1n8q:A (GLU663) to (GLY721) LIPOXYGENASE IN COMPLEX WITH PROTOCATECHUIC ACID | OXIDOREDUCTASE, LIPOXYGENASE, IRON,PROTOCATECHUIC ACID, 3,4- DIHYDROXYBENZOIC ACID, LOX COMPLEX, QUERCETIN
3e91:A (LEU250) to (GLY302) CRYSTAL STRUCTURE OF SARS-COV MPRO MUTANT IN P21 AT PH6.9 | SARS CORONAVIRUS PROTEASE, HYDROLASE
3e91:B (GLY251) to (CYS300) CRYSTAL STRUCTURE OF SARS-COV MPRO MUTANT IN P21 AT PH6.9 | SARS CORONAVIRUS PROTEASE, HYDROLASE
3ea8:A (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE TRIPLE MUTANT STI/A IN SPACE GROUP C2 | SARS CORONAVIRUS MAIN PROTEASE 3C-LIKE PROTEASE MUTANT EXTRA HELICAL DOMAIN, CYTOPLASM, HYDROLASE, MEMBRANE, METAL- BINDING, PROTEASE, RIBOSOMAL FRAMESHIFTING, RNA-BINDING, THIOL PROTEASE, TRANSMEMBRANE, ZINC, ZINC-FINGER
3eaj:A (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE QUADRUPLE MUTANT STIF/A WITH TWO MOLECULES IN ONE ASYMMETRIC UNIT | SARS CORONAVIRUS MAIN PROTEASE MUTANT EXTRA HELICAL DOMAIN, CYTOPLASM, HYDROLASE, MEMBRANE, METAL-BINDING, PROTEASE, RIBOSOMAL FRAMESHIFTING, RNA-BINDING, THIOL PROTEASE, TRANSMEMBRANE, ZINC, ZINC-FINGER
3eaj:B (THR201) to (LEU250) CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE QUADRUPLE MUTANT STIF/A WITH TWO MOLECULES IN ONE ASYMMETRIC UNIT | SARS CORONAVIRUS MAIN PROTEASE MUTANT EXTRA HELICAL DOMAIN, CYTOPLASM, HYDROLASE, MEMBRANE, METAL-BINDING, PROTEASE, RIBOSOMAL FRAMESHIFTING, RNA-BINDING, THIOL PROTEASE, TRANSMEMBRANE, ZINC, ZINC-FINGER
3eaj:B (LEU250) to (GLN299) CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE QUADRUPLE MUTANT STIF/A WITH TWO MOLECULES IN ONE ASYMMETRIC UNIT | SARS CORONAVIRUS MAIN PROTEASE MUTANT EXTRA HELICAL DOMAIN, CYTOPLASM, HYDROLASE, MEMBRANE, METAL-BINDING, PROTEASE, RIBOSOMAL FRAMESHIFTING, RNA-BINDING, THIOL PROTEASE, TRANSMEMBRANE, ZINC, ZINC-FINGER
2amd:A (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS_COV MPRO IN COMPLEX WITH AN INHIBITOR N9 | ANTI-PARALLEL B-BARREL, ANTI-PARALLEL A-HELICES, HYDROLASE
2amd:B (GLY251) to (GLY302) CRYSTAL STRUCTURE OF SARS_COV MPRO IN COMPLEX WITH AN INHIBITOR N9 | ANTI-PARALLEL B-BARREL, ANTI-PARALLEL A-HELICES, HYDROLASE
1a7u:B (ASP155) to (TRP205) CHLOROPEROXIDASE T | HALOPEROXIDASE, OXIDOREDUCTASE, PEROXIDASE, ALPHA/BETA HYDROLASE FOLD
2amp:B (PHE247) to (GLN295) CRYSTAL STRUCTURE OF PORCINE TRANSMISSIBLE GASTROENTERITIS VIRUS MPRO IN COMPLEX WITH AN INHIBITOR N1 | ANTI-PARALLEL B-BARREL, ANTI-PARALLEL A-HELICES, HYDROLASE
1a8u:A (ASP155) to (TRP205) CHLOROPEROXIDASE T/BENZOATE COMPLEX | HALOPEROXIDASE, OXIDOREDUCTASE, BENZOATE COMPLEX
3ebn:C (GLY251) to (ARG298) A SPECIAL DIMERIZATION OF SARS-COV MAIN PROTEASE C-TERMINAL DOMAIN DUE TO DOMAIN-SWAPPING | SARS, CORONAVIRUS, MAIN PROTEASE, CRYSTAL STRUCTURE, DIMERIZATION, N-FINGER, C-TERMINAL DOMAIN, HYDROLASE
3ebn:D (GLY251) to (ARG298) A SPECIAL DIMERIZATION OF SARS-COV MAIN PROTEASE C-TERMINAL DOMAIN DUE TO DOMAIN-SWAPPING | SARS, CORONAVIRUS, MAIN PROTEASE, CRYSTAL STRUCTURE, DIMERIZATION, N-FINGER, C-TERMINAL DOMAIN, HYDROLASE
1ngn:A (PRO430) to (ALA468) MISMATCH REPAIR IN METHYLATED DNA. STRUCTURE OF THE MISMATCH-SPECIFIC THYMINE GLYCOSYLASE DOMAIN OF METHYL-CPG- BINDING PROTEIN MBD4 | MISMACTH REPAIR IN METHYLATED DNA, DNA BINDING PROTEIN
4wmd:A (SER204) to (THR258) CRYSTAL STRUCTURE OF CATALYTICALLY INACTIVE MERS-COV 3CL PROTEASE (C148A) IN SPACEGROUP C2221 | 3CL PROTEASE, MERS, CORONAVIRUS, HYDROLASE
4wmd:B (GLN249) to (GLY302) CRYSTAL STRUCTURE OF CATALYTICALLY INACTIVE MERS-COV 3CL PROTEASE (C148A) IN SPACEGROUP C2221 | 3CL PROTEASE, MERS, CORONAVIRUS, HYDROLASE
4wmd:C (SER204) to (THR258) CRYSTAL STRUCTURE OF CATALYTICALLY INACTIVE MERS-COV 3CL PROTEASE (C148A) IN SPACEGROUP C2221 | 3CL PROTEASE, MERS, CORONAVIRUS, HYDROLASE
4wme:A (SER204) to (THR258) CRYSTAL STRUCTURE OF CATALYTICALLY INACTIVE MERS-COV 3CL PROTEASE (C148A) IN SPACEGROUP C2 | MERS, CORONAVIRUS, 3CL PROTEASE, HYDROLASE
4wme:B (SER204) to (THR258) CRYSTAL STRUCTURE OF CATALYTICALLY INACTIVE MERS-COV 3CL PROTEASE (C148A) IN SPACEGROUP C2 | MERS, CORONAVIRUS, 3CL PROTEASE, HYDROLASE
4wme:C (SER204) to (THR258) CRYSTAL STRUCTURE OF CATALYTICALLY INACTIVE MERS-COV 3CL PROTEASE (C148A) IN SPACEGROUP C2 | MERS, CORONAVIRUS, 3CL PROTEASE, HYDROLASE
4wme:D (SER204) to (THR258) CRYSTAL STRUCTURE OF CATALYTICALLY INACTIVE MERS-COV 3CL PROTEASE (C148A) IN SPACEGROUP C2 | MERS, CORONAVIRUS, 3CL PROTEASE, HYDROLASE
4wmf:A (GLN249) to (GLY302) CRYSTAL STRUCTURE OF CATALYTICALLY INACTIVE MERS-COV 3CL PROTEASE (C148A) IN SPACEGROUP P212121 | MES, 3CL PROTEASE, CORONAVIRUS, HYDROLASE
4wmf:B (SER204) to (THR258) CRYSTAL STRUCTURE OF CATALYTICALLY INACTIVE MERS-COV 3CL PROTEASE (C148A) IN SPACEGROUP P212121 | MES, 3CL PROTEASE, CORONAVIRUS, HYDROLASE
4wmf:C (SER204) to (THR258) CRYSTAL STRUCTURE OF CATALYTICALLY INACTIVE MERS-COV 3CL PROTEASE (C148A) IN SPACEGROUP P212121 | MES, 3CL PROTEASE, CORONAVIRUS, HYDROLASE
2op9:A (GLY251) to (CYS300) SUBSTRATE SPECIFICITY PROFILING AND IDENTIFICATION OF A NEW CLASS OF INHIBITOR FOR THE MAJOR PROTEASE OF THE SARS CORONAVIRUS | SARS, 3CLPRO, PROTEINASE, PROTEASE, HYDROLASE
2op9:B (GLY251) to (SER301) SUBSTRATE SPECIFICITY PROFILING AND IDENTIFICATION OF A NEW CLASS OF INHIBITOR FOR THE MAJOR PROTEASE OF THE SARS CORONAVIRUS | SARS, 3CLPRO, PROTEINASE, PROTEASE, HYDROLASE
3rwr:W (LEU635) to (GLN715) CRYSTAL STRUCTURE OF THE HUMAN XRCC4-XLF COMPLEX | COMPLEX-FILAMENT, NON-HOMOLOGOUS END-JOINING, DNA AND PROTEIN BINDING, DNA BINDING PROTEIN-PROTEIN BINDING COMPLEX
3eq5:L (CYS166) to (GLY209) CRYSTAL STRUCTURE OF FRAGMENT 137 TO 238 OF THE HUMAN SKI-LIKE PROTEIN | SKIL,SKI-LIKE PROTEIN,SNO,RECEPTOR SIGNALLING, TGF-BETA, SIGNALING PROTEIN, STRUCTURAL GENOMICS, SGC STOCKHOLM, STRUCTURAL GENOMICS CONSORTIUM, SGC
1nxh:A (VAL24) to (ALA62) X-RAY STRUCTURE: NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET TT87 | HYPOTHETICAL PROTEIN, DISULFIDE BONDS, HOMODIMER, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, UNKNOWN FUNCTION
4wwx:B (ASP792) to (LEU857) CRYSTAL STRUCTURE OF THE CORE RAG1/2 RECOMBINASE | V(D)J RECOMBINATION, RAG1/2, RECOMBINATION ACTIVATING GENE 1/2, CRYSTAL STRUCTURE., HYDROLASE, LIGASE
1o07:B (ALA98) to (TRP138) CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN Q120L/Y150E MUTANT OF AMPC AND A BETA-LACTAM INHIBITOR (MXG) | ENZYME INHIBITOR COMPLEX, BETA-LACTAMASE BETA-LACTAM COMPLEX, HYDROLASE
4wy3:A (GLY251) to (GLN299) STRUCTURE OF SARS-3CL PROTEASE COMPLEX WITH A PHENYLBENZOYL (R,S)-N- DECALIN TYPE INHIBITOR | HYDRASE PROTEINASE CONVERTING, DESIGNED INHIBITOR, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4hi3:B (GLY251) to (SER301) CRYSTAL STRUCTURE OF DIMERIC R298A MUTANT OF SARS CORONAVIRUS MAIN PROTEASE | CHYMOTRYPSIN-LIKE PROTEIN, PROTEASE, CYTOSOL, HYDROLASE
2p9v:B (ALA98) to (TRP138) STRUCTURE OF AMPC BETA-LACTAMASE WITH CROSS-LINKED ACTIVE SITE AFTER EXPOSURE TO SMALL MOLECULE INHIBITOR | BETA-LACTAMASE, CROSS-LINK, HYDROLASE
1bho:1 (THR185) to (GLY228) MAC-1 I DOMAIN MAGNESIUM COMPLEX | CELL ADHESION, INTEGRIN, I DOMAIN
1bhq:1 (THR185) to (GLY228) MAC-1 I DOMAIN CADMIUM COMPLEX | CELL ADHESION, INTEGRIN, I DOMAIN
3f9f:A (GLY251) to (CYS300) CRYSTAL STRUCTURE OF THE F140A MUTANT OF SARS-CORONOVIRUS 3C-LIKE PROTEASE AT PH 6.0 | PROTEASE, CYTOPLASM, HYDROLASE, MEMBRANE, METAL-BINDING, RIBOSOMAL FRAMESHIFTING, RNA-BINDING, THIOL PROTEASE, TRANSMEMBRANE, ZINC, ZINC-FINGER
3f9g:B (GLY251) to (CYS300) CRYSTAL STRUCTURE OF THE F140A MUTANT OF SARS-CORONOVIRUS 3C-LIKE PROTEASE AT PH 6.5 | PROTEASE, CYTOPLASM, HYDROLASE, MEMBRANE, METAL-BINDING, RIBOSOMAL FRAMESHIFTING, RNA-BINDING, THIOL PROTEASE, TRANSMEMBRANE, ZINC, ZINC-FINGER
2pg4:B (GLN9) to (GLY58) CRYSTAL STRUCTURE OF A PUTATIVE DNA BINDING PROTEIN (APE_0880A) FROM AEROPYRUM PERNIX K1 AT 2.21 A RESOLUTION | STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, DNA BINDING PROTEIN
4xfq:B (THR200) to (THR254) CRYSTAL STRUCTURE BASIS FOR PEDV 3C LIKE PROTEASE | PORCINE EPIDEMIC DIARRHEA VIRUS, 3C-LIKE PROTEASE, HYDROLASE
3fhj:F (PRO236) to (SER293) INDEPENDENT SATURATION OF THREE TRPRS SUBSITES GENERATES A PARTIALLY-ASSEMBLED STATE SIMILAR TO THOSE OBSERVED IN MOLECULAR SIMULATIONS | LIGAND-DEPENDENT DOMAIN REARRANGEMENT, MECHANISTIC PATHWAY, MOLECULAR SIMULATIONS, AMINOACYL-TRNA SYNTHETASE, ATP- BINDING, CYTOPLASM, LIGASE, NUCLEOTIDE-BINDING, PROTEIN BIOSYNTHESIS, TRANSLATION
3fkv:B (ALA98) to (TRP138) AMPC K67R MUTANT COMPLEXED WITH BENZO(B)THIOPHENE-2-BORONIC ACID (BZB) | AMPC, K67R, BETA-LACTAMASE, GENERAL BASE, ANTIBIOTIC RESISTANCE, PERIPLASM, HYDROLASE
3fkw:B (ALA98) to (TRP138) AMPC K67R MUTANT APO STRUCTURE | AMPC, K67R, BETA-LACTAMASE, GENERAL BASE, ANTIBIOTIC RESISTANCE, PERIPLASM, HYDROLASE
2pu4:A (ALA98) to (TRP138) AMPC BETA-LACAMASE WITH BOUND COVALENT OXADIAZOLE INHIBITOR | AMPC BETA-LACTAMASE OXADIAZOLE, HYDROLASE
3sn8:A (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEASE COMPLEXED WITH CM- FF-H (SOAKING) | 3C-LIKE PROTEINASE, PROTEASE, CM-FF-H, ACTIVE SITE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3sna:A (GLN244) to (GLN299) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEASE COMPLEXED WITH AC- NSFSQ-H (SOAKING) | 3C-LIKE PROTEINASE, PROTEASE, AC-NSFSQ-H, ACTIVE SITE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3snb:A (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEASE COMPLEXED WITH AC- DSFDQ-H (SOAKING) | 3C-LIKE PROTEINASE, PROTEASE, AC-DSFDQ-H, COVALENT BOUND, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3sne:A (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEASE COMPLEXED WITH AC- ESTLQ-H (SOAKING) | SARS CORONAVIRUS MAIN PROTEASE, 3C-LIKE PROTEINASE, PROTEASE, INHIBITOR AC-ESTLQ-H, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3fse:B (LEU165) to (GLY203) CRYSTAL STRUCTURE OF A TWO-DOMAIN PROTEIN CONTAINING DJ-1/THIJ/PFPI- LIKE AND FERRITIN-LIKE DOMAINS (AVA_4496) FROM ANABAENA VARIABILIS ATCC 29413 AT 1.90 A RESOLUTION | STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, HYDROLASE
2q1l:D (GLU489) to (ALA525) DESIGN AND SYNTHESIS OF PYRROLE-BASED, HEPATOSELECTIVE HMG-COA REDUCTASE INHIBITORS | OXIDOREDUCTASE, CHOLESTEROL BIOSYNTHESIS, HMG-COA, NADPH, STATIN
2q6c:C (THR487) to (ALA525) DESIGN AND SYNTHESIS OF NOVEL, CONFORMATIONALLY RESTRICTED HMG-COA REDUCTASE INHIBITORS | OXIDOREDUCTASE, CHOLESTEROL BIOSYNTHESIS, HMG-COA, NADPH, STATIN
2q6f:A (THR250) to (VAL301) CRYSTAL STRUCTURE OF INFECTIOUS BRONCHITIS VIRUS (IBV) MAIN PROTEASE IN COMPLEX WITH A MICHAEL ACCEPTOR INHIBITOR N3 | CORONAVIRUS; IBV; MAIN PROTEASE; 3C-LIKE PROTEINASE; MICHAEL ACCEPTOR INHIBITOR, HYDROLASE
2q6f:B (THR199) to (GLY260) CRYSTAL STRUCTURE OF INFECTIOUS BRONCHITIS VIRUS (IBV) MAIN PROTEASE IN COMPLEX WITH A MICHAEL ACCEPTOR INHIBITOR N3 | CORONAVIRUS; IBV; MAIN PROTEASE; 3C-LIKE PROTEINASE; MICHAEL ACCEPTOR INHIBITOR, HYDROLASE
2q6g:A (LEU250) to (GLY302) CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE H41A MUTANT IN COMPLEX WITH AN N-TERMINAL SUBSTRATE | CORONAVIRUS; SARS-COV; MAIN PROTEASE; 3C-LIKE PROTEINASE;SUBSTRATE, HYDROLASE
