3e5q:A (HIS190) to (ASN218) UNBOUND OXIDISED CPRK | CPRK, HALORESPIRATION, TRANSCRIPTIONAL REGULATOR, TRANSCRIPTION REGULATION
3e6p:H (ASP125) to (ASN159) CRYSTAL STRUCTURE OF HUMAN MEIZOTHROMBIN DESF1 | THROMBIN, MEIZOTHROMBIN, ALLOSTERY, LINKAGE, NA+ BINDING, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN
1a2c:H (ASP125) to (ASN159) STRUCTURE OF THROMBIN INHIBITED BY AERUGINOSIN298-A FROM A BLUE-GREEN ALGA | HYDROLASE, SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1a3e:H (ASP125) to (ASN159) COMPLEX OF HUMAN ALPHA-THROMBIN WITH THE BIFUNCTIONAL BORONATE INHIBITOR BOROLOG2 | COMPLEX (SERINE PROTEASE-INHIBITOR), HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1a46:H (ASP125) to (ASN159) THROMBIN COMPLEXED WITH HIRUGEN AND A BETA-STRAND MIMETIC INHIBITOR | COMPLEX (SERINE PROTEASE-INHIBITOR), HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1a4w:H (ASP125) to (ASN159) CRYSTAL STRUCTURES OF THROMBIN WITH THIAZOLE-CONTAINING INHIBITORS: PROBES OF THE S1' BINDING SITE | SERINE PROTEASE-INHIBITOR, BLOOD COAGULATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2ocv:B (ASP125) to (ASN159) STRUCTURAL BASIS OF NA+ ACTIVATION MIMICRY IN MURINE THROMBIN | SERINE PROTEASE, HYDROLASE
2od3:B (ASP125) to (ASN159) HUMAN THROMBIN CHIMERA WITH HUMAN RESIDUES 184A, 186, 186A, 186B, 186C AND 222 REPLACED BY MURINE THROMBIN EQUIVALENTS. | SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3rml:H (ASP125) to (ASN159) HUMAN THROMBIN IN COMPLEX WITH MI331 | SERINE PROTEASE, KRINGLE, HYDROLASE, BLOOD COAGULATION, BLOOD CLOTTING, CONVERTION OF FIBRINOGEN TO FIBRIN, HIRUDIN, BLOOD, GLYCOSYLATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3rmm:H (ASP125) to (ASN159) HUMAN THROMBIN IN COMPLEX WITH MI332 | SERINE PROTEASE, KRINGLE, HYDROLASE, BLOOD COAGULATION, BLOOD CLOTTING, CONVERTION OF FIBRINOGEN TO FIBRIN, HIRUDIN, GLYCOSYLATION, BLOOD, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3rmn:H (ASP125) to (ASN159) HUMAN THROMBIN IN COMPLEX WITH MI341 | SERINE PROTEASE, KRINGLE, HYDROLASE, BLOOD COAGULATION, BLOOD CLOTTING, CONVERTION OF FIBRINOGEN TO FIBRIN, HIRUDIN, GLYCOSYLATION, BLOOD, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1a61:H (ASP125) to (ASN159) THROMBIN COMPLEXED WITH A BETA-MIMETIC THIAZOLE-CONTAINING INHIBITOR | COMPLEX (SERINE PROTEASE-INHIBITOR), HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1a6d:A (GLY20) to (SER61) THERMOSOME FROM T. ACIDOPHILUM | THERMOPLASMA ACIDOPHILUM, GROUP II CHAPERONIN, CCT, TRIC, PROTEIN FOLDING, ATPASE, CHAPERONIN
4gvq:B (SER3) to (ASP37) X-RAY STRUCTURE OF THE ARCHAEOGLOBUS FULGIDUS METHENYL- TETRAHYDROMETHANOPTERIN CYCLOHYDROLASE IN COMPLEX WITH TETRAHYDROMETHANPTERIN | TETRAHYDROMETHANOPTERIN, HYDROLASE
4wgi:A (PRO-42) to (GLY-14) A SINGLE DIASTEREOMER OF A MACROLACTAM CORE BINDS SPECIFICALLY TO MYELOID CELL LEUKEMIA 1 (MCL1) | FUSION PROTEIN, MBP, TRANSPORT PROTEIN, TRANSPORT PROTEIN-INHIBITOR COMPLEX, APOPTOSIS-INHIBITOR COMPLEX
1a8i:A (ASP421) to (MET441) SPIROHYDANTOIN INHIBITOR OF GLYCOGEN PHOSPHORYLASE | GLYCOGEN PHOSPHORYLASE, GLUCOPYRANOSE SPIROHYDANTOIN, WATER STRUCTURE, INHIBITOR BINDING, ANTI-HYPERGLYCEMIC AGENT
3rpu:H (ASP138) to (GLU175) CRYSTAL STRUCTURE OF THE MUKE-MUKF COMPLEX | KLEISIN, SMC-ASSOCIATED PROTEINS, CHROMOSOME CONDENSATION AND SEGREGATION, MUKB, CELL CYCLE
2okj:A (ALA374) to (LYS419) THE X-RAY CRYSTAL STRUCTURE OF THE 67KDA ISOFORM OF GLUTAMIC ACID DECARBOXYLASE (GAD67) | PLP-DEPENDENT DECARBOXYLASE, LYASE
1ad8:H (ASP125) to (ASN159) COMPLEX OF THROMBIN WITH AND INHIBITOR CONTAINING A NOVEL P1 MOIETY | COMPLEX (SERINE PROTEASE-INHIBITOR), HYDROLASE, SERINE PROTEASE, COAGULANT, INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3ee0:B (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THE W215A/E217A MUTANT OF HUMAN THROMBIN (SPACE GROUP P2(1)2(1)2(1)) | SERINE PROTEASE, ACUTE PHASE, BLOOD COAGULATION, CALCIUM, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PHARMACEUTICAL, POLYMORPHISM, PROTEASE, SECRETED, ZYMOGEN
1aht:H (ASP125) to (ASN159) CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN COMPLEXED WITH HIRUGEN AND P-AMIDINOPHENYLPYRUVATE AT 1.6 ANGSTROMS RESOLUTION | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1nkq:A (SER160) to (GLY185) CRYSTAL STRUCTURE OF YEAST YNQ8, A FUMARYLACETOACETATE HYDROLASE FAMILY PROTEIN | DIMER, PSI, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC, STRUCTURAL GENOMICS, UNKNOWN FUNCTION
1nkq:C (SER160) to (GLY185) CRYSTAL STRUCTURE OF YEAST YNQ8, A FUMARYLACETOACETATE HYDROLASE FAMILY PROTEIN | DIMER, PSI, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC, STRUCTURAL GENOMICS, UNKNOWN FUNCTION
1nkq:F (SER460) to (GLY485) CRYSTAL STRUCTURE OF YEAST YNQ8, A FUMARYLACETOACETATE HYDROLASE FAMILY PROTEIN | DIMER, PSI, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC, STRUCTURAL GENOMICS, UNKNOWN FUNCTION
1nl3:B (ALA231) to (HIS263) CRYSTAL STRUCTURE OF THE SECA PROTEIN TRANSLOCATION ATPASE FROM MYCOBACTERIUM TUBERCULOSIS IN APO FORM | PREPROTEIN TRANSLOCATION, ATPASE, TRANSMEMBRANE TRANSPORT, HELICASE-LIKE MOTOR DOMAIN, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, TB STRUCTURAL GENOMICS CONSORTIUM, TBSGC, PROTEIN TRANSPORT
4wm7:A (SER165) to (PRO185) CRYSTAL STRUCTURE OF HUMAN ENTEROVIRUS D68 IN COMPLEX WITH PLECONARIL | ENTEROVIRUS, CAPSID, BETA JELLY ROLL, VIRUS, CAPSID-BINDING INHIBITOR
4wms:A (PRO-42) to (GLY-14) STRUCTURE OF APO MBP-MCL1 AT 1.9A | APOPTOSIS, PROTEIN-PROTEIN INTERACTION, CHIMERA PROTEIN
4h0e:B (ARG41) to (VAL67) CRYSTAL STRUCTURE OF MUTANT ORR3 IN COMPLEX WITH NTD OF ARAR | WINGED HELIX TURN HELIX, TRANSCRIPTION FACTOR, DNA, TRANSCRIPTION-DNA COMPLEX
3rwr:T (MET1) to (LEU24) CRYSTAL STRUCTURE OF THE HUMAN XRCC4-XLF COMPLEX | COMPLEX-FILAMENT, NON-HOMOLOGOUS END-JOINING, DNA AND PROTEIN BINDING, DNA BINDING PROTEIN-PROTEIN BINDING COMPLEX
1noi:B (VAL422) to (MET441) COMPLEX OF GLYCOGEN PHOSPHORYLASE WITH A TRANSITION STATE ANALOGUE NOJIRIMYCIN TETRAZOLE AND PHOSPHATE IN THE T AND R STATES | GLYCOGEN PHOSPHORYLASE, TRANSFERASE, GLYCOSYLTRANSFERASE
2oqi:A (ASN497) to (ILE529) HUMAN DIPEPTIDYL PEPTIDASE IV (DPP4) WITH PIPERIDINONE- CONSTRAINED PHENETHYLAMINE | SERINE-PEPTIDASE, INHIBITOR, HYDROLASE
2oqi:B (ASN497) to (ILE529) HUMAN DIPEPTIDYL PEPTIDASE IV (DPP4) WITH PIPERIDINONE- CONSTRAINED PHENETHYLAMINE | SERINE-PEPTIDASE, INHIBITOR, HYDROLASE
4wq6:B (ASN316) to (PRO345) THE CRYSTAL STRUCTURE OF HUMAN NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE (NAMPT) IN COMPLEX WITH N-(4-{(S)-[1-(2-METHYLPROPYL)PIPERIDIN-4- YL]SULFINYL}BENZYL)FURO[2,3-C]PYRIDINE-2-CARBOXAMIDE INHIBITOR (COMPOUND 21) | TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4h2x:A (GLY219) to (ARG258) CRYSTAL STRUCTURE OF ENGINEERED BRADYRHIZOBIUM JAPONICUM GLYCINE:[CARRIER PROTEIN] LIGASE COMPLEXED WITH CARRIER PROTEIN FROM AGROBACTERIUM TUMEFACIENS AND AN ANALOGUE OF GLYCYL ADENYLATE | LIGASE, ATP BINDING, GLYCINE BINDING, CARRIER PROTEIN, AMINOACYL-TRNA SYNTHETASE, SERYL-TRNA SYNTHETASE
1aqi:A (ARG323) to (TRP345) STRUCTURE OF ADENINE-N6-DNA-METHYLTRANSFERASE TAQI | METHYLTRANSFERASE, TRANSFERASE, RESTRICTION SYSTEM
1aqi:B (ARG323) to (TRP345) STRUCTURE OF ADENINE-N6-DNA-METHYLTRANSFERASE TAQI | METHYLTRANSFERASE, TRANSFERASE, RESTRICTION SYSTEM
1aqj:A (ARG323) to (TRP345) STRUCTURE OF ADENINE-N6-DNA-METHYLTRANSFERASE TAQI | METHYLTRANSFERASE, TRANSFERASE, RESTRICTION SYSTEM, DNA METHYLATION, SINEFUNGIN
1nrr:H (ASP125) to (ASN159) CRYSTALLOGRAPHIC STRUCTURES OF THROMBIN COMPLEXED WITH THROMBIN RECEPTOR PEPTIDES: EXISTENCE OF EXPECTED AND NOVEL BINDING MODES | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, BLOOD CLOTTING
2b5t:D (ASP125) to (ASN159) 2.1 ANGSTROM STRUCTURE OF A NONPRODUCTIVE COMPLEX BETWEEN ANTITHROMBIN, SYNTHETIC HEPARIN MIMETIC SR123781 AND TWO S195A THROMBIN MOLECULES | BLOOD COAGULATION, BLOOD CLOTTING
1nu9:A (ASP125) to (ASN159) STAPHYLOCOAGULASE-PRETHROMBIN-2 COMPLEX | THROMBIN NON-PROTEOLYTIC ACTIVATOR, ENDOCARDITIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEIN BINDING
1nug:B (HIS148) to (GLY178) 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
2oz6:A (LEU10) to (GLY35) CRYSTAL STRUCTURE OF VIRULENCE FACTOR REGULATOR FROM PSEUDOMONAS AERUGINOSA IN COMPLEX WITH CAMP | WINGED HELIX, HELIX-TURN-HELIX, TRANSCRIPTION FACTOR, CAMP-BINDING PROTEINS, CAMP RECEPTOR PROTEIN, NUCLEOTIDE BINDING PROTEINS, DNA- BINDING PROTEINS, DNA BINDING PROTEIN
3epc:1 (THR177) to (PRO197) CRYOEM STRUCTURE OF POLIOVIRUS RECEPTOR BOUND TO POLIOVIRUS TYPE 1 | CD155 STRUCTURE IMMUNOGLOBULIN SUPERFAMILY, POLIOVIRUS CAPSID JELLY ROLE, CELL ADHESION, CELL MEMBRANE, GLYCOPROTEIN, HOST-VIRUS INTERACTION, IMMUNOGLOBULIN DOMAIN, MEMBRANE, RECEPTOR, SECRETED, TRANSMEMBRANE, VIRAL PROTEIN
3epm:A (PRO180) to (GLY209) CRYSTAL STRUCTURE OF CAULOBACTER CRESCENTUS THIC | ALPHA-BETA BARREL, SAM SUPERFAMILY, THIAMINE BIOSYNTHESIS, BIOSYNTHETIC PROTEIN
3epm:B (PRO180) to (GLY209) CRYSTAL STRUCTURE OF CAULOBACTER CRESCENTUS THIC | ALPHA-BETA BARREL, SAM SUPERFAMILY, THIAMINE BIOSYNTHESIS, BIOSYNTHETIC PROTEIN
3epo:A (PRO180) to (GLY209) CRYSTAL STRUCTURE OF CAULOBACTER CRESCENTUS THIC COMPLEXED WITH HMP-P | ALPHA-BETA BARREL, SAM SUPERFAMILY, THIAMINE BIOSYNTHESIS, BIOSYNTHETIC PROTEIN
3epo:B (PRO180) to (GLY209) CRYSTAL STRUCTURE OF CAULOBACTER CRESCENTUS THIC COMPLEXED WITH HMP-P | ALPHA-BETA BARREL, SAM SUPERFAMILY, THIAMINE BIOSYNTHESIS, BIOSYNTHETIC PROTEIN
2b8k:A (SER754) to (ASN802) 12-SUBUNIT RNA POLYMERASE II | DNA-DIRECTED RNA POLYMERASE, DNA-DEPENDENT RNA POLYMERASE, CELLULAR RNA POLYMERASE, METAL-BINDING, NUCLEAR PROTEIN, TRANSCRIPTION, TRANSFERASE
1ny1:B (GLY45) to (GLY75) CRYSTAL STRUCTURE OF B. SUBTILIS POLYSACCHARIDE DEACETYLASE NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET SR127. | STRUCTURAL GENOMICS, POLYSACCHARIDE DEAC, PSI, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, UNKNOWN FUNCTION
1b5g:H (ASP125) to (ASN159) HUMAN THROMBIN COMPLEXED WITH NOVEL SYNTHETIC PEPTIDE MIMETIC INHIBITOR AND HIRUGEN | SERINE PROTEASE-INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3etr:B (LEU361) to (THR382) CRYSTAL STRUCTURE OF XANTHINE OXIDASE IN COMPLEX WITH LUMAZINE | PROTEIN-LIGAND COMPLEX, ENZYME CATALYSIS, SUBSTRATE ORIENTATION, FAD, FLAVOPROTEIN, IRON, IRON-SULFUR, METAL-BINDING, MOLYBDENUM, NAD, OXIDOREDUCTASE, PEROXISOME
4wyk:A (GLY504) to (ASN538) STRUCTURE OF THE LRR AND NTF2-LIKE DOMAINS OF NXF1 COMPLEXED WITH NXT1 | NUCLEAR EXPORT, TRANSPORT PROTEIN
1b7x:B (ASP125) to (ASN159) STRUCTURE OF HUMAN ALPHA-THROMBIN Y225I MUTANT BOUND TO D- PHE-PRO-ARG-CHLOROMETHYLKETONE | SERINE PROTEASE, HYDROLASE/HYDROLASE INHIBITOR COMPLEX
1bbr:N (ASP125) to (ASN159) THE STRUCTURE OF RESIDUES 7-16 OF THE A ALPHA CHAIN OF HUMAN FIBRINOGEN BOUND TO BOVINE THROMBIN AT 2.3 ANGSTROMS RESOLUTION | SERINE PROTEASE
1bcu:H (ASP125) to (ASN159) ALPHA-THROMBIN COMPLEXED WITH HIRUGEN AND PROFLAVIN | COMPLEX (SERINE PROTEASE INHIBITOR), HYDROLASE, SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4hk5:A (PRO18) to (LEU47) CRYSTAL STRUCTURE OF CORDYCEPS MILITARIS IDCASE IN APO FORM | PYRIMIDINE METABOLISM, DNA DECARBOXYLATION, IDCASE, DECARBOXYLASE, URACIL, LYASE
1o2f:A (ASP94) to (ASP123) COMPLEX OF ENZYME IIAGLC AND IIBGLC PHOSPHOCARRIER PROTEIN HPR FROM ESCHERICHIA COLI NMR, RESTRAINED REGULARIZED MEAN STRUCTURE | PHOSPHOTRANSFERASE, TRANSFERASE, KINASE, SUGAR TRANSPORT, COMPLEX (TRANSFERASE/PHOSPHOCARRIER)
1o2g:H (ASP125) to (ASN159) ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS | SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, BLOOD CLOTTING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, BLOOD CLOTTING, HYDROLASE-INHIBITOR COMPLEX
2bmf:A (THR408) to (LEU443) DENGUE VIRUS RNA HELICASE AT 2.4A | HYDROLASE, NUCLEOSIDE TRIPHOSPHATASE
4hnp:T (PHE18) to (THR51) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH VINYLKETONE CARMAPHYCIN ANALOGUE VNK1 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1o5l:A (ASP2) to (LYS22) CRYSTAL STRUCTURE OF TRANSCRIPTIONAL REGULATOR (TM1171) FROM THERMOTOGA MARITIMA AT 2.30 A RESOLUTION | TM1171, TRANSCRIPTIONAL REGULATOR, CRP FAMILY, STRUCTURAL GENOMICS, JCSG, PSI, PROTEIN STRUCTURE INITIATIVE, JOINT CENTER FOR STRUCTURAL GENOMICS, TRANSCRIPTION
3s7k:D (ASP125) to (ASN159) STRUCTURE OF THROMBIN MUTANT Y225P IN THE E FORM | SERINE PROTEASE, HYDROLASE
4x6z:G (PHE21) to (THR54) YEAST 20S PROTEASOME IN COMPLEX WITH PR-VI MODULATOR | 20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE
4x6z:U (PHE21) to (THR54) YEAST 20S PROTEASOME IN COMPLEX WITH PR-VI MODULATOR | 20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE
4hqm:B (THR48) to (TYR79) THE CRYSTAL STRUCTURE OF QSRR-MENADIONE COMPLEX | MENADIONE-MODIFIED PROTEIN, DNA, TRANSCRIPTION REGULATOR
4hrc:C (PHE16) to (GLU45) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE CARMAPHYCIN ANALOGUE 3 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4hrc:T (PHE18) to (THR51) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE CARMAPHYCIN ANALOGUE 3 | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4hrd:Q (PHE16) to (THR49) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH THE NATURAL PRODUCT CARMAPHYCIN A | PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4hri:B (SER179) to (PHE207) CRYSTAL STRUCTURE OF HETR IN COMPLEX WITH A 21-BP PALINDROMIC DNA AT THE UPSTREAM OF THE HETP PROMOTER FROM ANABAENA | CYANOBACTERIA, TRANSCRIPTIONAL FACTOR, HETEROCYST DIFFERENTIATION, HELIX-TURN-HELIX DNA-BINDING MOTIF, TRANSCRIPTION-DNA COMPLEX
2pfl:A (GLY528) to (GLY561) CRYSTAL STRUCTURE OF PFL FROM E.COLI | GLYCYL RADICAL ENZYME, TRANSFERASE, GLUCOSE METABOLISM, LYASE
2pfl:A (ARG712) to (ARG738) CRYSTAL STRUCTURE OF PFL FROM E.COLI | GLYCYL RADICAL ENZYME, TRANSFERASE, GLUCOSE METABOLISM, LYASE
2pfl:B (ARG712) to (ARG738) CRYSTAL STRUCTURE OF PFL FROM E.COLI | GLYCYL RADICAL ENZYME, TRANSFERASE, GLUCOSE METABOLISM, LYASE
2bvr:H (ASP125) to (ASN159) HUMAN THROMBIN COMPLEXED WITH FRAGMENT-BASED SMALL MOLECULES OCCUPYING THE S1 POCKET | SERINE PROTEASE, COAGULATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1of6:B (LEU208) to (LYS239) CRYSTAL STRUCTURE OF THE TYROSINE-REGULATED 3-DEOXY-D-ARABINO-HEPTULOSONATE-7-PHOSPHATE SYNTHASE FROM SACCHAROMYCES CEREVISIAE COMPLEXED WITH TYROSINE AND MANGANESE | BETA-ALPHA-BARREL, LYASE, SYNTHASE, ALDOLASE, SYNTHETASE
1of6:F (LEU208) to (LYS239) CRYSTAL STRUCTURE OF THE TYROSINE-REGULATED 3-DEOXY-D-ARABINO-HEPTULOSONATE-7-PHOSPHATE SYNTHASE FROM SACCHAROMYCES CEREVISIAE COMPLEXED WITH TYROSINE AND MANGANESE | BETA-ALPHA-BARREL, LYASE, SYNTHASE, ALDOLASE, SYNTHETASE
1c1u:H (ASP125) to (ASN164) RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES | ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS, PH DEPENDENCE, ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN, SERINE PROTEASE/INHIBITOR, BLOOD CLOTTING-HYDROLASE INHIBITOR COMPLEX
1c1w:H (ASP125) to (ASN164) RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES | ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS, PH DEPENDENCE, ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN, SERINE PROTEASE/INHIBITOR, BLOOD CLOTTING,HYDROLASE-HYDROLASE INHIBITOR COMPLEX, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
2bxt:H (ASP125) to (ASN159) DESIGN AND DISCOVERY OF NOVEL, POTENT THROMBIN INHIBITORS WITH A SOLUBILIZING CATIONIC P1-P2-LINKER | SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2plv:1 (THR177) to (PRO197) STRUCTURAL FACTORS THAT CONTROL CONFORMATIONAL TRANSITIONS AND SEROTYPE SPECIFICITY IN TYPE 3 POLIOVIRUS | PICORNAVIRUS, ICOSAHEDRAL VIRUS, VIRUS
3sdk:Q (PHE22) to (THR55) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 34 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3ffe:B (PRO549) to (PRO584) STRUCTURE OF ACHROMOBACTIN SYNTHETASE PROTEIN D, (ACSD) | ACSD, ADENYLATING ENZYME, SIDEROPHORE, STRUCTURAL GENOMICS, SCOTTISH STRUCTURAL PROTEOMICS FACILITY, SSPF, BIOSYNTHETIC PROTEIN
1c3o:A (ALA511) to (SER545) CRYSTAL STRUCTURE OF THE CARBAMOYL PHOSPHATE SYNTHETASE: SMALL SUBUNIT MUTANT C269S WITH BOUND GLUTAMINE | AMIDOTRANSFERASE, MICHAELIS COMPLEX, ATP-GRASP, LIGASE
1c3o:E (ALA511) to (SER545) CRYSTAL STRUCTURE OF THE CARBAMOYL PHOSPHATE SYNTHETASE: SMALL SUBUNIT MUTANT C269S WITH BOUND GLUTAMINE | AMIDOTRANSFERASE, MICHAELIS COMPLEX, ATP-GRASP, LIGASE
1c4y:2 (ASP125) to (ASN159) SELECTIVE NON-ELECTROPHILIC THROMBIN INHIBITORS | COMPLEX (SERINE PROTEASE-INHIBITOR), HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4i3e:B (LEU6) to (THR44) CRYSTAL STRUCTURE OF STAPHYLOCOCCAL IMPASE - I COMPLEXED WITH PRODUCTS. | IMPASE SPECIFIC PENTA LAYERED SANDWICH, ALPHA/BETA STRUCTURE, FIG SUPERFAMILY, DUAL SPECIFIC IMPASE/NADP(H) PHOSPHATASE, MAGNESIUM BINDING, HYDROLASE
2c2w:B (TYR77) to (ALA121) THE FLUORINASE FROM STREPTOMYCES CATTLEYA IS ALSO A CHLORINASE. STRUCTURE OF 5'-CHLORO-5'-DEOXYADENOSINE CRYSTALLISED IN THE FLUORINASE. | FLUORINASE, 5'-CHLORO-5'-DEOXYADENOSINE, FLA, BACTERIAL FLUORINATING ENZYME, BACTERIAL CHLORINATING ENZYME, STREPTOMYCES CATTLEYA, TRANSFERASE, CHLORINASE
2c2w:C (TYR77) to (ALA121) THE FLUORINASE FROM STREPTOMYCES CATTLEYA IS ALSO A CHLORINASE. STRUCTURE OF 5'-CHLORO-5'-DEOXYADENOSINE CRYSTALLISED IN THE FLUORINASE. | FLUORINASE, 5'-CHLORO-5'-DEOXYADENOSINE, FLA, BACTERIAL FLUORINATING ENZYME, BACTERIAL CHLORINATING ENZYME, STREPTOMYCES CATTLEYA, TRANSFERASE, CHLORINASE
4i3y:A (LEU6) to (THR44) CRYSTAL STRUCTURE OF STAPHYLOCOCCAL INOSITOL MONOPHOSPHATASE-1: 100 MM LICL SOAKED INHIBITORY COMPLEX | INOSITOL MONOPHOSPHATASE, PENTA LAYER REPEAT OF ALPHA/BETA STRETCHES, MAGNESIUM BINDING, CYTOPLASMIC, HYDROLASE
4i3y:B (THR5) to (THR44) CRYSTAL STRUCTURE OF STAPHYLOCOCCAL INOSITOL MONOPHOSPHATASE-1: 100 MM LICL SOAKED INHIBITORY COMPLEX | INOSITOL MONOPHOSPHATASE, PENTA LAYER REPEAT OF ALPHA/BETA STRETCHES, MAGNESIUM BINDING, CYTOPLASMIC, HYDROLASE
4i40:A (LEU6) to (THR44) CRYSTAL STRUCTURE OF STAPHYLOCOCCAL INOSITOL MONOPHOSPHATASE-1: 50MM LICL INHIBITED COMPLEX | INOSITOL MONOPHOSPHATASE-1, LI INHIBITION, MAGNESIUM BINDING, CYTOPLASMIC, HYDROLASE
4xjq:A (GLU276) to (LYS305) THE CATALYTIC MECHANISM OF HUMAN PARAINFLUENZA VIRUS TYPE 3 HAEMAGGLUTININ-NEURAMINIDASE REVEALED | HYDROLASE, HUMAN PARAINFLUENZA VIRUS 3 HAEMAGGLUTININ-NEURAMINIDASE, VIRAL ENVELOPE PROTEIN
4xjq:B (GLU276) to (LYS305) THE CATALYTIC MECHANISM OF HUMAN PARAINFLUENZA VIRUS TYPE 3 HAEMAGGLUTININ-NEURAMINIDASE REVEALED | HYDROLASE, HUMAN PARAINFLUENZA VIRUS 3 HAEMAGGLUTININ-NEURAMINIDASE, VIRAL ENVELOPE PROTEIN
3slf:B (VAL182) to (VAL213) CRYSTAL STRUCTURE OF BA2930 IN COMPLEX WITH ACCOA AND URACIL | STRUCTURAL GENOMICS, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID, ACETYLTRANSFERASE, TRANSFERASE
2pw8:H (ASP125) to (ASN159) CRYSTAL STRUCTURE OF SULFO-HIRUDIN COMPLEXED TO THROMBIN | THROMBIN, HIRUDIN, SULFOTYROSINE, HYDROLASE
1oo0:A (GLN55) to (THR102) CRYSTAL STRUCTURE OF THE DROSOPHILA MAGO NASHI-Y14 COMPLEX | RNA RECOGNITION MOTIF, SPLICING, PROTEIN COMPLEX, EXON JUNCTION COMPLEX, SIGNALING PROTEIN
2px9:B (THR51) to (PRO79) THE INTRINSIC AFFINITY BETWEEN E2 AND THE CYS DOMAIN OF E1 IN UBIQUITIN-LIKE MODIFICATIONS | NMR, UBIQUITINATION, SUMO, E1, E2, UBC9, SAE2, PROTEIN- PROTEIN INTERACTION, PARAMAGNETIC SPIN-LABELING, PROTEIN BINDING
4i7y:H (ASP125) to (ASN159) CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH A 27-MER APTAMER BOUND TO EXOSITE II | PROTEIN-DNA COMPLEX, SERINE PROTEASE, BLOOD COAGULATION, APTAMER, HYDROLASE-HYDROLASE INHIBITOR-DNA COMPLEX, SERINE PROTEASE FOLD, DNA APTAMER, BLOOD, G-QUADRUPLEX, DUPLEX-QUADRUPLEX JUNCTION
2c4t:B (TYR77) to (ALA121) X-RAY CRYSTAL STRUCTURE OF 5'-FLUORODEOXYADENOSINE SYNTHASE FROM STREPTOMYCES CATTLEYA COMPLEXED WITH AN INHIBITOR, AN ANALOGUE OF S-ADENOSYL METHIONINE | TRANSFERASE, FLUORINASE, 5'-FLUORODEOXYADENOSINE SYNTHASE, FLA, INHIBITOR, AZA, STREPTOMYCES CATTLEYA, SAM ANALOGUE
2c5h:A (TYR77) to (ALA121) X-RAY CRYSTAL STRUCTURE OF 5'-FLUORODEOXYADENOSINE SYNTHASE FROM STREPTOMYCES CATTLEYA COMPLEXED WITH 2'DEOXY-ADENOSINE | TRANSFERASE, FLUORINASE, 5'-FLUORODEOXYADENOSINE SYNTHASE, FLA, INHIBITOR, AZA, STREPTOMYCES CATTLEYA, SAM ANALOGUE
2c5h:B (TYR77) to (ALA121) X-RAY CRYSTAL STRUCTURE OF 5'-FLUORODEOXYADENOSINE SYNTHASE FROM STREPTOMYCES CATTLEYA COMPLEXED WITH 2'DEOXY-ADENOSINE | TRANSFERASE, FLUORINASE, 5'-FLUORODEOXYADENOSINE SYNTHASE, FLA, INHIBITOR, AZA, STREPTOMYCES CATTLEYA, SAM ANALOGUE
2c5h:C (TYR77) to (ALA121) X-RAY CRYSTAL STRUCTURE OF 5'-FLUORODEOXYADENOSINE SYNTHASE FROM STREPTOMYCES CATTLEYA COMPLEXED WITH 2'DEOXY-ADENOSINE | TRANSFERASE, FLUORINASE, 5'-FLUORODEOXYADENOSINE SYNTHASE, FLA, INHIBITOR, AZA, STREPTOMYCES CATTLEYA, SAM ANALOGUE
1cm5:A (ARG712) to (ARG738) CRYSTAL STRUCTURE OF C418A,C419A MUTANT OF PFL FROM E.COLI | GLYCYL RADICAL ENZYME, TRANSFERASE, GLUCOSE METABOLISM
1cm5:B (ARG712) to (ARG738) CRYSTAL STRUCTURE OF C418A,C419A MUTANT OF PFL FROM E.COLI | GLYCYL RADICAL ENZYME, TRANSFERASE, GLUCOSE METABOLISM
1cov:1 (THR161) to (PRO181) COXSACKIEVIRUS B3 COAT PROTEIN | COXSACKIEVIRUS B3, ICOSAHEDRAL VIRUS, VIRUS
3fto:A (PRO516) to (LEU557) CRYSTAL STRUCTURE OF OPPA IN A OPEN CONFORMATION | OLIGO-PEPTIDE BINDING, VOLUMINOUS BINDING CAVITY, VENUS FLY- TRAP, PEPTIDE BINDING PROTEIN
4ifd:C (SER60) to (GLU97) 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
2c8w:B (ASP125) to (ASN159) THROMBIN INHIBITORS | PROTEASE, BLOOD COAGULATION, THROMBIN, ACUTE PHASE, DISEASE MUTATION, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, PLASMA, SERINE PROTEASE, ZYMOGEN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2c8x:B (ASP125) to (ASN159) THROMBIN INHIBITORS | PROTEASE, BLOOD COAGULATION, THROMBIN, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2c8z:B (ASP125) to (ASN159) THROMBIN INHIBITORS | PROTEASE, BLOOD COAGULATION, THROMBIN, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2c90:B (ASP125) to (ASN159) THROMBIN INHIBITORS | PROTEASE, BLOOD COAGULATION, ACUTE PHASE, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, SERINE PROTEASE, ZYMOGEN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2c93:B (ASP125) to (ASN159) THROMBIN INHIBITORS | PROTEASE, BLOOD COAGULATION, THROMBIN, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1cy6:A (ARG493) to (ALA519) COMPLEX OF E.COLI DNA TOPOISOMERASE I WITH 3' THYMIDINE MONOPHOSPHATE | DNA TOPOISOMERASE, RELAXING ENZYME, ISOMERASE
1cy7:A (ARG493) to (ALA519) COMPLEX OF E.COLI DNA TOPOISOMERASE I WITH 5'-THYMIDINE MONOPHOSPHATE | DNA TOPOISOMERASE, RELAXING ENZYME, ISOMERASE
1cy8:A (THR496) to (ALA519) COMPLEX OF E.COLI DNA TOPOISOMERASE I WITH 5'-THYMIDINE MONOPHOSPHATE AND 3'-THYMIDINE MONOPHOSPHATE | DNA TOPOISOMERASE, RELAXING ENZYME, ISOMERASE
1p27:A (LYS54) to (THR101) CRYSTAL STRUCTURE OF THE HUMAN Y14/MAGOH COMPLEX | RNA-BINDING, NUCLEAR PROTEIN, MRNA SPLICING, RNA BINDING PROTEIN
2cc2:B (TYR77) to (ALA121) X-RAY CRYSTAL STRUCTURE OF 5'-FLUORODEOXYADENOSINE SYNTHASE FROM STREPTOMYCES CATTLEYA COMPLEXED WITH 5'DEOXYADENOSINE | FLUORINASE, 5'DEOXYADENOSINE, TRANSFERASE, FLA
4igl:A (SER1432) to (THR1458) STRUCTURE OF THE RHS-REPEAT CONTAINING BC COMPONENT OF THE SECRETED ABC TOXIN COMPLEX FROM YERSINIA ENTOMOPHAGA | BETA-PROPELLER, RHS, TOXIN COMPLEX, TOXIN TRANSPORTER/CHAPERONE, SECRETED, TOXIN
4igl:C (SER1432) to (THR1458) STRUCTURE OF THE RHS-REPEAT CONTAINING BC COMPONENT OF THE SECRETED ABC TOXIN COMPLEX FROM YERSINIA ENTOMOPHAGA | BETA-PROPELLER, RHS, TOXIN COMPLEX, TOXIN TRANSPORTER/CHAPERONE, SECRETED, TOXIN
1d3d:B (ASP158) to (ASN200) CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH BENZOTHIOPHENE INHIBITOR 4 | THROMBIN; BENZO[B]THIOPHENE; BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1d3p:B (ASP158) to (ASN200) CRYSTAL STRUCTURE OF HUMAN APLHA-THROMBIN IN COMPLEX WITH BENZO[B]THIOPHENE INHIBITOR 3 | THROMBIN, BENZO[B]THIOPHENE, BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1d3q:B (ASP158) to (ASN200) CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH BENZO[B]THIOPHENE INHIBITOR 2 | THROMBIN; BENZO[B]THIOPHENE, BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3sxw:A (ASP38) to (TYR76) CRYSTAL STRUCTURE OF ENGINEERED PROTEIN. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET OR69. | ENGINEERED PROTEIN, STRUCTURAL GENOMICS, PSI-BIOLOGY, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, ISOMERASE
1d4p:B (ASP158) to (ASN200) CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH 5- AMIDINOINDOLE-4-BENZYLPIPERIDINE INHIBITOR | THROMBIN; NONPEPTIDYL INHIBITOR; STRUCTURE-BASED DRUG DESIGN, BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3g1p:A (HIS225) to (GLY250) CRYSTALS STRUCTURE OF PHNP FROM E.COLI K-12 | PHNP, C-P LYASE, PHOSPHODIESTERASE, PHOSPHONATE UTILIZATION, ALKYLPHOSPHONATE UPTAKE
1d6w:A (ASP125) to (ASN159) STRUCTURE OF THROMBIN COMPLEXED WITH SELECTIVE NON-ELECTROPHILIC INHIBITORS HAVING CYCLOHEXYL MOIETIES AT P1 | HYDROLASE, THROMBIN, THROMBIN INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3g2n:A (ASP421) to (MET441) CRYSTAL STRUCTURE OF N-ACYLGLUCOSYLAMINE WITH GLYCOGEN PHOSPHORYLASE | GLYCOGEN PHOSPHORYLASE, AMIDE-1, 2, 3-TRIAZOLE BIOISOSTERISM, ACETYLATION, ALLOSTERIC ENZYME, CARBOHYDRATE METABOLISM, GLYCOGEN METABOLISM, GLYCOSYLTRANSFERASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, PYRIDOXAL PHOSPHATE, TRANSFERASE
3t00:A (PHE67) to (MET101) CRYSTAL STRUCTURE OF PHOSPHONOACETATE HYDROLASE FROM SINORHIZOBIUM MELILOTI 1021 IN COMPLEX WITH VANADATE | ALKALINE PHOSPHATASE SUPERFAMILY, TRANSITION STATE MIMIC, HYDROLASE
3t02:A (PHE67) to (MET101) CRYSTAL STRUCTURE OF PHOSPHONOACETATE HYDROLASE FROM SINORHIZOBIUM MELILOTI 1021 IN COMPLEX WITH PHOSPHONOACETATE | ALKALINE PHOSPHATASE SUPERFAMILY, HYDROLASE
4xr7:H (LEU630) to (SER662) STRUCTURE OF THE SACCHAROMYCES CEREVISIAE PAN2-PAN3 CORE COMPLEX | RNA DEGRADATION, DEADENYLATION, HYDROLASE, PSEUDOKINASE
1pc6:B (ALA69) to (GLY98) STRUCTURAL GENOMICS, NINB | STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, UNKNOWN FUNCTION
2qgx:B (SER19) to (LEU43) UBIQUITIN-CONJUGATING ENZYME E2Q | UBIQUITIN CONJUGATING PROTEIN, UBC, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, LIGASE
2ckj:C (ASN362) to (GLN384) HUMAN MILK XANTHINE OXIDOREDUCTASE | FAD, NAD, IRON, 2FE-2S, MOLYBDENUM, PEROXISOME, REVERSIBLE INTERCONVERSION, XANTHINE DEHYDROGENASE, XANTHINE OXIDOREDUCTASE, OXIDOREDUCTASE, XANTHINE OXIDASE, IRON- SULFUR, POLYMORPHISM, FLAVOPROTEIN, METAL-BINDING
4int:S (PHE19) to (LEU48) 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
4inu:E (PHE19) to (LEU48) YEAST 20S PROTEASOME IN COMPLEX WITH THE VINYL SULFONE LU112 | UPS, DRUG DISCOVERY, IRREVERSIBLE INHIBITION, NTN HYDROLASE, NON- LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4inu:S (PHE19) to (LEU48) YEAST 20S PROTEASOME IN COMPLEX WITH THE VINYL SULFONE LU112 | UPS, DRUG DISCOVERY, IRREVERSIBLE INHIBITION, NTN HYDROLASE, NON- LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2qky:B (SER498) to (ILE529) COMPLEX STRUCTURE OF DIPEPTIDYL PEPTIDASE IV AND A OXADIAZOLYL KETONE | BETA-PROPELLER, DIMER, AMINOPEPTIDASE, GLYCOPROTEIN, HYDROLASE, MEMBRANE, PROTEASE, SECRETED, SERINE PROTEASE, SIGNAL-ANCHOR, TRANSMEMBRANE
4iou:D (ASP196) to (LYS226) CRYSTAL STRUCTURE OF THE HIV-1 VIF BINDING, CATALYTICALLY ACTIVE DOMAIN OF APOBEC3F | CATALYTIC DOMAIN, CYTIDINE DEAMINASE, CYTIDINE DEAMINASE-LIKE, HYDROLASE, DNA BINDING, CYTIDINE DEAMINATION
3t3i:A (VAL422) to (MET441) GLYCOGEN PHOSPHORYLASE B IN COMPLEX WITH GLCCF3U | A+B PROTEIN, TRANSFERASE, MUSCLE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4xvk:A (ASP204) to (ARG253) BINARY COMPLEX OF HUMAN POLYMERASE NU AND DNA WITH THE FINGER DOMAIN CLOSED | POL NU, POLYMERASE, ERROR-PRONE DNA SYNTHESIS, TRANSFERASE-DNA COMPLEX
3gfi:A (THR65) to (ILE96) CRYSTAL STRUCTURE OF ST1710 COMPLEXED WITH ITS PROMOTER DNA | TRANSCRIPTION REGULATOR, ST1710, MARR, DNA-BINDING, TRANSCRIPTION, TRANSCRIPTION REGULATION, TRANSCRIPTION-DNA COMPLEX, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI
1pma:A (PHE22) to (SER56) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
1pma:C (PHE22) to (SER56) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
1pma:D (PHE22) to (SER56) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
1pma:E (LEU21) to (SER56) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
1pma:F (PHE22) to (SER56) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
1pma:G (PHE22) to (SER56) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
1pma:H (PHE22) to (ASP51) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
1pma:I (PHE22) to (SER56) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
1pma:J (PHE22) to (SER56) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
1pma:K (PHE22) to (SER56) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
1pma:L (PHE22) to (SER56) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
1pma:M (PHE22) to (SER56) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
1pma:N (PHE22) to (SER56) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
1pma:O (PHE22) to (SER56) PROTEASOME FROM THERMOPLASMA ACIDOPHILUM | PROTEASE, PROTEASOME, HYDROLASE
4xxo:A (ASP14) to (ASN57) CRYSTAL STRUCTURE OF HUMAN APOBEC3A | APOBEC, APOBEC3, DEAMINASE, DEAMINATION, APOLIPOPROTEIN B MRNA EDITING POLYPEPTIDE-LIKE 3, HYDROLASE
4xxo:B (ASP14) to (ASN57) CRYSTAL STRUCTURE OF HUMAN APOBEC3A | APOBEC, APOBEC3, DEAMINASE, DEAMINATION, APOLIPOPROTEIN B MRNA EDITING POLYPEPTIDE-LIKE 3, HYDROLASE
3gg4:A (ILE371) to (GLY402) THE CRYSTAL STRUCTURE OF GLYCEROL KINASE FROM YERSINIA PSEUDOTUBERCULOSIS | GLYCEROL KINASE, YERSINIA PSEUDOTUBERCULOSIS, STRUCTURE GENOMICS, 11200D1, KINASE, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC, TRANSFERASE
3t5f:H (ASP125) to (ASN159) HUMAN THROMBIN IN COMPLEX WITH MI340 | SERINE PROTEASE, KRINGLE, HYDROLASE, BLOOD COAGULATION, BLOOD CLOTTING, CONVERTION OF FIBRINOGEN TO FIBRIN, CLEAVAGE ON PAIRS OF BASIC RESIDUES, HIRUDIN, GLYCOSYLATION, BLOOD, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2qrq:A (ASP421) to (MET441) GLYCOGEN PHOSPHORYLASE B IN COMPLEX WITH (1R)-3'-(4- METHYLPHENYL)-SPIRO[1,5-ANHYDRO-D-GLUCITOL-1,5'- ISOXAZOLINE] | GLYCOGENOLYSIS, TYPE 2 DIABETES, ACETYLATION, ALLOSTERIC ENZYME, CARBOHYDRATE METABOLISM, GLYCOGEN METABOLISM, GLYCOSYLTRANSFERASE, NUCLEOTIDE-BINDING, PHOSPHORYLATION, PYRIDOXAL PHOSPHATE, TRANSFERASE
1dtk:A (ALA2) to (PHE33) THE NMR SOLUTION STRUCTURE OF DENDROTOXIN K FROM THE VENOM OF DENDROASPIS POLYLEPIS POLYLEPIS | PRESYNAPTIC NEUROTOXIN
3t6j:A (HIS568) to (SER608) STRUCTURE OF HUMAN DPPIII IN COMPLEX WITH THE OPIOID PEPTIDE TYNORPHIN, AT 3.0 ANGSTROMS | HUMAN DIPEPTIDYLPEPTIDASE III, ENTROPY BINDING, OPIOID PEPTIDE COMPLEX, DOMAIN MOTION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3gkn:B (GLU99) to (GLY120) INSIGHTS INTO THE ALKYL PEROXIDE REDUCTION ACTIVITY OF XANTHOMONAS CAMPESTRIS BACTERIOFERRITIN COMIGRATORY PROTEIN FROM THE TRAPPED INTERMEDIATE/LIGAND COMPLEX STRUCTURES | XANTHOMONAS CAMPESTRIS, BCP, PRX, ATYPICAL 2-CYS, OXIDOREDUCTASE
1e0f:E (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THE HUMAN ALPHA-THROMBIN-HAEMADIN COMPLEX: AN EXOSITE II-BINDING INHIBITOR | COAGULATION/CRYSTAL STRUCTURE/HEPARIN-B, COAGULATION/CRYSTAL STRUCTURE/HEPARIN-BINDING SITE/ HIRUDIN/THROMBIN INHIBITOR, HYDROLASE
4j00:B (SER179) to (LEU210) CRYSTAL STRUCTURE OF FISCHERELLA TRANSCRIPTION FACTOR HETR COMPLEXED WITH 24MER DNA TARGET | STRUCTURAL GENOMICS, PSI-BIOLOGY, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, HELIX-TURN-HELIX, DNA-BINDING DOMAIN, TRANSCRIPTION FACTOR, TRANSCRIPTION-DNA COMPLEX
4y1l:B (THR51) to (PRO79) UBC9 HOMODIMER THE MISSING LINK IN POLY-SUMO CHAIN FORMATION | UBC9, RWD, SUMOYLATION, HOMODIMER, SUMO, LIGASE-NUCLEAR PROTEIN COMPLEX
2d37:A (MET1) to (THR31) THE CRYSTAL STRUCTURE OF FLAVIN REDUCTASE HPAC COMPLEXED WITH NAD+ | FLAVIN REDUCTASE, OXIDOREDUCTASE
4j2n:C (THR18) to (VAL42) CRYSTAL STRUCTURE OF MYCOBACTERIOPHAGE PUKOVNIK XIS | WINGED-HELIX, DOMAN SWAP, FILAMENT, VIRAL PROTEIN
1e50:B (PRO36) to (SER65) AML1/CBF COMPLEX | TRANSCRIPTION FACTOR, TRANSCRIPTION
1e50:F (HIS37) to (SER65) AML1/CBF COMPLEX | TRANSCRIPTION FACTOR, TRANSCRIPTION
1e50:H (HIS37) to (SER65) AML1/CBF COMPLEX | TRANSCRIPTION FACTOR, TRANSCRIPTION
2r2m:B (ASP158) to (ASN194) 2-(2-CHLORO-6-FLUOROPHENYL)ACETAMIDES AS POTENT THROMBIN INHIBITORS | THROMBIN, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN, PROTEASE INHIBITOR, SERINE PROTEASE INHIBITOR, SULFATION, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4y5z:v (THR209) to (TYR254) T=1 CAPSID STRUCTURE OF SEMV NDEL65CP FUSED WITH B-DOMAIN OF S. AUREUS PROTEIN SPA AT THE N-TERMINUS (P1 CRYSTAL FORM) | COAT PROTEIN, CHIMERIC VLP, IN VITRO ASSEMBLY, VIRUS
3tda:A (GLY445) to (VAL495) COMPETITIVE REPLACEMENT OF THIORIDAZINE BY PRINOMASTAT IN CRYSTALS OF CYTOCHROME P450 2D6 | MONOOXYGENASE, HEME, PRINOMASTAT, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4y70:F (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAV-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y70:T (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAV-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
3tej:B (THR1049) to (ASN1064) CRYSTAL STRUCTURE OF A DOMAIN FRAGMENT INVOLVED IN PEPTIDE NATURAL PRODUCT BIOSYNTHESIS | NONRIBOSOMAL PEPTIDE, THIOESTERASE, CARRIER DOMAIN, ATP- BINDING, ENTEROBACTIN BIOSYNTHESIS, ION TRANSPORT, IRON, IRON TRANSPORT, LIGASE, MULTIFUNCTIONAL ENZYME, NUCLEOTIDE- BINDING, PHOSPHOPANTETHEINE, TRANSFERASE, TRANSPORT
4y77:F (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAF-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y77:T (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAF-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y78:F (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y78:T (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
2dfi:A (PRO245) to (ILE284) CRYSTAL STRUCTURE OF PF-MAP(1-292)-C | CHAMELEON SEQUENCE, FUSION PROTEIN, METHIONINE AMINOPEPTIDASE, PYROCOCCUS FURIOSUS, PF-MAP, HYDROLASE
