, SIGNALING PROTEIN
2b8w:B (GLY9) to (ALA23) CRYSTAL-STRUCTURE OF THE N-TERMINAL LARGE GTPASE DOMAIN OF HUMAN GUANYLATE BINDING PROTEIN 1 (HGBP1) IN COMPLEX WITH GMP/ALF4 | PROTEIN- GUANINE NUCLEOTIDE COMPLEX, SIGNALING PROTEIN
2b92:A (GLY9) to (ALA23) CRYSTAL-STRUCTURE OF THE N-TERMINAL LARGE GTPASE DOMAIN OF HUMAN GUANYLATE BINDING PROTEIN 1 (HGBP1) IN COMPLEX WITH GDP/ALF3 | PROTEIN- GUANINE NUCLEOTIDE COMPLEX, SIGNALING PROTEIN
2p2c:I (SER104) to (GLN127) INHIBITION OF CASPASE-2 BY A DESIGNED ANKYRIN REPEAT PROTEIN (DARPIN) | APOPTOSIS, CASPASE, CASPASE-2, INHIBITION, PROTEIN DESIGN, PROTEIN LIBRARIES, DESIGNED ANKYRIN REPEAT PROTEINS, RIBOSOME DISPLAY, HYDROLASE
1b0u:A (LYS6) to (LEU22) ATP-BINDING SUBUNIT OF THE HISTIDINE PERMEASE FROM SALMONELLA TYPHIMURIUM | ABC TRANSPORTER, HISTIDINE PERMEASE, TRANSPORT PROTEIN
4ww2:A (ASP167) to (ASN186) CRYSTAL STRUCTURE OF HUMAN TCR ALPHA CHAIN-TRAV21-TRAJ8, BETA CHAIN- TRBV7-8, ANTIGEN-PRESENTING GLYCOPROTEIN CD1D, AND BETA-2- MICROGLOBULIN | NATURAL KILLER T CELLS, IMMUNITY, IMMUNE SYSTEM
3eqt:B (GLN553) to (ASN581) CRYSTAL STRUCTURE OF HUMAN LGP2 C-TERMINAL DOMAIN IN COMPLEX WITH DSRNA | INNATE IMMUNITY, RIG-I-LIKE HELICASES, VIRAL RNA DETECTION, LGP2/DSRNA COMPLEX, ATP-BINDING, COILED COIL, CYTOPLASM, HELICASE, HYDROLASE, IMMUNE RESPONSE, NUCLEOTIDE-BINDING, POLYMORPHISM, RNA-BINDING, RNA BINDING PROTEIN/RNA COMPLEX
3eqv:A (GLU330) to (ASP346) CRYSTAL STRUCTURE OF PENICILLIN-BINDING PROTEIN 2 FROM NEISSERIA GONORRHOEAE CONTAINING FOUR MUTATIONS ASSOCIATED WITH PENICILLIN RESISTANCE | PENICILLIN-BINDING PROTEIN, CLASS B TRANSPEPTIDASE, PENICILLIN RESISTANCE, CELL DIVISION, CELL INNER MEMBRANE, CELL MEMBRANE, CELL SHAPE, CELL WALL BIOGENESIS/DEGRADATION, PEPTIDOGLYCAN SYNTHESIS, BIOSYNTHETIC PROTEIN
2bc9:A (GLY9) to (ALA23) CRYSTAL-STRUCTURE OF THE N-TERMINAL LARGE GTPASE DOMAIN OF HUMAN GUANYLATE BINDING PROTEIN 1 (HGBP1) IN COMPLEX WITH NON-HYDROLYSABLE GTP ANALOGUE GPPNHP | PROTEIN- GUANINE NUCLEOTIDE COMPLEX, SIGNALING PROTEIN
4he2:A (LYS112) to (THR134) CRYSTAL STRUCTURE OF HUMAN MUSCLE FRUCTOSE-1,6-BISPHOSPHATASE Q32R MUTANT COMPLEX WITH AMP | ALLOSTERIC ENZYME, HYDROLASE
2bdv:A (ALA56) to (ILE72) X-RAY CRYSTAL STRUCTURE OF PHAGE-RELATED PROTEIN BB2244 FROM BORDETELLA BRONCHISEPTICA. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET BOR24. | ALPHA-BETA PROTEIN, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, UNKNOWN FUNCTION
3s2c:K (LYS363) to (ASN388) STRUCTURE OF THE THERMOSTABLE GH51 ALPHA-L-ARABINOFURANOSIDASE FROM THERMOTOGA PETROPHILA RKU-1 | TIM-BARREL AND JELLY-ROLL DOMAINS, ALPHA-L-ARABINOFURANOSIDASE, GLYCOSYL HYDROLASE 51 FAMILY, HYDROLASE
4wzc:A (PRO44) to (TYR60) UNDERSTANDING EXTRADIOL DIOXYGENASE MECHANISM IN NAD+ BIOSYNTHESIS BY VIEWING CATALYTIC INTERMEDIATES - 2,3-CIS-4,5-TRANS ACMS BOUND TO I142A MUTANT HAO | BI-CUPIN IRON-BINDING, DIOXYGENASE, OXIDOREDUCTASE
3ewm:A (ILE4) to (LYS30) CRYSTAL STRUCTURE OF AN UNCHARACTERIZED SUGAR KINASE PH1459 FROM PYROCOCCUS HORIKOSHII | CARBOHYDRATE KINASE, PFKB FAMILY, PSI-II, 11207G, NYSGXRC, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, KINASE, TRANSFERASE
3ewm:B (LEU3) to (LYS30) CRYSTAL STRUCTURE OF AN UNCHARACTERIZED SUGAR KINASE PH1459 FROM PYROCOCCUS HORIKOSHII | CARBOHYDRATE KINASE, PFKB FAMILY, PSI-II, 11207G, NYSGXRC, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, KINASE, TRANSFERASE
4hlu:A (ARG2) to (LEU23) STRUCTURE OF THE ECFA-A' HETERODIMER BOUND TO ADP | MEMBRANE TRANSPORT, VITAMIN UPTAKE, ENERGY COUPLING FACTOR TRANSPORTER, ATPASE, ATP-BINDING CASETTE, HYDROLASE
4hlu:B (ARG2) to (LEU23) STRUCTURE OF THE ECFA-A' HETERODIMER BOUND TO ADP | MEMBRANE TRANSPORT, VITAMIN UPTAKE, ENERGY COUPLING FACTOR TRANSPORTER, ATPASE, ATP-BINDING CASETTE, HYDROLASE
4hnp:J (VAL13) to (LYS29) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH VINYLKETONE CARMAPHYCIN ANALOGUE VNK1 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4hnp:X (VAL13) to (LYS29) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH VINYLKETONE CARMAPHYCIN ANALOGUE VNK1 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4x6z:2 (VAL12) to (GLY30) YEAST 20S PROTEASOME IN COMPLEX WITH PR-VI MODULATOR | 20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE
4x6z:K (VAL12) to (LYS28) YEAST 20S PROTEASOME IN COMPLEX WITH PR-VI MODULATOR | 20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE
4x6z:N (VAL12) to (GLY30) YEAST 20S PROTEASOME IN COMPLEX WITH PR-VI MODULATOR | 20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE
4x6z:Y (VAL12) to (LYS28) YEAST 20S PROTEASOME IN COMPLEX WITH PR-VI MODULATOR | 20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE
1bs8:B (GLU579) to (CYS590) PEPTIDE DEFORMYLASE AS ZN2+ CONTAINING FORM IN COMPLEX WITH TRIPEPTIDE MET-ALA-SER | HYDROLASE, IRON METALLOPROTEASE; PROTEIN SYNTHESIS
4x8f:O (LYS3) to (PRO37) VIBRIO CHOLERAE O395 RIBOKINASE IN APO FORM | SUGAR KINASE, APO FORM, TRANSFERASE
4x8f:P (LYS3) to (PRO37) VIBRIO CHOLERAE O395 RIBOKINASE IN APO FORM | SUGAR KINASE, APO FORM, TRANSFERASE
4x9f:B (GLY208) to (LEU234) CRYSTAL STRUCTURE OF DSCAM1 ISOFORM 6.9, N-TERMINAL FOUR IG DOMAINS | IG FOLD, CELL ADHESION
4hrc:J (VAL13) to (LYS29) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE CARMAPHYCIN ANALOGUE 3 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4hrc:X (VAL13) to (LYS29) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE CARMAPHYCIN ANALOGUE 3 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4hrd:J (VAL13) to (LYS29) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH THE NATURAL PRODUCT CARMAPHYCIN A | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4hrd:M (VAL20) to (GLY38) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH THE NATURAL PRODUCT CARMAPHYCIN A | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4hrd:X (VAL13) to (LYS29) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH THE NATURAL PRODUCT CARMAPHYCIN A | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4xaj:D (ASN243) to (ASN269) CRYSTAL STRUCTURE OF HUMAN NR2E1/TLX | HELICAL SANWICH, TRANSPORT PROTEIN-TRANSCRIPTION COMPLEX
4hsj:A (PRO44) to (TYR60) 1.88 ANGSTROM X-RAY CRYSTAL STRUCTURE OF PICONLINIC-BOUND 3- HYDROXYANTHRANILATE-3,4-DIOXYGENASE | BI-CUPIN, DIOXYGENASE, OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4hsl:A (PRO44) to (TYR60) 2.00 ANGSTROM X-RAY CRYSTAL STRUCTURE OF SUBSTRATE-BOUND E110A 3- HYDROXYANTHRANILATE-3,4-DIOXYGENASE FROM CUPRIAVIDUS METALLIDURANS | BI-CUPIN IRON-BINDING, DIOXYGENASE, OXIDOREDUCTASE
4xb7:B (SER214) to (MET240) CRYSTAL STRUCTURE OF DSCAM1 ISOFORM 4.4, N-TERMINAL FOUR IG DOMAINS | IG FOLD, CELL ADHESION
4huq:A (ALA2) to (THR21) CRYSTAL STRUCTURE OF A TRANSPORTER | TRANSPORTER, HYDROLASE
2phd:D (ARG113) to (VAL129) CRYSTAL STRUCTURE DETERMINATION OF A SALICYLATE 1,2- DIOXYGENASE FROM PSEUDAMINOBACTER SALICYLATOXIDANS | BETA-SANDWICH, OXIDOREDUCTASE
2pi2:E (VAL25) to (MET56) FULL-LENGTH REPLICATION PROTEIN A SUBUNITS RPA14 AND RPA32 | FULL-LENGTH RPA14/32, SSDNA BINDING PROTEIN, OB-FOLD, DIOXANE, REPLICATION, DNA BINDING PROTEIN
4hvo:A (PRO44) to (TYR60) 1.75 ANGSTROM X-RAY CRYSTAL STRUCTURE OF CUFE RECONSTITUTED 3- HYDROXYANTHRANILATE-3,4-DIOXYGENASE FROM CUPRIAVIDUS METALLIDURANS | BI-CUPIN IRON-BINDING, DIOXYGENASE, OXIDOREDUCTASE
4hvq:A (PRO44) to (TYR60) X-RAY CRYSTAL STRUCTURE OF FECU RECONSTITUTED 3-HYDROXYANTHRANILATE-3, 4-DIOXYGENASE FROM CUPRIAVIDUS METALLIDURANS | BI-CUPIN IRON-BINDING, DIOXYGENASE, OXIDOREDUCTASE
3fe5:A (GLN216) to (GLN232) CRYSTAL STRUCTURE OF 3-HYDROXYANTHRANILATE 3,4-DIOXYGENASE FROM BOVINE KIDNEY | CUPIN, 3HAO, QUINOLINIC ACID, CYTOPLASM, DIOXYGENASE, IRON, METAL-BINDING, OXIDOREDUCTASE
3sdi:J (VAL12) to (LYS28) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 20 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3sdi:M (VAL11) to (GLY29) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 20 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3sdi:X (VAL12) to (LYS28) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 20 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3sdi:1 (VAL11) to (GLY29) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 20 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3sdk:J (VAL12) to (LYS28) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 34 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3sdk:M (VAL12) to (GLY30) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 34 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3sdk:X (VAL12) to (LYS28) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 34 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3sdk:1 (VAL12) to (GLY30) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 34 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2pn5:A (LYS1272) to (ASP1300) CRYSTAL STRUCTURE OF TEP1R | FULL-LENGTH MATURE PEPTIDE, IMMUNE SYSTEM
3set:A (ASN242) to (ASN268) NI-MEDIATED DIMER OF MALTOSE-BINDING PROTEIN A216H/K220H BY SYNTHETIC SYMMETRIZATION (FORM I) | METAL-MEDIATED SYNTHETIC SYMMETRIZATION, SYNTHETIC SYMMETRIZATION, SUGAR BINDING PROTEIN
3sev:A (ASN242) to (LEU263) ZN-MEDIATED TRIMER OF MALTOSE-BINDING PROTEIN E310H/K314H BY SYNTHETIC SYMMETRIZATION | METAL-MEDIATED SYNTHETIC SYMMETRIZATION, SYNTHETIC SYMMETRIZATION, SUGAR BINDING PROTEIN
3sev:E (ASN242) to (LEU263) ZN-MEDIATED TRIMER OF MALTOSE-BINDING PROTEIN E310H/K314H BY SYNTHETIC SYMMETRIZATION | METAL-MEDIATED SYNTHETIC SYMMETRIZATION, SYNTHETIC SYMMETRIZATION, SUGAR BINDING PROTEIN
1c77:A (VAL79) to (PRO105) STAPHYLOKINASE (SAK) DIMER | BETA-GRASP FAMILY, HYDROLASE
1c78:A (VAL79) to (PRO105) STAPHYLOKINASE (SAK) DIMER | BETA-GRASP FAMILY, HYDROLASE
1c79:A (VAL79) to (PRO105) STAPHYLOKINASE (SAK) DIMER | BETA-GRASP FAMILY, HYDROLASE
3fha:A (GLY496) to (GLY524) STRUCTURE OF ENDO-BETA-N-ACETYLGLUCOSAMINIDASE A | ENDO-A, GLYCOPROTEIN, MAN3GLCNAC-THIAZOLINE, GLCNAC-ASN, GLYCOSIDASE, HYDROLASE
3fha:C (GLY496) to (VAL523) STRUCTURE OF ENDO-BETA-N-ACETYLGLUCOSAMINIDASE A | ENDO-A, GLYCOPROTEIN, MAN3GLCNAC-THIAZOLINE, GLCNAC-ASN, GLYCOSIDASE, HYDROLASE
4xh3:A (ALA222) to (LYS250) MECHANISTIC INSIGHTS INTO ANCHORAGE OF THE CONTRACTILE RING FROM YEAST TO HUMANS | C2
2c1e:A (SER113) to (ASP135) CRYSTAL STRUCTURES OF CASPASE-3 IN COMPLEX WITH AZA-PEPTIDE MICHAEL ACCEPTOR INHIBITORS. | APOPTOSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, CYSTEINE-PROTEASE, THIOL PROTEASE, ZYMOGEN, CPP32, YAMA, AZA-PEPTIDE, MICHAEL ACCEPTOR, AZA-ASP, CLAN CD
3shj:J (VAL12) to (LYS28) PROTEASOME IN COMPLEX WITH HYDROXYUREA DERIVATIVE HU10 | UBIQUITIN, DRUG DEVELOPMENT, CANCER, IMMUNOLOGY, PROTEIN DEGRADATION, UNFOLDED PROTEIN SUBSTRATES, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3shj:M (VAL12) to (GLY30) PROTEASOME IN COMPLEX WITH HYDROXYUREA DERIVATIVE HU10 | UBIQUITIN, DRUG DEVELOPMENT, CANCER, IMMUNOLOGY, PROTEIN DEGRADATION, UNFOLDED PROTEIN SUBSTRATES, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3shj:X (VAL12) to (LYS28) PROTEASOME IN COMPLEX WITH HYDROXYUREA DERIVATIVE HU10 | UBIQUITIN, DRUG DEVELOPMENT, CANCER, IMMUNOLOGY, PROTEIN DEGRADATION, UNFOLDED PROTEIN SUBSTRATES, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3shj:1 (VAL12) to (GLY30) PROTEASOME IN COMPLEX WITH HYDROXYUREA DERIVATIVE HU10 | UBIQUITIN, DRUG DEVELOPMENT, CANCER, IMMUNOLOGY, PROTEIN DEGRADATION, UNFOLDED PROTEIN SUBSTRATES, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4i3p:A (PRO44) to (TYR60) 1.96 ANGSTROM X-RAY CRYSTAL STRUCTURE OF 3-HYDROXYANTHRANILATE-3,4- DIOXYGENASE BOUND WITH 3-AMINOSALICYLIC ACID FROM CUPRAAVIDUS METALLIDURANS | BI-CUPIN IRON-BINDING, DIOXYGENASE, OXIOREDUCTASE-SUBSTRATE COMPLEX
4xjc:A (GLY117) to (PRO137) DCTP DEAMINASE-DUTPASE FROM BACILLUS HALODURANS | BIFUNCTIONAL, TTP BINDING, COMPLEX, HYDROLASE
4xjc:C (GLY117) to (PRO137) DCTP DEAMINASE-DUTPASE FROM BACILLUS HALODURANS | BIFUNCTIONAL, TTP BINDING, COMPLEX, HYDROLASE
4xjc:E (GLY117) to (PRO137) DCTP DEAMINASE-DUTPASE FROM BACILLUS HALODURANS | BIFUNCTIONAL, TTP BINDING, COMPLEX, HYDROLASE
4xjc:B (GLY117) to (PRO137) DCTP DEAMINASE-DUTPASE FROM BACILLUS HALODURANS | BIFUNCTIONAL, TTP BINDING, COMPLEX, HYDROLASE
4xjc:D (GLY117) to (PRO137) DCTP DEAMINASE-DUTPASE FROM BACILLUS HALODURANS | BIFUNCTIONAL, TTP BINDING, COMPLEX, HYDROLASE
4xjc:F (GLY117) to (PRO137) DCTP DEAMINASE-DUTPASE FROM BACILLUS HALODURANS | BIFUNCTIONAL, TTP BINDING, COMPLEX, HYDROLASE
4i4n:F (ARG50) to (SER72) CRYSTAL STRUCTURE OF THE CATALYTIC CYS TO ALA MUTANT OF VCHSP31 FROM VIBRIO CHOLERAE | DIMER; ALPHA/BETA HYDROLASE, HEAT SHOCK PROTEIN, CHAPERONE, AMIDOPEPTIDASE, HYDROLASE
3skf:A (ASN293) to (PHE322) CRYSTAL STRUCTURE OF BETA-SITE APP-CLEAVING ENZYME 1 (BACE-WT) COMPLEX WITH (2S)-2-((3S)-3-(ACETYLAMINO)-3-(BUTAN-2-YL)-2-OXOPYRROLIDIN-1- YL)-N-((2S,3R)-3-HYDROXY-4-((3-METHOXYBENZYL)AMINO)-1-PHENYLBUTAN-2- YL)-4-PHENYLBUTANAMIDE | ALZHEIMER'S DISEASE, BACE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3skf:B (ASN293) to (PHE322) CRYSTAL STRUCTURE OF BETA-SITE APP-CLEAVING ENZYME 1 (BACE-WT) COMPLEX WITH (2S)-2-((3S)-3-(ACETYLAMINO)-3-(BUTAN-2-YL)-2-OXOPYRROLIDIN-1- YL)-N-((2S,3R)-3-HYDROXY-4-((3-METHOXYBENZYL)AMINO)-1-PHENYLBUTAN-2- YL)-4-PHENYLBUTANAMIDE | ALZHEIMER'S DISEASE, BACE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1ons:A (LYS47) to (SER69) CRYSTAL STRUCTURE OF ESCHERICHIA COLI HEAT SHOCK PROTEIN YEDU | HEAT SHOCK PROTEIN, STRESS RESPONSE, YEDU, HSP31, CHAPERONE, PROTEASE
1ope:A (ALA142) to (ILE159) DELETION MUTANT OF SUCCINYL-COA:3-KETOACID COA TRANSFERASE FROM PIG HEART | ALPHA/BETA PROTEIN, TRANSFERASE
1cms:A (LYS266) to (ASN291) THE THREE-DIMENSIONAL STRUCTURE OF RECOMBINANT BOVINE CHYMOSIN AT 2.3 ANGSTROMS RESOLUTION | HYDROLASE(ACID PROTEINASE)
2q11:B (THR59) to (GLY78) STRUCTURE OF BACE COMPLEXED TO COMPOUND 1 | BACE INHIBITOR COMPLEX, HYDROLASE
4ia5:A (ASP283) to (ASN309) HYDRATASE FROM LACTOBACILLUS ACIDOPHILUS - SEMET DERIVATIVE (APO LAH) | CONJUGATED LINOLEIC ACID, CLA, MCRA, ROSSMANN FOLD, FAD BINDING, HYDRATASE, FATTY ACID, IMMUNE SYSTEM
4ia6:A (ILE284) to (ASN309) HYDRATASE FROM LACTOBACILLUS ACIDOPHILUS IN A LIGAND BOUND FORM (LA LAH) | CONJUGATED LINOLEIC ACID, CLA, MCRA, ROSSMANN FOLD, FAD BINDING, HYDRATASE, FATTY ACID, IMMUNE SYSTEM
4ia6:B (ILE284) to (ASN309) HYDRATASE FROM LACTOBACILLUS ACIDOPHILUS IN A LIGAND BOUND FORM (LA LAH) | CONJUGATED LINOLEIC ACID, CLA, MCRA, ROSSMANN FOLD, FAD BINDING, HYDRATASE, FATTY ACID, IMMUNE SYSTEM
1oxt:B (MET1) to (LEU21) CRYSTAL STRUCTURE OF GLCV, THE ABC-ATPASE OF THE GLUCOSE ABC TRANSPORTER FROM SULFOLOBUS SOLFATARICUS | ABC-ATPASE, ATP-BINDING CASSETTE, ATPASE, GLCV, SULFOLOBUS SOLFATARICUS, TRANSPORT PROTEIN
1oxu:B (MET1) to (LEU21) CRYSTAL STRUCTURE OF GLCV, THE ABC-ATPASE OF THE GLUCOSE ABC TRANSPORTER FROM SULFOLOBUS SOLFATARICUS | ABC-ATPASE, ATP-BINDING CASSETTE, ATPASE, GLCV, SULFOLOBUS SOLFATARICUS, TRANSPORT PROTEIN
4ifd:C (LYS280) to (ALA332) CRYSTAL STRUCTURE OF AN 11-SUBUNIT EUKARYOTIC EXOSOME COMPLEX BOUND TO RNA | EXOSOME, RNA, RRP44, DIS3, PIN, RRP6, EXONUCLEASE, ENDONUCLEASE, HYDROLASE, NUCLEASE, RIBONUCLEASE, RNA PROCESSING, HYDROLASE-RNA COMPLEX
4xoa:E (ASN192) to (GLY220) CRYSTAL STRUCTURE OF A FIMH*DSG COMPLEX FROM E.COLI K12 IN SPACE GROUP P1 | TYPE I PILUS, CATCH-BOND, CELL ADHESION, LECTIN, UPEC, BACTERIAL ADHESIN, UTI, MANNOSE, ISOMERASE
2qcv:A (ASP12) to (LYS40) CRYSTAL STRUCTURE OF A PUTATIVE 5-DEHYDRO-2-DEOXYGLUCONOKINASE (IOLC) FROM BACILLUS HALODURANS C-125 AT 1.90 A RESOLUTION | PUTATIVE 5-DEHYDRO-2- DEOXYGLUCONOKINASE, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, TRANSFERASE
3syj:A (ASN401) to (THR418) CRYSTAL STRUCTURE OF THE HAEMOPHILUS INFLUENZAE HAP ADHESIN | BACTERIAL AGGREGATION AND BIOFILM FORMATION, SELF-ASSOCIATING AUTOTRANSPORTER (SAAT), OLIGOMERIZATION, BETA HELIX FOLD, MEMBRANE, CELL ADHESION
1dbd:A (GLU44) to (GLN63) E2 DNA-BINDING DOMAIN FROM PAPILLOMAVIRUS BPV-1 | DNA-BINDING DOMAIN, GENE REGULATION
1p9m:C (GLY164) to (SER184) CRYSTAL STRUCTURE OF THE HEXAMERIC HUMAN IL-6/IL-6 ALPHA RECEPTOR/GP130 COMPLEX | IG DOMAIN, FOUR HELIX BUNDLE, CYTOKINE, INTERLEUKIN-6, GP130, SIGNALING PROTEIN-CYTOKINE COMPLEX
4xrn:B (GLY51) to (LEU69) PILZ DOMAIN WITH C-DI-GMP OF A PROTEIN FROM PSEUDOMONAS AERUGINOSA | PILZ, C-DI-GMP, UNKNOWN FUNCTION
1pcx:A (MET550) to (MET568) CRYSTAL STRUCTURE OF THE COPII COAT SUBUNIT, SEC24, COMPLEXED WITH A PEPTIDE FROM THE SNARE PROTEIN BET1 | TRANSPORT PROTEIN
1pd0:A (MET550) to (GLY573) CRYSTAL STRUCTURE OF THE COPII COAT SUBUNIT, SEC24, COMPLEXED WITH A PEPTIDE FROM THE SNARE PROTEIN SED5 (YEAST SYNTAXIN-5) | TRANSPORT PROTEIN
1pd1:A (MET550) to (GLY573) CRYSTAL STRUCTURE OF THE COPII COAT SUBUNIT, SEC24, COMPLEXED WITH A PEPTIDE CONTAINING THE DXE CARGO SORTING SIGNAL OF YEAST SYS1 PROTEIN | TRANSPORT PROTEIN
4int:M (VAL20) to (GLY38) 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:a (VAL20) to (GLY38) 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:M (VAL20) to (GLY38) 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:a (VAL20) to (GLY38) 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
1dgg:A (MET212) to (TYR231) HUMAN ERYTHROCYTE CATALSE CYANIDE COMPLEX | CATALASE, HEME, NADPH, HYDROGEN PEROXIDE, CYANIDE, OXIDOREDUCTASE
3g7v:A (ASN241) to (ASN267) ISLET AMYLOID POLYPEPTIDE (IAPP OR AMYLIN) FUSED TO MALTOSE BINDING PROTEIN | NATIVE FOLD FOR AMYLOIDOGENIC PROTEIN, SUGAR TRANSPORT, TRANSPORT, AMIDATION, AMYLOID, CLEAVAGE ON PAIR OF BASIC RESIDUES, HORMONE, SECRETED, SUGAR BINDING PROTEIN
2qk5:B (ASN354) to (PHE383) STRUCTURE OF BACE1 BOUND TO SCH626485 | BACE1, PROTEASE, ALTERNATIVE SPLICING, ASPARTYL PROTEASE, GLYCOPROTEIN, HYDROLASE, MEMBRANE, TRANSMEMBRANE, ZYMOGEN
2qkl:A (PRO74) to (TRP107) THE CRYSTAL STRUCTURE OF FISSION YEAST MRNA DECAPPING ENZYME DCP1-DCP2 COMPLEX | PROTEIN-PROTEIN COMPLEX, HYDROLASE
2cnn:A (SER113) to (ASP135) CRYSTAL STRUCTURES OF CASPASE-3 IN COMPLEX WITH AZA-PEPTIDE EPOXIDE INHIBITORS. | THIOL PROTEASE, PHOSPHORYLATION, CYSTEINE-PROTEASE, PROTEASE- INHIBITOR COMPLEX, PROTEASE, EPOXIDES, TETRAMER, APOPTOSIS, AZA- PEPTIDE, EPOXYSUCCINYL, ICE, YAMA, CPP32, CLAN CD, AZA-ASP, ZYMOGEN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2ql5:A (PHE137) to (PRO158) CRYSTAL STRUCTURE OF CASPASE-7 WITH INHIBITOR AC-DMQD-CHO | CYSTEINE PROTEASE, APOPTOSIS, THIOL PROTEASE, ZYMOGEN, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
2ql5:C (PHE437) to (PRO458) CRYSTAL STRUCTURE OF CASPASE-7 WITH INHIBITOR AC-DMQD-CHO | CYSTEINE PROTEASE, APOPTOSIS, THIOL PROTEASE, ZYMOGEN, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
2ql9:A (CYS136) to (PRO158) CRYSTAL STRUCTURE OF CASPASE-7 WITH INHIBITOR AC-DQMD-CHO | CYSTEINE PROTEASE, APOPTOSIS, THIOL PROTEASE, ZYMOGEN, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
2ql9:C (PHE437) to (PRO458) CRYSTAL STRUCTURE OF CASPASE-7 WITH INHIBITOR AC-DQMD-CHO | CYSTEINE PROTEASE, APOPTOSIS, THIOL PROTEASE, ZYMOGEN, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
2qlb:A (PHE137) to (PRO158) CRYSTAL STRUCTURE OF CASPASE-7 WITH INHIBITOR AC-ESMD-CHO | CYSTEINE PROTEASE, APOPTOSIS, THIOL PROTEASE, ZYMOGEN, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
2qlj:A (CYS136) to (PRO158) CRYSTAL STRUCTURE OF CASPASE-7 WITH INHIBITOR AC-WEHD-CHO | CYSTEINE PROTEASE, APOPTOSIS, THIOL PROTEASE, ZYMOGEN, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4xsy:C (GLY248) to (VAL263) CRYSTAL STRUCTURE OF CBR 9379 BOUND TO ESCHERICHIA COLI RNA POLYMERASE HOLOENZYME | BACTERIAL RNA POLYMERASE ANTIBIOTIC COMPLEX, TRANSCRIPTION-ANTIBIOTIC COMPLEX
2qmg:A (ASN354) to (PHE383) STRUCTURE OF BACE BOUND TO SCH745966 | BACE1, PROTEASE, ALTERNATIVE SPLICING, ASPARTYL PROTEASE, GLYCOPROTEIN, HYDROLASE, MEMBRANE, TRANSMEMBRANE, ZYMOGEN
3gbu:A (LEU3) to (LYS30) CRYSTAL STRUCTURE OF AN UNCHARACTERIZED SUGAR KINASE PH1459 FROM PYROCOCCUS HORIKOSHII IN COMPLEX WITH ATP | CARBOHYDRATE KINASE, PFKB FAMILY, PSI-II, 11207G, NYSGXRC, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NEW YORK STRUCTURAL GENOMIX RESEARCH CONSORTIUM, KINASE, TRANSFERASE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS
3gbu:B (LEU3) to (LYS30) CRYSTAL STRUCTURE OF AN UNCHARACTERIZED SUGAR KINASE PH1459 FROM PYROCOCCUS HORIKOSHII IN COMPLEX WITH ATP | CARBOHYDRATE KINASE, PFKB FAMILY, PSI-II, 11207G, NYSGXRC, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NEW YORK STRUCTURAL GENOMIX RESEARCH CONSORTIUM, KINASE, TRANSFERASE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS
3gbu:D (LEU3) to (LYS30) CRYSTAL STRUCTURE OF AN UNCHARACTERIZED SUGAR KINASE PH1459 FROM PYROCOCCUS HORIKOSHII IN COMPLEX WITH ATP | CARBOHYDRATE KINASE, PFKB FAMILY, PSI-II, 11207G, NYSGXRC, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NEW YORK STRUCTURAL GENOMIX RESEARCH CONSORTIUM, KINASE, TRANSFERASE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS
4xtk:F (SER3) to (PRO31) STRUCTURE OF TM1797, A CAS1 PROTEIN FROM THERMOTOGA MARITIMA | CAS1, DNASE, PROKARYOTIC IMMUNE SYSTEM, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, HYDROLASE
4xtu:A (GLN231) to (SER258) MYCOBACTERIUM TUBERCULOSIS BIOTIN LIGASE COMPLEXED WITH BISUBSTRATE INHIBITOR (N-({[(1R,2S,3R,4R)-4-(6-AMINO-9H-PURIN-9-YL)-2,3- DIHYDROXYCYCLOPENTYL]METHYL}SULFAMOYL)-5-[(3AS,4S,6AR)-2- OXOHEXAHYDRO-1H-THIENO[3,4-D]IMIDAZOL-4-YL]PENTANAMIDE) | BIOTIN-PROTEIN LIGASE, BISUBSTRATE INHIBITOR, LIGASE-LIGASE INHIBITOR COMPLEX
4xtu:B (GLY230) to (SER258) MYCOBACTERIUM TUBERCULOSIS BIOTIN LIGASE COMPLEXED WITH BISUBSTRATE INHIBITOR (N-({[(1R,2S,3R,4R)-4-(6-AMINO-9H-PURIN-9-YL)-2,3- DIHYDROXYCYCLOPENTYL]METHYL}SULFAMOYL)-5-[(3AS,4S,6AR)-2- OXOHEXAHYDRO-1H-THIENO[3,4-D]IMIDAZOL-4-YL]PENTANAMIDE) | BIOTIN-PROTEIN LIGASE, BISUBSTRATE INHIBITOR, LIGASE-LIGASE INHIBITOR COMPLEX
4xtv:A (GLN231) to (SER258) MYCOBACTERIUM TUBERCULOSIS BIOTIN LIGASE COMPLEXED WITH BISUBSTRATE INHIBITOR 36 (N-({[(1R,3S)-3-(6-AMINO-9H-PURIN-9-YL) CYCLOPENTYL]METHYL}SULFAMOYL)-5-[(3AS,4S,6AR)-2-OXOHEXAHYDRO-1H- THIENO[3,4-D]IMIDAZOL-4-YL]PENTANAMIDE) | BIOTIN-PROTEIN LIGASE, BISUBSTRATE INHIBITOR, LIGASE-LIGASE INHIBITOR COMPLEX
4xtv:B (GLN231) to (SER258) MYCOBACTERIUM TUBERCULOSIS BIOTIN LIGASE COMPLEXED WITH BISUBSTRATE INHIBITOR 36 (N-({[(1R,3S)-3-(6-AMINO-9H-PURIN-9-YL) CYCLOPENTYL]METHYL}SULFAMOYL)-5-[(3AS,4S,6AR)-2-OXOHEXAHYDRO-1H- THIENO[3,4-D]IMIDAZOL-4-YL]PENTANAMIDE) | BIOTIN-PROTEIN LIGASE, BISUBSTRATE INHIBITOR, LIGASE-LIGASE INHIBITOR COMPLEX
4xtw:A (GLN231) to (SER258) MYCOBACTERIUM TUBERCULOSIS BIOTIN LIGASE COMPLEXED WITH BISUBSTRATE INHIBITOR 46 WITH AZIDE IN PLACE OF 2'OH | BIOTIN-PROTEIN LIGASE, BISUBSTRATE INHIBITOR, LIGASE-LIGASE INHIBITOR COMPLEX
4xty:A (GLN231) to (SER258) MYCOBACTERIUM TUBERCULOSIS BIOTIN LIGASE COMPLEXED WITH BISUBSTRATE INHIBITOR 63 WITH FLUORINE IN PLACE OF 2'OH | BIOTIN-PROTEIN LIGASE, BISUBSTRATE INHIBITOR, LIGASE-LIGASE INHIBITOR COMPLEX
4xty:B (GLY230) to (SER258) MYCOBACTERIUM TUBERCULOSIS BIOTIN LIGASE COMPLEXED WITH BISUBSTRATE INHIBITOR 63 WITH FLUORINE IN PLACE OF 2'OH | BIOTIN-PROTEIN LIGASE, BISUBSTRATE INHIBITOR, LIGASE-LIGASE INHIBITOR COMPLEX
4xtx:A (GLN231) to (SER258) MYCOBACTERIUM TUBERCULOSIS BIOTIN LIGASE COMPLEXED WITH BISUBSTRATE INHIBITOR 57 WITH AZIDE IN PLACE OF RIBOSE 2'OH | BIOTIN-PROTEIN LIGASE, BISUBSTRATE INHIBITOR, LIGASE-LIGASE INHIBITOR COMPLEX
4xtx:B (GLY230) to (SER258) MYCOBACTERIUM TUBERCULOSIS BIOTIN LIGASE COMPLEXED WITH BISUBSTRATE INHIBITOR 57 WITH AZIDE IN PLACE OF RIBOSE 2'OH | BIOTIN-PROTEIN LIGASE, BISUBSTRATE INHIBITOR, LIGASE-LIGASE INHIBITOR COMPLEX
4xu1:A (GLN231) to (SER258) MYCOBACTERIUM TUBERCULOSIS BIOTIN LIGASE COMPLEXED WITH BISUBSTRATE INHIBITOR 82 THAT INCORPORATES A MORPHOLINE IN PLACE OF THE RIBOSE | BIOTIN-PROTEIN LIGASE, BISUBSTRATE INHIBITOR, LIGASE-LIGASE INHIBITOR COMPLEX
4xu1:B (GLY230) to (SER258) MYCOBACTERIUM TUBERCULOSIS BIOTIN LIGASE COMPLEXED WITH BISUBSTRATE INHIBITOR 82 THAT INCORPORATES A MORPHOLINE IN PLACE OF THE RIBOSE | BIOTIN-PROTEIN LIGASE, BISUBSTRATE INHIBITOR, LIGASE-LIGASE INHIBITOR COMPLEX
4xu2:B (GLY230) to (SER258) MYCOBACTERIUM TUBERCULOSIS BIOTIN LIGASE COMPLEXED WITH BISUBSTRATE INHIBITOR 87 WITH A 3'DEOXY RIBOSE | BIOTIN-PROTEIN LIGASE, BISUBSTRATE INHIBITOR, LIGASE-LIGASE INHIBITOR COMPLEX
4xu3:A (GLN231) to (SER258) MYCOBACTERIUM TUBERCULOSIS BIOTIN LIGASE COMPLEXED WITH BISUBSTRATE INHIBITOR 90 THAT HAS AN ACYCLIC ETHER IN PLACE OF THE RIBOSE | BIOTIN-PROTEIN LIGASE, BISUBSTRATE INHIBITOR, LIGASE-LIGASE INHIBITOR COMPLEX
4xu3:B (GLY230) to (SER258) MYCOBACTERIUM TUBERCULOSIS BIOTIN LIGASE COMPLEXED WITH BISUBSTRATE INHIBITOR 90 THAT HAS AN ACYCLIC ETHER IN PLACE OF THE RIBOSE | BIOTIN-PROTEIN LIGASE, BISUBSTRATE INHIBITOR, LIGASE-LIGASE INHIBITOR COMPLEX
4irl:A (ASN242) to (LEU263) X-RAY STRUCTURE OF THE CARD DOMAIN OF ZEBRAFISH GBP-NLRP1 LIKE PROTEIN | CARD, DEATH FOLD SUPERFAMILY, SIX-HELIX BUNDLE, INFLAMMASOME, APOPTOSIS, INNATE IMMUNE SYSTEM, SIGNAL TRANSDUCTION
3gd4:A (GLY223) to (GLU253) CRYSTAL STRUCTURE OF THE REDUCED, NAD-BOUND FORM OF MURINE APOPTOSIS INDUCING FACTOR | ALPHA-BETA PROTEIN, ACETYLATION, APOPTOSIS, DNA-BINDING, FAD, FLAVOPROTEIN, MITOCHONDRION, NUCLEUS, OXIDOREDUCTASE, PHOSPHOPROTEIN, TRANSIT PEPTIDE
3gdb:A (GLY672) to (ILE700) CRYSTAL STRUCTURE OF SPR0440 GLYCOSIDE HYDROLASE DOMAIN, ENDO-D FROM STREPTOCOCCUS PNEUMONIAE R6 | ALPHA-BETA-BARRELS, CELL WALL, PEPTIDOGLYCAN-ANCHOR, SECRETED, HYDROLASE
2cu5:C (GLY29) to (VAL47) CRYSTAL STRUCTURE OF THE CONSERVED HYPOTHETICAL PROTEIN TT1486 FROM THERMUS THERMOPHILUS HB8 | THERMUS THERMOPHILUS HB8, CONSERVED HYPOTHETICAL PROTEIN, STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, UNKNOWN FUNCTION
2cun:A (ILE269) to (ASP287) CRYSTAL STRUCTURE OF PHOSPHOGLYCERATE KINASE FROM PYROCOCCUS HORIKOSHII OT3 | PHOSPHOGLYCERATE KINASE, STRUCTURAL GENOMICS, TANPAKU 3000, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, TRANSFERASE
2cun:B (ILE269) to (ASP287) CRYSTAL STRUCTURE OF PHOSPHOGLYCERATE KINASE FROM PYROCOCCUS HORIKOSHII OT3 | PHOSPHOGLYCERATE KINASE, STRUCTURAL GENOMICS, TANPAKU 3000, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, TRANSFERASE
4iug:A (PRO701) to (VAL735) CRYSTAL STRUCTURE OF BETA-GALACTOSIDASE FROM ASPERGILLUS ORYZAE IN COMPLEX WITH GALACTOSE | TIM BARREL, GLYCOSIDE HYDROLASE, HYDROLASE
2qry:A (ASP121) to (SER140) PERIPLASMIC THIAMIN BINDING PROTEIN | THIAMIN BINDING PROTEIN, PERIPLASMIC, ABC TRANSPORTER, TRANSPORT PROTEIN
2qry:B (ASP121) to (SER140) PERIPLASMIC THIAMIN BINDING PROTEIN | THIAMIN BINDING PROTEIN, PERIPLASMIC, ABC TRANSPORTER, TRANSPORT PROTEIN
2qry:C (ASP121) to (SER140) PERIPLASMIC THIAMIN BINDING PROTEIN | THIAMIN BINDING PROTEIN, PERIPLASMIC, ABC TRANSPORTER, TRANSPORT PROTEIN
2qry:D (ASP121) to (SER140) PERIPLASMIC THIAMIN BINDING PROTEIN | THIAMIN BINDING PROTEIN, PERIPLASMIC, ABC TRANSPORTER, TRANSPORT PROTEIN
2cwu:A (ARG267) to (PHE297) SUBSTRATE SCHIFF-BASE INTERMEDIATE OF COPPER AMINE OXIDASE FROM ARTHROBACTER GLOBIFORMIS | COPPER, AMINE OXIDASE, TOPAQUINONE, TPQ, CATALYTIC BASE, REACTION INTERMEDIATE, 2-PHENETHYLAMINE, OXIDOREDUCTASE
1po3:A (PHE558) to (ARG578) CRYSTAL STRUCTURE OF FERRIC CITRATE TRANSPORTER FECA IN COMPLEX WITH FERRIC CITRATE | OUTER MEMBRANE PROTEIN, BETA BARREL, TONB-DEPENDENT TRANSPORT, CITRATE, SIDEROPHORE, IRON
3t6y:B (SER43) to (ASN83) 5'-DIPHENYL NUCLEOSIDE INHIBITORS OF PLASMODIUM FALCIPARUM DUTPASE | DUTP BINDING, NUCLEUS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3gjr:A (SER113) to (ASP135) CASPASE-3 BINDS DIVERSE P4 RESIDUES IN PEPTIDES | ENZYME CATALYSIS, CYSTEINE PROTEASE, PROTEIN RECOGNITION, APOPTOSIS, HYDROLASE, PHOSPHOPROTEIN, PROTEASE, S-NITROSYLATION, THIOL PROTEASE, ZYMOGEN
3gjr:C (SER113) to (ASP135) CASPASE-3 BINDS DIVERSE P4 RESIDUES IN PEPTIDES | ENZYME CATALYSIS, CYSTEINE PROTEASE, PROTEIN RECOGNITION, APOPTOSIS, HYDROLASE, PHOSPHOPROTEIN, PROTEASE, S-NITROSYLATION, THIOL PROTEASE, ZYMOGEN
2czj:E (LEU58) to (ALA69) CRYSTAL STRUCTURE OF THE TRNA DOMAIN OF TMRNA FROM THERMUS THERMOPHILUS HB8 | SMPB, TMRNA, SSRA RNA, 10SA RNA, TRNA, TRANS-TRANSLATION, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, RNA BINDING PROTEIN-RNA COMPLEX
2qu3:A (CYS381) to (GLY396) BACE1 WITH COMPOUND 2 | BACE1, ACYLGUANIDINE, INHIBITOR, STRUCTURE, ALTERNATIVE SPLICING, ASPARTYL PROTEASE, GLYCOPROTEIN, HYDROLASE, MEMBRANE, PROTEASE, TRANSMEMBRANE, ZYMOGEN
1dyp:A (VAL66) to (LYS86) 1,3-ALPHA-1,4-BETA-D-GALACTOSE-4-SULFATE- 3,6-ANHYDRO-D-GALACTOSE 4 GALACTOHYDROLASE | HYDROLASE, KAPPA-CARRAGEENAN DOUBLE HELIX DEGRADATION
1ps9:A (VAL588) to (ALA616) THE CRYSTAL STRUCTURE AND REACTION MECHANISM OF E. COLI 2,4- DIENOYL COA REDUCTASE | IRON-SULFUR, TIM BARREL, FLAVODOXIN, FLAVIN, ELECTRON TRANSFER, HYDRIDE TRANSFER, OXIDOREDUCTASE
2d1w:B (ARG267) to (PHE297) SUBSTRATE SCHIFF-BASE INTERMEDIATE WITH TYRAMINE IN COPPER AMINE OXIDASE FROM ARTHROBACTER GLOBIFORMIS | COPPER, AMINE OXIDASE, TOPAQUINONE, TPQ, REACTION INTERMEDIATE, SUBSTRATE SCHIFF-BASE, OXIDOREDUCTASE
1pso:E (VAL265) to (PHE286) THE CRYSTAL STRUCTURE OF HUMAN PEPSIN AND ITS COMPLEX WITH PEPSTATIN | ACID PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1e0d:A (VAL228) to (LEU248) UDP-N-ACETYLMURAMOYL-L-ALANINE:D-GLUTAMATE LIGASE | LIGASE, PEPTIDOGLYCAN SYNTHESIS, MURD, ADP-FORMING ENZYME
4y1a:D (VAL172) to (ASN190) IMMUNE COMPLEX | TCR MHC, IMMUNE SYSTEM
1pv2:F (LYS48) to (THR71) NATIVE FORM 2 E.COLI CHAPERONE HSP31 | CHAPERONE, HEAT SHOCK PROTEIN, PUTATIVE CATALYTIC TRIAD, FLEXIBILITY, MONOCLINIC
4j1c:A (ASN354) to (ILE385) CRYSTAL STRUCTURE OF BACE-1 IN COMPLEX WITH 5-CYANO-PYRIDINE-2- CARBOXYLIC ACID [3-((S)-2-AMINO-5,5-DIFLUORO-4-FLUOROMETHYL-5,6- DIHYDRO-4H-[1,3]OXAZIN-4-YL)-4-FLUORO-PHENYL]-AMIDE | PROTEASE INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4j1e:A (ASN354) to (PHE383) CRYSTAL STRUCTURE OF BACE-1 IN COMPLEX WITH 5-CYANO-PYRIDINE-2- CARBOXYLIC ACID [3-((4S,6S)-2-AMINO-4-FLUOROMETHYL-6-TRIFLUOROMETHYL- 5,6-DIHYDRO-4H-[1,3]OXAZIN-4-YL)-4-FLUORO-PHENYL]-AMIDE | PROTEASE INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3go7:B (ARG15) to (PRO49) CRYSTAL STRUCTURE OF M. TUBERCULOSIS RIBOKINASE (RV2436) IN COMPLEX WITH RIBOSE | PHOSPHOFRUCTOKINASE, CARBOHYDRATE KINASE, KINASE, TRANSFERASE
2d40:B (GLY98) to (ILE114) CRYSTAL STRUCTURE OF Z3393 FROM ESCHERICHIA COLI O157:H7 | GENTISIC ACID, 1,2-DIOXYGENASE, BICUPIN, TETRAMER, MONTREAL-KINGSTON BACTERIAL STRUCTURAL GENOMICS INITIATIVE, BSGI, STRUCTURAL GENOMICS, OXIDOREDUCTASE
3gpj:J (VAL12) to (LYS28) 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:M (VAL12) to (GLY30) 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:X (VAL12) to (LYS28) 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:1 (VAL12) to (GLY30) 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
4j2x:C (GLN446) to (SER465) CSL (RBP-JK) WITH COREPRESSOR KYOT2 BOUND TO DNA | LIM DOMAIN CONTAINING PROTEIN, TRANSCRIPTION FACTOR COREPRESSOR, DNA BINDING, NUCLEUS, TRANSCRIPTION-DNA BINDING PROTEIN-DNA COMPLEX
3gpw:M (VAL12) to (GLY30) 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:1 (VAL12) to (GLY30) 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
2d9y:A (THR12) to (LYS30) SOLUTION STRUCTURE OF THE PH DOMAIN OF PEPP-3 FROM HUMAN | PH DOMAIN, PEPP-3, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, SIGNALING PROTEIN
4y69:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4y69:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2dcu:A (GLY233) to (VAL246) CRYSTAL STRUCTURE OF TRANSLATION INITIATION FACTOR AIF2BETAGAMMA HETERODIMER WITH GDP | PROTEIN COMPLEX, TRANSLATION
4y6a:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-PAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4y6a:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-PAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4y6v:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4y6v:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4y6z:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y6z:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y6z:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y6z:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