2q6g:B (THR201) to (LEU250) CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE H41A MUTANT IN COMPLEX WITH AN N-TERMINAL SUBSTRATE | CORONAVIRUS; SARS-COV; MAIN PROTEASE; 3C-LIKE PROTEINASE;SUBSTRATE, HYDROLASE
2q6g:B (LEU250) to (GLY302) CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE H41A MUTANT IN COMPLEX WITH AN N-TERMINAL SUBSTRATE | CORONAVIRUS; SARS-COV; MAIN PROTEASE; 3C-LIKE PROTEINASE;SUBSTRATE, HYDROLASE
2qc2:A (LEU250) to (GLY302) CRYSTAL STRUCTURE OF SEVERE ACUTE RESPIRATORY SYNDROME (SARS) 3C-LIKE PROTEASE ASN214ALA MUTANT | HYDROLASE
2qc2:B (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SEVERE ACUTE RESPIRATORY SYNDROME (SARS) 3C-LIKE PROTEASE ASN214ALA MUTANT | HYDROLASE
3szn:A (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEASE COMPLEXED WITH AN ALPHA, BETA-UNSATURATED ETHYL ESTER SG75 | SARS CORONAVIRUS MAIN PROTEASE, PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2qi9:A (PHE255) to (LYS323) ABC-TRANSPORTER BTUCD IN COMPLEX WITH ITS PERIPLASMIC BINDING PROTEIN BTUF | INNER MEMBRANE, MEMBRANE, TRANSMEMBRANE, TRANSPORT, ATP- BINDING, HYDROLASE, NUCLEOTIDE-BINDING, PERIPLASM, MEMBRANE PROTEIN
2qiq:A (GLY251) to (SER301) STRUCTURE-BASED DESIGN AND SYNTHESIS AND BIOLOGICAL EVALUATION OF PEPTIDOMIMETIC SARS-3CLPRO INHIBITORS | HYDROLASE, VIRAL PROTEIN
4xsx:E (ASN15) to (GLU79) CRYSTAL STRUCTURE OF CBR 703 BOUND TO ESCHERICHIA COLI RNA POLYMERASE HOLOENZYME | BACTERIAL RNA POLYMERASE ANTIBIOTIC COMPLEX, TRANSCRIPTION-ANTIBIOTIC COMPLEX
4xsx:K (ASN15) to (ALA78) CRYSTAL STRUCTURE OF CBR 703 BOUND TO ESCHERICHIA COLI RNA POLYMERASE HOLOENZYME | BACTERIAL RNA POLYMERASE ANTIBIOTIC COMPLEX, TRANSCRIPTION-ANTIBIOTIC COMPLEX
1dik:A (ASN768) to (VAL808) PYRUVATE PHOSPHATE DIKINASE | TRANSFERASE, KINASE, PHOSPHOTRANSFERASE
4xsy:E (ASN15) to (GLU79) CRYSTAL STRUCTURE OF CBR 9379 BOUND TO ESCHERICHIA COLI RNA POLYMERASE HOLOENZYME | BACTERIAL RNA POLYMERASE ANTIBIOTIC COMPLEX, TRANSCRIPTION-ANTIBIOTIC COMPLEX
4xsy:K (ASN15) to (ALA78) CRYSTAL STRUCTURE OF CBR 9379 BOUND TO ESCHERICHIA COLI RNA POLYMERASE HOLOENZYME | BACTERIAL RNA POLYMERASE ANTIBIOTIC COMPLEX, TRANSCRIPTION-ANTIBIOTIC COMPLEX
4iq4:A (ASP155) to (TRP205) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS, TRIPLE MUTANT, P21212 FORM | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRIC OLIGOMERIC DOMAINS, BIOMATERIALS, OXIDOREDUCTASE
4iq4:B (ASP155) to (TRP205) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS, TRIPLE MUTANT, P21212 FORM | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRIC OLIGOMERIC DOMAINS, BIOMATERIALS, OXIDOREDUCTASE
4iq4:C (ASP155) to (TRP205) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS, TRIPLE MUTANT, P21212 FORM | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRIC OLIGOMERIC DOMAINS, BIOMATERIALS, OXIDOREDUCTASE
1pi5:B (ALA98) to (TRP138) STRUCTURE OF N289A MUTANT OF AMPC IN COMPLEX WITH SM2, CARBOXYPHENYLGLYCYLBORONIC ACID BEARING THE CEPHALOTHIN R1 SIDE CHAIN | CRYSTAL STRUCTURE, ENZYME INHIBITOR COMPLEX, BETA-LACTAMASE, HYDROLASE
4xsz:E (ASN15) to (ALA78) CRYSTAL STRUCTURE OF CBR 9393 BOUND TO ESCHERICHIA COLI RNA POLYMERASE HOLOENZYME | BACTERIAL RNA POLYMERASE ANTIBIOTIC COMPLEX, TRANSCRIPTION-ANTIBIOTIC COMPLEX
4xsz:K (ASN15) to (ALA78) CRYSTAL STRUCTURE OF CBR 9393 BOUND TO ESCHERICHIA COLI RNA POLYMERASE HOLOENZYME | BACTERIAL RNA POLYMERASE ANTIBIOTIC COMPLEX, TRANSCRIPTION-ANTIBIOTIC COMPLEX
2qr1:G (MET74) to (GLY113) CRYSTAL STRUCTURE OF THE ADENYLATE SENSOR FROM AMP-ACTIVATED PROTEIN KINASE IN COMPLEX WITH ADP | AMPK, ADP, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, SERINE/THREONINE- PROTEIN KINASE, TRANSFERASE, CBS DOMAIN
2qrc:G (MET74) to (GLY113) CRYSTAL STRUCTURE OF THE ADENYLATE SENSOR FROM AMP-ACTIVATED PROTEIN KINASE IN COMPLEX WITH ADP AND AMP | AMPK, ADP, AMP, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, CBS DOMAIN
3gid:A (HIS589) to (GLY624) THE BIOTIN CARBOXYLASE (BC) DOMAIN OF HUMAN ACETYL-COA CARBOXYLASE 2 (ACC2) IN COMPLEX WITH SORAPHEN A | ATP BINDING, CARBOXYLASE, ATP-BINDING, BIOTIN, FATTY ACID BIOSYNTHESIS, LIGASE, LIPID SYNTHESIS, MANGANESE, MEMBRANE, METAL- BINDING, MULTIFUNCTIONAL ENZYME, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN
4ixj:A (GLY117) to (TYR176) THE STRUCTURE OF PILJ, A TYPE IV PILIN FROM CLOSTRIDIUM DIFFICILE | FILAMENT FORMATION, CELL ADHESION
2d2d:A (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS-COV MPRO IN COMPLEX WITH AN INHIBITOR I2 | ANTI-PARALLEL B-BARREL, ANTI-PARALLEL A-HELICES, HYDROLASE
2d2d:B (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS-COV MPRO IN COMPLEX WITH AN INHIBITOR I2 | ANTI-PARALLEL B-BARREL, ANTI-PARALLEL A-HELICES, HYDROLASE
1py2:A (SER6) to (LEU63) STRUCTURE OF A 60 NM SMALL MOLECULE BOUND TO A HOT SPOT ON IL-2 | IL-2, INTERLEUKIN 2, SMALL MOLECULE, HOT SPOT, MOLECULAR RECOGNITION, IMMUNE SYSTEM
1py2:C (LYS8) to (LEU63) STRUCTURE OF A 60 NM SMALL MOLECULE BOUND TO A HOT SPOT ON IL-2 | IL-2, INTERLEUKIN 2, SMALL MOLECULE, HOT SPOT, MOLECULAR RECOGNITION, IMMUNE SYSTEM
1py2:D (SER6) to (LEU63) STRUCTURE OF A 60 NM SMALL MOLECULE BOUND TO A HOT SPOT ON IL-2 | IL-2, INTERLEUKIN 2, SMALL MOLECULE, HOT SPOT, MOLECULAR RECOGNITION, IMMUNE SYSTEM
1q2w:A (GLY251) to (SER301) X-RAY CRYSTAL STRUCTURE OF THE SARS CORONAVIRUS MAIN PROTEASE | SARS-COV MAIN PROTEASE, THREE DOMAIN PROTEIN (TWO ANTIPARALLEL BETA BARRELS, ONE ALPHA HELICAL), HYDROLASE
1q2w:B (GLY251) to (SER301) X-RAY CRYSTAL STRUCTURE OF THE SARS CORONAVIRUS MAIN PROTEASE | SARS-COV MAIN PROTEASE, THREE DOMAIN PROTEIN (TWO ANTIPARALLEL BETA BARRELS, ONE ALPHA HELICAL), HYDROLASE
3tit:A (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEASE COMPLEXED WITH AN ALPHA, BETA-UNSATURATED ETHYL ESTER SG81 | SARS CORONAVIRUS MAIN PROTEASE, PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3tiu:A (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEASE COMPLEXED WITH AN ALPHA,BETA-UNSATURATED ETHYL ESTER INHIBITOR SG82 | CORONAVIRUS MAIN PROTEASE, PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4jdx:C (SER10) to (ILE74) STRUCTURE OF THE FLUORESCENCE RECOVERY PROTEIN FROM SYNECHOCYSTIS SP PCC 6803 | PHOTOPROTECTION, NON-PHOTOCHEMICAL QUENCHING, PROTEIN BINDING
3tlo:B (SER201) to (THR255) CRYSTAL STRUCTURE OF HCOV-NL63 3C-LIKE PROTEASE | HYDROLYSIS, HYDROLASE, PROTEIN BINDING
3tns:A (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEASE COMPLEXED WITH AN ALPHA, BETA-UNSATURATED ETHYL ESTER INHIBITOR SG83 | 3C-LIKE PROTEASE, PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3tnt:A (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEASE COMPLEXED WITH AN ALPHA, BETA-UNSATURATED ETHYL ESTER INHIBITOR SG85 | 3C-LIKE PROTEASE, PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2rcx:B (ALA98) to (TRP138) AMPC BETA-LACTAMASE IN COMPLEX WITH (1R)-1-(2-THIOPHEN-2-YL- ACETYLAMINO)-1-(3-(2-CARBOXYVINYL)-PHENYL) METHYLBORONIC ACID | AMPC, BETA-LACTAMASE, CEPHALOSPORINASE, SERINE HYDROLASE, ANTIBIOTIC RESISTANCE, PERIPLASM
4ydh:C (LEU35) to (PHE74) THE STRUCTURE OF HUMAN FMNL1 N-TERMINAL DOMAINS BOUND TO CDC42 | ACTIN CYTOSKELETON, GTPASE, FORMIN, SIGNALING PROTEIN
4jk1:E (ARG16) to (LEU80) X-RAY CRYSTAL STRUCTURE OF ESCHERICHIA COLI SIGMA70 HOLOENZYME IN COMPLEX WITH GUANOSINE TETRAPHOSPHATE (PPGPP) | TRANSCRIPTION, DNA, TRANSFERASE
4jk1:J (ARG16) to (ALA77) X-RAY CRYSTAL STRUCTURE OF ESCHERICHIA COLI SIGMA70 HOLOENZYME IN COMPLEX WITH GUANOSINE TETRAPHOSPHATE (PPGPP) | TRANSCRIPTION, DNA, TRANSFERASE
4jk2:E (ARG16) to (LEU80) X-RAY CRYSTAL STRUCTURE OF ESCHERICHIA COLI SIGMA70 HOLOENZYME IN COMPLEX WITH GUANOSINE PENTAPHOSPHATE (PPPGPP) | TRANSCRIPTION, DNA, TRANSFERASE
4yfk:E (ASN15) to (GLU79) ESCHERICHIA COLI RNA POLYMERASE IN COMPLEX WITH SQUARAMIDE COMPOUND 8. | SWITCH REGION, SQUARAMIDE, TRANSCRIPTION-INHIBITOR COMPLEX, TRANSCRIPTION-TRANSCRIPTION INHIBITOR COMPLEX
4yfk:K (ARG16) to (ALA78) ESCHERICHIA COLI RNA POLYMERASE IN COMPLEX WITH SQUARAMIDE COMPOUND 8. | SWITCH REGION, SQUARAMIDE, TRANSCRIPTION-INHIBITOR COMPLEX, TRANSCRIPTION-TRANSCRIPTION INHIBITOR COMPLEX
3h0q:A (ALA2118) to (ASN2178) CRYSTAL STRUCTURE OF THE CARBOXYLTRANSFERASE DOMAIN OF ACETYL-COENZYME A CARBOXYLASE IN COMPLEX WITH COMPOUND 3 | TRANSFERASE, ACETYL-COA CARBOXYLASE, CARBOXYLTRANSFERASE, INHIBITOR, LIGASE
4jkr:E (ASN15) to (GLU79) CRYSTAL STRUCTURE OF E. COLI RNA POLYMERASE IN COMPLEX WITH PPGPP | RNA POLYMERASE, TRANSCRIPTION REGULATION, TRANSCRIPTION, TRANSFERASE
4jkr:K (ASN15) to (GLU79) CRYSTAL STRUCTURE OF E. COLI RNA POLYMERASE IN COMPLEX WITH PPGPP | RNA POLYMERASE, TRANSCRIPTION REGULATION, TRANSCRIPTION, TRANSFERASE
4yfn:E (ARG16) to (GLU79) ESCHERICHIA COLI RNA POLYMERASE IN COMPLEX WITH SQUARAMIDE COMPOUND 14 (N-[3,4-DIOXO-2-(4-{[4-(TRIFLUOROMETHYL)BENZYL]AMINO}PIPERIDIN-1-YL) CYCLOBUT-1-EN-1-YL]-3,5-DIMETHYL-1,2-OXAZOLE-4-SULFONAMIDE) | SWITCH REGION, SQUARAMIDE, TRANSCRIPTION-TRANSCRIPTION INHIBITOR COMPLEX
4yfn:K (ARG16) to (ALA78) ESCHERICHIA COLI RNA POLYMERASE IN COMPLEX WITH SQUARAMIDE COMPOUND 14 (N-[3,4-DIOXO-2-(4-{[4-(TRIFLUOROMETHYL)BENZYL]AMINO}PIPERIDIN-1-YL) CYCLOBUT-1-EN-1-YL]-3,5-DIMETHYL-1,2-OXAZOLE-4-SULFONAMIDE) | SWITCH REGION, SQUARAMIDE, TRANSCRIPTION-TRANSCRIPTION INHIBITOR COMPLEX
4yfx:E (ASN15) to (GLU79) ESCHERICHIA COLI RNA POLYMERASE IN COMPLEX WITH MYXOPYRONIN B | SWITCH REGION, SQUARAMIDE, TRANSCRIPTION-TRANSCRIPTION INHIBITOR COMPLEX
4yfx:K (ASP18) to (LEU80) ESCHERICHIA COLI RNA POLYMERASE IN COMPLEX WITH MYXOPYRONIN B | SWITCH REGION, SQUARAMIDE, TRANSCRIPTION-TRANSCRIPTION INHIBITOR COMPLEX
4yg2:E (ASN15) to (GLU79) X-RAY CRYSTAL STRUCTUR OF ESCHERICHIA COLI RNA POLYMERASE SIGMA70 HOLOENZYME | RNA POLYMERASE, TRANSFERASE-TRANSCRIPTION COMPLEX
4yg2:K (ASN15) to (ALA78) X-RAY CRYSTAL STRUCTUR OF ESCHERICHIA COLI RNA POLYMERASE SIGMA70 HOLOENZYME | RNA POLYMERASE, TRANSFERASE-TRANSCRIPTION COMPLEX
3u1v:B (GLY237) to (SER293) X-RAY STRUCTURE OF DE NOVO DESIGN CYSTEINE ESTERASE FR29, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET OR52 | STRUCTURAL GENOMICS, PSI-BIOLOGY, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, FR29, DE NOVO DESIGN, UNKNOWN FUNCTION
3u1v:C (PRO236) to (GLU292) X-RAY STRUCTURE OF DE NOVO DESIGN CYSTEINE ESTERASE FR29, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET OR52 | STRUCTURAL GENOMICS, PSI-BIOLOGY, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, FR29, DE NOVO DESIGN, UNKNOWN FUNCTION
1qvn:A (SER4) to (LEU63) STRUCTURE OF SP4160 BOUND TO IL-2 V69A | IL-2 SMALL MOLECULE HOT SPOT, CYTOKINE
3hbj:A (THR158) to (LEU211) STRUCTURE OF UGT78G1 COMPLEXED WITH UDP | GLYCOSYLTRANSFERASE, GT-B FOLD, GT1, PHENYLPROPANOID METABOLISM, TRANSFERASE
4jxg:B (ALA98) to (TRP138) CRYSTAL STRUCTURE OF AMPC BETA-LACTAMASE FROM E. COLI IN COMPLEX WITH OXACILLIN | CEPHALOSPORINASE, BETA-LACTAMASE, SERINE HYDROLASE, ACYL-ENZYME COMPLEX, HYDROLASE-ANTIBIOTIC COMPLEX