2dfi:B (PRO245) to (THR282) CRYSTAL STRUCTURE OF PF-MAP(1-292)-C | CHAMELEON SEQUENCE, FUSION PROTEIN, METHIONINE AMINOPEPTIDASE, PYROCOCCUS FURIOSUS, PF-MAP, HYDROLASE
4y7k:A (PRO232) to (PRO252) STRUCTURE OF AN ARCHAEAL MECHANOSENSITIVE CHANNEL IN CLOSED STATE | MECHANOSENSITIVE CHANNEL, MECHANOSENSATION, MEMBRANE PROTEIN, TRANSPORT PROTEIN
4y7y:F (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAA-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y7y:T (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LAA-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y81:F (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAY-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y81:T (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAY-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y84:C (PHE16) to (THR49) YEAST 20S PROTEASOME IN COMPLEX WITH N3-A(4,4-F2P)NLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y84:F (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH N3-A(4,4-F2P)NLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y84:Q (PHE16) to (THR49) YEAST 20S PROTEASOME IN COMPLEX WITH N3-A(4,4-F2P)NLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y84:T (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH N3-A(4,4-F2P)NLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8g:C (PHE16) to (THR49) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APNLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8g:F (PHE18) to (SER52) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APNLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8g:Q (PHE16) to (THR49) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APNLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8g:T (PHE18) to (SER52) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APNLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
2di3:A (SER41) to (ILE72) CRYSTAL STRUCTURE OF THE TRANSCRIPTIONAL FACTOR CGL2915 FROM CORYNEBACTERIUM GLUTAMICUM | HELIX-TURN-HELIX, TRANSCRIPTION
4y8h:C (PHE16) to (THR49) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8h:F (PHE18) to (SER52) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8h:Q (PHE16) to (THR49) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8h:T (PHE18) to (SER52) YEAST 20S PROTEASOME IN COMPLEX WITH N3-APAL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8j:F (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8j:T (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH AC-LLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8l:F (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH AC-APLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8l:T (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH AC-APLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4jbi:A (ASN39) to (ASN87) 2.35A RESOLUTION STRUCTURE OF NADPH BOUND THERMOSTABLE ALCOHOL DEHYDROGENASE FROM PYROBACULUM AEROPHILUM | ALCOHOL DEHYDROGENASE, THERMOSTABILITY, ZINC BINDING, NADPH, OXIDOREDUCTASE
4jbi:G (ASN39) to (ASN87) 2.35A RESOLUTION STRUCTURE OF NADPH BOUND THERMOSTABLE ALCOHOL DEHYDROGENASE FROM PYROBACULUM AEROPHILUM | ALCOHOL DEHYDROGENASE, THERMOSTABILITY, ZINC BINDING, NADPH, OXIDOREDUCTASE
4jbi:J (ASN39) to (ASN87) 2.35A RESOLUTION STRUCTURE OF NADPH BOUND THERMOSTABLE ALCOHOL DEHYDROGENASE FROM PYROBACULUM AEROPHILUM | ALCOHOL DEHYDROGENASE, THERMOSTABILITY, ZINC BINDING, NADPH, OXIDOREDUCTASE
4jbi:M (ASN39) to (ASN87) 2.35A RESOLUTION STRUCTURE OF NADPH BOUND THERMOSTABLE ALCOHOL DEHYDROGENASE FROM PYROBACULUM AEROPHILUM | ALCOHOL DEHYDROGENASE, THERMOSTABILITY, ZINC BINDING, NADPH, OXIDOREDUCTASE
4y8o:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAF- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8o:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAF- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8q:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAY- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8q:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAY- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8s:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8s:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8t:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8t:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-PAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
1ecl:A (THR496) to (ALA519) AMINO TERMINAL 67KDA DOMAIN OF ESCHERICHIA COLI DNA TOPOISOMERASE I (RESIDUES 2-590 OF MATURE PROTEIN) CLONING ARTIFACT ADDS TWO RESIDUES TO THE AMINO-TERMINUS WHICH WERE NOT OBSERVED IN THE EXPERIMENTAL ELECTRON DENSITY (GLY-2, SER-1). | BACTERIAL TYPE I, DNA CLEAVAGE, STRAND PASSAGE, TOPOISOMERASE
4y9z:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA2-H116E MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y9z:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA2-H116E MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya2:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA2-H116N MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya2:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA2-H116N MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya4:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA2-H114D MUTANT | HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4jf7:D (ASP120) to (ASN183) STRUCTURE OF THE PARAINFLUENZA VIRUS 5 (PIV5) HEMAGGLUTININ- NEURAMINIDASE (HN) ECTODOMAIN | PARAMYXOVIRUS, PIV5, ATTACHMENT PROTEIN, HN, RECEPTOR BINDING PROTEIN, ECTODOMAIN, VIRAL PROTEIN
4ya7:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya7:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-LAE-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya9:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-LAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4ya9:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-LAD-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4jhc:A (THR84) to (VAL120) CRYSTAL STRUCTURE OF THE UNCHARACTERIZED MAF PROTEIN YCEF FROM E. COLI | MAF PROTEIN, PUTATIVE PYROPHOSPHATASE, CELL CYCLE
1ei6:C (ASN65) to (MET98) CRYSTAL STRUCTURE OF PHOSPHONOACETATE HYDROLASE COMPLEXED WITH PHOSPHONOFORMATE | PHOSPHONOACETATE, HYDROLASE, ZINC, CRYSTAL STRUCTURE
1qbv:H (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THROMBIN COMPLEXED WITH AN GUANIDINE-MIMETIC INHIBITOR | THROMBIN, INHIBITOR, 3DP, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3gyx:A (ASP114) to (GLY139) CRYSTAL STRUCTURE OF ADENYLYLSULFATE REDUCTASE FROM DESULFOVIBRIO GIGAS | ADENYLYLSULFATE REDUCTASE, OXIDOREDUCTASE
3gyx:C (ASP114) to (GLY139) CRYSTAL STRUCTURE OF ADENYLYLSULFATE REDUCTASE FROM DESULFOVIBRIO GIGAS | ADENYLYLSULFATE REDUCTASE, OXIDOREDUCTASE
3gyx:E (ASP114) to (GLY139) CRYSTAL STRUCTURE OF ADENYLYLSULFATE REDUCTASE FROM DESULFOVIBRIO GIGAS | ADENYLYLSULFATE REDUCTASE, OXIDOREDUCTASE
3gyx:I (ASP114) to (GLY139) CRYSTAL STRUCTURE OF ADENYLYLSULFATE REDUCTASE FROM DESULFOVIBRIO GIGAS | ADENYLYLSULFATE REDUCTASE, OXIDOREDUCTASE
3gyx:K (ASP114) to (GLY139) CRYSTAL STRUCTURE OF ADENYLYLSULFATE REDUCTASE FROM DESULFOVIBRIO GIGAS | ADENYLYLSULFATE REDUCTASE, OXIDOREDUCTASE
2rd5:A (SER135) to (PRO164) STRUCTURAL BASIS FOR THE REGULATION OF N-ACETYLGLUTAMATE KINASE BY PII IN ARABIDOPSIS THALIANA | PROTEIN-PROTEIN COMPLEX, REGULATION OF ARGININE BIOSYNTHESIS, NITROGEN METABOLISM, KINASE, TRANSFERASE, TRANSCRIPTION, TRANSCRIPTION REGULATION, PROTEIN BINDING
3tqd:A (GLU133) to (HIS158) STRUCTURE OF THE 3-DEOXY-D-MANNO-OCTULOSONATE CYTIDYLYLTRANSFERASE (KDSB) FROM COXIELLA BURNETII | CELL ENVELOPE, TRANSFERASE
4yes:B (ASP485) to (ASN527) THROMBIN IN COMPLEX WITH (S)-(4-CHLORO-2-((1-(5-METHYL-1H-PYRROLE-2- CARBONYL)PYRROLIDINE-2-CARBOXAMIDO)METHYL)PHENYL)METHANAMINIUM | SULFO-HIRUDIN, INHIBITOR, COMPLEX, THROMBIN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1eol:A (ASP125) to (ASN159) DESIGN OF P1' AND P3' RESIDUES OF TRIVALENT THROMBIN INHIBITORS AND THEIR CRYSTAL STRUCTURES | THROMBIN INHIBITORS, SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1qhr:B (ASP125) to (ASN159) NOVEL COVALENT ACTIVE SITE THROMBIN INHIBITORS | PROTEINASE, BLOOD COAGULATION, TRYPSIN LIKE PROTEINASE, COMPLEX (SERINE PROTEASE-INHIBITOR), BLOOD CLOTTING-HYDROLASE INHIBITOR COMPLEX
1qhs:A (GLY35) to (PRO66) CHLORAMPHENICOL PHOSPHOTRANSFERASE IN COMPLEX WITH CHLORAMPHENICOL FROM STREPTOMYCES VENEZUELAE | KINASE, ANTIBIOTIC RESISTANCE, PHOSPHORYLATION, MONONUCLEOTIDE BINDING FOLD, TRANSFERASE
1qhx:A (VAL36) to (PRO66) CHLORAMPHENICOL PHOSPHOTRANSFERASE IN COMPLEX WITH ATP FROM STREPTOMYCES VENEZUELAE | KINASE, ANTIBIOTIC RESISTANCE, PHOSPHORYLATION, MONONUCLEOTIDE BINDING FOLD, TRANSFERASE
1qhy:A (GLY35) to (PRO66) CHLORAMPHENICOL PHOSPHOTRANSFERASE FROM STREPTOMYCES VENEZUELAE IN COMPLEX WITH ATPGAMMAS AND CHLORAMPHENICOL | KINASE, ANTIBIOTIC RESISTANCE, PHOSPHORYLATION, MONONUCLEOTIDE BINDING FOLD, TRANSFERASE
1eqn:B (ASN175) to (ASP198) E.COLI PRIMASE CATALYTIC CORE | TOPRIM DOMAIN, ROSSMANN FOLD, TRANSFERASE
1qj6:B (ASP125) to (ASN159) NOVEL COVALENT ACTIVE SITE THROMBIN INHIBITORS | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, BLOOD COAGULATION-INHIBITOR COMPLEX, PROTEINASE, BLOOD COAGULATION, TRYPSIN LIKE PROTEINASE, PROTEASE-INHIBITOR COMPLEX, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
1etr:H (ASP125) to (ASN159) REFINED 2.3 ANGSTROMS X-RAY CRYSTAL STRUCTURE OF BOVINE THROMBIN COMPLEXES FORMED WITH THE BENZAMIDINE AND ARGININE-BASED THROMBIN INHIBITORS NAPAP, 4-TAPAP AND MQPA: A STARTING POINT FOR IMPROVING ANTITHROMBOTICS | SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1ets:H (ASP125) to (ASN159) REFINED 2.3 ANGSTROMS X-RAY CRYSTAL STRUCTURE OF BOVINE THROMBIN COMPLEXES FORMED WITH THE BENZAMIDINE AND ARGININE-BASED THROMBIN INHIBITORS NAPAP, 4-TAPAP AND MQPA: A STARTING POINT FOR IMPROVING ANTITHROMBOTICS | SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1ett:H (ASP125) to (ASN159) REFINED 2.3 ANGSTROMS X-RAY CRYSTAL STRUCTURE OF BOVINE THROMBIN COMPLEXES FORMED WITH THE BENZAMIDINE AND ARGININE-BASED THROMBIN INHIBITORS NAPAP, 4-TAPAP AND MQPA: A STARTING POINT FOR IMPROVING ANTITHROMBOTICS | SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3h1k:A (PRO71) to (ALA101) CHICKEN CYTOCHROME BC1 COMPLEX WITH ZN++ AND AN IODINATED DERIVATIVE OF KRESOXIM-METHYL BOUND | CYTOCHROME BC1, MEMBRANE PROTEIN, HEME PROTEIN, RIESKE IRON SULFUR PROTEIN, CYTOCHROME B, CYTOCHROME C1, COMPLEX III, UBIQUINONE, OXIDOREDUCTASE, REDOX ENZYME, ZINC,KRESOXIM-METHYL, RESPIRATORY CHAIN, ELECTRON TRANSPORT, HEME, INNER MEMBRANE IRON, MEMBRANE, METAL-BINDING, MITOCHONDRION, TRANSMEMBRANE, IRON, MITOCHONDRION INNER MEMBRANE, TRANSPORT, DISULFIDE BOND, IRON-SULFUR, TRANSIT PEPTIDE
3h1k:N (PRO71) to (ALA101) CHICKEN CYTOCHROME BC1 COMPLEX WITH ZN++ AND AN IODINATED DERIVATIVE OF KRESOXIM-METHYL BOUND | CYTOCHROME BC1, MEMBRANE PROTEIN, HEME PROTEIN, RIESKE IRON SULFUR PROTEIN, CYTOCHROME B, CYTOCHROME C1, COMPLEX III, UBIQUINONE, OXIDOREDUCTASE, REDOX ENZYME, ZINC,KRESOXIM-METHYL, RESPIRATORY CHAIN, ELECTRON TRANSPORT, HEME, INNER MEMBRANE IRON, MEMBRANE, METAL-BINDING, MITOCHONDRION, TRANSMEMBRANE, IRON, MITOCHONDRION INNER MEMBRANE, TRANSPORT, DISULFIDE BOND, IRON-SULFUR, TRANSIT PEPTIDE
1ex0:B (GLU198) to (GLY228) HUMAN FACTOR XIII, MUTANT W279F ZYMOGEN | TRANSGLUTAMINASE, BLOOD COAGULATION, MUTANT, W279F, OXYANION, TRANSFERASE
3tx1:A (SER125) to (LYS161) X-RAY CRYSTAL STRUCTURE OF LISTERIA MONOCYTOGENES EGD-E UDP-N- ACETYLENOLPYRUVYLGLUCOSAMINE REDUCTASE (MURB) | STRUCTURAL GENOMICS, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID, OXIDOREDUCTASE
4jr5:A (PRO317) to (PRO345) STRUCTURE-BASED IDENTIFICATION OF UREAS AS NOVEL NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE (NAMPT) INHIBITORS | TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
1qrk:B (GLU198) to (GLY228) HUMAN FACTOR XIII WITH STRONTIUM BOUND IN THE ION SITE | TRANSGLUTAMINASE, BLOOD COAGULATION, CALCIUM, STRONTIUM, TRANSFERASE
3h6f:A (PRO9) to (ALA43) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR HT1171 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6f:B (SER8) to (ALA43) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR HT1171 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6f:D (PRO9) to (ALA43) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR HT1171 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6f:I (PRO9) to (ALA43) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR HT1171 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6f:K (GLU10) to (ALA43) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR HT1171 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6f:S (SER8) to (ALA43) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR HT1171 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6f:Y (GLU10) to (ALA43) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR HT1171 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6f:1 (GLU10) to (ALA43) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR HT1171 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6i:B (SER8) to (ALA43) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6i:D (PRO9) to (ALA43) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6i:F (SER8) to (ALA43) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6i:I (PRO9) to (ALA43) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6i:K (PRO9) to (ALA43) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6i:M (SER8) to (ALA43) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6i:O (SER8) to (ALA43) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6i:Q (SER8) to (ALA43) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6i:S (SER8) to (ALA43) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6i:U (PRO9) to (ALA43) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
3h6i:1 (PRO9) to (ALA43) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME
4jsu:F (PHE18) to (THR51) 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:T (PHE18) to (THR51) 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
3h7f:A (ALA203) to (GLY239) CRYSTAL STRUCTURE OF SERINE HYDROXYMETHYLTRANSFERASE FROM MYCOBACTERIUM TUBERCULOSIS | MYCOBACTERIUM TUBERCULOSIS, SERINE HYDROXYMETHYLTRANSFERASE, ONE- CARBON METABOLISM, PYRIDOXAL PHOSPHATE, TRANSFERASE, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, SSGCID
3h7f:B (ALA203) to (GLY239) CRYSTAL STRUCTURE OF SERINE HYDROXYMETHYLTRANSFERASE FROM MYCOBACTERIUM TUBERCULOSIS | MYCOBACTERIUM TUBERCULOSIS, SERINE HYDROXYMETHYLTRANSFERASE, ONE- CARBON METABOLISM, PYRIDOXAL PHOSPHATE, TRANSFERASE, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, SSGCID
1f3z:A (ASP94) to (ASP123) IIAGLC-ZN COMPLEX | PHOSPHOTRANSFERASE, SIGNAL TRANSDUCTION, SUGAR TRANSPORT
3ha1:B (ASN358) to (ASN384) ALANINE RACEMASE FROM BACILLUS ANTHRACIS (AMES) | ALANINE RACEMASE, ISOMERASE, PLP, PYRIDOXAL PHOSPHATE
1fa9:A (ASP421) to (MET441) HUMAN LIVER GLYCOGEN PHOSPHORYLASE A COMPLEXED WITH AMP | PROTEIN-LIGAND COMPLEX, ALLOSTERIC PROTEIN, PHOSPHORYLATED PROTEIN, TRANSFERASE
3hbx:A (GLY248) to (ARG291) CRYSTAL STRUCTURE OF GAD1 FROM ARABIDOPSIS THALIANA | CALMODULIN-BINDING, DECARBOXYLASE, LYASE, PYRIDOXAL PHOSPHATE
3hbx:B (GLY248) to (ARG291) CRYSTAL STRUCTURE OF GAD1 FROM ARABIDOPSIS THALIANA | CALMODULIN-BINDING, DECARBOXYLASE, LYASE, PYRIDOXAL PHOSPHATE
3hbx:C (GLY248) to (ARG291) CRYSTAL STRUCTURE OF GAD1 FROM ARABIDOPSIS THALIANA | CALMODULIN-BINDING, DECARBOXYLASE, LYASE, PYRIDOXAL PHOSPHATE
3hbx:D (GLY248) to (ARG291) CRYSTAL STRUCTURE OF GAD1 FROM ARABIDOPSIS THALIANA | CALMODULIN-BINDING, DECARBOXYLASE, LYASE, PYRIDOXAL PHOSPHATE
3hbx:E (GLY248) to (ARG291) CRYSTAL STRUCTURE OF GAD1 FROM ARABIDOPSIS THALIANA | CALMODULIN-BINDING, DECARBOXYLASE, LYASE, PYRIDOXAL PHOSPHATE
3hbx:F (GLY248) to (ARG291) CRYSTAL STRUCTURE OF GAD1 FROM ARABIDOPSIS THALIANA | CALMODULIN-BINDING, DECARBOXYLASE, LYASE, PYRIDOXAL PHOSPHATE
2efw:B (HIS62) to (PHE90) CRYSTAL STRUCTURE OF THE RTP:NRB COMPLEX FROM BACILLUS SUBTILIS | PROTEIN-DNA COMPLEX, 'WINGED'-HELIX PROTEIN, DNA REPLICATION TERMINATION, REPLICATION FORK ARREST, REPLICATION-DNA COMPLEX
3u8p:B (LYS3) to (THR38) CYTOCHROME B562 INTEGRAL FUSION WITH EGFP | DIRECTED EVOLUTION, DOMAIN INSERTION, ENERGY TRANSFER, FLUORESCENCE QUENCHING, FLUORESCENT PROTEIN, ELECTRON TRANSPORT
3u8o:H (ASP442) to (ASN484) HUMAN THROMBIN COMPLEXED WITH D-PHE-PRO-D-ARG-D-THR | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3hf9:I (GLU10) to (GLU44) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME OPEN-GATE MUTANT MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, OPEN GATE, MUTANT, HYDROLASE, PROTEASOME
3hf9:K (ALA12) to (GLU44) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME OPEN-GATE MUTANT MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, OPEN GATE, MUTANT, HYDROLASE, PROTEASOME
3hf9:Y (GLN11) to (GLU44) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME OPEN-GATE MUTANT MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, OPEN GATE, MUTANT, HYDROLASE, PROTEASOME
3hf9:k (GLU310) to (GLU344) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME OPEN-GATE MUTANT MODIFIED BY INHIBITOR GL1 | BINDING SITES, OXAZOLIDIN-2-ONE, CRYSTALLOGRAPHY, X-RAY, MYCOBACTERIUM TUBERCULOSIS, PROTEASE INHIBITORS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, OPEN GATE, MUTANT, HYDROLASE, PROTEASOME
3hf9:o (GLU310) to (ALA343) 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
4ymd:A (SER116) to (LYS158) CL-K1 TRIMER BOUND TO MAN(ALPHA1-2)MAN | C-TYPE CARBOHYDRATE-RECOGNITION DOMAIN, COLLECTIN, C-TYPE LECTIN, SUGAR BINDING PROTEIN
4ymd:D (SER116) to (LYS158) CL-K1 TRIMER BOUND TO MAN(ALPHA1-2)MAN | C-TYPE CARBOHYDRATE-RECOGNITION DOMAIN, COLLECTIN, C-TYPE LECTIN, SUGAR BINDING PROTEIN
3hif:A (PRO9) to (GLN32) THE CRYSTAL STRUCTURE OF APO WILD TYPE CAP AT 3.6 A RESOLUTION. | HELIX-TURN-HELIX, CAMP BINDING DOMAIN, ACTIVATOR, CAMP, CAMP-BINDING, DNA-BINDING, NUCLEOTIDE-BINDING, TRANSCRIPTION, TRANSCRIPTION REGULATION, TRANSCRIPTION REGULATOR
1r8w:A (LYS742) to (GLN767) NATIVE STRUCTURE OF THE B12-INDEPENDENT GLYCEROL DEHYDRATASE FROM CLOSTRIDIUM BUTYRICUM | GLYCEROL DEHYDRATASE, RADICAL SAM, LYASE
1r8w:B (LYS742) to (GLN767) NATIVE STRUCTURE OF THE B12-INDEPENDENT GLYCEROL DEHYDRATASE FROM CLOSTRIDIUM BUTYRICUM | GLYCEROL DEHYDRATASE, RADICAL SAM, LYASE
2v4m:D (GLU349) to (LEU371) THE ISOMERASE DOMAIN OF HUMAN GLUTAMINE-FRUCTOSE-6- PHOSPHATE TRANSAMINASE 1 (GFPT1) IN COMPLEX WITH FRUCTOSE 6-PHOSPHATE | PHOSPHOPROTEIN, AMINOTRANSFERASE, FRUCTOSE 6-PHOSPHATE, ALTERNATIVE SPLICING, GLUTAMINE AMIDOTRANSFERASE, DIMER, ISOMERASE, SIS DOMAINS, TRANSFERASE
1fm0:D (SER39) to (PHE75) MOLYBDOPTERIN SYNTHASE (MOAD/MOAE) | MOLYBDENUM COFACTOR BIOSYNTHESIS, TRANSFERASE
4k3f:A (ASN132) to (LYS166) CRYSTAL STRUCTURE OF A PUTATIVE TONB-DEPENDENT RECEPTOR (PA5505) FROM PSEUDOMONAS AERUGINOSA PAO1 AT 1.60 A RESOLUTION | PERIPLASMIC METHIONINE BINDING PROTEIN, NLPA LIPOPROTEIN, PF03180 FAMILY, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-BIOLOGY, TRANSPORT PROTEIN
3hk6:D (ASP125) to (ASN159) CRYSTAL STRUCTURE OF MURINE THROMBIN MUTANT W215A/E217A (TWO MOLECULES IN THE ASYMMETRIC UNIT) | SERINE PROTEASE, ACUTE PHASE, BLOOD COAGULATION, CALCIUM, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISULFIDE BOND, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PROTEASE, ZYMOGEN
4ys0:A (SER277) to (THR307) CONFORMATIONAL CHANGES OF THE CLAMP OF THE PROTEIN TRANSLOCATION ATPASE SECA FROM THERMOTOGA MARITIMA | PROTEIN TRANSLOCATION, SECA, ATPASE, PROTEIN TRANSPORT
1fnt:G (GLN22) to (GLU50) CRYSTAL STRUCTURE OF THE 20S PROTEASOME FROM YEAST IN COMPLEX WITH THE PROTEASOME ACTIVATOR PA26 FROM TRYPANOSOME BRUCEI AT 3.2 ANGSTROMS RESOLUTION | MULTICATALYTIC PROTEINASE, 20S PROTEASOME, PROTEIN DEGRADATION, ANTIGEN PROCESSING, PROTEASE, PROTEASOME ACTIVATOR, CELL ADHESION, INTERFERON INDUCTION, HYDROLASE/HYDROLASE ACTIVATOR COMPLEX
1fnt:U (PHE21) to (GLU50) CRYSTAL STRUCTURE OF THE 20S PROTEASOME FROM YEAST IN COMPLEX WITH THE PROTEASOME ACTIVATOR PA26 FROM TRYPANOSOME BRUCEI AT 3.2 ANGSTROMS RESOLUTION | MULTICATALYTIC PROTEINASE, 20S PROTEASOME, PROTEIN DEGRADATION, ANTIGEN PROCESSING, PROTEASE, PROTEASOME ACTIVATOR, CELL ADHESION, INTERFERON INDUCTION, HYDROLASE/HYDROLASE ACTIVATOR COMPLEX
3hki:E (ASP125) to (ASN159) CRYSTAL STRUCTURE OF MURINE THROMBIN MUTANT W215A/E217A IN COMPLEX WITH THE EXTRACELLULAR FRAGMENT OF HUMAN PAR1 | SERINE PROTEASE, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISULFIDE BOND, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PROTEASE, ZYMOGEN, CELL MEMBRANE, G-PROTEIN COUPLED RECEPTOR, MEMBRANE, PHOSPHOPROTEIN, RECEPTOR, TRANSDUCER, TRANSMEMBRANE
3hkj:E (ASP125) to (ASN159) CRYSTAL STRUCTURE OF HUMAN THROMBIN MUTANT W215A/E217A IN COMPLEX WITH THE EXTRACELLULAR FRAGMENT OF HUMAN PAR1 | SERINE PROTEASE, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, DISULFIDE BOND, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PROTEASE, SECRETED, ZYMOGEN, CELL MEMBRANE, G-PROTEIN COUPLED RECEPTOR, MEMBRANE, PHOSPHOPROTEIN, RECEPTOR, TRANSDUCER, TRANSMEMBRANE
2exe:A (LEU200) to (GLY240) CRYSTAL STRUCTURE OF THE PHOSPHORYLATED CLK3 | DUAL-SPECIFICITY KINASE, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, TRANSFERASE
1fpc:H (ASP125) to (ASN159) ACTIVE SITE MIMETIC INHIBITION OF THROMBIN | SERINE PROTEASE-INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1rd3:B (ASP125) to (ASN159) 2.5A STRUCTURE OF ANTICOAGULANT THROMBIN VARIANT E217K | HYDROLASE
2v7t:B (TYR77) to (ALA121) X-RAY CRYSTAL STRUCTURE OF 5'-FLUORODEOXYADENOSINE SYNTHASE S158G MUTANT COMPLEXED WITH S-ADENOSYL-L-HOMOCYSTEINE AND CHLORIDE ION | TRANSFERASE, MECHANISM OF FLUORINATION, BIOSYNTHETIC PROTEIN
2v7u:A (TYR77) to (ALA121) X-RAY CRYSTAL STRUCTURE OF 5'-FLUORODEOXYADENOSINE SYNTHASE S158G MUTANT COMPLEXED WITH S-ADENOSYLMETHIONINE AND CHLORIDE ION | MECHANISM OF FLUORINATION, BIOSYNTHETIC PROTEIN, TRANSFERASE
2v7u:B (TYR77) to (ALA121) X-RAY CRYSTAL STRUCTURE OF 5'-FLUORODEOXYADENOSINE SYNTHASE S158G MUTANT COMPLEXED WITH S-ADENOSYLMETHIONINE AND CHLORIDE ION | MECHANISM OF FLUORINATION, BIOSYNTHETIC PROTEIN, TRANSFERASE
2v7u:C (TYR77) to (ALA121) X-RAY CRYSTAL STRUCTURE OF 5'-FLUORODEOXYADENOSINE SYNTHASE S158G MUTANT COMPLEXED WITH S-ADENOSYLMETHIONINE AND CHLORIDE ION | MECHANISM OF FLUORINATION, BIOSYNTHETIC PROTEIN, TRANSFERASE
2v7w:A (TYR77) to (ALA121) X-RAY CRYSTAL STRUCTURE OF 5'-FLUORODEOXYADENOSINE SYNTHASE S158G MUTANT COMPLEXED WITH 5'-FLUORODEOXYADENOSIN | FLUORINATION, TRANSFERASE, BIOSYNTHETIC PROTEIN
2v7w:B (TYR77) to (ALA121) X-RAY CRYSTAL STRUCTURE OF 5'-FLUORODEOXYADENOSINE SYNTHASE S158G MUTANT COMPLEXED WITH 5'-FLUORODEOXYADENOSIN | FLUORINATION, TRANSFERASE, BIOSYNTHETIC PROTEIN
2v7w:C (TYR77) to (ALA121) X-RAY CRYSTAL STRUCTURE OF 5'-FLUORODEOXYADENOSINE SYNTHASE S158G MUTANT COMPLEXED WITH 5'-FLUORODEOXYADENOSIN | FLUORINATION, TRANSFERASE, BIOSYNTHETIC PROTEIN
2v7v:B (TYR77) to (ALA121) X-RAY CRYSTAL STRUCTURE OF 5'-FLUORODEOXYADENOSINE SYNTHASE FROM STREPTOMYCES CATTLEYA COMPLEXED WITH 5'-FLUORODEOXYADENOSINE | TRANSFERASE, MECHANISM OF FLUORINATION, BIOSYNTHETIC PROTEIN
2v7v:C (TYR77) to (ALA121) X-RAY CRYSTAL STRUCTURE OF 5'-FLUORODEOXYADENOSINE SYNTHASE FROM STREPTOMYCES CATTLEYA COMPLEXED WITH 5'-FLUORODEOXYADENOSINE | TRANSFERASE, MECHANISM OF FLUORINATION, BIOSYNTHETIC PROTEIN
2v7x:A (TYR77) to (ALA121) X-RAY CRYSTAL STRUCTURE OF 5'-FLUORODEOXYADENOSINE SYNTHASE S158A MUTANT FROM STREPTOMYCES CATTLEYA COMPLEXED WITH THE PRODUCTS, FDA AND MET | FLUORINASE, TRANSFERASE, BIOSYNTHETIC PROTEIN
2v7x:B (TYR77) to (ALA121) X-RAY CRYSTAL STRUCTURE OF 5'-FLUORODEOXYADENOSINE SYNTHASE S158A MUTANT FROM STREPTOMYCES CATTLEYA COMPLEXED WITH THE PRODUCTS, FDA AND MET | FLUORINASE, TRANSFERASE, BIOSYNTHETIC PROTEIN
2v7x:C (TYR77) to (ALA121) X-RAY CRYSTAL STRUCTURE OF 5'-FLUORODEOXYADENOSINE SYNTHASE S158A MUTANT FROM STREPTOMYCES CATTLEYA COMPLEXED WITH THE PRODUCTS, FDA AND MET | FLUORINASE, TRANSFERASE, BIOSYNTHETIC PROTEIN
4yu2:D (ALA388) to (LEU405) CRYSTAL STRUCTURE OF DYRK1A WITH HARMINE-DERIVATIZED ANNH-75 INHIBITOR | TRANSFERASE, DYRK1A, DOWN SYNDROME, INHIBITOR, HARMINE, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC
2f16:F (PHE22) to (ILE54) 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:T (PHE22) to (ILE54) 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
3uk2:A (SER250) to (GLU278) THE STRUCTURE OF PANTOTHENATE SYNTHETASE FROM BURKHOLDERIA THAILANDENSIS | AMP, PANTOTHENATE SYNTHETASE, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, SSGCID, LIGASE
3uk2:B (SER250) to (GLU278) THE STRUCTURE OF PANTOTHENATE SYNTHETASE FROM BURKHOLDERIA THAILANDENSIS | AMP, PANTOTHENATE SYNTHETASE, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, SSGCID, LIGASE
1ftw:A (ASP421) to (MET441) STRUCTURES OF GLYCOGEN PHOSPHORYLASE-INHIBITOR COMPLEXES AND THE IMPLICATIONS FOR STRUCTURE-BASED DRUG DESIGN | TRANSFERASE, GLYCOGEN PHOSPHORYLASE, INHIBITOR COMPLEX, CATALYTIC SITE, DESIGN
2v9p:B (LEU492) to (ILE513) CRYSTAL STRUCTURE OF PAPILLOMAVIRUS E1 HEXAMERIC HELICASE DNA-FREE FORM | AAA+ MOLECULAR MOTOR, DNA REPLICATION, DNA TRANSLOCATION, NUCLEOTIDE-BINDING, DNA-BINDING, REPLICATION, EARLY PROTEIN, ATPASE, NUCLEUS, HELICASE, HYDROLASE, ATP-BINDING
2v9p:C (LEU492) to (ILE513) CRYSTAL STRUCTURE OF PAPILLOMAVIRUS E1 HEXAMERIC HELICASE DNA-FREE FORM | AAA+ MOLECULAR MOTOR, DNA REPLICATION, DNA TRANSLOCATION, NUCLEOTIDE-BINDING, DNA-BINDING, REPLICATION, EARLY PROTEIN, ATPASE, NUCLEUS, HELICASE, HYDROLASE, ATP-BINDING
2v9p:D (LEU492) to (ILE513) CRYSTAL STRUCTURE OF PAPILLOMAVIRUS E1 HEXAMERIC HELICASE DNA-FREE FORM | AAA+ MOLECULAR MOTOR, DNA REPLICATION, DNA TRANSLOCATION, NUCLEOTIDE-BINDING, DNA-BINDING, REPLICATION, EARLY PROTEIN, ATPASE, NUCLEUS, HELICASE, HYDROLASE, ATP-BINDING
2v9p:H (LEU492) to (ILE513) CRYSTAL STRUCTURE OF PAPILLOMAVIRUS E1 HEXAMERIC HELICASE DNA-FREE FORM | AAA+ MOLECULAR MOTOR, DNA REPLICATION, DNA TRANSLOCATION, NUCLEOTIDE-BINDING, DNA-BINDING, REPLICATION, EARLY PROTEIN, ATPASE, NUCLEUS, HELICASE, HYDROLASE, ATP-BINDING
2v9p:J (LEU492) to (ILE513) CRYSTAL STRUCTURE OF PAPILLOMAVIRUS E1 HEXAMERIC HELICASE DNA-FREE FORM | AAA+ MOLECULAR MOTOR, DNA REPLICATION, DNA TRANSLOCATION, NUCLEOTIDE-BINDING, DNA-BINDING, REPLICATION, EARLY PROTEIN, ATPASE, NUCLEUS, HELICASE, HYDROLASE, ATP-BINDING
1rk8:B (GLN55) to (THR102) STRUCTURE OF THE CYTOSOLIC PROTEIN PYM BOUND TO THE MAGO- Y14 CORE OF THE EXON JUNCTION COMPLEX | MRNA PROCESSING; RRM; RBD; NMD; OSKAR MRNA LOCALIZATION, TRANSLATION
2f3g:A (ASP94) to (ASP123) IIAGLC CRYSTAL FORM III | PHOSPHOTRANSFERASE, SIGNAL TRANSDUCTION, PHOSPHOCARRIER
2f3o:A (GLU730) to (TYR756) CRYSTAL STRUCTURE OF A GLYCYL RADICAL ENZYME FROM ARCHAEOGLOBUS FULGIDUS | PYRUVATE FORMATE LYASE, GLYCEROL DEHYDRATASE, PFL2, GLYCYL RADICAL, HYPERTHERMOPHILIC, UNKNOWN FUNCTION
4kbp:A (THR186) to (ALA243) KIDNEY BEAN PURPLE ACID PHOSPHATASE | PURPLE ACID PHOSPHATASE, HYDROLASE (PHOSPHORIC MONOESTER)
4kbp:C (THR186) to (ALA243) KIDNEY BEAN PURPLE ACID PHOSPHATASE | PURPLE ACID PHOSPHATASE, HYDROLASE (PHOSPHORIC MONOESTER)
4kbp:D (THR186) to (ALA243) KIDNEY BEAN PURPLE ACID PHOSPHATASE | PURPLE ACID PHOSPHATASE, HYDROLASE (PHOSPHORIC MONOESTER)
1rqp:B (TYR77) to (ALA121) CRYSTAL STRUCTURE AND MECHANISM OF A BACTERIAL FLUORINATING ENZYME | FLUORINASE, CENTRAL 7 STRANDED BETA SHEETS, ANTI-PARALLEL BETA SHEETS, TRANSFERASE
1rqp:C (TYR77) to (ALA121) CRYSTAL STRUCTURE AND MECHANISM OF A BACTERIAL FLUORINATING ENZYME | FLUORINASE, CENTRAL 7 STRANDED BETA SHEETS, ANTI-PARALLEL BETA SHEETS, TRANSFERASE
1rqr:B (TYR77) to (ALA121) CRYSTAL STRUCTURE AND MECHANISM OF A BACTERIAL FLUORINATING ENZYME, PRODUCT COMPLEX | FLUORINASE, CENTRAL 7 STRANDED BETA SHEETS, ANTI-PARALLEL BETA SHEETS, TRANSFERASE
3une:O (GLN20) to (SER53) MOUSE CONSTITUTIVE 20S PROTEASOME | 20S PROTEASOME COMPRISES 28 SUBUNITS, PROTEASE, CYTOSOL, HYDROLASE
3une:T (PHE21) to (GLU50) MOUSE CONSTITUTIVE 20S PROTEASOME | 20S PROTEASOME COMPRISES 28 SUBUNITS, PROTEASE, CYTOSOL, HYDROLASE
3une:v (PHE21) to (GLU50) MOUSE CONSTITUTIVE 20S PROTEASOME | 20S PROTEASOME COMPRISES 28 SUBUNITS, PROTEASE, CYTOSOL, HYDROLASE
3unf:F (GLN22) to (SER55) MOUSE 20S IMMUNOPROTEASOME IN COMPLEX WITH PR-957 | PROTEASOME, ANTIGEN PRESENTATION, DRUG DEVELOPMENT, PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3unf:T (GLN22) to (SER55) MOUSE 20S IMMUNOPROTEASOME IN COMPLEX WITH PR-957 | PROTEASOME, ANTIGEN PRESENTATION, DRUG DEVELOPMENT, PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2fao:A (ARG582) to (LYS606) CRYSTAL STRUCTURE OF PSEUDOMONAS AERUGINOSA LIGD POLYMERASE DOMAIN | POLYMERASE, PRIMASE, LIGASE, NHEJ, HYDROLASE/TRANSFERASE COMPLEX
4z1l:F (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH BELACTOSIN C DERIVATIVE 3 | HYDROLASE, PROTEASOME, INHIBITOR, BINDING ANALYSIS, LEAD STRUCTURE MOTIF, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4z1l:T (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH BELACTOSIN C DERIVATIVE 3 | HYDROLASE, PROTEASOME, INHIBITOR, BINDING ANALYSIS, LEAD STRUCTURE MOTIF, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2far:A (ARG582) to (LYS606) CRYSTAL STRUCTURE OF PSEUDOMONAS AERUGINOSA LIGD POLYMERASE DOMAIN WITH DATP AND MANGANESE | POLYMERASE, PRIMASE, LIGASE, NHEJ, DATP, HYDROLASE/TRANSFERASE COMPLEX
2far:B (ARG582) to (LYS606) CRYSTAL STRUCTURE OF PSEUDOMONAS AERUGINOSA LIGD POLYMERASE DOMAIN WITH DATP AND MANGANESE | POLYMERASE, PRIMASE, LIGASE, NHEJ, DATP, HYDROLASE/TRANSFERASE COMPLEX
3unh:F (GLN22) to (SER55) MOUSE 20S IMMUNOPROTEASOME | 20S PROTEASOME COMPRISES 28 SUBUNITS, PROTEASE, CYTOSOL, HYDROLASE
3unh:T (GLN22) to (SER55) MOUSE 20S IMMUNOPROTEASOME | 20S PROTEASOME COMPRISES 28 SUBUNITS, PROTEASE, CYTOSOL, HYDROLASE
1g30:B (ASP125) to (ASN159) THROMBIN INHIBITOR COMPLEX | BLOOD COAGULATION, FACTOR XA, INHIBITOR COMPLEXES, SERINE PROTEINASE, BLOOD COAGULATION CASCADE, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4kff:B (GLY324) to (LYS360) CRYSTAL STRUCTURE OF HANSENULA POLYMORPHA COPPER AMINE OXIDASE-1 REDUCED BY METHYLAMINE AT PH 8.5 | AMINE OXIDASE, OXIDOREDUCTASE, PEROXISOME
4kfn:B (PRO317) to (PRO345) STRUCTURE-BASED DISCOVERY OF NOVEL AMIDE-CONTAINING NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE (NAMPT) INHIBITORS | TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4kfo:A (PRO317) to (PRO345) STRUCTURE-BASED DISCOVERY OF NOVEL AMIDE-CONTAINING NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE (NAMPT) INHIBITORS | TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4kfo:B (PRO317) to (PRO345) STRUCTURE-BASED DISCOVERY OF NOVEL AMIDE-CONTAINING NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE (NAMPT) INHIBITORS | TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
2feq:H (ASP125) to (ASN159) ORALLY ACTIVE THROMBIN INHIBITORS | THROMBIN INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1ryp:U (PHE21) to (THR54) CRYSTAL STRUCTURE OF THE 20S PROTEASOME FROM YEAST AT 2.4 ANGSTROMS RESOLUTION | MULTICATALYTIC PROTEINASE, 20S PROTEASOME, PROTEIN DEGRADATION, ANTIGEN PROCESSING, HYDROLASE, PROTEASE
2fk4:A (GLU36) to (GLY57) SOLUTION STRUCTURE OF THE C-TERMINAL ZINC BINDING DOMAIN OF THE HPV16 E6 ONCOPROTEIN | ZINC BINDING DOMAIN, ONCOPROTEIN, METAL BINDING PROTEIN
4kkz:A (THR186) to (ALA243) THE CRYSTAL STRUCTURE OF RED KIDNEY BEAN PURPLE ACID PHOSPHATASE IN COMPLEX WITH DIETHYLENE GLYCOL MONOVANADATE | BETA BARREL, PHOSPHATASE, HYDROLASE, VANADATE, COTYLEDON CELLS
4kkz:B (THR186) to (ALA243) THE CRYSTAL STRUCTURE OF RED KIDNEY BEAN PURPLE ACID PHOSPHATASE IN COMPLEX WITH DIETHYLENE GLYCOL MONOVANADATE | BETA BARREL, PHOSPHATASE, HYDROLASE, VANADATE, COTYLEDON CELLS
4kkz:C (THR186) to (ALA243) THE CRYSTAL STRUCTURE OF RED KIDNEY BEAN PURPLE ACID PHOSPHATASE IN COMPLEX WITH DIETHYLENE GLYCOL MONOVANADATE | BETA BARREL, PHOSPHATASE, HYDROLASE, VANADATE, COTYLEDON CELLS
4kkz:D (THR186) to (ALA243) THE CRYSTAL STRUCTURE OF RED KIDNEY BEAN PURPLE ACID PHOSPHATASE IN COMPLEX WITH DIETHYLENE GLYCOL MONOVANADATE | BETA BARREL, PHOSPHATASE, HYDROLASE, VANADATE, COTYLEDON CELLS
3hs0:D (ASP432) to (ILE477) COBRA VENOM FACTOR (CVF) IN COMPLEX WITH HUMAN FACTOR B | SERINE PROTEASE, GLYCOSILATED, MULTI-DOMAIN, COMPLEMENT SYSTEM, CONVERTASE, COMPLEMENT ALTERNATE PATHWAY, COMPLEMENT PATHWAY, DISULFIDE BOND, GLYCOPROTEIN, IMMUNE RESPONSE, INFLAMMATORY RESPONSE, INNATE IMMUNITY, SECRETED, THIOESTER BOND, CLEAVAGE ON PAIR OF BASIC RESIDUES, GLYCATION, HYDROLASE, PROTEASE, SUSHI, ZYMOGEN, IMMUNE SYSTEM
1ggm:A (LEU5) to (PRO36) GLYCYL-TRNA SYNTHETASE FROM THERMUS THERMOPHILUS COMPLEXED WITH GLYCYL-ADENYLATE | AMINOACYL-TRNA SYNTHASE, LIGASE(SYNTHETASE), LIGASE
1ggm:B (LEU5) to (PRO36) GLYCYL-TRNA SYNTHETASE FROM THERMUS THERMOPHILUS COMPLEXED WITH GLYCYL-ADENYLATE | AMINOACYL-TRNA SYNTHASE, LIGASE(SYNTHETASE), LIGASE
1ghy:H (ASP125) to (ASN159) A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE | THREE-CENTERED, VERY SHORT HYDROGEN BOND, OXYANION HOLE WATER, SHIFT OF PKA OF HIS57, STRUCTURE-BASED DRUG DESIGN, SPECIFICITY, UROKINASE, TRYPSIN, THROMBIN, ZN+2-MEDIATED INHIBITION, BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1ghv:H (ASP125) to (ASN159) A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE | THREE-CENTERED, VERY SHORT HYDROGEN BOND, OXYANION HOLE WATER, SHIFT OF PKA OF HIS57, STRUCTURE-BASED DRUG DESIGN, SPECIFICITY, UROKINASE, TRYPSIN, THROMBIN, ZN+2-MEDIATED INHIBITION, BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1ghw:H (ASP125) to (ASN159) A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE | THREE-CENTERED, VERY SHORT HYDROGEN BOND, OXYANION HOLE WATER, SHIFT OF PKA OF HIS57, STRUCTURE-BASED DRUG DESIGN, SPECIFICITY, UROKINASE, TRYPSIN, THROMBIN, ZN+2-MEDIATED INHIBITION, BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1gj5:H (ASP125) to (ASN159) SELECTIVITY AT S1, H2O DISPLACEMENT, UPA, TPA, SER190/ALA190 PROTEASE, STRUCTURE-BASED DRUG DESIGN | THREE-CENTERED, VERY SHORT HYDROGEN BOND, OXYANION HOLE WATER, SHIFT OF PKA OF HIS57, STRUCTURE-BASED DRUG DESIGN, SPECIFICITY, UROKINASE, TRYPSIN, THROMBIN, ZN+2-MEDIATED INHIBITION, BLOOD CLOTTING, HYDROLASE,HYDROLASE-HYDROLASE INHIBITOR COMPLEX, BLOOD CLOTTING,HYDROLASE-INHIBITOR COMPLEX