3tec:E (ASP201) to (GLY223) CALCIUM BINDING TO THERMITASE. CRYSTALLOGRAPHIC STUDIES OF THERMITASE AT 0, 5 AND 100 MM CALCIUM | COMPLEX(SERINE PROTEINASE-INHIBITOR)
4y70:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAV-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y70:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAV-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y70:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAV-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y70:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAV-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y74:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y74:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y74:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y74:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y77:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAF-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y77:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAF-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y77:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAF-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y77:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAF-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y78:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y78:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y78:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y78:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4j70:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH THE BELACTOSIN DERIVATIVE 3E | PROTEASOME, DRUG DISCOVERY, IRREVERSIBLE INHIBITION, BETA-LACTONE, NTN HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4j70:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH THE BELACTOSIN DERIVATIVE 3E | PROTEASOME, DRUG DISCOVERY, IRREVERSIBLE INHIBITION, BETA-LACTONE, NTN HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4j70:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH THE BELACTOSIN DERIVATIVE 3E | PROTEASOME, DRUG DISCOVERY, IRREVERSIBLE INHIBITION, BETA-LACTONE, NTN HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4j70:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH THE BELACTOSIN DERIVATIVE 3E | PROTEASOME, DRUG DISCOVERY, IRREVERSIBLE INHIBITION, BETA-LACTONE, NTN HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4y7w:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y7w:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y7w:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y7w:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y7x:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAA-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y7x:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAA-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y7x:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAA-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y7x:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAA-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y7y:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAA-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y7y:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAA-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y7y:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAA-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y7y:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAA-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y80:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAI-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y80:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAI-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y80:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAI-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y80:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAI-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y81:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAY-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y81:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAY-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y81:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAY-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y81:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAY-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y82:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAY-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y82:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAY-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y82:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAY-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y82:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAY-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y84:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH N3-A(4,4-F2P)NLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y84:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH N3-A(4,4-F2P)NLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y84:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH N3-A(4,4-F2P)NLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y84:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH N3-A(4,4-F2P)NLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8g:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APNLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8g:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APNLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8g:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APNLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8g:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APNLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8h:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8h:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8h:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8h:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8j:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8j:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8j:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8j:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4jb7:A (VAL101) to (GLY120) 1.42 ANGSTROM RESOLUTION CRYSTAL STRUCTURE OF ACCESSORY COLONIZATION FACTOR ACFC (ACFC) IN COMPLEX WITH D-ASPARTIC ACID | ACCESSORY COLONIZATION FACTOR ACFC, VIRULENCE, PATHOGENESIS, CSGID, STRUCTURAL GENOMICS, NIAID, NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, ALPHA/BETA FOLD, CELLULAR PROCESSES, CELL INVASION
4y8l:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-APLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8l:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-APLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8l:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-APLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8l:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-APLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8m:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8m:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
1ea7:A (GLU226) to (ILE246) SPHERICASE | HYDROLASE, SERINE PROTEASE, SPHERICASE, SUBTILISIN LIKE PROTEASE
4y8n:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAE- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8n:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAE- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8o:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAF- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8o:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAF- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8o:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAF- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8o:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAF- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
2dmo:A (ALA9) to (ASN48) REFINED SOLUTION STRUCTURE OF THE 1ST SH3 DOMAIN FROM HUMAN NEUTROPHIL CYTOSOL FACTOR 2 (NCF-2) | SH3 DOMAIN, NEUTROPHIL CYTOSOL FACTOR, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, SIGNALING PROTEIN
4y8q:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAY- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8q:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAY- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8q:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAY- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8q:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAY- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8s:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8s:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8s:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8s:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8t:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8t:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8t:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8t:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8u:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-PAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8u:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-PAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y9y:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H116E MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4y9y:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H116E MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4y9z:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA2-H116E MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y9z:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H116E MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y9z:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA2-H116E MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y9z:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H116E MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya0:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H116E MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya0:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H116E MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya1:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H116N MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ya1:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H116N MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ya2:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA2-H116N MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya2:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H116N MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya2:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA2-H116N MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya2:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H116N MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya3:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H116N MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya4:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H114D MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ya4:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H114D MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ya7:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya7:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya7:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya7:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya9:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-LAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya9:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-LAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya9:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-LAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya9:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-LAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
1qak:A (THR352) to (ALA383) THE ACTIVE SITE BASE CONTROLS COFACTOR REACTIVITY IN ESCHERICHIA COLI AMINE OXIDASE : X-RAY CRYSTALLOGRAPHIC STUDIES WITH MUTATIONAL VARIANTS | OXIDOREDUCTASE, COPPER, TPQ, PERIPLASMIC, CATALYTIC BASE MUTANT
1qak:B (THR352) to (ALA383) THE ACTIVE SITE BASE CONTROLS COFACTOR REACTIVITY IN ESCHERICHIA COLI AMINE OXIDASE : X-RAY CRYSTALLOGRAPHIC STUDIES WITH MUTATIONAL VARIANTS | OXIDOREDUCTASE, COPPER, TPQ, PERIPLASMIC, CATALYTIC BASE MUTANT
1qal:A (THR352) to (ASN383) THE ACTIVE SITE BASE CONTROLS COFACTOR REACTIVITY IN ESCHERICHIA COLI AMINE OXIDASE : X-RAY CRYSTALLOGRAPHIC STUDIES WITH MUTATIONAL VARIANTS | MUSHROOM SHAPED HOMODIMER WITH MAINLY BETA STRUCTURE. THERE ARE 3 SMALL PERIPHERAL ALPHA/BETA DOMAINS., OXIDOREDUCTASE
3tpv:B (ILE179) to (LEU196) STRUCTURE OF PHIPA BOUND TO ADP | PERSISTENCE, MULTIDRUG TOLERANCE, HIPA, HIPB, TRANSFERASE
1qd5:A (VAL136) to (ARG157) OUTER MEMBRANE PHOSPHOLIPASE A FROM ESCHERICHIA COLI | ANTI-PARALLEL BETA BARREL, MEMBRANE PHOSPHOLIPASE, MEMBRANE PROTEIN
1qdm:C (LYS70) to (GLY87) CRYSTAL STRUCTURE OF PROPHYTEPSIN, A ZYMOGEN OF A BARLEY VACUOLAR ASPARTIC PROTEINASE. | ASPARTIC PROTEINASES, PHYTEPSIN, SAPOSIN-LIKE DOMAIN, ZYMOGEN STRUCTURE, HYDROLASE
1qdm:C (LYS273) to (ASP302) CRYSTAL STRUCTURE OF PROPHYTEPSIN, A ZYMOGEN OF A BARLEY VACUOLAR ASPARTIC PROTEINASE. | ASPARTIC PROTEINASES, PHYTEPSIN, SAPOSIN-LIKE DOMAIN, ZYMOGEN STRUCTURE, HYDROLASE
4jje:A (PHE114) to (ASP135) CASPASE-3 SPECIFIC UNNATURAL AMINO ACID PEPTIDES | PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1ej6:B (THR1173) to (TYR1198) REOVIRUS CORE | VIRUS, ICOSAHEDRAL, NON-EQUIVALENCE, DSRNA VIRUS, METHYLASE, METHYLTRANSFERASE, GUANYLYLTRANSFERASE, ZINC FINGER, ICOSAHEDRAL VIRUS
1ej6:C (THR1173) to (TYR1198) REOVIRUS CORE | VIRUS, ICOSAHEDRAL, NON-EQUIVALENCE, DSRNA VIRUS, METHYLASE, METHYLTRANSFERASE, GUANYLYLTRANSFERASE, ZINC FINGER, ICOSAHEDRAL VIRUS
2ren:A (LYS73) to (GLY90) STRUCTURE OF RECOMBINANT HUMAN RENIN, A TARGET FOR CARDIOVASCULAR- ACTIVE DRUGS, AT 2.5 ANGSTROMS RESOLUTION | HYDROLASE(ACID PROTEINASE)
3h0e:A (SER113) to (ASP135) 3,4-DIHYDROPYRIMIDO(1,2-A)INDOL-10(2H)-ONES AS POTENT NON- PEPTIDIC INHIBITORS OF CASPASE-3 | CASPASE-3, PROTEIN-INHIBITOR COMPLEX, APOPTOSIS, CYTOPLASM, HYDROLASE, PHOSPHOPROTEIN, POLYMORPHISM, PROTEASE, S- NITROSYLATION, THIOL PROTEASE, ZYMOGEN
4yed:B (GLY200) to (LYS223) TCDA (CSDL) | N6-THREONYLCARBAMOYLADENOSINE DEHYDRATASE TRNA MODIFICATION, LIGASE
4yed:C (GLY200) to (ALA221) TCDA (CSDL) | N6-THREONYLCARBAMOYLADENOSINE DEHYDRATASE TRNA MODIFICATION, LIGASE
4yed:D (GLY200) to (ALA221) TCDA (CSDL) | N6-THREONYLCARBAMOYLADENOSINE DEHYDRATASE TRNA MODIFICATION, LIGASE
4yfg:B (PRO232) to (ASN251) CRYSTAL STRUCTURE OF PTP DELTA MEA3/MEB MINUS VARIANT IG1-FN1 | SYNAPSE ORGANIZER, HYDROLASE
2e1p:A (GLU300) to (THR323) CRYSTAL STRUCTURE OF PRO-TK-SUBTILISIN | SUBTILISIN, SERINE PROTEASE, PRECURSOR, HYDROLASE
1epz:A (GLY58) to (LYS73) CRYSTAL STRUCTURE OF DTDP-6-DEOXY-D-XYLO-4-HEXULOASE 3,5-EPIMERASE FROM METHANOBACTERIUM THERMOAUTOTROPHICUM WITH BOUND LIGAND. | RACEMASE, DTDP-4-DEHYDRORHAMNOSE EPIMERASE, ISOMERASE
4yfk:I (ARG528) to (PRO590) ESCHERICHIA COLI RNA POLYMERASE IN COMPLEX WITH SQUARAMIDE COMPOUND 8. | SWITCH REGION, SQUARAMIDE, TRANSCRIPTION-INHIBITOR COMPLEX, TRANSCRIPTION-TRANSCRIPTION INHIBITOR COMPLEX
2rir:A (ASP59) to (GLN87) CRYSTAL STRUCTURE OF DIPICOLINATE SYNTHASE, A CHAIN, FROM BACILLUS SUBTILIS | STRUCTURAL GENOMICS, APC1343, DIPICOLINATE SYNTHASE, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, AMINO-ACID BIOSYNTHESIS, DIAMINOPIMELATE BIOSYNTHESIS, LYSINE BIOSYNTHESIS, SPORULATION, OXIDOREDUCTASE
2rir:C (ASP59) to (GLN87) CRYSTAL STRUCTURE OF DIPICOLINATE SYNTHASE, A CHAIN, FROM BACILLUS SUBTILIS | STRUCTURAL GENOMICS, APC1343, DIPICOLINATE SYNTHASE, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, AMINO-ACID BIOSYNTHESIS, DIAMINOPIMELATE BIOSYNTHESIS, LYSINE BIOSYNTHESIS, SPORULATION, OXIDOREDUCTASE
2rir:D (ASP59) to (GLN87) CRYSTAL STRUCTURE OF DIPICOLINATE SYNTHASE, A CHAIN, FROM BACILLUS SUBTILIS | STRUCTURAL GENOMICS, APC1343, DIPICOLINATE SYNTHASE, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, AMINO-ACID BIOSYNTHESIS, DIAMINOPIMELATE BIOSYNTHESIS, LYSINE BIOSYNTHESIS, SPORULATION, OXIDOREDUCTASE
2rir:G (ASP59) to (LEU85) CRYSTAL STRUCTURE OF DIPICOLINATE SYNTHASE, A CHAIN, FROM BACILLUS SUBTILIS | STRUCTURAL GENOMICS, APC1343, DIPICOLINATE SYNTHASE, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, AMINO-ACID BIOSYNTHESIS, DIAMINOPIMELATE BIOSYNTHESIS, LYSINE BIOSYNTHESIS, SPORULATION, OXIDOREDUCTASE
2rir:H (ASP59) to (LEU85) CRYSTAL STRUCTURE OF DIPICOLINATE SYNTHASE, A CHAIN, FROM BACILLUS SUBTILIS | STRUCTURAL GENOMICS, APC1343, DIPICOLINATE SYNTHASE, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, AMINO-ACID BIOSYNTHESIS, DIAMINOPIMELATE BIOSYNTHESIS, LYSINE BIOSYNTHESIS, SPORULATION, OXIDOREDUCTASE
4yfn:I (GLY248) to (VAL263) ESCHERICHIA COLI RNA POLYMERASE IN COMPLEX WITH SQUARAMIDE COMPOUND 14 (N-[3,4-DIOXO-2-(4-{[4-(TRIFLUOROMETHYL)BENZYL]AMINO}PIPERIDIN-1-YL) CYCLOBUT-1-EN-1-YL]-3,5-DIMETHYL-1,2-OXAZOLE-4-SULFONAMIDE) | SWITCH REGION, SQUARAMIDE, TRANSCRIPTION-TRANSCRIPTION INHIBITOR COMPLEX
3tuj:C (MSE1) to (GLN19) INWARD FACING CONFORMATIONS OF THE METNI METHIONINE ABC TRANSPORTER: DM CRYSTAL FORM | ABC-TRANSPORTER, TYPE I ABC TYPE IMPORTER,METHIONINE UPTAKE TRANSPORTER, MEMBRANE PROTEIN, AMINO-ACID TRANSPORT, ATP-BINDING, HYDROLASE, INNER MEMBRANE, HYDROLASE-TRANSPORT PROTEIN COMPLEX
3tuj:D (ILE2) to (GLN19) INWARD FACING CONFORMATIONS OF THE METNI METHIONINE ABC TRANSPORTER: DM CRYSTAL FORM | ABC-TRANSPORTER, TYPE I ABC TYPE IMPORTER,METHIONINE UPTAKE TRANSPORTER, MEMBRANE PROTEIN, AMINO-ACID TRANSPORT, ATP-BINDING, HYDROLASE, INNER MEMBRANE, HYDROLASE-TRANSPORT PROTEIN COMPLEX
3h1j:O (GLY20) to (LEU38) STIGMATELLIN-BOUND CYTOCHROME BC1 COMPLEX FROM CHICKEN | CYTOCHROME BC1, MEMBRANE PROTEIN, HEME PROTEIN, RIESKE IRON SULFUR PROTEIN, CYTOCHROME B, CYTOCHROME C1, COMPLEX III, MITOCHONDRIAL PROCESSING PROTEIN, UBIQUINONE, OXIDOREDUCTASE, REDOX ENZYM RESPIRATORY CHAIN, ELECTRON TRANSPORT, HEME, INNER MEMBRANE IRON, MEMBRANE, METAL-BINDING, MITOCHONDRION, TRANSMEMBRANE, STIGMATELLIN, IRON, MITOCHONDRION INNER MEMBRANE, RESPIRATORY CHAIN, TRANSPORT, DISULFIDE BOND, IRON-SULFUR, TRANSIT PEPTIDE
3h1l:O (GLY20) to (LEU38) CHICKEN CYTOCHROME BC1 COMPLEX WITH ASCOCHLORIN BOUND AT QO AND QI SITES | CYTOCHROME BC1, MEMBRANE PROTEIN, HEME PROTEIN, RIESKE IRON SULFUR PROTEIN, CYTOCHROME B, CYTOCHROME C1, COMPLEX III, ASCOCHLORIN, UBIQUINONE, OXIDOREDUCTASE, REDOX ENZYME, RESPIRATORY CHAIN, ELECTRON TRANSPORT, HEME, INNER MEMBRANE IRON, MEMBRANE, METAL-BINDING, MITOCHONDRION, TRANSMEMBRANE, IRON, MITOCHONDRION INNER MEMBRANE, TRANSPORT, 2FE-2S, DISULFIDE BOND, IRON-SULFUR, TRANSIT PEPTIDE
3tuz:D (MET1) to (GLN19) INWARD FACING CONFORMATIONS OF THE METNI METHIONINE ABC TRANSPORTER: CY5 SEMET SOAK CRYSTAL FORM | ABC-TRANSPORTER, TYPE I ABC TYPE IMPORTER,METHIONINE UPTAKE TRANSPORTER, MEMBRANE PROTEIN, AMINO-ACID TRANSPORT, ATP-BINDING, HYDROLASE, INNER MEMBRANE, HYDROLASE-TRANSPORT PROTEIN COMPLEX
1qlw:A (SER16) to (THR46) THE ATOMIC RESOLUTION STRUCTURE OF A NOVEL BACTERIAL ESTERASE | HYDROLASE(CARBOXYLIC ESTERASE), ESTERASE, ANISOTROPIC REFINEMENT, ATOMIC RESOLUTION, ALPHA/BETA HYDROLASE
2sak:A (VAL79) to (PRO105) STAPHYLOKINASE (SAKSTAR VARIANT) | PLASMINOGEN ACTIVATION, FIBRINOLYSIS, STAPHYLOKINASE, HYDROLASE, PLASMINOGEN ACTIVATOR
4jo5:A (ASP67) to (ILE87) CBM3A-L DOMAIN WITH FLANKING LINKERS FROM SCAFFOLDIN CIPA OF CELLULOSOME OF CLOSTRIDIUM THERMOCELLUM | CBM, SCAFFOLDING, CELLULOSE BINDING, BETA SANDWICH, THERMOPHILE, CIPA MODULE, CELLULOSE BINDING PROTEIN
4yg2:I (ARG528) to (PRO590) X-RAY CRYSTAL STRUCTUR OF ESCHERICHIA COLI RNA POLYMERASE SIGMA70 HOLOENZYME | RNA POLYMERASE, TRANSFERASE-TRANSCRIPTION COMPLEX
2e2u:A (ARG267) to (PHE297) SUBSTRATE SCHIFF-BASE ANALOGUE OF COPPER AMINE OXIDASE FROM ARTHROBACTER GLOBIFORMIS FORMED WITH 4-HYDROXYBENZYLHYDRAZINE | AMINE OXIDASE, TOPAQUINONE, TPQ, SUBSTRATE-SCHIFF BASE, 4- HYDROXYBENZYLHYDRAZINE, OXIDOREDUCTASE
2e2x:B (LYS1717) to (LYS1731) SEC14 HOMOLOGY MODULE OF NEUROFIBROMIN IN COMPLEX WITH PHOSPHATITYLETHANOLAMINE | SEC14, PH SUPERFOLD, PE, CRAL-TRIO DOMAIN, SIGNALING PROTEIN
4jr1:B (PHE137) to (PRO158) HUMAN PROCASPASE-7 BOUND TO AC-DEVD-CMK | PROTEASE, PROENZYME, PROTEIN-PEPTIDE COMPLEX, IRREVERSIBLE INHIBITOR, ACTIVITY BASED PROBE, CASPASE, APOPTOSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1qqt:A (GLY225) to (PHE250) METHIONYL-TRNA SYNTHETASE FROM ESCHERICHIA COLI | ROSSMANN FOLD, HELIX BUNDLE, TRNA LIGASE
1f1j:B (CYS436) to (PRO458) CRYSTAL STRUCTURE OF CASPASE-7 IN COMPLEX WITH ACETYL-ASP-GLU-VAL-ASP- CHO | CASPASE-7, CYSTEINE PROTEASE, HYDROLASE, APOPTOSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
1qqw:D (MET212) to (TYR231) CRYSTAL STRUCTURE OF HUMAN ERYTHROCYTE CATALASE | HEME PROTEIN, LATTICE CONTACT, WATER, NO NADP, OXIDOREDUCTASE
4jsq:M (VAL20) to (GLY38) 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:a (VAL20) to (GLY38) 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
3h6s:F (PRO72) to (ALA112) STRUCURE OF CLITOCYPIN - CATHEPSIN V COMPLEX | CATHEPSIN, CLITOCYPIN, KUNITZ INHIBITOR, CYSTEINE PROTEASE, DISULFIDE BOND, GLYCOPROTEIN, HYDROLASE, LYSOSOME, PROTEASE, THIOL PROTEASE, ZYMOGEN, HYDROLASE/HYDROLASE INHIBITOR COMPLEX
4jsu:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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
1qu0:B (GLY3082) to (ASN3100) CRYSTAL STRUCTURE OF THE FIFTH LAMININ G-LIKE MODULE OF THE MOUSE LAMININ ALPHA2 CHAIN | BETA SANDWICH, CALCIUM-BINDING PROTEIN, METAL BINDING PROTEIN
1qu0:C (GLY3082) to (ASN3100) CRYSTAL STRUCTURE OF THE FIFTH LAMININ G-LIKE MODULE OF THE MOUSE LAMININ ALPHA2 CHAIN | BETA SANDWICH, CALCIUM-BINDING PROTEIN, METAL BINDING PROTEIN
3h7l:A (GLY210) to (ASP241) CRYSTAL STRUCTURE OF ENDOGLUCANASE-RELATED PROTEIN FROM VIBRIO PARAHAEMOLYTICUS | ENDOGLUCANASE, DEHYDROGENASE, PSI-2, NYSGXRC, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, HYDROLASE
3h7l:B (GLY210) to (ASP241) CRYSTAL STRUCTURE OF ENDOGLUCANASE-RELATED PROTEIN FROM VIBRIO PARAHAEMOLYTICUS | ENDOGLUCANASE, DEHYDROGENASE, PSI-2, NYSGXRC, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, HYDROLASE
3h7l:C (GLY210) to (ASP241) CRYSTAL STRUCTURE OF ENDOGLUCANASE-RELATED PROTEIN FROM VIBRIO PARAHAEMOLYTICUS | ENDOGLUCANASE, DEHYDROGENASE, PSI-2, NYSGXRC, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, HYDROLASE
1qun:J (GLY222) to (LEU250) X-RAY STRUCTURE OF THE FIMC-FIMH CHAPERONE ADHESIN COMPLEX FROM UROPATHOGENIC E.COLI | CHAPERONE ADHESIN DONOR STRAND COMPLEMENTATION, CHAPERONE/STRUCTURAL PROTEIN COMPLEX
1qun:N (GLY222) to (LEU250) X-RAY STRUCTURE OF THE FIMC-FIMH CHAPERONE ADHESIN COMPLEX FROM UROPATHOGENIC E.COLI | CHAPERONE ADHESIN DONOR STRAND COMPLEMENTATION, CHAPERONE/STRUCTURAL PROTEIN COMPLEX
4jt0:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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
3h8l:A (GLY70) to (GLU101) THE FIRST X-RAY STRUCTURE OF A SULFIDE:QUINONE OXIDOREDUCTASE: INSIGHTS INTO SULFIDE OXIDATION MECHANISM | MEMBRANE PROTEIN, COMPLETE FORM, ROSSMAN-LIKE FOLD, OXIDOREDUCTASE
1qwl:B (MET193) to (TRP212) STRUCTURE OF HELICOBACTER PYLORI CATALASE | BETA BARREL, AZIDE COMPLEX, OXYFERRYL COMPLEX, OXIDOREDUCTASE
1qxp:B (ASN493) to (GLU512) CRYSTAL STRUCTURE OF A MU-LIKE CALPAIN | M-CALPAIN, MU-CALPAIN, CATALYTIC TRIAD, CA(2+) REQUIREMENT, HYDROLASE CHIMERA
2uy6:C (GLY75) to (ALA108) CRYSTAL STRUCTURE OF THE P PILUS ROD SUBUNIT PAPA | DONOR STRAND COMPLEMENTATION, PILI/N-TERMINAL EXTENSION, PILUS BIOGENESIS, DONOR-STRAND EXCHANGE, NTE, DSC, DSE, PAPA, PAPD, FIMBRIA, CHAPERONE
2uy7:H (THR76) to (ALA108) CRYSTAL STRUCTURE OF THE P PILUS ROD SUBUNIT PAPA | DONOR STRAND COMPLEMENTATION, PILI/N-TERMINAL EXTENSION, PILUS BIOGENESIS, DONOR-STRAND EXCHANGE, NTE, DSC, DSE, PAPA, PAPD, FIMBRIA, CHAPERONE
3hf9:L (GLY189) to (ASP204) 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
4ymb:A (PHE105) to (ALA136) STRUCTURE OF THE LIGAND-BINDING DOMAIN OF GLUK1 IN COMPLEX WITH THE ANTAGONIST CNG10111 | IONOTROPIC GLUTAMATE RECEPTOR, KAINATE RECEPTOR GLUK1, LIGAND-BINDING DOMAIN, ANTAGONIST, SIGNALING PROTEIN, FUSION PROTEIN
2v04:A (LYS220) to (ARG246) CRYSTAL STRUCTURE OF CHOLINE BINDING PROTEIN F FROM STREPTOCOCCUS PNEUMONIAE | CBPF, CHOLINE-BINDING-PROTEIN, LIPID-BINDING-PROTEIN
2v05:A (LYS220) to (ARG246) CRYSTAL STRUCTURE OF CHOLINE BINDING PROTEIN F FROM STREPTOCOCCUS PNEUMONIAE. CRYSTAL FORM II. | CBPF, CHOLINE-BINDING-PROTEIN, LIPID-BINDING-PROTEIN
2v1l:A (GLN71) to (LEU90) STRUCTURE OF THE CONSERVED HYPOTHETICAL PROTEIN VC1805 FROM PATHOGENICITY ISLAND VPI-2 OF VIBRIO CHOLERAE O1 BIOVAR ELTOR STR. N16961 SHARES STRUCTURAL HOMOLOGY WITH THE HUMAN P32 PROTEIN | PATHOGENICITY ISLAND, HYPOTHETICAL PROTEIN, UNKNOWN FUNCTION
2v2t:B (HIS109) to (PHE134) X-RAY STRUCTURE OF A NF-KB P50-RELB-DNA COMPLEX | 4-DIPHOSPHOCYTIDYL-2C-METHYL-D-ERYTHRITOL, AQUIFEX AEOLICUS, NUCLEOTIDE-BINDING, ISOPRENE BIOSYNTHESIS, TRANSCRIPTION, KINASE, TRANSFERASE, ATP-BINDING, NON-MEVALONATE
1fiv:A (ASN47) to (ARG64) STRUCTURE OF AN INHIBITOR COMPLEX OF PROTEINASE FROM FELINE IMMUNODEFICIENCY VIRUS | ACID PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1r6z:P (ASN240) to (ILE265) THE CRYSTAL STRUCTURE OF THE ARGONAUTE2 PAZ DOMAIN (AS A MBP FUSION) | DEVIANT OB FOLD, RNAI, GENE REGULATION
2erj:A (TYR135) to (TRP156) CRYSTAL STRUCTURE OF THE HETEROTRIMERIC INTERLEUKIN-2 RECEPTOR IN COMPLEX WITH INTERLEUKIN-2 | INTERLEUKIN-2, INTERLEUKIN-2 ALPHA RECEPTOR, INTERLEUKIN-2 BETA RECEPTOR, INTERLEUKIN-2 GAMMA RECEPTOR, IMMUNE SYSTEM-CYTOKINE COMPLEX
3hj6:A (ASP23) to (ARG51) STRUCTURE OF HALOTHERMOTHRIX ORENII FRUCTOKINASE (FRK) | FRUCTOKINASE, FRUCTOSE, KINASE, TRANSFERASE, CARBOHYDRATE METABOLISM
3hj6:B (ASP23) to (ARG51) STRUCTURE OF HALOTHERMOTHRIX ORENII FRUCTOKINASE (FRK) | FRUCTOKINASE, FRUCTOSE, KINASE, TRANSFERASE, CARBOHYDRATE METABOLISM
1fmu:A (LYS65) to (GLY82) STRUCTURE OF NATIVE PROTEINASE A IN P3221 SPACE GROUP. | PROTEINASE A, HYDROLASE
1fmx:A (TYR268) to (SER287) STRUCTURE OF NATIVE PROTEINASE A IN THE SPACE GROUP P21 | PROTEINASE A, HYDROLASE
2v5r:A (GLY210) to (LEU236) STRUCTURAL BASIS FOR DSCAM ISOFORM SPECIFICITY | DOWN SYNDROME CELL ADHESION MOLECULE DSCAM NEUROBIOLOGY SPL IMMUNOGLOBULIN DOMAIN, MEMBRANE, CELL ADHESION, DEVELOPMENTAL PROTEIN
2v5r:B (GLY210) to (LEU236) STRUCTURAL BASIS FOR DSCAM ISOFORM SPECIFICITY | DOWN SYNDROME CELL ADHESION MOLECULE DSCAM NEUROBIOLOGY SPL IMMUNOGLOBULIN DOMAIN, MEMBRANE, CELL ADHESION, DEVELOPMENTAL PROTEIN
4ytb:A (ASP431) to (TYR449) CRYSTAL STRUCTURE OF PORPHYROMONAS GINGIVALIS PEPTIDYLARGININE DEIMINASE (PPAD) IN COMPLEX WITH DIPEPTIDE ASP-GLN. | PEPTIDYLARGININE DEIMINASE, CITRULLINATION, HYDROLASE
2exj:C (LYS3) to (ASP15) STRUCTURE OF THE FAMILY43 BETA-XYLOSIDASE D128G MUTANT FROM GEOBACILLUS STEAROTHERMOPHILUS IN COMPLEX WITH XYLOBIOSE | GLYKOSIDASE, HYDROLSASE, XYLOSIDASE, FAMILY43, XYLOSE, HYDROLASE
2exw:F (SER28) to (ILE47) CRYSTAL STRUCTURE OF A ECCLC-FAB COMPLEX IN THE ABSENCE OF BOUND IONS | CLC FAMILY OF CL- CHANNELS AND TRANSPORTERS, H+/CL- ANTIPORTER, MEMBRANE PROTEIN/FAB COMPLEX
2f16:M (VAL12) to (GLY30) 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
2f16:1 (VAL12) to (GLY30) 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
1rhq:A (SER229) to (ASP257) CRYSTAL STRUCTURE OF THE COMPLEX OF CASPASE-3 WITH A BROMOMETHOXYPHENYL INHIBITOR | CYSTEINE PROTEASE, CASPASE-3, APOPAIN, CPP32, YAMA, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
1rhq:D (SER229) to (ASP257) CRYSTAL STRUCTURE OF THE COMPLEX OF CASPASE-3 WITH A BROMOMETHOXYPHENYL INHIBITOR | CYSTEINE PROTEASE, CASPASE-3, APOPAIN, CPP32, YAMA, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
1rhu:A (SER229) to (ASP257) CRYSTAL STRUCTURE OF THE COMPLEX OF CASPASE-3 WITH A 5,6,7 TRICYCLIC PEPTIDOMIMETIC INHIBITOR | CYSTEINE PROTEASE, CASPASE-3, APOPAIN, CPP32, YAMA, COMPLEX (PROTEASE-INHIBITOR), HYDROLASE
2v9x:G (GLY130) to (PRO151) E138D VARIANT OF ESCHERICHIA COLI DCTP DEAMINASE IN COMPLEX WITH DUTP | DUTPASE, HYDROLASE, DCTP DEAMINASE, NUCLEOTIDE METABOLISM
4k98:A (PHE345) to (GLU361) STRUCTURE OF TERNARY COMPLEX OF CGAS WITH DSDNA AND BOUND 5 -PPPG(2 ,5 )PG | NUCLEOTIDYLTRANSFERASE FOLD, TRANSFERASE-DNA COMPLEX
1rk2:A (SER6) to (VAL38) E. COLI RIBOKINASE COMPLEXED WITH RIBOSE AND ADP, SOLVED IN SPACE GROUP P212121 | CARBOHYDRATE KINASE, RIBOSE, TRANSFERASE, INDUCED FIT, DOMAIN RE-ARRANGEMENTS
1rl2:A (ASN142) to (ARG174) RIBOSOMAL PROTEIN L2 RNA-BINDING DOMAIN FROM BACILLUS STEAROTHERMOPHILUS | RIBOSOMAL PROTEIN, RNA-BINDING DOMAIN, PEPTIDYLTRANSFEREASE CENTER, X-RAY DIFFRACTION
1rot:A (ARG51) to (ASP67) STRUCTURE OF FKBP59-I, THE N-TERMINAL DOMAIN OF A 59 KDA FK506-BINDING PROTEIN, NMR, MINIMIZED AVERAGE STRUCTURE | ROTAMASE (ISOMERASE), DOMAIN I (N-TERM) OF A 59 KDA, FK506- BINDING PROTEIN, PEPTIDYL PROLYL CIS-TRANS ISOMERASE
1fyt:D (VAL158) to (ASN176) CRYSTAL STRUCTURE OF A COMPLEX OF A HUMAN ALPHA/BETA-T CELL RECEPTOR, INFLUENZA HA ANTIGEN PEPTIDE, AND MHC CLASS II MOLECULE, HLA-DR1 | PROTEIN-PROTEIN COMPLEX, IMMUNOGLOBULIN FOLD, IMMUNE SYSTEM
3un4:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH PR-957 (EPOXIDE) | PROTEASOME, ANTIGEN PRESENTATION, DRUG DEVELOPMENT, PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBTIOR COMPLEX
1g0v:A (TYR265) to (ILE286) THE STRUCTURE OF PROTEINASE A COMPLEXED WITH A IA3 MUTANT, MVV | PROTEINASE A, MVV, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1g0u:M (VAL12) to (GLY30) A GATED CHANNEL INTO THE PROTEASOME CORE PARTICLE | PROTEASOME, UBIQUITIN, DEGRADATION, PROTEASE, NTN-HYDROLASE
1g0u:X (VAL12) to (LYS28) A GATED CHANNEL INTO THE PROTEASOME CORE PARTICLE | PROTEASOME, UBIQUITIN, DEGRADATION, PROTEASE, NTN-HYDROLASE
1g0u:1 (VAL12) to (GLY30) A GATED CHANNEL INTO THE PROTEASOME CORE PARTICLE | PROTEASOME, UBIQUITIN, DEGRADATION, PROTEASE, NTN-HYDROLASE
2fak:J (VAL12) to (LYS28) CRYSTAL STRUCTURE OF SALINOSPORAMIDE A IN COMPLEX WITH THE YEAST 20S PROTEASOME | PROTEASOME, UBIQUITIN, DRUG DESIGN, INHIBITOR, PROTEASE, HYDROLASE
2fak:M (VAL12) to (GLY30) CRYSTAL STRUCTURE OF SALINOSPORAMIDE A IN COMPLEX WITH THE YEAST 20S PROTEASOME | PROTEASOME, UBIQUITIN, DRUG DESIGN, INHIBITOR, PROTEASE, HYDROLASE
2fak:X (VAL12) to (LYS28) CRYSTAL STRUCTURE OF SALINOSPORAMIDE A IN COMPLEX WITH THE YEAST 20S PROTEASOME | PROTEASOME, UBIQUITIN, DRUG DESIGN, INHIBITOR, PROTEASE, HYDROLASE
2fak:1 (VAL12) to (GLY30) CRYSTAL STRUCTURE OF SALINOSPORAMIDE A IN COMPLEX WITH THE YEAST 20S PROTEASOME | PROTEASOME, UBIQUITIN, DRUG DESIGN, INHIBITOR, PROTEASE, HYDROLASE
4z1l:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH BELACTOSIN C DERIVATIVE 3 | HYDROLASE, PROTEASOME, INHIBITOR, BINDING ANALYSIS, LEAD STRUCTURE MOTIF, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4z1l:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH BELACTOSIN C DERIVATIVE 3 | HYDROLASE, PROTEASOME, INHIBITOR, BINDING ANALYSIS, LEAD STRUCTURE MOTIF, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1g4m:B (ASP297) to (HIS353) CRYSTAL STRUCTURE OF BOVINE BETA-ARRESTIN 1 | SENSORY TRANSDUCTION, ALTERNATIVE SPLICING, SIGNALING PROTEIN
2fea:A (PHE95) to (TRP135) CRYSTAL STRUCTURE OF MTNX PHOSPHATASE FROM BACILLUS SUBTILIS AT 2.00 A RESOLUTION | 2633731, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI, HYDROLASE
2fea:B (PHE95) to (TRP135) CRYSTAL STRUCTURE OF MTNX PHOSPHATASE FROM BACILLUS SUBTILIS AT 2.00 A RESOLUTION | 2633731, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI, HYDROLASE
1g65:J (VAL12) to (LYS28) 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:X (VAL12) to (LYS28) 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
2ffv:A (VAL248) to (ASP269) HUMAN PPGALNACT-2 COMPLEXED WITH MANGANESE AND UDP | PPGALNACT; MUCIN; GLYCOSYLTRANSFERASE, TRANSFERASE