1fcm:A (ALA95) to (GLN133) CRYSTAL STRUCTURE OF THE E.COLI AMPC BETA-LACTAMASE MUTANT Q120L/Y150E COVALENTLY ACYLATED WITH THE INHIBITORY BETA-LACTAM, CLOXACILLIN | BETA-LACTAMASE BETA-LACTAM COMPLEX, ENZYME INHIBITOR COMPLEX, HYDROLASE-ANTIBIOTIC COMPLEX
4jym:A (TYR150) to (SER196) CRYSTAL STRUCTURE OF KAI2 IN COMPLEX WITH 3-METHYL-2H-FURO[2,3- C]PYRAN-2-ONE | ALPHA/BETA-HYDROLASE, HYDROLASE
4jym:B (TYR150) to (SER196) CRYSTAL STRUCTURE OF KAI2 IN COMPLEX WITH 3-METHYL-2H-FURO[2,3- C]PYRAN-2-ONE | ALPHA/BETA-HYDROLASE, HYDROLASE
1fco:B (ALA95) to (TRP135) CRYSTAL STRUCTURE OF THE E. COLI AMPC BETA-LACTAMASE COVALENTLY ACYLATED WITH THE INHIBITORY BETA-LACTAM, MOXALACTAM | BETA-LACTAMASE BETA-LACTAM COMPLEX, ENZYME INHIBITOR COMPLEX, HYDROLASE
4jyp:A (TYR150) to (GLN195) CRYSTAL STRUCTURE OF KAI2 APO FORM | ALPHA/BETA HYDROLASE, HYDROLASE
4jyp:B (TYR150) to (GLN195) CRYSTAL STRUCTURE OF KAI2 APO FORM | ALPHA/BETA HYDROLASE, HYDROLASE
4ylu:A (SER204) to (THR258) X-RAY STRUCTURE OF MERS-COV NSP5 PROTEASE BOUND WITH A NON-COVALENT INHIBITOR | PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ylu:B (GLN249) to (GLN299) X-RAY STRUCTURE OF MERS-COV NSP5 PROTEASE BOUND WITH A NON-COVALENT INHIBITOR | PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ylu:C (SER204) to (THR258) X-RAY STRUCTURE OF MERS-COV NSP5 PROTEASE BOUND WITH A NON-COVALENT INHIBITOR | PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ylu:D (THR248) to (GLY302) X-RAY STRUCTURE OF MERS-COV NSP5 PROTEASE BOUND WITH A NON-COVALENT INHIBITOR | PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4yo9:A (THR204) to (THR258) HKU4 3CLPRO UNBOUND STRUCTURE | HKU4 3CLPRO MPRO NSP5, HYDROLASE
4yo9:B (THR204) to (THR258) HKU4 3CLPRO UNBOUND STRUCTURE | HKU4 3CLPRO MPRO NSP5, HYDROLASE
4yoi:A (THR204) to (THR258) STRUCTURE OF HKU4 3CLPRO BOUND TO NON-COVALENT INHIBITOR 1A | HKU4 3CLPRO MPRO NSP5, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4yoi:B (THR204) to (THR258) STRUCTURE OF HKU4 3CLPRO BOUND TO NON-COVALENT INHIBITOR 1A | HKU4 3CLPRO MPRO NSP5, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4yoj:A (THR204) to (THR258) HKU4 3CLPRO BOUND TO NON-COVALENT INHIBITOR 2A | HKU4 3CLPRO MPRO NSP5, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4yoj:B (THR204) to (THR258) HKU4 3CLPRO BOUND TO NON-COVALENT INHIBITOR 2A | HKU4 3CLPRO MPRO NSP5, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3ubm:C (ASP295) to (MET324) FORMYL-COA:OXALATE COA-TRANSFERASE FROM ACETOBACTER ACETI | TRANSFERASE
2v6n:A (GLY251) to (GLN299) CRYSTAL STRUCTURES OF THE SARS-CORONAVIRUS MAIN PROTEINASE INACTIVATED BY BENZOTRIAZOLE COMPOUNDS | THIOL PROTEASE, RNA REPLICATION, MAIN PROTEINASE, RIBOSOMAL FRAMESHIFT, SARS, PROTEASE, HYDROLASE, POLYPROTEIN, VIRAL PROTEIN
1fsw:B (ALA98) to (TRP138) AMPC BETA-LACTAMASE FROM E. COLI COMPLEXED WITH INHIBITOR CEPHALOTHINBORONIC ACID | CEPHALOSPORINASE, BETA-LACTAMASE, SERINE HYDROLASE, HYDROLASE
1rrl:B (GLU663) to (GLY721) SOYBEAN LIPOXYGENASE (LOX-3) AT 93K AT 2.0 A RESOLUTION | OXIDOREDUCTASE, IRON METALLOPROTEIN, LIPOXYGENASE
1rwt:J (PRO170) to (PHE228) CRYSTAL STRUCTURE OF SPINACH MAJOR LIGHT-HARVESTING COMPLEX AT 2.72 ANGSTROM RESOLUTION | LIGHT-HARVESTING COMPLEX, MEMBRANE PROTEIN, PLANT, PHOTOSYNTHESIS
1g6h:A (PRO91) to (LYS121) CRYSTAL STRUCTURE OF THE ADP CONFORMATION OF MJ1267, AN ATP- BINDING CASSETTE OF AN ABC TRANSPORTER | BETA-CORE DOMAIN, ABC SPECIFIC-BETA-STRAND DOMAIN ALPHA- HELIX DOMAIN, TRANSPORT PROTEIN
2ffy:B (ALA98) to (TRP138) AMPC BETA-LACTAMASE N289A MUTANT IN COMPLEX WITH A BORONIC ACID DEACYLATION TRANSITION STATE ANALOG COMPOUND SM3 | AMPC; BETA-LACTAMASE; DEACYLATION; TRANSITION STATE; BORONIC ACID, HYDROLASE
2vj1:A (GLY251) to (GLN299) A STRUCTURAL VIEW OF THE INACTIVATION OF THE SARS- CORONAVIRUS MAIN PROTEINASE BY BENZOTRIAZOLE ESTERS | SARS, PROTEASE, HYDROLASE, POLYPROTEIN, THIOL PROTEASE, RIBOSOMAL FRAMESHIFT, SARS CORONAVIRUS MAIN PROTEINASE
2vj1:B (GLY251) to (ARG298) A STRUCTURAL VIEW OF THE INACTIVATION OF THE SARS- CORONAVIRUS MAIN PROTEINASE BY BENZOTRIAZOLE ESTERS | SARS, PROTEASE, HYDROLASE, POLYPROTEIN, THIOL PROTEASE, RIBOSOMAL FRAMESHIFT, SARS CORONAVIRUS MAIN PROTEINASE
1gd5:A (ARG45) to (SER105) SOLUTION STRUCTURE OF THE PX DOMAIN FROM HUMAN P47PHOX NADPH OXIDASE | ALPHA BETA,P47-PHOX,PX DOMAIN, PROTEIN BINDING
4kmu:E (ARG16) to (LEU80) X-RAY CRYSTAL STRUCTURE OF THE ESCHERICHIA COLI RNA POLYMERASE IN COMPLEX WITH RIFAMPIN | TRANSCRIPTION, DNA, RNA, TRANSFERASE-ANTIBIOTIC COMPLEX
4kn4:E (ASN15) to (LEU80) X-RAY CRYSTAL STRUCTURE OF THE ESCHERICHIA COLI RNA POLYMERASE IN COMPLEX WITH BENZOXAZINORIFAMYCIN-2B | TRANSCRIPTION, DNA, RNA, TRANSFERASE-ANTIBIOTIC COMPLEX
2fsg:A (ASP592) to (VAL669) COMPLEX SECA:ATP FROM ESCHERICHIA COLI | ATPASE, DNA-RNA HELICASE, PROTEIN TRANSLOCATION, SECA, PROTEIN TRANSPORT
3v3m:A (GLY251) to (GLN299) SEVERE ACUTE RESPIRATORY SYNDROME CORONAVIRUS (SARS-COV) 3CL PROTEASE IN COMPLEX WITH N-[(1R)-2-(TERT-BUTYLAMINO)-2-OXO-1-(PYRIDIN-3-YL) ETHYL]-N-(4-TERT-BUTYLPHENYL)FURAN-2-CARBOXAMIDE INHIBITOR. | CHYMOTRYPSIN LIKE FOLD, VIRAL POLYPEPTIDE PROTEASE, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4zh2:E (ASN15) to (GLU79) CRYSTAL STRUCTURE OF ESCHERICHIA COLI RNA POLYMERASE IN COMPLEX WITH CBR703 | RNA POLYMERASE, INHIBITOR, TRANSCRIPTION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4zh2:K (ASN15) to (ALA78) CRYSTAL STRUCTURE OF ESCHERICHIA COLI RNA POLYMERASE IN COMPLEX WITH CBR703 | RNA POLYMERASE, INHIBITOR, TRANSCRIPTION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4zh3:E (ASN15) to (GLU79) CRYSTAL STRUCTURE OF ESCHERICHIA COLI RNA POLYMERASE IN COMPLEX WITH CBRH16-BR | RNA POLYMERASE, INHIBITOR, TRANSCRIPTION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4zh3:K (ASN15) to (ALA78) CRYSTAL STRUCTURE OF ESCHERICHIA COLI RNA POLYMERASE IN COMPLEX WITH CBRH16-BR | RNA POLYMERASE, INHIBITOR, TRANSCRIPTION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4zh4:E (ASN15) to (GLU79) CRYSTAL STRUCTURE OF ESCHERICHIA COLI RNA POLYMERASE IN COMPLEX WITH CBRP18 | RNA POLYMERASE, INHIBITOR, TRANSCRIPTION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4zh4:K (ASN15) to (ALA78) CRYSTAL STRUCTURE OF ESCHERICHIA COLI RNA POLYMERASE IN COMPLEX WITH CBRP18 | RNA POLYMERASE, INHIBITOR, TRANSCRIPTION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
3vb4:B (GLY251) to (GLY302) CRYSTAL STRUCTURE OF SARS-COV 3C-LIKE PROTEASE WITH B4Z | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3vb5:B (LEU250) to (GLY302) CRYSTAL STRUCTURE OF SARS-COV 3C-LIKE PROTEASE WITH C4Z | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3vb6:A (GLY251) to (SER301) CRYSTAL STRUCTURE OF SARS-COV 3C-LIKE PROTEASE WITH C6Z | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3vb6:B (GLY251) to (GLY302) CRYSTAL STRUCTURE OF SARS-COV 3C-LIKE PROTEASE WITH C6Z | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3vb7:A (GLY251) to (SER301) CRYSTAL STRUCTURE OF SARS-COV 3C-LIKE PROTEASE WITH M4Z | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3vb7:B (GLY251) to (GLY302) CRYSTAL STRUCTURE OF SARS-COV 3C-LIKE PROTEASE WITH M4Z | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2gaf:D (ASN12) to (PHE47) CRYSTAL STRUCTURE OF THE VACCINIA POLYADENYLATE POLYMERASE HETERODIMER (APO FORM) | POLYADENYLATE POLYMERASE, POX VIRUS, NUCLEOTIDYLTRANSFERASE, HETERODIMER, PROCESSIVITY
4kxc:A (TRP408) to (SER472) CRYSTAL STRUCTURE OF HUMAN AMINOPEPTIDASE A COMPLEXED WITH GLUTAMATE | ZINC-AMINOPEPTIDASE, HYDROLASE
4kz9:B (ALA98) to (TRP138) CRYSTAL STRUCTURE OF AMPC BETA-LACTAMASE IN COMPLEX WITH FRAGMENT 41 ((4R,4AS,8AS)-4-PHENYLDECAHYDROQUINOLIN-4-OL) | AMPC BETA-LACTAMASE, CLASS C, HYDROLASE, CEPHALOSPORINASE
4kza:B (ALA98) to (TRP138) CRYSTAL STRUCTURE OF AMPC BETA-LACTAMASE IN COMPLEX WITH FRAGMENT 48 (3-(CYCLOPROPYLSULFAMOYL)THIOPHENE-2-CARBOXYLIC ACID) | AMPC BETA-LACTAMASE, CLASS C, HYDROLASE, CEPHALOSPORINASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
2gt7:A (GLY251) to (GLY302) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PEPTIDASE AT PH 6.0 IN THE SPACE GROUP P21 | CYSTEINE PEPTIDASE, 3C-LIKE, N-FINGER, CHYMOTRYPSIN-LIKE FOLD, LONG LOOP, ALPHA-HELICAL DOMAIN, DIMER, CATALYTIC DYAD, SPECIFICITY POCKETS, HYDROLASE
2gt7:B (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PEPTIDASE AT PH 6.0 IN THE SPACE GROUP P21 | CYSTEINE PEPTIDASE, 3C-LIKE, N-FINGER, CHYMOTRYPSIN-LIKE FOLD, LONG LOOP, ALPHA-HELICAL DOMAIN, DIMER, CATALYTIC DYAD, SPECIFICITY POCKETS, HYDROLASE
2gtb:A (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PEPTIDASE (WITH AN ADDITIONAL ALA AT THE N-TERMINUS OF EACH PROTOMER) INHIBITED BY AN AZA-PEPTIDE EPOXIDE IN THE SPACE GROUP P43212 | CYSTEINE PEPTIDASE, 3C-LIKE, N-FINGER, CHYMOTRYPSIN-LIKE FOLD, LONG LOOP, ALPHA-HELICAL DOMAIN, DIMER, CATALYTIC DYAD, SPECIFICITY POCKETS, HYDROLASE
2gz7:A (GLY251) to (GLN299) STRUCTURE-BASED DRUG DESIGN AND STRUCTURAL BIOLOGY STUDY OF NOVEL NONPEPTIDE INHIBITORS OF SARS-COV MAIN PROTEASE | SARS COV MAIN PROTEASE, HYDROLASE
2gz8:A (GLY251) to (GLN299) STRUCTURE-BASED DRUG DESIGN AND STRUCTURAL BIOLOGY STUDY OF NOVEL NONPEPTIDE INHIBITORS OF SARS-COV MAIN PROTEASE | SARS COV MAIN PROTEASE, HYDROLASE
2gz9:A (GLY251) to (GLN299) STRUCTURE-BASED DRUG DESIGN AND STRUCTURAL BIOLOGY STUDY OF NOVEL NONPEPTIDE INHIBITORS OF SARS-COV MAIN PROTEASE | SARS COV MAIN PROTEASE, HYDROLASE
4zuh:A (THR200) to (THR254) COMPLEX STRUCTURE OF PEDV 3CLPRO MUTANT (C144A) WITH A PEPTIDE SUBSTRATE. | 3C-LIKE PROTEASE, HYDROLASE-PEPTIDE COMPLEX
4zuh:B (THR200) to (THR254) COMPLEX STRUCTURE OF PEDV 3CLPRO MUTANT (C144A) WITH A PEPTIDE SUBSTRATE. | 3C-LIKE PROTEASE, HYDROLASE-PEPTIDE COMPLEX
4ljz:E (ASN15) to (GLU79) CRYSTAL STRUCTURE ANALYSIS OF THE E.COLI HOLOENZYME | DNA DIRECTED RNA POLYMERASE, TRANSFERASE
4ljz:K (ASN15) to (ALA78) CRYSTAL STRUCTURE ANALYSIS OF THE E.COLI HOLOENZYME | DNA DIRECTED RNA POLYMERASE, TRANSFERASE
4lk0:E (ARG16) to (GLU79) CRYSTAL STRUCTURE ANALYSIS OF THE E.COLI HOLOENZYME/T7 GP2 COMPLEX | DNA DIRECTED RNA POLYMERASE, TRANSFERASE
4lk0:K (ARG16) to (LEU80) CRYSTAL STRUCTURE ANALYSIS OF THE E.COLI HOLOENZYME/T7 GP2 COMPLEX | DNA DIRECTED RNA POLYMERASE, TRANSFERASE
2hdu:B (ALA98) to (TRP138) AMPC BETA-LACTAMASE IN COMPLEX WITH 2-ACETAMIDOTHIOPHENE-3- CARBOXYLIC ACID | AMPC BETA-LACTAMASE FRAGMENT-BASED DRUG DESIGN, HYDROLASE
4lk1:E (ASN15) to (GLU79) CRYSTAL STRUCTURE ANALYSIS OF THE E.COLI HOLOENZYME | TRANSFERASE
4lk1:K (ASN15) to (ALA78) CRYSTAL STRUCTURE ANALYSIS OF THE E.COLI HOLOENZYME | TRANSFERASE
3iwm:B (GLY251) to (CYS300) THE OCTAMERIC SARS-COV MAIN PROTEASE | SARS-COV, MAIN PROTEASE, OCTAMER, ACTIVE CONFORMATION, HYDROLASE
3iwm:C (LEU250) to (CYS300) THE OCTAMERIC SARS-COV MAIN PROTEASE | SARS-COV, MAIN PROTEASE, OCTAMER, ACTIVE CONFORMATION, HYDROLASE
3iwm:D (GLY251) to (CYS300) THE OCTAMERIC SARS-COV MAIN PROTEASE | SARS-COV, MAIN PROTEASE, OCTAMER, ACTIVE CONFORMATION, HYDROLASE
3iwo:B (ALA98) to (TRP138) X-RAY CRYSTAL STRUCTURE OF THE EXTENDED-SPECTRUM AMPC Y221G MUTANT BETA-LACTAMASE AT 1.90 ANGSTROM RESOLUTION | SERINE HYDROLASE, BETA-LACTAMASE, CEPHALOSPORINASE, EXTENDED-SPECTRUM ANTIBIOTIC RESISTANCE, ANTIBIOTIC RESISTANCE, HYDROLASE, PERIPLASM