3hwk:D (ARG357) to (ALA380) CRYSTAL STRUCTURE OF METHYLCITRATE SYNTHASE FROM MYCOBACTERIUM TUBERCULOSIS | NIAID, SSGCID, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, TUBERCLUOSIS, UW, SBRI, DECODE, ACYLTRANSFERASE, TRANSFERASE
3hwk:E (TRP361) to (ALA380) CRYSTAL STRUCTURE OF METHYLCITRATE SYNTHASE FROM MYCOBACTERIUM TUBERCULOSIS | NIAID, SSGCID, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, TUBERCLUOSIS, UW, SBRI, DECODE, ACYLTRANSFERASE, TRANSFERASE
1sb1:H (ASP125) to (ASN159) NOVEL NON-COVALENT THROMBIN INHIBITORS INCORPORATING P1 4,5,6,7- TETRAHYDROBENZOTHIAZOLE ARGININE SIDE CHAIN MIMETICS | THROMBIN, INHIBITION, HIRUGEN, SERINE PROTEASE INHIBITOR, BLOOD CLOTTING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ze8:C (GLY466) to (SER508) PBP ACCA FROM A. TUMEFACIENS C58 | PBP FROM C CLUSTER, TRANSPORT PROTEIN
4zg4:E (ALA2) to (SER24) MYOSIN VC PRE-POWERSTROKE | MYOSIN, PRE-POWERSTROKE, MOTOR PROTEIN
4zg9:B (LYS209) to (LEU244) STRUCTURAL BASIS FOR INHIBITION OF HUMAN AUTOTAXIN BY FOUR NOVEL COMPOUNDS | AUTOTAXIN, ENPP2, INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1sfq:B (ASP125) to (ASN159) FAST FORM OF THROMBIN MUTANT R(77A)A BOUND TO PPACK | SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1sfq:E (ASP125) to (ASN159) FAST FORM OF THROMBIN MUTANT R(77A)A BOUND TO PPACK | SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1sgi:B (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THE ANTICOAGULANT SLOW FORM OF THROMBIN | THROMBIN, ALLOSTERY, HYDROLASE
1shh:E (ASP125) to (ASN159) SLOW FORM OF THROMBIN BOUND WITH PPACK | SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4kr2:A (ALA68) to (PRO98) GLYCYL-TRNA SYNTHETASE IN COMPLEX WITH TRNA-GLY | ROSSMANN FOLD, AMINOACYLATION, TRNA-GLY, LIGASE-RNA COMPLEX
1gpa:A (ASP421) to (MET441) STRUCTURAL MECHANISM FOR GLYCOGEN PHOSPHORYLASE CONTROL BY PHOSPHORYLATION AND AMP | GLYCOGEN PHOSPHORYLASE
1gpa:B (ASP421) to (ALA442) STRUCTURAL MECHANISM FOR GLYCOGEN PHOSPHORYLASE CONTROL BY PHOSPHORYLATION AND AMP | GLYCOGEN PHOSPHORYLASE
1gpa:C (ASP421) to (MET441) STRUCTURAL MECHANISM FOR GLYCOGEN PHOSPHORYLASE CONTROL BY PHOSPHORYLATION AND AMP | GLYCOGEN PHOSPHORYLASE
1sl3:A (ASP125) to (ASN159) CRYSTAL STRUCTUE OF THROMBIN IN COMPLEX WITH A POTENT P1 HETEROCYCLE- ARYL BASED INHIBITOR | THROMBIN INHIBITOR COMPLEX, BLOOD CLOTTING, HYDROLASE-INHIBITOR COMPLEX, BLOOD CLOTTING,HYDROLASE-INHIBITOR COMPLEX
1grq:A (VAL36) to (PRO66) CHLORAMPHENICOL PHOSPHOTRANSFERASE IN COMPLEX WITH P-AMINO-CHLORAMPHENICOL FROM STREPTOMYCES VENEZUELAE | TRANSFERASE, KINASE, ANTIBIOTIC RESISTANCE, PHOSPHORYLATION, MONONUCLEOTIDE BINDING FOLD
1sr5:C (ASP125) to (ASN159) ANTITHROMBIN-ANHYDROTHROMBIN-HEPARIN TERNARY COMPLEX STRUCTURE | SERINE PROTEINASE INHIBITOR, ANTITHROMBIN ACTIVATION BY HEP ANHYDROTHROMBIN, PROTEIN-PROTEIN INTERACTIONS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2ga0:A (ALA42) to (THR86) VARIABLE SMALL PROTEIN 1 OF BORRELIA TURICATAE (VSPA OR VSP1) | HELICAL BUNDLE, NI(II) BINDING SITES, IMMUNE SYSTEM
2ga0:D (ALA42) to (THR86) VARIABLE SMALL PROTEIN 1 OF BORRELIA TURICATAE (VSPA OR VSP1) | HELICAL BUNDLE, NI(II) BINDING SITES, IMMUNE SYSTEM
2ga0:F (ALA42) to (THR86) VARIABLE SMALL PROTEIN 1 OF BORRELIA TURICATAE (VSPA OR VSP1) | HELICAL BUNDLE, NI(II) BINDING SITES, IMMUNE SYSTEM
2gai:A (THR464) to (PRO487) STRUCTURE OF FULL LENGTH TOPOISOMERASE I FROM THERMOTOGA MARITIMA IN TRICLINIC CRYSTAL FORM | TOPOISOMERASE, ZINC RIBBON, ISOMERASE
2gai:B (THR464) to (PRO487) STRUCTURE OF FULL LENGTH TOPOISOMERASE I FROM THERMOTOGA MARITIMA IN TRICLINIC CRYSTAL FORM | TOPOISOMERASE, ZINC RIBBON, ISOMERASE
2gaj:A (THR464) to (PRO487) STRUCTURE OF FULL LENGTH TOPOISOMERASE I FROM THERMOTOGA MARITIMA IN MONOCLINIC CRYSTAL FORM | TOPOISOMERASE, ZINC RIBBON, ISOMERASE
2gaj:B (THR464) to (PRO487) STRUCTURE OF FULL LENGTH TOPOISOMERASE I FROM THERMOTOGA MARITIMA IN MONOCLINIC CRYSTAL FORM | TOPOISOMERASE, ZINC RIBBON, ISOMERASE
1svl:B (LEU497) to (THR518) CO-CRYSTAL STRUCTURE OF SV40 LARGE T ANTIGEN HELICASE DOMAIN AND ADP | AAA+ FOLD, VIRAL PROTEIN
1gxd:C (HIS7) to (SER25) PROMMP-2/TIMP-2 COMPLEX | HYDROLASE, METALLOPROTEASE, ZYMOGEN, COLLAGEN DEGRADATION, EXTRACELLULAR MATRIX, GELATINASE A, MATRIX METALLOPROTEINASE 2, PROTEINASE INHIBITOR
2gce:C (GLU310) to (PRO328) THE 1,1-PROTON TRANSFER REACTION MECHANISM BY ALPHA- METHYLACYL-COA RACEMASE IS CATALYZED BY AN ASPARTATE/HISTIDINE PAIR AND INVOLVES A SMOOTH, METHIONINE- RICH SURFACE FOR BINDING THE FATTY ACYL MOIETY | ALPHA-METHYLACYL-COA RACEMASE, RACEMASE, COA TRANSFERASE, PROTON TRANSFER, COENZYME A, ISOMERASE
2gd0:D (GLU310) to (PRO328) THE 1,1-PROTON TRANSFER REACTION MECHANISM BY ALPHA-METHYLACYL-COA RACEMASE IS CATALYZED BY AN ASPARTATE/HISTIDINE PAIR AND INVOLVES A SMOOTH, METHIONINE-RICH SURFACE FOR BINDING THE FATTY ACYL MOIETY | ALPHA-METHYLACYL-COA RACEMASE, RACEMASE, COA TRANSFERASE, PROTON TRANSFER, COENZYME A, ISOMERASE
2gd2:A (GLU310) to (PRO328) THE 1,1-PROTON TRANSFER REACTION MECHANISM BY ALPHA-METHYLACYL-COA RACEMASE IS CATALYZED BY AN ASPARTATE/HISTIDINE PAIR AND INVOLVES A SMOOTH, METHIONINE-RICH SURFACE FOR BINDING THE FATTY ACYL MOIETY | ALPHA-METHYLACYL-COA RACEMASE, RACEMASE, COA TRANSFERASE, PROTON TRANSFER, COENZYME A, ISOMERASE
2gd2:C (GLU310) to (PRO328) THE 1,1-PROTON TRANSFER REACTION MECHANISM BY ALPHA-METHYLACYL-COA RACEMASE IS CATALYZED BY AN ASPARTATE/HISTIDINE PAIR AND INVOLVES A SMOOTH, METHIONINE-RICH SURFACE FOR BINDING THE FATTY ACYL MOIETY | ALPHA-METHYLACYL-COA RACEMASE, RACEMASE, COA TRANSFERASE, PROTON TRANSFER, COENZYME A, ISOMERASE
2gd2:D (GLU310) to (PRO328) THE 1,1-PROTON TRANSFER REACTION MECHANISM BY ALPHA-METHYLACYL-COA RACEMASE IS CATALYZED BY AN ASPARTATE/HISTIDINE PAIR AND INVOLVES A SMOOTH, METHIONINE-RICH SURFACE FOR BINDING THE FATTY ACYL MOIETY | ALPHA-METHYLACYL-COA RACEMASE, RACEMASE, COA TRANSFERASE, PROTON TRANSFER, COENZYME A, ISOMERASE
2gde:H (ASP125) to (ASN159) THROMBIN IN COMPLEX WITH INHIBITOR | THROMBIN, COMPLEX STRUCTURE, BLOOD CLOTTING-HYDROLASE INHIBITOR COMPLEX
3ve2:B (THR127) to (LYS169) THE 2.1 ANGSTROM CRYSTAL STRUCTURE OF TRANSFERRIN BINDING PROTEIN B (TBPB) FROM SEROGROUP B M982 NEISSERIA MENINGITIDIS | LIPOPROTEIN, TRANSFERRIN RECEPTOR, IRON ACQUISITION, VACCINE CANDIDATE, HOST PATHOGEN INTERACTION, BETA BARREL, RECEPTOR, TRANSFERRIN, OUTERMEMBRANE, TRANSFERRIN-BINDING PROTEIN
1h17:A (GLY528) to (GLY561) PYRUVATE FORMATE-LYASE (E.COLI) IN COMPLEX WITH COA AND THE SUBSTRATE ANALOG OXAMATE | LYASE, GLYCYL RADICAL ENZYME, TRANSFERASE, ACYLTRANSFERASE ACETYLATION
1h17:A (ARG712) to (ARG738) PYRUVATE FORMATE-LYASE (E.COLI) IN COMPLEX WITH COA AND THE SUBSTRATE ANALOG OXAMATE | LYASE, GLYCYL RADICAL ENZYME, TRANSFERASE, ACYLTRANSFERASE ACETYLATION
1h18:A (GLY528) to (GLY561) PYRUVATE FORMATE-LYASE (E.COLI) IN COMPLEX WITH PYRUVATE | LYASE, GLYCYL RADICAL ENZYME, TRANSFERASE, ACYLTRANSFERASE, ACETYLATION
1h18:A (ARG712) to (ARG738) PYRUVATE FORMATE-LYASE (E.COLI) IN COMPLEX WITH PYRUVATE | LYASE, GLYCYL RADICAL ENZYME, TRANSFERASE, ACYLTRANSFERASE, ACETYLATION
1h18:B (GLY528) to (GLY561) PYRUVATE FORMATE-LYASE (E.COLI) IN COMPLEX WITH PYRUVATE | LYASE, GLYCYL RADICAL ENZYME, TRANSFERASE, ACYLTRANSFERASE, ACETYLATION
1h18:B (GLU713) to (ARG738) PYRUVATE FORMATE-LYASE (E.COLI) IN COMPLEX WITH PYRUVATE | LYASE, GLYCYL RADICAL ENZYME, TRANSFERASE, ACYLTRANSFERASE, ACETYLATION
1t0f:A (LYS227) to (GLN261) CRYSTAL STRUCTURE OF THE TNSA/TNSC(504-555) COMPLEX | PROTEIN-PROTEIN COMPLEX, MIXED ALPHA-BETA, DNA BINDING PROTEIN
4l1p:B (ARG366) to (VAL402) CRYSTAL STRUCTURE OF HUMAN RTF1 PLUS3 DOMAIN | TUTOR, PLUS3, PEPTIDE BINDING PROTEIN, SPT5 CTR BINDING, TRANSCRIPTION, PAF1 COMPLEX, RTF1, ORF ASSOCIATION REGION, CHROMATIN
4l1u:D (SER365) to (VAL402) CRYSTAL STRUCTURE OF HUMAN RTF1 PLUS3 DOMAIN IN COMPLEX WITH SPT5 CTR PHOSPHOPEPTIDE | TUTOR, PLUS3, PEPTIDE BINDING PROTEIN, SPT5 CTR BINDING, TRANSCRIPTION, PAF1 COMPLEX, RTF1, ORF ASSOCIATION REGION, CHROMATIN, TRANSCRIPTION-PEPTIDE COMPLEX
4l1u:E (ARG366) to (VAL402) CRYSTAL STRUCTURE OF HUMAN RTF1 PLUS3 DOMAIN IN COMPLEX WITH SPT5 CTR PHOSPHOPEPTIDE | TUTOR, PLUS3, PEPTIDE BINDING PROTEIN, SPT5 CTR BINDING, TRANSCRIPTION, PAF1 COMPLEX, RTF1, ORF ASSOCIATION REGION, CHROMATIN, TRANSCRIPTION-PEPTIDE COMPLEX
4zlc:A (SER235) to (LEU266) CRYSTAL STRUCTURE OF THE ROQ DOMAIN OF HUMAN ROQUIN-2 | RNA BINDING PROTEIN
4zlc:B (SER235) to (LEU266) CRYSTAL STRUCTURE OF THE ROQ DOMAIN OF HUMAN ROQUIN-2 | RNA BINDING PROTEIN
4zlc:C (SER235) to (LEU266) CRYSTAL STRUCTURE OF THE ROQ DOMAIN OF HUMAN ROQUIN-2 | RNA BINDING PROTEIN
4zlc:D (SER235) to (LEU266) CRYSTAL STRUCTURE OF THE ROQ DOMAIN OF HUMAN ROQUIN-2 | RNA BINDING PROTEIN
4l4l:B (ASN316) to (PRO345) STRUCTURAL ANALYSIS OF A PHOSPHORIBOSYLATED INHIBITOR IN COMPLEX WITH HUMAN NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE | TRANSFERASE, INHIBITOR PRPP ADDUCT, ACTIVE SITE, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX
2gm9:A (VAL422) to (MET441) STRUCTURE OF RABBIT MUSCLE GLYCOGEN PHOSPHORYLASE IN COMPLEX WITH THIENOPYRROLE | GLYCOGEN PHOSPHORYLASE, TRANSFERASE
3if5:A (ILE28) to (CYS52) CRYSTAL STRUCTURE ANALYSIS OF MGLU | FRAGMENT, HYDROLASE
2gp9:B (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THE SLOW FORM OF THROMBIN IN A SELF- INHIBITED CONFORMATION | SERINE PROTEASE, HYDROLASE
2gpr:A (ASP87) to (ASP116) GLUCOSE PERMEASE IIA FROM MYCOPLASMA CAPRICOLUM | PHOSPHOTRANSFERASE, GLUCOSE PERMEASE, ENZYME IIA, MYCOPLASMA
3ih8:A (ILE28) to (GLY54) CRYSTAL STRUCTURE ANALYSIS OF MGLU IN ITS NATIVE FORM | SALT-TOLERANT GLUTAMINASE, HYDROLASE
3ih9:A (ILE28) to (CYS52) CRYSTAL STRUCTURE ANALYSIS OF MGLU IN ITS TRIS FORM | SALT-TOLERANT GLUTAMINASE, HYDROLASE
2grg:A (PRO6) to (GLY31) SOLUTION NMR STRUCTURE OF PROTEIN YNR034W-A FROM SACCHAROMYCES CEREVISIAE. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET YT727; ONTARIO CENTER FOR STRUCTURAL PROTEOMICS TARGET YST6499. | HELIX/BETA STRAND PROTEIN, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, UNKNOWN FUNCTION
1ta2:A (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THROMBIN IN COMPLEX WITH COMPOUND 1 | THROMBIN INHIBITOR COMPLEX, BLOOD CLOTTING, HYDROLASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
1ta6:A (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THROMBIN IN COMPLEX WITH COMPOUND 14B | THROMBIN INHIBITOR COMPLEX, BLOOD CLOTTING, HYDROLASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3vkg:A (PHE4679) to (LEU4705) X-RAY STRUCTURE OF AN MTBD TRUNCATION MUTANT OF DYNEIN MOTOR DOMAIN | AAA+ PROTEIN, MOLECULAR MOTOR, MICROTUBLES, MOTOR PROTEIN
4zs8:B (ARG58) to (VAL84) CRYSTAL STRUCTURE OF LIGAND-FREE, FULL LENGTH DASR | TRANSCRIPTION, REPRESSOR, BACTERIAL TRANSCRIPTION REGULATION, TRANSCRIPTION FACTOR, GNTR/HUTC FAMILY, WINGED HELIX-TURN-HELIX MOTIF, N-ACETYLGLUCOSAMINE UTILIZATION, LIGAND-FREE, MASTER REGULATOR
1hai:H (ASP125) to (ASN159) THE ISOMORPHOUS STRUCTURES OF PRETHROMBIN2, HIRUGEN-AND PPACK- THROMBIN: CHANGES ACCOMPANYING ACTIVATION AND EXOSITE BINDING TO THROMBIN | SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1hav:B (LYS105) to (SER131) HEPATITIS A VIRUS 3C PROTEINASE | POLYPROTEIN, COAT PROTEIN, CORE PROTEIN, RNA-DIRECTED RNA POLYMERASE, HYDROLASE, THIOL PROTEASE
1tbz:H (ASP125) to (ASN159) HUMAN THROMBIN WITH ACTIVE SITE N-METHYL-D PHENYLALANYL-N-[5- (AMINOIMINOMETHYL)AMINO]-1-{{BENZOTHIAZOLYL)CARBONYL] BUTYL]-L- PROLINAMIDE TRIFLUROACETATE AND EXOSITE-HIRUGEN | COMPLEX (SERINE PROTEASE-INHIBITOR), HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2gvg:B (ASN316) to (PRO345) CRYSTAL STRUCTURE OF HUMAN NMPRTASE AND ITS COMPLEX WITH NMN | NMPRTASE, VISFATIN, PBEF, CRYSTAL, CANCER, TRANSFERASE
3imn:A (THR170) to (GLU190) CRYSTAL STRUCTURE OF HEPARIN LYASE I FROM BACTEROIDES THETAIOTAOMICRON | JELLY ROLL, LYASE
1hbt:H (ASP125) to (ASN159) HUMAN ALPHA-THROMBIN COMPLEXED WITH A PEPTIDYL PYRIDINIUM METHYL KETONE CONTAINING BIVALENT INHIBITOR | SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1thp:B (ASP125) to (ASN159) STRUCTURE OF HUMAN ALPHA-THROMBIN Y225P MUTANT BOUND TO D-PHE-PRO-ARG- CHLOROMETHYLKETONE | SERINE PROTEASE, FPRCK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1thr:H (ASP125) to (ASN159) STRUCTURES OF THROMBIN COMPLEXES WITH A DESIGNED AND A NATURAL EXOSITE INHIBITOR | HYDROLASE(SERINE PROTEINASE)
2h1l:B (LEU497) to (GLN519) THE STRUCTURE OF THE ONCOPROTEIN SV40 LARGE T ANTIGEN AND P53 TUMOR SUPPRESSOR COMPLEX | P53 LOOP-3 CONFORMATION CHANGE, VIRAL PROTEIN
2h1l:E (LEU497) to (GLN519) THE STRUCTURE OF THE ONCOPROTEIN SV40 LARGE T ANTIGEN AND P53 TUMOR SUPPRESSOR COMPLEX | P53 LOOP-3 CONFORMATION CHANGE, VIRAL PROTEIN
2h1l:G (LEU497) to (ILE520) THE STRUCTURE OF THE ONCOPROTEIN SV40 LARGE T ANTIGEN AND P53 TUMOR SUPPRESSOR COMPLEX | P53 LOOP-3 CONFORMATION CHANGE, VIRAL PROTEIN
2h1l:K (LEU497) to (GLN519) THE STRUCTURE OF THE ONCOPROTEIN SV40 LARGE T ANTIGEN AND P53 TUMOR SUPPRESSOR COMPLEX | P53 LOOP-3 CONFORMATION CHANGE, VIRAL PROTEIN
3iqs:A (ASP198) to (ASN244) CRYSTAL STRUCTURE OF THE ANTI-VIRAL APOBEC3G CATALYTIC DOMAIN | FIVE BETA-STRANDS SURROUNDED BY SIX ALPHA-HELICES, ALTERNATIVE SPLICING, ANTIVIRAL DEFENSE, CYTOPLASM, HOST- VIRUS INTERACTION, HYDROLASE, METAL-BINDING, NUCLEUS, POLYMORPHISM, UBL CONJUGATION, ZINC
4lit:A (SER70) to (HIS99) STRUCTURE OF YCFD A RIBOSOMAL OXYGENASE FROM ESCHERICHIA COLI IN COMPLEX WITH COBALT AND 2-OXOGLUTARATE. | JMJC DOMAIN, DIOXYGENASE, HYDROXYLATION, OXIDOREDUCTASE
4liu:A (SER70) to (HIS99) STRUCTURE OF YCFD, A RIBOSOMAL OXYGENASE FROM ESCHERICHIA COLI. | JMJC DOMAIN, DIOXYGENASE, HYDROXYLATION, OXIDOREDUCTASE
1tmb:H (ASP125) to (ASN159) MOLECULAR BASIS FOR THE INHIBITION OF HUMAN ALPHA-THROMBIN BY THE MACROCYCLIC PEPTIDE CYCLOTHEONAMIDE A | SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1tmu:H (ASP125) to (ASN159) CHANGES IN INTERACTIONS IN COMPLEXES OF HIRUDIN DERIVATIVES AND HUMAN ALPHA-THROMBIN DUE TO DIFFERENT CRYSTAL FORMS | SERINE PROTEASE, PPACK INHIBITOR, BLOOD COAGULATION, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
1hl6:D (GLN55) to (SER103) A NOVEL MODE OF RBD-PROTEIN RECOGNITION IN THE Y14-MAGO COMPLEX | SIGNAL PROTEIN, RDB, EXON-EXON JUNCTION, OSKAR, RNP, NMD
1tom:H (ASP125) to (ASN159) ALPHA-THROMBIN COMPLEXED WITH HIRUGEN | HYDROLASE, SERINE PROTEASE, KRINGLE, DISEASE MUTATION, COMPLEX (HYDROLASE-INHIBITOR), HYDROLASE-HYDROLASE INHIBITOR COMPLEX, BLOOD COAGULATION-HYDROLASE INHIBITOR COMPLEX
1tq0:B (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THE POTENT ANTICOAGULANT THROMBIN MUTANT W215A/E217A IN FREE FORM | THROMBIN, ANTICOAGULANT, BLOOD CLOTTING
3vn4:A (THR441) to (LYS497) CRYSTAL STRUCTURE OF THE EXOSITE-CONTAINING FRAGMENT OF HUMAN ADAMTS13 (P475S MUTANT) | HYDROLASE
3vp6:A (ALA374) to (LYS419) STRUCTURAL CHARACTERIZATION OF GLUTAMIC ACID DECARBOXYLASE; INSIGHTS INTO THE MECHANISM OF AUTOINACTIVATION | CATALYTIC LOOP SWAP, LYASE
3vp6:B (ALA374) to (LYS419) STRUCTURAL CHARACTERIZATION OF GLUTAMIC ACID DECARBOXYLASE; INSIGHTS INTO THE MECHANISM OF AUTOINACTIVATION | CATALYTIC LOOP SWAP, LYASE
1tt7:B (TYR45) to (SER91) CRYSTAL STRUCTURE OF BACILLUS SUBTILIS PROTEIN YHFP | YHFP, ALCOHOL DEHYDROGENASE, ZN-DEPENDENT, NAD, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, PSI, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC, UNKNOWN FUNCTION
4zzg:G (PHE21) to (ILE53) YEAST 20S PROTEASOME IN COMPLEX WITH BLM-PEP ACTIVATOR | 20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE
4zzg:U (PHE21) to (SER55) YEAST 20S PROTEASOME IN COMPLEX WITH BLM-PEP ACTIVATOR | 20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE
1twx:B (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THE THROMBIN MUTANT D221A/D222K | THROMBIN, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2hoe:A (THR34) to (LEU68) CRYSTAL STRUCTURE OF N-ACETYLGLUCOSAMINE KINASE (TM1224) FROM THERMOTOGA MARITIMA AT 2.46 A RESOLUTION | TM1224, N-ACETYLGLUCOSAMINE KINASE (EC 2.7.1.59), STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, TRANSFERASE
2hpp:H (ASP125) to (ASN159) STRUCTURES OF THE NONCOVALENT COMPLEXES OF HUMAN AND BOVINE PROTHROMBIN FRAGMENT 2 WITH HUMAN PPACK-THROMBIN | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, SERINE PROTEINASE
2hpy:A (CYS167) to (ILE189) CRYSTALLOGRAPHIC MODEL OF LUMIRHODOPSIN | G PROTEIN-COUPLED RECEPTOR, VISUAL PIGMENT, SIGNALING PROTEIN
4lqi:F (PHE22) to (THR55) YEAST 20S PROTEASOME IN COMPLEX WITH VIBRALACTONE | BETA-LACTONE, INHIBITOR, NATURAL PRODUCT, TARGET IDENTIFICATION, NTN- PROTEASE, CELLULAR PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4lqi:T (PHE22) to (THR55) YEAST 20S PROTEASOME IN COMPLEX WITH VIBRALACTONE | BETA-LACTONE, INHIBITOR, NATURAL PRODUCT, TARGET IDENTIFICATION, NTN- PROTEASE, CELLULAR PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3vxe:H (ASP125) to (ASN159) HUMAN ALPHA-THROMBIN-BIVALIRUDIN COMPLEX AT PD5.0 | SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3vxf:H (ASP125) to (ASN159) X/N JOINT REFINEMENT OF HUMAN ALPHA-THROMBIN-BIVALIRUDIN COMPLEX PD5 | SERINE PROTEASE, HYDROLYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2wmq:A (ASN51) to (GLY89) CRYSTAL STRUCTURE OF CHECKPOINT KINASE 1 (CHK1) IN COMPLEX WITH INHIBITORS | SERINE/THREONINE-PROTEIN KINASE, POLYMORPHISM, PHOSPHOPROTEIN, UBL CONJUGATION, ISOPEPTIDE BOND, CHECKPOINT KINASE, NUCLEOTIDE-BINDING, SERINE/THREONINE KINASE, DNA DAMAGE, DNA REPAIR, ATP-BINDING, TRANSFERASE, CHK1, KINASE, NUCLEUS, CYTOPLASM, CELL CYCLE
4lts:B (PRO317) to (PRO345) DISCOVERY OF POTENT AND EFFICACIOUS CYANOGUANIDINE-CONTAINING NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE (NAMPT) INHIBITORS | TRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4lva:A (LEU318) to (PRO345) FRAGMENT-BASED IDENTIFICATION OF AMIDES DERIVED FROM TRANS-2-(PYRIDIN- 3-YL)CYCLOPROPANECARBOXYLIC ACID AS POTENT INHIBITORS OF HUMAN NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE (NAMPT) | TRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4lva:B (ASN316) to (PRO345) FRAGMENT-BASED IDENTIFICATION OF AMIDES DERIVED FROM TRANS-2-(PYRIDIN- 3-YL)CYCLOPROPANECARBOXYLIC ACID AS POTENT INHIBITORS OF HUMAN NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE (NAMPT) | TRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4lvb:B (ASN316) to (PRO345) FRAGMENT-BASED IDENTIFICATION OF AMIDES DERIVED FROM TRANS-2-(PYRIDIN- 3-YL)CYCLOPROPANECARBOXYLIC ACID AS POTENT INHIBITORS OF HUMAN NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE (NAMPT) | TRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4lwu:A (THR45) to (CYS73) THE 1.14A CRYSTAL STRUCTURE OF HUMANIZED XENOPUS MDM2 WITH RO5499252 | MDM2, SPIROINDOLINONE, E3 UBIQUITIN LIGASE, P53, NUCLEUS, LIGASE- LIGASE INHIBITOR COMPLEX
4lz1:H (ASP125) to (ASN159) X-RAY STRUCTURE OF THE COMPLEX BETWEEN HUMAN THROMBIN AND THE TBA DELETION MUTANT LACKING THYMINE 12 NUCLEOBASE | PROTEIN-DNA COMPLEX, BLOOD COAGULATION, APTAMER, INHIBITOR-DNA COMPLEX, DNA APTAMER, G-QUADRUPLEX, SERINE PROTEASE, HYDROLASE, ABASIC FURAN, DNA THYMINE NUCLEOBASE DELETION, BLOOD, HYDROLASE-DNA COMPLEX, HYDROLASE-HYDROLASE INHIBITOR-DNA COMPLEX
4lz4:D (ASP125) to (ASN159) X-RAY STRUCTURE OF THE COMPLEX BETWEEN HUMAN THROMBIN AND THE TBA DELETION MUTANT LACKING THYMINE 3 NUCLEOBASE | PROTEIN-DNA COMPLEX, DNA APTAMER, G-QUADRUPLEX, TBA DELETION MUTANT, SERINE PROTEASE, HYDROLASE, BLOOD COAGULATION, BLOOD, HYDROLASE-DNA COMPLEX, HYDROLASE-HYDROLASE INHIBITOR-DNA COMPLEX
1ubf:A (SER271) to (TYR295) MSRECA-ATPGS COMPLEX | RECOMBINATION, DNA-REPAIR
1udn:A (PHE177) to (GLY204) CRYSTAL STRUCTURE OF THE TRNA PROCESSING ENZYME RNASE PH FROM AQUIFEX AEOLICUS | TRANSFERASE, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, STRUCTURAL GENOMICS
1uds:A (ASN176) to (GLY204) CRYSTAL STRUCTURE OF THE TRNA PROCESSING ENZYME RNASE PH R126A MUTANT FROM AQUIFEX AEOLICUS | TRANSFERASE, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, STRUCTURAL GENOMICS
2wux:A (PHE191) to (PRO235) THE CRYSTAL STRUCTURE OF RECOMBINANT BACULOVIRUS POLYHEDRA | MICROCRYSTALS, POLYHEDRA, VIRAL PROTEIN, VIRAL OCCLUSION BODY, VIRAL CAPSID
2wuy:A (PHE191) to (PRO235) THE CRYSTAL STRUCTURE OF WILD-TYPE BACULOVIRUS POLYHEDRA | VIRAL PROTEIN, MICROCRYSTALS, POLYHEDRA, VIRUS, VIRAL OCCLUSION BODY, VIRAL CAPSID
2wuz:A (GLY424) to (ARG475) X-RAY STRUCTURE OF CYP51 FROM TRYPANOSOMA CRUZI IN COMPLEX WITH FLUCONAZOLE IN ALTERNATIVE CONFORMATION | OXIDOREDUCTASE, METHYLTRANSFERASE, P450, IRON, CYP51, METAL-BINDING, ERGOSTEROL BIOSYNTHESIS
2wv0:J (ARG48) to (VAL74) CRYSTAL STRUCTURE OF THE GNTR-HUTC FAMILY MEMBER YVOA FROM BACILLUS SUBTILIS | REPRESSOR, DNA-BINDING, TRANSCRIPTION, TRANSCRIPTION REGULATION, TRANSCRIPTIONAL REGULATOR, GNTR/HUTC FAMILY, CHORISMATE LYASE FOLD
3w7u:A (ASP510) to (LEU546) ESCHERICHIA COLI K12 YGJK COMPLEXED WITH GALACTOSE | GH63, PROCESSING ALPHA-GLUCOSIDASE I, ALPHA/ALPHA BARREL, HYDROLASE
3w7u:B (ASP510) to (LEU546) ESCHERICHIA COLI K12 YGJK COMPLEXED WITH GALACTOSE | GH63, PROCESSING ALPHA-GLUCOSIDASE I, ALPHA/ALPHA BARREL, HYDROLASE
3j1e:G (GLY28) to (THR69) CRYO-EM STRUCTURE OF 9-FOLD SYMMETRIC RATCPN-BETA IN APO STATE | GROUP II CHAPERONIN, CHAPERONE
3j1e:K (ALA34) to (THR69) CRYO-EM STRUCTURE OF 9-FOLD SYMMETRIC RATCPN-BETA IN APO STATE | GROUP II CHAPERONIN, CHAPERONE
3j1e:L (GLY28) to (THR69) CRYO-EM STRUCTURE OF 9-FOLD SYMMETRIC RATCPN-BETA IN APO STATE | GROUP II CHAPERONIN, CHAPERONE
3j1e:O (GLY28) to (THR69) CRYO-EM STRUCTURE OF 9-FOLD SYMMETRIC RATCPN-BETA IN APO STATE | GROUP II CHAPERONIN, CHAPERONE
3j1e:Q (GLY28) to (THR69) CRYO-EM STRUCTURE OF 9-FOLD SYMMETRIC RATCPN-BETA IN APO STATE | GROUP II CHAPERONIN, CHAPERONE
3j1f:C (ALA31) to (ILE68) CRYO-EM STRUCTURE OF 9-FOLD SYMMETRIC RATCPN-BETA IN ATP-BINDING STATE | GROUP II CHAPERONIN, CHAPERONE
3j1f:N (ALA31) to (THR69) CRYO-EM STRUCTURE OF 9-FOLD SYMMETRIC RATCPN-BETA IN ATP-BINDING STATE | GROUP II CHAPERONIN, CHAPERONE
3j1n:A (SER754) to (ASN802) CRYO-EM MAP OF A YEAST MINIMAL PREINITIATION COMPLEX INTERACTING WITH THE MEDIATOR HEAD MODULE | TRANSCRIPTION, MEDIATOR HEAD MODULE, PREINITIATION COMPLEX, TRANSFERASE
5aa6:B (GLY467) to (VAL511) HOMOHEXAMERIC STRUCTURE OF THE SECOND VANADATE-DEPENDENT BROMOPEROXIDASE (ANII) FROM ASCOPHYLLUM NODOSUM | OXIDOREDUCTASE, BROWN ALGAE, BROMOPEROXIDASE, VANADIUM-DEPENDANT HALOGENPEROXIDASE
2iei:B (ASP421) to (MET441) CRYSTAL STRUCTURE OF RABBIT MUSCLE GLYCOGEN PHOSPHORYLASE IN COMPLEX WITH 3,4-DIHYDRO-2-QUINOLONE | GLYCOGEN PHOSPHORYLASE, DIABETES, GLUCOSE, TRANSFERASE
3we3:B (SER1138) to (LEU1173) STRUCTURE OF BLM RQC DOMAIN BOUND TO AN ARSENATE ION | WINGED-HELIX, DNA HELICASE, DNA BINDING, DNA BINDING PROTEIN
2x1g:B (SER56) to (PHE100) CRYSTAL STRUCTURE OF IMPORTIN13 - MAGO-Y14 COMPLEX | TRANSPORT PROTEIN, DEVELOPMENTAL PROTEIN, MRNA PROCESSING, NUCLEAR TRANSPORT, MRNA SPLICING, MRNA TRANSPORT
2x1g:D (SER56) to (PHE100) CRYSTAL STRUCTURE OF IMPORTIN13 - MAGO-Y14 COMPLEX | TRANSPORT PROTEIN, DEVELOPMENTAL PROTEIN, MRNA PROCESSING, NUCLEAR TRANSPORT, MRNA SPLICING, MRNA TRANSPORT
5aeg:B (ASP597) to (ALA616) A BACTERIAL PROTEIN STUCTURE IN GLYCOSIDE HYDROLASE FAMILY 31. | HYDROLASE, GH31, ALPHA-SULFOQUINOVOSIDASE
5aek:U (THR369) to (THR398) CRYSTAL STRUCTURE OF THE HUMAN SENP2 C548S IN COMPLEX WITH THE HUMAN SUMO1 K48M F66W | HYDROLASE, SUMO, SENP, FOLDING EVOLUTION
2imz:A (ARG18) to (ALA42) CRYSTAL STRUCTURE OF MTU RECA INTEIN SPLICING DOMAIN | N-TERMINAL CYSTEINE SULFINIC ACID C-TERMINAL AMINOSUCCINIMIDE, HYDROLASE
3wgb:D (LEU172) to (GLY211) CRYSTAL STRUCTURE OF AEROMONAS JANDAEI L-ALLO-THREONINE ALDOLASE | LYASE, PYRIDOXAL-5'-PHOSPHATE, THREONINE ALDOLASE
3wgc:A (LEU172) to (GLY211) AEROMONAS JANDAEI L-ALLO-THREONINE ALDOLASE H128Y/S292R DOUBLE MUTANT | LYASE, PYRIDOXAL-5'-PHOSPHATE, THREONINE ALDOLASE
3wgc:B (LEU172) to (GLY211) AEROMONAS JANDAEI L-ALLO-THREONINE ALDOLASE H128Y/S292R DOUBLE MUTANT | LYASE, PYRIDOXAL-5'-PHOSPHATE, THREONINE ALDOLASE
5afy:H (ASP125) to (ASN159) THROMBIN IN COMPLEX WITH 3-CHLORO-BENZAMIDE | HYDROLASE, HYDROLASE INHIBITOR COMPLEX, SERINE PROTEASE, BLOOD COAGULATION, BLOOD CLOTTING, CONVERTION OF FIBRINOGEN TO FIBRIN, BLOOD CLOTTING INHIBITOR, THROMBIN INHIBITOR, FRAGMENT, GLYCOSYLATION, BLOOD
5afz:H (ASP125) to (ASN159) THROMBIN IN COMPLEX WITH (2R)-2-(BENZYLSULFONYLAMINO)-N-(2-( (4-CARBAMIMIDOYLPHENYL)METHYLAMINO)-2-OXO-PROPYL)-3-PHENYL- PROPANAMIDE | HYDROLASE, HYDROLASE INHIBITOR COMPLEX, SERINE PROTEASE, BLOOD COAGULATION, BLOOD CLOTTING, CONVERTION OF FIBRINOGEN TO FIBRIN, BLOOD CLOTTING INHIBITOR, THROMBIN INHIBITOR, FRAGMENT, GLYCOSYLATION, BLOOD
2io1:A (THR369) to (THR398) CRYSTAL STRUCTURE OF HUMAN SENP2 IN COMPLEX WITH PRESUMO-3 | SUMO, UBIQUITIN, SENP, ULP, COMPLEX, PROTEIN BINDING, HYDROLASE
2io1:C (THR369) to (THR398) CRYSTAL STRUCTURE OF HUMAN SENP2 IN COMPLEX WITH PRESUMO-3 | SUMO, UBIQUITIN, SENP, ULP, COMPLEX, PROTEIN BINDING, HYDROLASE
2io3:A (THR369) to (THR398) CRYSTAL STRUCTURE OF HUMAN SENP2 IN COMPLEX WITH RANGAP1- SUMO-2 | SUMO, UBIQUITIN, SENP, ULP, COMPLEX, PROTEIN BINDING, HYDROLASE
5ahj:F (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH MACYRANONE A | HYDROLASE, PROTEASOME, NATURAL PRODUCT, TARGET IDENTIFICATION, INHIBITION, BINDING ANALYSIS
5ahj:T (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH MACYRANONE A | HYDROLASE, PROTEASOME, NATURAL PRODUCT, TARGET IDENTIFICATION, INHIBITION, BINDING ANALYSIS
2ipc:A (THR233) to (HIS274) CRYSTAL STRUCTURE OF THE TRANSLOCATION ATPASE SECA FROM THERMUS THERMOPHILUS REVEALS A PARALLEL, HEAD-TO-HEAD DIMER | NUCLEOTIDE BINDING FOLD, ATPASE, PARALLEL DIMER, STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, TRANSPORT PROTEIN
2ipc:B (THR233) to (HIS274) CRYSTAL STRUCTURE OF THE TRANSLOCATION ATPASE SECA FROM THERMUS THERMOPHILUS REVEALS A PARALLEL, HEAD-TO-HEAD DIMER | NUCLEOTIDE BINDING FOLD, ATPASE, PARALLEL DIMER, STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, TRANSPORT PROTEIN
2ipc:C (THR233) to (HIS274) CRYSTAL STRUCTURE OF THE TRANSLOCATION ATPASE SECA FROM THERMUS THERMOPHILUS REVEALS A PARALLEL, HEAD-TO-HEAD DIMER | NUCLEOTIDE BINDING FOLD, ATPASE, PARALLEL DIMER, STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, TRANSPORT PROTEIN
2ipc:D (THR233) to (HIS274) CRYSTAL STRUCTURE OF THE TRANSLOCATION ATPASE SECA FROM THERMUS THERMOPHILUS REVEALS A PARALLEL, HEAD-TO-HEAD DIMER | NUCLEOTIDE BINDING FOLD, ATPASE, PARALLEL DIMER, STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, TRANSPORT PROTEIN
1v2i:A (ASP275) to (LYS305) STRUCTURE OF THE HEMAGGLUTININ-NEURAMINIDASE FROM HUMAN PARAINFLUENZA VIRUS TYPE III | PIV3 HN, NATIVE, ORTHORHOMBIC, HYDROLASE
1v2i:B (ASP275) to (LYS305) STRUCTURE OF THE HEMAGGLUTININ-NEURAMINIDASE FROM HUMAN PARAINFLUENZA VIRUS TYPE III | PIV3 HN, NATIVE, ORTHORHOMBIC, HYDROLASE
1v3c:A (ASP275) to (LYS305) STRUCTURE OF THE HEMAGGLUTININ-NEURAMINIDASE FROM HUMAN PARAINFLUENZA VIRUS TYPE III: COMPLEX WITH NEU5AC | PIV3 HN, NATIVE+NEU5AC, HEXAGONAL, HYDROLASE
1v3c:B (GLU276) to (LYS305) STRUCTURE OF THE HEMAGGLUTININ-NEURAMINIDASE FROM HUMAN PARAINFLUENZA VIRUS TYPE III: COMPLEX WITH NEU5AC | PIV3 HN, NATIVE+NEU5AC, HEXAGONAL, HYDROLASE
1v3e:A (GLU276) to (LYS305) STRUCTURE OF THE HEMAGGLUTININ-NEURAMINIDASE FROM HUMAN PARAINFLUENZA VIRUS TYPE III: COMPLEX WITH ZANAMAVIR | PIV3 HN, NATIVE+ZANAMAVIR, HEXAGONAL, HYDROLASE
1v3e:B (ASP275) to (LYS305) STRUCTURE OF THE HEMAGGLUTININ-NEURAMINIDASE FROM HUMAN PARAINFLUENZA VIRUS TYPE III: COMPLEX WITH ZANAMAVIR | PIV3 HN, NATIVE+ZANAMAVIR, HEXAGONAL, HYDROLASE
1j3q:A (GLU38) to (TYR75) CRYSTAL STRUCTURE OF THERMOCOCCUS LITORALIS PHOSPHOGRUCOSE ISOMERASE SOAKED WITH FESO4 | PHOSPHOGLUCOSE ISOMERASE, CUPIN SUPERFAMILY, IRON ION, ARCHAEA
2x7c:A (ASN29) to (ARG53) CRYSTAL STRUCTURE OF HUMAN KINESIN EG5 IN COMPLEX WITH (S)-ENASTRON | MICROTUBULE, ATP-BINDING, MOTOR PROTEIN, CELL DIVISION, MITOSIS, INHIBITOR, CELL CYCLE, NUCLEOTIDE-BINDING
2x9h:A (ASP21) to (GLU51) CRYSTAL STRUCTURE OF MYOSIN-2 MOTOR DOMAIN IN COMPLEX WITH ADP-METAVANADATE AND PENTACHLOROCARBAZOLE | NUCLEOTIDE-BINDING, MOTOR PROTEIN, ACTIN-BINDING, CONTRACTILE PROTEIN
1v95:A (THR68) to (ASN91) SOLUTION STRUCTURE OF ANTICODON BINDING DOMAIN FROM NUCLEAR RECEPTOR COACTIVATOR 5 (HUMAN KIAA1637 PROTEIN) | NUCLEAR RECEPTOR COACTIVATOR 5, COACTIVATOR INDEPENDENT OF AF-2 FUNCTION (CIA), STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, RNA BINDING PROTEIN
3wnu:A (ASN323) to (PRO348) THE CRYSTAL STRUCTURE OF CATALASE-PEROXIDASE, KATG, FROM SYNECHOCOCCUS PCC7942 | PEROXIDASE FAMILY, PEROXIDASE/CATALASE SUBFAMILY, OXIDOREDUCTASE, HEME B, FE, CROSS-LINK, COVALENT TRP-TYR-MET ADDUCT
1jd2:X (PHE22) to (GLU51) 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
1jd2:Z (PHE22) to (LEU51) 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
5amt:B (ASN53) to (PRO79) INTRACELLULAR GROWTH LOCUS PROTEIN E | TRANSPORT PROTEIN, BACTERIAL SECRETION SYSTEM, LIPOPROTEIN, IGLE, TSSJ, FRANCISELLA NOVICIDA
1jg8:B (ILE176) to (GLY215) CRYSTAL STRUCTURE OF THREONINE ALDOLASE (LOW-SPECIFICITY) | GLYCINE BIOSYNTHESIS, THREONINE ALDOLASE, PYRIDOXAL-5'- PHOSPHATE, CALCIUM BINDING SITE, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC, LYASE
5ao4:B (GLY357) to (ARG408) CRYSTAL STRUCTURE OF IN VITRO PHOSPHORYLATED HUMAN SAMHD1 (AMINO ACID RESIDUES 115-626) BOUND TO GTP | HYDROLASE, DEOXYNUCLEOSIDE TRIPHOSPHATE TRIPHOSPHOHYDROLASE, HIV RESTRICTION FACTOR
2j04:A (SER472) to (ASN508) THE TAU60-TAU91 SUBCOMPLEX OF YEAST TRANSCRIPTION FACTOR IIIC | BETA PROPELLER, TYPE 2 PROMOTERS, TRANSCRIPTION, HYPOTHETICAL PROTEIN, PREINITIATION COMPLEX, YEAST RNA POLYMERASE III, TRANSCRIPTION FACTOR IIIC
2j04:C (SER472) to (ASN508) THE TAU60-TAU91 SUBCOMPLEX OF YEAST TRANSCRIPTION FACTOR IIIC | BETA PROPELLER, TYPE 2 PROMOTERS, TRANSCRIPTION, HYPOTHETICAL PROTEIN, PREINITIATION COMPLEX, YEAST RNA POLYMERASE III, TRANSCRIPTION FACTOR IIIC
3wpz:A (GLY142) to (GLY176) MICROBACTERIUM SACCHAROPHILUM K-1 BETA-FRUCTOFURANOSIDASE MUTANT T47S/S200T/F447P/F470Y/P500S | GLYCOSIDE HYDROLASE FAMILY 68, BETA-PROPELLER, HYDROLASE
4mq1:C (ALA388) to (LEU405) THE CRYSTAL STRUCTURE OF DYRK1A WITH A BOUND PYRIDO[2,3-D]PYRIMIDINE INHIBITOR | DYRK1A, DYRK1B, KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4mq2:C (ALA388) to (LEU405) THE CRYSTAL STRUCTURE OF DYRK1A WITH A BOUND PYRIDO[2,3-D]PYRIMIDINE INHIBITOR | DYRK1A, DYRK1B, KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
3j67:A (GLU2452) to (LYS2476) STRUCTURAL MECHANISM OF THE DYNEIN POWERSTROKE (POST-POWERSTROKE STATE) | MOTOR PROTEIN
1vic:B (ASP132) to (ARG157) CRYSTAL STRUCTURE OF CMP-KDO SYNTHETASE | STRUCTURAL GENOMICS, TRANSFERASE
3j68:A (GLU2452) to (LYS2476) STRUCTURAL MECHANISM OF THE DYNEIN POWERSTROKE (PRE-POWERSTROKE STATE) | MOTOR PROTEIN
4mtj:B (LYS742) to (GLN767) STRUCTURE OF THE B12-INDEPENDENT GLYCEROL DEHYDRATASE WITH 1,2- PROPANEDIOL BOUND | PFL-LIKE GLYCYL RADICAL ENZYME, GLYCEROL/DIOL DEHYDRATASE, HYDROLASE
1vom:A (ASP21) to (GLU51) COMPLEX BETWEEN DICTYOSTELIUM MYOSIN AND MGADP AND VANADATE AT 1.9A RESOLUTION | MYOSIN, MOLECULAR MOTOR, TRANSITION-STATE ANALOG, MUSCLE PROTEIN
3wtu:G (PRO36) to (SER65) CRYSTAL STRUCTURE OF THE COMPLEX COMPRISED OF ETS1 (V170A), RUNX1, CBFBETA, AND THE TCRALPHA GENE ENHANCER DNA | PROTEIN-DNA COMPLEX, TRANSCRIPTION, DNA-BINDING, METHYLATION, NUCLEUS, PHOSPHOPROTEIN, TRANSCRIPTION REGULATION, ISOPEPTIDE BOND, PROTO-ONCOGENE, TRANSCRIPTION-DNA COMPLEX
3wty:G (PRO36) to (SER65) CRYSTAL STRUCTURE OF THE COMPLEX COMPRISED OF ETS1(G333P), RUNX1, CBFBETA, AND THE TCRALPHA GENE ENHANCER DNA | PROTEIN-DNA COMPLEX, DNA-BINDING, METHYLATION, NUCLEUS, PHOSPHOPROTEIN, TRANSCRIPTION REGULATION, ISOPEPTIDE BOND, PROTO- ONCOGENE, TRANSCRIPTION-DNA COMPLEX
3wus:A (TYR196) to (ARG235) CRYSTAL STRUCTURE OF THE VIF-BINDING DOMAIN OF HUMAN APOBEC3F | APOBEC3F, A3F, ZINC BINDING, HYDROLASE, ANTIVIRAL ENZYME, CYTIDINE DEAMINASE, DNA BINDING, HIV-1 VIF, SINGLE-STRANDED POLYNUCLEOTIDE
3wus:B (TYR196) to (ARG235) CRYSTAL STRUCTURE OF THE VIF-BINDING DOMAIN OF HUMAN APOBEC3F | APOBEC3F, A3F, ZINC BINDING, HYDROLASE, ANTIVIRAL ENZYME, CYTIDINE DEAMINASE, DNA BINDING, HIV-1 VIF, SINGLE-STRANDED POLYNUCLEOTIDE
1vq2:A (CYS49) to (LEU86) CRYSTAL STRUCTURE OF T4-BACTERIOPHAGE DEOXYCYTIDYLATE DEAMINASE, MUTANT R115E | HYDROLASE
5awg:B (LEU127) to (ALA149) CRYSTAL STRUCTURE OF HG-BOUND SUFB-SUFC-SUFD COMPLEX FROM ESCHERICHIA COLI | IRON-SULFUR CLUSTERS, IRON-SULFUR PROTEINS, ABC PROTEINS, ABC ATPASE, TRANSPORT PROTEIN-PROTEIN BINDING COMPLEX
1js3:A (ALA272) to (LYS317) CRYSTAL STRUCTURE OF DOPA DECARBOXYLASE IN COMPLEX WITH THE INHIBITOR CARBIDOPA | DOPA DECARBOXYLASE, CARBIDOPA, PARKINSON'S DISEASE, VITAMIN B6, LYASE
1js3:B (ALA272) to (LYS317) CRYSTAL STRUCTURE OF DOPA DECARBOXYLASE IN COMPLEX WITH THE INHIBITOR CARBIDOPA | DOPA DECARBOXYLASE, CARBIDOPA, PARKINSON'S DISEASE, VITAMIN B6, LYASE
3wxo:A (ASN323) to (PRO348) CRYSTAL STRUCTURE OF ISONIAZID BOUND KATG CATALASE PEROXIDASE FROM SYNECHOCOCCUS ELONGATUS PCC7942 | PEROXIDASE FAMILY, PEROXIDASE, CATALASE SUBFAMILY, OXIDOREDUCTASE PEROXIDASE, HEME B FE, CROSS-LINK, COVALENT TRP-TYR-MET ADDUCT, OXIDOREDUCTASE
3wxr:D (PHE18) to (THR51) YEAST 20S PROTEASOME WITH A MUTATION OF ALPHA7 SUBUNIT | UPS, 20S PROTEASOME, HYDROLASE, PROTEASE, 19S REGULATORY PARTICLE, MULTICATALYTIC PROTEASE
3wxr:G (PHE21) to (SER55) YEAST 20S PROTEASOME WITH A MUTATION OF ALPHA7 SUBUNIT | UPS, 20S PROTEASOME, HYDROLASE, PROTEASE, 19S REGULATORY PARTICLE, MULTICATALYTIC PROTEASE
4mza:A (GLU276) to (LYS305) CRYSTAL STRUCTURE OF HPIV3 HEMAGGLUTININ-NEURAMINIDASE | VIRAL ENVELOPE PROTEIN, VIRAL FUSION PROTEIN, HYDROLASE
4mza:B (GLU276) to (ARG303) CRYSTAL STRUCTURE OF HPIV3 HEMAGGLUTININ-NEURAMINIDASE | VIRAL ENVELOPE PROTEIN, VIRAL FUSION PROTEIN, HYDROLASE