1ryi:A (ARG296) to (ALA325) STRUCTURE OF GLYCINE OXIDASE WITH BOUND INHIBITOR GLYCOLATE | FLAVOPROTEIN; OXIDASE; PROTEIN-INHIBITOR COMPLEX, OXIDOREDUCTASE
1ryi:B (ARG296) to (ALA325) STRUCTURE OF GLYCINE OXIDASE WITH BOUND INHIBITOR GLYCOLATE | FLAVOPROTEIN; OXIDASE; PROTEIN-INHIBITOR COMPLEX, OXIDOREDUCTASE
1ryi:C (ARG296) to (ALA325) STRUCTURE OF GLYCINE OXIDASE WITH BOUND INHIBITOR GLYCOLATE | FLAVOPROTEIN; OXIDASE; PROTEIN-INHIBITOR COMPLEX, OXIDOREDUCTASE
1ryi:D (ARG296) to (ALA325) STRUCTURE OF GLYCINE OXIDASE WITH BOUND INHIBITOR GLYCOLATE | FLAVOPROTEIN; OXIDASE; PROTEIN-INHIBITOR COMPLEX, OXIDOREDUCTASE
1ryp:K (VAL12) to (LYS28) CRYSTAL STRUCTURE OF THE 20S PROTEASOME FROM YEAST AT 2.4 ANGSTROMS RESOLUTION | MULTICATALYTIC PROTEINASE, 20S PROTEASOME, PROTEIN DEGRADATION, ANTIGEN PROCESSING, HYDROLASE, PROTEASE
1ryp:N (VAL12) to (GLY30) CRYSTAL STRUCTURE OF THE 20S PROTEASOME FROM YEAST AT 2.4 ANGSTROMS RESOLUTION | MULTICATALYTIC PROTEINASE, 20S PROTEASOME, PROTEIN DEGRADATION, ANTIGEN PROCESSING, HYDROLASE, PROTEASE
4khz:E (ASN241) to (LEU262) CRYSTAL STRUCTURE OF THE MALTOSE-BINDING PROTEIN/MALTOSE TRANSPORTER COMPLEX IN AN PRE-TRANSLOCATION CONFORMATION BOUND TO MALTOHEPTAOSE | ABC TRANSPORTER, ATPASE MALTODEXTRIN TRANSPORTER, ATP BINDING MALTODEXTRIN BINDING, INNER MEMBRANE, TRANSPORT PROTEIN
2fh1:A (MET517) to (PRO533) C-TERMINAL HALF OF GELSOLIN SOAKED IN LOW CALCIUM AT PH 4.5 | GELSOLIN, CALCIUM, CONTRACTILE PROTEIN
2fh2:A (MET517) to (PRO533) C-TERMINAL HALF OF GELSOLIN SOAKED IN EGTA AT PH 4.5 | GELSOLIN, EGTA, CONTRACTILE PROTEIN
2fh2:C (MET517) to (PRO533) C-TERMINAL HALF OF GELSOLIN SOAKED IN EGTA AT PH 4.5 | GELSOLIN, EGTA, CONTRACTILE PROTEIN
2vgj:C (ASP121) to (GLY165) CRYSTAL STRUCTURE OF ACTINOMADURA R39 DD-PEPTIDASE COMPLEXED WITH A PEPTIDOGLYCAN-MIMETIC CEPHALOSPORIN | CELL WALL BIOGENESIS/DEGRADATION, ANTIBIOTIC RESISTANCE, PEPTIDOGLYCAN SYNTHESIS, PROTEASE, SECRETED, HYDROLASE, CELL SHAPE, CARBOXYPEPTIDASE, PENICILLIN-BINDING, ACTINOMADURA, PEPTIDOGLYCAN, TRANSPEPTIDASE
2vgk:C (ASP121) to (GLY165) CRYSTAL STRUCTURE OF ACTINOMADURA R39 DD-PEPTIDASE COMPLEXED WITH A PEPTIDOGLYCAN-MIMETIC CEPHALOSPORIN | CELL WALL BIOGENESIS/DEGRADATION, ANTIBIOTIC RESISTANCE, PEPTIDOGLYCAN SYNTHESIS, PROTEASE, SECRETED, HYDROLASE, CELL SHAPE, CARBOXYPEPTIDASE, PENICILLIN-BINDING, ACTINOMADURA, PEPTIDOGLYCAN, TRANSPEPTIDASE
1s02:A (ASP197) to (GLY219) EFFECTS OF ENGINEERED SALT BRIDGES ON THE STABILITY OF SUBTILISIN BPN' | HYDROLASE (SERINE PROTEINASE)
2fhg:H (GLY489) to (ASP504) CRYSTAL STRUCTURE OF MYCOBACTERIAL TUBERCULOSIS PROTEASOME | MULTI-PROTEIN, MULTI-SUBUNIT COMPLEX, PROTEASE, PROTEASOME, HYDROLASE
2fhg:E (GLY489) to (ASP504) CRYSTAL STRUCTURE OF MYCOBACTERIAL TUBERCULOSIS PROTEASOME | MULTI-PROTEIN, MULTI-SUBUNIT COMPLEX, PROTEASE, PROTEASOME, HYDROLASE
2fhg:G (GLY489) to (ASP504) CRYSTAL STRUCTURE OF MYCOBACTERIAL TUBERCULOSIS PROTEASOME | MULTI-PROTEIN, MULTI-SUBUNIT COMPLEX, PROTEASE, PROTEASOME, HYDROLASE
2fhg:J (GLY489) to (ASP504) CRYSTAL STRUCTURE OF MYCOBACTERIAL TUBERCULOSIS PROTEASOME | MULTI-PROTEIN, MULTI-SUBUNIT COMPLEX, PROTEASE, PROTEASOME, HYDROLASE
2fhg:N (GLY489) to (ASP504) CRYSTAL STRUCTURE OF MYCOBACTERIAL TUBERCULOSIS PROTEASOME | MULTI-PROTEIN, MULTI-SUBUNIT COMPLEX, PROTEASE, PROTEASOME, HYDROLASE
2fhg:V (GLY489) to (ASP504) CRYSTAL STRUCTURE OF MYCOBACTERIAL TUBERCULOSIS PROTEASOME | MULTI-PROTEIN, MULTI-SUBUNIT COMPLEX, PROTEASE, PROTEASOME, HYDROLASE
2fhg:X (GLY489) to (ASP504) CRYSTAL STRUCTURE OF MYCOBACTERIAL TUBERCULOSIS PROTEASOME | MULTI-PROTEIN, MULTI-SUBUNIT COMPLEX, PROTEASE, PROTEASOME, HYDROLASE
2fhg:2 (GLY489) to (ASP504) CRYSTAL STRUCTURE OF MYCOBACTERIAL TUBERCULOSIS PROTEASOME | MULTI-PROTEIN, MULTI-SUBUNIT COMPLEX, PROTEASE, PROTEASOME, HYDROLASE
3hqd:A (ALA230) to (VAL264) HUMAN KINESIN EG5 MOTOR DOMAIN IN COMPLEX WITH AMPPNP AND MG2+ | KINESIN, MOTOR DOMAIN, ATP HYDROLYSIS, MITOSIS, SPINDLE PROTEIN, ATP-BINDING, CELL CYCLE, CELL DIVISION, COILED COIL, MICROTUBULE, MOTOR PROTEIN, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM
2fme:A (SER36) to (ARG53) CRYSTAL STRUCTURE OF THE MITOTIC KINESIN EG5 (KSP) IN COMPLEX WITH MG-ADP AND (R)-4-(3-HYDROXYPHENYL)-N,N,7,8- TETRAMETHYL-3,4-DIHYDROISOQUINOLINE-2(1H)-CARBOXAMIDE | EG5 KSP MG-ADP COMPLEX INHIBITOR, CELL CYCLE
2fme:B (SER36) to (ARG53) CRYSTAL STRUCTURE OF THE MITOTIC KINESIN EG5 (KSP) IN COMPLEX WITH MG-ADP AND (R)-4-(3-HYDROXYPHENYL)-N,N,7,8- TETRAMETHYL-3,4-DIHYDROISOQUINOLINE-2(1H)-CARBOXAMIDE | EG5 KSP MG-ADP COMPLEX INHIBITOR, CELL CYCLE
1gfw:A (SER113) to (ASP135) THE 2.8 ANGSTROM CRYSTAL STRUCTURE OF CASPASE-3 (APOPAIN OR CPP32)IN COMPLEX WITH AN ISATIN SULFONAMIDE INHIBITOR. | X-RAY, CASPASE INHIBITOR, CASPASE-3, APOPAIN, ISTIN SULFONAMIDE, HYDROLASE
3hst:A (ASN249) to (LEU270) N-TERMINAL RNASE H DOMAIN OF RV2228C FROM MYCOBACTERIUM TUBERCULOSIS AS A FUSION PROTEIN WITH MALTOSE BINDING PROTEIN | RIBONUCLEASE H1, RV2228C N-TERMINAL DOMAIN, MYCOBACTERIUM, TUBERCULOSIS, FUSION PROTEIN, MALTOSE BINDING PROTEIN, HYDROLASE
4ze8:A (PRO485) to (SER508) PBP ACCA FROM A. TUMEFACIENS C58 | PBP FROM C CLUSTER, TRANSPORT PROTEIN
4ze8:B (PRO485) to (SER508) PBP ACCA FROM A. TUMEFACIENS C58 | PBP FROM C CLUSTER, TRANSPORT PROTEIN
4ze8:D (PRO485) to (SER508) PBP ACCA FROM A. TUMEFACIENS C58 | PBP FROM C CLUSTER, TRANSPORT PROTEIN
2vl4:A (LEU809) to (SER825) STRUCTURAL AND BIOCHEMICAL EVIDENCE FOR A BOAT-LIKE TRANSITION STATE IN BETA-MANNOSIDASES | LINEAR FREE ENERGY RELATIONSHIP, HYDROLASE, TRANSITION STATE MIMIC, MANNOSIDASE, GLYCOSIDE HYDROLASE
2vl6:C (VAL128) to (GLU154) STRUCTURAL ANALYSIS OF THE SULFOLOBUS SOLFATARICUS MCM PROTEIN N-TERMINAL DOMAIN | MCM, HELICASE, HYDROLASE, ZINC-FINGER, ATP-BINDING, DNA-BINDING, SSDNA BINDING, DNA REPLICATION, NUCLEOTIDE-BINDING, DNA BINDING PROTEIN
3hye:M (VAL12) to (GLY30) CRYSTAL STRUCTURE OF 20S PROTEASOME IN COMPLEX WITH HYDROXYLATED SALINOSPORAMIDE | CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, PROTEASOME, THREONINE PROTEASE, ISOPEPTIDE BOND, UBL CONJUGATION, ZYMOGEN
3hye:1 (VAL12) to (GLY30) CRYSTAL STRUCTURE OF 20S PROTEASOME IN COMPLEX WITH HYDROXYLATED SALINOSPORAMIDE | CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, PROTEASOME, THREONINE PROTEASE, ISOPEPTIDE BOND, UBL CONJUGATION, ZYMOGEN
1sel:A (GLU197) to (GLY219) CRYSTAL STRUCTURE OF SELENOSUBTILISIN AT 2.0-ANGSTROMS RESOLUTION | HYDROLASE(SERINE PROTEASE)
2vlj:D (VAL153) to (ASN171) THE STRUCTURAL DYNAMICS AND ENERGETICS OF AN IMMUNODOMINANT T-CELL RECEPTOR ARE PROGRAMMED BY ITS VBETA DOMAIN | IMMUNE SYSTEM, GLYCOPROTEIN, TRANSMEMBRANE, IMMUNE SYSTEM/RECEPTOR/COMPLEX, IMMUNOGLOBULIN DOMAIN, HOST-VIRUS INTERACTION, PYRROLIDONE CARBOXYLIC ACID, IMMUNE RESPONSE, IMMUNODOMINANCE, DISEASE MUTATION, MEMBRANE, SECRETED, RECEPTOR, GLYCATION, TCR, FLU, MHC, MHC I, T-CELL, COMPLEX
2fyf:A (GLY133) to (ALA150) STRUCTURE OF A PUTATIVE PHOSPHOSERINE AMINOTRANSFERASE FROM MYCOBACTERIUM TUBERCULOSIS | PLP-DEPENDENT ENZYME, DIMER, STRUCTURAL GENOMICS, MYCOBACTERIUM TUBERCULOSIS STRUCTURAL PROTEOMICS PROJECT, XMTB, TRANSFERASE
2vo5:A (LEU809) to (SER825) STRUCTURAL AND BIOCHEMICAL EVIDENCE FOR A BOAT-LIKE TRANSITION STATE IN BETA-MANNOSIDASES | GLYCOSIDE, HYDROLASE, MANNOSIDASE, TRANSITION STATE MIMIC, LINEAR FREE ENERGY RELATIONSHIP
2g21:B (LYS68) to (GLY85) KETOPIPERAZINE-BASED RENIN INHIBITORS: OPTIMIZATION OF THE "C" RING | PROTEIN-LIGAND COMPLEXES, HYDROLASE
1gpw:A (MET1) to (GLY30) STRUCTURAL EVIDENCE FOR AMMONIA TUNNELING ACROSS THE (BETA/ALPHA)8 BARREL OF THE IMIDAZOLE GLYCEROL PHOSPHATE SYNTHASE BIENZYME COMPLEX. | LYASE/TRANSFERASE, COMPLEX (LYASE/TRANSFERASE), HISTIDINE BIOSYNTHESIS, GLUTAMINASE, GLUTAMINE AMIDOTRANSFERASE, CYCLASE, AMMONIA CHANNEL
1gpw:D (GLU161) to (GLN176) STRUCTURAL EVIDENCE FOR AMMONIA TUNNELING ACROSS THE (BETA/ALPHA)8 BARREL OF THE IMIDAZOLE GLYCEROL PHOSPHATE SYNTHASE BIENZYME COMPLEX. | LYASE/TRANSFERASE, COMPLEX (LYASE/TRANSFERASE), HISTIDINE BIOSYNTHESIS, GLUTAMINASE, GLUTAMINE AMIDOTRANSFERASE, CYCLASE, AMMONIA CHANNEL
2vqu:A (LEU809) to (SER825) STRUCTURAL AND BIOCHEMICAL EVIDENCE FOR A BOAT-LIKE TRANSITION STATE IN BETA-MANNOSIDASES | LINEAR FREE ENERGY RELATIONSHIP, TRANSITION STATE MIMIC, MANNOSIDASE, GLYCOSIDE HYDROLASE, HYDROLASE
4zh3:C (GLY248) to (VAL263) CRYSTAL STRUCTURE OF ESCHERICHIA COLI RNA POLYMERASE IN COMPLEX WITH CBRH16-BR | RNA POLYMERASE, INHIBITOR, TRANSCRIPTION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4zh3:I (GLY248) to (VAL263) CRYSTAL STRUCTURE OF ESCHERICHIA COLI RNA POLYMERASE IN COMPLEX WITH CBRH16-BR | RNA POLYMERASE, INHIBITOR, TRANSCRIPTION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
1gqt:B (SER6) to (VAL38) ACTIVATION OF RIBOKINASE BY MONOVALENT CATIONS | CARBOHYDRATE KINASE, RIBOSE, TRANSFERASE, INDUCED FIT, BINDING OF MONOVALENT CATIONS, ACTIVATION BY MONOVALENT CATIONS
1smr:A (MET65) to (GLY82) THE 3-D STRUCTURE OF MOUSE SUBMAXILLARY RENIN COMPLEXED WITH A DECAPEPTIDE INHIBITOR CH-66 BASED ON THE 4-16 FRAGMENT OF RAT ANGIOTENSINOGEN | ASPARTIC PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1smr:C (MET65) to (GLY82) THE 3-D STRUCTURE OF MOUSE SUBMAXILLARY RENIN COMPLEXED WITH A DECAPEPTIDE INHIBITOR CH-66 BASED ON THE 4-16 FRAGMENT OF RAT ANGIOTENSINOGEN | ASPARTIC PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1smr:E (MET65) to (GLY82) THE 3-D STRUCTURE OF MOUSE SUBMAXILLARY RENIN COMPLEXED WITH A DECAPEPTIDE INHIBITOR CH-66 BASED ON THE 4-16 FRAGMENT OF RAT ANGIOTENSINOGEN | ASPARTIC PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1smr:G (MET65) to (GLY82) THE 3-D STRUCTURE OF MOUSE SUBMAXILLARY RENIN COMPLEXED WITH A DECAPEPTIDE INHIBITOR CH-66 BASED ON THE 4-16 FRAGMENT OF RAT ANGIOTENSINOGEN | ASPARTIC PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4zh4:I (GLY248) to (VAL263) CRYSTAL STRUCTURE OF ESCHERICHIA COLI RNA POLYMERASE IN COMPLEX WITH CBRP18 | RNA POLYMERASE, INHIBITOR, TRANSCRIPTION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
2vsa:A (ASN243) to (VAL314) STRUCTURE AND MODE OF ACTION OF A MOSQUITOCIDAL HOLOTOXIN | TOXIN, ADP-RIBOSYLTRANSFERASE, LECTIN, RICIN-B-LIKE DOMAIN
3i3y:D (ARG2) to (SER33) CRYSTAL STRUCTURE OF RIBOKINASE IN COMPLEX WITH D-RIBOSE FROM KLEBSIELLA PNEUMONIAE | TRANSFERASE,KINASE,SAD,RIBOSE,D-RIBOSE METABOLIC PROCESS,RIBOKINASE, PFKB FAMILY,11206L1,PSI-II,NYSGXRC, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, TRANSFERASE
4kuc:E (SER48) to (LEU69) CRYSTAL STRUCTURE OF RICIN-A CHAIN IN COMPLEX WITH THE ANTIBODY 6C2 | RNA-N-GLYCOSIDASE, HYDROLASE-IMMUNE SYSTEM COMPLEX
4kxc:A (GLU138) to (ARG158) CRYSTAL STRUCTURE OF HUMAN AMINOPEPTIDASE A COMPLEXED WITH GLUTAMATE | ZINC-AMINOPEPTIDASE, HYDROLASE
1gxm:A (SER591) to (TYR616) FAMILY 10 POLYSACCHARIDE LYASE FROM CELLVIBRIO CELLULOSA | LYASE, PECTATE, MECHANISM, ELIMINATION
4kyd:A (ASN241) to (LEU262) PARTIAL STRUCTURE OF THE C-TERMINAL DOMAIN OF THE HPIV4B PHOSPHOPROTEIN, FUSED TO MBP. | 3 HELIX BUNDLE, BINDING PROTEIN, VIRAL NUCLEOCAPSID, VIRAL PROTEIN
2gix:D (HIS226) to (PRO244) CYTOPLASMIC DOMAIN STRUCTURE OF KIR2.1 CONTAINING ANDERSEN'S MUTATION R218Q AND RESCUE MUTATION T309K | CYTOPLASMIC DOMAINS OF KIR2.1, ANDERSEN'S MUTATION, METAL TRANSPORT
3ibb:B (SER60) to (TYR83) PROPIONYL-COA CARBOXYLASE BETA SUBUNIT, D422A | ACCASE, PCCASE, ACC, PCC, PROPIONYL-COA, CT, CARBOXYLTRANSFERASE, POLYKETIDE, FATTY ACID, PKS, FAS, POLYKETIDE SYNTHASE, FATTY ACID SYNTHASE, CARBOXYLASE, BETA SUBUNIT, PCCB, ACYL-COA, ACYL-COA C ARBOXYLASE, STREPTOMCES, STREPTOMYCES COELICOLOR, BIOTIN, BIOSYNTHETIC PROTEIN
3ibb:F (SER60) to (TYR83) PROPIONYL-COA CARBOXYLASE BETA SUBUNIT, D422A | ACCASE, PCCASE, ACC, PCC, PROPIONYL-COA, CT, CARBOXYLTRANSFERASE, POLYKETIDE, FATTY ACID, PKS, FAS, POLYKETIDE SYNTHASE, FATTY ACID SYNTHASE, CARBOXYLASE, BETA SUBUNIT, PCCB, ACYL-COA, ACYL-COA C ARBOXYLASE, STREPTOMCES, STREPTOMYCES COELICOLOR, BIOTIN, BIOSYNTHETIC PROTEIN
3ibf:A (CYS136) to (PRO158) CRYSTAL STRUCTURE OF UNLIGANDED CASPASE-7 | PROTEIN STRUCTURE, ALTERNATIVE SPLICING, APOPTOSIS, CYTOPLASM, HYDROLASE, POLYMORPHISM, PROTEASE, THIOL PROTEASE, ZYMOGEN
3ibf:C (CYS436) to (PRO458) CRYSTAL STRUCTURE OF UNLIGANDED CASPASE-7 | PROTEIN STRUCTURE, ALTERNATIVE SPLICING, APOPTOSIS, CYTOPLASM, HYDROLASE, POLYMORPHISM, PROTEASE, THIOL PROTEASE, ZYMOGEN
2gmh:A (ASN106) to (PRO126) STRUCTURE OF PORCINE ELECTRON TRANSFER FLAVOPROTEIN- UBIQUINONE OXIDOREDUCTASE IN COMPLEXED WITH UBIQUINONE | ELECTRON-TRANSFER, OXIDOREDUCTASE, FLAVOPROTEIN, UBIQUINONE
3idx:G (ASP412) to (PRO437) CRYSTAL STRUCTURE OF HIV-GP120 CORE IN COMPLEX WITH CD4-BINDING SITE ANTIBODY B13, SPACE GROUP C222 | HIV-1, ANTIBODY, GP120, B13, ENVELOPE GLYCAN PROTEIN, CD4-BINDING SITE, AIDS, APOPTOSIS, CELL MEMBRANE, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISULFIDE BOND, ENVELOPE PROTEIN, FUSION PROTEIN, HOST- VIRUS INTERACTION, MEMBRANE, TRANSMEMBRANE, VIRAL IMMUNOEVASION, VIRION, IMMUNE SYSTEM
2w0c:L (THR230) to (THR254) X-RAY STRUCTURE OF THE ENTIRE LIPID-CONTAINING BACTERIOPHAGE PM2 | VIRUS, MEMBER OF PRD1-ADENO VIRAL LINEAGE, MEMBRANE-CONTAINING BACTERIOPHAGE, VIRUS VIRION, MEMBRANE, TRANSMEMBRANE, CAPSID PROTEIN
1t6e:X (TRP310) to (VAL328) CRYSTAL STRUCTURE OF THE TRITICUM AESTIVUM XYLANASE INHIBITOR I | TWO BETA-BARREL DOMAIN STRUCTURE, HYDROLASE INHIBITOR
1t6g:A (TRP310) to (VAL328) CRYSTAL STRUCTURE OF THE TRITICUM AESTIVUM XYLANASE INHIBITOR-I IN COMPLEX WITH ASPERGILLUS NIGER XYLANASE-I | PROTEIN-PROTEIN COMPLEX, TWO BETA-BARREL DOMAIN STRUCTURE, BETA-JELLY ROLL STRUCTURE, HYDROLASE INHIBITOR
1t6g:B (TRP310) to (VAL328) CRYSTAL STRUCTURE OF THE TRITICUM AESTIVUM XYLANASE INHIBITOR-I IN COMPLEX WITH ASPERGILLUS NIGER XYLANASE-I | PROTEIN-PROTEIN COMPLEX, TWO BETA-BARREL DOMAIN STRUCTURE, BETA-JELLY ROLL STRUCTURE, HYDROLASE INHIBITOR
3if9:B (ARG296) to (ALA325) CRYSTAL STRUCTURE OF GLYCINE OXIDASE G51S/A54R/H244A MUTANT IN COMPLEX WITH INHIBITOR GLYCOLATE | GO STRUCTURE, G51S/A54R/H244A, GLYCOLATE, FAD, FLAVOPROTEIN, OXIDOREDUCTASE
2gpl:M (VAL12) to (GLY30) TMC-95 BASED BIPHENYL-ETHER MACROCYCLES: SPECIFIC PROTEASOME INHIBITORS | PROTEASOMAL SUBUNIT FOLD REPRESENTS AN ANTIPARALLEL BETA- SHEET FLANKED BY HELICES; NTN-HYDROLASE
2gpl:1 (VAL12) to (GLY30) TMC-95 BASED BIPHENYL-ETHER MACROCYCLES: SPECIFIC PROTEASOME INHIBITORS | PROTEASOMAL SUBUNIT FOLD REPRESENTS AN ANTIPARALLEL BETA- SHEET FLANKED BY HELICES; NTN-HYDROLASE
3ih0:A (ILE4) to (GLU29) CRYSTAL STRUCTURE OF AN UNCHARACTERIZED SUGAR KINASE PH1459 FROM PYROCOCCUS HORIKOSHII IN COMPLEX WITH AMP-PNP | CARBOHYDRATE KINASE, PFKB FAMILY, PSI-II, 11207G, NYSGXRC,STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, KINASE, TRANSFERASE
3ih0:B (ILE4) to (GLU29) CRYSTAL STRUCTURE OF AN UNCHARACTERIZED SUGAR KINASE PH1459 FROM PYROCOCCUS HORIKOSHII IN COMPLEX WITH AMP-PNP | CARBOHYDRATE KINASE, PFKB FAMILY, PSI-II, 11207G, NYSGXRC,STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, KINASE, TRANSFERASE
1h80:A (TYR444) to (ASP467) 1,3-ALPHA-1,4-BETA-D-GALACTOSE-4-SULFATE- 3,6-ANHYDRO-D-GALACTOSE-2-SULFATE 4 GALACTOHYDROLASE | HYDROLASE, IOTA-CARRAGEENAN DOUBLE HELIX DEGRADATION
1h80:B (TYR444) to (ASP467) 1,3-ALPHA-1,4-BETA-D-GALACTOSE-4-SULFATE- 3,6-ANHYDRO-D-GALACTOSE-2-SULFATE 4 GALACTOHYDROLASE | HYDROLASE, IOTA-CARRAGEENAN DOUBLE HELIX DEGRADATION
4la2:A (GLY117) to (THR133) CRYSTAL STRUCTURE OF DIMETHYLSULPHONIOPROPIONATE (DMSP) LYASE DDDQ | CUPIN MOTIF, DMSP LYASE, LYASE
4la3:B (GLY117) to (THR133) CRYSTAL STRUCTURE OF DIMETHYLSULPHONIOPROPIONATE (DMSP) LYASE DDDQ Y131A IN COMPLEX WITH DMSP | CUPIN MOTIF, DMSP LYASE, LYASE
4zsm:A (ASN293) to (PHE322) BACE CRYSTAL STRUCTURE WITH BICYCLIC AMINOTHIAZINE FRAGMENT | ASPARTYL, PROTEASE, BETA-SECRETASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2w56:B (GLU71) to (ARG92) STRUCTURE OF THE HYPOTHETICAL PROTEIN VC0508 FROM VIBRIO CHOLERAE VSP-II PATHOGENICITY ISLAND | UNKNOWN FUNCTION
2gvc:B (SER253) to (ASN280) CRYSTAL STRUCTURE OF FLAVIN-CONTAINING MONOOXYGENASE (FMO)FROM S.POMBE AND SUBSTRATE (METHIMAZOLE) COMPLEX | FMO, FAD, METHIMAZOLE, OXYGENASE, PSI, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC, OXIDOREDUCTASE
2gvz:B (GLY1003) to (TYR1017) CRYSTAL STRUCTURE OF COMPLEX OF GS- WITH THE CATALYTIC DOMAINS OF MAMMALIAN ADENYLYL CYCLASE: COMPLEX WITH MANT- ATP AND MN | ADENYLYL CYCLASE, MANT-ATP, LYASE
3in4:A (THR121) to (GLU141) BACE1 WITH COMPOUND 38 | BACE-1, INHIBITOR, ALTERNATIVE SPLICING, ASPARTYL PROTEASE, DISULFIDE BOND, GLYCOPROTEIN, HYDROLASE, MEMBRANE, POLYMORPHISM, PROTEASE, TRANSMEMBRANE, ZYMOGEN
3ind:A (CYS381) to (GLY396) BACE1 WITH THE AMINOHYDANTOIN COMPOUND 29 | BACE1, XRAY, INHIBITOR, ALTERNATIVE SPLICING, ASPARTYL PROTEASE, DISULFIDE BOND, GLYCOPROTEIN, HYDROLASE, MEMBRANE, POLYMORPHISM, PROTEASE, TRANSMEMBRANE, ZYMOGEN
3ine:A (CYS381) to (GLY396) BACE1 WITH THE AMINOHYDANTOIN COMPOUND S-34 | BACE1, XRAY, INHIBITOR, ALTERNATIVE SPLICING, ASPARTYL PROTEASE, DISULFIDE BOND, GLYCOPROTEIN, HYDROLASE, MEMBRANE, POLYMORPHISM, PROTEASE, TRANSMEMBRANE, ZYMOGEN
1hei:B (ASP423) to (LEU451) STRUCTURE OF THE HEPATITIS C VIRUS RNA HELICASE DOMAIN | HELICASE, RNA, HEPATITIS, HCV, ATPASE, NTPASE
1th4:A (HIS210) to (TYR230) CRYSTAL STRUCTURE OF NADPH DEPLETED BOVINE LIVER CATALASE COMPLEXED WITH 3-AMINO-1,2,4-TRIAZOLE | BOVINE LIVER CATALASE, NADPH, 3-AMINO-1,2,4-TRIAZOLE, OXIDOREDUCTASE
1thm:A (VAL202) to (GLY223) CRYSTAL STRUCTURE OF THERMITASE AT 1.4 ANGSTROMS RESOLUTION | HYDROLASE(SERINE PROTEASE)
4zvo:C (CYS436) to (PRO458) CASPASE-7 VARIANT 4 (V4) WITH REPROGRAMMED SUBSTRATE SPECIFICITY DUE TO Y230V/W232Y/S234V/Q276D SUBSTITUTIONS BOUND TO VEID INHIBITOR. | DIRECTED EVOLUTION, PROTEASE, PEPTIDE INHIBITOR, DESIGNED ACTIVE SITE SPECIFICITY, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4zvp:C (PHE437) to (PRO458) CASPASE-7 VARIANT 2 (V2) WITH REPROGRAMMED SUBSTRATE SPECIFICITY DUE TO Y230V/W232M/Q276C SUBSTITUTIONS BOUND TO DEVD INHIBITOR. | DIRECTED EVOLUTION, PROTEASE, PEPTIDE INHIBITOR, DESIGNED ACTIVE SITE SPECIFICITY, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4zvq:C (PHE437) to (PRO458) CASPASE-7 VARIANT 2 (V2) WITH REPROGRAMMED SUBSTRATE SPECIFICITY DUE TO Y230V/W232M/Q276C SUBSTITUTIONS BOUND TO VEID INHIBITOR. | DIRECTED EVOLUTION, PROTEASE, PEPTIDE INHIBITOR, DESIGNED ACTIVE SITE SPECIFICITY, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4zvr:A (PHE137) to (PRO158) CASPASE-7 VARIANT 4 (V4) WITH REPROGRAMMED SUBSTRATE SPECIFICITY DUE TO Y230V/W232Y/S234V/Q276D SUBSTITUTIONS BOUND TO DEVD INHIBITOR. | DIRECTED EVOLUTION, PROTEASE, PEPTIDE INHIBITOR, DESIGNED ACTIVE SITE SPECIFICITY, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4zvr:C (PHE437) to (PRO458) CASPASE-7 VARIANT 4 (V4) WITH REPROGRAMMED SUBSTRATE SPECIFICITY DUE TO Y230V/W232Y/S234V/Q276D SUBSTITUTIONS BOUND TO DEVD INHIBITOR. | DIRECTED EVOLUTION, PROTEASE, PEPTIDE INHIBITOR, DESIGNED ACTIVE SITE SPECIFICITY, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4zvs:A (PHE137) to (PRO158) CASPASE-7 VARIANT 1 (V1) WITH REPROGRAMMED SUBSTRATE SPECIFICITY DUE TO Y230A/W232M/S234N SUBSTITUTIONS, BOUND TO DEVD INHIBITOR. | DIRECTED EVOLUTION, PROTEASE, PEPTIDE INHIBITOR, DESIGNED ACTIVE SITE SPECIFICITY, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4zvu:C (PHE437) to (PRO458) CASPASE-7 WILD-TYPE BOUND TO THE CASPASE-6 COGNATE TETRAPEPTIDE INHIBITOR AC-VEID-CHO | DIRECTED EVOLUTION, PROTEASE, PEPTIDE INHIBITOR, DESIGNED ACTIVE SITE SPECIFICITY, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4zx4:A (SER647) to (TYR674) X-RAY CRYSTAL STRUCTURE OF PFA-M1 IN COMPLEX WITH HYDROXAMIC ACID- BASED INHIBITOR 10O | M1 ALANYL-AMINOPEPTIDASE, PROTEASE, INHIBITOR, HYDROXAMIC ACID, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3vl9:A (GLU194) to (VAL216) CRYSTAL STRUCTURE OF XEG-XYLOGLUCAN | HYDROLASE
3vlb:C (THR213) to (GLU236) CRYSTAL STRUCTURE OF XEG-EDGP | CELL-WALL, PLANT PROTEIN-HYDROLASE COMPLEX
3vom:A (GLY133) to (ALA150) STRUCTURE OF A PUTATIVE PHOSPHOSERINE AMINOTRANSFERASE FROM MYCOBACTERIUM TUBERCULOSIS | PSAT, SERC, PLP-DEPENDENT ENZYME, PHOSPHOSERINE AMINOTRANSFERASE, TRANSFERASE
4zzg:K (VAL12) to (LYS28) YEAST 20S PROTEASOME IN COMPLEX WITH BLM-PEP ACTIVATOR | 20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE
4zzg:Y (VAL12) to (LYS28) YEAST 20S PROTEASOME IN COMPLEX WITH BLM-PEP ACTIVATOR | 20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE
4zzg:2 (VAL12) to (GLY30) YEAST 20S PROTEASOME IN COMPLEX WITH BLM-PEP ACTIVATOR | 20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE
4zzw:A (ASN89) to (GLY105) GEOTRICHUM CANDIDUM CEL7A STRUCTURE COMPLEX WITH CELLOBIOSE AT 1.5A | CELLOBIOHYDROLASE, CELLOBIOSE, HYDROLASE
4lna:A (GLY102) to (ILE127) CRYSTAL STRUCTURE OF PURINE NUCLEOSIDE PHOSPHORYLASE I FROM SPIROSOMA LINGUALE DSM 74, NYSGRC TARGET 029362 | STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NYSGRC,, PSI- BIOLOGY, NEW YORK STRUCTURAL GENOMICS RESEARCH CONSORTIUM, TRANSFERASE
2wjp:A (VAL228) to (LEU248) CRYSTAL STRUCTURE OF MURD LIGASE IN COMPLEX WITH D-GLU CONTAINING RHODANINE INHIBITOR | PEPTIDOGLYCAN SYNTHESIS, CELL WALL BIOGENESIS/DEGRADATION, CELL CYCLE, CELL DIVISION, LIGASE, CELL SHAPE SYNTHESIS
1tyy:A (LYS6) to (CYS28) CRYSTAL STRUCTURE OF AMINOIMIDAZOLE RIBOSIDE KINASE FROM SALMONELLA ENTERICA | RIBOKINASE FOLD, ALPHA/BETA, TRANSFERASE
2wke:A (ASP121) to (GLY165) CRYSTAL STRUCTURE OF THE ACTINOMADURA R39 DD-PEPTIDASE INHIBITED BY 6-BETA-IODOPENICILLANATE. | HYDROLASE, ANTIBIOTIC RESISTANCE, ACTINOMADURA, PENICILLIN BINDING, IODOPENICILLANATE
2wke:B (ASP121) to (GLY165) CRYSTAL STRUCTURE OF THE ACTINOMADURA R39 DD-PEPTIDASE INHIBITED BY 6-BETA-IODOPENICILLANATE. | HYDROLASE, ANTIBIOTIC RESISTANCE, ACTINOMADURA, PENICILLIN BINDING, IODOPENICILLANATE
2wke:D (ASP121) to (GLY165) CRYSTAL STRUCTURE OF THE ACTINOMADURA R39 DD-PEPTIDASE INHIBITED BY 6-BETA-IODOPENICILLANATE. | HYDROLASE, ANTIBIOTIC RESISTANCE, ACTINOMADURA, PENICILLIN BINDING, IODOPENICILLANATE
1tz3:A (LYS6) to (CYS28) CRYSTAL STRUCTURE OF AMINOIMIDAZOLE RIBOSIDE KINASE COMPLEXED WITH AMINOIMIDAZOLE RIBOSIDE | RIBOKINASE FOLD, ALPHA/BETA, TRANSFERASE
3iyp:F (GLY161) to (ASP183) THE INTERACTION OF DECAY-ACCELERATING FACTOR WITH ECHOVIRUS 7 | VIRUS, RECEPTOR, COMPLEX, ECHOVIRUS, DAF, ICOSAHEDRAL VIRUS
2wkw:A (SER16) to (THR46) ALCALIGENES ESTERASE COMPLEXED WITH PRODUCT ANALOGUE | HYDROLASE, HYDROLASE(CARBOXYLIC ESTERASE), ESTERASE, ATOMIC RESOLUTION, ALPHA/BETA HYDROLASE
2wkw:B (SER16) to (THR46) ALCALIGENES ESTERASE COMPLEXED WITH PRODUCT ANALOGUE | HYDROLASE, HYDROLASE(CARBOXYLIC ESTERASE), ESTERASE, ATOMIC RESOLUTION, ALPHA/BETA HYDROLASE
2wky:A (MET106) to (ALA136) CRYSTAL STRUCTURE OF THE LIGAND-BINDING CORE OF GLUR5 IN COMPLEX WITH THE AGONIST 4-AHCP | MEMBRANE PROTEIN, SYNAPSE, MEMBRANE, RECEPTOR, TRANSPORT, ION CHANNEL, RNA EDITING, GLYCOPROTEIN, CELL JUNCTION, IONOTROPIC GLUTAMATE RECEPTOR, ALTERNATIVE SPLICING, POSTSYNAPTIC CELL MEMBRANE, IONIC CHANNEL, CELL MEMBRANE, ION TRANSPORT, TRANSMEMBRANE, PHOSPHOPROTEIN, LIGAND-BINDING CORE
3vv7:A (CYS319) to (GLY334) CRYSTAL STRUCTURE OF BETA SECETASE IN COMPLEX WITH 2-AMINO-6-((1S,2R)- 2-(3'-METHOXYBIPHENYL-3-YL)CYCLOPROPYL)-3-METHYLPYRIMIDIN-4(3H)-ONE | ASPARTYL PROTEASE, BASE, BETA-SECRETASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4lqi:J (VAL12) to (LYS28) YEAST 20S PROTEASOME IN COMPLEX WITH VIBRALACTONE | BETA-LACTONE, INHIBITOR, NATURAL PRODUCT, TARGET IDENTIFICATION, NTN- PROTEASE, CELLULAR PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4lqi:M (VAL12) to (GLY30) YEAST 20S PROTEASOME IN COMPLEX WITH VIBRALACTONE | BETA-LACTONE, INHIBITOR, NATURAL PRODUCT, TARGET IDENTIFICATION, NTN- PROTEASE, CELLULAR PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4lqi:X (VAL12) to (LYS28) YEAST 20S PROTEASOME IN COMPLEX WITH VIBRALACTONE | BETA-LACTONE, INHIBITOR, NATURAL PRODUCT, TARGET IDENTIFICATION, NTN- PROTEASE, CELLULAR PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4lqi:a (VAL12) to (GLY30) YEAST 20S PROTEASOME IN COMPLEX WITH VIBRALACTONE | BETA-LACTONE, INHIBITOR, NATURAL PRODUCT, TARGET IDENTIFICATION, NTN- PROTEASE, CELLULAR PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3vxt:C (VAL152) to (ASN170) T36-5 TCR SPECIFIC FOR HLA-A24-NEF134-10 | HIV-1, NEF, IMMUNE SYSTEM, T CELL RECEPTOR, IMMUNOGLOBURIN DOMAIN, TCR, IMMUNE RESPONSE
4ltc:J (VAL13) to (LYS29) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH ENONE CARMAPHYCIN ANALOGUE 6 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ltc:M (VAL20) to (GLY38) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH ENONE CARMAPHYCIN ANALOGUE 6 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ltc:a (VAL20) to (GLY38) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH ENONE CARMAPHYCIN ANALOGUE 6 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1u8c:A (ASN806) to (SER824) A NOVEL ADAPTATION OF THE INTEGRIN PSI DOMAIN REVEALED FROM ITS CRYSTAL STRUCTURE | PSI DOMAIN, INTEGRIN, VITRONECTRIN RECEPTOR, CELL ADHESION
1ic0:E (VAL23) to (SER56) RED COPPER PROTEIN NITROSOCYANIN FROM NITROSOMONAS EUROPAEA | RED COPPER, CUPREDOXIN, BETA HAIRPIN, NITROSOCYANIN, NITROSOMONAS EUROPAEA, CU-MAD, METAL BINDING PROTEIN
5a5f:A (CYS227) to (LEU248) CRYSTAL STRUCTURE OF MURD LIGASE FROM ESCHERICHIA COLI IN COMPLEX WITH UMA AND ADP | LIGASE, PEPTIDOGLYCAN SYNTHESIS, ADP-FORMING ENZYME, CELL WALL, CELL SHAPE, CELL CYCLE, NUCLEOTIDE-BINDING, ATP- BINDING, CELL DIVISION, LIGAND, CONFORMATION
2i3s:A (ARG235) to (PRO253) BUB3 COMPLEX WITH BUB1 GLEBS MOTIF | WD40 PROTEIN, BETA-PROPELLER, GLEBS MOTIF, MITOTIC SPINDLE CHECKPOINT, CELL CYCLE
1ild:A (VAL136) to (ARG157) OUTER MEMBRANE PHOSPHOLIPASE A FROM ESCHERICHIA COLI N156A ACTIVE SITE MUTANT PH 4.6 | ANTI-PARALLEL BETA BARREL, MEMBRANE PHOSPHOLIPASE, MEMBRANE PROTEIN, SERINE HYDROLASE, N156A, HYDROLASE
1ilz:A (VAL136) to (ALA156) OUTER MEMBRANE PHOSPHOLIPASE A FROM ESCHERICHIA COLI N156A ACTIVE SITE MUTANT PH 6.1 | ANTI-PARALLEL BETA BARREL, MEMBRANE PHOSPHOLIPASE, MEMBRANE PROTEIN, SERINE HYDROLASE, CATALYTIC TRIAD, ASN ALA MUTATION, HYDROLASE
2ial:C (VAL150) to (ASN168) STRUCTURAL BASIS FOR RECOGNITION OF MUTANT SELF BY A TUMOR- SPECIFIC, MHC CLASS II-RESTRICTED TCR | X-RAY CRYSTALLOGRAPHY, MAJOR HISTOCOMPATIBILITY COMPLEX, T CELL RECEPTOR, T CELL STIMULATION, MELANOMA, TUMOR ANTIGEN, IMMUNE SYSTEM
3j1o:L (GLU159) to (ILE189) CRYO-EM MAP OF A YEAST MINIMAL PREINITIATION COMPLEX INTERACTING WITH THE MEDIATOR HEAD MODULE | RNA POLYMERASE II, MEDIATOR HEAD MODULE, PREINITIATION COMPLEX, TRANSCRIPTION
2wzc:A (VAL277) to (THR301) THE CATALYTICALLY ACTIVE FULLY CLOSED CONFORMATION OF HUMAN PHOSPHOGLYCERATE KINASE IN COMPLEX WITH ADP, 3PG AND ALUMINIUM TETRAFLUORIDE | HEREDITARY HEMOLYTIC ANEMIA, TRANSFERASE, PHOSPHOPROTEIN, KINASE, GLYCOLYSIS, NUCLEOTIDE-BINDING
2wzd:A (VAL277) to (THR301) THE CATALYTICALLY ACTIVE FULLY CLOSED CONFORMATION OF HUMAN PHOSPHOGLYCERATE KINASE K219A MUTANT IN COMPLEX WITH ADP, 3PG AND ALUMINIUM TRIFLUORIDE | TRANSFERASE, HEREDITARY HEMOLYTIC ANEMIA, PHOSPHOPROTEIN, KINASE, GLYCOLYSIS, NUCLEOTIDE-BINDING
4mb8:B (GLY22) to (ALA44) EVOLUTIONARY HISTORY AND METABOLIC INSIGHTS OF ANCIENT MAMMALIAN URICASES | URIC ACID OXIDASE, LYSOZOME, OXIDOREDUCTASE
4me3:A (PHE131) to (GLU151) 1.8 ANGSTROM CRYSTAL STRUCTURE OF THE N-TERMINAL DOMAIN OF AN ARCHAEAL MCM | AAA+, ZINC BINDING DOMAIN, HELICASE, REPLICATION
2x13:A (VAL278) to (THR302) THE CATALYTICALLY ACTIVE FULLY CLOSED CONFORMATION OF HUMAN PHOSPHOGLYCERATE KINASE IN COMPLEX WITH ADP AND 3PHOSPHOGLYCERATE | TRANSITION STATE ANALOGUE, HEREDITARY HEMOLYTIC ANEMIA, ATP-BINDING, KINASE, GLYCOLYSIS, TRANSFERASE, DISEASE MUTATION
2x14:A (VAL278) to (THR302) THE CATALYTICALLY ACTIVE FULLY CLOSED CONFORMATION OF HUMAN PHOSPHOGLYCERATE KINASE K219A MUTANT IN COMPLEX WITH AMP-PCP AND 3PG | TRANSITION STATE ANALOGUE, HEREDITARY HEMOLYTIC ANEMIA, ATP-BINDING, KINASE, GLYCOLYSIS, TRANSFERASE, DISEASE MUTATION
2x15:A (VAL278) to (THR302) THE CATALYTICALLY ACTIVE FULLY CLOSED CONFORMATION OF HUMAN PHOSPHOGLYCERATE KINASE IN COMPLEX WITH ADP AND 1,3- BISPHOSPHOGLYCERATE | TRANSITION STATE ANALOGUE, HEREDITARY HEMOLYTIC ANEMIA, PHOSPHOPROTEIN, KINASE, GLYCOLYSIS, TRANSFERASE, PHOSPHORYL TRANSFER, NUCLEOTIDE-BINDING
1iwn:A (GLN30) to (ALA48) CRYSTAL STRUCTURE OF THE OUTER MEMBRANE LIPOPROTEIN RECEPTOR LOLB COMPLEXED WITH PEGMME2000 | UNCLOSED BETA BARREL, LIPOPROTEIN, PROTEIN TRANSPORT
4mf3:A (PHE106) to (ALA137) CRYSTAL STRUCTURE OF HUMAN GRIK1 COMPLEXED WITH A 6-(TETRAZOLYL)ARYL DECAHYDROISOQUINOLINE ANTAGONIST | PROTEIN-LIGAND COMPLEX, LIGAND GATED ION CHANNEL, GLUTAMATE RECEPTOR, GLUTAMATE BINDING, NONE, MEMBRANE, SIGNALING PROTEIN
5ahj:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH MACYRANONE A | HYDROLASE, PROTEASOME, NATURAL PRODUCT, TARGET IDENTIFICATION, INHIBITION, BINDING ANALYSIS
5ahj:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH MACYRANONE A | HYDROLASE, PROTEASOME, NATURAL PRODUCT, TARGET IDENTIFICATION, INHIBITION, BINDING ANALYSIS
5ahj:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH MACYRANONE A | HYDROLASE, PROTEASOME, NATURAL PRODUCT, TARGET IDENTIFICATION, INHIBITION, BINDING ANALYSIS
5ahj:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH MACYRANONE A | HYDROLASE, PROTEASOME, NATURAL PRODUCT, TARGET IDENTIFICATION, INHIBITION, BINDING ANALYSIS
4mgq:A (GLY246) to (ILE264) PBXYN10C CBM APO | ENDO-XYLANASE, HYDROLASE
4mgu:A (GLY98) to (THR139) CRYSTAL STRUCTURE OF ACHETA DOMESTICUS DENSOVIRUS | VIRUS, JELLY-ROLL, DNV, VIRUS-DNA COMPLEX
3wia:C (HIS39) to (LYS61) CRYSTAL STRUCTURE OF THE N-TERMINAL 1-37 RESIDUES DELETED MUTANT OF GEOBACILLUS COPPER NITRITE REDUCTASE | CUPREDOXIN-FOLD, TRIMER, NITRITE REDUCTION, OXIDOREDUCTASE
3wir:B (GLY471) to (HIS487) CRYSTAL STRUCTURE OF KOJIBIOSE PHOSPHORYLASE COMPLEXED WITH GLUCOSE | (ALPHA/ALPHA)6 BARREL, PHOSPHORYLASE, TRANSFERASE
3wir:C (GLY471) to (HIS487) CRYSTAL STRUCTURE OF KOJIBIOSE PHOSPHORYLASE COMPLEXED WITH GLUCOSE | (ALPHA/ALPHA)6 BARREL, PHOSPHORYLASE, TRANSFERASE
2x5o:A (VAL228) to (LEU248) DISCOVERY OF NOVEL 5-BENZYLIDENERHODANINE- AND 5-BENZYLIDENE- THIAZOLIDINE-2,4-DIONE INHIBITORS OF MURD LIGASE | ATP-BINDING, CELL CYCLE, CELL DIVISION, CELL SHAPE, CELL WALL BIOGENESIS/DEGRADATION, LIGASE, PEPTIDOGLYCAN SYNTHESIS
2it1:B (GLU3) to (LEU19) STRUCTURE OF PH0203 PROTEIN FROM PYROCOCCUS HORIKOSHII | ATP BINDING PROTEIN, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, TRANSPORT PROTEIN
2iuk:B (ASP1131) to (VAL1152) CRYSTAL STRUCTURE OF SOYBEAN LIPOXYGENASE-D | IRON, DIOXYGENASE, METAL-BINDING, OXIDOREDUCTASE, OXYLIPIN BIOSYNTHESIS, SOYBEAN LIPOXYGENASE-D, FATTY ACID BIOSYNTHESIS, LIPID SYNTHESIS
2x8k:B (LEU127) to (GLY156) CRYSTAL STRUCTURE OF SPP1 DIT (GP 19.1) PROTEIN, A PARADIGM OF HUB ADSORPTION APPARATUS IN GRAM-POSITIVE INFECTING PHAGES. | VIRAL PROTEIN, DISTAL TAIL PROTEIN
2x8o:A (LYS200) to (ASP225) CRYSTAL STRUCTURE OF CBPF IN COMPLEX WITH ATROPINE BY SOAKING | CHOLINE-BINDING PROTEIN, LIPID-BINDING-PROTEIN
2x8p:A (LYS220) to (ARG246) CRYSTAL STRUCTURE OF CBPF IN COMPLEX WITH ATROPINE BY CO- CRYSTALLIZATION | CHOLINE-BINDING PROTEIN, LIPID-BINDING-PROTEIN
1jd2:M (VAL12) to (GLY30) 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
2ixj:A (VAL60) to (ALA78) RMLC P AERUGINOSA NATIVE | ISOMERASE, LIPOPOLYSACCHARIDE BIOSYNTHESIS, EPIMERISE, EPIMERASE, EPIMERIZE
2j0j:A (LYS255) to (SER269) CRYSTAL STRUCTURE OF A FRAGMENT OF FOCAL ADHESION KINASE CONTAINING THE FERM AND KINASE DOMAINS. | CELL MIGRATION, FERM, TRANSFERASE, INTEGRIN SIGNALING
5aor:A (VAL730) to (TRP756) STRUCTURE OF MLE RNA ADP ALF4 COMPLEX | HYDROLASE-RNA COMPLEX, HELICASE, DOSAGE COMPENSATION, MLE, DEAH, ROX
5aor:B (VAL730) to (TRP756) STRUCTURE OF MLE RNA ADP ALF4 COMPLEX | HYDROLASE-RNA COMPLEX, HELICASE, DOSAGE COMPENSATION, MLE, DEAH, ROX
2xdm:A (ASP121) to (GLY165) CRYSTAL STRUCTURE OF A COMPLEX BETWEEN ACTINOMADURA R39 DD PEPTIDASE AND A PEPTIDOGLYCAN MIMETIC BORONATE INHIBITOR | HYDROLASE-INHIBITOR COMPLEX, BORONIC ACID, PEPTIDOGLYCAN, HYDROLASE
2xdm:C (ASP121) to (GLY165) CRYSTAL STRUCTURE OF A COMPLEX BETWEEN ACTINOMADURA R39 DD PEPTIDASE AND A PEPTIDOGLYCAN MIMETIC BORONATE INHIBITOR | HYDROLASE-INHIBITOR COMPLEX, BORONIC ACID, PEPTIDOGLYCAN, HYDROLASE