3ixb:B (ALA98) to (TRP138) X-RAY CRYSTAL STRUCTURE OF THE EXTENDED-SPECTRUM AMPC E219K MUTANT BETA-LACTAMASE COMPLEXED WITH BENZO(B)THIOPHENE-2- BORONIC ACID (BZB) AT 1.63 ANGSTROM RESOLUTION | SERINE HYDROLASE, BETA-LACTAMASE, CEPHALOSPORINASE, EXTENDED-SPECTRUM ANTIBIOTIC RESISTANCE, ANTIBIOTIC RESISTANCE, HYDROLASE, PERIPLASM
4llg:E (ARG16) to (GLU79) CRYSTAL STRUCTURE ANALYSIS OF THE E.COLI HOLOENZYME/GP2 COMPLEX | TRANSFERASE
4llg:K (ARG16) to (ALA78) CRYSTAL STRUCTURE ANALYSIS OF THE E.COLI HOLOENZYME/GP2 COMPLEX | TRANSFERASE
1hw9:D (THR487) to (ALA525) COMPLEX OF THE CATALYTIC PORTION OF HUMAN HMG-COA REDUCTASE WITH SIMVASTATIN | PROTEIN-INHIBITOR COMPLEX, OXIDOREDUCTASE
1hwk:D (THR487) to (ALA525) COMPLEX OF THE CATALYTIC PORTION OF HUMAN HMG-COA REDUCTASE WITH ATORVASTATIN | PROTEIN-INHIBITOR COMPLEX, OXIDOREDUCTASE
2hob:A (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE WITH AUTHENTIC N AND C- TERMINI IN COMPLEX WITH A MICHAEL ACCEPTOR N3 | SARS-COV, MAIN PROTEASE, MICHAEL ACCEPTOR N3, VIRAL PROTEIN
3vvx:A (THR116) to (ASP169) CRYSTAL STRUCUTURE OF RAMR (TRANSCRIPTIONAL REGURATOR OF TETR FAMILY) FROM SALMONELLA TYPHIMURIUM | TETR TRANSCRIPTIONAL REGULATOR FAMILY, HTH-MOTIF, TRANSCRIPTIONAL REGURATOR, DNA BINDING, TRANSCRIPTION REGULATOR
3vvy:D (THR116) to (ASP169) CRYSTAL STRUCUTURE OF THE ETHIDIUM-BOUND FORM OF RAMR (TRANSCRIPTIONAL REGURATOR OF TETR FAMILY) FROM SALMONELLA TYPHIMURIUM | TETR TRANSCRIPTIONAL REGULATOR FAMILY, HTH-MOTIF, TRANSCRIPTIONAL REGULATOR, DNA BINDING, TRANSCRIPTION REGULATOR
3vvz:A (THR116) to (PRO170) CRYSTAL STRUCUTURE OF THE RHODAMINE 6G-BOUND FORM OF RAMR (TRANSCRIPTIONAL REGURATOR OF TETR FAMILY) FROM SALMONELLA TYPHIMURIUM | TETR TRANSCRIPTIONAL REGULATOR FAMILY, HTH-MOTIF, TRANSCRIPTIONAL REGULATOR, DNA BINDING, TRANSCRIPTION REGULATOR
3vvz:C (THR116) to (PRO170) CRYSTAL STRUCUTURE OF THE RHODAMINE 6G-BOUND FORM OF RAMR (TRANSCRIPTIONAL REGURATOR OF TETR FAMILY) FROM SALMONELLA TYPHIMURIUM | TETR TRANSCRIPTIONAL REGULATOR FAMILY, HTH-MOTIF, TRANSCRIPTIONAL REGULATOR, DNA BINDING, TRANSCRIPTION REGULATOR
3vvz:D (THR116) to (ASP169) CRYSTAL STRUCUTURE OF THE RHODAMINE 6G-BOUND FORM OF RAMR (TRANSCRIPTIONAL REGURATOR OF TETR FAMILY) FROM SALMONELLA TYPHIMURIUM | TETR TRANSCRIPTIONAL REGULATOR FAMILY, HTH-MOTIF, TRANSCRIPTIONAL REGULATOR, DNA BINDING, TRANSCRIPTION REGULATOR
3w06:A (TYR150) to (GLN195) CRYSTAL STRUCTURE OF ARABIDOPSIS THALIANA DWARF14 LIKE (ATD14L) | KARRIKIN SIGNALING, ALPHA/BETA HYDROLASE, KARRIKIN BINDING, HYDROLASE
4lv1:A (ALA98) to (ASN137) AMPC BETA-LACTAMASE IN COMPLEX WITH [1-(3-CHLOROPHENYL)-1H-PYRAZOL-4- YL] BORONIC ACID | AMPC BETA-LACTAMASE, CLASS C, HYDROLASE, BORONIC ACID, COVALENT INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4lv3:B (ALA98) to (TRP138) AMPC BETA-LACTAMASE IN COMPLEX WITH (3,5-DI-TERT-BUTYLPHENYL) BORONIC ACID | AMPC BETA-LACTAMASE, CLASS C, HYDROLASE, BORONIC ACID, COVALENT INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1iel:A (ALA98) to (TRP138) CRYSTAL STRUCTURE OF AMPC BETA-LACTAMASE FROM E. COLI IN COMPLEX WITH CEFTAZIDIME | CEPHALOSPORINASE, BETA-LACTAMASE, SERINE HYDROLASE
1uj1:A (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEINASE (3CLPRO) | ANTI-PARALLEL B-BARREL, ANTI-PARALLEL A-HELICES, HYDROLASE
1uj1:B (GLY251) to (GLY302) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEINASE (3CLPRO) | ANTI-PARALLEL B-BARREL, ANTI-PARALLEL A-HELICES, HYDROLASE
1uk2:A (THR201) to (GLY251) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEINASE (3CLPRO) AT PH8.0 | ANTI-PARALLEL B-BARREL, ANTI-PARALLEL A-HELICES, HYDROLASE
1uk2:A (GLY251) to (GLY302) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEINASE (3CLPRO) AT PH8.0 | ANTI-PARALLEL B-BARREL, ANTI-PARALLEL A-HELICES, HYDROLASE
1uk2:B (THR201) to (GLY251) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEINASE (3CLPRO) AT PH8.0 | ANTI-PARALLEL B-BARREL, ANTI-PARALLEL A-HELICES, HYDROLASE
1uk2:B (GLY251) to (ARG298) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEINASE (3CLPRO) AT PH8.0 | ANTI-PARALLEL B-BARREL, ANTI-PARALLEL A-HELICES, HYDROLASE
1uk3:A (GLY251) to (GLY302) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEINASE (3CLPRO) AT PH7.6 | ANTI-PARALLEL B-BARREL, ANTI-PARALLEL A-HELICES, HYDROLASE
1uk3:B (THR201) to (LEU250) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEINASE (3CLPRO) AT PH7.6 | ANTI-PARALLEL B-BARREL, ANTI-PARALLEL A-HELICES, HYDROLASE
1uk3:B (LEU250) to (GLN299) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEINASE (3CLPRO) AT PH7.6 | ANTI-PARALLEL B-BARREL, ANTI-PARALLEL A-HELICES, HYDROLASE
3j1e:S (THR100) to (LYS172) CRYO-EM STRUCTURE OF 9-FOLD SYMMETRIC RATCPN-BETA IN APO STATE | GROUP II CHAPERONIN, CHAPERONE
3wc2:B (LYS140) to (GLY198) CRYSTAL STRUCTURE OF C. ALBICANS TRNA(HIS) GUANYLYLTRANSFERASE (THG1) WITH A TRNA(PHE)(GUG) | TRANSFERASE-RNA COMPLEX
4mds:A (GLY251) to (SER301) DISCOVERY OF N-(BENZO[1,2,3]TRIAZOL-1-YL)-N-(BENZYL)ACETAMIDO)PHENYL) CARBOXAMIDES AS SEVERE ACUTE RESPIRATORY SYNDROME CORONAVIRUS (SARS- COV) 3CLPRO INHIBITORS: IDENTIFICATION OF ML300 AND NON-COVALENT NANOMOLAR INHIBITORS WITH AN INDUCED-FIT BINDING | CHYMOTRYPSIN-LIKE, PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4mea:A (PHE227) to (HIS270) CRYSTAL STRUCTURE OF THE CIF EPOXIDE HYDROLASE FROM ACINETOBACTER NOSOCOMIALIS | ALPHA/BETA HYDROLASE FOLD, EPOXIDE HYDROLASE, SECRETED, HYDROLASE
4mea:B (PHE227) to (SER269) CRYSTAL STRUCTURE OF THE CIF EPOXIDE HYDROLASE FROM ACINETOBACTER NOSOCOMIALIS | ALPHA/BETA HYDROLASE FOLD, EPOXIDE HYDROLASE, SECRETED, HYDROLASE
5ajd:G (GLU1570) to (GLU1629) NOT1 C-TERMINAL DOMAIN IN COMPLEX WITH NOT4 | TRANSCRIPTION, CCR4-NOT, NOT1, NOT4
1vbf:D (SER2) to (TYR38) CRYSTAL STRUCTURE OF PROTEIN L-ISOASPARTATE O-METHYLTRANSFERASE HOMOLOGUE FROM SULFOLOBUS TOKODAII | TRIMERIC COILED COIL ASSEMBLY, INTER-SUBUNIT DISULFIDE BRIDGE, PROTEIN REPAIR ENZYME, TRANSFERASE
2xoy:A (GLY542) to (GLY585) C-TERMINAL CYSTEINE-RICH DOMAIN OF HUMAN CHFR BOUND TO P(1), P(2)-DIADENOSINE-5'-PYROPHOSPHATE | LIGASE, ZINC-BINDING, PBZ, MITOSIS, ANTEPHASE CHECKPOINT
5b6o:A (GLY251) to (SER301) CRYSTAL STRUCTURE OF MS8104 | HYDROLASE, STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI
5b6o:B (GLY251) to (SER301) CRYSTAL STRUCTURE OF MS8104 | HYDROLASE, STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI
4net:A (THR101) to (ASP139) CRYSTAL STRUCTURE OF ADC-1 BETA-LACTAMASE | BETA-LACTAMASE, ANTIBIOTIC RESISTANCE, APO ENZYME, HYDROLASE
4net:B (THR101) to (TRP140) CRYSTAL STRUCTURE OF ADC-1 BETA-LACTAMASE | BETA-LACTAMASE, ANTIBIOTIC RESISTANCE, APO ENZYME, HYDROLASE
5bwk:M (LEU179) to (GLN229) 6.0 A CRYSTAL STRUCTURE OF A GET3-GET4-GET5 INTERMEDIATE COMPLEX FROM S.CEREVISIAE | TAIL-ANCHORED TARGETING, ATPASE, ELECTROSTATIC INTERACTION, HYDROLASE-TRANSPORT COMPLEX
2k7x:A (LEU250) to (GLN299) SOLUTION STRUCTURE OF C-TERMINAL DOMAIN OF SARS-COV MAIN PROTEASE | SOLUTION STRUCTURE, C-TERMINAL DOMAIN, MAIN PROTEASE, HYDROLASE
2kil:A (ILE4) to (LEU47) NMR STRUCTURE OF THE H103G MUTANT SO2144 H-NOX DOMAIN FROM SHEWANELLA ONEIDENSIS IN THE FE(II)CO LIGATION STATE | H-NOX, UNKNOWN FUNCTION
5byh:E (ARG16) to (LEU80) CRYSTAL STRUCTURE OF ESCHERICHIA COLI RNA POLYMERASE - SIGMA54 HOLOENZYME COMPLEX | SIGMA 54, RNA POLYMERASE, HOLOENZYME, TRANSCRIPTION, TRANSFERASE
2y3u:A (ASP120) to (ASN145) CRYSTAL STRUCTURE OF APO COLLAGENASE G FROM CLOSTRIDIUM HISTOLYTICUM AT 2.55 ANGSTROM RESOLUTION | HYDROLASE, GLUZINCIN, METALLOPROTEASE
1kds:B (ALA98) to (TRP138) X-RAY CRYSTAL STRUCTURE OF AMPC BETA-LACTAMASE FROM E. COLI IN COMPLEX WITH THE INHIBITOR 3-NITROPHENYLBORONIC ACID | CEPHALOSPORINASE, BETA-LACTAMASE, SERINE HYDROLASE, PHENYLBORONIC ACID INHIBITOR COMPLEX
1wof:A (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS-COV MPRO IN COMPLEX WITH AN INHIBITOR N1 | ANTI-PARALLEL B-BARREL, ANTI-PARALLEL A-HELICES, HYDROLASE
1wof:B (GLY251) to (GLY302) CRYSTAL STRUCTURE OF SARS-COV MPRO IN COMPLEX WITH AN INHIBITOR N1 | ANTI-PARALLEL B-BARREL, ANTI-PARALLEL A-HELICES, HYDROLASE
2yaz:E (ASN171) to (ASP223) THE CRYSTAL STRUCTURE OF LEISHMANIA MAJOR DUTPASE IN COMPLEX DUMP | HYDROLASE, LEISHMANIASIS
5c3n:A (SER204) to (GLY259) CRYSTAL STRUCTURE OF MERS CORONAVIRUS MAIN PROTEASE IN SPACEGROUP C2221 | MERS CORONAVIRUS, MAIN PROTEASE, 3CL PROTEASE, HYDROLASE
5c3n:B (SER204) to (GLY259) CRYSTAL STRUCTURE OF MERS CORONAVIRUS MAIN PROTEASE IN SPACEGROUP C2221 | MERS CORONAVIRUS, MAIN PROTEASE, 3CL PROTEASE, HYDROLASE
5c5n:A (GLY251) to (GLN299) STRUCTURE OF SARS-3CL PROTEASE COMPLEX WITH A PHENYL-BETA-ALANYL (R, S)-N-DECALIN TYPE INHIBITOR | HYDRASE PROTEINASE CONVERTING, DESIGNED INHIBITOR, HYDRASE-INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1kvl:B (ALA98) to (TRP138) X-RAY CRYSTAL STRUCTURE OF AMPC S64G MUTANT BETA-LACTAMASE IN COMPLEX WITH SUBSTRATE AND PRODUCT FORMS OF CEPHALOTHIN | AMIDE HYDROLASE, BETA-LACTAMASE, CEPHALOTHIN, SUBSTRATE- ENZYME COMPLEX, PRODUCT-ENZYME COMPLEX
3jcu:G (ALA172) to (PHE228) CRYO-EM STRUCTURE OF SPINACH PSII-LHCII SUPERCOMPLEX AT 3.2 ANGSTROM RESOLUTION | MEMBRANE PROTEIN
3jcu:g (ALA172) to (PHE228) CRYO-EM STRUCTURE OF SPINACH PSII-LHCII SUPERCOMPLEX AT 3.2 ANGSTROM RESOLUTION | MEMBRANE PROTEIN
1l0g:B (ALA98) to (TRP138) X-RAY CRYSTAL STRUCTURE OF AMPC S64G MUTANT BETA-LACTAMASE | AMIDE HYDROLASE, BETA-LACTAMASE, MUTANT ENZYME
2yna:A (THR204) to (THR258) CRYSTAL STRUCTURE OF THE MAIN PROTEASE OF CORONAVIRUS HKU4 | HYDROLASE, SARS
2yna:B (THR204) to (THR258) CRYSTAL STRUCTURE OF THE MAIN PROTEASE OF CORONAVIRUS HKU4 | HYDROLASE, SARS
2ynb:A (THR204) to (THR258) CRYSTAL STRUCTURE OF THE MAIN PROTEASE OF CORONAVIRUS HKU4 IN COMPLEX WITH A MICHAEL ACCEPTOR SG85 | HYDROLASE, SARS, MICHAEL ACCEPTOR
2ynb:B (THR204) to (THR258) CRYSTAL STRUCTURE OF THE MAIN PROTEASE OF CORONAVIRUS HKU4 IN COMPLEX WITH A MICHAEL ACCEPTOR SG85 | HYDROLASE, SARS, MICHAEL ACCEPTOR
5cky:O (LEU75) to (GLY115) CRYSTAL STRUCTURE OF THE MTERF1 R162A SUBSTITUTION BOUND TO THE TERMINATION SEQUENCE. | PROTEIN-DNA, TRANSCRIPTION FACTOR, MITOCHONDRIA, TERMINATION, TRANSCRIPTION-DNA COMPLEX
2z3c:A (GLY251) to (GLN299) A MECHANISTIC VIEW OF ENZYME INHIBITION AND PEPTIDE HYDROLYSIS IN THE ACTIVE SITE OF THE SARS-COV 3C-LIKE PEPTIDASE | BETA BARRELS, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2z3d:A (GLY251) to (GLN299) A MECHANISTIC VIEW OF ENZYME INHIBITION AND PEPTIDE HYDROLYSIS IN THE ACTIVE SITE OF THE SARS-COV 3C-LIKE PEPTIDASE | BETA BARRELS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2z3e:A (THR201) to (LEU250) A MECHANISTIC VIEW OF ENZYME INHIBITION AND PEPTIDE HYDROLYSIS IN THE ACTIVE SITE OF THE SARS-COV 3C-LIKE PEPTIDASE | SARS, 3C-LIKE PEPTIDASE, 3CL, MAIN PROTEINASE, VIRAL CYSTEINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, VIRAL PROTEIN