4mze:A (ASP275) to (LYS305) CRYSTAL STRUCTURE OF HPIV3 HEMAGGLUTININ-NEURAMINIDASE, H552Q/Q559R MUTANT | VIRAL ENVELOPE PROTEIN, VIRAL FUSION PROTEIN, HYDROLASE
4mze:B (GLU276) to (ARG303) CRYSTAL STRUCTURE OF HPIV3 HEMAGGLUTININ-NEURAMINIDASE, H552Q/Q559R MUTANT | VIRAL ENVELOPE PROTEIN, VIRAL FUSION PROTEIN, HYDROLASE
1jwa:D (SER39) to (GLY80) STRUCTURE OF THE ATP-BOUND MOEB-MOAD PROTEIN COMPLEX | MOEB: MODIFIED ROSSMANN FOLD; MOAD: UBIQUITIN-LIKE FOLD, LIGASE
1w17:B (LYS46) to (GLY75) STRUCTURE OF BACILLUS SUBTILIS PDAA, A FAMILY 4 CARBOHYDRATE ESTERASE. | HYDROLASE, FAMILY 4 CARBOHYDRATE ESTERASE, DEACETYLASE, PEPTIDOGLYCAN, NODB HOMOLOGY DOMAIN
1w1a:2 (GLY45) to (GLY75) STRUCTURE OF BACILLUS SUBTILIS PDAA IN COMPLEX WITH NAG, A FAMILY 4 CARBOHYDRATE ESTERASE. | FAMILY 4 CARBOHYDRATE ESTERASE, DEACETYLASE, PEPTIDOGLYCAN, NODB HOMOLOGY DOMAIN, HYDROLASE, SPORULATION
2xo8:A (ASP21) to (CYS49) CRYSTAL STRUCTURE OF MYOSIN-2 IN COMPLEX WITH TRIBROMODICHLOROPSEUDILIN | MOTOR PROTEIN
1w1m:A (SER175) to (THR212) STRUCTURE OF THE OCTAMERIC FLAVOENZYME VANILLYL-ALCOHOL OXIDASE: GLU502GLY MUTANT | FLAVOENZYME, OXIDOREDUCTASE, CATALYSIS, FAD
4n3l:H (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THROMBIN IN COMPLEX WITH A NOVEL GLUCOSE- CONJUGATED POTENT INHIBITOR | HYDROLASE(SERINE PROTEASE), COMPLEX THROMBIN-GLUCOSE-CONJUGATED INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5b6i:A (TYR77) to (ALA121) STRUCTURE OF FLUORINASE FROM STREPTOMYCES SP. MA37 | TRANSFERASE
5b6i:B (TYR77) to (ALA121) STRUCTURE OF FLUORINASE FROM STREPTOMYCES SP. MA37 | TRANSFERASE
5bnb:C (THR53) to (THR81) CRYSTAL STRUCTURE OF A UBE2S-UBIQUITIN CONJUGATE | UBIQUITIN-CONJUGATING ENZYME, E2 ENZYME, UBC DOMAIN, UBIQUITINATION, CELL CYCLE
2jhr:A (ASP21) to (CYS49) CRYSTAL STRUCTURE OF MYOSIN-2 MOTOR DOMAIN IN COMPLEX WITH ADP-METAVANADATE AND PENTABROMOPSEUDILIN | CONTRACTILE PROTEIN, CYTOPLASM, ALLOSTERIC, METHYLATION, COILED COIL, ATP-BINDING, MOTOR PROTEIN, ACTIN-BINDING, PHOSPHOPROTEIN, CALMODULIN-BINDING, NUCLEOTIDE-BINDING
4n9c:A (PRO317) to (PRO345) FRAGMENT-BASED DESIGN OF 3-AMINOPYRIDINE-DERIVED AMIDES AS POTENT INHIBITORS OF HUMAN NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE (NAMPT) | TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4n9f:F (HIS37) to (PRO70) CRYSTAL STRUCTURE OF THE VIF-CBFBETA-CUL5-ELOB-ELOC PENTAMERIC COMPLEX | ZINC FINGER MOTIF, STABILIZE VIF INTERACTION WITH CUL5, CUL5, TRANSCRIPTION-VIRAL PROTEIN COMPLEX, LIGASE-VIRAL PROTEIN COMPLEX
4n9f:o (HIS37) to (PRO70) CRYSTAL STRUCTURE OF THE VIF-CBFBETA-CUL5-ELOB-ELOC PENTAMERIC COMPLEX | ZINC FINGER MOTIF, STABILIZE VIF INTERACTION WITH CUL5, CUL5, TRANSCRIPTION-VIRAL PROTEIN COMPLEX, LIGASE-VIRAL PROTEIN COMPLEX
1w9j:A (ASP21) to (CYS49) MYOSIN II DICTYOSTELIUM DISCOIDEUM MOTOR DOMAIN S456Y BOUND WITH MGADP-ALF4 | MOLECULAR MOTOR, MYOSIN, ATPASE, MOTOR DOMAIN, MUTANT, MUSCLE CONTRACTION
1w9l:A (ASP21) to (CYS49) MYOSIN II DICTYOSTELIUM DISCOIDEUM MOTOR DOMAIN S456E BOUND WITH MGADP-ALF4 | MOLECULAR MOTOR, MYOSIN, POWERSTROKE, MOTOR DOMAIN, MUTANT, MUSCLE CONTRACTION
2jj9:A (ASP21) to (CYS49) CRYSTAL STRUCTURE OF MYOSIN-2 IN COMPLEX WITH ADP- METAVANADATE | CALMODULIN-BINDING, NUCLEOTIDE-BINDING, MOTOR PROTEIN, ACTIN-BINDING, PHOSPHOPROTEIN, MYOSIN, CYTOPLASM, ATP-ANALOG, METHYLATION, COILED COIL, ATP-BINDING, MOTOR-DOMAIN, CONTRACTILE PROTEIN
4ncr:A (THR122) to (PRO163) CRYSTAL STRUCTURE OF M. TUBERCULOSIS DPRE1 IN COMPLEX WITH PBTZ169 | DECAPRENYLPHOSPHORYL-BETA-D-RIBOSE OXIDASE, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
4ncr:B (THR122) to (PRO163) CRYSTAL STRUCTURE OF M. TUBERCULOSIS DPRE1 IN COMPLEX WITH PBTZ169 | DECAPRENYLPHOSPHORYL-BETA-D-RIBOSE OXIDASE, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
4ng2:H (THR18) to (LEU45) CRYSTAL STRUCTURE OF LASR LBD-QSLA COMPLEX FROM PSEUDOMONAS AERUGINOSA | QUORUM SENSING, ANTIACTIVATOR, TRANSCRIPTION REGULATOR
4ng2:I (THR18) to (LEU46) CRYSTAL STRUCTURE OF LASR LBD-QSLA COMPLEX FROM PSEUDOMONAS AERUGINOSA | QUORUM SENSING, ANTIACTIVATOR, TRANSCRIPTION REGULATOR
5bwo:A (PRO264) to (PHE294) CRYSTAL STRUCTURE OF HUMAN SIRT3 IN COMPLEX WITH A PALMITOYL H3K9 PEPTIDE | HYDROLASE, PEPTIDE-HYDROLASE COMPLEX
1kbp:A (THR186) to (ALA243) KIDNEY BEAN PURPLE ACID PHOSPHATASE | PURPLE ACID PHOSPHATASE, HYDROLASE (PHOSPHORIC MONOESTER)
1kbp:B (THR186) to (ALA243) KIDNEY BEAN PURPLE ACID PHOSPHATASE | PURPLE ACID PHOSPHATASE, HYDROLASE (PHOSPHORIC MONOESTER)
1kbp:C (THR186) to (ALA243) KIDNEY BEAN PURPLE ACID PHOSPHATASE | PURPLE ACID PHOSPHATASE, HYDROLASE (PHOSPHORIC MONOESTER)
1kbp:D (THR186) to (ALA243) KIDNEY BEAN PURPLE ACID PHOSPHATASE | PURPLE ACID PHOSPHATASE, HYDROLASE (PHOSPHORIC MONOESTER)
2ku1:A (PHE22) to (SER56) DYNAMIC REGULATION OF ARCHAEAL PROTEASOME GATE OPENING AS STUDIED BY TROSY-NMR | PROTEASOME, PROTEOLYSIS, GATING RESIDUES, CYTOPLASM, HYDROLASE, PROTEASE, THREONINE PROTEASE
2ku1:B (PHE22) to (SER56) DYNAMIC REGULATION OF ARCHAEAL PROTEASOME GATE OPENING AS STUDIED BY TROSY-NMR | PROTEASOME, PROTEOLYSIS, GATING RESIDUES, CYTOPLASM, HYDROLASE, PROTEASE, THREONINE PROTEASE
2ku1:C (PHE22) to (SER56) DYNAMIC REGULATION OF ARCHAEAL PROTEASOME GATE OPENING AS STUDIED BY TROSY-NMR | PROTEASOME, PROTEOLYSIS, GATING RESIDUES, CYTOPLASM, HYDROLASE, PROTEASE, THREONINE PROTEASE
2ku1:D (LEU21) to (SER56) DYNAMIC REGULATION OF ARCHAEAL PROTEASOME GATE OPENING AS STUDIED BY TROSY-NMR | PROTEASOME, PROTEOLYSIS, GATING RESIDUES, CYTOPLASM, HYDROLASE, PROTEASE, THREONINE PROTEASE
2ku1:E (PHE22) to (SER56) DYNAMIC REGULATION OF ARCHAEAL PROTEASOME GATE OPENING AS STUDIED BY TROSY-NMR | PROTEASOME, PROTEOLYSIS, GATING RESIDUES, CYTOPLASM, HYDROLASE, PROTEASE, THREONINE PROTEASE
2ku1:F (PHE22) to (SER56) DYNAMIC REGULATION OF ARCHAEAL PROTEASOME GATE OPENING AS STUDIED BY TROSY-NMR | PROTEASOME, PROTEOLYSIS, GATING RESIDUES, CYTOPLASM, HYDROLASE, PROTEASE, THREONINE PROTEASE
2ku1:G (PHE22) to (ASP51) DYNAMIC REGULATION OF ARCHAEAL PROTEASOME GATE OPENING AS STUDIED BY TROSY-NMR | PROTEASOME, PROTEOLYSIS, GATING RESIDUES, CYTOPLASM, HYDROLASE, PROTEASE, THREONINE PROTEASE
2ku2:A (PHE22) to (SER56) DYNAMIC REGULATION OF ARCHAEAL PROTEASOME GATE OPENING AS STUDIED BY TROSY-NMR | PROTEASOME, PROTEOLYSIS, GATING RESIDUES, CYTOPLASM, HYDROLASE, PROTEASE, THREONINE PROTEASE
2ku2:B (PHE22) to (SER56) DYNAMIC REGULATION OF ARCHAEAL PROTEASOME GATE OPENING AS STUDIED BY TROSY-NMR | PROTEASOME, PROTEOLYSIS, GATING RESIDUES, CYTOPLASM, HYDROLASE, PROTEASE, THREONINE PROTEASE
2ku2:C (PHE22) to (SER56) DYNAMIC REGULATION OF ARCHAEAL PROTEASOME GATE OPENING AS STUDIED BY TROSY-NMR | PROTEASOME, PROTEOLYSIS, GATING RESIDUES, CYTOPLASM, HYDROLASE, PROTEASE, THREONINE PROTEASE
2ku2:D (LEU21) to (SER56) DYNAMIC REGULATION OF ARCHAEAL PROTEASOME GATE OPENING AS STUDIED BY TROSY-NMR | PROTEASOME, PROTEOLYSIS, GATING RESIDUES, CYTOPLASM, HYDROLASE, PROTEASE, THREONINE PROTEASE
2ku2:E (PHE22) to (SER56) DYNAMIC REGULATION OF ARCHAEAL PROTEASOME GATE OPENING AS STUDIED BY TROSY-NMR | PROTEASOME, PROTEOLYSIS, GATING RESIDUES, CYTOPLASM, HYDROLASE, PROTEASE, THREONINE PROTEASE
2ku2:F (PHE22) to (SER56) DYNAMIC REGULATION OF ARCHAEAL PROTEASOME GATE OPENING AS STUDIED BY TROSY-NMR | PROTEASOME, PROTEOLYSIS, GATING RESIDUES, CYTOPLASM, HYDROLASE, PROTEASE, THREONINE PROTEASE
2ku2:G (PHE22) to (ASP51) DYNAMIC REGULATION OF ARCHAEAL PROTEASOME GATE OPENING AS STUDIED BY TROSY-NMR | PROTEASOME, PROTEOLYSIS, GATING RESIDUES, CYTOPLASM, HYDROLASE, PROTEASE, THREONINE PROTEASE
3zod:A (LYS137) to (THR163) CRYSTAL STRUCTURE OF FMN-BINDING PROTEIN (NP_142786.1) FROM PYROCOCCUS HORIKOSHII WITH BOUND BENZENE-1,4-DIOL | FMN-BINDING PROTEIN
3zog:A (LYS137) to (THR163) CRYSTAL STRUCTURE OF FMN-BINDING PROTEIN (NP_142786.1) FROM PYROCOCCUS HORIKOSHII WITH BOUND 1-CYCLOHEX-2-ENONE | OXIDOREDUCTASE, ELECTRON TRANSPORT
2l8l:A (ARG18) to (ALA42) STRUCTURE OF AN ENGINEERED SPLICING INTEIN MUTANT BASED ON MYCOBACTERIUM TUBERCULOSIS RECA | HYDROLASE
1wvc:A (ASN68) to (VAL87) ALPHA-D-GLUCOSE-1-PHOSPHATE CYTIDYLYLTRANSFERASE COMPLEXED WITH CTP | CDP-GLUCOSE PYROPHOSPHORYLASE, NUCLEOTIDYLTRANSFERASE, TRANSFERASE
4nn2:A (HIS302) to (CYS326) PROTEIN CRYSTAL STRUCTURE OF HUMAN BORJESON-FORSSMAN-LEHMANN SYNDROME ASSOCIATED PROTEIN PHF6 | ZINC FINGER, TRANSCRIPTION
4nnn:F (PHE18) to (THR51) YCP IN COMPLEX WITH MG132 | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, ALDEHYDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4nnn:T (PHE18) to (THR51) YCP IN COMPLEX WITH MG132 | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, ALDEHYDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4nnw:F (PHE18) to (THR51) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-KETOALDEHYDE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, KETOALDEHYDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4nnw:T (PHE18) to (THR51) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-KETOALDEHYDE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, KETOALDEHYDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no1:F (PHE18) to (THR51) 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:T (PHE18) to (THR51) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-B(OH)2 | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, BORONIC ACID, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no8:F (PHE18) to (THR51) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-KETOAMIDE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, KETOAMIDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no8:T (PHE18) to (THR51) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-KETOAMIDE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, REVERSIBLE INHIBITOR, KETOAMIDE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4npk:A (ASN514) to (VAL566) EXTENDED-SYNAPTOTAGMIN 2, C2A- AND C2B-DOMAINS, CALCIUM BOUND | CALCIUM/PHOSPHOLIPID BINDING PROTEIN, C2 DOMAIN, ER TO PLASMA MEMBRANE, MEMBRANE TRAFFIC, PROTEIN TARGETING, PLASMA MEMBRANE, MEMBRANE PROTEIN
2m0v:A (SER186) to (VAL200) COMPLEX STRUCTURE OF C-TERMINAL CFTR PEPTIDE AND EXTENDED PDZ2 DOMAIN FROM NHERF1 | PDZ DOMAIN, PROTEIN BINDING-PROTEIN BINDING COMPLEX
2mh9:A (SER72) to (VAL105) RESONANCE ASSIGNMENT OF RQC DOMAIN OF HUMAN BLOOM SYNDROME PROTEIN | WINGED HELIX, RQC, HYDROLASE
1kqm:A (ASN390) to (GLY413) SCALLOP MYOSIN S1-AMPPNP IN THE ACTIN-DETACHED CONFORMATION | ACTIN-DETACHED, MYOSIN, MECHANICS OF MOTOR, CONTRACTILE PROTEIN
1x74:C (GLU310) to (PRO328) ALPHA-METHYLACYL-COA RACEMASE FROM MYCOBACTERIUM TUBERCULOSIS- MUTATIONAL AND STRUCTURAL CHARACTERIZATION OF THE FOLD AND ACTIVE SITE | ALPHA-METHYLACYL-COA RACEMASE, RACEMASE, COA TRANSFERASE, COENZYME A, ISOMERASE
1x88:A (ASN29) to (ARG53) HUMAN EG5 MOTOR DOMAIN BOUND TO MG-ADP AND MONASTROL | SWITCH II, MOTOR DOMAIN, NECK LINKER, CELL CYCLE
2yfp:A (SER2) to (GLU32) STRUCTURE OF YELLOW-EMISSION VARIANT OF GFP | GREEN FLUORESCENT PROTEIN, YELLOW-EMISSION VARIANT, BIOLUMINESCENCE, PHOTOACTIVE PROTEIN, FLUORESCENT TAG, PHOTOSYNTHESIS
1xa0:B (ASN43) to (GLY90) CRYSTAL STRUCTURE OF MCSG TARGET APC35536 FROM BACILLUS STEAROTHERMOPHILUS | STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, MCSG, PSI, MIDWEST CENTER FOR STRUCTURAL GENOMICS, UNKNOWN FUNCTION
4nze:H (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THROMBIN IN COMPLEX WITH A NOVEL TETRA-O-ACETYL- GLUCOPYRANOSIDE-CONJUGATED POTENT INHIBITOR | HYDROLASE(SERINE PROTEASE), TETRA-O-ACETYL-GLUCOSE-CONJUGATED INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2nnn:J (ALA67) to (VAL96) CRYSTAL STRUCTURE OF PROBABLE TRANSCRIPTIONAL REGULATOR FROM PSEUDOMONAS AERUGINOSA | PSEUDOMONAS AERUGINOSA, PROBABLE TRANSCRIPTIONAL REGULATOR, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, TRANSCRIPTION
4o0z:A (PRO317) to (PRO345) STRUCTURAL AND BIOCHEMICAL ANALYSES OF THE CATALYSIS AND POTENCY IMPACT OF INHIBITOR PHOSPHORIBOSYLATION BY HUMAN NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE | TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4o10:B (PRO317) to (PRO345) STRUCTURAL AND BIOCHEMICAL ANALYSES OF THE CATALYSIS AND POTENCY IMPACT OF INHIBITOR PHOSPHORIBOSYLATION BY HUMAN NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE | TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4o12:A (PRO317) to (PRO345) STRUCTURAL AND BIOCHEMICAL ANALYSES OF THE CATALYSIS AND POTENCY IMPACT OF INHIBITOR PHOSPHORIBOSYLATION BY HUMAN NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE | TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4o13:A (PRO317) to (PRO345) THE CRYSTAL STRUCTURE OF NAMPT IN COMPLEX WITH GNE-618 | TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4o13:B (ASN316) to (PRO345) THE CRYSTAL STRUCTURE OF NAMPT IN COMPLEX WITH GNE-618 | TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4o14:A (ASN316) to (PRO345) STRUCTURAL BASIS FOR RESISTANCE TO DIVERSE CLASSES OF NAMPT INHIBITORS | TRANSFERASE
4o14:B (ASN316) to (PRO345) STRUCTURAL BASIS FOR RESISTANCE TO DIVERSE CLASSES OF NAMPT INHIBITORS | TRANSFERASE
4o15:A (ASN316) to (PRO345) THE CRYSTAL STRUCTURE OF A MUTANT NAMPT (S165F) IN COMPLEX WITH GNE- 618 | TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4o18:A (PRO317) to (PRO345) STRUCTURAL BASIS FOR RESISTANCE TO DIVERSE CLASSES OF NAMPT INHIBITORS | TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4o1d:A (ASN316) to (PRO345) STRUCTURAL BASIS FOR RESISTANCE TO DIVERSE CLASSES OF NAMPT INHIBITORS | TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4o1d:B (ASN316) to (PRO345) STRUCTURAL BASIS FOR RESISTANCE TO DIVERSE CLASSES OF NAMPT INHIBITORS | TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4o28:B (PRO317) to (PRO345) STRUCTURAL BASIS FOR RESISTANCE TO DIVERSE CLASSES OF NAMPT INHIBITORS | TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4o3m:A (SER1138) to (VAL1171) TERNARY COMPLEX OF BLOOM'S SYNDROME HELICASE | WINGED HELIX, HELICASE, HYDROLASE-DNA COMPLEX
1xgo:A (PRO245) to (ILE284) METHIONINE AMINOPEPTIDASE FROM HYPERTHERMOPHILE PYROCOCCUS FURIOSUS | AMINOPEPTIDASE, HYPERTHERMOPHILE
1l6y:B (SER13) to (GLU39) CRYSTAL STRUCTURE OF PORPHOBILINOGEN SYNTHASE COMPLEXED WITH THE INHIBITOR 4-OXOSEBACIC ACID | DEHYDRATASE, LYASE
1l9m:A (HIS148) to (GLY178) 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
1l9m:B (HIS148) to (GLY178) 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
5cfl:A (THR221) to (PRO239) CRYSTAL STRUCTURE OF ANEMONE STING (NEMATOSTELLA VECTENSIS) IN COMPLEX WITH 3', 3' C-DI-GMP, C[G(3', 5')PG(3', 5')P] | STING, CYCLIC-DINUCLEOTIDE BINDING DOMAIN, IMMUNE SYSTEM
3jz1:B (ASP125) to (ASN159) CRYSTAL STRUCTURE OF HUMAN THROMBIN MUTANT N143P IN E:NA+ FORM | SERINE PROTEASE, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, DISULFIDE BOND, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PROTEASE, SECRETED, ZYMOGEN
5cgg:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ALPHA- CHLOROACETAMIDE 1 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cgg:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ALPHA- CHLOROACETAMIDE 1 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cgh:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ALPHA- CHLOROACETAMIDE 5 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cgh:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ALPHA- CHLOROACETAMIDE 5 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cgi:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ONX 0914 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cgi:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-G48C MUTANT IN COMPLEX WITH ONX 0914 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4obv:B (GLY275) to (LYS320) RUMINOCOCCUS GNAVUS TRYPTOPHAN DECARBOXYLASE RUMGNA_01526 (ALPHA-FMT) | TYPE 1 PLP-DEPENDENT, DECARBOXYLASE, LYASE
2yvs:A (VAL43) to (ARG76) CRYSTAL STRUCTURE OF GLYCOLATE OXIDASE SUBUNIT GLCE FROM THERMUS THERMOPHILUS HB8 | GLYCOLATE OXIDASE SUBUNIT GLCE, OXIDOREDUCTASE
3k0l:A (ALA74) to (VAL103) CRYSTAL STRUCTURE OF PUTATIVE MARR FAMILY TRANSCRIPTIONAL REGULATOR FROM ACINETOBACTER SP. ADP | HELIX-TURN-HELIX, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, DNA-BINDING, TRANSCRIPTION, TRANSCRIPTION REGULATION, TRANSCRIPTION REGULATOR
2nyg:A (SER181) to (LYS215) CRYSTAL STRUCTURE OF YOKD PROTEIN FROM BACILLUS SUBTILIS | PFAM02522, NYSGXRC, 10116C, AMINOGLYCOSIDE 3-N- ACETYLTRANSFERASE, PSI-2, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, UNKNOWN FUNCTION
2nyg:E (PHE178) to (LYS215) CRYSTAL STRUCTURE OF YOKD PROTEIN FROM BACILLUS SUBTILIS | PFAM02522, NYSGXRC, 10116C, AMINOGLYCOSIDE 3-N- ACETYLTRANSFERASE, PSI-2, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, UNKNOWN FUNCTION
2nyg:F (ASP177) to (LYS215) CRYSTAL STRUCTURE OF YOKD PROTEIN FROM BACILLUS SUBTILIS | PFAM02522, NYSGXRC, 10116C, AMINOGLYCOSIDE 3-N- ACETYLTRANSFERASE, PSI-2, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, UNKNOWN FUNCTION
1lhc:H (ASP125) to (ASN159) HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BOROARG-OH | BLOOD COAGULATION, PLASMA, CALCIUM-BINDING, GLYCOPROTEIN, DUPLICATION, VITAMIN K, ZYMOGEN, GAMMA-CARBOXYGLUTAMIC ACID, ACUTE PHASE, LIVER, HYDROLASE, SERINE PROTEASE, KRINGLE, SIGNAL, DISEASE MUTATION, COMPLEX (SERINE PROTEASE/INHIBITOR)
1lhe:H (ASP125) to (ASN159) HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BORO-N- BUTYL-AMIDINO-GLYCINE-OH | BLOOD COAGULATION, PLASMA, CALCIUM-BINDING, GLYCOPROTEIN, DUPLICATION, VITAMIN K, ZYMOGEN, GAMMA-CARBOXYGLUTAMIC ACID, ACUTE PHASE, LIVER, HYDROLASE, SERINE PROTEASE, KRINGLE, SIGNAL, DISEASE MUTATION, COMPLEX (SERINE PROTEASE/INHIBITOR)
1lhf:H (ASP125) to (ASN159) HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BORO- HOMOLYS-OH | BLOOD COAGULATION, PLASMA, CALCIUM-BINDING, GLYCOPROTEIN, DUPLICATION, VITAMIN K, ZYMOGEN, GAMMA-CARBOXYGLUTAMIC ACID, ACUTE PHASE, LIVER, HYDROLASE, SERINE PROTEASE, KRINGLE, SIGNAL, DISEASE MUTATION, COMPLEX (SERINE PROTEASE/INHIBITOR)
2z1d:A (VAL265) to (LEU295) CRYSTAL STRUCTURE OF [NIFE] HYDROGENASE MATURATION PROTEIN, HYPD FROM THERMOCOCCUS KODAKARAENSIS | [NIFE] HYDROGENASE MATURATION, [4FE-4S] CLUSTER, THIOL REDOX, METAL BINDING PROTEIN
3k40:A (ALA271) to (LYS316) CRYSTAL STRUCTURE OF DROSOPHILA 3,4-DIHYDROXYPHENYLALANINE DECARBOXYLASE | PLP DEPENDENT PROTEIN, ALPHA BETA PROTEIN, ALTERNATIVE SPLICING, CATECHOLAMINE BIOSYNTHESIS, DECARBOXYLASE, LYASE, POLYMORPHISM, PYRIDOXAL PHOSPHATE, CG10697-PB ISOFORM B
3k40:B (ALA271) to (LYS316) CRYSTAL STRUCTURE OF DROSOPHILA 3,4-DIHYDROXYPHENYLALANINE DECARBOXYLASE | PLP DEPENDENT PROTEIN, ALPHA BETA PROTEIN, ALTERNATIVE SPLICING, CATECHOLAMINE BIOSYNTHESIS, DECARBOXYLASE, LYASE, POLYMORPHISM, PYRIDOXAL PHOSPHATE, CG10697-PB ISOFORM B
1lsh:A (LYS996) to (LEU1030) LIPID-PROTEIN INTERACTIONS IN LIPOVITELLIN | LIPOVITELLIN, VITELLOGENIN, LIPOPROTEIN, PLASMA APOLIPOPROTE APOLIPOPROTEIN B, APOB, MICROSOMAL TRIGLYCERIDE TRANSFER PR BOUNDARY LIPID, PHOSPHOLIPID STRUCTURE, LIPID BINDING PROTEIN
4a5m:A (THR53) to (TYR84) REDOX REGULATOR HYPR IN ITS OXIDIZED FORM | TRANSCRIPTION, ACTIVATOR, DNA-BINDING
4a5m:B (THR53) to (TYR84) REDOX REGULATOR HYPR IN ITS OXIDIZED FORM | TRANSCRIPTION, ACTIVATOR, DNA-BINDING
4a5m:C (THR53) to (TYR84) REDOX REGULATOR HYPR IN ITS OXIDIZED FORM | TRANSCRIPTION, ACTIVATOR, DNA-BINDING
4a5m:E (THR53) to (TYR84) REDOX REGULATOR HYPR IN ITS OXIDIZED FORM | TRANSCRIPTION, ACTIVATOR, DNA-BINDING
4a5m:F (THR53) to (TYR84) REDOX REGULATOR HYPR IN ITS OXIDIZED FORM | TRANSCRIPTION, ACTIVATOR, DNA-BINDING
4a5m:G (THR53) to (TYR84) REDOX REGULATOR HYPR IN ITS OXIDIZED FORM | TRANSCRIPTION, ACTIVATOR, DNA-BINDING
4a5t:S (GLU1) to (PHE15) STRUCTURAL BASIS FOR THE CONFORMATIONAL MODULATION | HYDROLASE, MULTI-DOMAIN CONFORMATIONAL CHANGE
1lw4:B (ILE172) to (GLY211) X-RAY STRUCTURE OF L-THREONINE ALDOLASE (LOW-SPECIFICITY) IN COMPLEX WITH L-ALLO-THREONINE | PYRIDOXAL-5-PHOSPHATE, PLP, ENZYME, PRODUCT COMPLEX, THREONINE, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC, LYASE
2zba:A (THR106) to (GLN164) CRYSTAL SRUCTURE OF F. SPOROTRICHIOIDES TRI101 COMPLEXED WITH COENZYME A AND T-2 | ACETYLTRANSFERASE, BAHD SUPERFAMILY, TRICHOTHECENE, DEOXYNIVALENOL, T-2, ACETYL COA, FUSARIUM, TRI101, TRANSFERASE
1xmn:B (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THROMBIN BOUND TO HEPARIN | BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1xmn:D (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THROMBIN BOUND TO HEPARIN | BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1xmn:H (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THROMBIN BOUND TO HEPARIN | BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2zcy:F (GLN23) to (ILE54) YEAST 20S PROTEASOME:SYRINGOLIN A-COMPLEX | ALPHA/BETA SANDWICH, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, PROTEASOME, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN
2zcy:T (GLN23) to (ILE54) YEAST 20S PROTEASOME:SYRINGOLIN A-COMPLEX | ALPHA/BETA SANDWICH, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, PROTEASOME, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN
2zdv:H (ASP125) to (ASN159) EXPLORING THROMBIN S1 POCKET | BLOOD CLOTTING/HYDROLASE INHIBITORS, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN, BLOOD CLOTTING-HYDROLASE INHIBITOR COMPLEX
2zf0:H (ASP125) to (ASN159) EXPLORING THROMBIN S1 POCKET | BLOOD CLOTTING/HYDROLASE INHIBITORS, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN, BLOOD CLOTTING-HYDROLASE INHIBITOR COMPLEX
2zfp:H (ASP125) to (ASN159) THROMBIN INIBITION | BLOOD CLOTTING/HYDROLASE INHIBITOR, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN, BLOOD CLOTTING-HYDROLASE INHIBITOR COMPLEX
2zfr:H (ASP125) to (ASN159) EXPLORING THROMBIN S3 POCKET | BLOOD CLOTTING/HYDROLASE INHIBITORS, ACUTE PHASE, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN, PROTEASE INHIBITOR, SERINE PROTEASE INHIBITOR, SULFATION, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
2zgb:H (ASP125) to (ASN159) THROMBIN INHIBITION | BLOOD CLOTTING, HYDROLASE INHIBITOR, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2zgx:H (ASP125) to (ASN159) THROMBIN INHIBITION | BLOOD CLOTTING, HYDROLASE INHIBITOR, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN, PROTEASE INHIBITOR, SERINE PROTEASE INHIBITOR, SULFATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2zhe:H (ASP125) to (ASN159) EXPLORING THROMBIN S3 POCKET | BLOOD COAGULATION, HYDROLASE INHIBITORS, ACUTE PHASE, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, PROTEASE INHIBITOR, SERINE PROTEASE INHIBITOR, SULFATION, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
2zhw:H (ASP125) to (ASN159) EXPLORING THROMBIN S3 POCKET | BLOOD COAGULATION, HYDROLASE INHIBITORS, ACUTE PHASE, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, PROTEASE INHIBITOR, SERINE PROTEASE INHIBITOR, SULFATION, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3kbp:A (THR186) to (ALA243) KIDNEY BEAN PURPLE ACID PHOSPHATASE | PURPLE ACID PHOSPHATASE, HYDROLASE (PHOSPHORIC MONOESTER)
3kbp:B (THR186) to (ALA243) KIDNEY BEAN PURPLE ACID PHOSPHATASE | PURPLE ACID PHOSPHATASE, HYDROLASE (PHOSPHORIC MONOESTER)
3kbp:C (THR186) to (ALA243) KIDNEY BEAN PURPLE ACID PHOSPHATASE | PURPLE ACID PHOSPHATASE, HYDROLASE (PHOSPHORIC MONOESTER)
3kbp:D (THR186) to (ALA243) KIDNEY BEAN PURPLE ACID PHOSPHATASE | PURPLE ACID PHOSPHATASE, HYDROLASE (PHOSPHORIC MONOESTER)
4oo1:C (SER60) to (ILE95) STRUCTURE OF AN RRP6-RNA EXOSOME COMPLEX BOUND TO POLY(A) RNA | RNA EXOSOME COMPLEX, RNA PROCESSING/DECAY, NUCLEUS, RNA BINDING PROTEIN-RNA COMPLEX, HYDROLASE-RNA COMPLEX
3kcq:C (CYS175) to (GLY200) CRYSTAL STRUCTURE OF PHOSPHORIBOSYLGLYCINAMIDE FORMYLTRANSFERASE FROM ANAPLASMA PHAGOCYTOPHILUM | STRUCTURAL GENOMICS, NIAID, TRANSFERASE, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, SSGCID
2zj3:A (GLU330) to (LEU352) ISOMERASE DOMAIN OF HUMAN GLUCOSE:FRUCTOSE-6-PHOSPHATE AMIDOTRANSFERASE | GLUCOSAMINE-6-PHOSPHATE SYNTHASE, ALDOSE/KETOSE ISOMERASE, CRYSTAL STRUCTURE, ROSSMANN-LIKE FOLD, TRANSFERASE, ALTERNATIVE SPLICING, AMINOTRANSFERASE, GLUTAMINE AMIDOTRANSFERASE, PHOSPHOPROTEIN
5cvl:A (ASN461) to (LEU529) WDR48 (UAF-1), RESIDUES 2-580 | WDR48, UAF1, WD-REPEAT, USP, DEUBIQUITINASE, DUB, PROTEIN BINDING
3kfd:D (ASP3) to (HIS40) TERNARY COMPLEX OF TGF-B1 REVEALS ISOFORM-SPECIFIC LIGAND RECOGNITION AND RECEPTOR RECRUITMENT IN THE SUPERFAMILY | TGF-BETA, TGF-B1, TGF-BETA RECEPTOR TYPE-1, TGF-BETA RECEPTOR TYPE-2, TBRII, TBRI, GROWTH FACTOR, RECEPTOR, SERINE/THREONINE-PROTEIN KINASE, CYTOKINE-CYTOKINE RECEPTOR COMPLEX
2znk:H (ASP125) to (ASN159) THROMBIN INHIBITION | BLOOD CLOTTING, HYDROLASE INHIBITOR, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, PROTEASE, SERINE PROTEASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
2zo3:H (ASP125) to (ASN159) BISPHENYLIC THROMBIN INHIBITORS | BLOOD CLOTTING, HYDROLASE INHIBITOR, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, SECRETED, SERINE PROTEASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5cz5:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA1-T1A MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cz5:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA1-T1A MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
2zrn:A (SER271) to (GLU296) MSRECA FORM IV | RECOMBINATION, RECA MUTANTS, DNA-REPAIR, ATP-BINDING, DNA DAMAGE, DNA RECOMBINATION, DNA REPAIR, DNA-BINDING, NUCLEOTIDE-BINDING, SOS RESPONSE, HYDROLASE
4oud:A (SER371) to (GLY414) ENGINEERED TYROSYL-TRNA SYNTHETASE WITH THE NONSTANDARD AMINO ACID L- 4,4-BIPHENYLALANINE | COMPLEX WITH L-TYROSINE, ROSSMANN FOLD, LIGASE, TRNA
4ad9:B (HIS254) to (ALA286) CRYSTAL STRUCTURE OF HUMAN LACTB2. | HYDROLASE, METALLO-BETA LACTAMASE, MITOCHONDRIA
5d0s:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-D166N MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0s:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-D166N MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0t:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-D166N MUTANT IN COMPLEX WITH MG132 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0t:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-D166N MUTANT IN COMPLEX WITH MG132 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
2zvz:B (ASP130) to (ILE153) STRUCTURE OF THE PERIPLASMIC DOMAIN OF MOTB FROM SALMONELLA (CRYSTAL FORM III) | 2-LAYER SANDWICH, BACTERIAL FLAGELLUM, CELL INNER MEMBRANE, CELL MEMBRANE, CHEMOTAXIS, FLAGELLAR ROTATION, MEMBRANE, TRANSMEMBRANE, MEMBRANE PROTEIN
5d0v:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-T1C MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0v:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-T1C MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0w:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-T1S MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5d0w:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-T1S MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4ae3:A (ASP21) to (CYS49) CRYSTAL STRUCTURE OF AMMOSAMIDE 272:MYOSIN-2 MOTOR DOMAIN COMPLEX | HYDROLASE, ATPASE, CONTRACTILE PROTEIN, ACTIN BINDING, MOTOR PROTEIN
5d0z:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-T1S MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5d0z:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-T1S MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
1mkx:H (ASP125) to (ASN159) THE CO-CRYSTAL STRUCTURE OF UNLIGANDED BOVINE ALPHA- THROMBIN AND PRETHROMBIN-2: MOVEMENT OF THE YPPW SEGMENT AND ACTIVE SITE RESIDUES UPON LIGAND BINDING | COMPLEX (BLOOD COAGULATION/PROENZYME), THROMBIN, PRETHROMBIN-2, PLASMA, SERINE PROTEASE
1mo4:A (SER270) to (GLU295) RECA-ATP-GAMMA-S COMPLEX | RECOMBINATION, DNA-REPAIR, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, TB STRUCTURAL GENOMICS CONSORTIUM, TBSGC, HYDROLASE
1mo5:A (SER270) to (GLU295) RECA-ATP-GAMMA-S-MG COMPLEX | RECOMBINATION, DNA-REPAIR, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, TB STRUCTURAL GENOMICS CONSORTIUM, TBSGC, HYDROLASE
3kol:A (THR56) to (GLU82) CRYSTAL STRUCTURE OF A GLYOXALASE/DIOXYGENASE FROM NOSTOC PUNCTIFORME | METAL ION BINDING, BLEOMYCIN RESISTANCE, NYSGXRC, PSI2, DIOXYGENASE, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS
1yau:A (PHE22) to (ARG55) STRUCTURE OF ARCHEABACTERIAL 20S PROTEASOME- PA26 COMPLEX | PROTEASOME 20S, PA26 PROTEASOME ACTIVATOR 11S, HYDROLASE-HYDROLASE ACTIVATOR COMPLEX
4p8c:A (THR122) to (PRO163) CRYSTAL STRUCTURE OF M. TUBERCULOSIS DPRE1 IN COMPLEX WITH THE NON- COVALENT INHIBITOR QN127 | DPRE1, INHIBITOR, COMPLEX, NON-COVALENT, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
4p8c:B (THR122) to (PRO163) CRYSTAL STRUCTURE OF M. TUBERCULOSIS DPRE1 IN COMPLEX WITH THE NON- COVALENT INHIBITOR QN127 | DPRE1, INHIBITOR, COMPLEX, NON-COVALENT, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
4p8h:A (THR122) to (PRO163) CRYSTAL STRUCTURE OF M. TUBERCULOSIS DPRE1 IN COMPLEX WITH THE NITRO- BENZOTHIAZOLE 6A | DPRE1, INHIBITOR, COMPLEX, COVALENT, NITRO-BENZOTHIAZOLE 6A, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4p8h:B (THR122) to (PRO163) CRYSTAL STRUCTURE OF M. TUBERCULOSIS DPRE1 IN COMPLEX WITH THE NITRO- BENZOTHIAZOLE 6A | DPRE1, INHIBITOR, COMPLEX, COVALENT, NITRO-BENZOTHIAZOLE 6A, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4p8k:A (THR122) to (PRO163) CRYSTAL STRUCTURE OF M. TUBERCULOSIS DPRE1 IN COMPLEX WITH THE NON- COVALENT INHIBITOR TY38C | DPRE1, INHIBITOR, COMPLEX, NON-COVALENT, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
4p8k:B (THR122) to (PRO163) CRYSTAL STRUCTURE OF M. TUBERCULOSIS DPRE1 IN COMPLEX WITH THE NON- COVALENT INHIBITOR TY38C | DPRE1, INHIBITOR, COMPLEX, NON-COVALENT, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
4p8l:A (THR122) to (PRO163) CRYSTAL STRUCTURE OF M. TUBERCULOSIS DPRE1 IN COMPLEX WITH THE NON- COVALENT INHIBITOR TY36C | DPRE1, INHIBITOR, COMPLEX, NON-COVALENT, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
4p8l:B (THR122) to (THR162) CRYSTAL STRUCTURE OF M. TUBERCULOSIS DPRE1 IN COMPLEX WITH THE NON- COVALENT INHIBITOR TY36C | DPRE1, INHIBITOR, COMPLEX, NON-COVALENT, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
4p8n:A (THR122) to (PRO163) CRYSTAL STRUCTURE OF M. TUBERCULOSIS DPRE1 IN COMPLEX WITH THE NON- COVALENT INHIBITOR QN118 | DPRE1, INHIBITOR, COMPLEX, NON-COVALENT, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
4p8n:B (THR122) to (PRO163) CRYSTAL STRUCTURE OF M. TUBERCULOSIS DPRE1 IN COMPLEX WITH THE NON- COVALENT INHIBITOR QN118 | DPRE1, INHIBITOR, COMPLEX, NON-COVALENT, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
4p8y:A (THR122) to (PRO163) CRYSTAL STRUCTURE OF M. TUBERCULOSIS DPRE1 IN COMPLEX WITH THE NON- COVALENT INHIBITOR TY21C | DPRE1, INHIBITOR, COMPLEX, NON-COVALENT, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
4p8y:B (THR122) to (PRO163) CRYSTAL STRUCTURE OF M. TUBERCULOSIS DPRE1 IN COMPLEX WITH THE NON- COVALENT INHIBITOR TY21C | DPRE1, INHIBITOR, COMPLEX, NON-COVALENT, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
5d7n:B (PRO264) to (PHE294) CRYSTAL STRUCTURE OF HUMAN SIRT3 AT AN IMPROVED RESOLUTION | HYDROLASE, SIRTUIN 3, DEACYLASE
5d7q:A (LEU206) to (PHE235) CRYSTAL STRUCTURE OF HUMAN SIRT2 IN COMPLEX WITH ADPR AND CHIC35 | HYDROLASE, HUMAN SIRT2, INHIBITOR COMPLEX, DEACYLASE
5d7q:B (PRO205) to (PHE235) CRYSTAL STRUCTURE OF HUMAN SIRT2 IN COMPLEX WITH ADPR AND CHIC35 | HYDROLASE, HUMAN SIRT2, INHIBITOR COMPLEX, DEACYLASE
5d7o:A (PRO205) to (PHE235) CRYSTAL STRUCTURE OF SIRT2-ADPR AT AN IMPROVED RESOLUTION | HYDROLASE, HUMAN SIRT2, DEACYLASE
5d7o:B (PRO205) to (PHE235) CRYSTAL STRUCTURE OF SIRT2-ADPR AT AN IMPROVED RESOLUTION | HYDROLASE, HUMAN SIRT2, DEACYLASE
1mu6:B (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THROMBIN IN COMPLEX WITH L-378,622 | HYDROLASE, BLOOD CLOTTING, HYDROLASE-BLOOD CLOTTING COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, BLOOD CLOTTING,HYDROLASE- INHIBITOR COMPLEX
5d7p:A (LEU206) to (PHE235) CRYSTAL STRUCTURE OF HUMAN SIRT2 IN COMPLEX WITH ADPR AND EX-243 | HYDROLASE, HUMAN SIRTUIN 2, INHIBITOR COMPLEX, DEACYLASE
5d7p:B (LEU206) to (PHE235) CRYSTAL STRUCTURE OF HUMAN SIRT2 IN COMPLEX WITH ADPR AND EX-243 | HYDROLASE, HUMAN SIRTUIN 2, INHIBITOR COMPLEX, DEACYLASE
3krd:M (SER8) to (GLU44) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME IN COMPLEX WITH FELLUTAMIDE B | BINDING SITES, MYCOBACTERIUM TUBERCULOSIS, PROTEIN SUBUNITS, SUBSTRATE SPECIFICITY, HYDROLASE, PROTEASOME, FELLUTAMIDE B, INHIBITION, PROTEASE, THREONINE PROTEASE, VIRULENCE, AUTOCATALYTIC CLEAVAGE, ZYMOGEN
1yf9:A (THR50) to (ASN78) STRUCTURAL ANALYSIS OF LEISHMANIA MAJOR UBIQUITIN CONJUGATING ENZYME E2 | SGPP, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, UBIQUITIN CONJUGATING ENZYME, STRUCTURAL GENOMICS OF PATHOGENIC PROTOZOA CONSORTIUM, UNKNOWN FUNCTION
1yf9:B (THR50) to (ASN78) STRUCTURAL ANALYSIS OF LEISHMANIA MAJOR UBIQUITIN CONJUGATING ENZYME E2 | SGPP, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, UBIQUITIN CONJUGATING ENZYME, STRUCTURAL GENOMICS OF PATHOGENIC PROTOZOA CONSORTIUM, UNKNOWN FUNCTION
1yf9:C (THR50) to (ASN78) STRUCTURAL ANALYSIS OF LEISHMANIA MAJOR UBIQUITIN CONJUGATING ENZYME E2 | SGPP, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, UBIQUITIN CONJUGATING ENZYME, STRUCTURAL GENOMICS OF PATHOGENIC PROTOZOA CONSORTIUM, UNKNOWN FUNCTION
5d95:B (VAL257) to (SER296) STRUCTURE OF THERMOSTABLE OMEGA-TRANSAMINASE | TRANSAMINASE, THERMOSTABLE, ENZYME, TRANSFERASE
5d98:B (GLU384) to (GLY406) INFLUENZA C VIRUS RNA-DEPENDENT RNA POLYMERASE - SPACE GROUP P43212 | RNA-DEPENDENT RNA POLYMERASE, INFLUENZA, INFLUENZA C VIRUS, NEGATIVE- STRAND VIRUS, TRANSFERASE-RNA COMPLEX
5d98:E (GLU384) to (GLY406) INFLUENZA C VIRUS RNA-DEPENDENT RNA POLYMERASE - SPACE GROUP P43212 | RNA-DEPENDENT RNA POLYMERASE, INFLUENZA, INFLUENZA C VIRUS, NEGATIVE- STRAND VIRUS, TRANSFERASE-RNA COMPLEX
1mw9:X (THR496) to (ALA519) CRYSTAL STRUCTURE OF H365R MUTANT OF 67 KDA N-TERMINAL FRAGMENT OF E. COLI DNA TOPOISOMERASE I | DNA TOPOISOMERASE, DECATENASE ENZYME, TOPRIM DOMAIN