2j30:A (PHE114) to (ASP135) THE ROLE OF LOOP BUNDLE HYDROGEN BONDS IN THE MATURATION AND ACTIVITY OF (PRO)CASPASE-3 | HYDROLASE, PRO-CASPASE3, THIOL PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2j31:A (SER113) to (ASP135) THE ROLE OF LOOP BUNDLE HYDROGEN BONDS IN THE MATURATION AND ACTIVITY OF(PRO)CASPASE-3 | CASPASE3 MUTANT E167A, THIOL PROTEASE, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3wu2:b (GLU364) to (ILE381) CRYSTAL STRUCTURE ANALYSIS OF PHOTOSYSTEM II COMPLEX | PSII, ELECTRON TRANSPORT, PHOTOSYNTHESIS, PHOTOSYSTEM, MEMBRANE COMPLEX, TRANSMEMBRANE ALPHA-HELIX, OXYGEN EVOLVING, WATER SPLITTING, IRON BINDING, CALCIUM BINDING, MANGANESE BINDING, CHLORIDE BINDING, FORMYLATION, HYDROXYLATION, THYLAKOID MEMBRANE
2xk1:D (ASP121) to (GLY165) CRYSTAL STRUCTURE OF A COMPLEX BETWEEN ACTINOMADURA R39 DD- PEPTIDASE AND A BORONATE INHIBITOR | HYDROLASE, PEPTIDOGLYCAN
3wwg:A (GLY222) to (ALA244) CRYSTAL STRUCTURE OF THE N-GLYCAN-DEFICIENT VARIANT N448A OF ISOPULLULANASE COMPLEXED WITH ISOPANOSE | BETA-HELIX, GLYCOSIDE HYDROLASE FAMILY 49, HYDROLASE
3wx6:B (ARG79) to (LYS112) CRYSTAL STRUCTURE OF TYPE SIX SECRETION SYSTEM PROTEIN | HEXAMERIC ASSEMBLY, HEXAMERIC RING, T6SS PROTEIN, UNKNOWN FUNCTION
1jsy:A (ASP297) to (HIS353) CRYSTAL STRUCTURE OF BOVINE ARRESTIN-2 | NONVISUAL ARRESTINS, BETA-ARRESTINS, DESENSITIZATION, ENDOCYTOSIS, DOWN-REGULATION, SIGNALING PROTEIN
3wxr:K (VAL12) to (LYS28) YEAST 20S PROTEASOME WITH A MUTATION OF ALPHA7 SUBUNIT | UPS, 20S PROTEASOME, HYDROLASE, PROTEASE, 19S REGULATORY PARTICLE, MULTICATALYTIC PROTEASE
3wxr:2 (VAL12) to (GLY30) YEAST 20S PROTEASOME WITH A MUTATION OF ALPHA7 SUBUNIT | UPS, 20S PROTEASOME, HYDROLASE, PROTEASE, 19S REGULATORY PARTICLE, MULTICATALYTIC PROTEASE
3j8f:2 (TYR100) to (GLU129) CRYO-EM RECONSTRUCTION OF POLIOVIRUS-RECEPTOR COMPLEX | POLIOVIRUS, RECEPTOR, PVR, CD155, VIRUS-SIGNALING PROTEIN COMPLEX
3j8k:F (GLU4) to (GLY20) TILTED STATE OF ACTIN, T2 | HELICAL POLYMER, ACTIN FILAMENT, STRUCTURAL PROTEIN
2xq1:F (MET202) to (TYR221) CRYSTAL STRUCTURE OF PEROXISOMAL CATALASE FROM THE YEAST HANSENULA POLYMORPHA | OXIDOREDUCTASE, HYDROGEN PEROXIDE DETOXIFICATION, PTS1
2xq1:G (ASN203) to (TYR221) CRYSTAL STRUCTURE OF PEROXISOMAL CATALASE FROM THE YEAST HANSENULA POLYMORPHA | OXIDOREDUCTASE, HYDROGEN PEROXIDE DETOXIFICATION, PTS1
2xrb:A (LEU199) to (TRP220) STRUCTURE OF THE N-TERMINAL FOUR DOMAINS OF THE COMPLEMENT REGULATOR RAT CRRY | IMMUNE SYSTEM, IMMUNOLOGY
2xrf:B (ASP162) to (SER185) CRYSTAL STRUCTURE OF HUMAN URIDINE PHOSPHORYLASE 2 | TRANSFERASE
3zcz:B (ASP121) to (GLY165) CRYSTAL STRUCTURE OF A COMPLEX BETWEEN ACTINOMADURA R39 DD- PEPTIDASE AND A TRIFLUOROKETONE INHIBITOR | HYDROLASE, INHIBITOR, PEPTIDOGLYCAN
3zcz:C (ASP121) to (GLY165) CRYSTAL STRUCTURE OF A COMPLEX BETWEEN ACTINOMADURA R39 DD- PEPTIDASE AND A TRIFLUOROKETONE INHIBITOR | HYDROLASE, INHIBITOR, PEPTIDOGLYCAN
1w50:A (THR59) to (GLU79) APO STRUCTURE OF BACE (BETA SECRETASE) | ALTERNATIVE SPLICING, ALZHEIMER'S DISEASE, ASPARTIC PROTEASE, ASPARTYL PROTEASE, BASE, BETA-SECRETASE, GLYCOPROTEIN, HYDROLASE, MEMAPSIN 2, SIGNAL, TRANSMEMBRANE, ZYMOGEN
1w50:A (ASN293) to (ILE324) APO STRUCTURE OF BACE (BETA SECRETASE) | ALTERNATIVE SPLICING, ALZHEIMER'S DISEASE, ASPARTIC PROTEASE, ASPARTYL PROTEASE, BASE, BETA-SECRETASE, GLYCOPROTEIN, HYDROLASE, MEMAPSIN 2, SIGNAL, TRANSMEMBRANE, ZYMOGEN
1w6h:B (GLY264) to (GLY291) NOVEL PLASMEPSIN II-INHIBITOR COMPLEX | MALARIA, DRUG, ASPARTIC PROTEASE, PLASMEPSIN, HYDROLASE, GLYCOPROTEIN
3zef:E (SER1403) to (THR1430) CRYSTAL STRUCTURE OF PRP8:AAR2 COMPLEX: SECOND CRYSTAL FORM AT 3.1 ANGSTROM RESOLUTION | TRANSLATION, PRE-MRNA SPLICING, SPLICEOSOME, U5 SNRNP
3zfd:A (SER208) to (ASP241) CRYSTAL STRUCTURE OF THE KIF4 MOTOR DOMAIN COMPLEXED WITH MG-AMPPNP | HYDROLASE, MOLECULAR MOTOR, ATPASE, MICROTUBULE
3zg2:A (ASP444) to (PRO464) STEROL 14 ALPHA-DEMETHYLASE (CYP51) FROM TRYPANOSOMA CRUZI IN COMPLEX WITH THE PYRIDINE INHIBITOR (S)-2-(4-CHLOROPHENYL)-2- (PYRIDIN-3-YL)-1-(4-(4-(TRIFLUOROMETHYL)PHENYL)PIPERAZIN-1-YL) ETHANONE (EPL-BS1246,UDO) | OXIDOREDUCTASE, MONOOXYGENASE, STEROL BIOSYNTHESIS, EUKARYOTIC MEMBRANES, CYTOCHROME P450 FOLD, ENDOPLASMIC RETICULUM MEMBRANE, INHIBITOR
1w8q:C (ASP121) to (GLY165) CRYSTAL STRUCTURE OF THE DD-TRANSPEPTIDASE-CARBOXYPEPTIDASE FROM ACTINOMADURA R39 | PENICILLIN-BINDING, PEPTIDOGLYCAN, ACTINOMADURA, TRANSPEPTIDASE, ANTIBIOTIC RESISTANCE, HYDROLASE
1k4z:A (CYS1483) to (PRO1503) C-TERMINAL DOMAIN OF CYCLASE ASSOCIATED PROTEIN | RIGHT-HANDED PARALLEL BETA-HELIX, INTERTWINED DIMER, ACTIN-BINDING, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, MEMBRANE PROTEIN
4ndz:B (ASN241) to (ILE266) STRUCTURE OF MALTOSE BINDING PROTEIN FUSION TO 2-O-SULFOTRANSFERASE WITH BOUND HEPTASACCHARIDE AND PAP | HEPARAN SULFATE, FUSION, TRANSPORT PROTEIN-TRANSFERASE COMPLEX
4ndz:C (ASN241) to (ILE266) STRUCTURE OF MALTOSE BINDING PROTEIN FUSION TO 2-O-SULFOTRANSFERASE WITH BOUND HEPTASACCHARIDE AND PAP | HEPARAN SULFATE, FUSION, TRANSPORT PROTEIN-TRANSFERASE COMPLEX
4ndz:D (ASN241) to (ILE266) STRUCTURE OF MALTOSE BINDING PROTEIN FUSION TO 2-O-SULFOTRANSFERASE WITH BOUND HEPTASACCHARIDE AND PAP | HEPARAN SULFATE, FUSION, TRANSPORT PROTEIN-TRANSFERASE COMPLEX
4ndz:E (ASN241) to (ILE266) STRUCTURE OF MALTOSE BINDING PROTEIN FUSION TO 2-O-SULFOTRANSFERASE WITH BOUND HEPTASACCHARIDE AND PAP | HEPARAN SULFATE, FUSION, TRANSPORT PROTEIN-TRANSFERASE COMPLEX
4ndz:F (ASN241) to (ILE266) STRUCTURE OF MALTOSE BINDING PROTEIN FUSION TO 2-O-SULFOTRANSFERASE WITH BOUND HEPTASACCHARIDE AND PAP | HEPARAN SULFATE, FUSION, TRANSPORT PROTEIN-TRANSFERASE COMPLEX
2xzd:A (SER113) to (ASP135) CASPASE-3 IN COMPLEX WITH AN INHIBITORY DARPIN-3.4 | HYDROLASE-PROTEIN BINDING COMPLEX, DE NOVO PROTEIN, APOPTOSIS, ANKYRIN REPEAT PROTEIN, RIBOSOME DISPLAY
2xzd:C (SER113) to (ASP135) CASPASE-3 IN COMPLEX WITH AN INHIBITORY DARPIN-3.4 | HYDROLASE-PROTEIN BINDING COMPLEX, DE NOVO PROTEIN, APOPTOSIS, ANKYRIN REPEAT PROTEIN, RIBOSOME DISPLAY
5bv1:A (ASN133) to (LEU151) CRYSTAL STRUCTURE OF A VPS33-VPS16 COMPLEX FROM CHAETOMIUM THERMOPHILUM | MEMBRANE TRAFFICKING, SM PROTEIN, HOPS COMPLEX, THERMOPHILE, TRANSPORT PROTEIN
2xzt:A (SER113) to (ASP135) CASPASE-3 IN COMPLEX WITH DARPIN-3.4_I78S | HYDROLASE-PROTEIN BINDING COMPLEX, DE NOVO PROTEIN, APOPTOSIS, ANKYRIN REPEAT PROTEIN, RIBOSOME DISPLAY
1wcs:A (THR581) to (ASN613) A MUTANT OF TRYPANOSOMA RANGELI SIALIDASE DISPLAYING TRANS- SIALIDASE ACTIVITY | TRANS-SIALIDASE, SIALIDASE, TRYPANOSOMA CRUZI, TRYPANOSOMA RANGELI, PROTEIN ENGINEERING, HYDROLASE
2y0b:A (PHE114) to (ASP135) CASPASE-3 IN COMPLEX WITH AN INHIBITORY DARPIN-3.4_S76R | HYDROLASE-PROTEIN BINDING COMPLEX, STRUCTURE-ACTIVITY RELATIONSHIP, ANKYRIN REPEAT PROTEIN, RIBOSOME DISPLAY, APOPTOSIS
2y0b:C (PHE114) to (ASP135) CASPASE-3 IN COMPLEX WITH AN INHIBITORY DARPIN-3.4_S76R | HYDROLASE-PROTEIN BINDING COMPLEX, STRUCTURE-ACTIVITY RELATIONSHIP, ANKYRIN REPEAT PROTEIN, RIBOSOME DISPLAY, APOPTOSIS
3ziw:A (GLY160) to (GLU198) CLOSTRIDIUM PERFRINGENS ENTEROTOXIN, D48A MUTATION AND N- TERMINAL 37 RESIDUES DELETED | TOXIN, BETA PORE-FORMING-TOXIN, CYTOTOXICITY MUTANT
3zix:A (GLY160) to (GLU198) CLOSTRIDIUM PERFRINGENS ENTEROTOXIN WITH THE N-TERMINAL 37 RESIDUES DELETED | TOXIN, BETA PORE-FORMING-TOXIN, CYTOTOXICITY MUTANT
5bx5:A (GLN330) to (TYR354) CRYSTAL STRUCTURE OF THERMOANAEROBACTERIUM XYLANOLYTICUM GH116 BETA- GLUCOSIDASE WITH GLUCOSE | THERMOANAEROBACTERIUM XYLANOLYTICUM LX-11, GH116, BETA-GLUCOSIDASE, GLUCOSE, HYDROLASE
1kat:V (GLY65) to (LEU97) SOLUTION STRUCTURE OF A PHAGE-DERIVED PEPTIDE ANTAGONIST IN COMPLEX WITH VASCULAR ENDOTHELIAL GROWTH FACTOR | PROTEIN-PEPTIDE COMPLEX, HOMODIMER, CYSTINE KNOT, CELL CYCLE, HORMONE/GROWTH FACTOR COMPLEX
1kat:W (GLY65) to (LEU97) SOLUTION STRUCTURE OF A PHAGE-DERIVED PEPTIDE ANTAGONIST IN COMPLEX WITH VASCULAR ENDOTHELIAL GROWTH FACTOR | PROTEIN-PEPTIDE COMPLEX, HOMODIMER, CYSTINE KNOT, CELL CYCLE, HORMONE/GROWTH FACTOR COMPLEX
2y4a:B (ASP121) to (GLY165) UNEXPECTED TRICOVALENT BINDING MODE OF BORONIC ACIDS WITHIN THE ACTIVE SITE OF A PENICILLIN BINDING PROTEIN | HYDROLASE, PEPTIDOGLYCAN, TETRAVALENT BORON
2y4a:D (ASP121) to (GLY165) UNEXPECTED TRICOVALENT BINDING MODE OF BORONIC ACIDS WITHIN THE ACTIVE SITE OF A PENICILLIN BINDING PROTEIN | HYDROLASE, PEPTIDOGLYCAN, TETRAVALENT BORON
2kr0:A (LEU23) to (PRO40) SOLUTION STRUCTURE OF THE PROTEASOME UBIQUITIN RECEPTOR RPN13 | PROTEASOME, UBIQUITIN, 19S REGULATOR, PROTEIN BINDING
2y55:D (ASP121) to (GLY165) UNEXPECTED TRICOVALENT BINDING MODE OF BORONIC ACIDS WITHIN THE ACTIVE SITE OF A PENICILLIN BINDING PROTEIN | HYDROLASE-INHIBITOR COMPLEX, PEPTIDOGLYCAN, HYDROLASE
2y59:C (ASP121) to (GLY165) UNEXPECTED TRICOVALENT BINDING MODE OF BORONIC ACIDS WITHIN THE ACTIVE SITE OF A PENICILLIN BINDING PROTEIN | HYDROLASE-INHIBITOR COMPLEX, PEPTIDOGLYCAN, HYDROLASE
2y59:D (ASP121) to (GLY165) UNEXPECTED TRICOVALENT BINDING MODE OF BORONIC ACIDS WITHIN THE ACTIVE SITE OF A PENICILLIN BINDING PROTEIN | HYDROLASE-INHIBITOR COMPLEX, PEPTIDOGLYCAN, HYDROLASE
2y68:A (VAL228) to (LEU248) STRUCTURE-BASED DESIGN OF A NEW SERIES OF D-GLUTAMIC ACID- BASED INHIBITORS OF BACTERIAL MURD LIGASE | ATP-BINDING, CELL CYCLE, CELL DIVISION, CELL SHAPE, CELL WALL, CELL WALL BIOGENESIS/DEGRADATION, LIGASE, NUCLEOTIDE-BINDING, PEPTIDOGLYCAN SYNTHESIS, UMA
2kxv:A (ARG100) to (ASP126) NMR STRUCTURE AND CALCIUM-BINDING PROPERTIES OF THE TELLURITE RESISTANCE PROTEIN TERD FROM KLEBSIELLA PNEUMONIAE | KP-TERD, TELLURITE RESISTANCE, CA2+ BINDING PROTEIN, CALCIUM SIGNALING, UNKNOWN FUNCTION
5c0x:C (LYS280) to (ALA332) STRUCTURE OF A 12-SUBUNIT NUCLEAR EXOSOME COMPLEX BOUND TO STRUCTURED RNA | HYDROLASE, RNA, NUCLEASE, PROTEIN-RNA COMPLEX, HYDROLASE-RNA COMPLEX
1kgc:D (VAL158) to (ASN176) IMMUNE RECEPTOR | T-CELL RECEPTOR, LC13 CLONE, IMMUNE SYSTEM
2y7i:B (TYR106) to (THR123) STRUCTURAL BASIS FOR HIGH ARGININE SPECIFICITY IN SALMONELLA TYPHIMURIUM PERIPLASMIC BINDING PROTEIN STM4351. | ARGININE-BINDING PROTEIN
2y7o:A (ASN190) to (ILE207) STRUCTURE OF N-TERMINAL DOMAIN OF CANDIDA ALBICANS ALS9-2 - G299W MUTANT | CELL ADHESION, ADHESIN, PEPTIDE BINDING PROTEIN
1ww5:B (GLY132) to (TYR157) AGROCYBE CYLINDRACEA GALECTIN COMPLEXED WITH 3'-SULFONYL LACTOSE | AGROCYBE CYLINDRACEA GALECTIN, FUNGAL GALECTIN, CARBOHYDRATE RECOGNITION DOMAIN, 3'-SULFATED LACTOSE, X-RAY CRYSTALLOGRAPHIC ANALYSIS, SUGAR BINDING PROTEIN
1ww5:D (GLY132) to (TYR157) AGROCYBE CYLINDRACEA GALECTIN COMPLEXED WITH 3'-SULFONYL LACTOSE | AGROCYBE CYLINDRACEA GALECTIN, FUNGAL GALECTIN, CARBOHYDRATE RECOGNITION DOMAIN, 3'-SULFATED LACTOSE, X-RAY CRYSTALLOGRAPHIC ANALYSIS, SUGAR BINDING PROTEIN
1ww6:C (GLY132) to (TYR157) AGROCYBE CYLINDRACEA GALECTIN COMPLEXED WITH LACTOSE | AGROCYBE CYLINDRACEA GALECTIN, FUNGAL GALECTIN, CARBOHYDRATE RECOGNITION DOMAIN, LACTOSE, X-RAY CRYSTALLOGRAPHIC ANALYSIS, SUGAR BINDING PROTEIN
4nnn:J (VAL13) to (LYS29) YCP IN COMPLEX WITH MG132 | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, ALDEHYDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4nnn:M (VAL20) to (GLY38) YCP IN COMPLEX WITH MG132 | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, ALDEHYDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4nnn:X (VAL13) to (LYS29) YCP IN COMPLEX WITH MG132 | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, ALDEHYDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4nnn:a (VAL20) to (GLY38) YCP IN COMPLEX WITH MG132 | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, ALDEHYDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4nnw:J (VAL13) to (LYS29) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-KETOALDEHYDE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, KETOALDEHYDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4nnw:M (VAL20) to (GLY38) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-KETOALDEHYDE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, KETOALDEHYDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4nnw:X (VAL13) to (LYS29) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-KETOALDEHYDE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, KETOALDEHYDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4nnw:a (VAL20) to (GLY38) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-KETOALDEHYDE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, KETOALDEHYDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no1:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-B(OH)2 | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, BORONIC ACID, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no6:J (VAL13) to (LYS29) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-VINYLSULFONE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, VINYLSULFONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no6:M (VAL20) to (GLY38) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-VINYLSULFONE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, VINYLSULFONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no6:X (VAL13) to (LYS29) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-VINYLSULFONE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, VINYLSULFONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no6:a (VAL20) to (GLY38) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-VINYLSULFONE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, VINYLSULFONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1wye:A (ALA2) to (HIS31) CRYSTAL STRUCTURE OF 2-KETO-3-DEOXYGLUCONATE KINASE (FORM 1) FROM SULFOLOBUS TOKODAII | ARCHEA, SULFOLOBUS TOKOKAI, TRANSFERASE
1wye:E (ALA2) to (HIS31) CRYSTAL STRUCTURE OF 2-KETO-3-DEOXYGLUCONATE KINASE (FORM 1) FROM SULFOLOBUS TOKODAII | ARCHEA, SULFOLOBUS TOKOKAI, TRANSFERASE
1kk1:A (GLY232) to (VAL245) STRUCTURE OF THE LARGE GAMMA SUBUNIT OF INITIATION FACTOR EIF2 FROM PYROCOCCUS ABYSSI-G235D MUTANT COMPLEXED WITH GDPNP-MG2+ | INITIATION OF TRANSLATION
1kjz:A (GLY232) to (VAL245) STRUCTURE OF THE LARGE GAMMA SUBUNIT OF INITIATION FACTOR EIF2 FROM PYROCOCCUS ABYSSI-G235D MUTANT | INITIATION OF TRANSLATION
1kk2:A (GLY232) to (VAL245) STRUCTURE OF THE LARGE GAMMA SUBUNIT OF INITIATION FACTOR EIF2 FROM PYROCOCCUS ABYSSI-G235D MUTANT COMPLEXED WITH GDP-MG2+ | INITIATION OF TRANSLATION
1kk3:A (GLY232) to (VAL245) STRUCTURE OF THE WILD-TYPE LARGE GAMMA SUBUNIT OF INITIATION FACTOR EIF2 FROM PYROCOCCUS ABYSSI COMPLEXED WITH GDP-MG2+ | INITIATION OF TRANSLATION
4no8:J (VAL13) to (LYS29) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-KETOAMIDE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, KETOAMIDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no8:M (VAL20) to (GLY38) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-KETOAMIDE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, KETOAMIDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no8:X (VAL13) to (LYS29) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-KETOAMIDE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, KETOAMIDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no8:a (VAL20) to (GLY38) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-KETOAMIDE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, KETOAMIDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1x0u:E (LYS55) to (TYR78) CRYSTAL STRUCTURE OF THE CARBOXYL TRANSFERASE SUBUNIT OF PUTATIVE PCC OF SULFOLOBUS TOKODAII | LYASE
3zvt:A (ASP121) to (GLY165) UNEXPECTED TRICOVALENT BINDING MODE OF BORONIC ACIDS WITHIN THE ACTIVE SITE OF A PENICILLIN BINDING PROTEIN | HYDROLASE, PEPTIDOGLYCAN, PENICILLIN-BINDING, TETRAVALENT BORON
3zvw:B (ASP121) to (GLY165) UNEXPECTED TRICOVALENT BINDING MODE OF BORONIC ACIDS WITHIN THE ACTIVE SITE OF A PENICILLIN BINDING PROTEIN | HYDROLASE, PEPTIDOGLYCAN, PENICILLIN-BINDING, TETRAVALENT BORON
3zvw:C (ASP121) to (GLY165) UNEXPECTED TRICOVALENT BINDING MODE OF BORONIC ACIDS WITHIN THE ACTIVE SITE OF A PENICILLIN BINDING PROTEIN | HYDROLASE, PEPTIDOGLYCAN, PENICILLIN-BINDING, TETRAVALENT BORON
2mpr:A (GLY245) to (ASN270) MALTOPORIN FROM SALMONELLA TYPHIMURIUM | OUTER MEMBRANE PROTEIN, OLIGOSACCHARIDE BINDING, SUGAR TRANSPORT, PHAGE RECOGNITION
2mpr:B (GLY245) to (ASN270) MALTOPORIN FROM SALMONELLA TYPHIMURIUM | OUTER MEMBRANE PROTEIN, OLIGOSACCHARIDE BINDING, SUGAR TRANSPORT, PHAGE RECOGNITION
2mpr:C (GLY245) to (ASN270) MALTOPORIN FROM SALMONELLA TYPHIMURIUM | OUTER MEMBRANE PROTEIN, OLIGOSACCHARIDE BINDING, SUGAR TRANSPORT, PHAGE RECOGNITION
4nww:A (SER44) to (ILE76) CRYSTAL STRUCTURE OF AN N-TERMINALLY TRUNCATED CAPSID PROTEIN MUTANT OF ORSAY VIRUS | BETA BARREL, VIRUS
2ygb:B (THR64) to (TYR86) STRUCTURE OF VACCINIA VIRUS D13 SCAFFOLDING PROTEIN | VIRAL PROTEIN, VIRAL EVOLUTION
2ygq:A (ALA171) to (PRO201) WIF DOMAIN-EPIDERMAL GROWTH FACTOR (EGF)-LIKE DOMAINS 1-3 OF HUMAN WNT INHIBITORY FACTOR 1 IN COMPLEX WITH 1,2-DIPALMITOYLPHOSPHATIDYLCHOLINE | SIGNALING PROTEIN, WNT SIGNALING PATHWAY, WNT ANTAGONIST, MORPHOGEN, CANCER, GLYCOSAMINOGLYCAN
1ktw:A (ASP447) to (ASP467) IOTA-CARRAGEENASE COMPLEXED TO IOTA-CARRAGEENAN FRAGMENTS | HYDROLASE, IOTA-CARRAGEENAN DOUBLE HELIX DEGRADATION
1ktw:B (ASN233) to (ASN261) IOTA-CARRAGEENASE COMPLEXED TO IOTA-CARRAGEENAN FRAGMENTS | HYDROLASE, IOTA-CARRAGEENAN DOUBLE HELIX DEGRADATION
3zx1:A (ASN81) to (TYR105) MULTICOPPER OXIDASE FROM CAMPYLOBACTER JEJUNI: A METALLO-OXIDASE | OXIDOREDUCTASE, LACCASE, METALLO-OXIDASE, CUPROUS OXIDASE
1xcg:E (ILE967) to (ASP983) CRYSTAL STRUCTURE OF HUMAN RHOA IN COMPLEX WITH DH/PH FRAGMENT OF PDZRHOGEF | X-RAY CRYSTALLOGRAPHY; REGULATION OF RHOA GTPASE; PROTEIN COMPLEX, SIGNALING PROTEIN ACTIVATOR/SIGNALING PROTEIN COMPLEX
5c7r:A (ASN241) to (LEU262) REVEALING SURFACE WATERS ON AN ANTIFREEZE PROTEIN BY FUSION PROTEIN CRYSTALLOGRAPHY | ANTIFREEZE PROTEIN, FUSION PROTEIN
3zyp:A (ASP66) to (PHE86) CELLULOSE INDUCED PROTEIN, CIP1 | METAL BINDING PROTEIN, CALCIUM-BINDING, CBM-CONTAINING, BETA SANDWICH JELLY ROLL, CARBOHYDRATE-BINDING
1kyi:M (VAL12) to (ASN30) 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:N (VAL12) to (ASN30) 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:O (VAL12) to (ASN30) 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:Q (VAL12) to (ASN30) 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:R (VAL12) to (ASN30) HSLUV (H. INFLUENZAE)-NLVS VINYL SULFONE INHIBITOR COMPLEX | PROKARYOTIC PROTEASOME, PROTEASE, AAA-PROTEIN, ATP-DEPENDENT CHAPERONE; CLP/HSP100, VINYL SULFONE INHIBITOR, CHAPERONE-HYDROLASE COMPLEX
5c97:A (ALA310) to (ASN330) INSULIN REGULATED AMINOPEPTIDASE | AMINOPEPTIDASE, ANTIGEN PRESENTATION, HYDROLASE, IRAP
1xdo:A (GLY431) to (THR457) CRYSTAL STRUCTURE OF ESCHERICHIA COLI POLYPHOSPHATE KINASE | POLYPHOSPHATE KINASE, PPK, E.COLI POLYPHOSPHATE KINASE, TRANSFERASE
1xe6:B (GLY264) to (ILE289) STRUCTURE OF PLASMEPSIN II IN COMPLEX OF AN PEPSTATIN ANALOGUE | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2ymw:B (LYS177) to (GLY197) STRUCTURE OF THE EPSILON-LYSINE OXIDASE FROM MARINOMONAS MEDITERRANEA | OXIDOREDUCTASE
1l9m:A (ASP621) to (ASP644) THREE-DIMENSIONAL STRUCTURE OF THE HUMAN TRANSGLUTAMINASE 3 ENZYME: BINDING OF CALCIUM IONS CHANGE STRUCTURE FOR ACTIVATION | ACTIVATION, CALCIUM BINDING, TRANSGLUTAMINASE, X-RAY STRUCTURE, TRANSFERASE
5cgg:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ALPHA- CHLOROACETAMIDE 1 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cgg:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ALPHA- CHLOROACETAMIDE 1 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cgg:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ALPHA- CHLOROACETAMIDE 1 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cgg:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ALPHA- CHLOROACETAMIDE 1 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4o9x:A (ARG1417) to (GLN1437) CRYSTAL STRUCTURE OF TCDB2-TCCC3 | BETA SHEET, COCOON, UNFOLDING, TC TOXIN, TOXIN
5cgh:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ALPHA- CHLOROACETAMIDE 5 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cgh:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ALPHA- CHLOROACETAMIDE 5 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cgh:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ALPHA- CHLOROACETAMIDE 5 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cgh:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ALPHA- CHLOROACETAMIDE 5 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
2yry:A (THR23) to (ARG42) SOLUTION STRUCTURE OF THE PH DOMAIN OF PLECKSTRIN HOMOLOGY DOMAIN-CONTAINING FAMILY A MEMBER 6 FROM HUMAN | PH DOMAIN, PEPP-3, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, SIGNALING PROTEIN
5cgi:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ONX 0914 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cgi:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ONX 0914 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cgi:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ONX 0914 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cgi:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ONX 0914 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cgm:B (SER228) to (THR250) STRUCTURE OF MYCOBACTERIUM THERMORESISTIBILE GLGE IN COMPLEX WITH MALTOSE AT 1.95A RESOLUTION | GLGE, MALTOSE, GH13, MALTOSYLTRANSFERASE, TRANSFERASE
2yz2:A (ARG2) to (LEU23) CRYSTAL STRUCTURE OF THE ABC TRANSPORTER IN THE COBALT TRANSPORT SYSTEM | ABC TRANSPORTER, COBALT TRANSPORT, ATP-BINDING PROTEIN, TM0222, HYDROLASE, INNER MEMBRANE, MEMBRANE, NUCLEOTIDE-BINDING, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI
5cjx:K (SER413) to (ALA436) CRYSTAL STRUCTURE OF 8ANC195 FAB IN COMPLEX WITH BG505 SOSIP.664 HIV-1 ENV TRIMER | HIV-1 ENV TRIMER, IG FOLD, ANTIBODY, VIRAL PROTEIN-IMMUNE SYSTEM COMPLEX
3k4z:A (PRO140) to (ASP167) CRYSTAL STRUCTURE OF THE CELLULOSOMAL CBM4 FROM CLOSTRIDIUM THERMOCELLUM CELLULASE CBHA | CELLULASE, CBHA, CLOSTRIDIUM THERMOCELLUM, CBM4, IG-LIKE, CELLULOSOME, CBM, SUGAR BINDING PROTEIN
1lnz:B (GLN112) to (GLY143) STRUCTURE OF THE OBG GTP-BINDING PROTEIN | GTPASE, OBG, STRINGENT FACTOR, STRESS RESPONSE, SPORULATION, LARGE G-PROTEIN, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC, CELL CYCLE
1ltl:A (ARG122) to (THR142) THE DODECAMER STRUCTURE OF MCM FROM ARCHAEAL M. THERMOAUTOTROPHICUM | REPLICATION
1ltl:B (ARG122) to (THR142) THE DODECAMER STRUCTURE OF MCM FROM ARCHAEAL M. THERMOAUTOTROPHICUM | REPLICATION
1ltl:C (ARG116) to (THR142) THE DODECAMER STRUCTURE OF MCM FROM ARCHAEAL M. THERMOAUTOTROPHICUM | REPLICATION
1ltl:E (ARG122) to (THR142) THE DODECAMER STRUCTURE OF MCM FROM ARCHAEAL M. THERMOAUTOTROPHICUM | REPLICATION
1ltl:F (ARG122) to (THR142) THE DODECAMER STRUCTURE OF MCM FROM ARCHAEAL M. THERMOAUTOTROPHICUM | REPLICATION
4ojl:A (PRO648) to (GLY671) 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
4ojp:B (PRO648) to (GLY671) CRYSTAL STRUCTURE OF PUTATIVE TAILSPIKE PROTEIN (TSP1, ORF210) FROM ESCHERICHIA COLI O157:H7 BACTERIOHAGE CBA120 IN COMPLEX WITH MALTOSE | PARALLEL BETA HELIX, PUTATIVE ENDO-GLYCOSIDASE, BACTERIAL POLYSACCHARIDE, PHAGE BASEPLATE, PHAGE TAIL, VIRAL PROTEIN
1lyw:F (LYS281) to (SER304) CATHEPSIN D AT PH 7.5 | ASPARTIC PROTEASE, HYDROLASE, GLYCOPROTEIN
1xnv:A (SER60) to (TYR83) ACYL-COA CARBOXYLASE BETA SUBUNIT FROM S. COELICOLOR (PCCB), APO FORM #1 | POLYKETIDE; POLYKETIDE SYNTHASE; ACYL-COA CARBOXYLASE; CARBOXYLTRANSFERASE, LIGASE
1xny:A (SER60) to (TYR83) BIOTIN AND PROPIONYL-COA BOUND TO ACYL-COA CARBOXYLASE BETA SUBUNIT FROM S. COELICOLOR (PCCB) | POLYKETIDE; POLYKETIDE SYNTHASE; ACYL-COA CARBOXYLASE; CARBOXYLTRANSFERASE, LIGASE
1xny:B (SER60) to (TYR83) BIOTIN AND PROPIONYL-COA BOUND TO ACYL-COA CARBOXYLASE BETA SUBUNIT FROM S. COELICOLOR (PCCB) | POLYKETIDE; POLYKETIDE SYNTHASE; ACYL-COA CARBOXYLASE; CARBOXYLTRANSFERASE, LIGASE
2zcy:M (VAL12) to (GLY30) YEAST 20S PROTEASOME:SYRINGOLIN A-COMPLEX | ALPHA/BETA SANDWICH, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, PROTEASOME, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN
2zcy:0 (VAL12) to (GLY30) YEAST 20S PROTEASOME:SYRINGOLIN A-COMPLEX | ALPHA/BETA SANDWICH, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, PROTEASOME, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN
1m1g:C (ASP44) to (LYS69) CRYSTAL STRUCTURE OF AQUIFEX AEOLICUS N-UTILIZATION SUBSTANCE G (NUSG), SPACE GROUP P2(1) | TRANSCRIPTION TERMINATION, ANTITERMINATION, KOW DOMAIN, RNP MOTIF, IMMUNOGLOBULIN FOLD, NUCLEIC ACID INTERACTION, PROTEIN-PROTEIN INTERACTION
1xo6:B (SER60) to (TYR83) ACYL-COA CARBOXYLASE BETA SUBUNIT FROM S. COELICOLOR (PCCB), APO FORM #3 | POLYKETIDE; POLYKETIDE SYNTHASE; ACYL-COA CARBOXYLASE; CARBOXYLTRANSFERASE, LIGASE
1xo6:C (SER60) to (TYR83) ACYL-COA CARBOXYLASE BETA SUBUNIT FROM S. COELICOLOR (PCCB), APO FORM #3 | POLYKETIDE; POLYKETIDE SYNTHASE; ACYL-COA CARBOXYLASE; CARBOXYLTRANSFERASE, LIGASE
1xo6:D (SER60) to (TYR83) ACYL-COA CARBOXYLASE BETA SUBUNIT FROM S. COELICOLOR (PCCB), APO FORM #3 | POLYKETIDE; POLYKETIDE SYNTHASE; ACYL-COA CARBOXYLASE; CARBOXYLTRANSFERASE, LIGASE
3k9f:A (VAL236) to (THR257) DETAILED STRUCTURAL INSIGHT INTO THE QUINOLONE-DNA CLEAVAGE COMPLEX OF TYPE IIA TOPOISOMERASES | QUINOLONE, TOPOISOMERASE, DNA, PROTEIN-DNA CLEAVAGE COMPLEX, STREPTOCOCCUS PNEUMONIAE, LEVOFLOXACIN, CELL MEMBRANE, DNA-BINDING, ISOMERASE, MEMBRANE, ATP-BINDING, NUCLEOTIDE-BINDING, ISOMERASE-DNA COMPLEX
3k9f:B (VAL236) to (THR257) DETAILED STRUCTURAL INSIGHT INTO THE QUINOLONE-DNA CLEAVAGE COMPLEX OF TYPE IIA TOPOISOMERASES | QUINOLONE, TOPOISOMERASE, DNA, PROTEIN-DNA CLEAVAGE COMPLEX, STREPTOCOCCUS PNEUMONIAE, LEVOFLOXACIN, CELL MEMBRANE, DNA-BINDING, ISOMERASE, MEMBRANE, ATP-BINDING, NUCLEOTIDE-BINDING, ISOMERASE-DNA COMPLEX
1m2v:B (MET550) to (GLY573) CRYSTAL STRUCTURE OF THE YEAST SEC23/24 HETERODIMER | ZINC-FINGER, BETA BARREL, VWA DOMAIN, GELSOLIN DOMAIN,, PROTEIN TRANSPORT
2zhr:B (ASN293) to (PHE322) CRYSTAL STRUCTURE OF BACE1 IN COMPLEX WITH OM99-2 AT PH 5.0 | OM99-2 COMPLEX, PH 5.0, ASPARTYL PROTEASE, GLYCOPROTEIN, MEMBRANE, PROTEASE, TRANSMEMBRANE, ZYMOGEN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1xrf:A (TYR10) to (ASP35) THE CRYSTAL STRUCTURE OF A NOVEL, LATENT DIHYDROOROTASE FROM AQUIFEX AEOLICUS AT 1.7 A RESOLUTION | DIHYDROOROTASE, AMIDOHYDROLASE, METALLOENZYME, PYRIMIDINE, HYDROLASE
1xs7:D (ASN293) to (PHE322) CRYSTAL STRUCTURE OF A CYCLOAMIDE-URETHANE-DERIVED NOVEL INHIBITOR BOUND TO HUMAN BRAIN MEMAPSIN 2 (BETA-SECRETASE). | BETA SECRETASE, MEMAPSIN2, BACE, ASP2, ASPARTIC PROTEASE, ACID PROTEASE, ALZHEIMER'S DISEASE, DRUG DESIGN, CRYSTALLOGRAPHY, HYDROLASE
2zja:A (PHE339) to (ARG356) ARCHAEAL DNA HELICASE HJM COMPLEXED WITH AMPPCP IN FORM 2 | RECA FOLD, ATP-BINDING, HELICASE, HYDROLASE, NUCLEOTIDE- BINDING
3kf8:D (SER21) to (CYS61) CRYSTAL STRUCTURE OF C. TROPICALIS STN1-TEN1 COMPLEX | OB FOLD
5cyf:A (ASP139) to (GLN162) CRYSTAL STRUCTURE OF ISOFORM 2 OF URIDINE PHOSPHORYLASE FROM SCHISTOSOMA MANSONI IN COMPLEX WITH CITRATE | TRANSFERASE
5cyg:B (ASP139) to (GLN162) CRYSTAL STRUCTURE OF ISOFORM 2 OF URIDINE PHOSPHORYLASE FROM SCHISTOSOMA MANSONI APO FORM | TRANSFERASE
3kg4:A (LYS55) to (VAL108) CRYSTAL STRUCTURE OF AN UNCHARACTERIZED PROTEIN FROM MANNHEIMIA SUCCINICIPRODUCENS | STRUCTURAL GENOMICS, UNKNOWN FUNCTION, PSI-2, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC
5cz6:M (VAL20) to (GLY38) 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:a (VAL20) to (GLY38) 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:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA1-T1A MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cz5:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA1-T1A MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cza:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-D166N MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5cza:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-D166N MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
1y12:A (GLY76) to (LEU102) STRUCTURE OF A HEMOLYSIN-COREGULATED PROTEIN FROM PSEUDOMONAS AERUGINOSA | PSEUDOMONAS AERUGINOSA, HEMOLYSIN-CORREGULATION, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, UNKNOWN FUNCTION
1y12:B (GLY76) to (LEU102) STRUCTURE OF A HEMOLYSIN-COREGULATED PROTEIN FROM PSEUDOMONAS AERUGINOSA | PSEUDOMONAS AERUGINOSA, HEMOLYSIN-CORREGULATION, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, UNKNOWN FUNCTION
4ozf:G (VAL170) to (ASN188) JR5.1 PROTEIN COMPLEX | IMMUNE RECEPTOR-LIGAND COMPLEX, IMMUNE SYSTEM
4ozh:G (VAL170) to (ASN188) S16 PROTEIN COMPLEX | IMMUNE RECEPTOR-LIGAND COMPLEX, IMMUNE SYSTEM
5d0s:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-D166N MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0s:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-D166N MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0s:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-D166N MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0s:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-D166N MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0t:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-D166N MUTANT IN COMPLEX WITH MG132 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0t:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-D166N MUTANT IN COMPLEX WITH MG132 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0t:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-D166N MUTANT IN COMPLEX WITH MG132 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0t:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-D166N MUTANT IN COMPLEX WITH MG132 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0v:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-T1C MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0v:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-T1C MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0w:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-T1S MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5d0w:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-T1S MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5d0x:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-T1S MUTANT IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
2zwo:C (GLU300) to (GLY322) CRYSTAL STRUCTURE OF CA2 SITE MUTANT OF PRO-S324A | SUBTILISIN, THERMOCOCCUS KODAKARAENSIS, CALCIUM ION, CALCIUM, HYDROLASE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN
5d0z:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-T1S MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0z:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-T1S MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0z:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-T1S MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4p0d:A (THR324) to (ASP374) THE T6 BACKBONE PILIN OF SEROTYPE M6 STREPTOCOCCUS PYOGENES HAS A MODULAR THREE-DOMAIN STRUCTURE DECORATED WITH VARIABLE LOOPS AND EXTENSIONS | IG-LIKE FOLDISOPEPTIDE BONDSORTASE MOTIFGRAM-POSITIVE PILI, STRUCTURAL PROTEIN
3km3:B (GLY125) to (PHE147) CRYSTAL STRUCTURE OF EOXYCYTIDINE TRIPHOSPHATE DEAMINASE FROM ANAPLASMA PHAGOCYTOPHILUM AT 2.1A RESOLUTION | SSGCID, NIH, NIAID, SBRI, UW, DECODE, DEOXYCYTIDINE TRIPHOSPHATE DEAMINASE, ANAPLASMA PHAGOCYTOPHILUM, IODIDE PHASING, HYDROLASE, NUCLEOTIDE METABOLISM, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE
5d3m:B (ALA2) to (GLY22) FOLATE ECF TRANSPORTER: AMPPNP BOUND STATE | ECF TRANSPORTER, FOLATE, MEMBRANE PROTEIN, VITAMIN TRANSPORT, TRANSPORT PROTEIN
5d3m:F (ALA2) to (GLY22) FOLATE ECF TRANSPORTER: AMPPNP BOUND STATE | ECF TRANSPORTER, FOLATE, MEMBRANE PROTEIN, VITAMIN TRANSPORT, TRANSPORT PROTEIN
1y8e:A (GLY218) to (PRO237) VCP:SURAMIN COMPLEX | BETA BARREL, VIRAL PROTEIN
1mpm:A (GLY245) to (ASN264) MALTOPORIN MALTOSE COMPLEX | MEMBRANE PROTEIN, SUGAR TRANSPORT, SPECIFIC PORIN, BETA BARREL
1mpm:B (GLY245) to (ASN264) MALTOPORIN MALTOSE COMPLEX | MEMBRANE PROTEIN, SUGAR TRANSPORT, SPECIFIC PORIN, BETA BARREL