2z3e:A (LEU250) to (GLN299) A MECHANISTIC VIEW OF ENZYME INHIBITION AND PEPTIDE HYDROLYSIS IN THE ACTIVE SITE OF THE SARS-COV 3C-LIKE PEPTIDASE | SARS, 3C-LIKE PEPTIDASE, 3CL, MAIN PROTEINASE, VIRAL CYSTEINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, VIRAL PROTEIN
2z94:A (GLY251) to (GLN299) COMPLEX STRUCTURE OF SARS-COV 3C-LIKE PROTEASE WITH TDT | COMPLEX, HYDROLASE
2z9g:A (GLY251) to (GLN299) COMPLEX STRUCTURE OF SARS-COV 3C-LIKE PROTEASE WITH PMA | COMPLEX, ATP-BINDING, CYTOPLASM, ENDONUCLEASE, EXONUCLEASE, HELICASE, HYDROLASE, MEMBRANE, METAL-BINDING, NUCLEASE, NUCLEOTIDE-BINDING, NUCLEOTIDYLTRANSFERASE, PROTEASE, RIBOSOMAL FRAMESHIFT, RNA REPLICATION, RNA-BINDING, RNA- DIRECTED RNA POLYMERASE, THIOL PROTEASE, TRANSFERASE, TRANSMEMBRANE, ZINC, ZINC-FINGER
2z9j:B (GLY251) to (GLY302) COMPLEX STRUCTURE OF SARS-COV 3C-LIKE PROTEASE WITH EPDTC | COMPLEX, ATP-BINDING, CYTOPLASM, ENDONUCLEASE, EXONUCLEASE, HELICASE, HYDROLASE, MEMBRANE, METAL-BINDING, NUCLEASE, NUCLEOTIDE-BINDING, NUCLEOTIDYLTRANSFERASE, PROTEASE, RIBOSOMAL FRAMESHIFT, RNA REPLICATION, RNA-BINDING, RNA- DIRECTED RNA POLYMERASE, THIOL PROTEASE, TRANSFERASE, TRANSMEMBRANE, ZINC, ZINC-FINGER
1lvo:B (PHE247) to (GLY298) STRUCTURE OF CORONAVIRUS MAIN PROTEINASE REVEALS COMBINATION OF A CHYMOTRYPSIN FOLD WITH AN EXTRA ALPHA- HELICAL DOMAIN | 3C LIKE, CORONA, PROTEINASE, CHYMOTRYPSIN, CYSTEINE HISTIDINE DYAD, BETA BARREL, HYDROLASE
1lvo:C (PHE247) to (GLY298) STRUCTURE OF CORONAVIRUS MAIN PROTEINASE REVEALS COMBINATION OF A CHYMOTRYPSIN FOLD WITH AN EXTRA ALPHA- HELICAL DOMAIN | 3C LIKE, CORONA, PROTEINASE, CHYMOTRYPSIN, CYSTEINE HISTIDINE DYAD, BETA BARREL, HYDROLASE
1lvo:D (SER200) to (PHE247) STRUCTURE OF CORONAVIRUS MAIN PROTEINASE REVEALS COMBINATION OF A CHYMOTRYPSIN FOLD WITH AN EXTRA ALPHA- HELICAL DOMAIN | 3C LIKE, CORONA, PROTEINASE, CHYMOTRYPSIN, CYSTEINE HISTIDINE DYAD, BETA BARREL, HYDROLASE
1lvo:D (PHE247) to (GLY298) STRUCTURE OF CORONAVIRUS MAIN PROTEINASE REVEALS COMBINATION OF A CHYMOTRYPSIN FOLD WITH AN EXTRA ALPHA- HELICAL DOMAIN | 3C LIKE, CORONA, PROTEINASE, CHYMOTRYPSIN, CYSTEINE HISTIDINE DYAD, BETA BARREL, HYDROLASE
1lvo:E (SER200) to (PHE247) STRUCTURE OF CORONAVIRUS MAIN PROTEINASE REVEALS COMBINATION OF A CHYMOTRYPSIN FOLD WITH AN EXTRA ALPHA- HELICAL DOMAIN | 3C LIKE, CORONA, PROTEINASE, CHYMOTRYPSIN, CYSTEINE HISTIDINE DYAD, BETA BARREL, HYDROLASE
1lvo:E (PHE247) to (MET296) STRUCTURE OF CORONAVIRUS MAIN PROTEINASE REVEALS COMBINATION OF A CHYMOTRYPSIN FOLD WITH AN EXTRA ALPHA- HELICAL DOMAIN | 3C LIKE, CORONA, PROTEINASE, CHYMOTRYPSIN, CYSTEINE HISTIDINE DYAD, BETA BARREL, HYDROLASE
1lvo:F (SER200) to (THR254) STRUCTURE OF CORONAVIRUS MAIN PROTEINASE REVEALS COMBINATION OF A CHYMOTRYPSIN FOLD WITH AN EXTRA ALPHA- HELICAL DOMAIN | 3C LIKE, CORONA, PROTEINASE, CHYMOTRYPSIN, CYSTEINE HISTIDINE DYAD, BETA BARREL, HYDROLASE
2zc2:A (ASN125) to (GLY172) CRYSTAL STRUCTURE OF DNAD-LIKE REPLICATION PROTEIN FROM STREPTOCOCCUS MUTANS UA159, GI 24377835, RESIDUES 127-199 | REPLICATION PROTEIN, DNAD-LIKE, GI 24377835, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG
2zc7:A (GLY98) to (TRP138) CRYSTAL STRUCTURE OF CLASS C BETA-LACTAMASE ACT-1 | TWO-DOMAIN STRUCTURE, HYDROLASE
2zc7:B (GLY98) to (TRP138) CRYSTAL STRUCTURE OF CLASS C BETA-LACTAMASE ACT-1 | TWO-DOMAIN STRUCTURE, HYDROLASE
4okp:B (ALA98) to (TRP138) CRYSTAL STRUCTURE OF AMPC BETA-LACTAMASE IN COMPLEX WITH THE PRODUCT FORM OF 7-AMINO-DESACETOXYCEPHALOSPORANIC ACID | AMPC BETA-LACTAMASE, CLASS C, HYDROLASE, CEPHALOSPORINASE
4old:B (ALA98) to (TRP138) CRYSTAL STRUCTURE OF AMPC BETA-LACTAMASE IN COMPLEX WITH THE PRODUCT FORM OF (6R,7R)-7-AMINO-8-OXO-5-THIA-1-AZABICYCLO[4.2.0]OCT-2-ENE-2- CARBOXYLIC ACID | AMPC BETA-LACTAMASE, CLASS C, HYDROLASE, CEPHALOSPORINASE
5csl:A (ALA2118) to (ASN2178) CRYSTAL STRUCTURE OF THE 500 KD YEAST ACETYL-COA CARBOXYLASE HOLOENZYME DIMER | ACETYL-COA CARBOXYLASE, LIGASE
5ctb:A (ARG2119) to (ASN2178) HUMANIZED YEAST ACC CARBOXYLTRANSFERASE DOMAIN BOUND TO 6,7-DIMETHYL- 1'-[(7-METHYL-1H-INDAZOL-5-YL)CARBONYL]SPIRO[CHROMENE-2,4'- PIPERIDIN]-4(3H)-ONE | ACC, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
1m4a:A (THR7) to (LEU63) CRYSTAL STRUCTURE OF HUMAN INTERLEUKIN-2 Y31C COVALENTLY MODIFIED AT C31 WITH (1H-INDOL-3-YL)-(2-MERCAPTO-ETHOXYIMINO)-ACETIC ACID | CYTOKINE, FOUR-HELIX BUNDLE, SMALL MOLECULE COMPLEX
1mb2:C (PRO236) to (SER293) CRYSTAL STRUCTURE OF TRYPTOPHANYL-TRNA SYNTHETASE COMPLEXED WITH TRYPTOPHAN IN AN OPEN CONFORMATION | AMINOACYL-TRNA SYNTHETASE, ROSSMANN FOLD, AMINO ACID BINDING SITE, LIGASE
1mc8:A (THR222) to (SER268) CRYSTAL STRUCTURE OF FLAP ENDONUCLEASE-1 R42E MUTANT FROM PYROCOCCUS HORIKOSHII | FLEXIBLE LOOP, HYDROLASE
2zu2:A (GLY243) to (GLY298) COMPLEX STRUCTURE OF COV 229E 3CL PROTEASE WITH EPDTC | PROTEASE-INHIBITOR COMPLEX, HYDROLASE, METAL-BINDING, PROTEASE, THIOL PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2zu2:B (GLU244) to (GLY298) COMPLEX STRUCTURE OF COV 229E 3CL PROTEASE WITH EPDTC | PROTEASE-INHIBITOR COMPLEX, HYDROLASE, METAL-BINDING, PROTEASE, THIOL PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2zu5:A (GLY251) to (GLN299) COMPLEX STRUCTURE OF SARS-COV 3CL PROTEASE WITH TG-0205486 | PROTEASE-INHIBITOR COMPLEX, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1mfz:A (THR202) to (ASP284) PARTIALLY REFINED 2.8 A CRYSTAL STRUCTURE OF GDP-MANNOSE DEHYDROGENASE FROM P. AERUGINOSA | ROSSMANN FOLD, DOMAIN-SWAPPED DIMER, ENZYME COMPLEX WITH COFACTOR AND PRODUCT, OXIDOREDUCTASE
1mfz:B (THR202) to (ASP284) PARTIALLY REFINED 2.8 A CRYSTAL STRUCTURE OF GDP-MANNOSE DEHYDROGENASE FROM P. AERUGINOSA | ROSSMANN FOLD, DOMAIN-SWAPPED DIMER, ENZYME COMPLEX WITH COFACTOR AND PRODUCT, OXIDOREDUCTASE
1mfz:C (THR202) to (ASP284) PARTIALLY REFINED 2.8 A CRYSTAL STRUCTURE OF GDP-MANNOSE DEHYDROGENASE FROM P. AERUGINOSA | ROSSMANN FOLD, DOMAIN-SWAPPED DIMER, ENZYME COMPLEX WITH COFACTOR AND PRODUCT, OXIDOREDUCTASE
1mfz:D (VAL203) to (ASP284) PARTIALLY REFINED 2.8 A CRYSTAL STRUCTURE OF GDP-MANNOSE DEHYDROGENASE FROM P. AERUGINOSA | ROSSMANN FOLD, DOMAIN-SWAPPED DIMER, ENZYME COMPLEX WITH COFACTOR AND PRODUCT, OXIDOREDUCTASE
1muu:A (THR202) to (ASP284) 2.0 A CRYSTAL STRUCTURE OF GDP-MANNOSE DEHYDROGENASE | ROSSMANN FOLD; DOMAIN-SWAPPED DIMER; ENZYME COMPLEX WITH COFACTOR AND PRODUCT, OXIDOREDUCTASE
1muu:B (THR202) to (ASP284) 2.0 A CRYSTAL STRUCTURE OF GDP-MANNOSE DEHYDROGENASE | ROSSMANN FOLD; DOMAIN-SWAPPED DIMER; ENZYME COMPLEX WITH COFACTOR AND PRODUCT, OXIDOREDUCTASE
1muu:C (THR202) to (ASP284) 2.0 A CRYSTAL STRUCTURE OF GDP-MANNOSE DEHYDROGENASE | ROSSMANN FOLD; DOMAIN-SWAPPED DIMER; ENZYME COMPLEX WITH COFACTOR AND PRODUCT, OXIDOREDUCTASE
1muu:D (THR202) to (ASP284) 2.0 A CRYSTAL STRUCTURE OF GDP-MANNOSE DEHYDROGENASE | ROSSMANN FOLD; DOMAIN-SWAPPED DIMER; ENZYME COMPLEX WITH COFACTOR AND PRODUCT, OXIDOREDUCTASE
1mxo:B (ALA98) to (TRP138) AMPC BETA-LACTAMASE IN COMPLEX WITH AN M.CARBOXYPHENYLGLYCYLBORONIC ACID BEARING THE CEPHALOTHIN R1 SIDE CHAIN | AMPC, BETA-LACTAMASE, CEPHALOSPORINASE, SERINE HYDROLASE
4pef:A (ASP272) to (TYR321) DBR1 IN COMPLEX WITH SULFATE | NUCLEASE, PHOSPHODIESTERASE, METALLOHYDROLASE, METALLOPHOSPHOESTERASE, LARIAT RNA, HYDROLASE, METALLOENZYME
4pef:B (ASP272) to (TYR321) DBR1 IN COMPLEX WITH SULFATE | NUCLEASE, PHOSPHODIESTERASE, METALLOHYDROLASE, METALLOPHOSPHOESTERASE, LARIAT RNA, HYDROLASE, METALLOENZYME
4pef:C (ASP272) to (TYR321) DBR1 IN COMPLEX WITH SULFATE | NUCLEASE, PHOSPHODIESTERASE, METALLOHYDROLASE, METALLOPHOSPHOESTERASE, LARIAT RNA, HYDROLASE, METALLOENZYME
4pef:E (ASP272) to (LYS320) DBR1 IN COMPLEX WITH SULFATE | NUCLEASE, PHOSPHODIESTERASE, METALLOHYDROLASE, METALLOPHOSPHOESTERASE, LARIAT RNA, HYDROLASE, METALLOENZYME
1z1i:A (GLY251) to (SER301) CRYSTAL STRUCTURE OF NATIVE SARS CLPRO | HYDROLASE
3lcb:A (TRP149) to (LYS191) THE CRYSTAL STRUCTURE OF ISOCITRATE DEHYDROGENASE KINASE/PHOSPHATASE IN COMPLEX WITH ITS SUBSTRATE, ISOCITRATE DEHYDROGENASE, FROM ESCHERICHIA COLI. | KINASE PHOSPHATASE, GLYOXYLATE BYPASS, HYDROLASEPROTEIN PHOSPHATASE, TRICARBOXYLIC ACID CYCLE, ISOCITRATE, TRANSFERASE, HYDROLASE
1zp9:A (ASP3) to (GLY46) CRYSTAL STRUCTURE OF FULL-LEGNTH A.FULGIDUS RIO1 SERINE KINASE BOUND TO ATP AND MN2+ IONS. | RIO1, RIOK1, SERINE KINASE, PROTEIN KINASE, MANGANESE, RIBOSOME BIOGENESIS, TRANSFERASE
1zp9:B (LYS2) to (GLY46) CRYSTAL STRUCTURE OF FULL-LEGNTH A.FULGIDUS RIO1 SERINE KINASE BOUND TO ATP AND MN2+ IONS. | RIO1, RIOK1, SERINE KINASE, PROTEIN KINASE, MANGANESE, RIBOSOME BIOGENESIS, TRANSFERASE
1zp9:D (GLU8) to (GLY46) CRYSTAL STRUCTURE OF FULL-LEGNTH A.FULGIDUS RIO1 SERINE KINASE BOUND TO ATP AND MN2+ IONS. | RIO1, RIOK1, SERINE KINASE, PROTEIN KINASE, MANGANESE, RIBOSOME BIOGENESIS, TRANSFERASE
1zth:A (ASP3) to (LYS45) CRYSTAL STRUCTURE OF A.FULGIDUS RIO1 SERINE PROTEIN KINASE BOUND TO ADP AND MANGANESE ION | PROTEIN KINASE, RIBOSOME BIOGENESIS, RRNA, ADP, MANGANESE, TRANSFERASE
1zth:B (ASP3) to (GLY46) CRYSTAL STRUCTURE OF A.FULGIDUS RIO1 SERINE PROTEIN KINASE BOUND TO ADP AND MANGANESE ION | PROTEIN KINASE, RIBOSOME BIOGENESIS, RRNA, ADP, MANGANESE, TRANSFERASE
1zth:C (GLU8) to (GLY46) CRYSTAL STRUCTURE OF A.FULGIDUS RIO1 SERINE PROTEIN KINASE BOUND TO ADP AND MANGANESE ION | PROTEIN KINASE, RIBOSOME BIOGENESIS, RRNA, ADP, MANGANESE, TRANSFERASE
5e2h:C (THR93) to (GLN131) CRYSTAL STRUCTURE OF D-ALANINE CARBOXYPEPTIDASE AMPC FROM MYCOBACTERIUM SMEGMATIS | STRUCTURAL GENOMICS, PSI-BIOLOGY, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, HYDROLASE
4aw6:A (SER397) to (HIS456) CRYSTAL STRUCTURE OF THE HUMAN NUCLEAR MEMBRANE ZINC METALLOPROTEASE ZMPSTE24 (FACE1) | HYDROLASE, M48 PEPTIDASE, INTEGRAL MEMBRANE PROTEIN, PRELAMIN A PROCESSING, AGEING, PROGERIA
4aw6:B (SER397) to (HIS456) CRYSTAL STRUCTURE OF THE HUMAN NUCLEAR MEMBRANE ZINC METALLOPROTEASE ZMPSTE24 (FACE1) | HYDROLASE, M48 PEPTIDASE, INTEGRAL MEMBRANE PROTEIN, PRELAMIN A PROCESSING, AGEING, PROGERIA
4aw6:D (SER397) to (HIS456) CRYSTAL STRUCTURE OF THE HUMAN NUCLEAR MEMBRANE ZINC METALLOPROTEASE ZMPSTE24 (FACE1) | HYDROLASE, M48 PEPTIDASE, INTEGRAL MEMBRANE PROTEIN, PRELAMIN A PROCESSING, AGEING, PROGERIA
4aw6:E (SER397) to (HIS456) CRYSTAL STRUCTURE OF THE HUMAN NUCLEAR MEMBRANE ZINC METALLOPROTEASE ZMPSTE24 (FACE1) | HYDROLASE, M48 PEPTIDASE, INTEGRAL MEMBRANE PROTEIN, PRELAMIN A PROCESSING, AGEING, PROGERIA
3ly8:A (ASN298) to (LEU337) CRYSTAL STRUCTURE OF MUTANT D471E OF THE PERIPLASMIC DOMAIN OF CADC | ALPHA/BETA DOMAIN, ALPHA DOMAIN, ACTIVATOR, DNA-BINDING, MEMBRANE, TRANSCRIPTION REGULATION, TRANSMEMBRANE, TWO-COMPONENT REGULATORY SYSTEM, SIGNALING PROTEIN
3aw0:A (GLY251) to (GLN299) STRUCTURE OF SARS 3CL PROTEASE WITH PEPTIDIC ALDEHYDE INHIBITOR | HYDROLASE PROTEINASE CONVERTING, DESIGNED INHIBITOR, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3aw1:A (GLY251) to (SER301) STRUCTURE OF SARS 3CL PROTEASE AUTO-PROTEOLYSIS RESISTANT MUTANT IN THE ABSENT OF INHIBITOR | HYDROLASE PROTEINASE CONVERTING, HYDROLASE
2a5a:A (GLY251) to (GLN299) CRYSTAL STRUCTURE OF UNBOUND SARS CORONAVIRUS MAIN PEPTIDASE IN THE SPACE GROUP C2 | CYSTEINE PEPTIDASE, 3C-LIKE, N-FINGER, CHYMOTRYPSIN-LIKE FOLD, LONG LOOP, ALPHA-HELICAL DOMAIN, DIMER, CATALYTIC DYAD, SPECIFICITY POCKETS, HYDROLASE