5d9a:B (GLU384) to (GLY406) INFLUENZA C VIRUS RNA-DEPENDENT RNA POLYMERASE - SPACE GROUP P212121 | RNA-DEPENDENT RNA POLYMERASE, INFLUENZA, INFLUENZA C VIRUS, NEGATIVE- STRAND VIRUS, VIRAL PROTEIN
5d9a:E (GLU384) to (GLY406) INFLUENZA C VIRUS RNA-DEPENDENT RNA POLYMERASE - SPACE GROUP P212121 | RNA-DEPENDENT RNA POLYMERASE, INFLUENZA, INFLUENZA C VIRUS, NEGATIVE- STRAND VIRUS, VIRAL PROTEIN
5d9a:H (GLU384) to (GLY406) INFLUENZA C VIRUS RNA-DEPENDENT RNA POLYMERASE - SPACE GROUP P212121 | RNA-DEPENDENT RNA POLYMERASE, INFLUENZA, INFLUENZA C VIRUS, NEGATIVE- STRAND VIRUS, VIRAL PROTEIN
5d9a:K (GLU384) to (GLY406) INFLUENZA C VIRUS RNA-DEPENDENT RNA POLYMERASE - SPACE GROUP P212121 | RNA-DEPENDENT RNA POLYMERASE, INFLUENZA, INFLUENZA C VIRUS, NEGATIVE- STRAND VIRUS, VIRAL PROTEIN
1yjg:A (LYS46) to (THR86) VARIABLE SMALL PROTEIN 1 OF BORRELIA TURICATAE (VSPA OR VSP1) | HELICAL BUNDLE, IMMUNE SYSTEM
1yjg:D (ASN47) to (THR86) VARIABLE SMALL PROTEIN 1 OF BORRELIA TURICATAE (VSPA OR VSP1) | HELICAL BUNDLE, IMMUNE SYSTEM
3kw0:D (TYR33) to (GLU64) CRYSTAL STRUCTURE OF CYSTEINE PEPTIDASE (NP_982244.1) FROM BACILLUS CEREUS ATCC 10987 AT 2.50 A RESOLUTION | CYSTEINE PEPTIDASE, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, HYDROLASE
1mzo:A (GLY528) to (GLY561) CRYSTAL STRUCTURE OF PYRUVATE FORMATE-LYASE WITH PYRUVATE | ENZYME-SUBSTRATE COMPLEX, TRANSFERASE
1mzo:A (GLU713) to (ARG738) CRYSTAL STRUCTURE OF PYRUVATE FORMATE-LYASE WITH PYRUVATE | ENZYME-SUBSTRATE COMPLEX, TRANSFERASE
1mzo:B (GLY528) to (GLY561) CRYSTAL STRUCTURE OF PYRUVATE FORMATE-LYASE WITH PYRUVATE | ENZYME-SUBSTRATE COMPLEX, TRANSFERASE
1mzo:B (GLU713) to (ARG738) CRYSTAL STRUCTURE OF PYRUVATE FORMATE-LYASE WITH PYRUVATE | ENZYME-SUBSTRATE COMPLEX, TRANSFERASE
1yle:A (ALA33) to (SER80) THE STRUCTURE OF ARGININE/ORNITHINE SUCCINYLTRANSFERASE SUBUNIT AI FROM PSEUDOMONAS AERUGINOSA. | PSEUDOMONAS AERUGINOSA, STRUCTURAL GENOMICS, ARGININE N- SUCCINYLTRANSFERASE, ACYLTRANSFERASE; ARGININE METABOLISM, PSI, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, TRANSFERASE
5dd8:B (GLY100) to (LEU132) THE CRYSTAL STRUCTURE OF HUCR MUTANT (HUCR-E48Q) FROM DEINOCOCCUS RADIODURANS | HUCR, TRANSCRIPTION FACTOR, MARR, TRANSCRIPTION REGULATOR
1ynk:H (ASN154) to (THR181) IDENTIFICATION OF KEY RESIDUES OF THE NC6.8 FAB ANTIBODY FRAGMENT BINDING TO SYNTHETIC SWEETENERS: CRYSTAL STRUCTURE OF NC6.8 CO-CRYSTALIZED WITH HIGH POTENCY SWEETENER COMPOUND SC45647 | SWEETENER COMPOUND, SC45657 AND NC174, IMMUNE SYSTEM
3kzl:B (VAL182) to (VAL213) CRYSTAL STRUCTURE OF BA2930 MUTANT (H183G) IN COMPLEX WITH ACCOA | PUTATIVE AMINOGLYCOSIDE N3-ACETYLTRANSFERASE, ACCOA, ACYLTRANSFERASE, STRUCTURAL GENOMICS, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID, TRANSFERASE
1yp3:D (GLU175) to (GLU197) CRYSTAL STRUCTURE OF POTATO TUBER ADP-GLUCOSE PYROPHOSPHORYLASE IN COMPLEX WITH ATP | ADP-GLUCOSE PYROPHOSPHORYLASE, ADP-GLUCOSE SYNTHASE, AGPASE B, ALPHA-D-GLUCOSE-1-PHOSPHATE ADENYL TRANSFERASE
1ypl:H (ASP125) to (ASN159) X-RAY CRYSTAL STRUCTURE OF THROMBIN INHIBITED BY SYNTHETIC CYANOPEPTIDE ANALOGUE RA-1008 | THROMBIN, INHIBITOR COMPLEX, BARREL, 6 STRANDED BETA-SHEET, BLOOD CLOTTING-HYDROLASE INHIBITOR COMPLEX
3l0q:A (ILE371) to (GLY402) THE CRYSTAL STRUCTURE OF XLYLULOSE KINASE FROM YERSINIA PSEUDOTUBERCULOSIS | XLYLULOSE KINASE, SGX, PSI, KINASE, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC
3l4d:D (GLY424) to (LYS474) CRYSTAL STRUCTURE OF STEROL 14-ALPHA DEMETHYLASE (CYP51) FROM LEISHMANIA INFANTUM IN COMPLEX WITH FLUCONAZOLE | STEROL 14-ALPHA DEMETHYLASE, CYP51, P450, HEME, OXIDOREDUCTASE, MONOOXYGENASE, ENDOPLASMIC RETICULUM, TRANSMEMBRANE PROTEIN, STEROL BIOSYNTHESIS, OBTUSIFOLIOL, LIPIDS, MEMBRANE, IRON
1n5x:A (LEU361) to (THR382) XANTHINE DEHYDROGENASE FROM BOVINE MILK WITH INHIBITOR TEI-6720 BOUND | OXIDOREDUCTASE, MOLYBDOPTERIN, TEI-6720, FLAVOPROTEIN, FAD, IRON- SULFUR CENTER, FE2/S2 CENTER
1n5x:B (LEU361) to (THR382) XANTHINE DEHYDROGENASE FROM BOVINE MILK WITH INHIBITOR TEI-6720 BOUND | OXIDOREDUCTASE, MOLYBDOPTERIN, TEI-6720, FLAVOPROTEIN, FAD, IRON- SULFUR CENTER, FE2/S2 CENTER
4akh:A (GLU2452) to (LYS2476) DYNEIN MOTOR DOMAIN - AMPPNP COMPLEX | MOTOR PROTEIN, MOTOR PROTEIN-TRANSFERASE COMPLEX, AAA+ PROTEIN, ASCE PROTEIN, MOTOR PROTEIN P-LOOP NTPASE, CYTOSKELETAL MOTOR
1yv3:A (ASP21) to (CYS49) THE STRUCTURAL BASIS OF BLEBBISTATIN INHIBITION AND SPECIFICITY FOR MYOSIN II | MYOSIN, BLEBBISTATIN, MYOSIN II INHIBITOR, MYOSIN-INHIBITOR COMPLEX, METASTABLE STATE, CONTRACTILE PROTEIN
4aki:A (GLU2452) to (LYS2476) DYNEIN MOTOR DOMAIN - LUAC DERIVATIVE | MOTOR PROTEIN, DYNEIN, DYNEIN HEAVY CHAIN, DYNEIN MOTOR DOMAIN, MOTOR PROTEIN AAA+ PROTEIN, ASCE PROTEIN, P-LOOP NTPASE, CYTOSKELETAL MOTOR
3ldi:B (PRO2) to (VAL34) CRYSTAL STRUCTURE OF APROTININ IN COMPLEX WITH SUCROSE OCTASULFATE: UNUSUAL INTERACTIONS AND IMPLICATION FOR HEPARIN BINDING | APROTININ, SUCROSE OCTASULFATE, DISULFIDE BOND, PROTEASE INHIBITOR, SECRETED, SERINE PROTEASE INHIBITOR, HYDROLASE INHIBITOR
3ldx:H (ASP125) to (ASN159) DISCOVERY AND CLINICAL EVALUATION OF RWJ-671818, A THROMBIN INHIBITOR WITH AN OXYGUANIDINE P1 MOTIF | BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, BLOOD COAGULATION,SERINE PROTEASE
1z7q:B (GLN20) to (SER51) 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:G (PHE21) to (GLU50) 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:P (GLN20) to (SER51) 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:U (PHE21) to (GLU50) 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
1z7s:1 (SER172) to (PRO192) THE CRYSTAL STRUCTURE OF COXSACKIEVIRUS A21 | PICORNAVIRUS, COXSACKIEVIRUS, A21, CAPSID PROTEIN, VIRAL PROTEIN, ICOSAHEDRAL VIRUS
4ptk:A (LEU6) to (THR44) CRYSTAL STRUCTURE OF STAPHYLOCOCCAL IMPASE-I COMPLEX WITH 3MG2+ AND PHOSPHATE | IMPASE PRODUCT COMPLEX, HYDROLASE
4ptk:B (LEU6) to (THR44) CRYSTAL STRUCTURE OF STAPHYLOCOCCAL IMPASE-I COMPLEX WITH 3MG2+ AND PHOSPHATE | IMPASE PRODUCT COMPLEX, HYDROLASE
1z8i:B (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THE THROMBIN MUTANT G193A BOUND TO PPACK | SERINE PROTEASE, OXYANION HOLE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ao9:A (GLU241) to (GLY279) BIOCHEMICAL PROPERTIES AND CRYSTAL STRUCTURE OF A NOVEL BETA-PHENYLALANINE AMINOTRANSFERASE FROM VARIOVORAX PARADOXUS | TRANSFERASE
5dsv:M (PHE21) to (VAL49) CRYSTAL STRUCTURE OF HUMAN PROTEASOME ALPHA7 TETRADECAMER | PROTEASOME, HYDROLASE
1zde:A (ALA93) to (MET134) 1.95 ANGSTROM CRYSTAL STRUCTURE OF A DNAE INTEIN PRECURSOR FROM SYNECHOCYSTIS SP. PCC 6803 | DNAE, INTEIN, SPLICING, PRECURSOR, TRANSFERASE
1zgi:A (ASP125) to (ASN159) THROMBIN IN COMPLEX WITH AN OXAZOLOPYRIDINE INHIBITOR 21 | THROMBIN, THROMBIN INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1zgv:A (ASP125) to (ASN159) THROMBIN IN COMPLEX WITH AN OXAZOLOPYRIDINE INHIBITOR 2 | THROMBIN, THROMBIN INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1zjk:A (ARG555) to (ASP589) CRYSTAL STRUCTURE OF THE ZYMOGEN CATALYTIC REGION OF HUMAN MASP-2 | BETA BARREL, MODULAR PROTEIN, HYDROLASE
5dy4:A (LEU206) to (PHE235) CRYSTAL STRUCTURE OF HUMAN SIRT2 IN COMPLEX WITH A BROMINATED 2ND GENERATION SIRREAL INHIBITOR AND NAD+ | HYDROLASE, HYDROLASE INHIBITOR COMPLEX
5dy5:A (LEU206) to (PHE235) CRYSTAL STRUCTURE OF HUMAN SIRT2 IN COMPLEX WITH A SIRREAL PROBE FRAGMENT | HYDROLASE, HYDROLASE INHIBITOR COMPLEX
4aso:A (SER53) to (LEU83) TUBR BOUND TO 24 BP OF TUBC FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, PARTITION, SEGREGATION
4aso:B (SER53) to (LEU83) TUBR BOUND TO 24 BP OF TUBC FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, PARTITION, SEGREGATION
4aso:C (SER53) to (LEU83) TUBR BOUND TO 24 BP OF TUBC FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, PARTITION, SEGREGATION
4aso:D (SER53) to (LEU83) TUBR BOUND TO 24 BP OF TUBC FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, PARTITION, SEGREGATION
4aso:E (SER53) to (LEU83) TUBR BOUND TO 24 BP OF TUBC FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, PARTITION, SEGREGATION
4aso:F (SER53) to (LEU83) TUBR BOUND TO 24 BP OF TUBC FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, PARTITION, SEGREGATION
4aso:G (SER53) to (LEU83) TUBR BOUND TO 24 BP OF TUBC FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, PARTITION, SEGREGATION
4aso:H (SER53) to (LEU83) TUBR BOUND TO 24 BP OF TUBC FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, PARTITION, SEGREGATION
4aso:I (SER53) to (LEU83) TUBR BOUND TO 24 BP OF TUBC FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, PARTITION, SEGREGATION
4aso:J (SER53) to (LEU83) TUBR BOUND TO 24 BP OF TUBC FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, PARTITION, SEGREGATION
4aso:K (SER53) to (LEU83) TUBR BOUND TO 24 BP OF TUBC FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, PARTITION, SEGREGATION
4aso:L (SER53) to (LEU83) TUBR BOUND TO 24 BP OF TUBC FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, PARTITION, SEGREGATION
4aso:M (SER53) to (LEU83) TUBR BOUND TO 24 BP OF TUBC FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, PARTITION, SEGREGATION
4aso:N (SER53) to (LEU83) TUBR BOUND TO 24 BP OF TUBC FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, PARTITION, SEGREGATION
4aso:O (SER53) to (LEU83) TUBR BOUND TO 24 BP OF TUBC FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, PARTITION, SEGREGATION
4aso:P (SER53) to (LEU83) TUBR BOUND TO 24 BP OF TUBC FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, PARTITION, SEGREGATION
4ass:A (SER53) to (LEU83) TUBR BOUND TO TUBC - 26 BP - FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, SEGREGATION, PARTITIONING
4ass:B (SER53) to (LEU83) TUBR BOUND TO TUBC - 26 BP - FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, SEGREGATION, PARTITIONING
4ass:C (SER53) to (LEU83) TUBR BOUND TO TUBC - 26 BP - FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, SEGREGATION, PARTITIONING
4ass:D (SER53) to (LEU83) TUBR BOUND TO TUBC - 26 BP - FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, SEGREGATION, PARTITIONING
4ass:E (SER53) to (LEU83) TUBR BOUND TO TUBC - 26 BP - FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, SEGREGATION, PARTITIONING
4ass:F (SER53) to (LEU83) TUBR BOUND TO TUBC - 26 BP - FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, SEGREGATION, PARTITIONING
4ass:G (SER53) to (LEU83) TUBR BOUND TO TUBC - 26 BP - FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, SEGREGATION, PARTITIONING
4ass:H (SER53) to (LEU83) TUBR BOUND TO TUBC - 26 BP - FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, SEGREGATION, PARTITIONING
4ass:I (SER53) to (LEU83) TUBR BOUND TO TUBC - 26 BP - FROM BACILLUS THURINGIENSIS SEROVAR ISRAELENSIS PBTOXIS | STRUCTURAL PROTEIN-DNA COMPLEX, SEGREGATION, PARTITIONING
4q48:B (ASP466) to (ALA493) STRUCTURE OF THE RECQ CATALYTIC CORE FROM DEINOCOCCUS RADIODURANS | DNA UNWINDING, HELICASE, DNA BINDING PROTEIN
4q4w:1 (SER179) to (PRO199) HIGH-RESOLUTION CRYSTAL STRUCTURE OF COXSACKIEVIRUS A24V | COXSACKIEVIRUS A24V, VIRUS
4q4v:1 (SER179) to (PRO199) CRYSTAL STRUCTURE OF COXSACKIEVIRUS A24V | COXSACKIEVIRUS A24V, VIRUS
4q4y:1 (SER179) to (PRO199) CRYSTAL STRUCTURE OF COXSACKIEVIRUS A24V SOAKED WITH DISIALYLLACTO-N- TETRAOSE (DSLNT) | COXSACKIEVIRUS A24V, VIRUS
4q4x:1 (SER179) to (PRO199) CRYSTAL STRUCTURE OF COXSACKIEVIRUS A24V SOAKED WITH 6'-SIALYLLACTOSE (6SL) | COXSACKIEVIRUS A24V, VIRUS
1zrb:A (ASP125) to (ASN159) THROMBIN IN COMPLEX WITH AN AZAFLUORENYL INHIBITOR 23B | THROMBIN; THROMBIN INHIBITOR COMPLEX, BLOOD CLOTTING, HYDROLASE- INHIBITOR COMPLEX, BLOOD CLOTTING,HYDROLASE-INHIBITOR COMPLEX
4q5t:A (THR146) to (LYS181) CRYSTAL STRUCTURE OF AN ATMB (PUTATIVE MEMBRANE LIPOPROTEIN) FROM STREPTOCOCCUS MUTANS UA159 AT 1.91 A RESOLUTION | METHIONINE-BINDING, NLPA LIPOPROTEIN, PF03180 FAMILY, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-BIOLOGY, TRANSPORT PROTEIN
5e2q:A (ALA567) to (ASP606) STRUCTURE OF HUMAN DPP3 IN COMPLEX WITH ANGIOTENSIN-II | COMPLEX, PEPTIDASE, ZINC-HYDROLASE, HYDROLASE
5e33:A (ALA567) to (ASP606) STRUCTURE OF HUMAN DPP3 IN COMPLEX WITH MET-ENKEPHALIN | COMPLEX, OPIOID-PEPTIDE, ZINC-HYDROLASE, PEPTIDASE, HYDROLASE
5e3a:A (ALA567) to (SER608) STRUCTURE OF HUMAN DPP3 IN COMPLEX WITH OPIOID PEPTIDE LEU-ENKEPHALIN | PEPTIDE-COMPLEX, ZINC-HYDROLASE, OPIOID-PEPTIDE, PEPTIDASE, HYDROLASE
5e3c:A (HIS568) to (ASP606) STRUCTURE OF HUMAN DPP3 IN COMPLEX WITH HEMORPHIN LIKE OPIOID PEPTIDE IVYPW | OPIOID-PEPTIDE, ZINC-HYDROLASE, PEPTIDASE, INHIBITOR COMPLEX, HYDROLASE
4q69:A (ASN281) to (VAL329) CRYSTAL STRUCTURE OF A SUSD HOMOLOG (BT2259) FROM BACTEROIDES THETAIOTAOMICRON VPI-5482 AT 2.50 A RESOLUTION | SUSD-LIKE_2 FAMILY, PF12771, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI- BIOLOGY, SUGAR BINDING PROTEIN
4q69:B (ASN281) to (VAL329) CRYSTAL STRUCTURE OF A SUSD HOMOLOG (BT2259) FROM BACTEROIDES THETAIOTAOMICRON VPI-5482 AT 2.50 A RESOLUTION | SUSD-LIKE_2 FAMILY, PF12771, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI- BIOLOGY, SUGAR BINDING PROTEIN
4ax9:H (ASP125) to (ASN159) HUMAN THROMBIN COMPLEXED WITH NAPSAGATRAN, RO0466240 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, HYDROLASE HYDROLASE INHIBITOR COMPLEX
3lu9:E (ASP125) to (ASN159) CRYSTAL STRUCTURE OF HUMAN THROMBIN MUTANT S195A IN COMPLEX WITH THE EXTRACELLULAR FRAGMENT OF HUMAN PAR1 | SERINE PROTEASE, ACUTE PHASE, BLOOD COAGULATION, CALCIUM, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, DISULFIDE BOND, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PHARMACEUTICAL, POLYMORPHISM, PROTEASE, SECRETED, ZYMOGEN, CELL MEMBRANE, G-PROTEIN COUPLED RECEPTOR, MEMBRANE, PHOSPHOPROTEIN, RECEPTOR, TRANSDUCER, TRANSMEMBRANE
4q6r:A (GLY320) to (SER367) CRYSTAL STRUCTURE OF HUMAN SPHINGOSINE-1-PHOSPHATE LYASE IN COMPLEX WITH INHIBITOR 6-[(2R)-4-(4-BENZYL-7-CHLOROPHTHALAZIN-1-YL)-2- METHYLPIPERAZIN-1-YL]PYRIDINE-3-CARBONITRILE | PLP, PYRIDOXAL 5-PHOSPHATE-DEPENDENT ENZYMES, LYASE-LYASE INHIBITOR COMPLEX
4q6r:B (GLY320) to (SER367) CRYSTAL STRUCTURE OF HUMAN SPHINGOSINE-1-PHOSPHATE LYASE IN COMPLEX WITH INHIBITOR 6-[(2R)-4-(4-BENZYL-7-CHLOROPHTHALAZIN-1-YL)-2- METHYLPIPERAZIN-1-YL]PYRIDINE-3-CARBONITRILE | PLP, PYRIDOXAL 5-PHOSPHATE-DEPENDENT ENZYMES, LYASE-LYASE INHIBITOR COMPLEX
1zy7:B (ASN417) to (LEU436) CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF AN ADENOSINE DEAMINASE THAT ACTS ON RNA (HADAR2) BOUND TO INOSITOL HEXAKISPHOSPHATE (IHP) | ALPHA/BETA DEAMINASE MOTIF, ZINC COORDINATION, IONSITOL HEXAKISPHOSPHATE, HYDROLASE
5e6m:A (ALA68) to (PRO98) CRYSTAL STRUCTURE OF HUMAN WILD TYPE GLYRS BOUND WITH TRNAGLY | AMINOACYL-TRNA SYNTHESES, GLYCYL-TRNA SYNTHETASE, TRNA, LIGASE-RNA COMPLEX
4ayy:B (ASP122) to (ASN164) HUMAN THROMBIN - INHIBITOR COMPLEX | HYDROLASE-INHIBITOR COMPLEX
4aze:A (ALA388) to (LEU405) HUMAN DYRK1A IN COMPLEX WITH LEUCETTINE L41 | TRANSFERASE
4aze:B (ALA388) to (LEU405) HUMAN DYRK1A IN COMPLEX WITH LEUCETTINE L41 | TRANSFERASE
4aze:C (ALA388) to (LEU405) HUMAN DYRK1A IN COMPLEX WITH LEUCETTINE L41 | TRANSFERASE
3ly6:B (SER152) to (GLY183) CRYSTAL STRUCTURE OF HUMAN TRANSGLUTAMINASE 2 COMPLEX WITH ADENOSINE 5' TRIPHOSPHATE | TRANSGLUTAMINASE, ACYLTRANSFERASE, DIABETES MELLITUS, DISEASE MUTATION, METAL-BINDING, PHOSPHOPROTEIN, TRANSFERASE
5e8e:H (ASP442) to (ASN484) CRYSTAL STRUCTURE OF THROMBIN BOUND TO AN EXOSITE 1-SPECIFIC IGA FAB | IMMUNE SYSTEM-HYDROLASE COMPLEX, IMMUNE SYSTEM, INHIBITOR
5e8m:A (PRO467) to (LEU495) CRYSTAL STRUCTURE OF HUMAN HEPARANASE | GLYCOSIDE HYDROLASE, APO, PROTEIN, SUGAR, HYDROLASE
5e9c:A (PRO467) to (LEU495) CRYSTAL STRUCTURE OF HUMAN HEPARANASE IN COMPLEX WITH HEPARIN TETRASACCHARIDE DP4 | GLYCOSIDE HYDROLASE, LIGAND 4, PROTEIN, SUGAR, HYDROLASE
2a45:B (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN THROMBIN AND THE CENTRAL "E" REGION OF FIBRIN | THROMBIN, FIBRIN, FRAGMENT E, THROMBIN-FIBRIN COMPLEX, COILED COILS, DISULFIDE RINGS, BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3ax7:A (LEU361) to (THR382) BOVINE XANTHINE OXIDASE, PROTEASE CLEAVED FORM | XANTHINE OXIDOREDUCTASE, XANTHINE OXIDASE, OXIDOREDUCTASE
3m46:B (ASP536) to (VAL557) THE CRYSTAL STRUCTURE OF THE D73A MUTANT OF GLYCOSIDE HYDROLASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174 | GLYCOSIDE HYDROLASE (FAMILY 31), STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MCSG, MIDWEST CENTER FOR STRUCTURAL GENOMICS, HYDROLASE
3b23:B (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THROMBIN-VARIEGIN COMPLEX: INSIGHTS OF A NOVEL MECHANISM OF INHIBITION AND DESIGN OF TUNABLE THROMBIN INHIBITORS | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qhw:A (ASP360) to (GLY386) CRYSTAL STRUCTURE OF A PUTATIVE TWO-DOMAIN SUGAR HYDROLASE (BACCAC_02064) FROM BACTEROIDES CACCAE ATCC 43185 AT 1.35 A RESOLUTION | TWO DOMAIN PROTEIN, GALACTOSE-BINDING DOMAIN-LIKE FOLD, CONCANAVALIN A-LIKE FOLD, PF11958 FAMILY, DUF3472, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-BIOLOGY, UNKNOWN FUNCTION
3m8e:A (SER53) to (LEU83) PROTEIN STRUCTURE OF TYPE III PLASMID SEGREGATION TUBR | WINGED HELIX-TURN-HELIX, ARSR FAMILY, DNA BINDING PROTEIN
4qhx:A (ASP360) to (GLY386) CRYSTAL STRUCTURE OF A PUTATIVE TWO-DOMAIN SUGAR HYDROLASE (BACCAC_02064) FROM BACTEROIDES CACCAE ATCC 43185 AT 1.80 A RESOLUTION | TWO DOMAIN PROTEIN, GALACTOSE-BINDING DOMAIN-LIKE FOLD, CONCANAVALIN A-LIKE FOLD, PF11958 FAMILY, DUF3472, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-BIOLOGY, UNKNOWN FUNCTION
4qi0:B (SER238) to (LEU269) X-RAY STRUCTURE OF THE ROQ DOMAIN FROM MURINE ROQUIN-1 | ROQ DOMAIN, WINGED-HELIX DOMAIN,RNA BINDING, TNF CDE RNA, RNA BINDING PROTEIN
3b39:B (PRO176) to (ASP198) STRUCTURE OF THE DNAG PRIMASE CATALYTIC DOMAIN BOUND TO SSDNA | PROTEIN-DNA COMPLEX, TOPRIM FOLD, DNA REPLICATION, DNA-DIRECTED RNA POLYMERASE, METAL-BINDING, NUCLEOTIDYLTRANSFERASE, PRIMOSOME, TRANSCRIPTION, TRANSFERASE, ZINC-FINGER, TRANSFERASE-DNA COMPLEX
3m9a:A (SER53) to (LEU83) PROTEIN STRUCTURE OF TYPE III PLASMID SEGREGATION TUBR | TUBR, WINGED HELIX-TURN-HELIX, PLASMID SEGREGATION, DNA BINDING PROTEIN
5egy:A (MET569) to (ASP606) STRUCTURE OF LIGAND FREE HUMAN DPP3 IN CLOSED FORM. | UNBOUND, PEPTIDASE, ZINC, HYDROLASE
5ehh:A (MET569) to (ASP606) STRUCTURE OF HUMAN DPP3 IN COMPLEX WITH ENDOMORPHIN-2. | INHIBITOR-COMPLEX, PEPTIDASE, ZINC-HYDROLASE, HYDROLASE
4bak:B (ASP158) to (ASN194) THROMBIN IN COMPLEX WITH INHIBITOR | HYDROLASE, THROMBIN INHIBITOR, SERINE PROTEASE
4ban:B (ASP158) to (ASN194) THROMBIN IN COMPLEX WITH INHIBITOR | SERINE PROTEASE, THROMBIN INHIBITOR, HYDROLASE
4bao:B (ASP158) to (ASN194) THROMBIN IN COMPLEX WITH INHIBITOR | SERINE PROTEASE, THROMBIN INHIBITOR, HYDROLASE
4baq:B (ASP158) to (ASN194) THROMBIN IN COMPLEX WITH INHIBITOR | SERINE PROTEASE, THROMBIN INHIBITOR, HYDROLASE
4qls:F (PHE18) to (THR51) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 11 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qls:T (PHE18) to (THR51) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 11 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlq:C (PHE16) to (THR49) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 8 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlq:F (PHE18) to (THR51) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 8 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlq:Q (PHE16) to (THR49) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 8 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlq:T (PHE18) to (THR51) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 8 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlt:F (PHE18) to (ILE50) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 2 (PR924) | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlt:T (PHE18) to (ILE50) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 2 (PR924) | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2afq:B (ASP125) to (ASN159) 1.9 ANGSTROM CRYTAL STRUCTURE OF WILD-TYPE HUMAN THROMBIN IN THE SODIUM FREE STATE | ALPHA-THROMBIN; COAGULATION; ALLOSTERY; PROTEASE; COAGULATION FACTOR II, BLOOD CLOTTING, HYDROLASE, BLOOD CLOTTING,HYDROLASE
2afq:D (ASP125) to (ASN159) 1.9 ANGSTROM CRYTAL STRUCTURE OF WILD-TYPE HUMAN THROMBIN IN THE SODIUM FREE STATE | ALPHA-THROMBIN; COAGULATION; ALLOSTERY; PROTEASE; COAGULATION FACTOR II, BLOOD CLOTTING, HYDROLASE, BLOOD CLOTTING,HYDROLASE
4qlu:F (PHE18) to (ILE50) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 9 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlu:T (PHE18) to (ILE50) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 9 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3mfx:B (THR73) to (ASP116) CRYSTAL STRUCTURE OF THE SENSORY BOX DOMAIN OF THE SENSORY- BOX/GGDEF PROTEIN SO_1695 FROM SHEWANELLA ONEIDENSIS, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET SOR288B | ALPHA-BETA PROTEIN, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, TRANSCRIPTION
3mg0:E (PHE22) to (LEU51) STRUCTURE OF YEAST 20S PROTEASOME WITH BORTEZOMIB | 20S PROTEASOME, HYDROLASE
3mg0:F (PHE22) to (THR55) STRUCTURE OF YEAST 20S PROTEASOME WITH BORTEZOMIB | 20S PROTEASOME, HYDROLASE
3mg0:S (PHE22) to (LEU51) STRUCTURE OF YEAST 20S PROTEASOME WITH BORTEZOMIB | 20S PROTEASOME, HYDROLASE
3mg6:F (PHE22) to (THR55) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 6 | 20S PROTEASOME, HYDROLASE
3mg7:T (PHE22) to (THR55) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 8 | 20S PROTEASOME, HYDROLASE
3b9j:B (LEU361) to (THR382) STRUCTURE OF XANTHINE OXIDASE WITH 2-HYDROXY-6-METHYLPURINE | OXIDOREDUCTASE, CATALYSIS, INTERMEDIATE, SUBSTRATE ORIENTATION, PEROXISOME
3mg8:Q (PHE22) to (THR55) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 16 | 20S PROTEASOME, HYDROLASE
3b9r:A (PHE407) to (GLY438) SERCA CA2+-ATPASE E2 ALUMINIUM FLUORIDE COMPLEX WITHOUT THAPSIGARGIN | CALCIUM PUMP, MEMBRANE PROTEIN, TRANSITION STATE, ALUMINIUM FLUORIDE, DEPHOSPHORYLATION, ALTERNATIVE SPLICING, ATP- BINDING, CALCIUM, CALCIUM TRANSPORT, ENDOPLASMIC RETICULUM, HYDROLASE, ION TRANSPORT, MAGNESIUM, METAL-BINDING, NUCLEOTIDE-BINDING, PHOSPHORYLATION, SARCOPLASMIC RETICULUM, TRANSMEMBRANE, TRANSPORT
3mjx:A (ASP21) to (CYS49) CRYSTAL STRUCTURE OF MYOSIN-2 MOTOR DOMAIN IN COMPLEX WITH ADP- METAVANADATE AND BLEBBISTATIN | CONTRACTILE PROTEIN, ALLOSTERIC, METHYLATION, ATP-BINDING, MOTOR PROTEIN, ACTIN-BINDING, PHOSPHOPROTEIN, ADP-METAVANADATE, CALMODULIN-BINDING, NUCLEOTIDE-BINDING, BLEBBISTATIN, MYOSIN, STRUCTURAL PROTEIN
3mkd:A (ASP21) to (GLU51) CRYSTAL STRUCTURE OF MYOSIN-2 DICTYOSTELIUM DISCOIDEUM MOTOR DOMAIN S456Y MUTANT IN COMPLEX WITH ADP-ORTHOVANADATE | CONTRACTILE PROTEIN, ALLOSTERIC, METHYLATION, ATP-BINDING, MOTOR PROTEIN, ACTIN-BINDING, PHOSPHOPROTEIN, ADP-ORTHOVANADATE, CALMODULIN-BINDING, NUCLEOTIDE-BINDING, MYOSIN
3mka:D (SER8) to (GLU44) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME WITH PROPETIDE AND AN T1A MUTATION AT BETA-SUBUNIT | MYCOBACTERIUM TUBERCULOSIS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, PROPEPTIDE, PROTEIN MATURATION, PROTEASOME ASSEMBLY, HYDROLASE
3mka:I (PRO9) to (GLU44) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME WITH PROPETIDE AND AN T1A MUTATION AT BETA-SUBUNIT | MYCOBACTERIUM TUBERCULOSIS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, PROPEPTIDE, PROTEIN MATURATION, PROTEASOME ASSEMBLY, HYDROLASE
3mka:K (SER8) to (GLU44) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME WITH PROPETIDE AND AN T1A MUTATION AT BETA-SUBUNIT | MYCOBACTERIUM TUBERCULOSIS, PROTEASOME ENDOPEPTIDASE COMPLEX, PROTEIN SUBUNITS, PROPEPTIDE, PROTEIN MATURATION, PROTEASOME ASSEMBLY, HYDROLASE
3mkk:A (ASP536) to (GLU559) THE CRYSTAL STRUCTURE OF THE D307A MUTANT OF GLYCOSIDE HYDROLASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174 IN COMPLEX WITH ISOMALTOSE | ISOMALTOSE, STRUCTURAL COMPLEX, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MCSG, MIDWEST CENTER FOR STRUCTURAL GENOMICS, HYDROLASE
3mkk:B (ASP536) to (GLU559) THE CRYSTAL STRUCTURE OF THE D307A MUTANT OF GLYCOSIDE HYDROLASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174 IN COMPLEX WITH ISOMALTOSE | ISOMALTOSE, STRUCTURAL COMPLEX, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MCSG, MIDWEST CENTER FOR STRUCTURAL GENOMICS, HYDROLASE
3bei:B (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THE SLOW FORM OF THROMBIN IN A SELF_INHIBITED CONFORMATION | SERINE PROTEASE, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, SECRETED, ZYMOGEN
3bf6:H (ASP125) to (ASN159) THROMBIN:SURAMIN COMPLEX | THROMBIN, SURAMIN, BLOOD, COAGULATION, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN
5erc:A (HIS410) to (TYR443) X-RAY CRYSTAL STRUCTURE OF BRPF1 PZP DOMAIN | READER DOMAIN, METHYLLYSINE, DNA, H3 HISTONE, TRANSCRIPTION
3mnq:A (ASP21) to (CYS49) CRYSTAL STRUCTURE OF MYOSIN-2 MOTOR DOMAIN IN COMPLEX WITH ADP- METAVANADATE AND RESVERATROL | MYOSIN, MOTOR DOMAIN, RESVERATROL, ALLOSTERIC, INHIBITOR, ACTIVATOR, CONTRACTILE PROTEIN, ATP-BINDING, ACTIN-BINDING, PHOSPHOPROTEIN, CALMODULIN-BINDING, NUCLEOTIDE-BINDING, MOTOR PROTEIN, MOTOR PROTEIN-INHIBITOR COMPLEX
4bgd:A (SER1795) to (THR1846) CRYSTAL STRUCTURE OF BRR2 IN COMPLEX WITH THE JAB1/MPN DOMAIN OF PRP8 | TRANSCRIPTION, SPLICEOSOME, RNA HELICASE, U5 SNRNP, RETINITIS PIGMENTOSA
5eud:A (GLY278) to (ARG325) S1P LYASE BACTERIAL SURROGATE BOUND TO N-(1-(4-(3-HYDROXYPROP-1-YN-1- YL)PHENYL)-2-((4-METHOXY-2,5-DIMETHYLBENZYL)AMINO)ETHYL)-5- METHYLISOXAZOLE-3-CARBOXAMIDE | S1P LYASE BACTERIAL SURROGATE, LYASE
5eud:B (GLY278) to (ARG325) S1P LYASE BACTERIAL SURROGATE BOUND TO N-(1-(4-(3-HYDROXYPROP-1-YN-1- YL)PHENYL)-2-((4-METHOXY-2,5-DIMETHYLBENZYL)AMINO)ETHYL)-5- METHYLISOXAZOLE-3-CARBOXAMIDE | S1P LYASE BACTERIAL SURROGATE, LYASE
5eue:A (GLY278) to (ARG325) S1P LYASE BACTERIAL SURROGATE BOUND TO N-(2-((4-METHOXY-2,5- DIMETHYLBENZYL)AMINO)-1-PHENYLETHYL)-5-METHYLISOXAZOLE-3-CARBOXAMIDE | S1P LYASE BACTERIAL SURROGATE, LYASE
5eue:B (GLY278) to (ARG325) S1P LYASE BACTERIAL SURROGATE BOUND TO N-(2-((4-METHOXY-2,5- DIMETHYLBENZYL)AMINO)-1-PHENYLETHYL)-5-METHYLISOXAZOLE-3-CARBOXAMIDE | S1P LYASE BACTERIAL SURROGATE, LYASE
3bii:D (SER39) to (PHE75) CRYSTAL STRUCTURE OF ACTIVATED MPT SYNTHASE | MPT SYNTHASE, MOCO BIOSYNTHESIS, MOAE, MOAD, UBIQUITIN-LIKE, BETA-HAMMERHEAD FOLD, MOLYBDENUM COFACTOR BIOSYNTHESIS, TRANSFERASE
4qv1:F (PHE18) to (THR51) YCP BETA5-M45A MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qv1:T (PHE18) to (THR51) YCP BETA5-M45A MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4quy:F (PHE18) to (THR51) YCP BETA5-A49S-MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4quy:T (PHE18) to (THR51) YCP BETA5-A49S-MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv0:F (VAL24) to (THR51) YCP BETA5-A49T-A50V-DOUBLE MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv0:T (VAL24) to (THR51) YCP BETA5-A49T-A50V-DOUBLE MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
3bj8:C (THR37) to (TYR77) SPERMINE/SPERMIDINE N1-ACETYLTRANSFERASE FROM MOUSE: CRYSTAL STRUCTURE OF A TERNARY COMPLEX REVEALS SOLVENT-MEDIATED SPERMINE BINDING | SSAT, COA, SPERMINE, TERNARY COMPLEX, ACYLTRANSFERASE, CYTOPLASM, TRANSFERASE
5ew1:H (ASP125) to (ASN159) HUMAN THROMBIN SANDWICHED BETWEEN TWO DNA APTAMERS: HD22 AND HD1- DELTAT3 | PROTEIN-DNA COMPLEX, BLOOD COAGULATION, DNA APTAMER, DNA-INHIBITOR, G-QUADRUPLEX, DUPLEX-QUADRUPLEX JUNCTION, SERINE PROTEASE, HYDROLASE, ABASIC FURAN, HYDROLASE-DNA COMPLEX
5ew2:H (ASP125) to (ASN159) HUMAN THROMBIN SANDWICHED BETWEEN TWO DNA APTAMERS: HD22 AND HD1- DELTAT12 | PROTEIN-DNA COMPLEX, BLOOD COAGULATION, DNA APTAMER, DNA-INHIBITOR, G-QUADRUPLEX, DUPLEX-QUADRUPLEX JUNCTION, SERINE PROTEASE, HYDROLASE, ABASIC FURAN, HYDROLASE-DNA COMPLEX
4qv3:F (PHE18) to (THR51) YCP BETA5-M45V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv3:T (PHE18) to (THR51) YCP BETA5-M45V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv5:F (VAL24) to (THR51) YCP BETA5-M45I MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv5:T (VAL24) to (THR51) YCP BETA5-M45I MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv6:F (PHE18) to (THR51) YCP BETA5-A49V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv6:T (PHE18) to (THR51) YCP BETA5-A49V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv7:F (VAL24) to (THR51) YCP BETA5-A50V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv7:T (VAL24) to (THR51) YCP BETA5-A50V MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv8:F (VAL24) to (THR51) YCP BETA5-C52F MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv8:T (VAL24) to (THR51) YCP BETA5-C52F MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv9:F (VAL24) to (THR51) YCP BETA5-C63F MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qv9:T (VAL24) to (THR51) YCP BETA5-C63F MUTANT | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE
4qvm:F (PHE18) to (THR51) YCP BETA5-M45A MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvm:T (PHE18) to (THR51) YCP BETA5-M45A MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvn:E (PHE19) to (LEU48) YCP BETA5-M45V MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvn:F (PHE18) to (THR51) YCP BETA5-M45V MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvn:S (GLN20) to (LEU48) YCP BETA5-M45V MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvn:T (PHE18) to (THR51) YCP BETA5-M45V MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvp:E (PHE19) to (LEU48) YCP BETA5-M45T MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvp:S (PHE19) to (LEU48) YCP BETA5-M45T MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qvq:E (PHE19) to (LEU48) YCP BETA5-M45I MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4qvq:S (PHE19) to (LEU48) YCP BETA5-M45I MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4blt:A (SER28) to (ASP60) P4 PROTEIN FROM BACTERIOPHAGE PHI12 S292A MUTANT IN COMPLEX WITH AMPCPP | HYDROLASE, CYSTOVIRIDAE
4qvw:F (PHE18) to (THR51) YCP BETA5-A49S-MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4qvw:T (PHE18) to (THR51) YCP BETA5-A49S-MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5eyh:A (LEU6) to (THR44) CRYSTAL STRUCTURE OF IMPASE/NADP PHOSPHATASE COMPLEXED WITH NADP AND CA2+ AT PH 7.0 | IMPASE, FIG SUPERFAMILY, SUBSTRATE BOUND COMPLEX, PHOSPHATASE, HYDROLASE
4bmm:B (GLN425) to (ARG475) CRYSTAL STRUCTURE OF TRYPANOSOMA CRUZI CYP51 BOUND TO THE INHIBITOR (R)-N-(3-(1H-INDOL-3-YL)-1-OXO-1-(PYRIDIN-4- YLAMINO)PROPAN-2-YL)- 2',3,5'-TRIFLUORO-(1,1'-BIPHENYL)-4-CARBOXAMIDE | OXIDOREDUCTASE, STEROL BIOSYNTHESIS, CHAGAS DISEASE
4qw1:F (PHE18) to (THR51) YCP BETA5-A50V MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw1:T (PHE18) to (THR51) YCP BETA5-A50V MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw5:F (PHE18) to (THR51) YCP BETA5-M45A MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw5:T (PHE18) to (THR51) YCP BETA5-M45A MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw4:F (PHE18) to (THR51) YCP IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw4:T (PHE18) to (THR51) YCP IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw6:F (PHE18) to (THR51) YCP BETA5-M45V MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw6:T (PHE18) to (THR51) YCP BETA5-M45V MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwj:F (PHE18) to (SER52) YCP BETA5-A49T-MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwj:T (PHE18) to (SER52) YCP BETA5-A49T-MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwf:F (PHE18) to (THR51) YCP BETA5-M45I MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwf:T (PHE18) to (THR51) YCP BETA5-M45I MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwk:F (PHE18) to (THR51) YCP BETA5-A49T-A50V-DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwk:T (PHE18) to (THR51) YCP BETA5-A49T-A50V-DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwl:F (PHE18) to (THR51) YCP BETA5-A50V MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwl:T (PHE18) to (THR51) YCP BETA5-A50V MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwr:F (PHE18) to (THR51) YCP BETA5-C52F MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwr:T (PHE18) to (THR51) YCP BETA5-C52F MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qws:F (PHE18) to (THR51) YCP BETA5-C63F MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qws:T (PHE18) to (THR51) YCP BETA5-C63F MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwu:F (PHE18) to (THR51) YCP BETA5-C52F MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwu:T (PHE18) to (THR51) YCP BETA5-C52F MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5f24:B (LEU6) to (THR44) CRYSTAL STRUCTURE OF DUAL SPECIFIC IMPASE/NADP PHOSPHATASE BOUND WITH D-INOSITOL-1-PHOSPHATE | IMPASE/NADP PHOSPHATASE, SUBSTRATE BOUND COMPLEX, FIG SUPERFAMILY, PHOSPHATASE, HYDROLASE
4qwx:F (PHE18) to (THR51) YCP IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwx:T (PHE18) to (THR51) YCP IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qxj:F (PHE18) to (THR51) YCP BETA5-M45A MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qxj:T (PHE18) to (THR51) YCP BETA5-M45A MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz0:F (PHE18) to (THR51) YCP BETA5-M45V MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz0:T (PHE18) to (THR51) YCP BETA5-M45V MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz2:F (PHE18) to (THR51) YCP BETA5-M45I MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz2:T (PHE18) to (THR51) YCP BETA5-M45I MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz3:F (PHE18) to (THR51) YCP BETA5-A49V MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz3:T (PHE18) to (THR51) YCP BETA5-A49V MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3myh:X (ASP21) to (CYS49) INSIGHTS INTO THE IMPORTANCE OF HYDROGEN BONDING IN THE GAMMA- PHOSPHATE BINDING POCKET OF MYOSIN: STRUCTURAL AND FUNCTIONAL STUDIES OF SER236 | S1DC, MYOSIN, S236A, STRUCTURAL PROTEIN