1mpm:C (GLY245) to (ASN264) MALTOPORIN MALTOSE COMPLEX | MEMBRANE PROTEIN, SUGAR TRANSPORT, SPECIFIC PORIN, BETA BARREL
1mpo:A (GLY245) to (ASN264) MALTOPORIN MALTOHEXAOSE COMPLEX | MEMBRANE PROTEIN, SPECIFIC PORIN, BETA BARREL MEMBRANE PROTEIN, SUGAR TRANSPORT, BETA BARREL
1mpo:B (GLY245) to (ASN264) MALTOPORIN MALTOHEXAOSE COMPLEX | MEMBRANE PROTEIN, SPECIFIC PORIN, BETA BARREL MEMBRANE PROTEIN, SUGAR TRANSPORT, BETA BARREL
1mpo:C (GLY245) to (ASN264) MALTOPORIN MALTOHEXAOSE COMPLEX | MEMBRANE PROTEIN, SPECIFIC PORIN, BETA BARREL MEMBRANE PROTEIN, SUGAR TRANSPORT, BETA BARREL
1mpq:A (GLY245) to (ASN264) MALTOPORIN TREHALOSE COMPLEX | MEMBRANE PROTEIN, SPECIFIC PORIN, BETA BARREL, SUGAR TRANSPORT
1mpq:B (GLY245) to (ASN264) MALTOPORIN TREHALOSE COMPLEX | MEMBRANE PROTEIN, SPECIFIC PORIN, BETA BARREL, SUGAR TRANSPORT
1mpq:C (GLY245) to (ASN264) MALTOPORIN TREHALOSE COMPLEX | MEMBRANE PROTEIN, SPECIFIC PORIN, BETA BARREL, SUGAR TRANSPORT
1mpr:A (GLY245) to (ALA269) MALTOPORIN FROM SALMONELLA TYPHIMURIUM | MEMBRANE PROTEIN, SUGAR TRANSPORT, SPECIFIC PORIN, BETA BARREL
1mpr:B (GLY245) to (ALA269) MALTOPORIN FROM SALMONELLA TYPHIMURIUM | MEMBRANE PROTEIN, SUGAR TRANSPORT, SPECIFIC PORIN, BETA BARREL
1mpr:C (GLY245) to (ALA269) MALTOPORIN FROM SALMONELLA TYPHIMURIUM | MEMBRANE PROTEIN, SUGAR TRANSPORT, SPECIFIC PORIN, BETA BARREL
1mql:G (SER266) to (PRO289) BHA OF UKR/63 | INFLUENZA A VIRUS, VIRAL PROTEIN
1mqs:A (GLN155) to (LEU173) CRYSTAL STRUCTURE OF SLY1P IN COMPLEX WITH AN N-TERMINAL PEPTIDE OF SED5P | SM-PROTEIN, SNARE, SYNTAXIN, ENDOCYTOSIS/EXOCYTOSIS COMPLEX
3kpt:B (ARG317) to (GLU343) CRYSTAL STRUCTURE OF BCPA, THE MAJOR PILIN SUBUNIT OF BACILLUS CEREUS | INTRAMOLECULAR AMIDE BOND, PILIN SUBUNIT, BETA SHEET
4p9s:A (ASN359) to (ILE388) CRYSTAL STRUCTURE OF THE MATURE FORM OF RAT DMGDH | DIMETHYLGLYCINE DEHYDROGENASE, RAT, OXIDOREDUCTASE
4paa:B (ASN359) to (ILE388) CRYSTAL STRUCTURE OF THE MATURE FORM OF RAT DMGDH COMPLEXED WITH TETRAHYDROFOLATE | DIMETHYLGLYCINE DEHYDROGENASE, RAT, TETRAHYDROFOLATE
1yfu:A (PRO44) to (TYR60) CRYSTAL STRUCTURE OF 3-HYDROXYANTHRANILATE-3,4-DIOXYGENASE FROM RALSTONIA METALLIDURANS | CUPIN, OXIDOREDUCTASE
1yfx:A (PRO44) to (TYR60) CRYSTAL STRUCTURE OF 3-HYDROXYANTHRANILATE-3,4-DIOXYGENASE FROM RALSTONIA METALLIDURANS COMPLEXED WITH 4-CHLORO-3-HYDROXYANTHRANILIC ACID AND NO | CUPIN, OXIDOREDUCTASE
1yfy:A (PRO44) to (TYR60) CRYSTAL STRUCTURE OF 3-HYDROXYANTHRANILATE-3,4-DIOXYGENASE FROM RALSTONIA METALLIDURANS COMPLEXED WITH 3-HYDROXYANTHRANILIC ACID | CUPIN, OXIDOREDUCTASE
3ku4:D (GLN156) to (ASN178) TRAPPING OF AN OXOCARBENIUM ION INTERMEDIATE IN UP CRYSTALS | OXOCARBENIUM ION, GLYCAL, PYRIMIDINE SALVAGE, URIDINE PHOSPHORYLASE, TRANSFERASE
4pew:A (THR532) to (GLN553) STRUCTURE OF SACTELAM55A FROM STREPTOMYCES SP. SIREXAA-E | BETA-1, 3-GLUCANASE, SECRETED, BIOMASS DEGRADATION, GH55, EXO-BETA-1, HYDROLASE
5dfm:A (ASN241) to (LEU262) STRUCTURE OF TETRAHYMENA TELOMERASE P19 FUSED TO MBP | TELOMERASE, P19, CST COMPLEX, TEN1, OB-FOLD, OLIGONUCLEOTIDE BINDING FOLD, NUCLEAR PROTEIN
4ph8:B (GLY50) to (ASP83) CRYSTAL STRUCTURE OF AGGA, THE MAJOR SUBUNIT OF AGGREGATIVE ADHERENCE FIMBRIAE TYPE I (AAF/I) FROM THE ESCHERICHIA COLI O4H104 | CELL ADHESION, BETA SANDWICH, DONOR-STRAND COMPLEMENTATION, FIBRONECTIN BINDING
3l1a:B (GLY230) to (SER258) STRUCTURAL ORDERING OF DISORDERED LIGAND BINDING LOOPS OF BIOTIN PROTEIN LIGASE INTO ACTIVE CONFORMATIONS AS A CONSEQUENCE OF DEHYDRATION | BIOTIN PROTEIN LIGASE, DEHYDRATED CRYSTALS, LIGASE
5dgr:A (GLY209) to (ALA240) CRYSTAL STRUCTURE OF GH9 EXO-BETA-D-GLUCOSAMINIDASE PBPRA0520, GLUCOSAMINE COMPLEX | GLYCOSIDE HYDROLASE FAMILY 9, ALPHA-ALPHA-6 BARREL, EXO-D-BETA- GLUCOSAMINIDASE, HYDROLASE
5dgr:B (GLY209) to (ALA240) CRYSTAL STRUCTURE OF GH9 EXO-BETA-D-GLUCOSAMINIDASE PBPRA0520, GLUCOSAMINE COMPLEX | GLYCOSIDE HYDROLASE FAMILY 9, ALPHA-ALPHA-6 BARREL, EXO-D-BETA- GLUCOSAMINIDASE, HYDROLASE
5dgq:A (GLY209) to (ALA240) CRYSTAL STRUCTURE OF GH9 EXO-BETA-D-GLUCOSAMINIDASE PBPRA0520 | GLYCOSIDE HYDROLASE FAMILY 9, ALPHA-ALPHA-6 BARREL, EXO-D-BETA- GLUCOSAMINIDASE, HYDROLASE
5dgq:B (GLY209) to (ALA240) CRYSTAL STRUCTURE OF GH9 EXO-BETA-D-GLUCOSAMINIDASE PBPRA0520 | GLYCOSIDE HYDROLASE FAMILY 9, ALPHA-ALPHA-6 BARREL, EXO-D-BETA- GLUCOSAMINIDASE, HYDROLASE
3l38:A (CYS381) to (GLY396) BACE1 IN COMPLEX WITH THE AMINOPYRIDINE COMPOUND 44 | BETA-SECRETASE, BACE-1, AMINOPYRIDINE, INHIBITOR, ASPARTYL PROTEASE, DISULFIDE BOND, PROTEASE, TRANSMEMBRANE, ZYMOGEN, HYDROLASE
1yrq:J (THR11) to (VAL32) STRUCTURE OF THE READY OXIDIZED FORM OF [NIFE]-HYDROGENASE | NIB STATE, HYDROXIDE BRIDGE, OXIDOREDUCTASE
3afh:A (HIS154) to (ASP180) CRYSTAL STRUCTURE OF THERMOTOGA MARITIMA NONDISCRIMINATING GLUTAMYL- TRNA SYNTHETASE IN COMPLEX WITH A GLUTAMYL-AMP ANALOG | PROTEIN-SUBSTRATE COMPLEX, NON-DISCRIMINATING GLUTAMYL-TRNA SYNTHETASE, AMINOACYL-TRNA SYNTHETASE, ATP-BINDING, LIGASE, NUCLEOTIDE-BINDING, PROTEIN BIOSYNTHESIS
3l58:B (ASN354) to (PHE383) STRUCTURE OF BACE BOUND TO SCH589432 | BACE1, ALZHEIMERS, ALTERNATIVE SPLICING, ASPARTYL PROTEASE, DISULFIDE BOND, ENDOPLASMIC RETICULUM, ENDOSOME, GLYCOPROTEIN, GOLGI APPARATUS, HYDROLASE, MEMBRANE, POLYMORPHISM, PROTEASE, TRANSMEMBRANE, ZYMOGEN
3l5d:B (THR120) to (GLY139) STRUCTURE OF BACE BOUND TO SCH723873 | BACE1, ALZHEIMERS, ALTERNATIVE SPLICING, ASPARTYL PROTEASE, DISULFIDE BOND, ENDOPLASMIC RETICULUM, ENDOSOME, GLYCOPROTEIN, GOLGI APPARATUS, HYDROLASE, MEMBRANE, POLYMORPHISM, PROTEASE, TRANSMEMBRANE, ZYMOGEN
5dki:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH ALKYNE-PI | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, TARGET DELIVERY, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5dki:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH ALKYNE-PI | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, TARGET DELIVERY, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5dkj:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH OCTREOTIDE-PI | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, TARGET DELIVERY, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5dkj:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH OCTREOTIDE-PI | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, TARGET DELIVERY, PROTEASOME, INHIBITOR, BINDING ANALYSIS
1z15:A (GLY326) to (ASP342) CRYSTAL STRUCTURE ANALYSIS OF PERIPLASMIC LEU/ILE/VAL-BINDING PROTEIN IN SUPEROPEN FORM | PERIPLASMIC BINDING PROTEINS, ALPHA-BETA FOLD, ALIPHATIC AMINO ACID BINDING PROTEIN, TRANSPORT PROTEIN
3l87:A (GLY140) to (GLY166) THE CRYSTAL STRUCTURE OF SMU.143C FROM STREPTOCOCCUS MUTANS UA159 | DEF, PEPTIDE DEFORMYLASE, HYDROLASE, IRON, METAL-BINDING, PROTEIN BIOSYNTHESIS
3l89:O (GLY96) to (TRP116) HUMAN ADENOVIRUS TYPE 21 KNOB IN COMPLEX WITH DOMAINS SCR1 AND SCR2 OF CD46 (MEMBRANE COFACTOR PROTEIN, MCP) | ADENOVIRUS, FIBER KNOB, VIRAL PROTEIN, MEMBRANE COFACTOR PROTEIN, MCP, VIRUS RECEPTOR COMPLEX, SCR, SHORT CONSENSUS REPEAT, CCP, COMPLEMENT CONTROL PROTEIN, COMPLEMENT PATHWAY, GLYCOPROTEIN, HOST-VIRUS INTERACTION, IMMUNE RESPONSE, INNATE IMMUNITY, SUSHI2, VIRAL PROTEIN-PROTEIN BINDING COMPLEX
3l89:P (GLY96) to (TRP116) HUMAN ADENOVIRUS TYPE 21 KNOB IN COMPLEX WITH DOMAINS SCR1 AND SCR2 OF CD46 (MEMBRANE COFACTOR PROTEIN, MCP) | ADENOVIRUS, FIBER KNOB, VIRAL PROTEIN, MEMBRANE COFACTOR PROTEIN, MCP, VIRUS RECEPTOR COMPLEX, SCR, SHORT CONSENSUS REPEAT, CCP, COMPLEMENT CONTROL PROTEIN, COMPLEMENT PATHWAY, GLYCOPROTEIN, HOST-VIRUS INTERACTION, IMMUNE RESPONSE, INNATE IMMUNITY, SUSHI2, VIRAL PROTEIN-PROTEIN BINDING COMPLEX
3l89:Q (GLY96) to (TRP116) HUMAN ADENOVIRUS TYPE 21 KNOB IN COMPLEX WITH DOMAINS SCR1 AND SCR2 OF CD46 (MEMBRANE COFACTOR PROTEIN, MCP) | ADENOVIRUS, FIBER KNOB, VIRAL PROTEIN, MEMBRANE COFACTOR PROTEIN, MCP, VIRUS RECEPTOR COMPLEX, SCR, SHORT CONSENSUS REPEAT, CCP, COMPLEMENT CONTROL PROTEIN, COMPLEMENT PATHWAY, GLYCOPROTEIN, HOST-VIRUS INTERACTION, IMMUNE RESPONSE, INNATE IMMUNITY, SUSHI2, VIRAL PROTEIN-PROTEIN BINDING COMPLEX
3l89:R (GLY96) to (TRP116) HUMAN ADENOVIRUS TYPE 21 KNOB IN COMPLEX WITH DOMAINS SCR1 AND SCR2 OF CD46 (MEMBRANE COFACTOR PROTEIN, MCP) | ADENOVIRUS, FIBER KNOB, VIRAL PROTEIN, MEMBRANE COFACTOR PROTEIN, MCP, VIRUS RECEPTOR COMPLEX, SCR, SHORT CONSENSUS REPEAT, CCP, COMPLEMENT CONTROL PROTEIN, COMPLEMENT PATHWAY, GLYCOPROTEIN, HOST-VIRUS INTERACTION, IMMUNE RESPONSE, INNATE IMMUNITY, SUSHI2, VIRAL PROTEIN-PROTEIN BINDING COMPLEX
3l89:X (GLY96) to (TRP116) HUMAN ADENOVIRUS TYPE 21 KNOB IN COMPLEX WITH DOMAINS SCR1 AND SCR2 OF CD46 (MEMBRANE COFACTOR PROTEIN, MCP) | ADENOVIRUS, FIBER KNOB, VIRAL PROTEIN, MEMBRANE COFACTOR PROTEIN, MCP, VIRUS RECEPTOR COMPLEX, SCR, SHORT CONSENSUS REPEAT, CCP, COMPLEMENT CONTROL PROTEIN, COMPLEMENT PATHWAY, GLYCOPROTEIN, HOST-VIRUS INTERACTION, IMMUNE RESPONSE, INNATE IMMUNITY, SUSHI2, VIRAL PROTEIN-PROTEIN BINDING COMPLEX
4pof:A (ASN169) to (ASP209) PFMCM N-TERMINAL DOMAIN WITHOUT DNA | OB-FOLD, DNA REPLICATION, REPLICATION, DNA BINDING PROTEIN
4pof:B (ASN169) to (ASP209) PFMCM N-TERMINAL DOMAIN WITHOUT DNA | OB-FOLD, DNA REPLICATION, REPLICATION, DNA BINDING PROTEIN
4pof:D (ASN169) to (ASP209) PFMCM N-TERMINAL DOMAIN WITHOUT DNA | OB-FOLD, DNA REPLICATION, REPLICATION, DNA BINDING PROTEIN
4pof:E (ASN169) to (ASP209) PFMCM N-TERMINAL DOMAIN WITHOUT DNA | OB-FOLD, DNA REPLICATION, REPLICATION, DNA BINDING PROTEIN
5do2:B (LYS496) to (ALA520) COMPLEX STRUCTURE OF MERS-RBD BOUND WITH 4C2 ANTIBODY | RECEPTOR-BINDING DOMAIN OF MERS-COV SPIKE, 4C2 ANTIBODY, NEURALIZATION, RECEPTOR-BINDING BLOCKING., VIRAL PROTEIN-IMMUNE SYSTEM COMPLEX
3akz:A (GLY153) to (ASP180) CRYSTAL STRUCTURE OF THERMOTOGA MARITIMA NONDISCRIMINATING GLUTAMYL- TRNA SYNTHETASE IN COMPLEX WITH TRNAGLN AND A GLUTAMYL-AMP ANALOG | PROTEIN-RNA COMPLEX, LIGASE-RNA COMPLEX
1z7q:K (VAL13) to (LYS29) 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:Y (VAL13) to (LYS29) 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
1z8l:A (LEU116) to (SER142) CRYSTAL STRUCTURE OF PROSTATE-SPECIFIC MEMBRANE ANTIGEN, A TUMOR MARKER AND PEPTIDASE | DIMERIC PROTEIN WITH THREE DOMAINS OF TYPE A+B, HYDROLASE
1z8l:B (LEU116) to (SER142) CRYSTAL STRUCTURE OF PROSTATE-SPECIFIC MEMBRANE ANTIGEN, A TUMOR MARKER AND PEPTIDASE | DIMERIC PROTEIN WITH THREE DOMAINS OF TYPE A+B, HYDROLASE
1z8l:C (LEU116) to (SER142) CRYSTAL STRUCTURE OF PROSTATE-SPECIFIC MEMBRANE ANTIGEN, A TUMOR MARKER AND PEPTIDASE | DIMERIC PROTEIN WITH THREE DOMAINS OF TYPE A+B, HYDROLASE
1z8l:D (LEU116) to (SER142) CRYSTAL STRUCTURE OF PROSTATE-SPECIFIC MEMBRANE ANTIGEN, A TUMOR MARKER AND PEPTIDASE | DIMERIC PROTEIN WITH THREE DOMAINS OF TYPE A+B, HYDROLASE
5dqx:A (VAL156) to (ARG177) CRYSTAL STRUCTURE OF SALMONELLA TYPHI - OMPLA WITH INHERENT BOUND COFACTOR | OUTER MEMBRANE PHOSPHOLIPASE A, OMPLA, MEMBRANE PROTEIN, SALMONELLA TYPHI, HYDROLASE, STRUCTURAL PROTEIN
5dqx:B (VAL156) to (ARG177) CRYSTAL STRUCTURE OF SALMONELLA TYPHI - OMPLA WITH INHERENT BOUND COFACTOR | OUTER MEMBRANE PHOSPHOLIPASE A, OMPLA, MEMBRANE PROTEIN, SALMONELLA TYPHI, HYDROLASE, STRUCTURAL PROTEIN
3amt:A (ILE344) to (GLU379) CRYSTAL STRUCTURE OF THE TIAS-TRNA(ILE2)-ATP COMPLEX | TIAS, TRNA(ILE2), MODIFICATION, RNA BINDING PROTEIN-RNA COMPLEX
4q0y:A (ARG31) to (ASP61) CRYSTAL STRUCTURE OF A THIOESTERASE-LIKE PROTEIN (CLOSPO_01618) FROM CLOSTRIDIUM SPOROGENES ATCC 15579 AT 1.70 A RESOLUTION | ORPHAN, HOT DOG/THIOESTERASE-LIKE FOLD, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-BIOLOGY, UNKNOWN FUNCTION
4q1s:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH KENDOMYCIN | PROTEASOME, NATURAL PRODUCT, QUINONE METHIDE, COVALENT BINDING, EXOSITE, HYDROLASE-TOXIN COMPLEX
4q1s:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH KENDOMYCIN | PROTEASOME, NATURAL PRODUCT, QUINONE METHIDE, COVALENT BINDING, EXOSITE, HYDROLASE-TOXIN COMPLEX
4q1s:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH KENDOMYCIN | PROTEASOME, NATURAL PRODUCT, QUINONE METHIDE, COVALENT BINDING, EXOSITE, HYDROLASE-TOXIN COMPLEX
3apm:A (ASN409) to (LEU425) CRYSTAL STRUCTURE OF THE HUMAN SNP PAD4 PROTEIN | ALPHA/BETA-PROPELLER, IMMUNOGLOBULIN-LIKE, ARGININE CITRULLINATION, HYDROLASE, PROTEIN-ARGININE DEIMINASE, POST-TRANSLATIONAL MODIFICATION, CALCIUM BINDING, HISTONE BINDING, BENZOYL-L-ARGININE AMIDE BINDING, NUCLEUS
4axx:A (VAL278) to (THR302) THE CATALYTICALLY ACTIVE FULLY CLOSED CONFORMATION OF HUMAN PHOSPHOGLYCERATE KINASE IN COMPLEX WITH ADP 3-PHOSPHOGLYCERATE AND BERYLLIUM TRIFLUORIDE | GROUND STATE ANALOGUE, HEREDITARY HEMOLYTIC ANEMIA, PHOSPHOPROTEIN, GLYCOLYSIS, TRANSFERASE, PHOSPHORYL TRANSFER, NUCLEOTIDE-BINDING
3at8:A (GLU236) to (PRO256) CRYSTAL STRUCTURE OF THE KIR3.2 CYTOPLASMIC DOMAIN (NA+-FREE CRYSTAL SOAKED IN 10 MM BARIUM CHLORIDE) | CYTOPLASMIC ASSEMBLY, BETA-BARREL, ION TRANSPORT, G PROTEIN BETA- GAMMA SUBUNITS, TRANSPORT PROTEIN
3at9:A (GLU236) to (PRO256) CRYSTAL STRUCTURE OF THE KIR3.2 CYTOPLASMIC DOMAIN (NA+-FREE CRYSTAL SOAKED IN 10 MM BARIUM CHLORIDE AND 10 MM MAGNESIUM CHLORIDE) | CYTOPLASMIC ASSEMBLY, BETA-BARREL, ION TRANSPORT, G PROTEIN BETA- GAMMA SUBUNITS, TRANSPORT PROTEIN
3atd:A (GLU236) to (PRO256) CRYSTAL STRUCTURE OF THE KIR3.2 CYTOPLASMIC DOMAIN (NA+-FREE CRYSTAL SOAKED IN 10 MM GADOLINIUM CHLORIDE AND 10 MM MAGNESIUM CHLORIDE) | CYTOPLASMIC ASSEMBLY, BETA-BARREL, ION TRANSPORT, G PROTEIN BETA- GAMMA SUBUNITS, TRANSPORT PROTEIN
3ate:A (GLU236) to (PRO256) CRYSTAL STRUCTURE OF THE KIR3.2 CYTOPLASMIC DOMAIN (NA+-FREE CRYSTAL SOAKED IN 10 MM PRASEODYMIUM (III) ACETATE) | CYTOPLASMIC ASSEMBLY, BETA-BARREL, ION TRANSPORT, G PROTEIN BETA- GAMMA SUBUNITS, TRANSPORT PROTEIN
3aup:B (TRP328) to (LEU346) CRYSTAL STRUCTURE OF BASIC 7S GLOBULIN FROM SOYBEAN | PEPSIN-LIKE FOLD, PLANT PROTEIN
4b0b:A (VAL139) to (GLU158) CRYSTAL STRUCTURE OF 3-HYDROXYDECANOYL-ACYL CARRIER PROTEIN DEHYDRATASE (FABA) FROM PSEUDOMONAS AERUGINOSA IN COMPLEX WITH 3-(PYRIDIN-2-YLOXY)ANILINE | LYASE, FATTY ACID BIOSYNTHESIS, BACTERIAL VIRULENCE, DRUG DISCOVERY
3lyr:A (GLY119) to (THR156) HUMAN EARLY B-CELL FACTOR 1 (EBF1) DNA-BINDING DOMAIN | IMMUNOGLOBULIN (IG)-LIKE DOMAIN, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, ACTIVATOR, DEVELOPMENTAL PROTEIN, DNA- BINDING, METAL-BINDING, NUCLEUS, TRANSCRIPTION, TRANSCRIPTION REGULATION, ZINC-FINGER, TRANSCRIPTION ACTIVATOR
4b4x:B (ASP121) to (GLY165) CRYSTAL STRUCTURE OF A COMPLEX BETWEEN ACTINOMADURA R39 DD- PEPTIDASE AND A SULFONAMIDE BORONATE INHIBITOR | HYDROLASE, PEPTIDOGLYCAN
4b4x:C (ASP121) to (GLY165) CRYSTAL STRUCTURE OF A COMPLEX BETWEEN ACTINOMADURA R39 DD- PEPTIDASE AND A SULFONAMIDE BORONATE INHIBITOR | HYDROLASE, PEPTIDOGLYCAN
4b4z:C (ASP121) to (GLY165) CRYSTAL STRUCTURE OF A COMPLEX BETWEEN ACTINOMADURA R39 DD-PEPTIDASE AND A SULFONAMIDE BORONATE INHIBITOR | HYDROLASE, BORONIC ACID, PEPTIDOGLYCAN
4qf9:A (PHE105) to (ALA136) STRUCTURE OF GLUK1 LIGAND-BINDING DOMAIN (S1S2) IN COMPLEX WITH (S)-2- AMINO-4-(2,3-DIOXO-1,2,3,4-TETRAHYDROQUINOXALIN-6-YL)BUTANOIC ACID AT 2.28 A RESOLUTION | KAINATE RECEPTOR LIGAND-BINDING DOMAIN, GLUK1-S1S2, ANTAGONIST, MEMBRANE PROTEIN
4qf9:B (PHE105) to (ALA136) STRUCTURE OF GLUK1 LIGAND-BINDING DOMAIN (S1S2) IN COMPLEX WITH (S)-2- AMINO-4-(2,3-DIOXO-1,2,3,4-TETRAHYDROQUINOXALIN-6-YL)BUTANOIC ACID AT 2.28 A RESOLUTION | KAINATE RECEPTOR LIGAND-BINDING DOMAIN, GLUK1-S1S2, ANTAGONIST, MEMBRANE PROTEIN
4qg5:C (LYS489) to (LYS507) CRYSTAL STRUCTURE OF PHOSPHOGLUCOMUTASE FROM LEISHMANIA MAJOR AT 3.5 ANGSTROM RESOLUTION | PHOSPHOHEXOMUTASE, PHOSPHOTRANSFERASE, METAL-BINDING REGION, ALPHA AND BETA PROTEINS, ISOMERASE
4b7g:A (GLN207) to (TRP226) STRUCTURE OF A BACTERIAL CATALASE | OXIDOREDUCTASE, CATALASE INHIBITION
4b7g:B (GLN207) to (TRP226) STRUCTURE OF A BACTERIAL CATALASE | OXIDOREDUCTASE, CATALASE INHIBITION
4b7h:A (GLN207) to (TRP226) STRUCTURE OF A HIGHDOSE LIGANDED BACTERIAL CATALASE | OXIDOREDUCTASE, CATALASE INHIBITION
4b7h:B (GLN207) to (TRP226) STRUCTURE OF A HIGHDOSE LIGANDED BACTERIAL CATALASE | OXIDOREDUCTASE, CATALASE INHIBITION
4b7h:C (GLN207) to (TRP226) STRUCTURE OF A HIGHDOSE LIGANDED BACTERIAL CATALASE | OXIDOREDUCTASE, CATALASE INHIBITION
4b7h:D (GLN207) to (TRP226) STRUCTURE OF A HIGHDOSE LIGANDED BACTERIAL CATALASE | OXIDOREDUCTASE, CATALASE INHIBITION
2a9g:A (ALA275) to (PHE294) STRUCTURE OF C406A ARGININE DEIMINASE IN COMPLEX WITH L-ARGININE | ARGININE DEGRADATION PATHWAY, L-ARGININE DEIMINASE, CATALYTIC MECHANISM, HYDROLASE
3mdj:A (HIS99) to (PRO119) ER AMINOPEPTIDASE, ERAP1, BOUND TO THE ZINC AMINOPEPTIDASE INHIBITOR, BESTATIN | AMINOPEPTIDASE, ZN BINDING PROTEIN, ER, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qls:J (VAL13) to (LYS29) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 11 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qls:M (VAL20) to (GLY38) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 11 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qls:X (VAL13) to (LYS29) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 11 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qls:a (VAL20) to (GLY38) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 11 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlq:J (VAL13) to (LYS29) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 8 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlq:M (VAL20) to (GLY38) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 8 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlq:X (VAL13) to (LYS29) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 8 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlq:a (VAL20) to (GLY38) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 8 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlt:J (VAL13) to (LYS29) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 2 (PR924) | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlt:M (VAL20) to (GLY38) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 2 (PR924) | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlt:X (VAL13) to (LYS29) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 2 (PR924) | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlt:a (VAL20) to (GLY38) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 2 (PR924) | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlu:J (VAL13) to (LYS29) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 9 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlu:M (VAL20) to (GLY38) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 9 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlu:X (VAL13) to (LYS29) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 9 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlu:a (VAL20) to (GLY38) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 9 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlz:B (ASN39) to (ILE78) THE STRUCTURE OF INORGANIC PYROPHOSPHATASE FROM SCHISTOSOMA JAPONICUM | PYROPHOSPHATASE, HYDROLASE, METAL BINDING PROTEIN
3mfm:A (SER60) to (TYR83) CRYSTAL STRUCTURES AND MUTATIONAL ANALYSES OF ACYL-COA CARBOXYLASE SUBUNIT OF STREPTOMYCES COELICOLOR | ACCASE, PCCASE, ACC, PCC, PROPIONYL-COA, CT, CARBOXYLTRANSFERASE, POLYKETIDE, FATTY ACID, PKS, FAS, POLYKETIDE SYNTHASE, FATTY ACID SYNTHASE, CARBOXYLASE, BETA SUBUNIT, PCCB, ACYL-COA, ACYL-COA CARBOXYLASE, BIOTIN, LIGASE
3mg0:M (VAL12) to (GLY30) STRUCTURE OF YEAST 20S PROTEASOME WITH BORTEZOMIB | 20S PROTEASOME, HYDROLASE
3mg0:1 (VAL12) to (GLY30) STRUCTURE OF YEAST 20S PROTEASOME WITH BORTEZOMIB | 20S PROTEASOME, HYDROLASE
3mg4:J (VAL12) to (LYS28) STRUCTURE OF YEAST 20S PROTEASOME WITH COMPOUND 1 | 20S PROTEASOME, HYDROLASE
3mg4:X (VAL12) to (LYS28) STRUCTURE OF YEAST 20S PROTEASOME WITH COMPOUND 1 | 20S PROTEASOME, HYDROLASE
3mg4:Z (PHE11) to (SER28) STRUCTURE OF YEAST 20S PROTEASOME WITH COMPOUND 1 | 20S PROTEASOME, HYDROLASE
3mg6:J (VAL12) to (LYS28) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 6 | 20S PROTEASOME, HYDROLASE
3mg6:L (ALA12) to (SER28) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 6 | 20S PROTEASOME, HYDROLASE
3mg6:M (VAL12) to (GLY30) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 6 | 20S PROTEASOME, HYDROLASE
3mg6:X (VAL12) to (LYS28) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 6 | 20S PROTEASOME, HYDROLASE
3mg6:1 (VAL12) to (GLY30) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 6 | 20S PROTEASOME, HYDROLASE
3mg7:J (VAL12) to (LYS28) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 8 | 20S PROTEASOME, HYDROLASE
3mg7:M (VAL12) to (GLY30) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 8 | 20S PROTEASOME, HYDROLASE
3mg7:X (VAL12) to (LYS28) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 8 | 20S PROTEASOME, HYDROLASE
3mg7:1 (VAL12) to (GLY30) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 8 | 20S PROTEASOME, HYDROLASE
3mg8:J (VAL12) to (LYS28) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 16 | 20S PROTEASOME, HYDROLASE
3mg8:M (VAL12) to (GLY30) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 16 | 20S PROTEASOME, HYDROLASE
3mg8:X (VAL12) to (LYS28) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 16 | 20S PROTEASOME, HYDROLASE
3mg8:1 (VAL12) to (GLY30) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 16 | 20S PROTEASOME, HYDROLASE
3mln:A (GLY119) to (THR156) DNA BINDING DOMAIN OF EARLY B-CELL FACTOR 1 (EBF1) BOUND TO DNA (CRYSTAL FORM II) | TRANSCRIPTION FACTOR, PSEUDO-IG-FOLD, ZN-FINGER, ZN-KNUCKLE, DNA, TRANSCRIPTION-DNA COMPLEX, EBF, EBF-1
5es4:E (PHE895) to (ASN940) RE-REFINEMENT OF INTEGRIN ALPHAXBETA2 ECTODOMAIN IN THE CLOSED/BENT CONFORMATION | COMPLEMENT RECEPTOR-4 ALPHAXBETA2, CELL ADHESION
4qtx:A (SER113) to (ASP135) CASPASE-3 Y195A | ALLOSTERIC NETWORKS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qu5:A (SER113) to (ASP135) CASPASE-3 T140V | ALLOSTERIC NETWORK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qu8:A (PHE114) to (ASP135) CASPASE-3 M61A V266H | ALLOSTERIC NETWORK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qu9:A (PHE114) to (ASP135) CASPASE-3 F128A | ALLOSTERIC NETWORK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qub:A (PHE114) to (ASP135) CASPASE-3 K137A | ALLOSTERIC NETWORK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qui:B (PHE114) to (ASP135) CASPASE-3 F128AV266H | ALLOSTERIC NETWORK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qul:C (SER113) to (ASP135) CASPASE-3 F55W | ALLOSTERIC NETWORK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qux:M (VAL20) to (GLY38) YCP BETA5-A49T-MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qux:X (VAL13) to (LYS29) YCP BETA5-A49T-MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qux:a (VAL20) to (GLY38) YCP BETA5-A49T-MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
5ev0:A (GLY19) to (SER38) CRYSTAL STRUCTURE OF RAGWEED PROFILIN AMB A 8 IN COMPLEX WITH POLY- PRO14 | ALLERGEN
5ev0:B (GLY19) to (SER38) CRYSTAL STRUCTURE OF RAGWEED PROFILIN AMB A 8 IN COMPLEX WITH POLY- PRO14 | ALLERGEN
4qv1:M (VAL20) to (GLY38) YCP BETA5-M45A MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qv1:a (VAL20) to (GLY38) YCP BETA5-M45A MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5eve:A (GLY19) to (SER38) CRYSTAL STRUCTURE OF AMB A 8 IN COMPLEX WITH POLY-PRO10 | ALLERGEN
4qv0:J (VAL13) to (LYS29) YCP BETA5-A49T-A50V-DOUBLE MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv0:M (VAL20) to (GLY38) YCP BETA5-A49T-A50V-DOUBLE MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv0:X (VAL13) to (LYS29) YCP BETA5-A49T-A50V-DOUBLE MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv0:a (VAL20) to (GLY38) YCP BETA5-A49T-A50V-DOUBLE MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv3:M (VAL20) to (GLY38) YCP BETA5-M45V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv3:a (VAL20) to (GLY38) YCP BETA5-M45V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv4:M (VAL20) to (GLY38) YCP BETA5-M45T MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv4:X (VAL13) to (LYS29) YCP BETA5-M45T MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv4:a (VAL20) to (GLY38) YCP BETA5-M45T MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv5:M (VAL20) to (GLY38) YCP BETA5-M45I MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv5:a (VAL20) to (GLY38) YCP BETA5-M45I MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv6:J (VAL13) to (LYS29) YCP BETA5-A49V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv6:X (VAL13) to (LYS29) YCP BETA5-A49V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv7:J (VAL13) to (LYS29) YCP BETA5-A50V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv7:M (VAL20) to (GLY38) YCP BETA5-A50V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv7:X (VAL13) to (LYS29) YCP BETA5-A50V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv7:a (VAL20) to (GLY38) YCP BETA5-A50V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv8:M (VAL20) to (GLY38) YCP BETA5-C52F MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv8:a (VAL20) to (GLY38) YCP BETA5-C52F MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv9:M (VAL20) to (GLY38) YCP BETA5-C63F MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv9:a (VAL20) to (GLY38) YCP BETA5-C63F MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qvh:A (ASN242) to (LEU263) CRYSTAL STRUCTURE OF THE ESSENTIAL MYCOBACTERIUM TUBERCULOSIS PHOSPHOPANTETHEINYL TRANSFERASE PPTT, SOLVED AS A FUSION PROTEIN WITH MALTOSE BINDING PROTEIN | A/B-FOLD, PHOSPHOPANTETHEINYL TRANSFERASE, ACYL CARRIER PROTEIN, PEPTIDYL CARRIER PROTEIN, TRANSFERASE
4qvl:J (VAL13) to (LYS29) YCP IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvl:M (VAL20) to (GLY38) YCP IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvl:X (VAL13) to (LYS29) YCP IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvl:a (VAL20) to (GLY38) YCP IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvm:J (VAL13) to (LYS29) YCP BETA5-M45A MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvm:M (VAL20) to (GLY38) YCP BETA5-M45A MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvm:X (VAL13) to (LYS29) YCP BETA5-M45A MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvm:a (VAL20) to (GLY38) YCP BETA5-M45A MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvn:J (VAL13) to (LYS29) YCP BETA5-M45V MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvn:M (VAL20) to (GLY38) YCP BETA5-M45V MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvn:a (VAL20) to (GLY38) YCP BETA5-M45V MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvp:J (VAL13) to (LYS29) YCP BETA5-M45T MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvp:M (VAL20) to (GLY38) YCP BETA5-M45T MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvp:X (VAL13) to (LYS29) YCP BETA5-M45T MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvp:a (VAL20) to (GLY38) YCP BETA5-M45T MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvq:J (VAL13) to (LYS29) YCP BETA5-M45I MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4qvq:M (VAL20) to (GLY38) YCP BETA5-M45I MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4qvq:X (VAL13) to (LYS29) YCP BETA5-M45I MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4qvq:a (VAL20) to (GLY38) YCP BETA5-M45I MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4qvv:J (VAL13) to (LYS29) YCP BETA5-A49V MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvv:M (VAL20) to (GLY38) YCP BETA5-A49V MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvv:X (VAL13) to (LYS29) YCP BETA5-A49V MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvv:a (VAL20) to (GLY38) YCP BETA5-A49V MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvw:M (VAL20) to (GLY38) YCP BETA5-A49S-MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4qvw:X (VAL13) to (LYS29) YCP BETA5-A49S-MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4qvw:a (VAL20) to (GLY38) YCP BETA5-A49S-MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4qvy:J (VAL13) to (LYS29) YCP BETA5-A49T-MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvy:M (VAL20) to (GLY38) YCP BETA5-A49T-MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvy:X (VAL13) to (LYS29) YCP BETA5-A49T-MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvy:a (VAL20) to (GLY38) YCP BETA5-A49T-MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw0:M (VAL20) to (GLY38) YCP BETA5-A49T-A50V-DOUBLE MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw0:a (VAL20) to (GLY38) YCP BETA5-A49T-A50V-DOUBLE MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw5:J (VAL13) to (LYS29) YCP BETA5-M45A MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw5:M (VAL20) to (GLY38) YCP BETA5-M45A MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw5:X (VAL13) to (LYS29) YCP BETA5-M45A MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw5:a (VAL20) to (GLY38) YCP BETA5-M45A MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw4:J (VAL13) to (LYS29) YCP IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw4:M (VAL20) to (GLY38) YCP IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw4:X (VAL13) to (LYS29) YCP IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw4:a (VAL20) to (GLY38) YCP IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw6:J (VAL13) to (LYS29) YCP BETA5-M45V MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw6:M (VAL20) to (GLY38) YCP BETA5-M45V MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw6:X (VAL13) to (LYS29) YCP BETA5-M45V MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw6:a (VAL20) to (GLY38) YCP BETA5-M45V MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwj:J (VAL13) to (LYS29) YCP BETA5-A49T-MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwj:M (VAL20) to (GLY38) YCP BETA5-A49T-MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwj:X (VAL13) to (LYS29) YCP BETA5-A49T-MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwj:a (VAL20) to (GLY38) YCP BETA5-A49T-MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwf:J (VAL13) to (LYS29) YCP BETA5-M45I MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwf:X (VAL13) to (LYS29) YCP BETA5-M45I MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwf:a (VAL20) to (GLY38) YCP BETA5-M45I MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwg:J (VAL13) to (LYS29) YCP BETA5-A49V MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwg:X (VAL13) to (LYS29) YCP BETA5-A49V MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwk:J (VAL13) to (LYS29) YCP BETA5-A49T-A50V-DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwk:X (VAL13) to (LYS29) YCP BETA5-A49T-A50V-DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwl:M (VAL20) to (GLY38) YCP BETA5-A50V MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwl:a (VAL20) to (GLY38) YCP BETA5-A50V MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwr:J (VAL13) to (LYS29) YCP BETA5-C52F MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwr:M (VAL20) to (GLY38) YCP BETA5-C52F MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwr:X (VAL13) to (LYS29) YCP BETA5-C52F MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwr:a (VAL20) to (GLY38) YCP BETA5-C52F MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qws:J (VAL13) to (LYS29) YCP BETA5-C63F MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qws:X (VAL13) to (LYS29) YCP BETA5-C63F MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwu:J (VAL13) to (LYS29) YCP BETA5-C52F MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwu:M (VAL20) to (GLY38) YCP BETA5-C52F MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwu:X (VAL13) to (LYS29) YCP BETA5-C52F MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwu:a (VAL20) to (GLY38) YCP BETA5-C52F MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3bra:A (THR59) to (GLY78) BACE-1 COMPLEXED WITH COMPOUND 1 | ALZHEIMER'S DISEASE, ASPARTIC PROTEASE, BETA-SECRETASE, MEMAPSIN 2, FRAGMENT SCREEN, ALTERNATIVE SPLICING, ASPARTYL PROTEASE, GLYCOPROTEIN, HYDROLASE, MEMBRANE, TRANSMEMBRANE, ZYMOGEN