2a5i:A (THR201) to (GLY251) CRYSTAL STRUCTURES OF SARS CORONAVIRUS MAIN PEPTIDASE INHIBITED BY AN AZA-PEPTIDE EPOXIDE IN THE SPACE GROUP C2 | CYSTEINE PEPTIDASE, 3C-LIKE, N-FINGER, CHYMOTRYPSIN-LIKE FOLD, LONG LOOP, ALPHA-HELICAL DOMAIN, DIMER, CATALYTIC DYAD, SPECIFICITY POCKETS, AZA-PEPTIDE EPOXIDE, SUBSTRATE-LIKE INHIBITOR, C-S COVALENT BOND, EPOXIDE STEREOCHEMISTRY, HYDROLASE
2a5i:A (GLY251) to (GLN299) CRYSTAL STRUCTURES OF SARS CORONAVIRUS MAIN PEPTIDASE INHIBITED BY AN AZA-PEPTIDE EPOXIDE IN THE SPACE GROUP C2 | CYSTEINE PEPTIDASE, 3C-LIKE, N-FINGER, CHYMOTRYPSIN-LIKE FOLD, LONG LOOP, ALPHA-HELICAL DOMAIN, DIMER, CATALYTIC DYAD, SPECIFICITY POCKETS, AZA-PEPTIDE EPOXIDE, SUBSTRATE-LIKE INHIBITOR, C-S COVALENT BOND, EPOXIDE STEREOCHEMISTRY, HYDROLASE
2a5k:A (GLY251) to (SER301) CRYSTAL STRUCTURES OF SARS CORONAVIRUS MAIN PEPTIDASE INHIBITED BY AN AZA-PEPTIDE EPOXIDE IN SPACE GROUP P212121 | CYSTEINE PEPTIDASE, 3C-LIKE, N-FINGER, CHYMOTRYPSIN-LIKE FOLD, LONG LOOP, ALPHA-HELICAL DOMAIN, DIMER, CATALYTIC DYAD, SPECIFICITY POCKETS, AZA-PEPTIDE EPOXIDE, SUBSTRATE- LIKE INHIBITOR, C-S COVALENT BOND, EPOXIDE STEREOCHEMISTRY, HYDROLASE
2a5k:B (LEU250) to (CYS300) CRYSTAL STRUCTURES OF SARS CORONAVIRUS MAIN PEPTIDASE INHIBITED BY AN AZA-PEPTIDE EPOXIDE IN SPACE GROUP P212121 | CYSTEINE PEPTIDASE, 3C-LIKE, N-FINGER, CHYMOTRYPSIN-LIKE FOLD, LONG LOOP, ALPHA-HELICAL DOMAIN, DIMER, CATALYTIC DYAD, SPECIFICITY POCKETS, AZA-PEPTIDE EPOXIDE, SUBSTRATE- LIKE INHIBITOR, C-S COVALENT BOND, EPOXIDE STEREOCHEMISTRY, HYDROLASE
3m3s:A (LEU250) to (GLY302) CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE ASN214ALA MUTANT WITH AUTHORIZE N-TERMINUS | SARS CORONAVIRUS PROTEASE N214A MUTATION, HYDROLASE
3m3s:B (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE ASN214ALA MUTANT WITH AUTHORIZE N-TERMINUS | SARS CORONAVIRUS PROTEASE N214A MUTATION, HYDROLASE
4qes:A (ASP155) to (TRP205) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS, QUADRUPLE MUTANT, I222 FORM | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, OXIDOREDUCTASE, VIRAL PROTEIN
4qes:B (ASP155) to (TRP205) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS, QUADRUPLE MUTANT, I222 FORM | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, OXIDOREDUCTASE, VIRAL PROTEIN
4qes:C (ASP155) to (TRP205) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS, QUADRUPLE MUTANT, I222 FORM | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, OXIDOREDUCTASE, VIRAL PROTEIN
3m7k:A (CYS24) to (SER75) CRYSTAL STRUCTURE OF PACI-DNA ENZYME PRODUCT COMPLEX | HNH RESTRICTION ENDONUCLEASE, BETA-BETA-ALPHA-METAL ACTIVE SITE, 8 BASE-PAIR RARE CUTTER, HYDROLASE-DNA COMPLEX
4qlo:A (GLY178) to (HIS239) CRYSTAL STRUCTURE OF HOMOSERINE O-ACETYLTRANSFERASE FROM STAPHYLOCOCCUS AUREUS | ROSSMANN FOLD, ACETYLTRANSFERASE, ACETYLCO-A BINDING, TRANSFERASE
3mva:O (LEU75) to (GLY115) CRYSTAL STRUCTURE OF HUMAN MTERF1 BOUND TO THE TERMINATION SEQUENCE | ALL ALPHA-HELIX, PROTEIN-DNA, TRANSCRIPTION FACTOR, TERMINATION, MITOCHONDRIA, TRANSCRIPTION-DNA COMPLEX
3mvb:O (LEU76) to (GLY115) CRYSTAL STRUCTURE OF A TRIPLE RFY MUTANT OF HUMAN MTERF1 BOUND TO THE TERMINATION SEQUENCE | ALL ALPHA-HELIX, PROTEIN-DNA, TRANSCRIPTION FACTOR, TERMINATION, MITOCHONDRIA, TRANSCRIPTION-DNA COMPLEX
3n6s:A (LEU75) to (GLY115) CRYSTAL STRUCTURE OF HUMAN MITOCHONDRIAL MTERF IN COMPLEX WITH A 15- MER DNA ENCOMPASSING THE TRNALEU(UUR) BINDING SEQUENCE | MITOCHONDRIAL TRANSCRIPTION TERMINATION FACTOR-DNA COMPLEX, MITOCHONDRIAL REPLICATION PAUSING-DNA COMPLEX, LEFT-HANDED HELICAL TANDEM REPEAT, PROTEIN-DNA COMPLEX, TRANSCRIPTION, REPLICATION-DNA COMPLEX
3c4c:B (SER614) to (GLY672) B-RAF KINASE IN COMPLEX WITH PLX4720 | B-RAF, BRAF, RAF, PROTO-ONCOGENE, SERINE/THREONINE KINASE, ATP-BINDING, CARDIOMYOPATHY, CYTOPLASM, DISEASE MUTATION, METAL-BINDING, NUCLEOTIDE-BINDING, PHORBOL-ESTER BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, ZINC, ZINC-FINGER
3cd5:D (THR487) to (ALA525) THERMODYNAMIC AND STRUCTURE GUIDED DESIGN OF STATIN HMG-COA REDUCTASE INHIBITORS | OXIDOREDUCTASE, CHOLESTEROL BIOSYNTHESIS, HMG-COA, NADPH, STATIN, ALTERNATIVE SPLICING, ENDOPLASMIC RETICULUM, GLYCOPROTEIN, LIPID SYNTHESIS, MEMBRANE, PEROXISOME, POLYMORPHISM, STEROID BIOSYNTHESIS, TRANSMEMBRANE
3cd7:D (GLU489) to (ALA525) THERMODYNAMIC AND STRUCTURE GUIDED DESIGN OF STATIN HMG-COA REDUCTASE INHIBITORS | OXIDOREDUCTASE, CHOLESTEROL BIOSYNTHESIS, HMG-COA, NADPH, STATIN, ALTERNATIVE SPLICING, ENDOPLASMIC RETICULUM, GLYCOPROTEIN, LIPID SYNTHESIS, MEMBRANE, PEROXISOME, POLYMORPHISM, STEROID BIOSYNTHESIS, TRANSMEMBRANE
4rea:A (SER553) to (GLY622) A NUCLEASE DNA COMPLEX | HJC, TPR, SAP, STRUCTURAL SPECIFIC NUCLEASE, FANCD2, NUCLEUS, HYDROLASE-DNA COMPLEX
4rsp:A (SER204) to (THR258) X-RAY STRUCTURE OF MERS-COV NSP5 PROTEASE BOUND WITH A DESIGNED INHIBITOR | PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5fwk:A (THR94) to (VAL139) ATOMIC CRYOEM STRUCTURE OF HSP90-CDC37-CDK4 COMPLEX | SIGNALING PROTEIN, HSP90, CDC37, CDK4, CHAPERONE, KINASE, UNFOLDING
5fwl:A (THR94) to (VAL139) ATOMIC CRYOEM STRUCTURE OF HSP90-CDC37-CDK4 COMPLEX | HSP90, CDC37, CDK4, CHAPERONE, KINASE, UNFOLDING
5fwm:A (THR94) to (VAL139) ATOMIC CRYOEM STRUCTURE OF HSP90-CDC37-CDK4 COMPLEX | HSP90, CDC37, CDK4, CHAPERONE, KINASE, UNFOLDING
5fwp:A (THR94) to (VAL139) ATOMIC CRYOEM STRUCTURE OF HSP90-CDC37-CDK4 COMPLEX | HSP90, CDC37, CDK4, CHAPERONE, KINASE, UNFOLDING
3o86:B (ALA98) to (TRP138) CRYSTAL STRUCTURE OF AMPC BETA-LACTAMASE IN COMPLEX WITH A SULFONAMIDE BORONIC ACID INHIBITOR | CONTAINS ALPHA HELICES AND A BETA SANDWICH / BETA-LACTAMASE-LIKE FOLD / AMPC BETA-LACTAMASE, CLASS C, HYDROLASE, CEPHALOSPORINASE
3o87:B (ALA98) to (TRP138) CRYSTAL STRUCTURE OF AMPC BETA-LACTAMASE IN COMPLEX WITH A SULFONAMIDE BORONIC ACID INHIBITOR | CONTAINS ALPHA HELICES AND A BETA SANDWICH / BETA-LACTAMASE-LIKE FOLD / AMPC BETA-LACTAMASE, CLASS C, HYDROLASE, CEPHALOSPORINASE
3o88:B (ALA98) to (TRP138) CRYSTAL STRUCTURE OF AMPC BETA-LACTAMASE IN COMPLEX WITH A SULFONAMIDE BORONIC ACID INHIBITOR | CONTAINS ALPHA HELICES AND A BETA SANDWICH / BETA-LACTAMASE-LIKE FOLD / AMPC BETA-LACTAMASE, CLASS C, HYDROLASE, CEPHALOSPORINASE
4s20:E (ASN15) to (GLU74) STRUCTURAL BASIS FOR TRANSCRIPTION REACTIVATION BY RAPA | DNA-DIRECTED RNA POLYMERASE, TRANSCRIPTION TRANSFERASE, DNA TRANSLOCASE, ATPASE, TRANSFERASE-DNA-RNA COMPLEX
4s20:J (ASN15) to (GLU76) STRUCTURAL BASIS FOR TRANSCRIPTION REACTIVATION BY RAPA | DNA-DIRECTED RNA POLYMERASE, TRANSCRIPTION TRANSFERASE, DNA TRANSLOCASE, ATPASE, TRANSFERASE-DNA-RNA COMPLEX
3d62:A (GLY251) to (SER301) DEVELOPMENT OF BROAD-SPECTRUM HALOMETHYL KETONE INHIBITORS AGAINST CORONAVIRUS MAIN PROTEASE 3CLPRO | MAIN PROTEASE 3CLPRO, SARS, INHIBITOR, 95990, ATP-BINDING, ENDONUCLEASE, EXONUCLEASE, HELICASE, HYDROLASE, MEMBRANE, METAL- BINDING, NUCLEASE, NUCLEOTIDE-BINDING, NUCLEOTIDYLTRANSFERASE, RNA REPLICATION, RNA-BINDING, RNA-DIRECTED RNA POLYMERASE, THIOL PROTEASE, TRANSFERASE, TRANSMEMBRANE, ZINC-FINGER
4cz8:B (SER5) to (ARG62) STRUCTURE OF THE SODIUM PROTON ANTIPORTER PANHAP FROM PYROCOCCUS ABYSSII AT PH 8. | MEMBRANE PROTEIN, ANTIPORTER, TRANSPORTER, EXCHANGER, CPA
4tww:A (GLY251) to (GLN299) STRUCTURE OF SARS-3CL PROTEASE COMPLEX WITH A BROMOBENZOYL (S,R)-N- DECALIN TYPE INHIBITOR | HYDRASE PROTEINASE CONVERTING, DESIGNED INHIBITOR, HYDRASE-INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4tww:B (THR201) to (GLY251) STRUCTURE OF SARS-3CL PROTEASE COMPLEX WITH A BROMOBENZOYL (S,R)-N- DECALIN TYPE INHIBITOR | HYDRASE PROTEINASE CONVERTING, DESIGNED INHIBITOR, HYDRASE-INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4tww:B (GLY251) to (SER301) STRUCTURE OF SARS-3CL PROTEASE COMPLEX WITH A BROMOBENZOYL (S,R)-N- DECALIN TYPE INHIBITOR | HYDRASE PROTEINASE CONVERTING, DESIGNED INHIBITOR, HYDRASE-INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4twy:A (GLY251) to (GLN299) STRUCTURE OF SARS-3CL PROTEASE COMPLEX WITH A PHENYLBENZOYL (S,R)-N- DECALIN TYPE INHIBITOR | HYDRASE PROTEINASE CONVERTING, DESIGNED INHIBITOR, HYDRASE-INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4u0t:A (THR99) to (TRP138) CRYSTAL STRUCTURE OF ADC-7 BETA-LACTAMASE | CEPHALOSPORINASE, BETA-LACTAMASE, HYDROLASE
4u0t:G (THR99) to (TRP138) CRYSTAL STRUCTURE OF ADC-7 BETA-LACTAMASE | CEPHALOSPORINASE, BETA-LACTAMASE, HYDROLASE
4u0x:A (THR99) to (TRP138) STRUCTURE OF ADC-7 BETA-LACTAMASE IN COMPLEX WITH BORONIC ACID INHIBITOR S02030 | BETA-LACTAMASE, BORONIC ACID INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4u0x:C (THR99) to (TRP138) STRUCTURE OF ADC-7 BETA-LACTAMASE IN COMPLEX WITH BORONIC ACID INHIBITOR S02030 | BETA-LACTAMASE, BORONIC ACID INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4u0x:D (THR99) to (TRP138) STRUCTURE OF ADC-7 BETA-LACTAMASE IN COMPLEX WITH BORONIC ACID INHIBITOR S02030 | BETA-LACTAMASE, BORONIC ACID INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4d9j:A (ASP155) to (TRP205) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, DE NOVO PROTEIN
4d9j:B (ASP155) to (TRP205) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, DE NOVO PROTEIN
4d9j:D (ASP155) to (TRP205) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, DE NOVO PROTEIN
4d9j:E (ASP155) to (TRP205) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, DE NOVO PROTEIN
4d9j:F (ASP155) to (TRP205) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, DE NOVO PROTEIN
4d9j:G (ASP155) to (TRP205) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, DE NOVO PROTEIN
4d9j:I (ASP155) to (TRP205) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, DE NOVO PROTEIN
4d9j:J (ASP155) to (TRP205) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, DE NOVO PROTEIN
4d9j:L (ASP155) to (TRP205) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, DE NOVO PROTEIN
3duh:D (VAL102) to (THR167) STRUCTURE OF INTERLEUKIN-23 | FOUR-HELIX BUNDLE CYTOKINE, IG DOMAIN, CYTOKINE, GLYCOPROTEIN, IMMUNOGLOBULIN DOMAIN, SECRETED, ANTIVIRAL DEFENSE, IMMUNE RESPONSE, INFLAMMATORY RESPONSE, INNATE IMMUNITY, TISSUE REMODELING, IMMUNE SYSTEM, IMMUNE SYSTEM-CYTOKINE COMPLEX
4dnq:D (TYR151) to (SER196) CRYSTAL STRUCTURE OF DAD2 S96A MUTANT | ALPHA/BETA HYDROLASE, HYDROLASE
4dnq:H (TYR151) to (SER196) CRYSTAL STRUCTURE OF DAD2 S96A MUTANT | ALPHA/BETA HYDROLASE, HYDROLASE
3e40:A (HIS73) to (TRP99) Q138F HINCII BOUND TO GTTAAC AND COCRYSTALLIZED WITH 5 MM CA2+ | PROTEIN-DNA COMPLEX, ENDONUCLEASE, INDIRECT READOUT, HYDROLASE, NUCLEASE, RESTRICTION SYSTEM, HYDROLASE/DNA COMPLEX
3e44:A (GLY72) to (TRP99) Q138F HINCII BOUND TO CLEAVED DNA (GTT | AAC) AND MN2+ | PROTEIN-DNA COMPLEX, ENDONUCLEASE, INDIRECT READOUT, HYDROLASE, NUCLEASE, RESTRICTION SYSTEM, HYDROLASE/DNA COMPLEX
5hyo:A (PHE199) to (THR254) X-RAY STRUCTURE OF UNBOUND PORCINE EPIDEMIC DIARRHEA VIRUS 3CLPRO | PEDV, 3CLPRO, CORONAVIRUS, MPRO, VIRAL PROTEIN