4qz4:F (PHE18) to (THR51) YCP BETA5-A49S MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz4:T (PHE18) to (THR51) YCP BETA5-A49S MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz5:F (PHE18) to (THR51) YCP BETA5-A49T-MUTANT IN COMPLEX WITH ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz5:T (PHE18) to (THR51) YCP BETA5-A49T-MUTANT IN COMPLEX WITH ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz6:T (PHE18) to (THR51) 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:F (PHE18) to (THR51) YCP BETA5-C52F MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qzw:T (PHE18) to (THR51) YCP BETA5-C52F MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qzx:F (PHE18) to (THR51) YCP BETA5-C63F MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qzx:T (PHE18) to (THR51) YCP BETA5-C63F MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r00:F (PHE18) to (THR51) YCP BETA5-C52F MUTANT IN COMPLEX WITH OMURALIDE | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r00:T (PHE18) to (THR51) YCP BETA5-C52F MUTANT IN COMPLEX WITH OMURALIDE | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qzz:F (PHE18) to (THR51) YCP IN COMPLEX WITH OMURALIDE | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qzz:T (PHE18) to (THR51) YCP IN COMPLEX WITH OMURALIDE | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r02:C (PHE16) to (THR49) YCP IN COMPLEX WITH BSC4999 (ALPHA-KETO PHENYLAMIDE) | CANCER, PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, REVERSIBLE COVALENT LIGAND, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3by6:A (ASN47) to (ILE72) CRYSTAL STRUCTURE OF A TRANSCRIPTIONAL REGULATOR FROM OENOCOCCUS OENI | TRANSCRIPTIONAL REGULATOR, STRUCTURAL GENOMICS, PSI-2, MCSG, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, DNA- BINDING, TRANSCRIPTION REGULATION, TRANSCRIPTION REGULATOR
3by6:B (ASN45) to (ILE72) CRYSTAL STRUCTURE OF A TRANSCRIPTIONAL REGULATOR FROM OENOCOCCUS OENI | TRANSCRIPTIONAL REGULATOR, STRUCTURAL GENOMICS, PSI-2, MCSG, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, DNA- BINDING, TRANSCRIPTION REGULATION, TRANSCRIPTION REGULATOR
3by6:C (PRO46) to (ILE72) CRYSTAL STRUCTURE OF A TRANSCRIPTIONAL REGULATOR FROM OENOCOCCUS OENI | TRANSCRIPTIONAL REGULATOR, STRUCTURAL GENOMICS, PSI-2, MCSG, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, DNA- BINDING, TRANSCRIPTION REGULATION, TRANSCRIPTION REGULATOR
3by6:E (ASN45) to (ILE72) CRYSTAL STRUCTURE OF A TRANSCRIPTIONAL REGULATOR FROM OENOCOCCUS OENI | TRANSCRIPTIONAL REGULATOR, STRUCTURAL GENOMICS, PSI-2, MCSG, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, DNA- BINDING, TRANSCRIPTION REGULATION, TRANSCRIPTION REGULATOR
3bz7:A (ASP21) to (CYS49) CRYSTAL STRUCTURES OF (S)-(-)-BLEBBISTATIN ANALOGS BOUND TO DICTYOSTELIUM DISCOIDEUM MYOSIN II | MYOSIN INHIBITOR, MOTOR DOMAIN, BLEBBISTATIN ANALOGUE, ACTIN-BINDING, ATP-BINDING, CALMODULIN-BINDING, COILED COIL, CYTOPLASM, METHYLATION, MOTOR PROTEIN, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, CONTRACTILE PROTEIN
3bz8:A (ASP21) to (GLU51) CRYSTAL STRUCTURES OF (S)-(-)-BLEBBISTATIN ANALOGS BOUND TO DICTYOSTELIUM DISCOIDEUM MYOSIN II | MYOSIN INHIBITOR, MOTOR DOMAIN, BLEBBISTATIN ANALOGUE, ACTIN-BINDING, ATP-BINDING, CALMODULIN-BINDING, COILED COIL, CYTOPLASM, METHYLATION, MOTOR PROTEIN, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, CONTRACTILE PROTEIN
5fau:A (ASN799) to (PHE825) WILD-TYPE CHOLINE TMA LYASE IN COMPLEX WITH CHOLINE | RADICAL, LYASE, BARREL
5fau:B (ASN799) to (PHE825) WILD-TYPE CHOLINE TMA LYASE IN COMPLEX WITH CHOLINE | RADICAL, LYASE, BARREL
5fau:D (ASN799) to (PHE825) WILD-TYPE CHOLINE TMA LYASE IN COMPLEX WITH CHOLINE | RADICAL, LYASE, BARREL
5fav:A (ASN799) to (PHE825) E491Q MUTANT OF CHOLINE TMA-LYASE | MUTANT, RADICAL, LYASE
5fav:B (ASN799) to (PHE825) E491Q MUTANT OF CHOLINE TMA-LYASE | MUTANT, RADICAL, LYASE
5faw:A (ASN799) to (PHE825) T502A MUTANT OF CHOLINE TMA-LYASE | MUTANT, RADICAL, LYASE
5faw:B (ASN799) to (PHE825) T502A MUTANT OF CHOLINE TMA-LYASE | MUTANT, RADICAL, LYASE
3c1k:A (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THROMBIN IN COMPLEX WITH INHIBITOR 15 | THROMBIN, THROMBIN INHIBITOR COMPLEX, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN, PROTEASE INHIBITOR, SERINE PROTEASE INHIBITOR, SULFATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5fay:A (ASN799) to (PHE825) Y208F MUTANT OF CHOLINE TMA-LYASE | MUTANT, RADICAL, LYASE
5fay:B (ASN799) to (PHE825) Y208F MUTANT OF CHOLINE TMA-LYASE | MUTANT, RADICAL, LYASE
4bup:A (MET165) to (LYS208) A NOVEL ROUTE TO PRODUCT SPECIFICITY IN THE SUV4-20 FAMILY OF HISTONE H4K20 METHYLTRANSFERASES | TRANSFERASE, EPIGENETICS, HISTONE
4bup:B (LYS164) to (LYS208) A NOVEL ROUTE TO PRODUCT SPECIFICITY IN THE SUV4-20 FAMILY OF HISTONE H4K20 METHYLTRANSFERASES | TRANSFERASE, EPIGENETICS, HISTONE
4bwk:B (THR596) to (VAL627) STRUCTURE OF NEUROSPORA CRASSA PAN3 PSEUDOKINASE | GENE REGULATION, DEADENYLASE, PAN2, MIRNA, MRNA DECAY
4bwx:B (THR596) to (VAL627) STRUCTURE OF NEUROSPORA CRASSA PAN3 PSEUDOKINASE MUTANT | GENE REGULATION, DEADENYLASE, PAN2, MIRNA, MRNA DECAY
4r3o:A (TYR23) to (ASP58) HUMAN CONSTITUTIVE 20S PROTEASOME | HYDROLASE
4r3o:B (VAL19) to (GLU48) HUMAN CONSTITUTIVE 20S PROTEASOME | HYDROLASE
4r3o:G (PHE21) to (GLU50) HUMAN CONSTITUTIVE 20S PROTEASOME | HYDROLASE
4r3o:O (TYR23) to (ASP58) HUMAN CONSTITUTIVE 20S PROTEASOME | HYDROLASE
4r3o:P (VAL19) to (GLU48) HUMAN CONSTITUTIVE 20S PROTEASOME | HYDROLASE
4r3o:U (PHE21) to (SER55) HUMAN CONSTITUTIVE 20S PROTEASOME | HYDROLASE
5fgd:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-H(-2)L-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgd:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-H(-2)L-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fg7:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA2-T1A MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5fg7:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA2-T1A MUTANT | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5fgf:F (PHE18) to (THR51) 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:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-H(-2)A-T1A-K81R TRIPLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
3n75:A (VAL334) to (GLY382) X-RAY CRYSTAL STRUCTURE OF THE ESCHERICHIA COLI INDUCIBLE LYSINE DECARBOXYLASE LDCI | PYRIDOXAL-5'-PHOSPHATE DEPENDENT DECARBOXYLASE, ACID STRESS RESPONSE, STRINGENT RESPONSE, GUANOSINE TETRAPHOSPHATE (PPGPP), LYASE
3n75:B (VAL334) to (GLY382) X-RAY CRYSTAL STRUCTURE OF THE ESCHERICHIA COLI INDUCIBLE LYSINE DECARBOXYLASE LDCI | PYRIDOXAL-5'-PHOSPHATE DEPENDENT DECARBOXYLASE, ACID STRESS RESPONSE, STRINGENT RESPONSE, GUANOSINE TETRAPHOSPHATE (PPGPP), LYASE
3n75:C (VAL334) to (GLY382) X-RAY CRYSTAL STRUCTURE OF THE ESCHERICHIA COLI INDUCIBLE LYSINE DECARBOXYLASE LDCI | PYRIDOXAL-5'-PHOSPHATE DEPENDENT DECARBOXYLASE, ACID STRESS RESPONSE, STRINGENT RESPONSE, GUANOSINE TETRAPHOSPHATE (PPGPP), LYASE
3n75:D (VAL334) to (GLY382) X-RAY CRYSTAL STRUCTURE OF THE ESCHERICHIA COLI INDUCIBLE LYSINE DECARBOXYLASE LDCI | PYRIDOXAL-5'-PHOSPHATE DEPENDENT DECARBOXYLASE, ACID STRESS RESPONSE, STRINGENT RESPONSE, GUANOSINE TETRAPHOSPHATE (PPGPP), LYASE
3n75:E (VAL334) to (GLY382) X-RAY CRYSTAL STRUCTURE OF THE ESCHERICHIA COLI INDUCIBLE LYSINE DECARBOXYLASE LDCI | PYRIDOXAL-5'-PHOSPHATE DEPENDENT DECARBOXYLASE, ACID STRESS RESPONSE, STRINGENT RESPONSE, GUANOSINE TETRAPHOSPHATE (PPGPP), LYASE
3n7z:D (GLU33) to (ALA60) CRYSTAL STRUCTURE OF ACETYLTRANSFERASE FROM BACILLUS ANTHRACIS | PSI2, MCSG, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, TRANSFERASE
4by0:A (GLN425) to (ARG475) CRYSTAL STRUCTURE OF TRYPANOSOMA CRUZI CYP51 BOUND TO THE INHIBITOR (R)-N-(3-(1H-INDOL-3-YL)-1-OXO-1-(PYRIDIN-4- YLAMINO)PROPAN-2-YL)-3,3'-DIFLUORO-(1,1'-BIPHENYL)-4- CARBOXAMIDE | OXIDOREDUCTASE, STEROL 14-DEMETHYLASE, STEROL BIOSYNTHESIS, CHAGAS DISEASE
5fhs:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fhs:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fiu:A (TYR77) to (ALA121) BINDING AND STRUCTURAL STUDIES OF A 5,5-DIFLUOROMETHYL ADENOSINE NUCLEOSIDE WITH THE FLUORINASE ENZYME | TRANSFERASE, FLUORINASE, DIFLUOROMETHYL, ISOTHERMAL TITRATION CALORIMETRY,
5fiu:B (TYR77) to (ALA121) BINDING AND STRUCTURAL STUDIES OF A 5,5-DIFLUOROMETHYL ADENOSINE NUCLEOSIDE WITH THE FLUORINASE ENZYME | TRANSFERASE, FLUORINASE, DIFLUOROMETHYL, ISOTHERMAL TITRATION CALORIMETRY,
5fiu:C (TYR77) to (ALA121) BINDING AND STRUCTURAL STUDIES OF A 5,5-DIFLUOROMETHYL ADENOSINE NUCLEOSIDE WITH THE FLUORINASE ENZYME | TRANSFERASE, FLUORINASE, DIFLUOROMETHYL, ISOTHERMAL TITRATION CALORIMETRY,
3ncw:A (THR898) to (GLY920) CRYSTAL STRUCTURE OF EHEC O157:H7 INTIMIN | CELL MEMBRANE, CELL ADHESION, IMMUNOGLOBULIN-LIKE FOLD, C-TYPE AND LECTIN-LIKE FOLD
3ncw:D (THR898) to (PRO919) CRYSTAL STRUCTURE OF EHEC O157:H7 INTIMIN | CELL MEMBRANE, CELL ADHESION, IMMUNOGLOBULIN-LIKE FOLD, C-TYPE AND LECTIN-LIKE FOLD
3ncx:A (THR898) to (GLY920) CRYSTAL STRUCTURE OF EHEC O157:H7 INTIMIN MUTANT | INTIMIN TIR, CELL ADHESION
3ncx:B (THR898) to (GLY920) CRYSTAL STRUCTURE OF EHEC O157:H7 INTIMIN MUTANT | INTIMIN TIR, CELL ADHESION
4rft:M (THR137) to (GLN161) T=1 SUBVIRAL PARTICLE OF GROUPER NERVOUS NECROSIS VIRUS CAPSID PROTEIN DELETION MUTANT (DELTA 1-34 & 218-338) | VIRUS, SHELL DOMAIN
3ci7:D (PRO2) to (VAL34) CRYSTAL STRUCTURE OF A SIMPLIFIED BPTI CONTAINING 20 ALANINES | SEQUENCE SIMPLIFICATION, BOVINE PANCREATIC TRYPSIN INHIBITOR, STRUCTURE, HYDROLASE INHIBITOR
4rgr:A (ALA74) to (VAL103) CRYSTAL STRUCTURE OF PUTATIVE MARR FAMILY TRANSCRIPTIONAL REGULATOR HCAR FROM ACINETOBACTER SP. ADP | STRUCTURAL GENOMICS, PSI-BIOLOGY, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, WINGED HELIX-TURN-HELIX, TRANSCRIPTION
4rgu:B (ALA74) to (VAL103) CRYSTAL STRUCTURE OF PUTATIVE MARR FAMILY TRANSCRIPTIONAL REGULATOR HCAR FROM ACINETOBACTER SP. ADP COMPLEXED WITH FERULIC ACID | STRUCTURAL GENOMICS, PSI-BIOLOGY, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, WINGED HELIX-TURN-HELIX, TRANSCRIPTION
4rgx:A (ALA74) to (VAL103) CRYSTAL STRUCTURE OF PUTATIVE MARR FAMILY TRANSCRIPTIONAL REGULATOR HCAR FROM ACINETOBACTER SP. ADP COMPLEXED WITH 3,4-DIHYDROXY BEZOIC ACID | STRUCTURAL GENOMICS, PSI-BIOLOGY, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, WINGED HELIX-TURN-HELIX, TRANSCRIPTION
4c4a:A (SER187) to (VAL211) CRYSTAL STRUCTURE OF MOUSE PROTEIN ARGININE METHYLTRANSFERASE 7 IN COMPLEX WITH SAH | TRANSFERASE
5fmo:L (VAL104) to (THR126) CRYSTAL STRUCTURE AND PROTEOMICS ANALYSIS OF EMPTY VIRUS LIKE PARTICLES OF COWPEA MOSAIC VIRUS | VIRUS, CPMV, EVLPS
3cki:B (HIS7) to (VAL24) CRYSTAL STRUCTURE OF THE TACE-N-TIMP-3 COMPLEX | EXTRA-CELLULAR MATRIX, CATALYTIC ZINC, SA-SB LOOP, ALTERNATIVE SPLICING, CLEAVAGE ON PAIR OF BASIC RESIDUES, GLYCOPROTEIN, MEMBRANE, METAL-BINDING, METALLOPROTEASE, NOTCH SIGNALING PATHWAY, PHOSPHOPROTEIN, PROTEASE, SH3- BINDING, TRANSMEMBRANE, ZYMOGEN, DISEASE MUTATION, EXTRACELLULAR MATRIX, METALLOENZYME INHIBITOR, METALLOPROTEASE INHIBITOR, SECRETED, SENSORY TRANSDUCTION, VISION, HYDROLASE, HYDROLASE INHIBITOR
4rkj:B (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THROMBIN MUTANT S195T (FREE FORM) | TRYPSIN-LIKE PROTEASES, CATALYSIS, ALLOSTERIC REGULATION, HYDROLASE
4ccg:B (THR44) to (THR72) STRUCTURE OF AN E2-E3 COMPLEX | LIGASE
4ccl:B (SER36) to (HIS65) X-RAY STRUCTURE OF E. COLI YCFD | OXIDOREDUCTASE, 2OG AND IRON DEPENDENT OXYGENASE
3nrz:K (LEU361) to (THR382) CRYSTAL STRUCTURE OF BOVINE XANTHINE OXIDASE IN COMPLEX WITH HYPOXANTHINE | XANTHINE OXIDASE, HYPOXANTHINE, SUBSTRATE ORIENTATION, HYDROXYLASE, OXIDOREDUCTASE
3ns1:B (ASN362) to (THR382) CRYSTAL STRUCTURE OF BOVINE XANTHINE OXIDASE IN COMPLEX WITH 6- MERCAPTOPURINE | XANTHINE OXIDASE, HYPOXANTHINE, SUBSTRATE ORIENTATION, HYDROXYLASE, OXIDOREDUCTASE
3nsx:A (ASP536) to (GLU559) THE CRYSTAL STRUCTURE OF THE THE CRYSTAL STRUCTURE OF THE D420A MUTANT OF THE ALPHA-GLUCOSIDASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174 | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, ACARBOSE, ALPHA-GLUCOSE, STRUCTURAL COMPLEX, HYDROLASE
3nsx:B (ASP536) to (GLU559) THE CRYSTAL STRUCTURE OF THE THE CRYSTAL STRUCTURE OF THE D420A MUTANT OF THE ALPHA-GLUCOSIDASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174 | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, ACARBOSE, ALPHA-GLUCOSE, STRUCTURAL COMPLEX, HYDROLASE
3nuk:A (ASP536) to (GLU559) THE CRYSTAL STRUCTURE OF THE W169Y MUTANT OF ALPHA-GLUCOSIDASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174 | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, (BETA/ALPHA)8 BARREL, GLYCOSYLE HYDROLYSIS, HYDROLASE
3nuk:B (ASP536) to (GLU559) THE CRYSTAL STRUCTURE OF THE W169Y MUTANT OF ALPHA-GLUCOSIDASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174 | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, (BETA/ALPHA)8 BARREL, GLYCOSYLE HYDROLYSIS, HYDROLASE
3nvv:K (LEU361) to (THR382) CRYSTAL STRUCTURE OF BOVINE XANTHINE OXIDASE IN COMPLEX WITH ARSENITE | HYDROXYLASE, HOMODIMER, XANTHINE OXIDASE, ARSENITE, OXIDOREDUCTASE
3nvy:K (LEU361) to (THR382) CRYSTAL STRUCTURE OF BOVINE XANTHINE OXIDASE IN COMPLEX WITH QUERCETIN | HYDROXYLASE, HOMODIMER, XANTHINE OXIDASE, QUERCETIN, OXIDOREDUCTASE
3nvz:K (LEU361) to (THR382) CRYSTAL STRUCTURE OF BOVINE XANTHINE OXIDASE IN COMPLEX WITH INDOLE-3- ALDEHYDE | HYDROXYLASE, HOMODIMER, XANTHINE OXIDASE, INDOLE-3-ALDEHYDE, OXIDOREDUCTASE
4ch2:D (ASP442) to (ASN484) LOW-SALT CRYSTAL STRUCTURE OF A THROMBIN-GPIBALPHA PEPTIDE COMPLEX | HYDROLASE-PEPTIDE COMPLEX
3csk:A (GLN576) to (ASP615) STRUCTURE OF DPP III FROM SACCHAROMYCES CEREVISIAE | ZN-HYDROLASE, AMINODIPEPTIDASE, HEXXGH-MOTIF, AMINOPEPTIDASE, HYDROLASE, METAL-BINDING, METALLOPROTEASE, PROTEASE
4ch8:B (ASP442) to (ASN484) HIGH-SALT CRYSTAL STRUCTURE OF A THROMBIN-GPIBALPHA PEPTIDE COMPLEX | HYDROLASE-PEPTIDE COMPLEX, COMPLEX
4ch8:D (ASP442) to (ASN484) HIGH-SALT CRYSTAL STRUCTURE OF A THROMBIN-GPIBALPHA PEPTIDE COMPLEX | HYDROLASE-PEPTIDE COMPLEX, COMPLEX
4ch8:F (ASP442) to (ASN484) HIGH-SALT CRYSTAL STRUCTURE OF A THROMBIN-GPIBALPHA PEPTIDE COMPLEX | HYDROLASE-PEPTIDE COMPLEX, COMPLEX
4ch8:H (ASP442) to (ASN484) HIGH-SALT CRYSTAL STRUCTURE OF A THROMBIN-GPIBALPHA PEPTIDE COMPLEX | HYDROLASE-PEPTIDE COMPLEX, COMPLEX
3cuq:D (PRO70) to (TRP101) INTEGRATED STRUCTURAL AND FUNCTIONAL MODEL OF THE HUMAN ESCRT-II COMPLEX | ESCRT, SORTING, MBV, VPS, NUCLEUS, PROTEIN TRANSPORT, TRANSCRIPTION, TRANSCRIPTION REGULATION, TRANSPORT, ENDOSOME, LIPID-BINDING
3cuv:A (VAL422) to (MET441) TRACKING STRUCTURE ACTIVITY RELATIONSHIPS OF GLYCOGEN PHOSPHORYLASE INHIBITORS: SYNTHESIS, KINETIC AND CRYSTALLOGRAPHIC EVALUATION OF ANALOGUES OF N-(-D- GLUCOPYRANOSYL)-N'-OXAMIDES | GLYCOGEN PHOSPHORYLASE, STRUCTURE, CATALYTIC SITE, RATIONAL INHIBITOR DESIGN, ACETYLATION, ALLOSTERIC ENZYME, CARBOHYDRATE METABOLISM, GLYCOGEN METABOLISM, GLYCOSYLTRANSFERASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, PYRIDOXAL PHOSPHATE, TRANSFERASE
3nzw:T (PHE22) to (ILE54) 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
4ckn:B (ASP208) to (ASP256) STRUCTURE OF AN N-TERMINAL FRAGMENT OF LEISHMANIA SAS-6 CONTAINING PARTS OF ITS COILED COIL DOMAIN, F257E MUTANT | STRUCTURAL PROTEIN, BASAL BODY, CENTRIOLE, CARTWHEEL, TRYPANOSOMATIDS
3d0s:B (GLU189) to (SER214) CAMP RECEPTOR PROTEIN FROM M.TUBERCULOSIS, CAMP-FREE FORM | CAMP RECEPTOR PROTEIN (CRP), DIMER, INACTIVE(APO, UNLIGANDED) FORM, ALLOSTERY, DNA BINDING, CYCLIC AMP, TRANSCRIPTION REGULATION, CATABOLITE GENE ACTIVATOR PROTEIN, DNA-BINDING, NUCLEOTIDE-BINDING, TRANSCRIPTION
3d29:F (PHE22) to (ILE54) 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:T (PHE22) to (ILE54) 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
4cqj:C (TYR77) to (ALA121) FLUORINASE SUBSTRATE FLEXIBILITY ENABLES LAST STEP AQUEOUS AND AMBIENT 18F FLUORINATION OF A RGD PEPTIDE FOR POSITRON EMISSION TOMOGRAPHY | TRANSFERASE
3d3i:B (LYS511) to (LEU546) CRYSTAL STRUCTURAL OF ESCHERICHIA COLI K12 YGJK, A GLUCOSIDASE BELONGING TO GLYCOSIDE HYDROLASE FAMILY 63 | GH63, PROCESSING ALPHA-GLUCOSIDASE, ALPHA/ALPHA BARREL, HYDROLASE
4cr3:C (GLN21) to (GLU49) DEEP CLASSIFICATION OF A LARGE CRYO-EM DATASET DEFINES THE CONFORMATIONAL LANDSCAPE OF THE 26S PROTEASOME | HYDROLASE, AAA-ATPASE, ATP-ANALOG, CLASSIFICATION
4cr3:D (ILE17) to (GLU47) DEEP CLASSIFICATION OF A LARGE CRYO-EM DATASET DEFINES THE CONFORMATIONAL LANDSCAPE OF THE 26S PROTEASOME | HYDROLASE, AAA-ATPASE, ATP-ANALOG, CLASSIFICATION
4cr3:F (GLN21) to (LEU49) DEEP CLASSIFICATION OF A LARGE CRYO-EM DATASET DEFINES THE CONFORMATIONAL LANDSCAPE OF THE 26S PROTEASOME | HYDROLASE, AAA-ATPASE, ATP-ANALOG, CLASSIFICATION
4cr3:G (ASN20) to (THR54) DEEP CLASSIFICATION OF A LARGE CRYO-EM DATASET DEFINES THE CONFORMATIONAL LANDSCAPE OF THE 26S PROTEASOME | HYDROLASE, AAA-ATPASE, ATP-ANALOG, CLASSIFICATION
4cr4:D (ILE17) to (LEU52) DEEP CLASSIFICATION OF A LARGE CRYO-EM DATASET DEFINES THE CONFORMATIONAL LANDSCAPE OF THE 26S PROTEASOME | HYDROLASE, AAA-ATPASE, ATP-ANALOG, CLASSIFICATION
4cr4:F (PHE20) to (ASP54) DEEP CLASSIFICATION OF A LARGE CRYO-EM DATASET DEFINES THE CONFORMATIONAL LANDSCAPE OF THE 26S PROTEASOME | HYDROLASE, AAA-ATPASE, ATP-ANALOG, CLASSIFICATION
4cr4:G (PHE21) to (THR54) DEEP CLASSIFICATION OF A LARGE CRYO-EM DATASET DEFINES THE CONFORMATIONAL LANDSCAPE OF THE 26S PROTEASOME | HYDROLASE, AAA-ATPASE, ATP-ANALOG, CLASSIFICATION
4cug:A (THR40) to (GLY72) RHODOTHERMUS MARINUS YCFD-LIKE RIBOSOMAL PROTEIN L16 ARGINYL HYDROXYLASE IN COMPLEX SUBSTRATE FRAGMENT | TRANSLATION, 2-OXOGLUTARATE AND IRON DEPENDENT OXYGENASE, DOUBLE STRANDED BETA HELIX FOLD
4tm3:C (THR103) to (PRO133) KUTZNERIA SP. 744 ORNITHINE N-HYDROXYLASE, KTZI-FADOX-BR | HYDROXYLASE, FLAVIN, ORNITHINE, MONOOXYGENASE
4tm3:D (ARG104) to (ALA130) KUTZNERIA SP. 744 ORNITHINE N-HYDROXYLASE, KTZI-FADOX-BR | HYDROXYLASE, FLAVIN, ORNITHINE, MONOOXYGENASE
3da9:B (ASP158) to (ASN194) CRYSTAL STRUCTURE OF THROMBIN IN COMPLEX WITH INHIBITOR | THROMBIN, INHIBITOR COMPLEX, ACUTE PHASE, BLOOD COAGULATION, CALCIUM, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PHARMACEUTICAL, POLYMORPHISM, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN
3oev:T (ASN21) to (THR55) STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 25 | 20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4cyi:A (ILE580) to (VAL610) CHAETOMIUM THERMOPHILUM PAN3 | TRANSFERASE
4cyi:B (ILE580) to (VAL610) CHAETOMIUM THERMOPHILUM PAN3 | TRANSFERASE
4cyi:C (ILE580) to (VAL610) CHAETOMIUM THERMOPHILUM PAN3 | TRANSFERASE
4cyi:D (ILE580) to (VAL610) CHAETOMIUM THERMOPHILUM PAN3 | TRANSFERASE
4cyi:F (ILE580) to (VAL610) CHAETOMIUM THERMOPHILUM PAN3 | TRANSFERASE
3dhk:H (ASP125) to (ASN159) BISPHENYLIC THROMBIN INHIBITORS | BLOOD CLOTTING/HYDROLASE INHIBITOR, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN, BLOOD CLOTTING-HYDROLASE INHIBITOR COMPLEX
4ttx:F (PRO103) to (LYS138) N-TERMINAL DOMAIN OF C. REINHARDTII SAS-6 HOMOLOG BLD12P VARIANT G94C K146C (NN19) | HOMODIMER, STABILIZATION, MUTATION, CENTRIOLE SAS-6, CARTWHEEL, STRUCTURAL PROTEIN, BETA-SANDWICH, ALPHA-BETA PROTEIN, CENTRIOLAR
3drh:A (PRO516) to (ASP558) CRYSTAL STRUCTURE OF LACTOCOCCAL OPPA CO-CRYSTALLIZED WITH LEU- ENKEPHALIN IN AN OPEN CONFORMATION | OLIGO-PEPTIDE BINDING, VOLUMINOUS BINDING CAVITY, VENUS FLY-TRAP, PEPTIDE BINDING PROTEIN
3drk:A (PRO516) to (ASP558) CRYSTAL STRUCTURE OF LACTOCOCCAL OPPA CO-CRYSTALLIZED WITH NEUROPEPTIDE S IN AN OPEN CONFORMATION | OLIGO-PEPTIDE BINDING, VOLUMINOUS BINDING CAVITY, VENUS FLY-TRAP, PEPTIDE BINDING PROTEIN
3dri:A (PRO516) to (ASP558) CRYSTAL STRUCTURE OF LACTOCOCCAL OPPA CO-CRYSTALLIZED WITH AN OCTAMER PEPTIDE IN AN OPEN CONFORMATION | OLIGO-PEPTIDE BINDING, VOLUMINOUS BINDING CAVITY, VENUS FLY-TRAP, PEPTIDE BINDING PROTEIN
4u2v:D (SER2) to (GLY31) BAK BH3-IN-GROOVE DIMER (GFP) | APOPTOSIS, BAK, BCL-2
3owc:A (HIS53) to (LEU84) CRYSTAL STRUCTURE OF GNAT SUPERFAMILY PROTEIN PA2578 FROM PSEUDOMONAS AERUGINOSA | STRUCTURAL GENOMICS, PSI-BIOLOGY, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, ACYL-COA N- ACYLTRANSFERASE (NAT), GNAT, ACETYLTRANSFERASE, TRANSFERASE
4dg4:F (PRO2) to (PHE33) HUMAN MESOTRYPSIN-S39Y COMPLEXED WITH BOVINE PANCREATIC TRYPSIN INHIBITOR (BPTI) | HUMAN MESOTRYPSIN, CANONICAL INHIBITOR, BPTI, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4dii:H (ASP125) to (ASN159) X-RAY STRUCTURE OF THE COMPLEX BETWEEN HUMAN ALPHA THROMBIN AND THROMBIN BINDING APTAMER IN THE PRESENCE OF POTASSIUM IONS | PROTEIN-DNA COMPLEX, SERINE PROTEASE, BLOOD COAGULATION, APTAMER, HYDROLASE-HYDROLASE INHIBITOR-DNA COMPLEX, SERINE PROTEASE FOLD, DNA APTAMER, BLOOD, G-QUADRUPLEX
3p17:H (ASP125) to (ASN159) THROMBIN INHIBITION BY PYRIDIN DERIVATIVES | SERINE PROTEASE, KRINGLE, DISULFIDE BONDS, BLOOD COAGULATION, BLOOD CLOTTING, CONVERTION OF FIBRINOGEN TO FIBRIN, CLEAVAGE ON PAIRS OF BASIC RESIDUES, THROMBIN INHIBITOR, GLYCOSYLATION, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3p2u:A (HIS225) to (GLY250) CRYSTAL STRUCTURE OF PHNP IN COMPLEX WITH ORTHOVANADATE | PHOSPHODIESTERASE, HYDROLASE
3p6z:B (ASP485) to (ASN527) STRUCTURAL BASIS OF THROMBIN MEDIATED FACTOR V ACTIVATION: ESSENTIAL ROLE OF THE HIRUDIN-LIKE SEQUENCE GLU666-GLU672 FOR PROCESSING AT THE HEAVY CHAIN-B DOMAIN JUNCTION | TRYPSIN-LIKE SERINE PROTEINASE, BLOOD COAGULATION, N-GLYCOSYLATION, BLOOD PLASMA, PPACK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3p6z:H (ASP485) to (ASN527) STRUCTURAL BASIS OF THROMBIN MEDIATED FACTOR V ACTIVATION: ESSENTIAL ROLE OF THE HIRUDIN-LIKE SEQUENCE GLU666-GLU672 FOR PROCESSING AT THE HEAVY CHAIN-B DOMAIN JUNCTION | TRYPSIN-LIKE SERINE PROTEINASE, BLOOD COAGULATION, N-GLYCOSYLATION, BLOOD PLASMA, PPACK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5ht0:B (PRO160) to (GLU201) CRYSTAL STRUCTURE OF AN ANTIBIOTIC_NAT FAMILY AMINOGLYCOSIDE ACETYLTRANSFERASE HMB0038 FROM AN UNCULTURED SOIL METAGENOMIC SAMPLE IN COMPLEX WITH COENZYME A | ANTIBIOTIC_NAT FAMILY, ACETYLTRANSFERASE, AMINOGLYCOSIDE, ANTIBIOTIC RESISTANCE, METAGENOME, SOIL, COENZYME A, CSGID, TRANSFERASE, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES
3e3n:D (ASP421) to (MET441) THE GLYCOGEN PHOSPHORYLASE B R STATE- AMP COMPLEX | GLYCOGENOLYSIS, INHIBITION, TYPE 2 DIABETES, ALLOSTERIC ENZYME, CARBOHYDRATE METABOLISM, GLYCOGEN METABOLISM, GLYCOSYLTRANSFERASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, PYRIDOXAL PHOSPHATE, TRANSFERASE
3e3n:H (VAL422) to (MET441) THE GLYCOGEN PHOSPHORYLASE B R STATE- AMP COMPLEX | GLYCOGENOLYSIS, INHIBITION, TYPE 2 DIABETES, ALLOSTERIC ENZYME, CARBOHYDRATE METABOLISM, GLYCOGEN METABOLISM, GLYCOSYLTRANSFERASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, PYRIDOXAL PHOSPHATE, TRANSFERASE
3pay:D (PRO288) to (ILE318) 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:F (PHE22) to (THR55) 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:T (PHE22) to (THR55) 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
3e4f:A (VAL182) to (VAL213) CRYSTAL STRUCTURE OF BA2930- A PUTATIVE AMINOGLYCOSIDE N3- ACETYLTRANSFERASE FROM BACILLUS ANTHRACIS | N3-ACETYLTRANSFERASE, BACILLUS ANTHRACIS, ANTRAX, TRANSFERASE, STRUCTURAL GENOMICS, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID
4dsy:B (THR186) to (ALA243) CRYSTAL STRUCTURE OF RED KIDNEY BEAN PURPLE ACID PHOSPHATASE IN COMPLEX WITH MAYBRIDGE FRAGMENT CC24201 | PHOSPHATASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4dsy:C (THR186) to (ALA243) CRYSTAL STRUCTURE OF RED KIDNEY BEAN PURPLE ACID PHOSPHATASE IN COMPLEX WITH MAYBRIDGE FRAGMENT CC24201 | PHOSPHATASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4dsy:D (GLU187) to (ALA243) CRYSTAL STRUCTURE OF RED KIDNEY BEAN PURPLE ACID PHOSPHATASE IN COMPLEX WITH MAYBRIDGE FRAGMENT CC24201 | PHOSPHATASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4dt2:B (GLU187) to (ALA243) CRYSTAL STRUCTURE OF RED KIDNEY BEAN PURPLE ACID PHOSPHATASE IN COMPLEX WITH MAYBRIDGE FRAGMENT CC27209 | PHOSPHATASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4dt2:C (THR186) to (ALA243) CRYSTAL STRUCTURE OF RED KIDNEY BEAN PURPLE ACID PHOSPHATASE IN COMPLEX WITH MAYBRIDGE FRAGMENT CC27209 | PHOSPHATASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4dt2:D (THR186) to (ALA243) CRYSTAL STRUCTURE OF RED KIDNEY BEAN PURPLE ACID PHOSPHATASE IN COMPLEX WITH MAYBRIDGE FRAGMENT CC27209 | PHOSPHATASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4dt7:B (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THROMBIN BOUND TO THE ACTIVATION DOMAIN QEDQVDPRLIDGKMTRRGDS OF PROTEIN C | SERINE PROTEASE, HYDROLASE
4dt7:D (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THROMBIN BOUND TO THE ACTIVATION DOMAIN QEDQVDPRLIDGKMTRRGDS OF PROTEIN C | SERINE PROTEASE, HYDROLASE
4udw:H (ASP125) to (ASN159) THROMBIN IN COMPLEX WITH 1-(2R)-2-AMINO-3-PHENYL-PROPANOYL- N-(2,5DICHLOROPHENYL)METHYLPYRROLIDINE-2-CARBOXAMIDE | HYDROLASE, HYDROLASE INHIBITOR COMPLEX, SERINE PROTEASE, BLOOD COAGULATION, BLOOD CLOTTING, CONVERTION OF FIBRINOGEN TO FIBRIN, BLOOD CLOTTING INHIBITOR, THROMBIN INHIBITOR, FRAGMENT, GLYCOSYLATION, BLOOD
4ufe:H (ASP125) to (ASN159) THROMBIN IN COMPLEX WITH (2R)-2-(BENZYLSULFONYLAMINO)-N-(2-( (4-CARBAMIMIDOYLPHENYL)METHYLAMINO)-2-OXO-BUTYL)-3-PHENYL- PROPANAMIDE | HYDROLASE, HYDROLASE INHIBITOR COMPLEX, SERINE PROTEASE, BLOOD COAGULATION, BLOOD CLOTTING, CONVERTION OF FIBRINOGEN TO FIBRIN, BLOOD CLOTTING INHIBITOR, THROMBIN INHIBITOR, PREORGANIZATION, GLYCOSYLATION, BLOOD
4uff:H (ASP125) to (ASN159) THROMBIN IN COMPLEX WITH (2R)-2-(BENZYLSULFONYLAMINO)-N-(2-( (4-CARBAMIMIDOYLPHENYL)METHYLAMINO)-2-OXO-ETHYL)-N-METHYL- 3-PHENYL-PROPANAMIDE | HYDROLASE, HYDROLASE INHIBITOR COMPLEX, SERINE PROTEASE, BLOOD COAGULATION, BLOOD CLOTTING, CONVERTION OF FIBRINOGEN TO FIBRIN, BLOOD CLOTTING INHIBITOR, THROMBIN INHIBITOR, PREORGANIZATION, GLYCOSYLATION, BLOOD
4ufg:H (ASP125) to (ASN159) THROMBIN IN COMPLEX WITH (2R)-2-(BENZYLSULFONYLAMINO)-N-(( 1S)-2-((4-CARBAMIMIDOYLPHENYL)METHYLAMINO)-1-METHYL-2-OXO- ETHYL)-N-METHYL-3-PHENYL-PROPANAMIDE ETHANE | HYDROLASE, HYDROLASE INHIBITOR COMPLEX, SERINE PROTEASE, BLOOD COAGULATION, BLOOD CLOTTING, CONVERTION OF FIBRINOGEN TO FIBRIN, BLOOD CLOTTING INHIBITOR, THROMBIN INHIBITOR, PREORGANIZATION, GLYCOSYLATION, BLOOD
3pfl:A (ARG712) to (ARG738) CRYSTAL STRUCTURE OF PFL FROM E.COLI IN COMPLEX WITH SUBSTRATE ANALOGUE OXAMATE | GLYCYL RADICAL ENZYME, TRANSFERASE, GLUCOSE METABOLISM, LYASE/TRANSFERASE COMPLEX
3pfl:B (ARG712) to (ARG738) CRYSTAL STRUCTURE OF PFL FROM E.COLI IN COMPLEX WITH SUBSTRATE ANALOGUE OXAMATE | GLYCYL RADICAL ENZYME, TRANSFERASE, GLUCOSE METABOLISM, LYASE/TRANSFERASE COMPLEX
3pft:B (THR9) to (SER39) CRYSTAL STRUCTURE OF UNTAGGED C54A MUTANT FLAVIN REDUCTASE (DSZD) IN COMPLEX WITH FMN FROM MYCOBACTERIUM GOODII | FLAVIN REDUCTASE, DESULFURIZATION, OXIDOREDUCTASE
3pha:A (ASP536) to (VAL557) THE CRYSTAL STRUCTURE OF THE W169Y MUTANT OF ALPHA-GLUCOSIDASE (GH31 FAMILY) FROM RUMINOCOCCUS OBEUM ATCC 29174 IN COMPLEX WITH ACARBOSE | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, STRUCTURALCOMPLEX, MCSG, MIDWEST CENTER FOR STRUCTURAL GENOMICS, HYDROLASE, (BETA/ALPHA)8-BARREL, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3pha:B (ASP536) to (GLU559) THE CRYSTAL STRUCTURE OF THE W169Y MUTANT OF ALPHA-GLUCOSIDASE (GH31 FAMILY) FROM RUMINOCOCCUS OBEUM ATCC 29174 IN COMPLEX WITH ACARBOSE | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, STRUCTURALCOMPLEX, MCSG, MIDWEST CENTER FOR STRUCTURAL GENOMICS, HYDROLASE, (BETA/ALPHA)8-BARREL, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3pha:C (ASP536) to (GLU559) THE CRYSTAL STRUCTURE OF THE W169Y MUTANT OF ALPHA-GLUCOSIDASE (GH31 FAMILY) FROM RUMINOCOCCUS OBEUM ATCC 29174 IN COMPLEX WITH ACARBOSE | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, STRUCTURALCOMPLEX, MCSG, MIDWEST CENTER FOR STRUCTURAL GENOMICS, HYDROLASE, (BETA/ALPHA)8-BARREL, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3pha:D (ASP536) to (GLU559) THE CRYSTAL STRUCTURE OF THE W169Y MUTANT OF ALPHA-GLUCOSIDASE (GH31 FAMILY) FROM RUMINOCOCCUS OBEUM ATCC 29174 IN COMPLEX WITH ACARBOSE | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, STRUCTURALCOMPLEX, MCSG, MIDWEST CENTER FOR STRUCTURAL GENOMICS, HYDROLASE, (BETA/ALPHA)8-BARREL, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5i2g:B (ALA796) to (LEU821) 1,2-PROPANEDIOL DEHYDRATION IN ROSEBURIA INULINIVORANS; STRUCTURAL BASIS FOR SUBSTRATE AND ENANTIOMER SELECTIVITY | DIOL DEHYDRATASE, GLYCYL RADICAL ENZYMES, ENZYME STRUCTURE, LYASE
5i31:A (TYR509) to (PHE565) CRYSTAL STRUCTURE OF HUMAN NIEMANN-PICK C1 PROTEIN | MEMBRANE PROTEIN
3pmh:B (ASP125) to (ASN159) MECHANISM OF SULFOTYROSINE-MEDIATED GLYCOPROTEIN IB INTERACTION WITH TWO DISTINCT ALPHA-THROMBIN SITES | SULFATED TYROSINE RESIDUES, LEUCINE RICH REPEATS, PROTEASE PLATELET RECEPTOR OF THROMBIN, THROMBIN BINDING, PLATELET SURFACE, BLOOD CLOTING, HYDROLASE-INHIBITOR COMPLEX
4e05:H (ASP442) to (ASN484) ANOPHELIN FROM THE MALARIA VECTOR INHIBITS THROMBIN THROUGH A NOVEL REVERSE-BINDING MECHANISM | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4e06:H (ASP442) to (ASN484) ANOPHELIN FROM THE MALARIA VECTOR INHIBITS THROMBIN THROUGH A NOVEL REVERSE-BINDING MECHANISM | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3poc:A (ASP536) to (GLU559) THE CRYSTAL STRUCTURE OF THE D307A MUTANT OF ALPHA-GLUCOSIDASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174 IN COMPLEX WITH ACARBOSE | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, MULTI-DOMAIN, ALPHA- GLUCOSIDASE, CYTOPLASMIC, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3poc:B (ASP536) to (GLU559) THE CRYSTAL STRUCTURE OF THE D307A MUTANT OF ALPHA-GLUCOSIDASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174 IN COMPLEX WITH ACARBOSE | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, MULTI-DOMAIN, ALPHA- GLUCOSIDASE, CYTOPLASMIC, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4e7r:H (ASP125) to (ASN159) THROMBIN IN COMPLEX WITH 3-AMIDINOPHENYLALANINE INHIBITOR | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, SERINE PROTEASE, KRINGLE, HYDROLASE, BLOOD COAGULATION, BLOOD CLOTTING, CONVERTION OF FIBRINOGEN TO FIBRIN, BLOOD CLOTTING INHIBITOR, THROMBIN INHIBITOR, GLYCOSYLATION, BLOOD
4uun:A (ALA242) to (PRO288) TRICHOMONAS VAGINALIS LACTATE DEHYDROGENASE IN COMPLEX WITH NADH | OXIDOREDUCTASE
4eck:A (VAL557) to (GLY597) CRYSTAL STRUCTURE OF THE TOXOPLASMA GONDII TS-DHFR | BIFUNCTIONAL, TRANSFERASE, OXIDOREDUCTASE
5iko:A (ASP421) to (MET441) CRYSTAL STRUCTURE OF HUMAN BRAIN GLYCOGEN PHOSPHORYLASE | GP, GLYCOGEN PHOSPHORYLASE, GLYCOGEN METABOLISM, GLYCOGEN DISEASE, GLYCOSYLTRANSFERASE, NUCLEOTIDE-BINDING, ALLOSTERIC ENZYME, TRANSFERASE
3pwt:A (THR496) to (ALA519) CRYSTAL STRUCTURE OF MUTANT E.COLI TOPOISOMERASE IA | TOPOISOMERASE, DNA RELAXATION, ISOMERASE
3q16:C (VAL334) to (GLY382) LINKAGE BETWEEN THE BACTERIAL ACID STRESS AND STRINGENT RESPONSES: THE STRUCTURE OF THE INDUCIBLE LYSINE DECARBOXYLASE | ASPARTATE AMINOTRANFERASE, CHEY, PLP, PYRIDOXAL-5-PHOSPHATE, INDUCIBLE LYSINE DECARBOXYLASE, LYASE
3q24:A (LEU228) to (ILE275) X-RAY CRYSTAL STRUCTURE OF THE N4 MINI-VRNAP AND P2_7A PROMOTER TRANSCRIPTION INITIATION COMPLEX WITH PPPGPG AND PYROPHOSPHATE: PRODUCT COMPLEX | PROTEIN-DNA COMPLEX, TWO-METAL CATALYSIS, DE NOVO TRANSCRIPTION INITIATION, NUCLEOTIDYLTRANSFERASE, INITIATION COMPLEX, DNA-HAIRPIN, VIRION RNA POLYMERASE, TRANSFERASE-DNA-RNA COMPLEX
3q24:B (LEU228) to (ILE275) X-RAY CRYSTAL STRUCTURE OF THE N4 MINI-VRNAP AND P2_7A PROMOTER TRANSCRIPTION INITIATION COMPLEX WITH PPPGPG AND PYROPHOSPHATE: PRODUCT COMPLEX | PROTEIN-DNA COMPLEX, TWO-METAL CATALYSIS, DE NOVO TRANSCRIPTION INITIATION, NUCLEOTIDYLTRANSFERASE, INITIATION COMPLEX, DNA-HAIRPIN, VIRION RNA POLYMERASE, TRANSFERASE-DNA-RNA COMPLEX
5ire:A (ASP155) to (THR179) THE CRYO-EM STRUCTURE OF ZIKA VIRUS | ZIKA VIRUS, VIRUS
5ire:E (ASP155) to (THR179) THE CRYO-EM STRUCTURE OF ZIKA VIRUS | ZIKA VIRUS, VIRUS
5irg:A (ASN59) to (LEU92) REVERSE TRANSCRIPTASE DOMAIN OF GROUP II INTRON MATURASE FROM ROSEBURIA INTESTINALIS IN P212121 SPACE GROUP | GROUP II INTRON, MATURASE, REVERSE TRANSCRIPTASE, RNA BINDING PROTEIN
5ix1:A (THR73) to (GLY98) CRYSTAL STRUCTURE OF MOUSE MORC3 ATPASE-CW CASSETTE IN COMPLEX WITH AMPPNP AND H3K4ME3 PEPTIDE | MORC3, ATPASE, CW DOMAIN, H3K4ME3, TRANSCRIPTION
5ix1:B (THR73) to (GLY98) CRYSTAL STRUCTURE OF MOUSE MORC3 ATPASE-CW CASSETTE IN COMPLEX WITH AMPPNP AND H3K4ME3 PEPTIDE | MORC3, ATPASE, CW DOMAIN, H3K4ME3, TRANSCRIPTION
5ix2:A (THR73) to (GLY98) CRYSTAL STRUCTURE OF MOUSE MORC3 ATPASE-CW CASSETTE IN COMPLEX WITH AMPPNP AND UNMODIFIED H3 PEPTIDE | MORC3, ATPASE, CW DOMAIN, H3, TRANSCRIPTION
5ix2:B (THR73) to (GLY98) CRYSTAL STRUCTURE OF MOUSE MORC3 ATPASE-CW CASSETTE IN COMPLEX WITH AMPPNP AND UNMODIFIED H3 PEPTIDE | MORC3, ATPASE, CW DOMAIN, H3, TRANSCRIPTION
4ex4:A (ASP281) to (THR312) THE STRUCTURE OF GLCB FROM MYCOBACTERIUM LEPRAE | SSGCID, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, MALATE SYNTHASE, MYCOBACTERIUM LEPRAE, NIAID, NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES, SYNTHASE, TRANSFERASE
4f4q:A (THR129) to (PRO170) CRYSTAL STRUCTURE OF M. SMEGMATIS DPRE1 IN COMPLEX WITH FAD AND COVALENTLY BOUND BTZ043 | FAD DOMAIN, OXIDASE, BTZ043 COVALENTLY BOUND TO CYS394, OXIDOREDUCTASE
4uze:B (VAL176) to (HIS214) R66A MUTANT OF FAD SYNTHETASE FROM CORYNEBACTERIUM AMMONIAGENES | TRANSFERASE, RIBOFLAVIN KINASE, NUCLEOTIDE-BINDING, ATP-BINDING, MULTIFUNCTIONAL ENZYME, NUCLEOTIDYLTRANSFERASE
4feh:A (THR122) to (PRO163) MYCOBACTERIUM TUBERCULOSIS DPRE1 - HEXAGONAL CRYSTAL FORM | ALPHA+BETA, OXIDOREDUCTASE, DECAPRENYLPHOSPHORYL-BETA-D-RIBOSE
3qtv:H (ASP125) to (ASN159) THROMBIN INHIBITION BY PYRIDIN DERIVATIVES | SERINE PROTEASE, KRINGLE, HYDROLASE, BLOOD COAGULATION, BLOOD CLOTTING, CONVERTION OF FIBRINOGEN TO FIBRIN, CLEAVAGE ON PAIRS OF BASIC RESIDUES, BLOOD CLOTTING INHIBITOR, THROMBIN INHIBITOR, GLYCOSYLATION, BLOOD, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3qz2:A (ALA608) to (VAL631) THE STRUCTURE OF CYSTEINE-FREE HUMAN INSULIN DEGRADING ENZYME | INSULIN DEGRADING ENZYME, HYDROLASE