4qwx:J (VAL13) to (LYS29) YCP IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwx:M (VAL20) to (GLY38) YCP IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwx:X (VAL13) to (LYS29) YCP IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwx:a (VAL20) to (GLY38) YCP IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qxj:J (VAL13) to (LYS29) YCP BETA5-M45A MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qxj:X (VAL13) to (LYS29) YCP BETA5-M45A MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3bts:A (SER227) to (PRO255) CRYSTAL STRUCTURE OF A TERNARY COMPLEX OF THE TRANSCRIPTIONAL REPRESSOR GAL80P (GAL80S0 [G301R]) AND THE ACIDIC ACTIVATION DOMAIN OF GAL4P (AA 854-874) FROM SACCHAROMYCES CEREVISIAE WITH NAD | EUKARYOTIC TRANSCRIPTION COMPLEX, NAD, ROSSMANN FOLD, ACETYLATION, CARBOHYDRATE METABOLISM, DNA-BINDING, GALACTOSE METABOLISM, REPRESSOR, TRANSCRIPTION REGULATION, ACTIVATOR, METAL-BINDING, NUCLEUS, PHOSPHOPROTEIN, ZINC
3bts:B (SER227) to (PRO255) CRYSTAL STRUCTURE OF A TERNARY COMPLEX OF THE TRANSCRIPTIONAL REPRESSOR GAL80P (GAL80S0 [G301R]) AND THE ACIDIC ACTIVATION DOMAIN OF GAL4P (AA 854-874) FROM SACCHAROMYCES CEREVISIAE WITH NAD | EUKARYOTIC TRANSCRIPTION COMPLEX, NAD, ROSSMANN FOLD, ACETYLATION, CARBOHYDRATE METABOLISM, DNA-BINDING, GALACTOSE METABOLISM, REPRESSOR, TRANSCRIPTION REGULATION, ACTIVATOR, METAL-BINDING, NUCLEUS, PHOSPHOPROTEIN, ZINC
3btu:C (SER227) to (PRO255) CRYSTAL STRUCTURE OF THE SUPER-REPRESSOR MUTANT OF GAL80P FROM SACCHAROMYCES CEREVISIAE; GAL80(S2) [E351K] | EUKARYOTIC TRANSCRIPTION COMPLEX, ACETYLATION, CARBOHYDRATE METABOLISM, DNA-BINDING, GALACTOSE METABOLISM, REPRESSOR, TRANSCRIPTION REGULATION
4qz0:J (VAL13) to (LYS29) YCP BETA5-M45V MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz0:M (VAL20) to (GLY38) YCP BETA5-M45V MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz0:X (VAL13) to (LYS29) YCP BETA5-M45V MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz0:a (VAL20) to (GLY38) YCP BETA5-M45V MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5f6r:A (ILE140) to (THR159) CO-CRYSTAL STRUCTURE OF 3-HYDROXYDECANOYL-(ACYL CARRIER PROTEIN) DEHYDRATASE FROM YERSINIA PESTIS WITH 5-BENZOYLPENTANOIC ACID | LYASE, ALPHA-BETA FOLD, STRUCTURAL GENOMICS, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID
3buf:A (THR59) to (GLY78) BACE-1 COMPLEXED WITH COMPOUND 2 | ALZHEIMER'S DISEASE, ASPARTIC PROTEASE, BETA-SECRETASE, MEMAPSIN 2, FRAGMENT SCREEN, ALTERNATIVE SPLICING, ASPARTYL PROTEASE, GLYCOPROTEIN, HYDROLASE, MEMBRANE, TRANSMEMBRANE, ZYMOGEN
3buh:A (ASN293) to (ILE324) BACE-1 COMPLEXED WITH COMPOUND 4 | ALZHEIMER'S DISEASE, ASPARTIC PROTEASE, BETA-SECRETASE, MEMAPSIN 2, FRAGMENT SCREEN, ALTERNATIVE SPLICING, ASPARTYL PROTEASE, GLYCOPROTEIN, HYDROLASE, MEMBRANE, TRANSMEMBRANE, ZYMOGEN
4qz2:J (VAL13) to (LYS29) YCP BETA5-M45I MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz2:X (VAL13) to (LYS29) YCP BETA5-M45I MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz3:J (VAL13) to (LYS29) YCP BETA5-A49V MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz3:X (VAL13) to (LYS29) YCP BETA5-A49V MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz4:J (VAL13) to (LYS29) YCP BETA5-A49S MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz4:M (VAL20) to (GLY38) YCP BETA5-A49S MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz4:X (VAL13) to (LYS29) YCP BETA5-A49S MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz4:a (VAL20) to (GLY38) YCP BETA5-A49S MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz5:J (VAL13) to (LYS29) YCP BETA5-A49T-MUTANT IN COMPLEX WITH ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz5:M (VAL20) to (GLY38) YCP BETA5-A49T-MUTANT IN COMPLEX WITH ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz5:X (VAL13) to (LYS29) YCP BETA5-A49T-MUTANT IN COMPLEX WITH ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz5:a (VAL20) to (GLY38) YCP BETA5-A49T-MUTANT IN COMPLEX WITH ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz6:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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:J (VAL13) to (LYS29) YCP BETA5-C52F MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qzw:X (VAL13) to (LYS29) YCP BETA5-C52F MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qzx:J (VAL13) to (LYS29) YCP BETA5-C63F MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qzx:X (VAL13) to (LYS29) YCP BETA5-C63F MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r00:J (VAL13) to (LYS29) YCP BETA5-C52F MUTANT IN COMPLEX WITH OMURALIDE | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r00:M (VAL20) to (GLY38) YCP BETA5-C52F MUTANT IN COMPLEX WITH OMURALIDE | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r00:X (VAL13) to (LYS29) YCP BETA5-C52F MUTANT IN COMPLEX WITH OMURALIDE | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r00:a (VAL20) to (GLY38) YCP BETA5-C52F MUTANT IN COMPLEX WITH OMURALIDE | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qzz:M (VAL20) to (GLY38) YCP IN COMPLEX WITH OMURALIDE | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qzz:a (VAL20) to (GLY38) YCP IN COMPLEX WITH OMURALIDE | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r02:J (VAL13) to (LYS29) YCP IN COMPLEX WITH BSC4999 (ALPHA-KETO PHENYLAMIDE) | CANCER, PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, REVERSIBLE COVALENT LIGAND, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r02:M (VAL20) to (GLY38) YCP IN COMPLEX WITH BSC4999 (ALPHA-KETO PHENYLAMIDE) | CANCER, PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, REVERSIBLE COVALENT LIGAND, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r02:X (VAL13) to (LYS29) YCP IN COMPLEX WITH BSC4999 (ALPHA-KETO PHENYLAMIDE) | CANCER, PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, REVERSIBLE COVALENT LIGAND, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r02:a (VAL20) to (GLY38) YCP IN COMPLEX WITH BSC4999 (ALPHA-KETO PHENYLAMIDE) | CANCER, PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, REVERSIBLE COVALENT LIGAND, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r17:J (VAL13) to (LYS29) LIGAND-INDUCED AZIRIDINE-FORMATION AT SUBUNIT BETA5 OF THE YEAST 20S PROTEASOME | PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, UMPOLUNG, CROSSLINK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r17:M (VAL20) to (GLY38) LIGAND-INDUCED AZIRIDINE-FORMATION AT SUBUNIT BETA5 OF THE YEAST 20S PROTEASOME | PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, UMPOLUNG, CROSSLINK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r17:X (VAL13) to (LYS29) LIGAND-INDUCED AZIRIDINE-FORMATION AT SUBUNIT BETA5 OF THE YEAST 20S PROTEASOME | PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, UMPOLUNG, CROSSLINK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r17:a (VAL20) to (GLY38) LIGAND-INDUCED AZIRIDINE-FORMATION AT SUBUNIT BETA5 OF THE YEAST 20S PROTEASOME | PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, UMPOLUNG, CROSSLINK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r18:M (VAL20) to (GLY38) 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:a (VAL20) to (GLY38) LIGAND-INDUCED LYS33-THR1 CROSSLINKING AT SUBUNIT BETA5 OF THE YEAST 20S PROTEASOME | PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, UMPOLUNG, CROSSLINK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4bvy:A (GLN36) to (SER61) CRYSTAL STRUCTURE OF THE AIMP3-MRS N-TERMINAL DOMAIN COMPLEX | LIGASE-TRANSLATION COMPLEX, AIMP3, MRS
5feg:A (GLY17) to (SER36) CRYSTAL STRUCTURE OF THE DIMERIC ALLERGEN PROFILIN (HEV B 8) | ACTIN BINDING PROTEIN, ALLERGEN, ALLERGY, CROSS-REACTIVITY, HEV B 8
4r3d:A (CYS209) to (ILE237) CRYSTAL STRUCTURE OF MERS CORONAVIRUS PAPAIN LIKE PROTEASE | BETA STRANDS, ZINC FINGER, HYDROLASE
5fgd:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-H(-2)L-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgd:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-H(-2)L-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgd:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-H(-2)L-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgd:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-H(-2)L-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4r52:A (PRO44) to (TYR60) 1.5 ANGSTROM CRYSTAL STRUCTURE OF 3-HYDROXYANTHRANILATE-3,4- DIOXYGENASE FROM CUPRIAVIDUS METALLIDURANS | CUPIN RUBREDOXIN, OXIDOREDUCTASE
5fg7:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-T1A MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5fg7:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-T1A MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5fg9:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-T(-2)V MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5fg9:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-T(-2)V MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3c4n:A (ALA348) to (GLY375) CRYSTAL STRUCTURE OF DR_0571 PROTEIN FROM DEINOCOCCUS RADIODURANS IN COMPLEX WITH ADP. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET DRR125 | ALPHA-BETA PROTEIN, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, UNKNOWN FUNCTION
3c4n:B (ALA348) to (GLY375) CRYSTAL STRUCTURE OF DR_0571 PROTEIN FROM DEINOCOCCUS RADIODURANS IN COMPLEX WITH ADP. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET DRR125 | ALPHA-BETA PROTEIN, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, UNKNOWN FUNCTION
5fge:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-H(-2)T-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fge:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-H(-2)T-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fge:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-H(-2)T-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fge:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-H(-2)T-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgf:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-H(-2)A-T1A-K81R TRIPLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fhs:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fhs:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fhs:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fhs:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
3n95:D (ASN-129) to (LEU-108) CRYSTAL STRUCTURE OF HUMAN CRFR2 ALPHA EXTRACELLULAR DOMAIN IN COMPLEX WITH UROCORTIN 2 | CLASS B-GPCR, EXTRACELLULAR DOMAIN, CRFR2 ALPHA EXTRACELLULAR DOMAIN, NEUROPEPTIDE,SELECTIVITY, MEMBRANE PROTEIN, HORMONE
4bzi:E (MET550) to (GLY573) THE STRUCTURE OF THE COPII COAT ASSEMBLED ON MEMBRANES | TRANSPORT PROTEIN, SECRETION, TRAFFICKING, SEC23, SEC24, SAR1
4bzi:L (MET550) to (GLY573) THE STRUCTURE OF THE COPII COAT ASSEMBLED ON MEMBRANES | TRANSPORT PROTEIN, SECRETION, TRAFFICKING, SEC23, SEC24, SAR1
4bzi:M (MET550) to (GLY573) THE STRUCTURE OF THE COPII COAT ASSEMBLED ON MEMBRANES | TRANSPORT PROTEIN, SECRETION, TRAFFICKING, SEC23, SEC24, SAR1
3cb5:A (GLY259) to (ASP301) CRYSTAL STRUCTURE OF THE S. POMBE PEPTIDASE HOMOLOGY DOMAIN OF FACT COMPLEX SUBUNIT SPT16 (FORM A) | PEPTIDASE HOMOLOGY DOMAIN, HISTONE BINDING MODULE, HISTONE H3/H4 CHAPERONE, PITA-BREAD FOLD, CHROMOSOMAL PROTEIN, DNA DAMAGE, DNA REPAIR, DNA REPLICATION, NUCLEUS, TRANSCRIPTION, TRANSCRIPTION REGULATION
3cb5:B (GLY259) to (ASP301) CRYSTAL STRUCTURE OF THE S. POMBE PEPTIDASE HOMOLOGY DOMAIN OF FACT COMPLEX SUBUNIT SPT16 (FORM A) | PEPTIDASE HOMOLOGY DOMAIN, HISTONE BINDING MODULE, HISTONE H3/H4 CHAPERONE, PITA-BREAD FOLD, CHROMOSOMAL PROTEIN, DNA DAMAGE, DNA REPAIR, DNA REPLICATION, NUCLEUS, TRANSCRIPTION, TRANSCRIPTION REGULATION
4r91:A (THR120) to (GLY139) BACE-1 IN COMPLEX WITH (R)-4-(2-CYCLOHEXYLETHYL)-4-(((1S,3R)-3- (CYCLOPENTYLAMINO)CYCLOHEXYL)METHYL)-1-METHYL-5-OXOIMIDAZOLIDIN-2- IMINIUM | ASPARTIC PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r99:D (VAL160) to (PHE201) CRYSTAL STRUCTURE OF A URICASE FROM BACILLUS FASTIDIOUS | BACILLUS FASTIDIOUS URICASE, FOLD, STABILITY, HYDROLASE
3nbn:A (GLN406) to (SER425) CRYSTAL STRUCTURE OF A DIMER OF NOTCH TRANSCRIPTION COMPLEX TRIMERS ON HES1 DNA | PROMOTER REGIONS, NOTCH1, CSL, RBPJ, MASTERMIND, TRANSCRIPTION FACTORS, TRANSCRIPTION, TRANSCRIPTIONAL ACTIVATION, TRANSCRIPTION- DNA COMPLEX
3nbn:D (GLN406) to (SER425) CRYSTAL STRUCTURE OF A DIMER OF NOTCH TRANSCRIPTION COMPLEX TRIMERS ON HES1 DNA | PROMOTER REGIONS, NOTCH1, CSL, RBPJ, MASTERMIND, TRANSCRIPTION FACTORS, TRANSCRIPTION, TRANSCRIPTIONAL ACTIVATION, TRANSCRIPTION- DNA COMPLEX
3cgb:A (ASP73) to (SER104) PYRIDINE NUCLEOTIDE COMPLEXES WITH BACILLUS ANTHRACIS COENZYME A- DISULFIDE REDUCTASE: A STRUCTURAL ANALYSIS OF DUAL NAD(P)H SPECIFICITY | COENZYME A, FLAVIN ADENINE DINUCLEOTIDE, SELENOMETHIONINE, FAD, FLAVOPROTEIN, OXIDOREDUCTASE
3cgd:A (ASP73) to (SER104) PYRIDINE NUCLEOTIDE COMPLEXES WITH BACILLUS ANTHRACIS COENZYME A- DISULFIDE REDUCTASE: A STRUCTURAL ANALYSIS OF DUAL NAD(P)H SPECIFICITY | COENZYME A, FLAVIN ADENINE DINUCLEOTIDE, NICOTINAMIDE ADENINE DINUCLEOTIDE, FAD, FLAVOPROTEIN, OXIDOREDUCTASE
5fmh:A (GLY224) to (GLU254) CRYSTAL STRUCTURE OF THE E405K MUTANT OF HUMAN APOPTOSIS INDUCING FACTOR | APOPTOSIS, APOPTOSIS INDUCING FACTOR, FLAVOPROTEIN, OXIDOREDUCTASE, MITOCHIONDRIA
4ri8:A (VAL777) to (SER813) FAN1 NUCLEASE BOUND TO 5' PHOSPHORYLATED P(DG)/3'(DT-DT-DT-DT) DOUBLE FLAP DNA | NUCLEASE, HYDROLASE-DNA COMPLEX
4ri8:B (VAL777) to (SER813) FAN1 NUCLEASE BOUND TO 5' PHOSPHORYLATED P(DG)/3'(DT-DT-DT-DT) DOUBLE FLAP DNA | NUCLEASE, HYDROLASE-DNA COMPLEX
4rib:B (VAL777) to (LEU811) FAN1 NUCLEASE BOUND TO 5' PHOSPHORYLATED P(DT) SINGLE FLAP DNA | NUCLEASE, HYDROLASE-DNA COMPLEX
5fs6:A (GLY224) to (GLU254) CRYSTAL STRUCTURE OF THE V243L MUTANT OF HUMAN APOPTOSIS INDUCING FACTOR | OXIDOREDUCTASE, MITOCHONDRIA, FLAVOPROTEIN
4ccf:A (GLY307) to (ARG336) STRUCTURE OF RESPIRATORY SYNCYTIAL VIRUS F PROTEIN HEAD DOMAIN | VIRAL PROTEIN
4ccf:C (GLY307) to (ARG336) STRUCTURE OF RESPIRATORY SYNCYTIAL VIRUS F PROTEIN HEAD DOMAIN | VIRAL PROTEIN
4ccf:E (GLY307) to (ARG336) STRUCTURE OF RESPIRATORY SYNCYTIAL VIRUS F PROTEIN HEAD DOMAIN | VIRAL PROTEIN
4ccf:F (GLY307) to (ARG336) STRUCTURE OF RESPIRATORY SYNCYTIAL VIRUS F PROTEIN HEAD DOMAIN | VIRAL PROTEIN
3nst:A (ARG113) to (VAL129) CRYSTAL STRUCTURE OF SALICYLATE 1,2-DIOXYGENASE G106A MUTANT FROM PSEUDOAMINOBACTER SALICYLATOXIDANS | BETA-BARREL, CUPINS, OXIDOREDUCTASE
3cpx:A (ARG59) to (GLY83) CRYSTAL STRUCTURE OF PUTATIVE M42 GLUTAMYL AMINOPEPTIDASE (YP_676701.1) FROM CYTOPHAGA HUTCHINSONII ATCC 33406 AT 2.39 A RESOLUTION | YP_676701.1, PUTATIVE M42 GLUTAMYL AMINOPEPTIDASE, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, HYDROLASE
3cpx:B (ARG59) to (GLY83) CRYSTAL STRUCTURE OF PUTATIVE M42 GLUTAMYL AMINOPEPTIDASE (YP_676701.1) FROM CYTOPHAGA HUTCHINSONII ATCC 33406 AT 2.39 A RESOLUTION | YP_676701.1, PUTATIVE M42 GLUTAMYL AMINOPEPTIDASE, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, HYDROLASE
3nul:A (GLY17) to (SER36) PROFILIN I FROM ARABIDOPSIS THALIANA | PROFILIN, CYTOSKELETON, ACTIN BINDING PROTEIN
3nvc:A (ARG113) to (VAL129) CRYSTAL STRUCTURE OF SALICYLATE 1,2-DIOXYGENASE G106A MUTANT FROM PSEUDOAMINOBACTER SALICYLATOXIDANS IN COMPLEX WITH SALICYLATE | BETA-BARREL, OXIDOREDUCTASE
5fv9:D (THR246) to (ASP269) CRYSTAL STRUCTURE OF GALNAC-T2 IN COMPLEX WITH COMPOUND 16D | TRANSFERASE
3nwl:C (MET211) to (TYR230) THE CRYSTAL STRUCTURE OF THE P212121 FORM OF BOVINE LIVER CATALASE PREVIOUSLY CHARACTERIZED BY ELECTRON MICROSCOPY | OXIOREDUCTASE, NADPH, HEME B, OXIDOREDUCTASE
3nyc:A (GLU1298) to (ALA1328) CRYSTAL STRUCTURE OF PSEUDOMONAS AERUGINOSA D-ARGININE DEHYDROGENASE | D-ARGININE DEHYDROGENASE, FAD, IMINO-ARGININE, OXIDOREDUCTASE
4ru4:C (LYS454) to (ASN482) CRYSTAL STRUCTURE OF THE TAILSPIKE PROTEIN GP49 FROM PSEUDOMONAS PHAGE LKA1 | TAIL SPIKE PROTEIN, BASEPLATE, PHAGE LKA1, LYASE, STRUCTURAL PROTEIN
4ru4:C (THR529) to (LEU551) CRYSTAL STRUCTURE OF THE TAILSPIKE PROTEIN GP49 FROM PSEUDOMONAS PHAGE LKA1 | TAIL SPIKE PROTEIN, BASEPLATE, PHAGE LKA1, LYASE, STRUCTURAL PROTEIN
3nzj:J (VAL12) to (LYS28) 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:M (VAL12) to (GLY30) 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:X (VAL12) to (LYS28) 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:1 (VAL12) to (GLY30) 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:J (VAL12) to (LYS28) 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:M (VAL12) to (GLY30) 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:X (VAL12) to (LYS28) 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:1 (VAL12) to (GLY30) 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:M (VAL12) to (GLY30) 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
3d29:1 (VAL12) to (GLY30) 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
4cr3:X (VAL7) to (GLY31) DEEP CLASSIFICATION OF A LARGE CRYO-EM DATASET DEFINES THE CONFORMATIONAL LANDSCAPE OF THE 26S PROTEASOME | HYDROLASE, AAA-ATPASE, ATP-ANALOG, CLASSIFICATION
4s37:A (ASP37) to (GLY82) CRYSTAL STRUCTURE OF R2 PYOCIN MEMBRANE-PIERCING SPIKE | CELL PUNCTURING DEVICE, TRIMER, BETA-HELIX, IRON-BINDING, OUTER CELL MEMBRANE PIERCING, METAL BINDING PROTEIN
3d4o:B (ASP59) to (LEU85) CRYSTAL STRUCTURE OF DIPICOLINATE SYNTHASE SUBUNIT A (NP_243269.1) FROM BACILLUS HALODURANS AT 2.10 A RESOLUTION | NP_243269.1, DIPICOLINATE SYNTHASE SUBUNIT A, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, ALANINE DEHYDROGENASE/PNT, C-TERMINAL DOMAIN COMPLEX, OXIDOREDUCTASE
3d4o:D (ASP59) to (LEU85) CRYSTAL STRUCTURE OF DIPICOLINATE SYNTHASE SUBUNIT A (NP_243269.1) FROM BACILLUS HALODURANS AT 2.10 A RESOLUTION | NP_243269.1, DIPICOLINATE SYNTHASE SUBUNIT A, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, ALANINE DEHYDROGENASE/PNT, C-TERMINAL DOMAIN COMPLEX, OXIDOREDUCTASE
4tlv:F (VAL205) to (ASN256) CARDS TOXIN, NICKED | MYCOPLASMA PNEUMONIAE, VIRULENCE, ATYPICAL PNEUMONIA, COMMUNITY ACQUIRED RESPIRATORY DISTRESS SYNDROME, ADP-RIBOSYL TRANSFERASE, TOXIN, TRANSFERASE
4cvu:A (GLY882) to (ASP901) STRUCTURE OF FUNGAL BETA-MANNOSIDASE FROM GLYCOSIDE HYDROLASE FAMILY 2 OF TRICHODERMA HARZIANUM | HYDROLASE
3odx:A (VAL649) to (GLU665) CRYSTAL STRUCTURE OF AN N-TERMINALLY TRUNCATED LINKER-DH/PH DOMAINS OF P115-RHOGEF | REGULATION OF RHOA GTPASE, RHOGEF, DH, PH, RHO, SIGNALING PROTEIN
3oeu:J (VAL12) to (LYS28) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 24 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3oeu:M (VAL12) to (GLY30) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 24 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3oev:J (VAL12) to (LYS28) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 25 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3oev:M (VAL12) to (GLY30) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 25 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3oev:X (VAL12) to (LYS28) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 25 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3oev:1 (VAL12) to (GLY30) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 25 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3deh:C (SER113) to (ASP135) CRYSTAL STRUCTURES OF CASPASE-3 WITH BOUND ISOQUINOLINE-1,3, 4-TRIONE DERIVATIVE INHIBITORS | CASPASE-3, ISOQUINOLINE-1, 3, 4-TRIONE DERIVATIVES, INACTIVATION, PROTEIN-INHIBITOR COMPLEX, CYTOPLASM, HYDROLASE, APOPTOSIS, PHOSPHOPROTEIN, POLYMORPHISM, PROTEASE, S-NITROSYLATION, THIOL PROTEASE, ZYMOGEN
3deh:D (SER113) to (ASP135) CRYSTAL STRUCTURES OF CASPASE-3 WITH BOUND ISOQUINOLINE-1,3, 4-TRIONE DERIVATIVE INHIBITORS | CASPASE-3, ISOQUINOLINE-1, 3, 4-TRIONE DERIVATIVES, INACTIVATION, PROTEIN-INHIBITOR COMPLEX, CYTOPLASM, HYDROLASE, APOPTOSIS, PHOSPHOPROTEIN, POLYMORPHISM, PROTEASE, S-NITROSYLATION, THIOL PROTEASE, ZYMOGEN
3dei:B (SER113) to (ASP135) CRYSTAL STRUCTURES OF CASPASE-3 WITH BOUND ISOQUINOLINE-1,3, 4-TRIONE DERIVATIVE INHIBITORS | CASPASE-3, ISOQUINOLINE-1, 3, 4-TRIONE DERIVATIVES, INACTIVATION, PROTEIN-INHIBITOR COMPLEX, APOPTOSIS, CYTOPLASM, HYDROLASE, PHOSPHOPROTEIN, POLYMORPHISM, PROTEASE, S-NITROSYLATION, THIOL PROTEASE, ZYMOGEN
3dei:C (SER113) to (ASP135) CRYSTAL STRUCTURES OF CASPASE-3 WITH BOUND ISOQUINOLINE-1,3, 4-TRIONE DERIVATIVE INHIBITORS | CASPASE-3, ISOQUINOLINE-1, 3, 4-TRIONE DERIVATIVES, INACTIVATION, PROTEIN-INHIBITOR COMPLEX, APOPTOSIS, CYTOPLASM, HYDROLASE, PHOSPHOPROTEIN, POLYMORPHISM, PROTEASE, S-NITROSYLATION, THIOL PROTEASE, ZYMOGEN
3dei:D (SER113) to (ASP135) CRYSTAL STRUCTURES OF CASPASE-3 WITH BOUND ISOQUINOLINE-1,3, 4-TRIONE DERIVATIVE INHIBITORS | CASPASE-3, ISOQUINOLINE-1, 3, 4-TRIONE DERIVATIVES, INACTIVATION, PROTEIN-INHIBITOR COMPLEX, APOPTOSIS, CYTOPLASM, HYDROLASE, PHOSPHOPROTEIN, POLYMORPHISM, PROTEASE, S-NITROSYLATION, THIOL PROTEASE, ZYMOGEN
3dej:D (SER113) to (ASP135) CRYSTAL STRUCTURES OF CASPASE-3 WITH BOUND ISOQUINOLINE-1,3, 4-TRIONE DERIVATIVE INHIBITORS | CASPASE-3, ISOQUINOLINE-1, 3, 4-TRIONE DERIVATIVES, INACTIVATION, PROTEIN-INHIBITOR COMPLEX, APOPTOSIS, CYTOPLASM, HYDROLASE, PHOSPHOPROTEIN, POLYMORPHISM, PROTEASE, S-NITROSYLATION, THIOL PROTEASE, ZYMOGEN
3dek:A (SER113) to (ASP135) CRYSTAL STRUCTURES OF CASPASE-3 WITH BOUND ISOQUINOLINE-1,3, 4-TRIONE DERIVATIVE INHIBITORS | CASPASE-3, ISOQUINOLINE-1, 3, 4-TRIONE DERIVATIVES, INACTIVATION, PROTEIN-INHIBITOR COMPLEX, APOPTOSIS, CYTOPLASM, HYDROLASE, PHOSPHOPROTEIN, POLYMORPHISM, PROTEASE, S-NITROSYLATION, THIOL PROTEASE, ZYMOGEN
3dek:B (SER113) to (ASP135) CRYSTAL STRUCTURES OF CASPASE-3 WITH BOUND ISOQUINOLINE-1,3, 4-TRIONE DERIVATIVE INHIBITORS | CASPASE-3, ISOQUINOLINE-1, 3, 4-TRIONE DERIVATIVES, INACTIVATION, PROTEIN-INHIBITOR COMPLEX, APOPTOSIS, CYTOPLASM, HYDROLASE, PHOSPHOPROTEIN, POLYMORPHISM, PROTEASE, S-NITROSYLATION, THIOL PROTEASE, ZYMOGEN
3dek:C (SER113) to (ASP135) CRYSTAL STRUCTURES OF CASPASE-3 WITH BOUND ISOQUINOLINE-1,3, 4-TRIONE DERIVATIVE INHIBITORS | CASPASE-3, ISOQUINOLINE-1, 3, 4-TRIONE DERIVATIVES, INACTIVATION, PROTEIN-INHIBITOR COMPLEX, APOPTOSIS, CYTOPLASM, HYDROLASE, PHOSPHOPROTEIN, POLYMORPHISM, PROTEASE, S-NITROSYLATION, THIOL PROTEASE, ZYMOGEN
3dek:D (SER113) to (ASP135) CRYSTAL STRUCTURES OF CASPASE-3 WITH BOUND ISOQUINOLINE-1,3, 4-TRIONE DERIVATIVE INHIBITORS | CASPASE-3, ISOQUINOLINE-1, 3, 4-TRIONE DERIVATIVES, INACTIVATION, PROTEIN-INHIBITOR COMPLEX, APOPTOSIS, CYTOPLASM, HYDROLASE, PHOSPHOPROTEIN, POLYMORPHISM, PROTEASE, S-NITROSYLATION, THIOL PROTEASE, ZYMOGEN
3og2:A (ARG706) to (THR740) NATIVE CRYSTAL STRUCTURE OF TRICHODERMA REESEI BETA-GALACTOSIDASE | TIM BARREL DOMAIN, GLYCOSIDE HYDROLASE, FAMILY 35, GLYCOPROTEIN, HYDROLASE
4d0t:D (THR246) to (ASP269) GALNAC-T2 CRYSTAL SOAKED WITH UDP-GALNAC, EA2 PEPTIDE AND MANGANESE | TRANSFERASE, RETAINING GALNAC-T2, SUBSTRATE-GUIDED SNI-TYPE REACTION, QM/MM METADYNAMICS, BI-BI KINETIC MECHANISM, SUBSTRATE SPECIFICITY, PROTEIN X-RAY CRYSTALLOGRAPHY, ACETAMIDO GROUP
3ogr:A (ARG706) to (THR740) COMPLEX STRUCTURE OF BETA-GALACTOSIDASE FROM TRICHODERMA REESEI WITH GALACTOSE | TIM BARREL DOMAIN, GLYCOSIDE HYDROLASE, FAMILY 35, GLYCOPROTEIN, HYDROLASE
3dhw:D (ILE2) to (LEU21) CRYSTAL STRUCTURE OF METHIONINE IMPORTER METNI | ABC-TRANSPORTER, METHIONINE UPTAKE TRANSPORTER, MEMBRANE PROTEIN, AMINO-ACID TRANSPORT, INNER MEMBRANE, TRANSMEMBRANE, ATP-BINDING, HYDROLASE, NUCLEOTIDE-BINDING, MEMBRANE PROTEIN-HYDROLASE COMPLEX
3dhw:G (MET1) to (GLN19) CRYSTAL STRUCTURE OF METHIONINE IMPORTER METNI | ABC-TRANSPORTER, METHIONINE UPTAKE TRANSPORTER, MEMBRANE PROTEIN, AMINO-ACID TRANSPORT, INNER MEMBRANE, TRANSMEMBRANE, ATP-BINDING, HYDROLASE, NUCLEOTIDE-BINDING, MEMBRANE PROTEIN-HYDROLASE COMPLEX
5gkn:A (HIS210) to (TYR230) CATALASE STRUCTURE DETERMINED BY ELECTRON CRYSTALLOGRAPHY OF THIN 3D CRYSTALS | OXIDOREDUCTASE, HEME, NADPH
5gkn:C (MET211) to (TYR230) CATALASE STRUCTURE DETERMINED BY ELECTRON CRYSTALLOGRAPHY OF THIN 3D CRYSTALS | OXIDOREDUCTASE, HEME, NADPH
3djd:B (SER330) to (CYS360) CRYSTAL STRUCTURE OF THE DEGLYCATING ENZYME FRUCTOSAMINE OXIDASE FROM ASPERGILLUS FUMIGATUS (AMADORIASE II) | FRUCTOSYL-AMINO ACID, AMADORIASE, DEGLYCATION, OXIDOREDUCTASE, FRUCTOSAMINE OXIDASE
4d3i:A (GLY214) to (ALA232) STRUCTURE OF BACILLUS SUBTILIS NITRIC OXIDE SYNTHASE IN COMPLEX WITH 6,6'-((5-(AMINOMETHYL)-1,3-PHENYLENE)BIS( ETHANE-2,1-DIYL))BIS(4-METHYLPYRIDIN-2-AMINE) | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, INHIBITOR
4txh:A (ASP139) to (GLN162) CRYSTAL STRUCTURE OF URIDINE PHOSPHORYLASE FROM SCHISTOSOMA MANSONI IN APO FORM | URIDINE PHOSPHORYLASE, TRANSFERASE
4txh:B (ASP139) to (GLN162) CRYSTAL STRUCTURE OF URIDINE PHOSPHORYLASE FROM SCHISTOSOMA MANSONI IN APO FORM | URIDINE PHOSPHORYLASE, TRANSFERASE
4txh:C (ASP139) to (GLN162) CRYSTAL STRUCTURE OF URIDINE PHOSPHORYLASE FROM SCHISTOSOMA MANSONI IN APO FORM | URIDINE PHOSPHORYLASE, TRANSFERASE
4txl:C (ASP139) to (GLN162) CRYSTAL STRUCTURE OF URIDINE PHOSPHORYLASE FROM SCHISTOSOMA MANSONI IN COMPLEX WITH URACIL | URIDINE PHOSPHORYLASE, TRANSFERASE
4txl:D (ASP139) to (GLN162) CRYSTAL STRUCTURE OF URIDINE PHOSPHORYLASE FROM SCHISTOSOMA MANSONI IN COMPLEX WITH URACIL | URIDINE PHOSPHORYLASE, TRANSFERASE
4txl:A (ASP139) to (GLN162) CRYSTAL STRUCTURE OF URIDINE PHOSPHORYLASE FROM SCHISTOSOMA MANSONI IN COMPLEX WITH URACIL | URIDINE PHOSPHORYLASE, TRANSFERASE
4txm:A (ASP139) to (GLN162) CRYSTAL STRUCTURE OF URIDINE PHOSPHORYLASE FROM SCHISTOSOMA MANSONI IN COMPLEX WITH THYMINE | URIDINE PHOSPHORYLASE, TRANSFERASE
4txm:B (ASP139) to (GLN162) CRYSTAL STRUCTURE OF URIDINE PHOSPHORYLASE FROM SCHISTOSOMA MANSONI IN COMPLEX WITH THYMINE | URIDINE PHOSPHORYLASE, TRANSFERASE
4txn:A (ASP139) to (GLN162) CRYSTAL STRUCTURE OF URIDINE PHOSPHORYLASE FROM SCHISTOSOMA MANSONI IN COMPLEX WITH 5-FLUOROURACIL | URIDINE PHOSPHORYLASE, TRANSFERASE
4txn:B (ASP139) to (GLN162) CRYSTAL STRUCTURE OF URIDINE PHOSPHORYLASE FROM SCHISTOSOMA MANSONI IN COMPLEX WITH 5-FLUOROURACIL | URIDINE PHOSPHORYLASE, TRANSFERASE
4txn:C (ASP139) to (GLN162) CRYSTAL STRUCTURE OF URIDINE PHOSPHORYLASE FROM SCHISTOSOMA MANSONI IN COMPLEX WITH 5-FLUOROURACIL | URIDINE PHOSPHORYLASE, TRANSFERASE
4txn:D (ASP139) to (GLN162) CRYSTAL STRUCTURE OF URIDINE PHOSPHORYLASE FROM SCHISTOSOMA MANSONI IN COMPLEX WITH 5-FLUOROURACIL | URIDINE PHOSPHORYLASE, TRANSFERASE
5gv0:A (MET338) to (CYS364) CRYSTAL STRUCTURE OF THE MEMBRANE-PROXIMAL DOMAIN OF MOUSE LYSOSOME- ASSOCIATED MEMBRANE PROTEIN 1 (LAMP-1) | MEMBRANE PROTEIN
4d5q:A (SER90) to (GLY105) HYPOCREA JECORINA CEL7A (WILD TYPE) SOAKED WITH XYLOPENTAOSE. | HYDROLASE, GLYCOSIDE HYDROLASE, CELLOBIOHYDROLASE, CELLULASE. INHIBITION, XYLOOLIGOSACCHARIDES
4tz3:A (THR532) to (GLN553) ENSEMBLE REFINEMENT OF THE E502A VARIANT OF SACTELAM55A FROM STREPTOMYCES SP. SIREXAA-E IN COMPLEX WITH LAMINARITETRAOSE | EXO-BETA-1, 3-GLUCANASE, BETA-1, GH55, LAMINARITETRAOSE, SECRETED, BIOMASS DEGRADATION, HYDROLASE
4tz5:A (VAL335) to (GLY355) ENSEMBLE REFINEMENT OF THE E502A VARIANT OF SACTELAM55A FROM STREPTOMYCES SP. SIREXAA-E IN COMPLEX WITH LAMINARIHEXAOSE | EXO-BETA-1, 3-GLUCANASE, BETA-1, GH55, LAMINARITETRAOSE, SECRETED, BIOMASS DEGRADATION, HYDROLASE
4tz5:B (THR532) to (GLN553) ENSEMBLE REFINEMENT OF THE E502A VARIANT OF SACTELAM55A FROM STREPTOMYCES SP. SIREXAA-E IN COMPLEX WITH LAMINARIHEXAOSE | EXO-BETA-1, 3-GLUCANASE, BETA-1, GH55, LAMINARITETRAOSE, SECRETED, BIOMASS DEGRADATION, HYDROLASE
4d94:A (LYS1293) to (ASP1321) CRYSTAL STRUCTURE OF TEP1R | PLASMODIUM REFRACTORY ALLELE, IMMUNE SYSTEM, FULL-LENGTH PROTEIN, THIOESTER, MACROGLOBULIN DOMAINS, COMPONENT OF INNATE IMMUNE RESPONSE BY THE OPSINIZATION AND MELANIZATION OF PATHOGENS
3or2:A (ALA316) to (GLY342) CRYSTAL STRUCTURE OF DISSIMILATORY SULFITE REDUCTASE II (DSRII) | DISSIMILATORY SULFITE REDUCTASE, SULFATE REDUCTION, OXIDOREDUCTASE
5hca:A (ASP304) to (THR328) GLOBULAR DOMAIN OF THE ENTAMOEBA HISTOLYTICA CALRETICULIN IN COMPLEX WITH GLUCOSE | CHAPERONE, LEGUME LECTIN DOMAIN, SUGAR BINDING PROTEIN
5hcb:A (ASP304) to (THR328) GLOBULAR DOMAIN OF THE ENTAMOEBA HISTOLYTICA CALRETICULIN IN COMPLEX WITH GLUCOSE | CHAPERONE, LEGUME LECTIN DOMAIN, SUGAR BINDING PROTEIN, FUSION PROTEIN
5hcb:B (ASP304) to (THR328) GLOBULAR DOMAIN OF THE ENTAMOEBA HISTOLYTICA CALRETICULIN IN COMPLEX WITH GLUCOSE | CHAPERONE, LEGUME LECTIN DOMAIN, SUGAR BINDING PROTEIN, FUSION PROTEIN
4u33:A (ALA233) to (THR255) STRUCTURE OF MTB GLGE BOUND TO MALTOSE | COMPLEX WILD-TYPE MALTOSE MALTOSYL-TRANSFERASE, TRANSFERASE
4u33:C (ALA233) to (THR255) STRUCTURE OF MTB GLGE BOUND TO MALTOSE | COMPLEX WILD-TYPE MALTOSE MALTOSYL-TRANSFERASE, TRANSFERASE
4u33:E (ALA233) to (THR255) STRUCTURE OF MTB GLGE BOUND TO MALTOSE | COMPLEX WILD-TYPE MALTOSE MALTOSYL-TRANSFERASE, TRANSFERASE
4u3t:B (GLU330) to (ARG345) CRYSTAL STRUCTURE OF THE TRANSPEPTIDASE DOMAIN OF NEISSERIA GONORRHOEAE PENICILLIN-BINDING PROTEIN 2 DERIVED FROM THE PENICILLIN- RESISTANT STRAIN 6140 | PENICILLIN-BINDING PROTEIN, TRANSPEPTIDASE DOMAIN, PEPTIDOGLYCAN SYNTHESIS, ANTIBIOTIC RESISTANCE
3oxu:D (GLY1107) to (ILE1120) COMPLEMENT COMPONENTS FACTOR H CCP19-20 AND C3D IN COMPLEX | C3D-ALPHA-ALPHA BARREL, COMPLEMENT COMPONENT, FACTOR H, IMMUNE SYSTEM
3dy3:M (VAL12) to (GLY30) 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
3dy3:1 (VAL12) to (GLY30) 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
3p0e:A (ASP162) to (SER185) STRUCTURE OF HUPP2 IN AN ACTIVE CONFORMATION WITH BOUND 5- BENZYLACYCLOURIDINE | URIDINE PHOSPHORYLASE, TRANSFERASE
3p0e:D (ASP162) to (SER185) STRUCTURE OF HUPP2 IN AN ACTIVE CONFORMATION WITH BOUND 5- BENZYLACYCLOURIDINE | URIDINE PHOSPHORYLASE, TRANSFERASE
3p0e:E (ASP162) to (SER185) STRUCTURE OF HUPP2 IN AN ACTIVE CONFORMATION WITH BOUND 5- BENZYLACYCLOURIDINE | URIDINE PHOSPHORYLASE, TRANSFERASE
3p0e:F (ASP162) to (SER185) STRUCTURE OF HUPP2 IN AN ACTIVE CONFORMATION WITH BOUND 5- BENZYLACYCLOURIDINE | URIDINE PHOSPHORYLASE, TRANSFERASE
3p0f:A (ASP162) to (SER185) STRUCTURE OF HUPP2 IN AN INACTIVE CONFORMATION WITH BOUND 5- BENZYLACYCLOURIDINE | URIDINE PHOSPHORYLASE, TRANSFERASE
3p6a:A (VAL649) to (GLU665) CRYSTAL STRUCTURE OF THE DH/PH DOMAINS OF P115-RHOGEF (R399E MUTANT) | REGULATION OF RHOA GTPASE, RHOGEF, DH, PH, RHO, SIGNALING PROTEIN
3p6b:A (PRO160) to (PRO193) THE CRYSTAL STRUCTURE OF CELK CBM4 FROM CLOSTRIDIUM THERMOCELLUM | BETA-SANDWICH, CARBOHYDRATE BINDING, SUGAR BINDING PROTEIN
3e1t:A (ILE280) to (GLY302) STRUCTURE AND ACTION OF THE MYXOBACTERIAL CHONDROCHLOREN HALOGENASE CNDH, A NEW VARIANT OF FAD-DEPENDENT HALOGENASES | FAD DEPENDENT HALOGENASE, FLAVOPROTEIN
3p7z:A (LYS1717) to (LYS1731) CRYSTAL STRUCTURE OF THE NEUROFIBROMIN SEC14-PH MODULE CONTAINING THE PATIENT DERIVED MUTATION I1584V | SEC14 HOMOLGY DOMAIN, PLECKSTRIN HOMOLOGY DOMAIN, BINDING OF GLYCEROPHOSPHOLIPIDS, GLYCEROPHOSPHOLIPIDS, CYTOPLASMATIC, LIPID BINDING PROTEIN
3e3h:B (SER30) to (THR45) CRYSTAL STRUCTURE OF THE OP HYDROLASE MUTANT FROM BREVUNDIMONAS DIMINUTA | OP HYDROLASE MUTANT, MEMBRANE, METAL-BINDING, PLASMID, ZINC
4ub6:B (GLU364) to (ILE381) NATIVE STRUCTURE OF PHOTOSYSTEM II (DATASET-1) BY A FEMTOSECOND X-RAY LASER | MEMBRANE PROTEIN, ELECTRON TRANSPORT, PHOTOSYNTHESIS, OXYGEN EVOLUTION, WATER SPLITTING, PHOTO SYSTEM II
4ub6:b (GLU364) to (ILE381) NATIVE STRUCTURE OF PHOTOSYSTEM II (DATASET-1) BY A FEMTOSECOND X-RAY LASER | MEMBRANE PROTEIN, ELECTRON TRANSPORT, PHOTOSYNTHESIS, OXYGEN EVOLUTION, WATER SPLITTING, PHOTO SYSTEM II
4ub8:B (GLU364) to (ILE381) NATIVE STRUCTURE OF PHOTOSYSTEM II (DATASET-2) BY A FEMTOSECOND X-RAY LASER | PHOTOSYNTHESIS, ELECTRON TRANSPORT, OXYGEN EVOLUTION, WATER SPLITTING, PHOTO SYSTEM II
4ub8:b (GLU364) to (ILE381) NATIVE STRUCTURE OF PHOTOSYSTEM II (DATASET-2) BY A FEMTOSECOND X-RAY LASER | PHOTOSYNTHESIS, ELECTRON TRANSPORT, OXYGEN EVOLUTION, WATER SPLITTING, PHOTO SYSTEM II
3pay:C (PHE140) to (ARG171) CRYSTAL STRUCTURE OF A PUTATIVE ADHESIN (BACOVA_04077) FROM BACTEROIDES OVATUS AT 2.50 A RESOLUTION | STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-BIOLOGY, CELL ADHESION
3e47:M (VAL12) to (GLY30) 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
3e47:1 (VAL12) to (GLY30) 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
3e4w:A (THR160) to (PHE179) CRYSTAL STRUCTURE OF A 33KDA CATALASE-RELATED PROTEIN FROM MYCOBACTERIUM AVIUM SUBSP. PARATUBERCULOSIS. P2(1)2(1)2(1) CRYSTAL FORM. | HEME ENZYME, CATALASE, PEROXIDASE, OXIDOREDUCTASE