5hyo:B (PHE247) to (MET296) X-RAY STRUCTURE OF UNBOUND PORCINE EPIDEMIC DIARRHEA VIRUS 3CLPRO | PEDV, 3CLPRO, CORONAVIRUS, MPRO, VIRAL PROTEIN
4e3j:A (ALA98) to (ASN137) CRYSTAL STRUCTURE OF AMPC BETA-LACTAMASE IN COMPLEX WITH A DESIGNED 4- TETRAZOLYL BENZENE SULFONAMIDE BORONIC ACID INHIBITOR | AMPC BETA-LACTAMASE, CLASS C, HYDROLASE, CEPHALOSPORINASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4e3n:B (ALA98) to (TRP138) CRYSTAL STRUCTURE OF AMPC BETA-LACTAMASE IN COMPLEX WITH A 2- TRIFLUOROMETHYL-4-TETRAZOLYL BENZENE SULFONAMIDE BORONIC ACID INHIBITOR | AMPC BETA-LACTAMASE, CLASS C, CEPHALOSPORINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4e3o:B (ALA98) to (TRP138) CRYSTAL STRUCTURE OF AMPC BETA-LACTAMASE IN COMPLEX WITH A SMALL CHLOROMETHYL SULFONAMIDE BORONIC ACID INHIBITOR | AMPC BETA-LACTAMASE, CLASS C, CEPHALOSPORINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4e9h:A (PRO456) to (ALA494) STRUCTURE OF GLYCOSYLASE DOMAIN OF MBD4 BOUND TO 5HMU CONTAINING DNA | HHH DNA GLYCOSYLASE FAMILY, HYDROLASE-DNA COMPLEX
4ea4:A (PRO456) to (ALA494) STRUCTURE OF THE GLYCOSYLASE DOMAIN OF MBD4 BOUND TO 5HMU-CONTAINING DNA | HHH DNA GLYCOSYLASE FAMILY, HYDROLASE-DNA COMPLEX
4ea5:A (PRO456) to (ALA494) STRUCTURE OF THE GLYCOSLYASE DOMAIN OF MBD4 BOUND TO A 5HMU CONTAINING DNA | HHH DNA GLYCOSYLASE FAMILY, HYDROLASE-DNA COMPLEX
3pwq:C (THR58) to (TRP123) THE PHENYLACETYL-COA MONOOXYGENASE PAAAC SUBCOMPLEX | PROTEIN-PROTEIN COMPLEX, STRUCTURAL GENOMICS, MONTREAL-KINGSTON BACTERIAL STRUCTURAL GENOMICS INITIATIVE, BSGI, FERRITIN-LIKE FOLD, BACTERIAL MULTICOMPONENT MONOOXYGENASE, OXIDOREDUCTASE
3pwq:H (THR58) to (TRP123) THE PHENYLACETYL-COA MONOOXYGENASE PAAAC SUBCOMPLEX | PROTEIN-PROTEIN COMPLEX, STRUCTURAL GENOMICS, MONTREAL-KINGSTON BACTERIAL STRUCTURAL GENOMICS INITIATIVE, BSGI, FERRITIN-LIKE FOLD, BACTERIAL MULTICOMPONENT MONOOXYGENASE, OXIDOREDUCTASE
5ipl:E (ASN15) to (LEU80) SIGMAS-TRANSCRIPTION INITIATION COMPLEX WITH 4-NT NASCENT RNA | TRANSCRIPTION INITIATION, RNA POLYMERASE, GENERAL STRESS SIGMA FACTOR, PYROPHOSPHATE RELEASE, TRANSCRIPTION, TRANSFERASE-DNA-RNA COMPLEX
5ipm:E (ASN15) to (LEU80) SIGMAS-TRANSCRIPTION INITIATION COMPLEX WITH 4-NT NASCENT RNA | TRANSCRIPTION INITIATION, RNA POLYMERASE, GENERAL STRESS SIGMA FACTOR, PYROPHOSPHATE RELEASE, TRANSCRIPTION, TRANSFERASE-DNA-RNA COMPLEX
5ipn:E (ASN15) to (LEU80) SIGMAS-TRANSCRIPTION INITIATION COMPLEX WITH 4-NT NASCENT RNA | TRANSCRIPTION INITIATION, RNA POLYMERASE, GENERAL STRESS SIGMA FACTOR, PYROPHOSPHATE RELEASE, TRANSCRIPTION, TRANSFERASE-DNA-RNA COMPLEX
4etw:A (PHE136) to (LYS184) STRUCTURE OF THE ENZYME-ACP SUBSTRATE GATEKEEPER COMPLEX REQUIRED FOR BIOTIN SYNTHESIS | ESTERASE, HYDROLASE
4etw:C (PHE136) to (LYS184) STRUCTURE OF THE ENZYME-ACP SUBSTRATE GATEKEEPER COMPLEX REQUIRED FOR BIOTIN SYNTHESIS | ESTERASE, HYDROLASE
4ew0:A (PRO430) to (ALA468) MOUSE MBD4 GLYCOSYLASE DOMAIN IN COMPLEX WITH A G:5HMU (5- HYDROXYMETHYLURACIL) MISMATCH | 5-HYDROXYMETHYLURACIL, DEAMINATION, 5-METHYLCYTOSINE, ACTIVE DNA DEMETHYLATION, HELIX-HAIRPIN-HELIX, DNA GLYCOSYLASE, HYDROLASE-DNA COMPLEX
4f49:A (SER200) to (THR254) 2.25A RESOLUTION STRUCTURE OF TRANSMISSIBLE GASTROENTERITIS VIRUS PROTEASE CONTAINING A COVALENTLY BOUND DIPEPTIDYL INHIBITOR | PROTEASE, ANTIVIRAL INHIBITORS, DIPEPTIDYL INHIBITOR, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4f49:B (PHE247) to (GLY298) 2.25A RESOLUTION STRUCTURE OF TRANSMISSIBLE GASTROENTERITIS VIRUS PROTEASE CONTAINING A COVALENTLY BOUND DIPEPTIDYL INHIBITOR | PROTEASE, ANTIVIRAL INHIBITORS, DIPEPTIDYL INHIBITOR, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4f49:C (PHE247) to (GLN295) 2.25A RESOLUTION STRUCTURE OF TRANSMISSIBLE GASTROENTERITIS VIRUS PROTEASE CONTAINING A COVALENTLY BOUND DIPEPTIDYL INHIBITOR | PROTEASE, ANTIVIRAL INHIBITORS, DIPEPTIDYL INHIBITOR, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3re4:A (ASP3) to (GLY46) CRYSTAL STRUCTURE OF ARCHAEOGLOBUS FULGIDUS RIO1 KINASE BOUND TO TOYOCAMYCIN. | ATYPICAL KINASE, TRANSFERASE-ANTIBIOTIC COMPLEX
3re4:B (ASP3) to (GLY46) CRYSTAL STRUCTURE OF ARCHAEOGLOBUS FULGIDUS RIO1 KINASE BOUND TO TOYOCAMYCIN. | ATYPICAL KINASE, TRANSFERASE-ANTIBIOTIC COMPLEX
5syt:A (SER397) to (HIS456) CRYSTAL STRUCTURE OF ZMPSTE24 | HYDROLASE, MEMBRANE PROTEIN, CAAX PROTEASE, ZINC METALLOPROTEASE, STE24, ISOPRENYLATION, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MEMBRANE PROTEIN STRUCTURAL BIOLOGY CONSORTIUM, MPSBC
3ea7:A (GLY251) to (SER301) CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE TRIPLE MUTANT STI/A IN SPACE GROUP P21 | SARS-COV MAIN PROTEASE MUTANT, 3C-LIKE PROTEASE MUTANT, EXTRA HELICAL DOMAIN MUTATION, CYTOPLASM, HYDROLASE, MEMBRANE, METAL-BINDING, PROTEASE, RIBOSOMAL FRAMESHIFTING, RNA-BINDING, THIOL PROTEASE, TRANSMEMBRANE, ZINC, ZINC- FINGER
3ea7:B (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE TRIPLE MUTANT STI/A IN SPACE GROUP P21 | SARS-COV MAIN PROTEASE MUTANT, 3C-LIKE PROTEASE MUTANT, EXTRA HELICAL DOMAIN MUTATION, CYTOPLASM, HYDROLASE, MEMBRANE, METAL-BINDING, PROTEASE, RIBOSOMAL FRAMESHIFTING, RNA-BINDING, THIOL PROTEASE, TRANSMEMBRANE, ZINC, ZINC- FINGER
2amq:B (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS_COV MPRO IN COMPLEX WITH AN INHIBITOR N3 | ANTI-PARALLEL B-BARREL, ANTI-PARALLEL A-HELICES, HYDROLASE
2oox:G (MET74) to (GLY113) CRYSTAL STRUCTURE OF THE ADENYLATE SENSOR FROM AMP-ACTIVATED PROTEIN KINASE COMPLEXED WITH AMP | AMPK, KINASE, AMP, TRANSFERASE
3er8:C (ILE13) to (PHE47) CRYSTAL STRUCTURE OF THE HETERODIMERIC VACCINIA VIRUS MRNA POLYADENYLATE POLYMERASE COMPLEX WITH TWO FRAGMENTS OF RNA | POLYADENYLATE POLYMERASE, TRANSLOCATION, SINGLE TRANDED RNA POLY(A) POLYMERASE, RNA PROTEIN COMPLEX, PROCESSIVITY, HETERODIMER, NUCLEOTIDYLTRANSFERASE, POXVIRUS; METHYLTRANSFERASE, MRNA CAPPING, MRNA PROCESSING, S-ADENOSYL-L-METHIONINE, TRANSCRIPTION, TRANSFERASE, TRANSFERASE/DNA, RNA COMPLEX, TRANSFERASE-DNA
3er8:D (ILE13) to (PHE47) CRYSTAL STRUCTURE OF THE HETERODIMERIC VACCINIA VIRUS MRNA POLYADENYLATE POLYMERASE COMPLEX WITH TWO FRAGMENTS OF RNA | POLYADENYLATE POLYMERASE, TRANSLOCATION, SINGLE TRANDED RNA POLY(A) POLYMERASE, RNA PROTEIN COMPLEX, PROCESSIVITY, HETERODIMER, NUCLEOTIDYLTRANSFERASE, POXVIRUS; METHYLTRANSFERASE, MRNA CAPPING, MRNA PROCESSING, S-ADENOSYL-L-METHIONINE, TRANSCRIPTION, TRANSFERASE, TRANSFERASE/DNA, RNA COMPLEX, TRANSFERASE-DNA
4x00:B (LEU162) to (ALA203) X-RAY CRYSTAL STRUCTURE OF A PUTATIVE ARYL ESTERASE FROM BURKHOLDERIA CENOCEPACIA | HYDROLASE, ARYL ESTERASE, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, SSGCID
4x00:D (LEU162) to (ALA203) X-RAY CRYSTAL STRUCTURE OF A PUTATIVE ARYL ESTERASE FROM BURKHOLDERIA CENOCEPACIA | HYDROLASE, ARYL ESTERASE, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, SSGCID
1brt:A (ASP155) to (TRP205) BROMOPEROXIDASE A2 MUTANT M99T | HALOPEROXIDASE, OXIDOREDUCTASE, PEROXIDASE, ALPHA/BETA HYDROLASE FOLD, MUTANT M99T
3f9h:A (GLY251) to (CYS300) CRYSTAL STRUCTURE OF THE F140A MUTANT OF SARS-CORONOVIRUS 3C-LIKE PROTEASE AT PH 7.6 | PROTEASE, CYTOPLASM, HYDROLASE, MEMBRANE, METAL-BINDING, RIBOSOMAL FRAMESHIFTING, RNA-BINDING, THIOL PROTEASE, TRANSMEMBRANE, ZINC, ZINC-FINGER
3f9h:B (LEU250) to (CYS300) CRYSTAL STRUCTURE OF THE F140A MUTANT OF SARS-CORONOVIRUS 3C-LIKE PROTEASE AT PH 7.6 | PROTEASE, CYTOPLASM, HYDROLASE, MEMBRANE, METAL-BINDING, RIBOSOMAL FRAMESHIFTING, RNA-BINDING, THIOL PROTEASE, TRANSMEMBRANE, ZINC, ZINC-FINGER
2bx4:A (GLY251) to (CYS300) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEINASE (P21212) | HYDROLASE, ANTI-PARALLEL B-BARREL, ANTI-PARALLEL A- HELICES, VIRAL PROTEIN
3snd:A (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEASE COMPLEXED WITH AC- ESTLQ-H (COCRYSTALLIZATION) | 3C-LIKE PROTEINASE, PROTEASE, AC-ESTLQ-H, ACTIVE SITE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3snd:B (GLY251) to (GLY302) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEASE COMPLEXED WITH AC- ESTLQ-H (COCRYSTALLIZATION) | 3C-LIKE PROTEINASE, PROTEASE, AC-ESTLQ-H, ACTIVE SITE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
2q6d:A (THR199) to (THR259) CRYSTAL STRUCTURE OF INFECTIOUS BRONCHITIS VIRUS (IBV) MAIN PROTEASE | CORONAVIRUS; IBV; MAIN PROTEASE; 3C-LIKE PROTEINASE, HYDROLASE
2q6d:B (SER249) to (VAL304) CRYSTAL STRUCTURE OF INFECTIOUS BRONCHITIS VIRUS (IBV) MAIN PROTEASE | CORONAVIRUS; IBV; MAIN PROTEASE; 3C-LIKE PROTEINASE, HYDROLASE
2q6d:C (THR250) to (ASN299) CRYSTAL STRUCTURE OF INFECTIOUS BRONCHITIS VIRUS (IBV) MAIN PROTEASE | CORONAVIRUS; IBV; MAIN PROTEASE; 3C-LIKE PROTEINASE, HYDROLASE
3fzd:A (GLY251) to (CYS300) MUTATION OF ASN28 DISRUPTS THE ENZYMATIC ACTIVITY AND DIMERIZATION OF SARS 3CLPRO | SARS, SARS 3CLPRO, PROTEASE, SARS-COV MPRO, DIMERIZATION, ANALYTICAL ULTRACENTRIFUGATION, CYTOPLASM, HYDROLASE, MEMBRANE, METAL-BINDING, RIBOSOMAL FRAMESHIFTING, RNA-BINDING, THIOL PROTEASE, TRANSMEMBRANE, ZINC, ZINC-FINGER
1p9u:B (PHE247) to (MET296) CORONAVIRUS MAIN PROTEINASE (3CLPRO) STRUCTURE: BASIS FOR DESIGN OF ANTI-SARS DRUGS | SARS-COV, HCOV, TGEV, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1p9u:C (PHE247) to (GLY298) CORONAVIRUS MAIN PROTEINASE (3CLPRO) STRUCTURE: BASIS FOR DESIGN OF ANTI-SARS DRUGS | SARS-COV, HCOV, TGEV, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1p9u:D (SER200) to (PHE247) CORONAVIRUS MAIN PROTEINASE (3CLPRO) STRUCTURE: BASIS FOR DESIGN OF ANTI-SARS DRUGS | SARS-COV, HCOV, TGEV, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1p9u:D (PHE247) to (GLY298) CORONAVIRUS MAIN PROTEINASE (3CLPRO) STRUCTURE: BASIS FOR DESIGN OF ANTI-SARS DRUGS | SARS-COV, HCOV, TGEV, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1p9u:E (SER200) to (PHE247) CORONAVIRUS MAIN PROTEINASE (3CLPRO) STRUCTURE: BASIS FOR DESIGN OF ANTI-SARS DRUGS | SARS-COV, HCOV, TGEV, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1p9u:E (PHE247) to (MET296) CORONAVIRUS MAIN PROTEINASE (3CLPRO) STRUCTURE: BASIS FOR DESIGN OF ANTI-SARS DRUGS | SARS-COV, HCOV, TGEV, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1p9u:F (PHE247) to (MET296) CORONAVIRUS MAIN PROTEINASE (3CLPRO) STRUCTURE: BASIS FOR DESIGN OF ANTI-SARS DRUGS | SARS-COV, HCOV, TGEV, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ybq:B (LEU403) to (VAL480) RAT GLUT5 WITH FV IN THE OUTWARD-OPEN FORM | SUGAR TRANSPORTER, MAJOR FACILITATOR SUPERFAMILY, TRANSPORT PROTEIN- IMMUNE SYSTEM COMPLEX
2duc:A (GLY251) to (GLY302) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEINASE(3CLPRO) | HYDROLASE, SARS CORONAVIRUS MAIN PROTEINASE, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI
2duc:B (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEINASE(3CLPRO) | HYDROLASE, SARS CORONAVIRUS MAIN PROTEINASE, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI
2rdc:A (GLY73) to (ARG150) CRYSTAL STRUCTURE OF A PUTATIVE LIPID BINDING PROTEIN (GSU0061) FROM GEOBACTER SULFURREDUCENS PCA AT 1.80 A RESOLUTION | STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, LIPID BINDING PROTEIN