3r89:A (ILE3) to (ILE25) CRYSTAL STRUCTURE OF OROTIDINE 5-PHOSPHATE DECARBOXYLASE FROM ANAEROCOCCUS PREVOTII DSM 20548 | PSI-BIOLOGY, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, OROTIDINE 5-PHOSPHATE DECARBOXYLASE, LYASE
5jdu:B (ASP125) to (ASN159) CRYSTAL STRUCTURE FOR HUMAN THROMBIN MUTANT D189A | SERINE PROTEASE, COAGULATION, CONFORMATIONAL EQUILIBRIUM, HYDROLASE
5jdu:D (ASP125) to (ASN159) CRYSTAL STRUCTURE FOR HUMAN THROMBIN MUTANT D189A | SERINE PROTEASE, COAGULATION, CONFORMATIONAL EQUILIBRIUM, HYDROLASE
3rbf:B (ALA273) to (LYS317) CRYSTAL STRUCTURE OF HUMAN AROMATIC L-AMINO ACID DECARBOXYLASE (AADC) IN THE APO FORM | APO ENZYME, APO FORM, OPEN CONFORMATION, OPEN DIMER, EXPOSED, CONFORMATIONAL CHANGE, PARKINSON, AADC DEFICIENCY, DDC, DECARBOXYLASE, PLP BINDING, LYASE
3rbl:A (ALA272) to (LYS317) CRYSTAL STRUCTURE OF HUMAN AROMATIC L-AMINO ACID DECARBOXYLASE (AADC) IN THE APO FORM | APO ENZYME, APO FORM, OPEN CONFORMATION, OPEN DIMER, EXPOSED, CONFORMATIONAL CHANGE, PARKINSON, AADC DEFICIENCY, DDC,, DECARBOXYLASE, PLP, L-DOPA, LYASE
3rbl:B (ALA272) to (LYS317) CRYSTAL STRUCTURE OF HUMAN AROMATIC L-AMINO ACID DECARBOXYLASE (AADC) IN THE APO FORM | APO ENZYME, APO FORM, OPEN CONFORMATION, OPEN DIMER, EXPOSED, CONFORMATIONAL CHANGE, PARKINSON, AADC DEFICIENCY, DDC,, DECARBOXYLASE, PLP, L-DOPA, LYASE
3rch:B (GLY276) to (LYS317) CRYSTAL STRUCTURE OF HUMAN AROMATIC L-AMINO ACID DECARBOXYLASE (AADC) IN THE OPEN CONFORMATION WITH LLP AND PLP BOUND TO CHAIN-A AND CHAIN- B RESPECTIVELY | APO ENZYME, APO FORM, OPEN CONFORMATION, OPEN DIMER, EXPOSED, CONFORMATIONAL CHANGE, PARKINSON, AADC DEFICIENCY, DDC, LLP, PLP, DECARBOXYLASE, L-DOPA, INTERNAL ALDIMINE, SHIFF BASE, LYASE
5jhr:F (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH THE PEPTIDIC EPOXYKETONE INHIBITOR 27 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5jhr:T (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH THE PEPTIDIC EPOXYKETONE INHIBITOR 27 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5jhs:F (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH THE PEPTIDIC EPOXYKETONE INHIBITOR 15 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5jhs:T (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH THE PEPTIDIC EPOXYKETONE INHIBITOR 15 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5jm8:D (ASP11) to (ILE40) THE STRUCTURE OF ATP-BOUND AEROBACTIN SYNTHETASE IUCA FROM A HYPERVIRULENT PATHOTYPE OF KLEBSIELLA PNEUMONIAE | AEROBACTIN NIS SYNTHETASE, LIGASE
4fsx:A (GLU146) to (LEU188) CRYSTAL STRUCTURE OF SE-SUBSTITUTED ZEA MAYS ZMET2 IN COMPLEX WITH SAH | CHROMODOMAIN, BAH DOMAIN, DNA METHYLTRANSFERASE DOMAIN, H3K9ME2 BINDING, TRANSFERASE
4ft4:B (ALA143) to (LEU188) CRYSTAL STRUCTURE OF ZEA MAYS ZMET2 IN COMPLEX H3(1-32)K9ME2 PEPTIDE AND SAH | CHROMODOMAIN, BAH DOMAIN, DNA METHYLTRANSFERASE DOMAIN, H3K9ME2 BINDING, METHYLATION, TRANSFERASE
4ft4:A (ALA143) to (LEU188) CRYSTAL STRUCTURE OF ZEA MAYS ZMET2 IN COMPLEX H3(1-32)K9ME2 PEPTIDE AND SAH | CHROMODOMAIN, BAH DOMAIN, DNA METHYLTRANSFERASE DOMAIN, H3K9ME2 BINDING, METHYLATION, TRANSFERASE
4g3t:A (THR129) to (PRO170) MYCOBACTERIUM SMEGMATIS DPRE1 - HEXAGONAL CRYSTAL FORM | VAO SUPERFAMILY, OXIDOREDUCTASE
4g3u:A (THR129) to (PRO170) MYCOBACTERIUM SMEGMATIS DPRE1 - MONOCLINIC CRYSTAL FORM | VAO SUPERFAMILY, OXIDOREDUCTASE
4g3u:B (THR129) to (PRO170) MYCOBACTERIUM SMEGMATIS DPRE1 - MONOCLINIC CRYSTAL FORM | VAO SUPERFAMILY, OXIDOREDUCTASE
4g4s:G (PHE22) to (VAL50) STRUCTURE OF PROTEASOME-PBA1-PBA2 COMPLEX | ALPHA BETA, NTN-HYDROLASE, PEPTIDE BINDING, HYDROLASE-CHAPERONE COMPLEX
5k1b:B (GLY463) to (LEU529) CRYSTAL STRUCTURE OF THE UAF1/USP12 COMPLEX IN F222 SPACE GROUP | WD40 DOMAIN, SUMO-LIKE DOMAIN, UBIQUITIN-SPECIFIC PROTEASE 12, USP12, USP1-ASSOCIATED FACTOR 1, DEUBIQUITINATING ENZYME, DUB, PROTEIN BINDING-HYDROLASE COMPLEX
5k1r:A (GLY237) to (ARG285) STRUCTURE OF BURKHOLDERIA PSEUDOMALLEI K96243 SPHINGOSINE-1-PHOSPHATE LYASE BPSS2021 | SPHINGOSINE-1-PHOSPHATE SPHINGOSINE-1-PHOSPHATE LYASE BURKHOLDERIA PSEUDOMALLEI PLP, LYASE
5k1r:B (GLY237) to (ARG285) STRUCTURE OF BURKHOLDERIA PSEUDOMALLEI K96243 SPHINGOSINE-1-PHOSPHATE LYASE BPSS2021 | SPHINGOSINE-1-PHOSPHATE SPHINGOSINE-1-PHOSPHATE LYASE BURKHOLDERIA PSEUDOMALLEI PLP, LYASE
5k2x:A (ASP216) to (ASP241) CRYSTAL STRUCTURE OF M. TUBERCULOSIS USPC (TETRAGONAL CRYSTAL FORM) | MYCOBACTERIUM TUBERCULOSIS, ABC TRANSPORTER, SOLUTE BINDING PROTEIN, TRANSPORT PROTEIN
5k2y:A (ASP216) to (ASP241) CRYSTAL STRUCTURE OF M. TUBERCULOSIS USPC (MONOCLINIC CRYSTAL FORM) | MYCOBACTERIUM TUBERCULOSIS, ABC TRANSPORTER, SOLUTE BINDING PROTEIN, TRANSPORT PROTEIN
5k81:E (ASP13) to (GLY56) CRYSTAL STRUCTURE OF A PRIMATE APOBEC3G N-TERMINAL DOMAIN | APOBEC3G, VIF, HIV, APOBEC, HYDROLASE
5k82:B (ASP13) to (LYS57) CRYSTAL STRUCTURE OF A PRIMATE APOBEC3G N-TERMINAL DOMAIN | APOBEC3G, VIF, HIV, APOBEC, HYDROLASE
5k82:C (ASP13) to (LYS57) CRYSTAL STRUCTURE OF A PRIMATE APOBEC3G N-TERMINAL DOMAIN | APOBEC3G, VIF, HIV, APOBEC, HYDROLASE
5k82:D (ASP13) to (LYS57) CRYSTAL STRUCTURE OF A PRIMATE APOBEC3G N-TERMINAL DOMAIN | APOBEC3G, VIF, HIV, APOBEC, HYDROLASE
5k8p:A (ALA92) to (TYR120) ZN2+/TETRAHEDRAL INTERMEDIATE-BOUND R289A 5-NITROANTHRANILATE AMINOHYDROLASE | NITROAROMATICS, DEAMINASE, METALLOENZYME, HYDROLASE
5k8p:B (ALA92) to (GLY119) ZN2+/TETRAHEDRAL INTERMEDIATE-BOUND R289A 5-NITROANTHRANILATE AMINOHYDROLASE | NITROAROMATICS, DEAMINASE, METALLOENZYME, HYDROLASE
5k8p:H (ALA92) to (TYR120) ZN2+/TETRAHEDRAL INTERMEDIATE-BOUND R289A 5-NITROANTHRANILATE AMINOHYDROLASE | NITROAROMATICS, DEAMINASE, METALLOENZYME, HYDROLASE
5kbj:G (LYS78) to (LYS112) STRUCTURE OF REP-DNA COMPLEX | REPLICATION INITIATION, REP PROTEIN, S. AUREUS, TRANSCRIPTION-DNA COMPLEX
4gam:F (PRO404) to (CYS426) COMPLEX STRUCTURE OF METHANE MONOOXYGENASE HYDROXYLASE AND REGULATORY SUBUNIT | METHANE MONOOXYGENASE, HYDROXYLASE, REGULATORY SUBUNIT B, OXIDOREDUCTASE
4gb3:1 (THR161) to (PRO181) HUMAN COXSACKIEVIRUS B3 STRAIN RD COAT PROTEIN | CAPSID PROTEIN, VIRUS
5kdp:A (ASN799) to (PHE825) E491A MUTANT OF CHOLINE TMA-LYASE | MUTANT, RADICAL, LYASE
5kdp:C (ASN799) to (PHE825) E491A MUTANT OF CHOLINE TMA-LYASE | MUTANT, RADICAL, LYASE
4gfc:B (ASP86) to (PHE118) N-TERMINAL COILED-COIL DIMER OF C.ELEGANS SAS-6, CRYSTAL FORM B | BETA-SANDWICH, ALPHA-BETA PROTEIN, STRUCTURAL PROTEIN, CYTOPLASMIC, CENTRIOLAR, CENTRAL TUBE
4gl9:F (LEU121) to (PRO152) CRYSTAL STRUCTURE OF INHIBITORY PROTEIN SOCS3 IN COMPLEX WITH JAK2 KINASE DOMAIN AND FRAGMENT OF GP130 INTRACELLULAR DOMAIN | KINASE INHIBITOR RECEPTOR CYTOKINE SIGNALLING, PHOSPHORYLATION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
5kl0:A (SER375) to (LYS396) CRYSTAL STRUCTURE OF PHOSPHOGLUCOMUTASE FROM XANTHOMONAS CITRI CITRI COMPLEXED WITH GLUCOSE-1,6-BIPHOSPHATE | PHOSPHOGLUCOMUTASE CITRUS CANKER, ISOMERASE
4gmj:D (ASP59) to (PHE99) STRUCTURE OF HUMAN NOT1 MIF4G DOMAIN CO-CRYSTALLIZED WITH CAF1 | CCR4-NOT, MRNA DECAY, DEADENYLASE, TRANSCRIPTION, RNA BINDING PROTEIN
5ktg:A (SER2) to (GLY31) CRYSTAL STRUCTURE OF MOUSE BAK BH3-IN-GROOVE HOMODIMER (GFP) | BCL-2 FAMILY PROTEINS, MITOCHONDRIAL OUTER MEMBRANE PERMEABILIZATION, APOPTOSIS REGULATORS, PORE-FORMING PROTEINS, APOPTOSIS
5kwl:1 (LYS169) to (PRO197) EXPANDED POLIOVIRUS IN COMPLEX WITH VHH 10E | POLIOVIRUS, VHH, NANOBODY, 80S, EXPANDED, SINGLE DOMAIN ANTIBODY, VIRUS-IMMUNE SYSTEM COMPLEX
5kwy:A (HIS510) to (ASN568) STRUCTURE OF HUMAN NPC1 MIDDLE LUMENAL DOMAIN BOUND TO NPC2 | HUMAN PROTEIN COMPLEX, NPC1, NPC2, TRANSPORT PROTEIN
5l2r:A (PRO516) to (ASP548) CRYSTAL STRUCTURE OF FUMARATE HYDRATASE FROM LEISHMANIA MAJOR | FUMARATE HYDRATASE FE-S CLUSTER, LYASE
5l2r:B (PRO516) to (ASP548) CRYSTAL STRUCTURE OF FUMARATE HYDRATASE FROM LEISHMANIA MAJOR | FUMARATE HYDRATASE FE-S CLUSTER, LYASE
5l52:F (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 14 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l52:T (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 14 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l54:F (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 16 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l54:T (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 16 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l55:E (PHE19) to (LEU48) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 18 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l55:S (PHE19) to (LEU48) YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE INHIBITOR 18 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
5l5d:F (PHE18) to (THR51) 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:T (PHE18) to (THR51) 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
5l5i:F (PHE18) to (THR51) 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
5l5u:E (PHE19) to (LEU48) 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:F (PHE18) to (THR51) 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:S (PHE19) to (LEU48) 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:T (PHE18) to (THR51) 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
5l5x:F (PHE18) to (THR51) '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
5l65:F (PHE18) to (THR51) 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:T (PHE18) to (THR51) 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
5l6a:F (PHE18) to (THR51) 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:F (PHE18) to (THR51) 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:T (PHE18) to (THR51) 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
5l8e:A (ASN461) to (LEU529) STRUCTURE OF UAF1 | WDR48 ACTIVATES USP1/12/46 B PROPELLAR, STRUCTURAL PROTEIN
5l8w:B (GLY463) to (LEU529) STRUCTURE OF USP12-UB-PRG/UAF1 | DUB-ACTIVATOR COMPLEX USP1 PARALOG, STRUCTURAL PROTEIN
5le5:G (TYR23) to (ASP58) NATIVE HUMAN 20S PROTEASOME AT 1.8 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5le5:O (VAL19) to (GLU48) NATIVE HUMAN 20S PROTEASOME AT 1.8 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5le5:U (TYR23) to (ASP58) NATIVE HUMAN 20S PROTEASOME AT 1.8 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lex:A (VAL19) to (GLU48) NATIVE HUMAN 20S PROTEASOME IN MG-ACETATE AT 2.2 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lex:B (TYR19) to (GLU48) NATIVE HUMAN 20S PROTEASOME IN MG-ACETATE AT 2.2 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lex:C (PHE17) to (GLU46) NATIVE HUMAN 20S PROTEASOME IN MG-ACETATE AT 2.2 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lex:E (HIS20) to (GLN53) NATIVE HUMAN 20S PROTEASOME IN MG-ACETATE AT 2.2 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lex:G (TYR23) to (ASP58) NATIVE HUMAN 20S PROTEASOME IN MG-ACETATE AT 2.2 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lex:O (GLN20) to (SER53) NATIVE HUMAN 20S PROTEASOME IN MG-ACETATE AT 2.2 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lex:Q (PHE17) to (GLU46) NATIVE HUMAN 20S PROTEASOME IN MG-ACETATE AT 2.2 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lex:U (TYR23) to (ASP58) NATIVE HUMAN 20S PROTEASOME IN MG-ACETATE AT 2.2 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5ley:E (HIS20) to (SER54) HUMAN 20S PROTEASOME COMPLEX WITH OPROZOMIB AT 1.9 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5ley:G (TYR23) to (ASP58) HUMAN 20S PROTEASOME COMPLEX WITH OPROZOMIB AT 1.9 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5ley:O (VAL19) to (GLU48) HUMAN 20S PROTEASOME COMPLEX WITH OPROZOMIB AT 1.9 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5ley:U (TYR23) to (ASP58) HUMAN 20S PROTEASOME COMPLEX WITH OPROZOMIB AT 1.9 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lez:A (VAL19) to (GLU48) HUMAN 20S PROTEASOME COMPLEX WITH OPROZOMIB IN MG-ACETATE AT 2.2 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lez:C (PHE17) to (GLU46) HUMAN 20S PROTEASOME COMPLEX WITH OPROZOMIB IN MG-ACETATE AT 2.2 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lez:E (HIS20) to (GLN53) HUMAN 20S PROTEASOME COMPLEX WITH OPROZOMIB IN MG-ACETATE AT 2.2 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lez:G (TYR23) to (ASP58) HUMAN 20S PROTEASOME COMPLEX WITH OPROZOMIB IN MG-ACETATE AT 2.2 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lez:O (VAL19) to (GLU48) HUMAN 20S PROTEASOME COMPLEX WITH OPROZOMIB IN MG-ACETATE AT 2.2 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lez:U (TYR23) to (ASP58) HUMAN 20S PROTEASOME COMPLEX WITH OPROZOMIB IN MG-ACETATE AT 2.2 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf0:A (VAL19) to (GLU48) HUMAN 20S PROTEASOME COMPLEX WITH EPOXOMICIN AT 2.4 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf0:C (PHE17) to (GLU46) HUMAN 20S PROTEASOME COMPLEX WITH EPOXOMICIN AT 2.4 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf0:E (HIS20) to (GLN53) HUMAN 20S PROTEASOME COMPLEX WITH EPOXOMICIN AT 2.4 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf0:G (TYR23) to (ASP58) HUMAN 20S PROTEASOME COMPLEX WITH EPOXOMICIN AT 2.4 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf0:U (TYR23) to (ASP58) HUMAN 20S PROTEASOME COMPLEX WITH EPOXOMICIN AT 2.4 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf1:A (VAL19) to (GLU48) HUMAN 20S PROTEASOME COMPLEX WITH DIHYDROEPONEMYCIN AT 2.0 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf1:E (HIS20) to (GLN53) HUMAN 20S PROTEASOME COMPLEX WITH DIHYDROEPONEMYCIN AT 2.0 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf1:G (TYR23) to (ASP58) HUMAN 20S PROTEASOME COMPLEX WITH DIHYDROEPONEMYCIN AT 2.0 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf1:O (VAL19) to (GLU48) HUMAN 20S PROTEASOME COMPLEX WITH DIHYDROEPONEMYCIN AT 2.0 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf1:U (TYR23) to (ASP58) HUMAN 20S PROTEASOME COMPLEX WITH DIHYDROEPONEMYCIN AT 2.0 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf3:A (VAL19) to (GLU48) HUMAN 20S PROTEASOME COMPLEX WITH BORTEZOMIB AT 2.1 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf3:E (HIS20) to (GLN53) HUMAN 20S PROTEASOME COMPLEX WITH BORTEZOMIB AT 2.1 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf3:G (TYR23) to (ASP58) HUMAN 20S PROTEASOME COMPLEX WITH BORTEZOMIB AT 2.1 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf3:O (VAL19) to (GLU48) HUMAN 20S PROTEASOME COMPLEX WITH BORTEZOMIB AT 2.1 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf3:U (TYR23) to (ASP58) HUMAN 20S PROTEASOME COMPLEX WITH BORTEZOMIB AT 2.1 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf4:A (VAL19) to (GLU48) HUMAN 20S PROTEASOME COMPLEX WITH DELANZOMIB AT 2.0 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf4:E (HIS20) to (GLN53) HUMAN 20S PROTEASOME COMPLEX WITH DELANZOMIB AT 2.0 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf4:G (TYR23) to (ASP58) HUMAN 20S PROTEASOME COMPLEX WITH DELANZOMIB AT 2.0 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf4:O (VAL19) to (GLU48) HUMAN 20S PROTEASOME COMPLEX WITH DELANZOMIB AT 2.0 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf4:U (TYR23) to (ASP58) HUMAN 20S PROTEASOME COMPLEX WITH DELANZOMIB AT 2.0 ANGSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf7:A (VAL19) to (GLU48) HUMAN 20S PROTEASOME COMPLEX WITH IXAZOMIB AT 2.0 ANSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf7:E (HIS20) to (GLN53) HUMAN 20S PROTEASOME COMPLEX WITH IXAZOMIB AT 2.0 ANSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf7:G (TYR23) to (ASP58) HUMAN 20S PROTEASOME COMPLEX WITH IXAZOMIB AT 2.0 ANSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf7:O (VAL19) to (GLU48) HUMAN 20S PROTEASOME COMPLEX WITH IXAZOMIB AT 2.0 ANSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lf7:U (TYR23) to (ASP58) HUMAN 20S PROTEASOME COMPLEX WITH IXAZOMIB AT 2.0 ANSTROM | PROTEASOME, MULTICATALYTIC PROTEINASE, NTN-HYDROLASE, HYDROLASE
5lof:A (PRO-42) to (GLY-14) CRYSTAL STRUCTURE OF THE MBP-MCL1 COMPLEX WITH HIGHLY SELECTIVE AND POTENT INHIBITOR OF MCL1 | APOPTOSIS-INHIBITOR COMPLEX, MCL-1, S S63845, MBP
5ltt:E (PHE19) to (LEU48) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; R57T)IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5ltt:F (PHE18) to (THR51) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; R57T)IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5ltt:S (PHE19) to (LEU48) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; R57T)IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5ltt:T (PHE18) to (THR51) YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138; R57T)IN COMPLEX WITH PR-924 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5svl:A (ASP228) to (THR263) CRYSTAL STRUCTURE OF THE ATP-GATED HUMAN P2X3 ION CHANNEL IN THE ATP- BOUND, CLOSED (DESENSITIZED) STATE | MEMBRANE PROTEIN, ION CHANNEL, DESENSITIZED STATE
5svm:A (ASP228) to (THR263) CRYSTAL STRUCTURE OF THE ATP-GATED HUMAN P2X3 ION CHANNEL BOUND TO AGONIST 2-METHYLTHIO-ATP IN THE DESENSITIZED STATE | MEMBRANE PROTEIN, ION CHANNEL, DESENSITIZED STATE
5svp:A (ASP228) to (THR263) ANOMALOUS SULFUR SIGNAL REVEALS THE POSITION OF AGONIST 2-METHYLTHIO- ATP BOUND TO THE ATP-GATED HUMAN P2X3 ION CHANNEL IN THE DESENSITIZED STATE | ION CHANNEL, DESENSITIZED STATE, ANOMALOUS SIGNAL, MEMBRANE PROTEIN
5t0h:M (PHE21) to (LEU54) STRUCTURAL BASIS FOR DYNAMIC REGULATION OF THE HUMAN 26S PROTEASOME | UBIQUITIN-PROTEASOME SYSTEM, AAA-ATPASE, HYDROLASE
5t0i:G (TYR23) to (PRO57) STRUCTURAL BASIS FOR DYNAMIC REGULATION OF THE HUMAN 26S PROTEASOME | UBIQUITIN-PROTEASOME SYSTEM, AAA-ATPASE, HYDROLASE
5t0i:H (LEU19) to (GLN52) STRUCTURAL BASIS FOR DYNAMIC REGULATION OF THE HUMAN 26S PROTEASOME | UBIQUITIN-PROTEASOME SYSTEM, AAA-ATPASE, HYDROLASE
5t0i:M (PHE21) to (SER55) STRUCTURAL BASIS FOR DYNAMIC REGULATION OF THE HUMAN 26S PROTEASOME | UBIQUITIN-PROTEASOME SYSTEM, AAA-ATPASE, HYDROLASE
5t0j:M (PHE21) to (SER55) STRUCTURAL BASIS FOR DYNAMIC REGULATION OF THE HUMAN 26S PROTEASOME | UBIQUITIN-PROTEASOME SYSTEM, AAA-ATPASE, HYDROLASE
7gpb:D (ASP421) to (MET441) STRUCTURAL MECHANISM FOR GLYCOGEN PHOSPHORYLASE CONTROL BY PHOSPHORYLATION AND AMP | GLYCOGEN PHOSPHORYLASE
7kme:H (ASP125) to (ASN159) CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN INHIBITED WITH SEL2711. | SELECTIDE INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
8kme:2 (ASP125) to (ASN159) CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN INHIBITED WITH SEL2770. | THROMBIN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, SELECTIDE
1a0h:E (ASP442) to (ASN484) THE X-RAY CRYSTAL STRUCTURE OF PPACK-MEIZOTHROMBIN DESF1: KRINGLE/THROMBIN AND CARBOHYDRATE/KRINGLE/THROMBIN INTERACTIONS AND LOCATION OF THE LINKER CHAIN | SERINE PROTEASE, COAGULATION, THROMBIN, PROTHROMBIN, MEIZOTHROMBIN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3rmo:H (ASP125) to (ASN159) HUMAN THROMBIN IN COMPLEX WITH MI004 | SERINE PROTEASE, KRINGLE, HYDROLASE, BLOOD COAGULATION, BLOOD CLOTTING, CONVERTION OF FIBRINOGEN, HIRUDIN, GLYCOSYLATION, BLOOD, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1ncr:A (ASP157) to (SER180) THE STRUCTURE OF RHINOVIRUS 16 WHEN COMPLEXED WITH PLECONARIL, AN ANTIVIRAL COMPOUND | HRV16, RHINOVIRUS, PLECONARIL, PICONAVIRUS, ICOSAHEDRAL VIRUS
3edx:F (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THE W215A/E217A MUTANT OF MURINE THROMBIN | SERINE PROTEASE, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PROTEASE, ZYMOGEN
1nkt:A (ALA231) to (HIS263) CRYSTAL STRUCTURE OF THE SECA PROTEIN TRANSLOCATION ATPASE FROM MYCOBACTERIUM TUBERCULOSIS COMPLEX WITH ADPBS | PREPROTEIN TRANSLOCATION, ATPASE, TRANSMEMBRANE TRANSPORT, HELICASE-LIKE MOTOR DOMAIN, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, TB STRUCTURAL GENOMICS CONSORTIUM, TBSGC, PROTEIN TRANSPORT
1ai8:H (ASP125) to (ASN159) HUMAN ALPHA-THROMBIN TERNARY COMPLEX WITH THE EXOSITE INHIBITOR HIRUGEN AND ACTIVE SITE INHIBITOR PHCH2OCO-D-DPA-PRO-BOROMPG | SERINE PROTEINASE, BLOOD COAGULATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, BLOOD COAGULATION-HYDROLASE INHIBITOR COMPLEX
1nro:H (ASP125) to (ASN159) CRYSTALLOGRAPHIC STRUCTURES OF THROMBIN COMPLEXED WITH THROMBIN RECEPTOR PEPTIDES: EXISTENCE OF EXPECTED AND NOVEL BINDING MODES | SERINE PROTEINASE/RECEPTOR
1nrp:H (ASP125) to (ASN159) CRYSTALLOGRAPHIC STRUCTURES OF THROMBIN COMPLEXED WITH THROMBIN RECEPTOR PEPTIDES: EXISTENCE OF EXPECTED AND NOVEL BINDING MODES | SERINE PROTEINASE/RECEPTOR
1nu7:F (ASP125) to (ASN159) STAPHYLOCOAGULASE-THROMBIN COMPLEX | THROMBIN NON-PROTEOLYTIC ACTIVATOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEIN BINDING
3eo1:F (ASP3) to (GLY46) STRUCTURE OF THE FAB FRAGMENT OF GC-1008 IN COMPLEX WITH TRANSFORMING GROWTH FACTOR-BETA 3 | ANTIBODY-CYTOKINE COMPLEX, GROWTH FACTOR, FAB FRAGMENT, CARDIOMYOPATHY, CLEAVAGE ON PAIR OF BASIC RESIDUES, GLYCOPROTEIN, MITOGEN, POLYMORPHISM, SECRETED, IMMUNE SYSTEM/CYTOKINE COMPLEX
3eo1:L (ASP3) to (GLY46) STRUCTURE OF THE FAB FRAGMENT OF GC-1008 IN COMPLEX WITH TRANSFORMING GROWTH FACTOR-BETA 3 | ANTIBODY-CYTOKINE COMPLEX, GROWTH FACTOR, FAB FRAGMENT, CARDIOMYOPATHY, CLEAVAGE ON PAIR OF BASIC RESIDUES, GLYCOPROTEIN, MITOGEN, POLYMORPHISM, SECRETED, IMMUNE SYSTEM/CYTOKINE COMPLEX
4ham:A (PRO49) to (ILE75) CRYSTAL STRUCTURE OF TRANSCRIPTIONAL ANTITERMINATOR FROM LISTERIA MONOCYTOGENES EGD-E | STRUCTURAL GENOMICS, PSI-BIOLOGY, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, WINGED HELIX-TURN-HELIX, FOUR HELIX BUNDLE, TRANSCRIPTIONAL REGULATOR, TRANSCRIPTION
3epn:A (PRO180) to (GLY209) CRYSTAL STRUCTURE OF CAULOBACTER CRESCENTUS THIC COMPLEXED WITH IMIDAZOLE RIBONUCLEOTIDE | ALPHA-BETA BARREL, SAM SUPERFAMILY, THIAMINE BIOSYNTHESIS, BIOSYNTHETIC PROTEIN
3epn:B (PRO180) to (GLY209) CRYSTAL STRUCTURE OF CAULOBACTER CRESCENTUS THIC COMPLEXED WITH IMIDAZOLE RIBONUCLEOTIDE | ALPHA-BETA BARREL, SAM SUPERFAMILY, THIAMINE BIOSYNTHESIS, BIOSYNTHETIC PROTEIN
3eq0:H (ASP125) to (ASN159) THROMBIN INHIBITOR | BLOOD CLOTTING, HYDROLASE INHIBITOR, ACUTE PHASE, BLOOD COAGULATION, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4x4m:C (LYS414) to (SER440) STRUCTURE OF FCGAMMARI IN COMPLEX WITH FC REVEALS THE IMPORTANCE OF GLYCAN RECOGNITION FOR HIGH AFFINITY IGG BINDING | IMMUNE SYSTEM
3f68:H (ASP125) to (ASN159) THROMBIN INHIBITION | BLOOD CLOTTING, HYDROLASE INHIBITOR, ACUTE PHASE, BLOOD COAGULATION, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, PROTEASE INHIBITOR, SERINE PROTEASE INHIBITOR, SULFATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3s8p:B (ASN171) to (LYS216) CRYSTAL STRUCTURE OF THE SET DOMAIN OF HUMAN HISTONE-LYSINE N- METHYLTRANSFERASE SUV420H1 IN COMPLEX WITH S-ADENOSYL-L-METHIONINE | SET DOMAIN, HISTONE METHYLTRANSFERASE, TRANSCRIPTION REGULATION, HISTONE LYSINE, SAM, METHYLATION, NUCLEUS, CHROMOSOME, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, TRANSFERASE
2pgq:B (ASP125) to (ASN159) HUMAN THROMBIN MUTANT C191A-C220A IN COMPLEX WITH THE INHIBITOR PPACK | SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1c4u:2 (ASP125) to (ASN159) SELECTIVE NON ELECTROPHILIC THROMBIN INHIBITORS WITH CYCLOHEXYL MOIETIES. | COMPLEX (SERINE PROTEASE-INHIBITOR), HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1oop:A (THR163) to (PRO183) THE CRYSTAL STRUCTURE OF SWINE VESICULAR DISEASE VIRUS | PICORNAVIRUS STRUCTURE, VIRUS/VIRAL PROTEIN, VIRUS-RECEPTOR INTERACTIONS, HOST ADAPTATION, CAR, DAF, COXSACKIEVIRUS, X- RAY DIFFRACTION, ICOSAHEDRAL VIRUS
3fvy:A (HIS568) to (ASP606) CRYSTAL STRUCTURE OF HUMAN DIPEPTIDYL PEPTIDASE III | SGC, DPP3, DIPEPTIDYL PEPTIDASE III, AMINOPEPTIDASE, HYDROLASE, METAL-BINDING, METALLOPROTEASE, PHOSPHOPROTEIN, PROTEASE, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM
2c8y:B (ASP125) to (ASN159) THROMBIN INHIBITORS | PROTEASE, BLOOD COAGULATION, THROMBIN, ACUTE PHASE, DISEASE MUTATION, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, PLASMA, SERINE PROTEASE, ZYMOGEN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1cy4:A (ARG493) to (ALA519) COMPLEX OF E.COLI DNA TOPOISOMERASE I WITH 5'PTPTPTP3' | DNA TOPOISOMERASE, RELAXING ENZYME, ISOMERASE
2cbx:C (TYR77) to (ALA121) X-RAY CRYSTAL STRUCTURE OF 5'-FLUORODEOXYADENOSINE SYNTHASE FROM STREPTOMYCES CATTLEYA COMPLEXED WITH BETA-D- ERYTHROFURANOSYL-ADENOSINE | TRANSFERASE, FLUORINASE, 5'-FLUORODEOXYADENOSINE SYNTHASE, FLA, INHIBITOR, AZA, STREPTOMYCES CATTLEYA, SAM ANALOGUE
1d3t:B (ASP158) to (ASN200) CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH BENZO[B]THIOPHENE INHIBITOR 1 | THROMBIN; BENZO[B]THIOPHENE, BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3g2i:A (ASP421) to (MET441) CRYSTAL STRUCTURE OF 1-(BETA-D-GLUCOPYRANOSYL)-4- SUBSTITUTED-1,2,3-TRIAZOLE | GLYCOGEN PHOSPHORYLASE, AMIDE-1, 2, 3-TRIAZOLE BIOISOSTERISM, ACETYLATION, ALLOSTERIC ENZYME, CARBOHYDRATE METABOLISM, GLYCOGEN METABOLISM, GLYCOSYLTRANSFERASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, PYRIDOXAL PHOSPHATE, TRANSFERASE
1dpp:A (HIS452) to (ASP494) DIPEPTIDE BINDING PROTEIN COMPLEX WITH GLYCYL-L-LEUCINE | CHEMOTAXIS, COMPLEX (BINDING PROTEIN/PEPTIDE) COMPLEX, PEPTIDE BINDING PROTEIN
1dpp:C (HIS452) to (ASP494) DIPEPTIDE BINDING PROTEIN COMPLEX WITH GLYCYL-L-LEUCINE | CHEMOTAXIS, COMPLEX (BINDING PROTEIN/PEPTIDE) COMPLEX, PEPTIDE BINDING PROTEIN
1dpp:E (HIS452) to (ASP494) DIPEPTIDE BINDING PROTEIN COMPLEX WITH GLYCYL-L-LEUCINE | CHEMOTAXIS, COMPLEX (BINDING PROTEIN/PEPTIDE) COMPLEX, PEPTIDE BINDING PROTEIN
1dpp:G (HIS452) to (ASP494) DIPEPTIDE BINDING PROTEIN COMPLEX WITH GLYCYL-L-LEUCINE | CHEMOTAXIS, COMPLEX (BINDING PROTEIN/PEPTIDE) COMPLEX, PEPTIDE BINDING PROTEIN
3gic:B (ASP125) to (ASN159) STRUCTURE OF THROMBIN MUTANT DELTA(146-149E) IN THE FREE FORM | SERINE PROTEASE, CHYMOTRYPSIN FOLD, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, DISULFIDE BOND, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PROTEASE, SECRETED, ZYMOGEN
1ppb:H (ASP125) to (ASN159) THE REFINED 1.9 ANGSTROMS CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN: INTERACTION WITH D-PHE-PRO-ARG CHLOROMETHYLKETONE AND SIGNIFICANCE OF THE TYR-PRO-PRO-TRP INSERTION SEGMENT | SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1dwe:H (ASP125) to (ASN159) CRYSTALLOGRAPHIC ANALYSIS AT 3.0-ANGSTROMS RESOLUTION OF THE BINDING TO HUMAN THROMBIN OF FOUR ACTIVE SITE-DIRECTED INHIBITORS | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, SERINE PROTEINASE
3gls:A (PRO264) to (PHE294) CRYSTAL STRUCTURE OF HUMAN SIRT3 | NAD DEPENDENT DEACETYLASE, SIRTUIN, APO STRUCTURE, HYDROLASE, METAL-BINDING, MITOCHONDRION, NAD, POLYMORPHISM, TRANSIT PEPTIDE, ZINC
3gls:D (PRO264) to (PHE294) CRYSTAL STRUCTURE OF HUMAN SIRT3 | NAD DEPENDENT DEACETYLASE, SIRTUIN, APO STRUCTURE, HYDROLASE, METAL-BINDING, MITOCHONDRION, NAD, POLYMORPHISM, TRANSIT PEPTIDE, ZINC
4y75:F (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAF-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y75:T (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAF-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8i:F (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8i:T (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH AC-PLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8k:F (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH H-APLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4y8k:T (PHE18) to (THR51) YEAST 20S PROTEASOME IN COMPLEX WITH H-APLL-EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS
4jbh:D (ASN39) to (ASN87) 2.2A RESOLUTION STRUCTURE OF COBALT AND ZINC BOUND THERMOSTABLE ALCOHOL DEHYDROGENASE FROM PYROBACULUM AEROPHILUM | ALCOHOL DEHYDROGENASE, THERMOSTABILITY, ZINC BINDING, OXIDOREDUCTASE
4y8p:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAL- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8p:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAL- EP | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4y8r:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA2-H116D MUTANT | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS
4y8r:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA2-H116D MUTANT | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS
1qj1:B (ASP125) to (ASN159) NOVEL COVALENT ACTIVE SITE THROMBIN INHIBITORS | BLOOD COAGULATION-INHIBITOR, PROTEINASE, TRYPSIN LIKE PROTEINASE, PROTEASE-INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1qj7:B (ASP125) to (ASN159) NOVEL COVALENT ACTIVE SITE THROMBIN INHIBITORS | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, BLOOD COAGULATION-INHIBITOR COMPLEX, PROTEINASE, BLOOD COAGULATION, TRYPSIN LIKE PROTEINASE, PROTEASE-INHIBITOR COMPLEX, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3u9a:H (ASP125) to (ASN159) HUMAN THROMBIN IN COMPLEX WITH MI330 | SERINE PROTEASE, KRINGLE, HYDROLASE, BLOOD COAGULATION, BLOOD CLOTTING, CONVERTION OF FIBRINOGEN TO FIBRIN, CLEAVAGE ON PAIRS OF BASIC RESIDUES, HIRUDIN, GLYCOSYLATION, BLOOD, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3hk3:B (ASP125) to (ASN159) CRYSTAL STRUCTURE OF MURINE THROMBIN MUTANT W215A/E217A (ONE MOLECULE IN THE ASYMMETRIC UNIT) | SERINE PROTEASE, ACUTE PHASE, BLOOD COAGULATION, CALCIUM, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISULFIDE BOND, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PROTEASE, ZYMOGEN
3unb:T (GLN22) to (SER55) 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:c (VAL19) to (GLU48) 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:h (GLN22) to (SER55) 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:v (GLN22) to (SER55) 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
2faq:A (ARG582) to (LYS606) CRYSTAL STRUCTURE OF PSEUDOMONAS AERUGINOSA LIGD POLYMERASE DOMAIN WITH ATP AND MANGANESE | POLYMERASE, PRIMASE, LIGASE, NHEJ, ATP, HYDROLASE/TRANSFERASE COMPLEX
2faq:B (ARG582) to (LYS606) CRYSTAL STRUCTURE OF PSEUDOMONAS AERUGINOSA LIGD POLYMERASE DOMAIN WITH ATP AND MANGANESE | POLYMERASE, PRIMASE, LIGASE, NHEJ, ATP, HYDROLASE/TRANSFERASE COMPLEX
2fhh:D (SER8) to (GLU44) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PROTEASOME IN COMPLEX WITH A PEPTIDYL BORONATE INHIBITOR MLN-273 | MULTI-SUBUNIT PROTEIN ASSEMBLY, INHIBITOR-COMPLEX, HYDROLASE
3utu:H (ASP125) to (ASN159) HIGH AFFINITY INHIBITOR OF HUMAN THROMBIN | SERINE PROTEASE, BLOOD CLOTTING, FIBRINOPEPTIDE A, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
1ggr:A (ASP94) to (ASP123) COMPLEX OF ENZYME IIAGLC AND THE HISTIDINE-CONTAINING PHOSPHOCARRIER PROTEIN HPR FROM ESCHERICHIA COLI NMR, RESTRAINED REGULARIZED MEAN STRUCTURE | PHOSPHOTRANSFERASE, TRANSFERASE, KINASE, SUGAR TRANSPORT, COMPLEX (TRANSFERASE/PHOSPHOCARRIER)
1glb:F (ASP94) to (ASP123) STRUCTURE OF THE REGULATORY COMPLEX OF ESCHERICHIA COLI IIIGLC WITH GLYCEROL KINASE | PHOSPHOTRANSFERASE
4kty:A (GLU198) to (GLY228) FIBRIN-STABILIZING FACTOR WITH A BOUND LIGAND | TRANSGLUTAMINASE, COAGULATION, TRANSFERASE, ACYLTRANSFERASE, LIGAND, CALCIUM IONS, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4kty:B (GLU198) to (GLY228) FIBRIN-STABILIZING FACTOR WITH A BOUND LIGAND | TRANSGLUTAMINASE, COAGULATION, TRANSFERASE, ACYLTRANSFERASE, LIGAND, CALCIUM IONS, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
2g97:A (ASN316) to (PRO345) CRYSTAL STRUCTURE OF VISFATIN/PRE-B CELL COLONY ENHANCING FACTOR 1/NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE IN COMPLEX WITH THE SPECIFIC INHIBITOR FK-866 | VISFATIN, PBEF, NAMPRTASE, FK-866, RATTUS NORVEGICUS, TRANSFERASE
2vx3:C (ALA388) to (LEU405) CRYSTAL STRUCTURE OF THE HUMAN DUAL SPECIFICITY TYROSINE- PHOSPHORYLATION-REGULATED KINASE 1A | SERINE/THREONINE-PROTEIN KINASE, MINIBRAIN HOMOLOG, NUCLEOTIDE-BINDING, TRANSFERASE, PHOSPHOPROTEIN, TYROSINE-PROTEIN KINASE, CASP8, KINASE
1svm:B (LEU497) to (THR518) CO-CRYSTAL STRUCTURE OF SV40 LARGE T ANTIGEN HELICASE DOMAIN AND ATP | AAA+ FOLD, VIRAL PROTEIN
1svm:E (LEU497) to (ARG517) CO-CRYSTAL STRUCTURE OF SV40 LARGE T ANTIGEN HELICASE DOMAIN AND ATP | AAA+ FOLD, VIRAL PROTEIN
4kxz:E (ALA4) to (GLY46) CRYSTAL STRUCTURE OF TGFB2 IN COMPLEX WITH GC2008. | CYSTEINE KNOT, FAB, VARIOUS GROWTH FUNCTIONS (TGF-BETA), TGF-BETA ANTAGONIST (GC2008), TGF-BETA RECEPTORS, IMMUNE SYSTEM
2gd6:C (GLU310) to (PRO328) THE 1,1-PROTON TRANSFER REACTION MECHANISM BY ALPHA-METHYLACYL-COA RACEMASE IS CATALYZED BY AN ASPARTATE/HISTIDINE PAIR AND INVOLVES A SMOOTH, METHIONINE-RICH SURFACE FOR BINDING THE FATTY ACYL MOIETY | ALPHA-METHYLACYL-COA RACEMASE, RACEMASE, COA TRANSFERASE, PROTON TRANSFER, COENZYME A, ISOMERASE
1h16:A (GLY528) to (GLY561) PYRUVATE FORMATE-LYASE (E.COLI) IN COMPLEX WITH PYRUVATE AND COA | LYASE, GLYCYL RADICAL ENZYME, TRANSFERASE, ACYLTRANSFERASE
1h16:A (ARG712) to (ARG738) PYRUVATE FORMATE-LYASE (E.COLI) IN COMPLEX WITH PYRUVATE AND COA | LYASE, GLYCYL RADICAL ENZYME, TRANSFERASE, ACYLTRANSFERASE
1t4u:H (ASP158) to (ASN194) CRYSTAL STRUCTURE ANALYSIS OF A NOVEL OXYGUANIDINE BOUND TO THROMBIN | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1h9d:B (HIS37) to (SER65) AML1/CBF-BETA/DNA COMPLEX | TRANSCRIPTION FACTOR
1h9d:D (HIS37) to (SER65) AML1/CBF-BETA/DNA COMPLEX | TRANSCRIPTION FACTOR
2gvj:A (PRO317) to (PRO345) CRYSTAL STRUCTURE OF HUMAN NMPRTASE IN COMPLEX WITH FK866 | NMPRTASE, VISFATIN, PBEF, CANCER, FK866, TRANSFERASE
2w82:A (TYR140) to (TYR165) THE STRUCTURE OF ARDA | DNA MIMIC, REPLICATION INHIBITOR
2w82:B (TYR140) to (VAL164) THE STRUCTURE OF ARDA | DNA MIMIC, REPLICATION INHIBITOR
2w82:D (TYR140) to (VAL164) THE STRUCTURE OF ARDA | DNA MIMIC, REPLICATION INHIBITOR
2h6b:A (LEU25) to (PRO46) CRYSTAL STRUCTURE OF OXIDIZED CPRK IN COMPLEX WITH O- CHLOROPHENOLACETIC ACID | HALORESPIRATION, DNA BINDING, CHLORINATED LIGAND, CHLOROPHENOL, CPRK, HELIX-TURN-HELIX, DNA BINDING PROTEIN
2h9t:H (ASP125) to (ASN159) CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN IN COMPLEX WITH SURAMIN | THROMBIN, COAGULATION FACTOR II, SURAMIN, INHIBITOR, HYDROLASE
1tq7:B (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THE ANTICOAGULANT THROMBIN MUTANT W215A/E217A BOUND TO PPACK | THROMBIN, ANTICOAGULANT, BLOOD CLOTTING, PPACK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2wcr:B (GLN115) to (ARG145) CRYSTAL STRUCTURE OF TIP-ALPHA N34 (HP0596) FROM HELICOBACTER PYLORI AT PH8 | HP0596, TIP-ALPHA, HELICOBACTER PYLORI, IMMUNE SYSTEM