3e4w:B (THR160) to (PHE179) CRYSTAL STRUCTURE OF A 33KDA CATALASE-RELATED PROTEIN FROM MYCOBACTERIUM AVIUM SUBSP. PARATUBERCULOSIS. P2(1)2(1)2(1) CRYSTAL FORM. | HEME ENZYME, CATALASE, PEROXIDASE, OXIDOREDUCTASE
3e4y:A (THR160) to (PHE179) CRYSTAL STRUCTURE OF A 33KDA CATALASE-RELATED PROTEIN FROM MYCOBACTERIUM AVIUM SUBSP. PARATUBERCULOSIS. I2(1)2(1)2(1) CRYSTAL FORM | HEME ENZYME, CATALASE, PEROXIDASE, OXIDOREDUCTASE
5hxv:F (ASN203) to (SER223) THE CRYSTAL STRUCTURE OF THERMOSTABLE XYLANASE MUTANT | GLYCOSIDE HYDROLASE FAMILY 11 ENDO-XYLANASE, HYDROLASE
5hxv:J (ASN203) to (THR221) THE CRYSTAL STRUCTURE OF THERMOSTABLE XYLANASE MUTANT | GLYCOSIDE HYDROLASE FAMILY 11 ENDO-XYLANASE, HYDROLASE
5hxv:K (ASN203) to (SER223) THE CRYSTAL STRUCTURE OF THERMOSTABLE XYLANASE MUTANT | GLYCOSIDE HYDROLASE FAMILY 11 ENDO-XYLANASE, HYDROLASE
4ueq:S (THR11) to (VAL32) STRUCTURE OF THE V74C LARGE SUBUNIT MUTANT OF D. FRUCTOSOVORANS NIFE-HYDROGENASE | OXIDOREDUCTASE, NIFE-HYDROGENASE MUTANT, NICKEL-CARBOXAMIDO BOND, OXYGEN- TOLERANCE
4du5:A (VAL29) to (LYS55) CRYSTAL STRUCTURE OF PFKB PROTEIN FROM POLAROMONAS SP. JS666 | STRUCTURAL GENOMICS, PSI-BIOLOGY, NEW YORK STRUCTURAL GENOMICS RESEARCH CONSORTIUM, NYSGRC, TRANSFERASE
3pgk:A (VAL275) to (THR297) THE STRUCTURE OF YEAST PHOSPHOGLYCERATE KINASE AT 0.25 NM RESOLUTION | PHOSPHOTRANSFERASE(CARBOXYL AS ACCEPTOR), TRANSFERASE
3pl2:A (GLU9) to (TYR38) CRYSTAL STRUCTURE OF A 5-KETO-2-DEOXYGLUCONOKINASE (NCGL0155, CGL0158) FROM CORYNEBACTERIUM GLUTAMICUM ATCC 13032 KITASATO AT 1.89 A RESOLUTION | PFKB PFAM MOTIF, INOSITOL PHOSPHATE METABOLISM, RIBOKINASE-LIKE FOLD, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-BIOLOGY, TRANSFERASE
3pl2:B (GLU9) to (TYR38) CRYSTAL STRUCTURE OF A 5-KETO-2-DEOXYGLUCONOKINASE (NCGL0155, CGL0158) FROM CORYNEBACTERIUM GLUTAMICUM ATCC 13032 KITASATO AT 1.89 A RESOLUTION | PFKB PFAM MOTIF, INOSITOL PHOSPHATE METABOLISM, RIBOKINASE-LIKE FOLD, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-BIOLOGY, TRANSFERASE
3pl2:C (GLU9) to (LYS37) CRYSTAL STRUCTURE OF A 5-KETO-2-DEOXYGLUCONOKINASE (NCGL0155, CGL0158) FROM CORYNEBACTERIUM GLUTAMICUM ATCC 13032 KITASATO AT 1.89 A RESOLUTION | PFKB PFAM MOTIF, INOSITOL PHOSPHATE METABOLISM, RIBOKINASE-LIKE FOLD, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-BIOLOGY, TRANSFERASE
3pl2:D (GLU9) to (LYS37) CRYSTAL STRUCTURE OF A 5-KETO-2-DEOXYGLUCONOKINASE (NCGL0155, CGL0158) FROM CORYNEBACTERIUM GLUTAMICUM ATCC 13032 KITASATO AT 1.89 A RESOLUTION | PFKB PFAM MOTIF, INOSITOL PHOSPHATE METABOLISM, RIBOKINASE-LIKE FOLD, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-BIOLOGY, TRANSFERASE
4e0x:B (MET106) to (VAL137) CRYSTAL STRUCTURE OF THE KAINATE RECEPTOR GLUK1 LIGAND-BINDING DOMAIN IN COMPLEX WITH KAINATE IN THE ABSENCE OF GLYCEROL | IONOTROPIC GLUTAMATE RECEPTOR, GLUK1, LIGAND-BINDING DOMAIN, AGONIST, MEMBRANE PROTEIN
4uow:B (ALA9) to (LEU29) CRYSTAL STRUCTURE OF THE TITIN M10-OBSCURIN IG DOMAIN 1 COMPLEX | TRANSFERASE-STRUCTURAL PROTEIN COMPLEX, TRANSFERASE, SARCOMERE, IMMUNOGLOBULIN DOMAIN, LIMB-GIRDLE MUSCULAR DYSTROPHY
4upt:B (ALA334) to (ALA352) 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
5iag:A (PHE114) to (ASP135) CASPASE 3 V266Q | ALLOSTERY, SATURATION MUTAGENESIS, CONFORMATIONAL SELECTION, NATIVE ENSEMBLE, PROTEIN SOLVATION, PROTEIN STRUCTURE, PROTEIN DYNAMICS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5ibc:A (PHE114) to (ASP135) CASPASE 3 V266I | ALLOSTERY, SATURATION MUTAGENESIS, CONFORMATIONAL SELECTION, NATIVE ENSEMBLE, PROTEIN SOLVATION, PROTEIN STRUCTURE, PROTEIN DYNAMICS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5ibp:A (PHE114) to (ASP135) CASPASE 3 V266M | ALLOSTERY, SATURATION MUTAGENESIS, CONFORMATIONAL SELECTION, NATIVE ENSEMBLE, PROTEIN SOLVATION, PROTEIN STRUCTURE, PROTEIN DYNAMICS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5ic4:A (SER113) to (ASP135) CRYSTAL STRUCTURE OF CASPASE-3 DEVE PEPTIDE COMPLEX | APOPTOSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5ic4:E (SER113) to (ASP135) CRYSTAL STRUCTURE OF CASPASE-3 DEVE PEPTIDE COMPLEX | APOPTOSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5ic6:A (PHE137) to (PRO158) CRYSTAL STRUCTURE OF CASPASE-7 DEVE PEPTIDE COMPLEX | APOPTOSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4uqy:A (ALA170) to (PRO195) COEVOLUTION OF THE ATPASE CLPV, THE TSSB-TSSC SHEATH AND THE ACCESSORY HSIE PROTEIN DISTINGUISHES TWO TYPE VI SECRETION CLASSES | PROTEIN TRANSPORT, SECRETION, SHEATH, DISASSEMBLY, REGULATION, BACTERIAL
4uqz:A (ALA170) to (PRO195) COEVOLUTION OF THE ATPASE CLPV, THE TSSB-TSSC SHEATH AND THE ACCESSORY HSIE PROTEIN DISTINGUISHES TWO TYPE VI SECRETION CLASSES | PROTEIN TRANSPORT, SECRETION, SHEATH, DISASSEMBLY, REGULATION, BACTERIAL
3pq6:D (MET269) to (PHE288) STRUCTURE OF I274C VARIANT OF E. COLI KATE[] - IMAGES 25-30 | CATALASE, I274C VARIANT, HEME ORIENTATION, X-RAY DAMAGE, OXIDOREDUCTASE
5ig9:D (GLY162) to (VAL183) CRYSTAL STRUCTURE OF MACROCYCLASE MDNC BOUND WITH PRECURSOR PEPTIDE MDNA FROM MICROCYSTIS AERUGINOSA MRC | RIPP, MACROCYCLASE, PRECURSOR PEPTIDE, LIGASE
4usx:B (GLY790) to (ALA812) THE STRUCTURE OF THE C-TERMINAL YADA-LIKE DOMAIN OF BPSL2063 FROM BURKHOLDERIA PSEUDOMALLEI | TRANSPORT PROTEIN, YADA-LIKE HEAD DOMAIN
3psg:A (VAL265) to (ASP290) THE HIGH RESOLUTION CRYSTAL STRUCTURE OF PORCINE PEPSINOGEN | HYDROLASE(ACID PROTEINASE ZYMOGEN)
4ebu:A (MET1) to (GLY25) CRYSTAL STRUCTURE OF A SUGAR KINASE (TARGET EFI-502312) FROM OCEANICOLA GRANULOSUS, WITH BOUND AMP/ADP CRYSTAL FORM I | PUTATIVE SUGAR KINASE, ENZYME FUNCTION INITIATIVE, EFI, STRUCTURAL GENOMICS, TRANSFERASE
3puz:B (SER3) to (SER19) CRYSTAL STRUCTURE OF A PRE-TRANSLOCATION STATE MBP-MALTOSE TRANSPORTER COMPLEX BOUND TO AMP-PNP | ATP BINDING CASSETTE, NUCLEOTIDE BINDING DOMAIN, SUBSTRATE BINDING PROTEIN, ABC TRANSPORTER, IMPORTER, ATPASE, ATP BINDING, MALTODEXTRIN BINDING, TRANSMEMBRANE INTEGRAL MEMBRANE, TRANSPORT PROTEIN, MEMBRANE PROTEIN
4ehk:A (PHE114) to (ASP135) ALLOSTERIC MODULATION OF CASPASE-3 THROUGH MUTAGENESIS | CASPASE, APOPTOSIS, ALLOSTERIC INHIBITION, PROTEIN ENSEMBLES, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ehl:A (SER113) to (ASP135) ALLOSTERIC MODULATION OF CASPASE-3 THROUGH MUTAGENESIS | CASPASE, APOPTOSIS, ALLOSTERIC INHIBITION, PROTEIN ENSEMBLES, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3q27:A (ASN242) to (LEU263) CYRSTAL STRUCTURE OF HUMAN ALPHA-SYNUCLEIN (32-57) FUSED TO MALTOSE BINDING PROTEIN (MBP) | FUSION PROTEIN, AMYLOID, SUGAR BINDING PROTEIN, PROTEIN FIBRIL
5iqs:B (GLN145) to (ILE161) WELO5 BOUND TO FE(II), CL, AND 2-OXOGLUTARATE | METALLOENZYME HALOGENASE 2-OXOGLUTARATE, OXIDOREDUCTASE
5iqt:C (GLN145) to (ILE161) WELO5 BOUND TO FE(II), CL, 2-OXOGLUTARATE, AND 12-EPIFISCHERINDOLE U | METALLOENZYME HALOGENASE 2-OXOGLUTARATE, OXIDOREDUCTASE
5iu2:A (ASP126) to (GLY147) DISCOVERY OF IMIDAZOQUINOLINES AS A NOVEL CLASS OF POTENT, SELECTIVE AND IN VIVO EFFICACIOUS COT KINASE INHIBITORS | COT, TPL-2, MAP3K8, KINASE, INHIBITOR, COMPLEX, TRANSFERASE
5iu2:B (ASP126) to (GLY147) DISCOVERY OF IMIDAZOQUINOLINES AS A NOVEL CLASS OF POTENT, SELECTIVE AND IN VIVO EFFICACIOUS COT KINASE INHIBITORS | COT, TPL-2, MAP3K8, KINASE, INHIBITOR, COMPLEX, TRANSFERASE
4eu2:K (VAL12) to (LYS28) CRYSTAL STRUCTURE OF 20S PROTEASOME WITH NOVEL INHIBITOR K-7174 | PROTEASOME INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4eu2:Y (VAL12) to (LYS28) CRYSTAL STRUCTURE OF 20S PROTEASOME WITH NOVEL INHIBITOR K-7174 | PROTEASOME INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4eu2:2 (VAL12) to (GLY30) CRYSTAL STRUCTURE OF 20S PROTEASOME WITH NOVEL INHIBITOR K-7174 | PROTEASOME INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4eum:A (MET1) to (GLY25) CRYSTAL STRUCTURE OF A SUGAR KINASE (TARGET EFI-502132) FROM OCEANICOLA GRANULOSUS WITH BOUND AMP, CRYSTAL FORM II | PUTATIVE SUGAR KINASE, ENZYME FUNCTION INITIATIVE, EFI, STRUCTURAL GENOMICS, TRANSFERASE
5iy0:A (ASN169) to (ASP209) PFMCM N-TERMINAL DOMAIN DOUBLE HEXAMER | REPLICATION, DNA BINDING PROTEIN, REPLICATION DNA BINDING PROTEIN
5iy0:B (ASN169) to (ASP209) PFMCM N-TERMINAL DOMAIN DOUBLE HEXAMER | REPLICATION, DNA BINDING PROTEIN, REPLICATION DNA BINDING PROTEIN
5iy0:C (ASN169) to (ASP209) PFMCM N-TERMINAL DOMAIN DOUBLE HEXAMER | REPLICATION, DNA BINDING PROTEIN, REPLICATION DNA BINDING PROTEIN
5iy0:D (ASN169) to (ASP209) PFMCM N-TERMINAL DOMAIN DOUBLE HEXAMER | REPLICATION, DNA BINDING PROTEIN, REPLICATION DNA BINDING PROTEIN
5iy0:E (ASN169) to (ASP209) PFMCM N-TERMINAL DOMAIN DOUBLE HEXAMER | REPLICATION, DNA BINDING PROTEIN, REPLICATION DNA BINDING PROTEIN
5iy0:F (ASN169) to (ASP209) PFMCM N-TERMINAL DOMAIN DOUBLE HEXAMER | REPLICATION, DNA BINDING PROTEIN, REPLICATION DNA BINDING PROTEIN
3qe5:B (GLY1398) to (LYS1417) COMPLETE STRUCTURE OF STREPTOCOCCUS MUTANS ANTIGEN I/II CARBOXY- TERMINUS | DE-VARIANT IMMUNOGLOBULIN-LIKE FOLD, IGG-LIKE FOLD, ADHERENCE TO HUMAN TOOTH, SALIVARY AGGLUTININ, EXTRACELLULAR, STREPTOCOCCUS, ANTIGEN I/II, CELL ADHESION
5iyx:A (ASN580) to (LYS615) CRYSTAL STRUCTURE OF THE ARABIDOPSIS RECEPTOR KINASE HAESA IN COMPLEX WITH THE PEPTIDE HORMONE IDA AND THE CO-RECEPTOR SERK1 | MEMBRANE RECEPTOR KINASE, PEPTIDE HORMONE RECEPTOR, SIGNALING COMPLEX, PLANT DEVELOPMENT, ORGAN SHEDDING, SIGNALING PROTEIN
5j5j:A (ILE218) to (ASN236) CRYSTAL STRUCTURE OF A CHIMERA OF HUMAN DESMOCOLLIN-2 EC1 AND HUMAN DESMOGLEIN-2 EC2-EC5 | EXTRACELLULAR CADHERIN DOMAIN, CELL ADHESION, DESMOSOME, CELL SURFACE
3qjg:C (GLY137) to (VAL160) EPIDERMIN BIOSYNTHESIS PROTEIN EPID FROM STAPHYLOCOCCUS AUREUS | STRUCTURAL GENOMICS, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID, OXIDOREDUCTASE
3qjg:I (GLY137) to (ASN159) EPIDERMIN BIOSYNTHESIS PROTEIN EPID FROM STAPHYLOCOCCUS AUREUS | STRUCTURAL GENOMICS, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID, OXIDOREDUCTASE
3qjg:L (GLY137) to (VAL160) EPIDERMIN BIOSYNTHESIS PROTEIN EPID FROM STAPHYLOCOCCUS AUREUS | STRUCTURAL GENOMICS, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID, OXIDOREDUCTASE
5j7u:D (SER472) to (GLN508) FAUSTOVIRUS MAJOR CAPSID PROTEIN | VIRUS, CAPSID, DOUBLE JELLY-ROLL, VIRAL PROTEIN
3qnf:A (HIS99) to (PRO119) CRYSTAL STRUCTURE OF THE OPEN STATE OF HUMAN ENDOPLASMIC RETICULUM AMINOPEPTIDASE 1 ERAP1 | STRUCTURAL GENOMICS CONSORTIUM, SGC, GLYCOPROTEIN, METAL-BINDING, METALLOPROTEASE, PROTEASE, ADAPTIVE IMMUNITY, HYDROLASE
3qnf:B (HIS99) to (PRO119) CRYSTAL STRUCTURE OF THE OPEN STATE OF HUMAN ENDOPLASMIC RETICULUM AMINOPEPTIDASE 1 ERAP1 | STRUCTURAL GENOMICS CONSORTIUM, SGC, GLYCOPROTEIN, METAL-BINDING, METALLOPROTEASE, PROTEASE, ADAPTIVE IMMUNITY, HYDROLASE
4fdg:B (LYS134) to (GLU154) CRYSTAL STRUCTURE OF AN ARCHAEAL MCM FILAMENT | HYDROLASE
4fdg:A (LYS134) to (GLU154) CRYSTAL STRUCTURE OF AN ARCHAEAL MCM FILAMENT | HYDROLASE
4fdg:C (LYS134) to (GLU154) CRYSTAL STRUCTURE OF AN ARCHAEAL MCM FILAMENT | HYDROLASE
4fdg:D (LYS134) to (GLU154) CRYSTAL STRUCTURE OF AN ARCHAEAL MCM FILAMENT | HYDROLASE
4fdg:E (LYS134) to (GLU154) CRYSTAL STRUCTURE OF AN ARCHAEAL MCM FILAMENT | HYDROLASE
4fdl:A (CYS136) to (PRO158) CRYSTAL STRUCTURE OF CASPASE-7 | CYSTEINE PROTEASE, CENTRAL CAVITY, HYDROLASE
3qs1:A (GLU65) to (GLY82) CRYSTAL STRUCTURE OF KNI-10006 COMPLEX OF PLASMEPSIN I (PMI) FROM PLASMODIUM FALCIPARUM | ASPARTIC PROTEASE, MALARIA, KNI, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3qs1:B (GLU65) to (GLY82) CRYSTAL STRUCTURE OF KNI-10006 COMPLEX OF PLASMEPSIN I (PMI) FROM PLASMODIUM FALCIPARUM | ASPARTIC PROTEASE, MALARIA, KNI, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ffv:C (SER28) to (TRP46) CRYSTAL STRUCTURE OF DIPEPTIDYL PEPTIDASE IV (DPP4, DPP-IV, CD26) IN COMPLEX WITH 11A19 FAB | HYDROLASE, HYDROLASE-IMMUNE SYSTEM, INHIBITOR COMPLEX
5j92:B (ALA191) to (LEU209) CRYSTAL STRUCTURE OF A PUTATIVE ALPHA-KETOGLUTARATE DEPENDENT 2,4-D DIOXYGENASE FROM BURKHOLDERIA XENOVORANS | SSGCID, ALPHA-KETOGLUTARATE DEPENDENT DIOXYGENASE, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, OXIDOREDUCTASE
5j92:C (ALA191) to (LEU209) CRYSTAL STRUCTURE OF A PUTATIVE ALPHA-KETOGLUTARATE DEPENDENT 2,4-D DIOXYGENASE FROM BURKHOLDERIA XENOVORANS | SSGCID, ALPHA-KETOGLUTARATE DEPENDENT DIOXYGENASE, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, OXIDOREDUCTASE
5j92:D (ALA191) to (LEU209) CRYSTAL STRUCTURE OF A PUTATIVE ALPHA-KETOGLUTARATE DEPENDENT 2,4-D DIOXYGENASE FROM BURKHOLDERIA XENOVORANS | SSGCID, ALPHA-KETOGLUTARATE DEPENDENT DIOXYGENASE, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, OXIDOREDUCTASE
3r6l:C (CYS270) to (LEU293) CASPASE-2 T380A BOUND WITH AC-VDVAD-CHO | HYDROLASE, APOPTOSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3r7s:A (CYS270) to (LEU293) CRYSTAL STRUCTURE OF APO CASPASE2 | HYDROLASE, APOPTOSIS
5jc7:A (THR878) to (LYS906) CRYSTAL STRUCTURE OF CHICKEN MDA5 WITH 5'P 24-MER DSRNA AND ADP-MG2+ AT 2.75 A RESOLUTION. | INNATE IMMUNE PATTERN RECOGNITION RECEPTOR, RIG-I LIKE HELICASE, DSRNA DEPENDENT ATPASE, ZINC-CONTAINING CTD DOMAIN, IMMUNE SYSTEM
5jhr:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH THE PEPTIDIC EPOXYKETONE INHIBITOR 27 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5jhr:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH THE PEPTIDIC EPOXYKETONE INHIBITOR 27 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5jhr:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH THE PEPTIDIC EPOXYKETONE INHIBITOR 27 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5jhr:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH THE PEPTIDIC EPOXYKETONE INHIBITOR 27 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5jhs:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH THE PEPTIDIC EPOXYKETONE INHIBITOR 15 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5jhs:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH THE PEPTIDIC EPOXYKETONE INHIBITOR 15 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
3re8:A (ASN212) to (TYR230) STRUCTURAL AND KINETIC ANALYSIS OF THE BEEF LIVER CATALASE INTERACTING WITH NITRIC OXIDE | THE 5-COORDINATED HEME PROTEIN, DISPROPORTIONATION OF THE HYDROGEN PEROXIDE, OXIDOREDUCATASE, OXIDOREDUCTASE
3re8:C (MET211) to (TYR230) STRUCTURAL AND KINETIC ANALYSIS OF THE BEEF LIVER CATALASE INTERACTING WITH NITRIC OXIDE | THE 5-COORDINATED HEME PROTEIN, DISPROPORTIONATION OF THE HYDROGEN PEROXIDE, OXIDOREDUCATASE, OXIDOREDUCTASE
5jon:A (ASN-128) to (ASN-102) CRYSTAL STRUCTURE OF THE UNLIGANDED FORM OF HCN2 CNBD | HCN CHANNELS, CYCLIC NUCLEOTIDE REGULATED CHANNELS, CYCLIC NUCLEOTIDE BINDING DOMAIN, TRANSPORT PROTEIN
5jp4:A (PRO74) to (TRP107) CRYSTAL STRUCTURE OF S. POMBE DCP1 IN COMPLEX WITH THE DECAPPING ENHANCER EDC | EVH1, COMPLEX, MRNA, DECAPPING, HYDROLASE, PEPTIDE BINDING PROTEIN
3rj1:E (GLU159) to (ILE189) ARCHITECTURE OF THE MEDIATOR HEAD MODULE | MEDIATOR, RNA POLYMERAS II, POL II, RNAP, MED, HEAD MODULE, MEDIATOR HEAD, REGULATOR, HELICAL BUNDLE, TRANSCRIPTIONAL REGULATION, RNA POLYMERASE II, TBP, NUCLEUS, TRANSCRIPTION
3rj1:L (GLU159) to (ILE189) ARCHITECTURE OF THE MEDIATOR HEAD MODULE | MEDIATOR, RNA POLYMERAS II, POL II, RNAP, MED, HEAD MODULE, MEDIATOR HEAD, REGULATOR, HELICAL BUNDLE, TRANSCRIPTIONAL REGULATION, RNA POLYMERASE II, TBP, NUCLEUS, TRANSCRIPTION
3rj1:S (GLU159) to (ILE189) ARCHITECTURE OF THE MEDIATOR HEAD MODULE | MEDIATOR, RNA POLYMERAS II, POL II, RNAP, MED, HEAD MODULE, MEDIATOR HEAD, REGULATOR, HELICAL BUNDLE, TRANSCRIPTIONAL REGULATION, RNA POLYMERASE II, TBP, NUCLEUS, TRANSCRIPTION
4fwj:A (LYS48) to (ASN93) NATIVE STRUCTURE OF LSD2/AOF1/KDM1B IN SPACEGROUP OF I222 AT 2.9A | LSD2, FAD, HISTONE DEMETHYLASE, C4H2C2, CW, EPIGENETIC, OXIDOREDUCTASE
4fzc:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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
5jzm:A (ARG50) to (SER72) STRUCTURE OF WILD TYPE AMIDASE FROM VIBRIO CHOLERAE 0395 AT LOW TEMPARATURE AT 1.8 ANGSTROMS RESOLUTION. | HEAT SHOCK PROTEIN, LYASE
5jzm:E (ARG50) to (SER72) STRUCTURE OF WILD TYPE AMIDASE FROM VIBRIO CHOLERAE 0395 AT LOW TEMPARATURE AT 1.8 ANGSTROMS RESOLUTION. | HEAT SHOCK PROTEIN, LYASE
5jzo:A (ARG50) to (SER72) STRUCTURE OF WILD TYPE AMIDASE AT HIGH TEMPERATURE AT 2.5 ANGSTROM RESOLUTION | HEAT SHOCK PROTEIN, LYASE
4g4s:N (VAL12) to (GLY30) STRUCTURE OF PROTEASOME-PBA1-PBA2 COMPLEX | ALPHA BETA, NTN-HYDROLASE, PEPTIDE BINDING, HYDROLASE-CHAPERONE COMPLEX
4g8e:A (ASP167) to (SER187) CRYSTAL STRUCTURE OF CLONE18 TCR | TCR, T CELL, CD1B, GMM, LIPID RECOGNITION, IMMUNE SYSTEM
4gid:B (ASN341) to (PHE370) STRUCTURE OF BETA-SECRETASE COMPLEXED WITH INHIBITOR | ASPARTIC PROTEASE, BETA SECRETASE, APP, BACE, A-BETA, PROTEASE, MEMAPSIN, ALZHEIMER, DRUG DESIGN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5knn:B (LEU167) to (PRO186) EVOLUTIONARY GAIN OF ALANINE MISCHARGING TO NON-COGNATE TRNAS WITH A G4:U69 BASE PAIR | TRNA SYNTHETASE, LIGASE
5knn:F (LEU167) to (PRO186) EVOLUTIONARY GAIN OF ALANINE MISCHARGING TO NON-COGNATE TRNAS WITH A G4:U69 BASE PAIR | TRNA SYNTHETASE, LIGASE
4gqa:A (ARG207) to (GLU241) CRYSTAL STRUCTURE OF NAD BINDING OXIDOREDUCTASE FROM KLEBSIELLA PNEUMONIAE | STRUCTURAL GENOMICS, PSI-BIOLOGY, NEW YORK STRUCTURAL GENOMICS RESEARCH CONSORTIUM, NYSGRC, NAD(P)-BINDING ROSSMANN-FOLD DOMAIN, OXIDOREDUCTASE, NAD BINDING
4gqa:B (ARG207) to (GLU241) CRYSTAL STRUCTURE OF NAD BINDING OXIDOREDUCTASE FROM KLEBSIELLA PNEUMONIAE | STRUCTURAL GENOMICS, PSI-BIOLOGY, NEW YORK STRUCTURAL GENOMICS RESEARCH CONSORTIUM, NYSGRC, NAD(P)-BINDING ROSSMANN-FOLD DOMAIN, OXIDOREDUCTASE, NAD BINDING
4gqa:C (ARG207) to (GLU241) CRYSTAL STRUCTURE OF NAD BINDING OXIDOREDUCTASE FROM KLEBSIELLA PNEUMONIAE | STRUCTURAL GENOMICS, PSI-BIOLOGY, NEW YORK STRUCTURAL GENOMICS RESEARCH CONSORTIUM, NYSGRC, NAD(P)-BINDING ROSSMANN-FOLD DOMAIN, OXIDOREDUCTASE, NAD BINDING
4gqa:D (ARG207) to (GLU241) CRYSTAL STRUCTURE OF NAD BINDING OXIDOREDUCTASE FROM KLEBSIELLA PNEUMONIAE | STRUCTURAL GENOMICS, PSI-BIOLOGY, NEW YORK STRUCTURAL GENOMICS RESEARCH CONSORTIUM, NYSGRC, NAD(P)-BINDING ROSSMANN-FOLD DOMAIN, OXIDOREDUCTASE, NAD BINDING
5kum:A (HIS227) to (PRO245) CRYSTAL STRUCTURE OF INWARD RECTIFIER KIR2.2 K62W MUTANT IN COMPLEX WITH PIP2 | METAL TRANSPORT, KIR 2.2 K62W MUTANT STRUCTURE
5l52:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 14 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l52:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 14 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l52:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 14 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l52:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 14 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l54:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 16 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l54:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 16 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l54:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 16 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l54:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 16 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l55:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 18 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l55:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 18 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l55:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 18 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l55:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 18 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l5a:M (VAL20) to (GLY38) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; R57T) | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5l5a:X (VAL13) to (LYS29) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; R57T) | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5l5a:a (VAL20) to (GLY38) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; R57T) | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5l5b:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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:J (VAL13) to (LYS29) 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:X (VAL13) to (LYS29) 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
5l5j:J (VAL13) to (LYS29) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 14 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5j:M (VAL20) to (GLY38) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 14 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5j:X (VAL13) to (LYS29) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 14 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5j:a (VAL20) to (GLY38) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 14 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5l5o:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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:J (VAL13) to (LYS29) '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:M (VAL20) to (GLY38) '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:X (VAL13) to (LYS29) '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:a (VAL20) to (GLY38) '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:M (VAL20) to (GLY38) 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:a (VAL20) to (GLY38) 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:J (VAL13) to (LYS29) '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:X (VAL13) to (LYS29) '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:M (VAL20) to (GLY38) 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:a (VAL20) to (GLY38) 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:M (VAL20) to (GLY38) 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:a (VAL20) to (GLY38) 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:M (VAL20) to (GLY38) 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:a (VAL20) to (GLY38) 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:M (VAL20) to (GLY38) 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:a (VAL20) to (GLY38) 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:M (VAL20) to (GLY38) 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:a (VAL20) to (GLY38) 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:M (VAL20) to (GLY38) 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:a (VAL20) to (GLY38) 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:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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
5ldf:M (ASN241) to (ILE266) MALTOSE BINDING PROTEIN GENETICALLY FUSED TO DODECAMERIC GLUTAMINE SYNTHETASE | FUSION PROTEIN, CHIMERA, DODECAMER, SYMMETRIZED CONSTRUCT, LIGASE
5ldf:N (ASN241) to (ILE266) MALTOSE BINDING PROTEIN GENETICALLY FUSED TO DODECAMERIC GLUTAMINE SYNTHETASE | FUSION PROTEIN, CHIMERA, DODECAMER, SYMMETRIZED CONSTRUCT, LIGASE
5ldf:O (ASN241) to (ILE266) MALTOSE BINDING PROTEIN GENETICALLY FUSED TO DODECAMERIC GLUTAMINE SYNTHETASE | FUSION PROTEIN, CHIMERA, DODECAMER, SYMMETRIZED CONSTRUCT, LIGASE
5ldf:P (ASN241) to (ILE266) MALTOSE BINDING PROTEIN GENETICALLY FUSED TO DODECAMERIC GLUTAMINE SYNTHETASE | FUSION PROTEIN, CHIMERA, DODECAMER, SYMMETRIZED CONSTRUCT, LIGASE
5ldf:Q (ASN241) to (ILE266) MALTOSE BINDING PROTEIN GENETICALLY FUSED TO DODECAMERIC GLUTAMINE SYNTHETASE | FUSION PROTEIN, CHIMERA, DODECAMER, SYMMETRIZED CONSTRUCT, LIGASE
5ldf:R (ASN241) to (ILE266) MALTOSE BINDING PROTEIN GENETICALLY FUSED TO DODECAMERIC GLUTAMINE SYNTHETASE | FUSION PROTEIN, CHIMERA, DODECAMER, SYMMETRIZED CONSTRUCT, LIGASE
5ldf:S (ASN241) to (ILE266) MALTOSE BINDING PROTEIN GENETICALLY FUSED TO DODECAMERIC GLUTAMINE SYNTHETASE | FUSION PROTEIN, CHIMERA, DODECAMER, SYMMETRIZED CONSTRUCT, LIGASE
5ldf:T (ASN241) to (ILE266) MALTOSE BINDING PROTEIN GENETICALLY FUSED TO DODECAMERIC GLUTAMINE SYNTHETASE | FUSION PROTEIN, CHIMERA, DODECAMER, SYMMETRIZED CONSTRUCT, LIGASE
5ldf:U (ASN241) to (ILE266) MALTOSE BINDING PROTEIN GENETICALLY FUSED TO DODECAMERIC GLUTAMINE SYNTHETASE | FUSION PROTEIN, CHIMERA, DODECAMER, SYMMETRIZED CONSTRUCT, LIGASE
5ldf:V (ASN241) to (ILE266) MALTOSE BINDING PROTEIN GENETICALLY FUSED TO DODECAMERIC GLUTAMINE SYNTHETASE | FUSION PROTEIN, CHIMERA, DODECAMER, SYMMETRIZED CONSTRUCT, LIGASE
5ldf:W (ASN241) to (ILE266) MALTOSE BINDING PROTEIN GENETICALLY FUSED TO DODECAMERIC GLUTAMINE SYNTHETASE | FUSION PROTEIN, CHIMERA, DODECAMER, SYMMETRIZED CONSTRUCT, LIGASE
5ldf:X (ASN241) to (ILE266) MALTOSE BINDING PROTEIN GENETICALLY FUSED TO DODECAMERIC GLUTAMINE SYNTHETASE | FUSION PROTEIN, CHIMERA, DODECAMER, SYMMETRIZED CONSTRUCT, LIGASE
5lf0:L (ALA21) to (THR37) HUMAN 20S PROTEASOME COMPLEX WITH EPOXOMICIN AT 2.4 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lk5:J (ASP309) to (THR333) CRYSTAL STRUCTURE OF THE GLOBULAR DOMAIN OF HUMAN CALRETICULIN MUTANT D71K | CALCIUM-BINDING PROTEIN
5ln4:B (GLY43) to (GLY66) CRYSTAL STRUCTURE OF SELF-COMPLEMENTED PSAA, THE MAJOR SUBUNIT OF PH 6 ANTIGEN FROM YERSINIA PESTS, IN COMPLEX WITH CHOLINE | IG-LIKE FOLD, BETA SANDWICH, DONOR-STRAND COMPLEMENTATION, CELL ADHESION
5lrx:E (PRO206) to (PHE224) STRUCTURE OF A20 OTU DOMAIN BOUND TO UBIQUITIN | HYDROLASE, PROTEASE, DEUBIQUITINASE, OTU DOMAIN
5ltt:J (VAL13) to (LYS29) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; R57T)IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5ltt:M (VAL20) to (GLY38) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; R57T)IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5ltt:X (VAL13) to (LYS29) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; R57T)IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5ltt:a (VAL20) to (GLY38) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; R57T)IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5m3m:B (LEU130) to (PHE153) FREE MONOMERIC RNA POLYMERASE I AT 4.0A RESOLUTION | RNA POLYMERASE I, TRANSCRIPTION
5pep:A (VAL266) to (ASP291) X-RAY ANALYSES OF ASPARTIC PROTEASES. II. THREE-DIMENSIONAL STRUCTURE OF THE HEXAGONAL CRYSTAL FORM OF PORCINE PEPSIN AT 2.3 ANGSTROMS RESOLUTION | HYDROLASE(ACID PROTEINASE)
5sz9:B (ASN189) to (VAL225) STRUCTURE-BASED DESIGN OF A NEW SERIES OF N-PIPERIDIN-3-YLPYRIMIDINE- 5-CARBOXAMIDES AS RENIN INHIBITORS | PROTEIN-LIGAND COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5t0h:S (ALA21) to (THR37) STRUCTURAL BASIS FOR DYNAMIC REGULATION OF THE HUMAN 26S PROTEASOME | UBIQUITIN-PROTEASOME SYSTEM, AAA-ATPASE, HYDROLASE
1nbc:A (ASP50) to (ILE70) BACTERIAL TYPE 3A CELLULOSE-BINDING DOMAIN | CELLULOSE DEGRADATION, CELLULOSE-BINDING DOMAIN, CELLULOSOME, SCAFOLDIN
1nbc:B (ASP50) to (ILE70) BACTERIAL TYPE 3A CELLULOSE-BINDING DOMAIN | CELLULOSE DEGRADATION, CELLULOSE-BINDING DOMAIN, CELLULOSOME, SCAFOLDIN
3ed1:B (GLU111) to (SER130) CRYSTAL STRUCTURE OF RICE GID1 COMPLEXED WITH GA3 | ALPHA/BETA HYDROLASE, LIPASE, GIBBERELLIN SIGNALING PATHWAY, HYDROLASE, NUCLEUS, RECEPTOR, HYDROLASE RECEPTOR
2aug:A (LYS484) to (HIS501) CRYSTAL STRUCTURE OF THE GRB14 SH2 DOMAIN | PHOSPHORYLATION, SH2 DOMAIN, SIGNALING PROTEIN
4wmv:A (ASN45) to (LEU66) STRUCTURE OF MBP-MCL1 BOUND TO LIGAND 4 AT 2.4A | APOPTOSIS, PROTEIN-PROTEIN INTERACTION
4h4v:A (VAL74) to (GLY103) CRYSTAL STRUCTURE OF FERREDOXIN REDUCTASE, BPHA4 E175C/T176R/Q177G MUTANT (OXIDIZED FORM) | FLAVOPROTEIN, OXIDOREDUCTASE
4h4z:A (VAL74) to (GLY103) CRYSTAL STRUCTURE OF FERREDOXIN REDUCTASE, BPHA4 E175Q/T176R/Q177G MUTANT (OXIDIZED FORM) | FLAVOPROTEIN, OXIDOREDUCTASE
1nro:H (ARG206) to (TYR228) CRYSTALLOGRAPHIC STRUCTURES OF THROMBIN COMPLEXED WITH THROMBIN RECEPTOR PEPTIDES: EXISTENCE OF EXPECTED AND NOVEL BINDING MODES | SERINE PROTEINASE/RECEPTOR
1nuw:A (LYS1112) to (THR1134) FRUCTOSE-1,6-BISPHOSPHATASE COMPLEX WITH MAGNESIUM, FRUCTOSE-6- PHOSPHATE AND PHOSPHATE AT PH 9.6 | BISPHOSPHATASE, ALLOSTERIC ENZYMES, GLUCONEOGENESIS, HYDROLASE
3euf:B (GLN157) to (LYS179) CRYSTAL STRUCTURE OF BAU-BOUND HUMAN URIDINE PHOSPHORYLASE 1 | NUCLEOSIDE PHOSPHORYLASE, URIDINE RESCUE, 5- BENZYLACYCLOURIDINE, ALTERNATIVE SPLICING, GLYCOSYLTRANSFERASE, TRANSFERASE
4wzg:A (ASP184) to (ARG209) STRUCTURE OF HUMAN ATG101 | AUTOPHAGY, ULK1 COMPLEX, HORMA DOMAIN, ATG13 BINDING, PROTEIN BINDING
3s2v:B (PHE105) to (ALA136) CRYSTAL STRUCTURE OF THE LIGAND BINDING DOMAIN OF GLUK1 IN COMPLEX WITH AN ANTAGONIST (S)-1-(2'-AMINO-2'-CARBOXYETHYL)-3-[(2- CARBOXYTHIEN-3-YL)METHYL]THIENO[3,4-D]PYRIMIDIN-2,4-DIONE AT 2.5 A RESOLUTION | ANTAGONIST, IONOTROPIC GLUTAMATE RECEPTOR, MEMBRANE PROTEIN
2pbw:A (MET106) to (ALA136) CRYSTAL STRUCTURE OF THE LIGAND-BINDING CORE OF IGLUR5 IN COMPLEX WITH THE PARTIAL AGONIST DOMOIC ACID AT 2.5 A RESOLUTION | AGONIST COMPLEX, MEMBRANE PROTEIN
2pbw:B (MET106) to (ALA136) CRYSTAL STRUCTURE OF THE LIGAND-BINDING CORE OF IGLUR5 IN COMPLEX WITH THE PARTIAL AGONIST DOMOIC ACID AT 2.5 A RESOLUTION | AGONIST COMPLEX, MEMBRANE PROTEIN
3ses:A (ASN242) to (LEU263) CU-MEDIATED DIMER OF MALTOSE-BINDING PROTEIN A216H/K220H BY SYNTHETIC SYMMETRIZATION | METAL-MEDIATED SYNTHETIC SYMMETRIZATION, SYNTHETIC SYMMETRIZATION, SUGAR BINDING PROTEIN
1ojw:B (GLY161) to (ASP183) DECAY ACCELERATING FACTOR (CD55): THE STRUCTURE OF AN INTACT HUMAN COMPLEMENT REGULATOR. | REGULATOR OF COMPLEMENT PATHWAY, REGULATOR OF COMPLEMENT, DECAY ACCELERATION OF C3/C5 CONVERTASES, PATHOGEN RECEPTOR, SHORT CONSENSUS REPEAT DOMAINS
1ojy:A (GLY161) to (ASP183) DECAY ACCELERATING FACTOR (CD55): THE STRUCTURE OF AN INTACT HUMAN COMPLEMENT REGULATOR. | REGULATOR OF COMPLEMENT PATHWAY, REGULATOR OF COMPLEMENT, DECAY ACCELERATION OF C3/C5 CONVERTASES, PATHOGEN RECEPTOR, SHORT CONSENSUS REPEAT DOMAINS, PLASMA, GLYCOPROTEIN, MEMBRANE, GPI-ANCHOR
1ojy:B (GLY161) to (ASP183) DECAY ACCELERATING FACTOR (CD55): THE STRUCTURE OF AN INTACT HUMAN COMPLEMENT REGULATOR. | REGULATOR OF COMPLEMENT PATHWAY, REGULATOR OF COMPLEMENT, DECAY ACCELERATION OF C3/C5 CONVERTASES, PATHOGEN RECEPTOR, SHORT CONSENSUS REPEAT DOMAINS, PLASMA, GLYCOPROTEIN, MEMBRANE, GPI-ANCHOR
3sjg:A (LEU116) to (THR141) HUMAN GLUTAMATE CARBOXYPEPTIDASE II (E424A INACTIVE MUTANT ) IN COMPLEX WITH N-ACETYL-ASPARTYL-AMINOOCTANOIC ACID | HYDROLASE, METALLOPEPTIDASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4idj:A (LYS273) to (ASN293) S.AUREUS A-HEMOLYSIN MONOMER IN COMPLEX WITH FAB | HEMOLYSIN COMPLEX WITH FAB, CYTOLYTIC PROTEIN, FAB, SECRETED, IMMUNE SYSTEM
1oxs:C (ARG3) to (ALA20) CRYSTAL STRUCTURE OF GLCV, THE ABC-ATPASE OF THE GLUCOSE ABC TRANSPORTER FROM SULFOLOBUS SOLFATARICUS | ABC-ATPASE, ATP-BINDING CASSETTE, ATPASE, GLCV, SULFOLOBUS SOLFATARICUS, TRANSPORT PROTEIN
1oyv:A (GLU197) to (GLY219) CRYSTAL STRUCTURE OF TOMATO INHIBITOR-II IN A TERNARY COMPLEX WITH SUBTILISIN CARLSBERG | SERINE PROTEINASE INHIBITOR, TERNARY COMPLEX, MULTIDOMAIN INHIBITOR, POTATO II FAMILY, HYDROLASE
4xr8:A (ASN242) to (LEU263) CRYSTAL STRUCTURE OF THE HPV16 E6/E6AP/P53 TERNARY COMPLEX AT 2.25 A RESOLUTION | HUMAN PAPILLOMAVIRUS 16, E6 ONCOPROTEIN, UBIQUITIN-LIGASE E6AP, TUMOR SUPPRESSOR P53, P53 DEGRADATION, VIRAL PROTEIN-ANTITUMOR PROTEIN, VIRAL PROTEIN- ANTITUMOR PROTEIN COMPLEX
4xr8:B (ASN242) to (LEU263) CRYSTAL STRUCTURE OF THE HPV16 E6/E6AP/P53 TERNARY COMPLEX AT 2.25 A RESOLUTION | HUMAN PAPILLOMAVIRUS 16, E6 ONCOPROTEIN, UBIQUITIN-LIGASE E6AP, TUMOR SUPPRESSOR P53, P53 DEGRADATION, VIRAL PROTEIN-ANTITUMOR PROTEIN, VIRAL PROTEIN- ANTITUMOR PROTEIN COMPLEX
2cnk:A (SER113) to (ASP135) CRYSTAL STRUCTURES OF CASPASE-3 IN COMPLEX WITH AZA-PEPTIDE EPOXIDE INHIBITORS. | THIOL PROTEASE, PHOSPHORYLATION, CYSTEINE-PROTEASE, COMPLEX (PROTEASE-INHIBITOR), PROTEASE, EPOXIDES, TETRAMER, APOPTOSIS, HYDROLASE, AZA-PEPTIDE, EPOXYSUCCINYL, ICE, YAMA, CPP32, CLAN CD, AZA-ASP, ZYMOGEN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2ql7:A (PHE137) to (PRO158) CRYSTAL STRUCTURE OF CASPASE-7 WITH INHIBITOR AC-IEPD-CHO | CYSTEINE PROTEASE, APOPTOSIS, THIOL PROTEASE, ZYMOGEN, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4xtz:A (GLN231) to (SER258) MYCOBACTERIUM TUBERCULOSIS BIOTIN LIGASE COMPLEXED WITH BISUBSTRATE INHIBITOR 69 THAT HAS A FLUORINE IN PLACE OF THE RIBOSE 2'OH | BIOTIN-PROTEIN LIGASE, BISUBSTRATE INHIBITOR, LIGASE-LIGASE INHIBITOR COMPLEX