4yog:A (THR204) to (THR258) HKU4-3CLPRO BOUND TO NON-COVALENT INHIBITOR 3B | HKU4 3CLPRO MPRO NSP5, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4yog:B (THR204) to (THR258) HKU4-3CLPRO BOUND TO NON-COVALENT INHIBITOR 3B | HKU4 3CLPRO MPRO NSP5, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4kn7:E (ARG16) to (LEU80) X-RAY CRYSTAL STRUCTURE OF THE ESCHERICHIA COLI RNA POLYMERASE IN COMPLEX WITH BENZOXAZINORIFAMYCIN-2C | TRANSCRIPTION, DNA, RNA, TRANSFERASE-ANTIBIOTIC COMPLEX
3vb3:A (GLY251) to (SER301) CRYSTAL STRUCTURE OF SARS-COV 3C-LIKE PROTEASE IN APO FORM | HYDROLASE
3vb3:B (GLY251) to (SER301) CRYSTAL STRUCTURE OF SARS-COV 3C-LIKE PROTEASE IN APO FORM | HYDROLASE
3vdx:C (ASP155) to (TRP205) STRUCTURE OF A 16 NM PROTEIN CAGE DESIGNED BY FUSING SYMMETRIC OLIGOMERIC DOMAINS | PROTEIN DESIGN, BIONANOTECHNOLOGY, PROTEIN ASSEMBLY, SYMMETRY, BIOMATERIALS, DE NOVO PROTEIN
4kz6:A (ALA98) to (TRP138) CRYSTAL STRUCTURE OF AMPC BETA-LACTAMASE IN COMPLEX WITH FRAGMENT 13 ((2R,6R)-6-METHYL-1-(3-SULFANYLPROPANOYL)PIPERIDINE-2-CARBOXYLIC ACID) | AMPC BETA-LACTAMASE, CLASS C, HYDROLASE, CEPHALOSPORINASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3iho:A (PRO456) to (ALA494) THE C-TERMINAL GLYCOSYLASE DOMAIN OF HUMAN MBD4 | MBD4, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, DNA DAMAGE, DNA REPAIR, DNA-BINDING, HYDROLASE, NUCLEUS
4zro:A (PHE247) to (MET296) 2.1 A X-RAY STRUCTURE OF FIPV-3CLPRO BOUND TO COVALENT INHIBITOR | CORONAVIRUS, MAIN PROTEASE, 3CLPRO, MPRO, FIPV, FCOV, INHIBITOR COMPLEX, FELINE INFECTIOUS PERITONITIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4zro:B (SER200) to (THR254) 2.1 A X-RAY STRUCTURE OF FIPV-3CLPRO BOUND TO COVALENT INHIBITOR | CORONAVIRUS, MAIN PROTEASE, 3CLPRO, MPRO, FIPV, FCOV, INHIBITOR COMPLEX, FELINE INFECTIOUS PERITONITIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4zro:D (PHE247) to (GLY298) 2.1 A X-RAY STRUCTURE OF FIPV-3CLPRO BOUND TO COVALENT INHIBITOR | CORONAVIRUS, MAIN PROTEASE, 3CLPRO, MPRO, FIPV, FCOV, INHIBITOR COMPLEX, FELINE INFECTIOUS PERITONITIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2gx4:A (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS CORONAVIRUS 3CL PROTEASE INHIBITOR COMPLEX | SARS, 3CL PROTEASE, INHIBITOR COMPLEX, HYDROLASE
2h2z:A (GLY251) to (GLN299) CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE WITH AUTHENTIC N AND C-TERMINI | SARS, MAIN PROTEASE, AUTHENTIC N AND C TERMINI, VIRAL PROTEIN
1hu9:A (GLN665) to (ASN713) LIPOXYGENASE-3 (SOYBEAN) COMPLEX WITH 4-HYDROPEROXY-2- METHOXY-PHENOL | OXIDOREDUCTASE, METALLOPROTEIN, FE(III) COMPLEX, PURPLE LIPOXYGENASE, ENZYME INHIBITOR
1uk4:A (LEU250) to (GLY302) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEINASE (3CLPRO) COMPLEXED WITH AN INHIBITOR | ANTI-PARALLEL B-BARREL, ANTI-PARALLEL A-HELICES, AN INHIBITOR, HYDROLASE
1uk4:B (LEU250) to (GLY302) CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEINASE (3CLPRO) COMPLEXED WITH AN INHIBITOR | ANTI-PARALLEL B-BARREL, ANTI-PARALLEL A-HELICES, AN INHIBITOR, HYDROLASE
5c5o:A (GLY251) to (GLN299) STRUCTURE OF SARS-3CL PROTEASE COMPLEX WITH A PHENYL-BETA-ALANYL (S, R)-N-DECALIN TYPE INHIBITOR | HYDRASE PROTEINASE CONVERTING, DESIGNED INHIBITOR, HYDRASE-INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5c5o:B (GLY251) to (CYS300) STRUCTURE OF SARS-3CL PROTEASE COMPLEX WITH A PHENYL-BETA-ALANYL (S, R)-N-DECALIN TYPE INHIBITOR | HYDRASE PROTEINASE CONVERTING, DESIGNED INHIBITOR, HYDRASE-INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2ypt:A (SER397) to (HIS456) CRYSTAL STRUCTURE OF THE HUMAN NUCLEAR MEMBRANE ZINC METALLOPROTEASE ZMPSTE24 MUTANT (E336A) IN COMPLEX WITH A SYNTHETIC CSIM TETRAPEPTIDE FROM THE C-TERMINUS OF PRELAMIN A | HYDROLASE-PEPTIDE COMPLEX, M48 PEPTIDASE, INTEGRAL MEMBRANE PROTEIN, PRELAMIN A PROCESSING, AGEING, PROGERIA
2ypt:B (SER397) to (HIS456) CRYSTAL STRUCTURE OF THE HUMAN NUCLEAR MEMBRANE ZINC METALLOPROTEASE ZMPSTE24 MUTANT (E336A) IN COMPLEX WITH A SYNTHETIC CSIM TETRAPEPTIDE FROM THE C-TERMINUS OF PRELAMIN A | HYDROLASE-PEPTIDE COMPLEX, M48 PEPTIDASE, INTEGRAL MEMBRANE PROTEIN, PRELAMIN A PROCESSING, AGEING, PROGERIA
2ypt:D (SER397) to (HIS456) CRYSTAL STRUCTURE OF THE HUMAN NUCLEAR MEMBRANE ZINC METALLOPROTEASE ZMPSTE24 MUTANT (E336A) IN COMPLEX WITH A SYNTHETIC CSIM TETRAPEPTIDE FROM THE C-TERMINUS OF PRELAMIN A | HYDROLASE-PEPTIDE COMPLEX, M48 PEPTIDASE, INTEGRAL MEMBRANE PROTEIN, PRELAMIN A PROCESSING, AGEING, PROGERIA
2ypt:E (SER397) to (HIS456) CRYSTAL STRUCTURE OF THE HUMAN NUCLEAR MEMBRANE ZINC METALLOPROTEASE ZMPSTE24 MUTANT (E336A) IN COMPLEX WITH A SYNTHETIC CSIM TETRAPEPTIDE FROM THE C-TERMINUS OF PRELAMIN A | HYDROLASE-PEPTIDE COMPLEX, M48 PEPTIDASE, INTEGRAL MEMBRANE PROTEIN, PRELAMIN A PROCESSING, AGEING, PROGERIA
4ofh:A (PRO456) to (ALA494) STRUCTURAL BASIS FOR THYMINE GLYCOSYLASE ACTIVITY ON T:O6-METHYLG MISMATCH BY METHYL-CPG BINDING DOMAIN PROTEIN 4: IMPLICATIONS FOR ROLES OF ARG468 IN MISMATCH RECOGNITION AND CATALYSIS | PROTEIN-DNA COMPLEX, MISMATCH, THYMINE GLYCOSYLASE, HYDROLASE-DNA COMPLEX
2z9k:A (GLY251) to (SER301) COMPLEX STRUCTURE OF SARS-COV 3C-LIKE PROTEASE WITH JMF1600 | COMPLEX, ATP-BINDING, CYTOPLASM, ENDONUCLEASE, EXONUCLEASE, HELICASE, HYDROLASE, MEMBRANE, METAL-BINDING, NUCLEASE, NUCLEOTIDE-BINDING, NUCLEOTIDYLTRANSFERASE, PROTEASE, RIBOSOMAL FRAMESHIFT, RNA REPLICATION, RNA-BINDING, RNA- DIRECTED RNA POLYMERASE, THIOL PROTEASE, TRANSFERASE, TRANSMEMBRANE, ZINC, ZINC-FINGER
2z9k:B (GLY251) to (GLN299) COMPLEX STRUCTURE OF SARS-COV 3C-LIKE PROTEASE WITH JMF1600 | COMPLEX, ATP-BINDING, CYTOPLASM, ENDONUCLEASE, EXONUCLEASE, HELICASE, HYDROLASE, MEMBRANE, METAL-BINDING, NUCLEASE, NUCLEOTIDE-BINDING, NUCLEOTIDYLTRANSFERASE, PROTEASE, RIBOSOMAL FRAMESHIFT, RNA REPLICATION, RNA-BINDING, RNA- DIRECTED RNA POLYMERASE, THIOL PROTEASE, TRANSFERASE, TRANSMEMBRANE, ZINC, ZINC-FINGER
2z9l:A (GLY251) to (SER301) COMPLEX STRUCTURE OF SARS-COV 3C-LIKE PROTEASE WITH JMF1586 | COMPLEX, HYDROLASE
2z9l:B (GLY251) to (GLN299) COMPLEX STRUCTURE OF SARS-COV 3C-LIKE PROTEASE WITH JMF1586 | COMPLEX, HYDROLASE
1xtj:A (SER45) to (GLY82) STRUCTURE OF HUMAN UAP56 IN COMPLEX WITH ADP | ALPHA-BETA FOLD, GENE REGULATION
1mv8:A (THR202) to (ASP284) 1.55 A CRYSTAL STRUCTURE OF A TERNARY COMPLEX OF GDP-MANNOSE DEHYDROGENASE FROM PSUEDOMONAS AERUGINOSA | ROSSMANN FOLD, DOMAIN-SWAPPED DIMER, ENZYME COMPLEX WITH COFACTOR AND PRODUCT, OXIDOREDUCTASE
1mv8:B (THR202) to (ASP284) 1.55 A CRYSTAL STRUCTURE OF A TERNARY COMPLEX OF GDP-MANNOSE DEHYDROGENASE FROM PSUEDOMONAS AERUGINOSA | ROSSMANN FOLD, DOMAIN-SWAPPED DIMER, ENZYME COMPLEX WITH COFACTOR AND PRODUCT, OXIDOREDUCTASE
1mv8:C (THR202) to (ASP284) 1.55 A CRYSTAL STRUCTURE OF A TERNARY COMPLEX OF GDP-MANNOSE DEHYDROGENASE FROM PSUEDOMONAS AERUGINOSA | ROSSMANN FOLD, DOMAIN-SWAPPED DIMER, ENZYME COMPLEX WITH COFACTOR AND PRODUCT, OXIDOREDUCTASE
1mv8:D (THR202) to (ASP284) 1.55 A CRYSTAL STRUCTURE OF A TERNARY COMPLEX OF GDP-MANNOSE DEHYDROGENASE FROM PSUEDOMONAS AERUGINOSA | ROSSMANN FOLD, DOMAIN-SWAPPED DIMER, ENZYME COMPLEX WITH COFACTOR AND PRODUCT, OXIDOREDUCTASE
4peg:A (LYS273) to (TYR321) DBR1 IN COMPLEX WITH GUANOSINE-5'-MONOPHOSPHATE | NUCLEASE, PHOSPHODIESTERASE, METALLOHYDROLASE, METALLOPHOSPHOESTERASE, LARIAT RNA, HYDROLASE, METALLOENZYME
4peg:B (ASP272) to (TYR321) DBR1 IN COMPLEX WITH GUANOSINE-5'-MONOPHOSPHATE | NUCLEASE, PHOSPHODIESTERASE, METALLOHYDROLASE, METALLOPHOSPHOESTERASE, LARIAT RNA, HYDROLASE, METALLOENZYME
4peg:D (ASP272) to (TYR321) DBR1 IN COMPLEX WITH GUANOSINE-5'-MONOPHOSPHATE | NUCLEASE, PHOSPHODIESTERASE, METALLOHYDROLASE, METALLOPHOSPHOESTERASE, LARIAT RNA, HYDROLASE, METALLOENZYME
4peg:E (ASP272) to (TYR321) DBR1 IN COMPLEX WITH GUANOSINE-5'-MONOPHOSPHATE | NUCLEASE, PHOSPHODIESTERASE, METALLOHYDROLASE, METALLOPHOSPHOESTERASE, LARIAT RNA, HYDROLASE, METALLOENZYME
5dnw:A (TYR150) to (PHE194) CRYSTAL STRUCTURE OF KAI2-LIKE PROTEIN FROM STRIGA (APO STATE 1) | KAI2 KARRIKIN STRIGA, HYDROLASE
3lyb:B (GLY42) to (GLN66) STRUCTURE OF PUTATIVE ENDORIBONUCLEASE(KP1_3112) FROM KLEBSIELLA PNEUMONIAE | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC, HYDROLASE
4qd4:B (THR101) to (TRP140) STRUCTURE OF ADC-68, A NOVEL CARBAPENEM-HYDROLYZING CLASS C EXTENDED- SPECTRUM -LACTAMASE FROM ACINETOBACTER BAUMANNII | BETA-LACTAMASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, HYDROLASE
3ckd:C (SER284) to (SER325) CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF THE SHIGELLA TYPE III EFFECTOR IPAH | E3 UBIQUITIN LIGASE, HELICAL, TYPE III EFFECTOR, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, LIGASE
3d23:B (LEU246) to (GLY299) MAIN PROTEASE OF HCOV-HKU1 | MAIN PROTEASE, ATP-BINDING, ENDONUCLEASE, EXONUCLEASE, HELICASE, MEMBRANE, METAL-BINDING, NUCLEASE, NUCLEOTIDE-BINDING, NUCLEOTIDYLTRANSFERASE, PROTEASE, RNA REPLICATION, RNA-BINDING, RNA- DIRECTED RNA POLYMERASE, THIOL PROTEASE, TRANSFERASE, TRANSMEMBRANE, ZINC-FINGER, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3d23:A (LEU246) to (GLY299) MAIN PROTEASE OF HCOV-HKU1 | MAIN PROTEASE, ATP-BINDING, ENDONUCLEASE, EXONUCLEASE, HELICASE, MEMBRANE, METAL-BINDING, NUCLEASE, NUCLEOTIDE-BINDING, NUCLEOTIDYLTRANSFERASE, PROTEASE, RNA REPLICATION, RNA-BINDING, RNA- DIRECTED RNA POLYMERASE, THIOL PROTEASE, TRANSFERASE, TRANSMEMBRANE, ZINC-FINGER, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3d23:C (LEU246) to (GLY299) MAIN PROTEASE OF HCOV-HKU1 | MAIN PROTEASE, ATP-BINDING, ENDONUCLEASE, EXONUCLEASE, HELICASE, MEMBRANE, METAL-BINDING, NUCLEASE, NUCLEOTIDE-BINDING, NUCLEOTIDYLTRANSFERASE, PROTEASE, RNA REPLICATION, RNA-BINDING, RNA- DIRECTED RNA POLYMERASE, THIOL PROTEASE, TRANSFERASE, TRANSMEMBRANE, ZINC-FINGER, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3d23:D (LEU246) to (GLY299) MAIN PROTEASE OF HCOV-HKU1 | MAIN PROTEASE, ATP-BINDING, ENDONUCLEASE, EXONUCLEASE, HELICASE, MEMBRANE, METAL-BINDING, NUCLEASE, NUCLEOTIDE-BINDING, NUCLEOTIDYLTRANSFERASE, PROTEASE, RNA REPLICATION, RNA-BINDING, RNA- DIRECTED RNA POLYMERASE, THIOL PROTEASE, TRANSFERASE, TRANSMEMBRANE, ZINC-FINGER, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3e3y:A (HIS73) to (TRP99) Q138F HINCII BOUND TO GTTAAC AND COCRYSTALLIZED WITH 5 MM CA2+ | PROTEIN-DNA COMPLEX, ENDONUCLEASE, INDIRECT READOUT, HYDROLASE, NUCLEASE, RESTRICTION SYSTEM, HYDROLASE/DNA COMPLEX
3pvr:A (THR58) to (CYS137) THE PHENYLACETYL-COA MONOOXYGENASE PAAAC SUBCOMPLEX WITH BENZOYL-COA | PROTEIN-PROTEIN COMPLEX, FERRETIN-LIKE FOLD, BACTERIAL MULTICOMPONENT MONOOXYGENASE, STRUCTURAL GENOMICS, MONTREAL-KINGSTON BACTERIAL STRUCTURAL GENOMICS INITIATIVE, BSGI, OXIDOREDUCTASE
3pvy:A (LEU59) to (TRP123) THE PHENYLACETYL-COA MONOOXYGENASE PAAAC SUBCOMPLEX WITH COENZYME A | PROTEIN-PROTEIN COMPLEX, FERRITIN-LIKE FOLD, BACTERIAL MULTICOMPONENT MONOOXYGENASE, STRUCTURAL GENOMICS, MONTREAL-KINGSTON BACTERIAL STRUCTURAL GENOMICS INITIATIVE, BSGI, OXIDOREDUCTASE
4g12:B (ARG27) to (HIS65) CRYSTAL STRUCTURE OF PUTATIVE TETR FAMILY TRANSCRIPTIONAL REGULATOR, FAD35R, FROM MYCOBACTERIUM TUBERCULOSIS | OHM FOLD, FATTY ACID BINDING DOMAIN, DNA BINDING PROTEIN