2wff:3 (THR134) to (PRO163) EQUINE RHINITIS A VIRUS | VIRUS, CAPSID, PICORNAVIRUS
5a0q:B (LEU18) to (GLU48) CRYO-EM REVEALS THE CONFORMATION OF A SUBSTRATE ANALOGUE IN THE HUMAN 20S PROTEASOME CORE | HYDROLASE, PROTEASOME, 20S, ADAAHX3L3VS, LIGAND, INHIBITOR, DRUG DESIGN
5a0q:F (HIS20) to (LEU49) CRYO-EM REVEALS THE CONFORMATION OF A SUBSTRATE ANALOGUE IN THE HUMAN 20S PROTEASOME CORE | HYDROLASE, PROTEASOME, 20S, ADAAHX3L3VS, LIGAND, INHIBITOR, DRUG DESIGN
5a0q:P (LEU18) to (GLU48) CRYO-EM REVEALS THE CONFORMATION OF A SUBSTRATE ANALOGUE IN THE HUMAN 20S PROTEASOME CORE | HYDROLASE, PROTEASOME, 20S, ADAAHX3L3VS, LIGAND, INHIBITOR, DRUG DESIGN
5a0q:T (HIS20) to (LEU49) CRYO-EM REVEALS THE CONFORMATION OF A SUBSTRATE ANALOGUE IN THE HUMAN 20S PROTEASOME CORE | HYDROLASE, PROTEASOME, 20S, ADAAHX3L3VS, LIGAND, INHIBITOR, DRUG DESIGN
4lnm:A (ILE170) to (GLY209) STRUCTURE OF ESCHERICHIA COLI THREONINE ALDOLASE IN COMPLEX WITH SERINE | THREONINE ALDOLASE, VITAMIN B6, PLP, ALDIMINE, FOLD TYPE 1, AMINO ACID SYNTHESIS, LYASE
3vyr:B (VAL265) to (LEU295) CRYSTAL STRUCTURE OF THE HYPC-HYPD COMPLEX | [NIFE] HYDROGENASE MATURATION, METAL BINDING PROTEIN
5a2m:H (ASP125) to (ASN159) THROMBIN INHIBITOR | HYDROLASE, HYDROLASE INHIBITOR COMPLEX, SERINE PROTEASE, BLOOD COAGULATION, BLOOD CLOTTING, CONVERTION OF FIBRINOGEN TO FIBRIN, BLOOD CLOTTING INHIBITOR, THROMBIN INHIBITOR, PREORGANIZATION, GLYCOSYLATION, BLOOD
4lv9:A (PRO317) to (PRO345) FRAGMENT-BASED IDENTIFICATION OF AMIDES DERIVED FROM TRANS-2-(PYRIDIN- 3-YL)CYCLOPROPANECARBOXYLIC ACID AS POTENT INHIBITORS OF HUMAN NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE (NAMPT) | TRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4lvg:B (ASN316) to (PRO345) FRAGMENT-BASED IDENTIFICATION OF AMIDES DERIVED FROM TRANS-2-(PYRIDIN- 3-YL)CYCLOPROPANECARBOXYLIC ACID AS POTENT INHIBITORS OF HUMAN NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE (NAMPT) | TRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
1ubg:A (SER271) to (TYR295) MSRECA-DATP COMPLEX | RECOMBINATION, DNA-REPAIR
1uea:D (HIS7) to (GLY25) MMP-3/TIMP-1 COMPLEX | PROTEINASE, ZINC-ENDOPEPTIDASE, PROTEINASE INHIBITOR, COMPLEX, MMPS (MATRIX METALLO PROTEINASES) TIMPS (TISSUE INHIBITOR OF METALLO PROTEINASES), METZINCINS, COMPLEX (METALLOPROTEASE/INHIBITOR)
5a5b:C (GLN21) to (GLU49) STRUCTURE OF THE 26S PROTEASOME-UBP6 COMPLEX | HYDROLASE, CONFORMATIONAL SWITCHING, PROTEIN DEGRADATION, PROTEOSTASIS, QUALITY CONTROL, UBP6, USP14
5a5b:D (ILE17) to (GLU47) STRUCTURE OF THE 26S PROTEASOME-UBP6 COMPLEX | HYDROLASE, CONFORMATIONAL SWITCHING, PROTEIN DEGRADATION, PROTEOSTASIS, QUALITY CONTROL, UBP6, USP14
5a5b:F (GLN21) to (LEU49) STRUCTURE OF THE 26S PROTEASOME-UBP6 COMPLEX | HYDROLASE, CONFORMATIONAL SWITCHING, PROTEIN DEGRADATION, PROTEOSTASIS, QUALITY CONTROL, UBP6, USP14
5a5b:G (ASN20) to (THR54) STRUCTURE OF THE 26S PROTEASOME-UBP6 COMPLEX | HYDROLASE, CONFORMATIONAL SWITCHING, PROTEIN DEGRADATION, PROTEOSTASIS, QUALITY CONTROL, UBP6, USP14
3w7x:B (LYS511) to (LEU546) CRYSTAL STRUCTURE OF E. COLI YGJK D324N COMPLEXED WITH MELIBIOSE | GH63, PROCESSING ALPHA-GLUCOSIDASE I, ALPHA/ALPHA BARREL, HYDROLASE
2ia2:C (THR49) to (LEU75) THE CRYSTAL STRUCTURE OF A PUTATIVE TRANSCRIPTIONAL REGULATOR RHA06195 FROM RHODOCOCCUS SP. RHA1 | SAD, TRANSCRIPTIONAL REGULATOR, PSI-2, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, TRANSCRIPTION
3j17:A (GLU964) to (ALA990) STRUCTURE OF A TRANSCRIBING CYPOVIRUS BY CRYO-ELECTRON MICROSCOPY | DSRNA VIRUS REOVIRIDAE TRANSCRIBING CYPOVIRUS, VIRUS
5a9k:B (LEU492) to (ILE513) STRUCTURAL BASIS FOR DNA STRAND SEPARATION BY A HEXAMERIC REPLICATIVE HELICASE | HYDROLASE, DNA REPLICATION FORK
5a9k:C (LEU492) to (ILE513) STRUCTURAL BASIS FOR DNA STRAND SEPARATION BY A HEXAMERIC REPLICATIVE HELICASE | HYDROLASE, DNA REPLICATION FORK
5a9k:D (LEU492) to (ILE513) STRUCTURAL BASIS FOR DNA STRAND SEPARATION BY A HEXAMERIC REPLICATIVE HELICASE | HYDROLASE, DNA REPLICATION FORK
3j1c:G (ARG20) to (THR60) CRYO-EM STRUCTURE OF 9-FOLD SYMMETRIC RATCPN-ALPHA IN APO STATE | GROUP II CHAPERONIN, CHAPERONE
3j1c:K (ALA22) to (THR60) CRYO-EM STRUCTURE OF 9-FOLD SYMMETRIC RATCPN-ALPHA IN APO STATE | GROUP II CHAPERONIN, CHAPERONE
3we2:A (SER1138) to (LEU1173) STRUCTURE OF BLM RQC DOMAIN BOUND TO A PHOSPHATE ION | WINGED-HELIX, DNA HELICASE, DNA BINDING, DNA BINDING PROTEIN
3we2:B (SER1138) to (LEU1173) STRUCTURE OF BLM RQC DOMAIN BOUND TO A PHOSPHATE ION | WINGED-HELIX, DNA HELICASE, DNA BINDING, DNA BINDING PROTEIN
5aed:A (ASP597) to (ALA616) A BACTERIAL PROTEIN STRUCTURE IN GLYCOSIDE HYDROLASE FAMILY 31 | HYDROLASE, GH31, ALPHA-SULFOQUINOVOSIDASE
5aed:B (ASP597) to (ALA616) A BACTERIAL PROTEIN STRUCTURE IN GLYCOSIDE HYDROLASE FAMILY 31 | HYDROLASE, GH31, ALPHA-SULFOQUINOVOSIDASE
5aee:A (ASP597) to (ALA616) A BACTERIAL PROTEIN STRUCTURE IN GLYCOSIDE HYDROLASE FAMILY 31 | HYDROLASE, GH31, ALPHA-SULFOQUINOVOSIDASE
5aee:B (ASP597) to (ALA616) A BACTERIAL PROTEIN STRUCTURE IN GLYCOSIDE HYDROLASE FAMILY 31 | HYDROLASE, GH31, ALPHA-SULFOQUINOVOSIDASE
5af3:B (ARG29) to (LEU68) X-RAY CRYSTAL STRUCTURE OF RV2018 FROM MYCOBACTERIUM TUBERCULOSIS | MYCOBACTERIUM TUBERCULOSIS, DNA BINDING, TA SYSTEM
1v3b:A (GLU276) to (LYS305) STRUCTURE OF THE HEMAGGLUTININ-NEURAMINIDASE FROM HUMAN PARAINFLUENZA VIRUS TYPE III | PIV3 HN, NATIVE, HEXAGONAL, HYDROLASE
1v3b:B (ASP275) to (LYS305) STRUCTURE OF THE HEMAGGLUTININ-NEURAMINIDASE FROM HUMAN PARAINFLUENZA VIRUS TYPE III | PIV3 HN, NATIVE, HEXAGONAL, HYDROLASE
5an8:A (ALA319) to (ALA344) CRYO-ELECTRON MICROSCOPY STRUCTURE OF RABBIT TRPV2 ION CHANNEL | TRANSPORT PROTEIN, TRP CHANNEL
5an8:B (ALA319) to (ALA344) CRYO-ELECTRON MICROSCOPY STRUCTURE OF RABBIT TRPV2 ION CHANNEL | TRANSPORT PROTEIN, TRP CHANNEL
5an8:C (ALA319) to (ALA344) CRYO-ELECTRON MICROSCOPY STRUCTURE OF RABBIT TRPV2 ION CHANNEL | TRANSPORT PROTEIN, TRP CHANNEL
5an8:D (ALA319) to (ALA344) CRYO-ELECTRON MICROSCOPY STRUCTURE OF RABBIT TRPV2 ION CHANNEL | TRANSPORT PROTEIN, TRP CHANNEL
2xel:A (ASP21) to (CYS49) MOLECULAR MECHANISM OF PENTACHLOROPSEUDILIN MEDIATED INHIBITION OF MYOSIN MOTOR ACTIVITY | CONTRACTILE PROTEIN, ALLOSTERIC INHIBITOR, NON-HYDROYLSABLE ATP ANALOGUE, MOTOR PROTEIN
1w0f:A (MET445) to (SER495) CRYSTAL STRUCTURE OF HUMAN CYTOCHROME P450 3A4 | OXIDOREDUCTASE, NIFEDIPINE OXIDASE, CYTOCHROME P450, ELECTRON TRANSPORT, MONOOXYGENASE
4n43:B (PRO171) to (PRO196) HUMAN ENTEROVIRUS 71 UNCOATING INTERMEDIATE CAPTURED AT ATOMIC RESOLUTION | HAND-FOOT-AND-MOUTH DISEASE, PICORNAVIRUS, HUMAN ENTEROVIRUS 71, UNCOATING INTERMEDIATE, ICOSAHEDRAL VIRUS, POCKET FACTOR, VIRUS
2jh6:D (ASP125) to (ASN159) HUMAN THROMBIN HIRUGEN INHIBITOR COMPLEX | GLYCOPROTEIN, SERINE PROTEASE, KRINGLE, ZYMOGEN, THROMBIN, PROTEASE, DISEASE MUTATION, BLOOD COAGULATION, GAMMA-CARBOXYGLUTAMIC ACID, PROTEASE INHIBITOR, SERINE PROTEASE INHIBITOR, SULFATION, ACUTE PHASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2jhb:A (GLU41) to (SER67) CORE BINDING FACTOR BETA | CORE BINDING FACTOR, TRANSCRIPTION FACTOR, GENE REGULATION
4n9i:A (ASP8) to (GLY33) CRYSTAL STRUCTURE OF TRANSCRIPTION REGULATION PROTEIN CRP COMPLEXED WITH CGMP | DNA BINDING, TRANSCRIPTION REGULATOR
1k5m:A (SER1170) to (TYR1190) CRYSTAL STRUCTURE OF A HUMAN RHINOVIRUS TYPE 14:HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 V3 LOOP CHIMERIC VIRUS MN- III-2 | ENGINEERED RHINOVIRUS, HIV-1 V3 LOOP, BETA TURNS, ICOSAHEDRAL VIRUS
1wcm:A (SER754) to (ASN802) COMPLETE 12-SUBUNIT RNA POLYMERASE II AT 3.8 ANG | DNA-BINDING, DNA-DIRECTED RNA POLYMERASE, DNA-DEPENDENT RNA POLYMERASE, CELLULAR RNA POLYMERASE, MULTISUBUNIT CO, METAL- BINDING, NUCLEAR PROTEIN, REPEAT, TRANSCRIPTION, PHOSPHORYLATION, TRANSFERASE, ZINC, ZINC-FINGER
5bxn:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA2-G170A MUTANT IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, IMMUNODEFICIENCY, PROTEASOME, MUTANT, ASSEMBLY DEFECT
5bxn:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA2-G170A MUTANT IN COMPLEX WITH BORTEZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, IMMUNODEFICIENCY, PROTEASOME, MUTANT, ASSEMBLY DEFECT
5c17:A (ASN51) to (LEU80) CRYSTAL STRUCTURE OF THE MERCURY-BOUND FORM OF MERB2 | BACTERIAL PROTEINS, CYSTEINE, LYASES, MERCURY, LYASE
2y6p:A (ASP124) to (ARG149) EVIDENCE FOR A TWO-METAL-ION-MECHANISM IN THE KDO-CYTIDYLYLTRANSFERASE KDSB | TRANSFERASE, LIPID A
2y6p:B (ASP124) to (ARG149) EVIDENCE FOR A TWO-METAL-ION-MECHANISM IN THE KDO-CYTIDYLYLTRANSFERASE KDSB | TRANSFERASE, LIPID A
2y6p:C (ASP124) to (ARG149) EVIDENCE FOR A TWO-METAL-ION-MECHANISM IN THE KDO-CYTIDYLYLTRANSFERASE KDSB | TRANSFERASE, LIPID A
1wv0:A (ASP421) to (MET441) CRYSTALLOGRAPHIC STUDIES ON ACYL UREAS, A NEW CLASS OF INHIBITORS OF GLYCOGEN PHOSPHORYLASE. BROAD SPECIFICITY OF THE ALLOSTERIC SITE | GLYCOGENOLYSIS, TYPE 2 DIABETES, TRANSFERASE
4no9:C (PHE16) to (THR49) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-EPOXYKETONE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, EPOXYKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no9:F (PHE18) to (THR51) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-EPOXYKETONE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, EPOXYKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no9:Q (PHE16) to (THR49) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-EPOXYKETONE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, EPOXYKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4no9:T (PHE18) to (THR51) YCP IN COMPLEX WITH Z-LEU-LEU-LEU-EPOXYKETONE | PROTEASOME, PEPTIDE ELECTROPHILE, BINDING ANALYSIS, IRREVERSIBLE INHIBITOR, EPOXYKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4nub:A (SER36) to (HIS65) CRYSTAL STRUCTURE OF ESCHERICHIA COLI RIBOSOMAL OXYGENASE YCFD | STRUCTURAL GENOMICS, MONTREAL-KINGSTON BACTERIAL STRUCTURAL GENOMICS INITIATIVE, BSGI, JELLY ROLL, CUPIN, BETA-BARREL, 2OG/FE2+ DEPENDENT OXYGENASE, RIBOSOMAL PROTEIN L-16, OXIDOREDUCTASE
2mp0:B (ASP394) to (ASP423) PROTEIN PHOSPHORYLATION UPON A FLEETING ENCOUNTER | EIN EIIAGLC COMPLEX, TRANSFERASE
4o1b:B (ASN316) to (PRO345) THE CRYSTAL STRUCTURE OF A MUTANT NAMPT (G217R) IN COMPLEX WITH AN INHIBITOR APO866 | TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
2yim:A (GLU310) to (PRO328) THE ENOLISATION CHEMISTRY OF A THIOESTER-DEPENDENT RACEMASE: THE 1.4 A CRYSTAL STRUCTURE OF A COMPLEX WITH A PLANAR REACTION INTERMEDIATE ANALOGUE | ISOMERASE, METHYL-COA RACEMASE, TRANSITION STATE, MOLECULAR DYNAMICS, QM/MM, OXYANION HOLE
2yim:C (GLU310) to (PRO328) THE ENOLISATION CHEMISTRY OF A THIOESTER-DEPENDENT RACEMASE: THE 1.4 A CRYSTAL STRUCTURE OF A COMPLEX WITH A PLANAR REACTION INTERMEDIATE ANALOGUE | ISOMERASE, METHYL-COA RACEMASE, TRANSITION STATE, MOLECULAR DYNAMICS, QM/MM, OXYANION HOLE
3jrm:A (PHE22) to (ASP51) CRYSTAL STRUCTURE OF ARCHAEAL 20S PROTEASOME IN COMPLEX WITH MUTATED P26 ACTIVATOR | 20S PROTEASOME, PA26, CYTOPLASM, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE, HYDROLASE/HYDROLASE ACTIVATOR COMPLEX
3jrm:G (PHE22) to (ASP51) CRYSTAL STRUCTURE OF ARCHAEAL 20S PROTEASOME IN COMPLEX WITH MUTATED P26 ACTIVATOR | 20S PROTEASOME, PA26, CYTOPLASM, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE, HYDROLASE/HYDROLASE ACTIVATOR COMPLEX
3jw4:B (SER70) to (VAL100) THE STRUCTURE OF A PUTATIVE MARR FAMILY TRANSCRIPTIONAL REGULATOR FROM CLOSTRIDIUM ACETOBUTYLICUM | MARR, EMRR, TRANSCRIPTIONAL REGULATOR, DNA-BINDING PROTEIN, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, DNA-BINDING, TRANSCRIPTION, TRANSCRIPTION REGULATION, TRANSCRIPTION REGULATOR
4obu:E (GLY275) to (LYS320) RUMINOCOCCUS GNAVUS TRYPTOPHAN DECARBOXYLASE RUMGNA_01526 (APO) | TYPE 1 PLP-DEPENDENT, DECARBOXYLASE, TRYPTOPHAN, LYASE
4obu:U (GLY275) to (LYS320) RUMINOCOCCUS GNAVUS TRYPTOPHAN DECARBOXYLASE RUMGNA_01526 (APO) | TYPE 1 PLP-DEPENDENT, DECARBOXYLASE, TRYPTOPHAN, LYASE
4obu:G (GLY275) to (LYS320) RUMINOCOCCUS GNAVUS TRYPTOPHAN DECARBOXYLASE RUMGNA_01526 (APO) | TYPE 1 PLP-DEPENDENT, DECARBOXYLASE, TRYPTOPHAN, LYASE
4obu:H (GLY275) to (LYS320) RUMINOCOCCUS GNAVUS TRYPTOPHAN DECARBOXYLASE RUMGNA_01526 (APO) | TYPE 1 PLP-DEPENDENT, DECARBOXYLASE, TRYPTOPHAN, LYASE
4obu:F (GLY275) to (LYS320) RUMINOCOCCUS GNAVUS TRYPTOPHAN DECARBOXYLASE RUMGNA_01526 (APO) | TYPE 1 PLP-DEPENDENT, DECARBOXYLASE, TRYPTOPHAN, LYASE
4obu:B (GLY275) to (LYS320) RUMINOCOCCUS GNAVUS TRYPTOPHAN DECARBOXYLASE RUMGNA_01526 (APO) | TYPE 1 PLP-DEPENDENT, DECARBOXYLASE, TRYPTOPHAN, LYASE
4obu:C (GLY275) to (LYS320) RUMINOCOCCUS GNAVUS TRYPTOPHAN DECARBOXYLASE RUMGNA_01526 (APO) | TYPE 1 PLP-DEPENDENT, DECARBOXYLASE, TRYPTOPHAN, LYASE
2zc9:H (ASP125) to (ASN159) THROMBIN IN COMPLEX WITH INHIBITOR | BLOOD CLOTTING/SERINE PROTEASE INHIBITORS, SECRETED, SULFATION, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, ZYMOGEN, BLOOD CLOTTING-HYDROLASE INHIBITOR COMPLEX
2zhf:H (ASP125) to (ASN159) EXPLORING THROMBIN S3 POCKET | BLOOD COAGULATION, HYDROLASE INHIBITORS, ACUTE PHASE, CLEAVAGE ON PAIR OF BASIC RESIDUES, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, PROTEASE INHIBITOR, SERINE PROTEASE INHIBITOR, SULFATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2ziq:H (ASP125) to (ASN159) THROMBIN INHIBITION | BLOOD CLOTTING, HYDROLASE INHIBITOR, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2zqk:B (THR152) to (GLY174) CRYSTAL STRUCTURE OF INTIMIN-TIR68 COMPLEX | PROTEIN-PROTEIN COMPLEX, UNIQUE INTIMIN-TIR TRIMER INTERMEDIATE, CELL MEMBRANE, CELL OUTER MEMBRANE, MEMBRANE, TRANSMEMBRANE, VIRULENCE, RECEPTOR, CELL ADHESION
5cz9:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-D17N MUTANT IN COMPLEX WITH CARFILZOMIB; PROPEPTIDE EXPRESSED IN TRANS | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5cz9:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-D17N MUTANT IN COMPLEX WITH CARFILZOMIB; PROPEPTIDE EXPRESSED IN TRANS | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
1mh0:A (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THE ANTICOAGULANT SLOW FORM OF THROMBIN | THROMBIN, ALLOSTERY, SODIUM BINDING, SERINE PROTEASE, BLOOD CLOTTING
1mh0:B (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THE ANTICOAGULANT SLOW FORM OF THROMBIN | THROMBIN, ALLOSTERY, SODIUM BINDING, SERINE PROTEASE, BLOOD CLOTTING
2zwk:C (THR152) to (GLY174) CRYSTAL STRUCTURE OF INTIMIN-TIR90 COMPLEX | PROTEIN-PROTEIN COMPLEX, UNIQUE INTIMIN-TIR OCTAMER INTERMEDIATE, CELL MEMBRANE, CELL OUTER MEMBRANE, MEMBRANE, TRANSMEMBRANE, VIRULENCE, RECEPTOR, CELL ADHESION
4p8m:A (THR122) to (PRO163) CRYSTAL STRUCTURE OF M. TUBERCULOSIS DPRE1 IN COMPLEX WITH THE NON- COVALENT INHIBITOR QN114 | DPRE1, INHIBITOR, COMPLEX, NON-COVALENT, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
4p8m:B (THR122) to (PRO163) CRYSTAL STRUCTURE OF M. TUBERCULOSIS DPRE1 IN COMPLEX WITH THE NON- COVALENT INHIBITOR QN114 | DPRE1, INHIBITOR, COMPLEX, NON-COVALENT, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
4p8p:A (THR122) to (PRO163) CRYSTAL STRUCTURE OF M. TUBERCULOSIS DPRE1 IN COMPLEX WITH THE NON- COVALENT INHIBITOR QN127 | DPRE1, INHIBITOR, COMPLEX, NON-COVALENT, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
4p8p:B (THR122) to (PRO163) CRYSTAL STRUCTURE OF M. TUBERCULOSIS DPRE1 IN COMPLEX WITH THE NON- COVALENT INHIBITOR QN127 | DPRE1, INHIBITOR, COMPLEX, NON-COVALENT, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
4p8t:A (THR122) to (PRO163) CRYSTAL STRUCTURE OF M. TUBERCULOSIS DPRE1 IN COMPLEX WITH THE NON- COVALENT INHIBITOR QN129 | DPRE1, INHIBITOR, COMPLEX, NON-COVALENT, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
4p8t:B (THR122) to (PRO163) CRYSTAL STRUCTURE OF M. TUBERCULOSIS DPRE1 IN COMPLEX WITH THE NON- COVALENT INHIBITOR QN129 | DPRE1, INHIBITOR, COMPLEX, NON-COVALENT, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
3aaf:A (THR1011) to (ALA1042) STRUCTURE OF WRN RQC DOMAIN BOUND TO DOUBLE-STRANDED DNA | HELIX-TURN-HELIX, WINGED-HELIX, PROTEIN-DNA COMPLEX, DNA-BINDING, HELICASE, DNA BINDING PROTEIN-DNA COMPLEX
3aaf:B (THR1011) to (ALA1042) STRUCTURE OF WRN RQC DOMAIN BOUND TO DOUBLE-STRANDED DNA | HELIX-TURN-HELIX, WINGED-HELIX, PROTEIN-DNA COMPLEX, DNA-BINDING, HELICASE, DNA BINDING PROTEIN-DNA COMPLEX
4pfd:A (THR122) to (PRO163) CRYSTAL STRUCTURE OF M. TUBERCULOSIS IN COMPLEX WITH A CBT - NON- COVALENT ADDUCT | DPRE1, INHIBITOR, COVALENT, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4pfd:B (THR122) to (PRO163) CRYSTAL STRUCTURE OF M. TUBERCULOSIS IN COMPLEX WITH A CBT - NON- COVALENT ADDUCT | DPRE1, INHIBITOR, COVALENT, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
5deq:B (LYS179) to (PHE212) CRYSTAL STRUCTURE OF TRANSCRIPTIONAL FACTOR ARAR FROM BACTEROIDES THETAIOTAOMICRON VPI IN COMPLEX WITH L-ARABINOSE | STRUCTURAL GENOMICS, PSI-BIOLOGY, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, TRANSCRIPTION REGULATOR
4pjk:A (ASP21) to (CYS49) DICTY MYOSIN II R238E.E459R MUTANT (WITH ADP.PI) IN THE PI RELEASE STATE | MOTOR DOMAIN MUTANT, MOTOR PROTEIN
3ako:E (LYS3) to (GLY31) CRYSTAL STRUCTURE OF THE REASSEMBLED VENUS | VENUS, FLUORESCENT PROTEIN, GFP
3lfk:D (PRO63) to (LEU89) A REPORTED ARCHAEAL MECHANOSENSITIVE CHANNEL IS A STRUCTURAL HOMOLOG OF MARR-LIKE TRANSCRIPTIONAL REGULATORS | MULTIPLE ANTIBIOTIC RESISTANCE REGULATOR, TRANSCRIPTIONAL REGULATOR, WINGED HELIX-TURN-HELIX MOTIF, MECHANOSENSITIVE CHANNEL, UNKNOWN FUNCTION
1z8j:B (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THE THROMBIN MUTANT G193P BOUND TO PPACK | SERINE PROTEASE, OXYANION HOLE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3m1v:B (THR264) to (ASP297) STRUCTURAL INSIGHT INTO METHYL-COENZYME M REDUCTASE CHEMISTRY USING COENZYME B ANALOGUES | METHYL-COENZYME M REDUCTASE, METAL-BINDING, METHANOGENESIS, METHYLATION, NICKEL, TRANSFERASE
3m2u:B (THR264) to (ASP297) STRUCTURAL INSIGHT INTO METHYL-COENZYME M REDUCTASE CHEMISTRY USING COENZYME B ANALOGUES | METHYL-COENZYME M REDUCTASE, NICKEL, METAL-BINDING, METHANOGENESIS, METHYLATION, TRANSFERASE
3m6d:A (ASP536) to (GLU559) THE CRYSTAL STRUCTURE OF THE D307A MUTANT OF GLYCOSIDE HYDROLASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174 | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MCSG, MIDWEST CENTER FOR STRUCTURAL GENOMICS, HYDROLASE
3m6d:B (ASP536) to (GLU559) THE CRYSTAL STRUCTURE OF THE D307A MUTANT OF GLYCOSIDE HYDROLASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174 | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MCSG, MIDWEST CENTER FOR STRUCTURAL GENOMICS, HYDROLASE
3mad:A (GLY278) to (ARG325) CRYSTAL STRUCTURE OF STSPL (SYMMETRIC FORM) | CARBOXY-LYASE ACTIVITY, PYRIDOXAL PHOSPHATE, LYASE
3mad:B (GLY278) to (ARG325) CRYSTAL STRUCTURE OF STSPL (SYMMETRIC FORM) | CARBOXY-LYASE ACTIVITY, PYRIDOXAL PHOSPHATE, LYASE
4bam:B (ASP158) to (ASN194) THROMBIN IN COMPLEX WITH INHIBITOR | THROMBIN INHIBITOR, HYDROLASE
4qlv:C (PHE16) to (THR49) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 17 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlv:F (PHE18) to (ILE50) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 17 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlv:Q (PHE16) to (THR49) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 17 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qlv:T (PHE18) to (ILE50) YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 17 | PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3bd7:A (VAL422) to (MET441) GLYCOGEN PHOSPHORYLASE COMPLEX WITH 1(-D-GLUCOPYRANOSYL) THYMINE | GLYCOGENOLYSIS, TYPE 2 DIABETES, ALLOSTERIC ENZYME, CARBOHYDRATE METABOLISM, GLYCOGEN METABOLISM, GLYCOSYLTRANSFERASE, NUCLEOTIDE- BINDING, PHOSPHOPROTEIN, PYRIDOXAL PHOSPHATE, TRANSFERASE
4qw3:T (PHE18) to (THR51) YCP BETA5-C63F MUTANT IN COMPLEX WITH BORTEZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw7:F (PHE18) to (THR51) YCP BETA5-M45T MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qw7:T (PHE18) to (THR51) YCP BETA5-M45T MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwi:F (PHE18) to (THR51) YCP BETA5-A49S-MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qwi:T (PHE18) to (THR51) YCP BETA5-A49S-MUTANT IN COMPLEX WITH CARFILZOMIB | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz1:F (PHE18) to (THR51) YCP BETA5-M45T MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qz1:T (PHE18) to (THR51) YCP BETA5-M45T MUTANT IN COMPLEX WITH THE EPOXYKETONE INHIBITOR ONX 0914 | CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5f7p:A (GLY42) to (PHE78) ROK REPRESSOR LMO0178 FROM LISTERIA MONOCYTOGENES | REPRESSOR, OPEN READING FRAME, KINASE, STRUCTURAL GENOMICS, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID, TRANSCRIPTION
3n04:A (ASP536) to (GLU559) THE CRYSTAL STRUCTURE OF THE ALPHA-GLUCOSIDASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174 | STRUCTURAL GENOMICS, PSI-2,PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, HYDROLASE
3n04:B (ASP536) to (GLU559) THE CRYSTAL STRUCTURE OF THE ALPHA-GLUCOSIDASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174 | STRUCTURAL GENOMICS, PSI-2,PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, HYDROLASE
3bz9:A (ASP21) to (CYS49) CRYSTAL STRUCTURES OF (S)-(-)-BLEBBISTATIN ANALOGS BOUND TO DICTYOSTELIUM DISCOIDEUM MYOSIN II | MYOSIN INHIBITOR, MOTOR DOMAIN, BLEBBISTATIN ANALOGUE, ACTIN-BINDING, ATP-BINDING, CALMODULIN-BINDING, COILED COIL, CYTOPLASM, METHYLATION, MOTOR PROTEIN, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, CONTRACTILE PROTEIN
5fga:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5fga:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) | HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5fgg:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-L(-49S)_D17N DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgg:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA5-L(-49S)_D17N DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgi:F (PHE18) to (THR51) YEAST 20S PROTEASOME BETA1-T1A BETA2-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
5fgi:T (PHE18) to (THR51) YEAST 20S PROTEASOME BETA1-T1A BETA2-T1A DOUBLE MUTANT IN COMPLEX WITH CARFILZOMIB | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS
4r67:G (PHE21) to (SER55) HUMAN CONSTITUTIVE 20S PROTEASOME IN COMPLEX WITH CARFILZOMIB | HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r67:U (PHE21) to (SER55) HUMAN CONSTITUTIVE 20S PROTEASOME IN COMPLEX WITH CARFILZOMIB | HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r67:i (PHE21) to (SER55) HUMAN CONSTITUTIVE 20S PROTEASOME IN COMPLEX WITH CARFILZOMIB | HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4r67:w (PHE21) to (GLU50) HUMAN CONSTITUTIVE 20S PROTEASOME IN COMPLEX WITH CARFILZOMIB | HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3c91:A (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:B (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:C (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:D (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:E (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:F (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:G (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:O (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:P (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:Q (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:R (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:S (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:T (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c91:U (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH AN OPEN GATE | PROTEIN PEPTIDE COMPLEX, PEPTIDE NOT MODELED., HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:A (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:B (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:C (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:D (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:E (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:F (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:G (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:O (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:P (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:Q (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:R (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:S (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:T (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3c92:U (PHE22) to (SER56) THERMOPLASMA ACIDOPHILUM 20S PROTEASOME WITH A CLOSED GATE | PROTEIN COMPLEX, HYDROLASE, PROTEASE, PROTEASOME, THREONINE PROTEASE
3nc4:A (VAL422) to (MET441) THE BINDING OF BETA-D-GLUCOPYRANOSYL-THIOSEMICARBAZONE DERIVATIVES TO GLYCOGEN PHOSPHORYLASE: A NEW CLASS OF INHIBITORS | GLYCOGENOLYSIS, TYPE 2 DIABETES, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
3neu:A (PRO48) to (VAL74) THE CRYSTAL STRUCTURE OF A FUNCTIONALLY-UNKNOWN PROTEIN LIN1836 FROM LISTERIA INNOCUA CLIP11262 | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, UNKNOWN FUNCTION
4rgs:A (ALA74) to (VAL103) CRYSTAL STRUCTURE OF PUTATIVE MARR FAMILY TRANSCRIPTIONAL REGULATOR HCAR FROM ACINETOBACTER SP. ADP COMPLEXED WITH VANILIN | STRUCTURAL GENOMICS, PSI-BIOLOGY, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, WINGED HELIX-TURN-HELIX, TRANSCRIPTION
5fmg:C (TYR19) to (ASP48) STRUCTURE AND FUNCTION BASED DESIGN OF PLASMODIUM-SELECTIVE PROTEASOME INHIBITORS | HYDROLASE, PROTEASOME, 20S, PLASMODIUM, MALARIA, INHIBITOR, DRUG DESIGN, CRYO-EM
5fmg:D (LEU17) to (GLU46) STRUCTURE AND FUNCTION BASED DESIGN OF PLASMODIUM-SELECTIVE PROTEASOME INHIBITORS | HYDROLASE, PROTEASOME, 20S, PLASMODIUM, MALARIA, INHIBITOR, DRUG DESIGN, CRYO-EM
5fmg:Q (TYR19) to (ASP48) STRUCTURE AND FUNCTION BASED DESIGN OF PLASMODIUM-SELECTIVE PROTEASOME INHIBITORS | HYDROLASE, PROTEASOME, 20S, PLASMODIUM, MALARIA, INHIBITOR, DRUG DESIGN, CRYO-EM
5fmg:R (LEU17) to (GLU46) STRUCTURE AND FUNCTION BASED DESIGN OF PLASMODIUM-SELECTIVE PROTEASOME INHIBITORS | HYDROLASE, PROTEASOME, 20S, PLASMODIUM, MALARIA, INHIBITOR, DRUG DESIGN, CRYO-EM
4cdg:A (SER1138) to (VAL1171) CRYSTAL STRUCTURE OF THE BLOOM'S SYNDROME HELICASE BLM IN COMPLEX WITH NANOBODY | HYDROLASE
4rmj:A (PRO205) to (PHE235) HUMAN SIRT2 IN COMPLEX WITH ADP RIBOSE AND NICOTINAMIDE | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4cfi:A (SER227) to (THR252) 3D STRUCTURE OF FLIC FROM BURKHOLDERIA PSEUDOMALLEI | STRUCTURAL PROTEIN, FLAGELLA, EPITOPE, IMMUNE RESPONSE
3nzx:T (PHE22) to (THR55) 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
4s2a:A (PRO180) to (GLY209) CRYSTAL STRUCTURE OF CAULOBACTER CRESCENTUS THIC WITH FE4S4 CLUSTER AT REMOTE SITE (HOLO FORM) | ALPHA-BETA BARREL, RADICAL SAM SUPERFAMILY, IRON-SULFUR CLUSTER, THIAMIN, VITAMIN B1, VITAMIN B12, DOMAIN SWAPPING, ADOMET AND GLUTAMATE MUTASE, LYASE
4cr2:F (GLN21) to (ALA53) DEEP CLASSIFICATION OF A LARGE CRYO-EM DATASET DEFINES THE CONFORMATIONAL LANDSCAPE OF THE 26S PROTEASOME | HYDROLASE, AAA-ATPASE, ATP-ANALOG, CLASSIFICATION
4cr2:G (PHE21) to (THR54) DEEP CLASSIFICATION OF A LARGE CRYO-EM DATASET DEFINES THE CONFORMATIONAL LANDSCAPE OF THE 26S PROTEASOME | HYDROLASE, AAA-ATPASE, ATP-ANALOG, CLASSIFICATION
3ddw:A (ASP421) to (MET441) CRYSTAL STRUCTURE OF GLYCOGEN PHOSPHORYLASE COMPLEXED WITH AN ANTHRANILIMIDE BASED INHIBITOR GSK055 | GLYCOGEN PHOSPHORYLASE, GP, DIABETES, ALLOSTERIC ENZYME, CARBOHYDRATE METABOLISM, DISEASE MUTATION, GLYCOGEN METABOLISM, GLYCOGEN STORAGE DISEASE, GLYCOSYLTRANSFERASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, PYRIDOXAL PHOSPHATE, TRANSFERASE
5gjq:C (VAL19) to (SER53) STRUCTURE OF THE HUMAN 26S PROTEASOME BOUND TO USP14-UBAL | PROTEIN COMPLEX, HUMAN PROTEASOME, HYDROLASE
5gjq:E (PHE17) to (GLU46) STRUCTURE OF THE HUMAN 26S PROTEASOME BOUND TO USP14-UBAL | PROTEIN COMPLEX, HUMAN PROTEASOME, HYDROLASE
5gjq:i (VAL19) to (GLU48) STRUCTURE OF THE HUMAN 26S PROTEASOME BOUND TO USP14-UBAL | PROTEIN COMPLEX, HUMAN PROTEASOME, HYDROLASE
3ojl:A (GLY50) to (ALA72) NATIVE STRUCTURE OF THE UDP-N-ACETYL-MANNOSAMINE DEHYDROGENASE CAP5O FROM STAPHYLOCOCCUS AUREUS | ROSSMANN FOLD, BINARY COMPLEX, COFACTOR NAD, DIMER, OXIDOREDUCTION, OXIDOREDUCTASE
3ojl:B (LEU51) to (ALA72) NATIVE STRUCTURE OF THE UDP-N-ACETYL-MANNOSAMINE DEHYDROGENASE CAP5O FROM STAPHYLOCOCCUS AUREUS | ROSSMANN FOLD, BINARY COMPLEX, COFACTOR NAD, DIMER, OXIDOREDUCTION, OXIDOREDUCTASE
3dy4:F (GLN23) to (ILE54) 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:T (GLN23) to (ILE54) CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH SPIROLACTACYSTIN | PROTEASOME, INHIBITOR, PROTEIN DEGRADATION, UBIQUITIN-PROTEASOME- PATHWAY, HYDROLASE, NUCLEUS, PROTEASE, THREONINE PROTEASE, PHOSPHOPROTEIN, ZYMOGEN
4dhl:B (THR186) to (ALA243) CRYSTAL STRUCTURE OF RED KIDNEY BEAN PURPLE ACID PHOSPHATASE IN COMPLEX WITH MAYBRIDGE FRAGMENT MO07123 | CATALYTIC C DOMAIN, N TERMINAL DOMAIN, PHOSPHATASE, ACID PHOSPHATASE, PHOSPHORIC MONOESTER HYDROLASES, HYDROLASE, MO07123, MAYBRIDGE, FRAGMENT, LYSOSOME
4dhl:C (THR186) to (ALA243) CRYSTAL STRUCTURE OF RED KIDNEY BEAN PURPLE ACID PHOSPHATASE IN COMPLEX WITH MAYBRIDGE FRAGMENT MO07123 | CATALYTIC C DOMAIN, N TERMINAL DOMAIN, PHOSPHATASE, ACID PHOSPHATASE, PHOSPHORIC MONOESTER HYDROLASES, HYDROLASE, MO07123, MAYBRIDGE, FRAGMENT, LYSOSOME
3p70:B (ASP485) to (ASN527) STRUCTURAL BASIS OF THROMBIN-MEDIATED FACTOR V ACTIVATION: ESSENTIAL ROLE OF THE HIRUDIN-LIKE SEQUENCE GLU666-GLU672 FOR PROCESSING AT THE HEAVY CHAIN-B DOMAIN JUNCTION | TRYPSIN-LIKE SERINE PROTEINASE, BLOOD COAGULATION, N-GLYCOSYLATION, BLOOD PLASMA, HYDROLASE
3p70:D (ASP485) to (ASN527) STRUCTURAL BASIS OF THROMBIN-MEDIATED FACTOR V ACTIVATION: ESSENTIAL ROLE OF THE HIRUDIN-LIKE SEQUENCE GLU666-GLU672 FOR PROCESSING AT THE HEAVY CHAIN-B DOMAIN JUNCTION | TRYPSIN-LIKE SERINE PROTEINASE, BLOOD COAGULATION, N-GLYCOSYLATION, BLOOD PLASMA, HYDROLASE
4ueh:H (ASP125) to (ASN159) THROMBIN IN COMPLEX WITH BENZAMIDINE | HYDROLASE, HYDROLASE INHIBITOR COMPLEX, SERINE PROTEASE, BLOOD COAGULATION, BLOOD CLOTTING, CONVERTION OF FIBRINOGEN TO FIBRIN, BLOOD CLOTTING INHIBITOR, THROMBIN INHIBITOR, FRAGMENT, GLYCOSYLATION, BLOOD
4uey:A (HIS137) to (VAL178) STRUCTURE OF THE PERIPLASMIC DOMAIN PHOQ DOUBLE MUTANT ( W104C-A128C) | SIGNALING PROTEIN, SIGNAL TRANSDUCTION, PHOQ, PERIPLASMIC DOMAIN, HAMP DOMAIN, HISTIDINE KINASE
4e1o:A (ALA274) to (LYS319) HUMAN HISTIDINE DECARBOXYLASE COMPLEX WITH HISTIDINE METHYL ESTER (HME) | HISTIDINE DECARBOXYLASE, LYASE
4e1o:B (ALA274) to (LYS319) HUMAN HISTIDINE DECARBOXYLASE COMPLEX WITH HISTIDINE METHYL ESTER (HME) | HISTIDINE DECARBOXYLASE, LYASE
4e1o:C (ALA274) to (LYS319) HUMAN HISTIDINE DECARBOXYLASE COMPLEX WITH HISTIDINE METHYL ESTER (HME) | HISTIDINE DECARBOXYLASE, LYASE
4e1o:D (ALA274) to (LYS319) HUMAN HISTIDINE DECARBOXYLASE COMPLEX WITH HISTIDINE METHYL ESTER (HME) | HISTIDINE DECARBOXYLASE, LYASE
4e1o:E (ALA274) to (LYS319) HUMAN HISTIDINE DECARBOXYLASE COMPLEX WITH HISTIDINE METHYL ESTER (HME) | HISTIDINE DECARBOXYLASE, LYASE
4e1o:F (ALA274) to (LYS319) HUMAN HISTIDINE DECARBOXYLASE COMPLEX WITH HISTIDINE METHYL ESTER (HME) | HISTIDINE DECARBOXYLASE, LYASE
3qdz:B (ASP125) to (ASN159) CRYSTAL STRUCTURE OF THE HUMAN THROMBIN MUTANT D102N IN COMPLEX WITH THE EXTRACELLULAR FRAGMENT OF HUMAN PAR4. | SERINE PROTEASE, PROTEIN FUNCTION, PROTEASE-ACTIVATED RECEPTORS, HYDROLASE-HYDROLASE RECEPTOR COMPLEX
4fdp:A (THR122) to (PRO163) MYCOBACTERIUM TUBERCULOSIS DPRE1 - MONOCLINIC CRYSTAL FORM | ALPHA+BETA, OXIDOREDUCTASE, DECAPRENYLPHOSPHORYL-BETA-D-RIBOSE
4fdp:B (THR122) to (PRO163) MYCOBACTERIUM TUBERCULOSIS DPRE1 - MONOCLINIC CRYSTAL FORM | ALPHA+BETA, OXIDOREDUCTASE, DECAPRENYLPHOSPHORYL-BETA-D-RIBOSE
5k1a:D (ASN461) to (LEU529) CRYSTAL STRUCTURE OF THE UAF1-USP12 COMPLEX IN C2 SPACE GROUP | WD40 DOMAIN, UBIQUITIN-SPECIFIC PROTEASE 12, USP12, USP1-ASSOCIATED FACTOR 1, USP1, DEUBIQUITINATING ENZYME, DUB, SUMO-LIKE DOMAIN, SLD, HYDROLASE
5k1a:F (ASN461) to (LEU529) CRYSTAL STRUCTURE OF THE UAF1-USP12 COMPLEX IN C2 SPACE GROUP | WD40 DOMAIN, UBIQUITIN-SPECIFIC PROTEASE 12, USP12, USP1-ASSOCIATED FACTOR 1, USP1, DEUBIQUITINATING ENZYME, DUB, SUMO-LIKE DOMAIN, SLD, HYDROLASE
5k1a:H (ASN461) to (LEU529) CRYSTAL STRUCTURE OF THE UAF1-USP12 COMPLEX IN C2 SPACE GROUP | WD40 DOMAIN, UBIQUITIN-SPECIFIC PROTEASE 12, USP12, USP1-ASSOCIATED FACTOR 1, USP1, DEUBIQUITINATING ENZYME, DUB, SUMO-LIKE DOMAIN, SLD, HYDROLASE
5k1c:B (ASN461) to (LEU529) CRYSTAL STRUCTURE OF THE UAF1/WDR20/USP12 COMPLEX | WD40 REPEAT DOMAIN, WDR20, USP12, UAF1, WDR48, DEUBIQUITINATING ENZYME, UBIQUITIN-SPECIFIC PROTEASE, USP1-ASSOCIATED FACTOR 1, HYDROLASE
5k8n:A (ALA92) to (GLY119) 5NAA-BOUND 5-NITROANTHRANILATE AMINOHYDROLASE | NITROAROMATICS, DEAMINASE, METALLOENZYME, HYDROLASE
5k8n:B (ALA92) to (GLY119) 5NAA-BOUND 5-NITROANTHRANILATE AMINOHYDROLASE | NITROAROMATICS, DEAMINASE, METALLOENZYME, HYDROLASE
5k8n:D (ALA92) to (GLY119) 5NAA-BOUND 5-NITROANTHRANILATE AMINOHYDROLASE | NITROAROMATICS, DEAMINASE, METALLOENZYME, HYDROLASE
5k8n:E (ALA92) to (GLY119) 5NAA-BOUND 5-NITROANTHRANILATE AMINOHYDROLASE | NITROAROMATICS, DEAMINASE, METALLOENZYME, HYDROLASE
5k8n:F (ALA92) to (GLY119) 5NAA-BOUND 5-NITROANTHRANILATE AMINOHYDROLASE | NITROAROMATICS, DEAMINASE, METALLOENZYME, HYDROLASE
5k8n:G (ALA92) to (GLY119) 5NAA-BOUND 5-NITROANTHRANILATE AMINOHYDROLASE | NITROAROMATICS, DEAMINASE, METALLOENZYME, HYDROLASE
5k8n:H (ALA92) to (GLY119) 5NAA-BOUND 5-NITROANTHRANILATE AMINOHYDROLASE | NITROAROMATICS, DEAMINASE, METALLOENZYME, HYDROLASE
5l5e:F (PHE18) to (THR51) 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
5l5r:T (PHE18) to (THR51) 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
5t0g:G (GLN24) to (PRO57) STRUCTURAL BASIS FOR DYNAMIC REGULATION OF THE HUMAN 26S PROTEASOME | UBIQUITIN-PROTEASOME SYSTEM, AAA-ATPASE, HYDROLASE
5t0g:J (GLN18) to (GLU46) STRUCTURAL BASIS FOR DYNAMIC REGULATION OF THE HUMAN 26S PROTEASOME | UBIQUITIN-PROTEASOME SYSTEM, AAA-ATPASE, HYDROLASE
5t0g:M (PHE21) to (SER55) STRUCTURAL BASIS FOR DYNAMIC REGULATION OF THE HUMAN 26S PROTEASOME | UBIQUITIN-PROTEASOME SYSTEM, AAA-ATPASE, HYDROLASE