4xtz:B (GLY230) to (SER258) MYCOBACTERIUM TUBERCULOSIS BIOTIN LIGASE COMPLEXED WITH BISUBSTRATE INHIBITOR 69 THAT HAS A FLUORINE IN PLACE OF THE RIBOSE 2'OH | BIOTIN-PROTEIN LIGASE, BISUBSTRATE INHIBITOR, LIGASE-LIGASE INHIBITOR COMPLEX
4xu0:A (GLN231) to (SER258) MYCOBACTERIUM TUBERCULOSIS BIOTIN LIGASE COMPLEXED WITH BISUBSTRATE INHIBITOR 73 THAT HAS A 2'-METHYL ON THE RIBOSE | BIOTIN-PROTEIN LIGASE, BISUBSTRATE INHIBITOR, LIGASE-LIGASE INHIBITOR COMPLEX
4xu0:B (GLN231) to (SER258) MYCOBACTERIUM TUBERCULOSIS BIOTIN LIGASE COMPLEXED WITH BISUBSTRATE INHIBITOR 73 THAT HAS A 2'-METHYL ON THE RIBOSE | BIOTIN-PROTEIN LIGASE, BISUBSTRATE INHIBITOR, LIGASE-LIGASE INHIBITOR COMPLEX
1pm4:A (THR41) to (GLY68) CRYSTAL STRUCTURE OF YERSINIA PSEUDOTUBERCULOSIS-DERIVED MITOGEN (YPM) | JELLY ROLL FOLD, TOXIN
3gjq:A (SER113) to (ASP135) CASPASE-3 BINDS DIVERSE P4 RESIDUES IN PEPTIDES | ENZYME CATALYSIS, CYSTEINE PROTEASE, PROTEIN RECOGNITION, APOPTOSIS, CYTOPLASM, HYDROLASE, PHOSPHOPROTEIN, POLYMORPHISM, PROTEASE, S-NITROSYLATION, THIOL PROTEASE, ZYMOGEN
2d4q:B (LYS1717) to (LYS1731) CRYSTAL STRUCTURE OF THE SEC-PH DOMAIN OF THE HUMAN NEUROFIBROMATOSIS TYPE 1 PROTEIN | CRAL_TRIO, PH, TRITON X-100, BETA HAIRPIN, SEC14, SIGNALING PROTEIN
3gpt:M (VAL12) to (GLY30) 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:1 (VAL12) to (GLY30) 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
2r2d:A (PRO32) to (ASP58) STRUCTURE OF A QUORUM-QUENCHING LACTONASE (AIIB) FROM AGROBACTERIUM TUMEFACIENS | LACTONASE, N-ACYL HOMPSERINE LACTONE, DI-NUCLEAR ZINC CENTER, QUORUM QUENCHING, AIIB, PHOSPHATE, AGROBACTERIUM TUMEFACIENS, HYDROLASE
3tdd:J (VAL12) to (LYS28) 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:M (VAL12) to (GLY30) 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:X (VAL12) to (LYS28) 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:1 (VAL12) to (GLY30) 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
4y75:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAF-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y75:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAF-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y75:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAF-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y75:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAF-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8i:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8i:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8i:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8i:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8k:J (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH H-APLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8k:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH H-APLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8k:X (VAL13) to (LYS29) YEAST 20S PROTEASOME IN COMPLEX WITH H-APLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8k:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH H-APLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
2dkh:A (ALA98) to (ARG119) CRYSTAL STRUCTURE OF 3-HYDROXYBENZOATE HYDROXYLASE FROM COMAMONAS TESTOSTERONI, IN COMPLEX WITH THE SUBSTRATE | 3-HYDROXYBENZOATE HYDROXYLASE, FLAVOPROTEIN, MONOOXYGENASE, SUBSTRATE COMPLEX, OXIDOREDUCTASE
2dki:A (ALA98) to (ARG119) CRYSTAL STRUCTURE OF 3-HYDROXYBENZOATE HYDROXYLASE FROM COMAMONAS TESTOSTERONI, UNDER PRESSURE OF XENON GAS (12 ATM) | 3-HYDROXYBENZOATE HYDROXYLASE, FLAVOPROTEIN, MONOOXYGENASE, XENON DERIVATIVE, OXIDOREDUCTASE
2dmr:A (SER395) to (LYS421) DITHIONITE REDUCED DMSO REDUCTASE FROM RHODOBACTER CAPSULATUS | REDUCTASE, DMSO, MOLYBDOPTERIN, DITHIONITE, MONOXO
4y8p:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAL- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8p:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAL- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8p:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAL- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8p:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAL- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8r:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H116D MUTANT | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS
4y8r:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H116D MUTANT | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS
4ya5:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya5:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
3trs:B (GLY125) to (PRO143) THE CRYSTAL STRUCTURE OF ASPERGILLOGLUTAMIC PEPTIDASE FROM ASPERGILLUS NIGER | ASPERGILLOGLUTAMIC PEPTIDASE, GLUTAMIC PEPTIDASE, BETA SANDWICH STRUCTURE, HYDROLASE
3h1i:B (GLY20) to (GLU39) STIGMATELLIN AND ANTIMYCIN BOUND CYTOCHROME BC1 COMPLEX FROM CHICKEN | CYTOCHROME BC1, MEMBRANE PROTEIN, HEME PROTEIN, RIESKE IRON SULFUR PROTEIN, CYTOCHROME B, CYTOCHROME C1, COMPLEX III, MITOCHONDRIAL PROCESSING PROTEASE, UBIQUINONE, OXIDOREDUCTASE, REDOX ENZYME, RESPIRATORY CHAIN, STIGMATELLIN, ANTIMYCIN, ELECTRON TRANSPORT, HEME, IRON, MEMBRANE, METAL-BINDING, MITOCHONDRION, MITOCHONDRION INNER MEMBRANE, TRANSMEMBRANE, TRANSPORT, DISULFIDE BOND, IRON- SULFUR, TRANSIT PEPTIDE
3h1p:A (PHE137) to (PRO158) MATURE CASPASE-7 I213A WITH DEVD-CHO INHIBITOR BOUND TO ACTIVE SITE | PROTEASE, COMPENSATORY MECHANISM, APOPTOSIS, CELL DEATH, CYSTEINE PROTEASE, THIOL PROTEASE, ZYMOGEN, HYDROLASE-INHIBITOR COMPLEX
1qw7:A (SER30) to (THR45) STRUCTURE OF AN ENGINEERED ORGANOPHOSPHOROUS HYDROLASE WITH INCREASED ACTIVITY TOWARD HYDROLYSIS OF PHOSPHOTHIOLATE BONDS | ORGANOPHOSPHOROUS HYDROLASE, PHOSPHOTRIESTERASE, VX, RVX, 4- METHYLBENZYLPHOSPHONATE, MUTANT
1qw7:B (SER30) to (THR45) STRUCTURE OF AN ENGINEERED ORGANOPHOSPHOROUS HYDROLASE WITH INCREASED ACTIVITY TOWARD HYDROLYSIS OF PHOSPHOTHIOLATE BONDS | ORGANOPHOSPHOROUS HYDROLASE, PHOSPHOTRIESTERASE, VX, RVX, 4- METHYLBENZYLPHOSPHONATE, MUTANT
3hd8:A (TRP312) to (VAL330) CRYSTAL STRUCTURE OF THE TRITICUM AESTIVUM XYLANASE INHIBITOR-IIA IN COMPLEX WITH BACILLUS SUBTILIS XYLANASE | TWO BETA-BARREL DOMAIN, BETA-JELLY ROLL, HYDROLASE INHIBITOR- HYDROLASE COMPLEX, PROTEIN-PROTEIN COMPLEX, XYLAN DEGRADATION, GLYCOSIDASE, HYDROLASE
3hd8:C (TRP312) to (VAL330) CRYSTAL STRUCTURE OF THE TRITICUM AESTIVUM XYLANASE INHIBITOR-IIA IN COMPLEX WITH BACILLUS SUBTILIS XYLANASE | TWO BETA-BARREL DOMAIN, BETA-JELLY ROLL, HYDROLASE INHIBITOR- HYDROLASE COMPLEX, PROTEIN-PROTEIN COMPLEX, XYLAN DEGRADATION, GLYCOSIDASE, HYDROLASE
2v0z:O (ASN178) to (THR216) CRYSTAL STRUCTURE OF RENIN WITH INHIBITOR 10 (ALISKIREN) | GLYCOPROTEIN, INHIBITOR-COMPLEX, ASPARTYL PROTEASE, ZYMOGEN, PROTEASE, HYDROLASE, POLYMORPHISM, ALTERNATIVE SPLICING, HYDROLASE(ACID PROTEINASE), CLEAVAGE ON PAIR OF BASIC RESIDUES
1ree:A (ASP170) to (SER190) ENDO-1,4-BETA-XYLANASE II COMPLEX WITH 3,4-EPOXYBUTYL-BETA- D-XYLOSIDE | XYLANASE, XYLAN DEGRADATION, HYDROLASE
3unb:Z (SER21) to (THR37) 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:2 (SER21) to (THR37) 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
2fhh:C (GLY489) to (ASP504) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME IN COMPLEX WITH A PEPTIDYL BORONATE INHIBITOR MLN-273 | MULTI-SUBUNIT PROTEIN ASSEMBLY, INHIBITOR-COMPLEX, HYDROLASE
2fhh:G (GLY489) to (ASP504) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME IN COMPLEX WITH A PEPTIDYL BORONATE INHIBITOR MLN-273 | MULTI-SUBUNIT PROTEIN ASSEMBLY, INHIBITOR-COMPLEX, HYDROLASE
2fhh:J (GLY489) to (ASP504) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME IN COMPLEX WITH A PEPTIDYL BORONATE INHIBITOR MLN-273 | MULTI-SUBUNIT PROTEIN ASSEMBLY, INHIBITOR-COMPLEX, HYDROLASE
2fhh:P (GLY489) to (ASP504) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME IN COMPLEX WITH A PEPTIDYL BORONATE INHIBITOR MLN-273 | MULTI-SUBUNIT PROTEIN ASSEMBLY, INHIBITOR-COMPLEX, HYDROLASE
2fhh:R (GLY489) to (ASP504) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME IN COMPLEX WITH A PEPTIDYL BORONATE INHIBITOR MLN-273 | MULTI-SUBUNIT PROTEIN ASSEMBLY, INHIBITOR-COMPLEX, HYDROLASE
2fhh:V (GLY489) to (ASP504) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME IN COMPLEX WITH A PEPTIDYL BORONATE INHIBITOR MLN-273 | MULTI-SUBUNIT PROTEIN ASSEMBLY, INHIBITOR-COMPLEX, HYDROLASE
2fhh:2 (GLY489) to (ASP504) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME IN COMPLEX WITH A PEPTIDYL BORONATE INHIBITOR MLN-273 | MULTI-SUBUNIT PROTEIN ASSEMBLY, INHIBITOR-COMPLEX, HYDROLASE
3v4h:A (GLY76) to (PHE101) CRYSTAL STRUCTURE OF A TYPE VI SECRETION SYSTEM EFFECTOR FROM YERSINIA PESTIS | STRUCTURAL GENOMICS, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID, UNKNOWN FUNCTION
2vr4:A (LEU809) to (SER825) TRANSITION-STATE MIMICRY IN MANNOSIDE HYDROLYSIS: CHARACTERISATION OF TWENTY SIX INHIBITORS AND INSIGHT INTO BINDING FROM LINEAR FREE ENERGY RELATIONSHIPS AND 3-D STRUCTURE | LINEAR FREE ENERGY RELATIONSHIP, HYDROLASE, TRANSITION STATE MIMIC, MANNOSIDASE, GLYCOSIDE HYDROLASE
4kty:A (SER644) to (ASN662) FIBRIN-STABILIZING FACTOR WITH A BOUND LIGAND | TRANSGLUTAMINASE, COAGULATION, TRANSFERASE, ACYLTRANSFERASE, LIGAND, CALCIUM IONS, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
1gxo:A (SER591) to (TYR616) MUTANT D189A OF FAMILY 10 POLYSACCHARIDE LYASE FROM CELLVIBRIO CELLULOSA IN COMPLEX WITH TRIGALATURONIC ACID | LYASE, PECTATE, MECHANISM, ELIMINATION
2gh0:C (GLN185) to (ASP209) GROWTH FACTOR/RECEPTOR COMPLEX | CYSTINE-KNOT, HELIX BUNDLE, HORMONE-GROWTH FACTOR COMPLEX
4l2n:A (PRO44) to (TYR60) UNDERSTANDING EXTRADIOL DIOXYGENASE MECHANISM IN NAD+ BIOSYNTHESIS BY VIEWING CATALYTIC INTERMEDIATES - LIGAND-FREE STRUCTURE | BI-CUPIN IRON-BINDING, DIOXYGENASE, OXIDOREDUCTASE
2gqw:A (VAL74) to (GLY103) CRYSTAL STRUCTURE OF FERREDOXIN REDUCTASE, BPHA4 (OXIDIZED FORM) | FLAVOPROTEIN, OXIDOREDUCTASE
1hc1:A (GLY410) to (HIS453) CRYSTAL STRUCTURE OF HEXAMERIC HAEMOCYANIN FROM PANULIRUS INTERRUPTUS REFINED AT 3.2 ANGSTROMS RESOLUTION | OXYGEN TRANSPORT
4zvt:C (CYS436) to (PRO458) CASPASE-7 VARIANT 1 (V1) WITH REPROGRAMMED SUBSTRATE SPECIFICITY DUE TO Y230A/W232M/S234N SUBSTITUTIONS, BOUND TO VEID INHIBITOR. | DIRECTED EVOLUTION, PROTEASE, PEPTIDE INHIBITOR, DESIGNED ACTIVE SITE SPECIFICITY, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2h65:C (SER113) to (ASP135) CRYSTAL STRUSTURE OF CASPASE-3 WITH INHIBITOR AC-VDVAD-CHO | ENZYME CATALYSIS, CYSTEINE PROTEASE, APOPTOSIS, INDUCED FIT, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1ibz:D (ASN27) to (LYS55) RED COPPER PROTEIN NITROSOCYANIN FROM NITROSOMONAS EUROPAEA | RED COPPER, CUPREDOXIN, BETA HAIRPIN, NITROSOCYANIN, NITROSOMONAS EUROPAEA, METAL BINDING PROTEIN
5a5b:X (VAL7) to (GLY31) STRUCTURE OF THE 26S PROTEASOME-UBP6 COMPLEX | HYDROLASE, CONFORMATIONAL SWITCHING, PROTEIN DEGRADATION, PROTEOSTASIS, QUALITY CONTROL, UBP6, USP14
3j24:B (GLY161) to (ASP183) CRYOEM RECONSTRUCTION OF COMPLEMENT DECAY-ACCELERATING FACTOR | BLOOD GROUP ANTIGEN, COMPLEMENT PATHWAY, GLYCOPROTEIN, GPI-ANCHOR, IMMUNE RESPONSE, INNATE IMMUNITY, LIPOPROTEIN, MEMBRANE, SUSHI, IMMUNE SYSTEM
2inw:B (ARG17) to (ALA45) CRYSTAL STRUCTURE OF Q83JN9 FROM SHIGELLA FLEXNERI AT HIGH RESOLUTION. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET SFR137. | Q83JN9 X-RAY NESG SFR137, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, UNKNOWN FUNCTION
5akb:A (ALA743) to (MET759) MUTS IN COMPLEX WITH THE N-TERMINAL DOMAIN OF MUTL - CRYSTAL FORM 1 | DNA BINDING PROTEIN, HYDROLASE, DNA MISMATCH REPAIR, COMPLEX, SLIDING CLAMP, CROSSLINKING
1j71:A (VAL268) to (PHE289) STRUCTURE OF THE EXTRACELLULAR ASPARTIC PROTEINASE FROM CANDIDA TROPICALIS YEAST. | CANDIDA TROPICALIS ASPARTIC PROTEASE, SAPT1, HYDROLASE
2j32:A (PHE114) to (ASP135) THE ROLE OF LOOP BUNDLE HYDROGEN BONDS IN THE MATURATION AND ACTIVITY OF(PRO)CASPASE-3 | PRO-CASPASE3, THIOL PROTEASE, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2xln:B (ASP121) to (GLY165) CRYSTAL STRUCTURE OF A COMPLEX BETWEEN ACTINOMADURA R39 DD-PEPTIDASE AND A BORONATE INHIBITOR | HYDROLASE, PEPTIDOGLYCAN
2xln:C (ASP121) to (GLY165) CRYSTAL STRUCTURE OF A COMPLEX BETWEEN ACTINOMADURA R39 DD-PEPTIDASE AND A BORONATE INHIBITOR | HYDROLASE, PEPTIDOGLYCAN
1jxq:D (CYS230) to (VAL258) STRUCTURE OF CLEAVED, CARD DOMAIN DELETED CASPASE-9 | PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5bou:M (VAL20) to (GLY38) 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:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH A BETA1 / BETA2 SPECIFIC NON- PEPTIDIC SULFONAMIDE LIGAND | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, NON-COVALENT LIGAND, BINDING ANALYSIS
5bxl:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-G170A MUTANT | HYDROLASE, IMMUNODEFICIENCY, PROTEASOME, MUTANT, ASSEMBLY DEFECT
5bxl:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-G170A MUTANT | HYDROLASE, IMMUNODEFICIENCY, PROTEASOME, MUTANT, ASSEMBLY DEFECT
5bxn:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA2-G170A MUTANT IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, IMMUNODEFICIENCY, PROTEASOME, MUTANT, ASSEMBLY DEFECT
5bxn:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-G170A MUTANT IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, IMMUNODEFICIENCY, PROTEASOME, MUTANT, ASSEMBLY DEFECT
5bxn:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA2-G170A MUTANT IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, IMMUNODEFICIENCY, PROTEASOME, MUTANT, ASSEMBLY DEFECT
5bxn:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA2-G170A MUTANT IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, IMMUNODEFICIENCY, PROTEASOME, MUTANT, ASSEMBLY DEFECT
5bz0:A (ILE196) to (VAL225) CRYSTAL STRUCTURE OF IBV PAPAIN-LIKE PROTEASE PLPRO C101S MUTANT IN COMPLEX WITH UBIQUITIN | IBV, PAPAIN-LIKE PROTEASE, UBIQUITIN, DUB, HYDROLASE-PROTEIN BINDING COMPLEX
5c1c:A (GLY71) to (GLY89) CRYSTAL STRUCTURE OF THE PECTIN METHYLESTERASE FROM ASPERGILLUS NIGER IN DEGLYCOSYLATED FORM | PARALLEL BETA HELIX, PECTIN METHYLESTERASE, HYDROLASE
4no9:J (VAL13) to (LYS29) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-EPOXYKETONE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, EPOXYKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no9:M (VAL20) to (GLY38) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-EPOXYKETONE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, EPOXYKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no9:X (VAL13) to (LYS29) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-EPOXYKETONE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, EPOXYKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no9:a (VAL20) to (GLY38) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-EPOXYKETONE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, EPOXYKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1xdp:B (GLY431) to (THR457) CRYSTAL STRUCTURE OF THE E.COLI POLYPHOSPHATE KINASE IN COMPLEX WITH AMPPNP | E.COLI POLYPHOSPHATE KINASE, PPK, PPK COMPLEX WITH AMPPNP, AMPPNP, TRANSFERASE
5cgf:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-G48C MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5cgf:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-G48C MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5cim:B (SER228) to (THR250) STRUCTURE OF MYCOBACTERIUM THERMORESISTIBILE GLGE IN COMPLEX WITH MALTOSE (COCRYSTALLISATION WITH MALTOSE-1-PHOSPHATE) AT 3.32A RESOLUTION | GLGE, MALTOSE, GH13, MALTOSYLTRANSFERASE, TRANSFERASE
4a6a:F (GLY121) to (TRP141) A115V VARIANT OF DCTP DEAMINASE-DUTPASE FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH DTTP | HYDROLASE, DEOXY-RIBONUCLEOTIDE METABOLISM, DTTP INHIBITION
4a6a:H (GLY121) to (TRP141) A115V VARIANT OF DCTP DEAMINASE-DUTPASE FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH DTTP | HYDROLASE, DEOXY-RIBONUCLEOTIDE METABOLISM, DTTP INHIBITION
4a6a:I (GLY121) to (TRP141) A115V VARIANT OF DCTP DEAMINASE-DUTPASE FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH DTTP | HYDROLASE, DEOXY-RIBONUCLEOTIDE METABOLISM, DTTP INHIBITION
4a6a:K (GLY121) to (TRP141) A115V VARIANT OF DCTP DEAMINASE-DUTPASE FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH DTTP | HYDROLASE, DEOXY-RIBONUCLEOTIDE METABOLISM, DTTP INHIBITION
4a6a:L (GLY121) to (TRP141) A115V VARIANT OF DCTP DEAMINASE-DUTPASE FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH DTTP | HYDROLASE, DEOXY-RIBONUCLEOTIDE METABOLISM, DTTP INHIBITION
1xnw:C (SER60) to (TYR83) ACYL-COA CARBOXYLASE BETA SUBUNIT FROM S. COELICOLOR (PCCB), APO FORM #2, MUTANT D422I | POLYKETIDE; POLYKETIDE SYNTHASE; ACYL-COA CARBOXYLASE; CARBOXYLTRANSFERASE, LIGASE
4om9:A (ASN333) to (ASP350) X-RAY CRYSTAL STRUCTURE OF THE PASSENGER DOMAIN OF PLASMID ENCODED TOXIN, AN AUTROTANSPORTER ENTEROTOXIN FROM ENTEROAGGREGATIVE ESCHERICHIA COLI (EAEC) | BETA-HELIX, PEPTIDASE, ALPHA-FODRIN, HYDROLASE, EAEC, PLASMID ENCODED TOXIN(PET)
5cz4:M (VAL20) to (GLY38) YEAST 20S PROTEASOME AT 2.3 A RESOLUTION | HYDROLASE-HYDROLASE COMPLEX, UBIQUITIN-DEGRADATION SYSTEM, PROTEASOME, NTN-HYDROLASE, THR-PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5cz4:a (VAL20) to (GLY38) YEAST 20S PROTEASOME AT 2.3 A RESOLUTION | HYDROLASE-HYDROLASE COMPLEX, UBIQUITIN-DEGRADATION SYSTEM, PROTEASOME, NTN-HYDROLASE, THR-PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5cz7:M (VAL20) to (GLY38) 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:a (VAL20) to (GLY38) 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:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-L(-49)S-K33A MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cz8:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-L(-49)S-K33A MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cz9:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-D17N MUTANT IN COMPLEX WITH CARFILZOMIB; PROPEPTIDE EXPRESSED IN TRANS | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cz9:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-D17N MUTANT IN COMPLEX WITH CARFILZOMIB; PROPEPTIDE EXPRESSED IN TRANS | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cz9:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-D17N MUTANT IN COMPLEX WITH CARFILZOMIB; PROPEPTIDE EXPRESSED IN TRANS | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cz9:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-D17N MUTANT IN COMPLEX WITH CARFILZOMIB; PROPEPTIDE EXPRESSED IN TRANS | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4pab:A (ASN359) to (ILE388) CRYSTAL STRUCTURE OF THE PRECURSOR FORM OF RAT DMGDH COMPLEXED WITH TETRAHYDROFOLATE | DIMETHYLGLYCINE DEHYDROGENASE, RAT, TETRAHYDROFOLATE, OXIDOREDUCTASE
4pab:B (ASN359) to (ILE388) CRYSTAL STRUCTURE OF THE PRECURSOR FORM OF RAT DMGDH COMPLEXED WITH TETRAHYDROFOLATE | DIMETHYLGLYCINE DEHYDROGENASE, RAT, TETRAHYDROFOLATE, OXIDOREDUCTASE
3l3a:A (CYS381) to (GLY396) BACE-1 WITH THE AMINOPYRIDINE COMPOUND 32 | BETA-SECRETASE, BACE-1, INHIBITOR, AMINOPYRIDINE, ASPARTYL PROTEASE, DISULFIDE BOND, PROTEASE, TRANSMEMBRANE, HYDROLASE
1yu6:B (GLU197) to (THR216) CRYSTAL STRUCTURE OF THE SUBTILISIN CARLSBERG:OMTKY3 COMPLEX | PROTEIN PROTEINASE INHIBITOR, PROTEASE, HYDROLASE
4pqk:C (ASN242) to (LEU263) C-TERMINAL DOMAIN OF DNA BINDING PROTEIN | DNA BINDING PROTEIN
4pqk:D (ASN242) to (LEU263) C-TERMINAL DOMAIN OF DNA BINDING PROTEIN | DNA BINDING PROTEIN
3ak5:A (GLY393) to (ASN410) HEMOGLOBIN PROTEASE (HBP) PASSENGER MISSING DOMAIN-2 | AUTOTRANSPORTER, BETA HELIX, MUTANT, HYDROLASE
3ak5:C (SER372) to (SER391) HEMOGLOBIN PROTEASE (HBP) PASSENGER MISSING DOMAIN-2 | AUTOTRANSPORTER, BETA HELIX, MUTANT, HYDROLASE
5dqt:C (SER16) to (PRO45) CRYSTAL STRUCTURE OF CAS-DNA-22 COMPLEX | PROTEIN-DNA COMPLEX, HYDROLASE-DNA COMPLEX
5dqt:B (SER16) to (PRO45) CRYSTAL STRUCTURE OF CAS-DNA-22 COMPLEX | PROTEIN-DNA COMPLEX, HYDROLASE-DNA COMPLEX
5dqt:L (VAL15) to (PRO45) CRYSTAL STRUCTURE OF CAS-DNA-22 COMPLEX | PROTEIN-DNA COMPLEX, HYDROLASE-DNA COMPLEX
5dqt:K (MET17) to (PRO45) CRYSTAL STRUCTURE OF CAS-DNA-22 COMPLEX | PROTEIN-DNA COMPLEX, HYDROLASE-DNA COMPLEX
5dqt:J (MET17) to (PRO45) CRYSTAL STRUCTURE OF CAS-DNA-22 COMPLEX | PROTEIN-DNA COMPLEX, HYDROLASE-DNA COMPLEX
1zsh:A (ASP297) to (HIS353) CRYSTAL STRUCTURE OF BOVINE ARRESTIN-2 IN COMPLEX WITH INOSITOL HEXAKISPHOSPHATE (IP6) | NONVISUAL ARRESTINS, BETA-ARRESTINS, SIGNAL TRANSDUCTION, SIGNALING PROTEIN
5e64:C (PRO197) to (GLU232) HEMAGGLUTININ-ESTERASE-FUSION PROTEIN STRUCTURE OF INFLUENZA D VIRUS | INFLUENZA VIRUS, HEF, SURFACE, HYDROLASE
5e7c:B (GLU364) to (ILE381) MACROMOLECULAR DIFFRACTIVE IMAGING USING IMPERFECT CRYSTALS - BRAGG DATA | PHOTOSYSTEM II, XFEL, SFX, PHOTOSYNTHESIS
3lyy:B (ALA57) to (ASP70) CRYSTAL STRUCTURE OF THE MUCBP DOMAIN OF THE ADHESION PROTEIN PEPE_0118 FROM PEDIOCOCCUS PENTOSACEUS. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET ID PTR41A | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, CELL WALL, PEPTIDOGLYCAN-ANCHOR, CELL ADHESION
3m13:A (LYS310) to (ALA340) CRYSTAL STRUCTURE OF THE LYS265ARG PEG-CRYSTALLIZED MUTANT OF MONOMERIC SARCOSINE OXIDASE | FLAVOPROTEIN OXIDASE, FAD, OXIDOREDUCTASE, FLAVOPROTEIN
3m13:C (ARG311) to (ALA340) CRYSTAL STRUCTURE OF THE LYS265ARG PEG-CRYSTALLIZED MUTANT OF MONOMERIC SARCOSINE OXIDASE | FLAVOPROTEIN OXIDASE, FAD, OXIDOREDUCTASE, FLAVOPROTEIN
4b7f:A (GLN207) to (TRP226) STRUCTURE OF A LIGANDED BACTERIAL CATALASE | OXIDOREDUCTASE, NITRIC OXIDE, CATALASE INHIBITION
4b7f:B (GLN207) to (TRP226) STRUCTURE OF A LIGANDED BACTERIAL CATALASE | OXIDOREDUCTASE, NITRIC OXIDE, CATALASE INHIBITION
4b7f:C (GLN207) to (TRP226) STRUCTURE OF A LIGANDED BACTERIAL CATALASE | OXIDOREDUCTASE, NITRIC OXIDE, CATALASE INHIBITION
4b7f:D (GLN207) to (TRP226) STRUCTURE OF A LIGANDED BACTERIAL CATALASE | OXIDOREDUCTASE, NITRIC OXIDE, CATALASE INHIBITION
4qlv:J (VAL13) to (LYS29) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 17 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlv:X (VAL13) to (LYS29) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 17 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4bdr:B (MET534) to (ALA684) CRYSTAL STRUCTURE OF THE GLUK2 R775A LBD DIMER IN COMPLEX WITH KAINATE | METAL TRANSPORT, KAINATE RECEPTOR
3bdm:M (VAL12) to (GLY30) YEAST 20S PROTEASOME:GLIDOBACTIN A-COMPLEX | PROTEASOME, UBIQUITIN, PROTEOLYSIS, PATHOGEN, VIRULENCE FACTOR, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN
3bdm:0 (VAL12) to (GLY30) YEAST 20S PROTEASOME:GLIDOBACTIN A-COMPLEX | PROTEASOME, UBIQUITIN, PROTEOLYSIS, PATHOGEN, VIRULENCE FACTOR, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN
4que:A (SER113) to (ASP135) CASPASE-3 Y195FV266H | ALLOSTERIC NETWORK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw3:J (VAL13) to (LYS29) YCP BETA5-C63F MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw3:M (VAL20) to (GLY38) YCP BETA5-C63F MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw3:X (VAL13) to (LYS29) YCP BETA5-C63F MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw3:a (VAL20) to (GLY38) YCP BETA5-C63F MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw7:J (VAL13) to (LYS29) YCP BETA5-M45T MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw7:M (VAL20) to (GLY38) YCP BETA5-M45T MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw7:a (VAL20) to (GLY38) YCP BETA5-M45T MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwi:J (VAL13) to (LYS29) YCP BETA5-A49S-MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwi:M (VAL20) to (GLY38) YCP BETA5-A49S-MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwi:X (VAL13) to (LYS29) YCP BETA5-A49S-MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwi:a (VAL20) to (GLY38) YCP BETA5-A49S-MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3btv:A (SER227) to (PRO255) CRYSTAL STRUCTURE OF THE SUPER-REPRESSOR MUTANT OF GAL80P FROM SACCHAROMYCES CEREVISIAE; GAL80(S0)-[G301R] | EUKARYOTIC TRANSCRIPTION REPRESSOR, ACETYLATION, CARBOHYDRATE METABOLISM, DNA-BINDING, GALACTOSE METABOLISM, TRANSCRIPTION REGULATION
3btv:B (SER227) to (PRO255) CRYSTAL STRUCTURE OF THE SUPER-REPRESSOR MUTANT OF GAL80P FROM SACCHAROMYCES CEREVISIAE; GAL80(S0)-[G301R] | EUKARYOTIC TRANSCRIPTION REPRESSOR, ACETYLATION, CARBOHYDRATE METABOLISM, DNA-BINDING, GALACTOSE METABOLISM, TRANSCRIPTION REGULATION
4qz1:J (VAL13) to (LYS29) YCP BETA5-M45T MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz1:X (VAL13) to (LYS29) YCP BETA5-M45T MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5fga:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5fga:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5fgg:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-L(-49S)_D17N DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgg:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-L(-49S)_D17N DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgg:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-L(-49S)_D17N DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgg:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-L(-49S)_D17N DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgh:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) IN COMPLEX WITH MG132 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgh:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) IN COMPLEX WITH MG132 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgh:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) IN COMPLEX WITH MG132 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgh:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) IN COMPLEX WITH MG132 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgi:J (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA1-T1A BETA2-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgi:M (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA1-T1A BETA2-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgi:X (VAL13) to (LYS29) YEAST 20S PROTEASOME BETA1-T1A BETA2-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgi:a (VAL20) to (GLY38) YEAST 20S PROTEASOME BETA1-T1A BETA2-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4r67:1 (ALA21) to (THR37) HUMAN CONSTITUTIVE 20S PROTEASOME IN COMPLEX WITH CARFILZOMIB | HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4cel:A (SER90) to (GLY105) ACTIVE-SITE MUTANT D214N DETERMINED AT PH 6.0 WITH NO LIGAND BOUND IN THE ACTIVE SITE | CELLULOSE DEGRADATION, HYDROLASE, GLYCOSIDASE, GLYCOPROTEIN
4cel:B (SER90) to (GLY105) ACTIVE-SITE MUTANT D214N DETERMINED AT PH 6.0 WITH NO LIGAND BOUND IN THE ACTIVE SITE | CELLULOSE DEGRADATION, HYDROLASE, GLYCOSIDASE, GLYCOPROTEIN
4rur:M (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH THE ALKALOID INDOLO-PHAKELLIN (4) | PROTEASOME, ALKALOID, REVERSIBLE INHIBITION, DRUG DISCOVERY, HALOGEN BONDING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4rur:a (VAL20) to (GLY38) YEAST 20S PROTEASOME IN COMPLEX WITH THE ALKALOID INDOLO-PHAKELLIN (4) | PROTEASOME, ALKALOID, REVERSIBLE INHIBITION, DRUG DISCOVERY, HALOGEN BONDING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3nzx:M (VAL12) to (GLY30) 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:X (VAL12) to (LYS28) 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:1 (VAL12) to (GLY30) 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
3d82:C (GLY39) to (VAL55) CRYSTAL STRUCTURE OF A CUPIN-2 DOMAIN CONTAINING PROTEIN (SFRI_3543) FROM SHEWANELLA FRIGIDIMARINA NCIMB 400 AT 2.05 A RESOLUTION | STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, METAL BINDING PROTEIN
3d82:E (GLY39) to (VAL55) CRYSTAL STRUCTURE OF A CUPIN-2 DOMAIN CONTAINING PROTEIN (SFRI_3543) FROM SHEWANELLA FRIGIDIMARINA NCIMB 400 AT 2.05 A RESOLUTION | STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, METAL BINDING PROTEIN
5gjq:f (ARG1) to (ASP26) STRUCTURE OF THE HUMAN 26S PROTEASOME BOUND TO USP14-UBAL | PROTEIN COMPLEX, HUMAN PROTEASOME, HYDROLASE
3ogv:A (ARG706) to (THR740) COMPLEX STRUCTURE OF BETA-GALACTOSIDASE FROM TRICHODERMA REESEI WITH PETG | TIM BARREL DOMAIN, GLYCOSIDE HYDROLASE, FAMILY 35, GLYCOPROTEIN, HYDROLASE
4txj:A (ASP139) to (GLN162) CRYSTAL STRUCTURE OF URIDINE PHOSPHORYLASE FROM SCHISTOSOMA MANSONI IN COMPLEX WITH THYMIDINE | URIDINE PHOSPHORYLASE THYMIDINE, TRANSFERASE
4txj:B (ASP139) to (GLN162) CRYSTAL STRUCTURE OF URIDINE PHOSPHORYLASE FROM SCHISTOSOMA MANSONI IN COMPLEX WITH THYMIDINE | URIDINE PHOSPHORYLASE THYMIDINE, TRANSFERASE
4txj:C (ASP139) to (GLN162) CRYSTAL STRUCTURE OF URIDINE PHOSPHORYLASE FROM SCHISTOSOMA MANSONI IN COMPLEX WITH THYMIDINE | URIDINE PHOSPHORYLASE THYMIDINE, TRANSFERASE
4txj:D (ASP139) to (GLN162) CRYSTAL STRUCTURE OF URIDINE PHOSPHORYLASE FROM SCHISTOSOMA MANSONI IN COMPLEX WITH THYMIDINE | URIDINE PHOSPHORYLASE THYMIDINE, TRANSFERASE
3dy4:M (VAL12) to (GLY30) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH SPIROLACTACYSTIN | PROTEASOME, INHIBITOR, PROTEIN DEGRADATION, UBIQUITIN-PROTEASOME- PATHWAY, HYDROLASE, NUCLEUS, PROTEASE, THREONINE PROTEASE, PHOSPHOPROTEIN, ZYMOGEN
3dy4:1 (VAL12) to (GLY30) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH SPIROLACTACYSTIN | PROTEASOME, INHIBITOR, PROTEIN DEGRADATION, UBIQUITIN-PROTEASOME- PATHWAY, HYDROLASE, NUCLEUS, PROTEASE, THREONINE PROTEASE, PHOSPHOPROTEIN, ZYMOGEN
3pcx:A (PHE114) to (ASP135) CASPASE-3 E246A, K242A DOUBLE MUTANT | SALT BRIDGE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3pd1:A (PHE114) to (ASP135) CASPASE-3 K242A | SALT BRIDGE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5iab:A (PHE114) to (ASP135) CASPASE 3 V266D | ALLOSTERY, SATURATION MUTAGENESIS, CONFORMATIONAL SELECTION, NATIVE ENSEMBLE, PROTEIN SOLVATION, PROTEIN STRUCTURE, PROTEIN DYNAMICS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5ik4:A (GLY3082) to (ASN3100) LAMININ A2LG45 C-FORM, APO. | EXTRACELLULAR MATRIX, LIGAND BINDING, LG DOMAIN, STRUCTURAL PROTEIN
4fca:A (SER124) to (LYS146) THE CRYSTAL STRUCTURE OF A FUNCTIONALLY UNKNOWN CONSERVED PROTEIN FROM BACILLUS ANTHRACIS STR. AMES. | STRUCTURAL GENOMICS, THE CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID, NIAID, NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES, UNKNOWN FUNCTION
3qtl:C (GLU196) to (THR215) STRUCTURAL BASIS FOR DUAL-INHIBITION MECHANISM OF A NON-CLASSICAL KAZAL-TYPE SERINE PROTEASE INHIBITOR FROM HORSESHOE CRAB IN COMPLEX WITH SUBTILISIN | SERINE PROTEASE -KAZAL TYPE SERINE PROTEASE INHIBITOR COMPLEX, HYDROLASE INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5jod:B (GLU67) to (GLY84) STRUCTURE OF PROPLASMEPSIN IV FROM PLASMODIUM FALCIPARUM | MALARIA, HYDROLASE
4fzg:M (VAL20) to (GLY38) 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:a (VAL20) to (GLY38) 20S YEAST PROTEASOME IN COMPLEX WITH GLIDOBACTIN | UBIQUITIN, PROTEASOME, DRUG DEVELOPMENT, INHIBITOR, NATURAL PRODUCT, N-TERMINAL NUCLEOPHILIC HYDROLASE, PROTEIN DEGRADATION, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5kai:b (GLN338) to (VAL356) NH3-BOUND RT XFEL STRUCTURE OF PHOTOSYSTEM II 500 MS AFTER THE 2ND ILLUMINATION (2F) AT 2.8 A RESOLUTION | PHOTOSYSTEMS, TRANSMEMBRANE, ROOM TEMPERATURE, ELECTRON TRANSPORT
4gk7:M (VAL11) to (GLY29) 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:a (VAL11) to (GLY29) 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
5l5e:J (VAL13) to (LYS29) 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:X (VAL13) to (LYS29) 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:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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:J (VAL13) to (LYS29) 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:X (VAL13) to (LYS29) 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:J (VAL13) to (LYS29) 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:M (VAL20) to (GLY38) 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:X (VAL13) to (LYS29) 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:a (VAL20) to (GLY38) 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:M (VAL20) to (GLY38) 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:a (VAL20) to (GLY38) 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