2aim:A (HIS159) to (GLY212) CRUZAIN INHIBITED WITH BENZOYL-ARGININE-ALANINE-FLUOROMETHYLKETONE | CYSTEINE PROTEASE, TRYPANOSOMA CRUZI, PROTEINASE, PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1nb3:B (HIS159) to (VAL212) CRYSTAL STRUCTURE OF STEFIN A IN COMPLEX WITH CATHEPSIN H: N-TERMINAL RESIDUES OF INHIBITORS CAN ADAPT TO THE ACTIVE SITES OF ENDO-AND EXOPEPTIDASES | CYSTEINE PROTEINASE, AMINOPEPTIDASE, CYSTATIN, ENZYME-INHIBITOR COMPLEX, HYDROLASE
2avw:E (ILE260) to (SER329) CRYSTAL STRUCTURE OF MONOCLINIC FORM OF STREPTOCOCCUS MAC-1 | MAC-1, HYDROLASE
2bdl:A (HIS162) to (MET215) CATHEPSIN K COMPLEXED WITH A PYRROLIDINE KETOAMIDE-BASED INHIBITOR | CATHEPSIN, CYSTEINE PROTEASE, CATK, CATO, HYDROLASE
2p86:A (HIS162) to (GLY215) THE HIGH RESOLUTION CRYSTAL STRUCTURE OF ROHEDSAIN, THE MAJOR CATHEPSIN L PROTEASE FROM T. BRUCEI RHODESIENSE, BOUND TO INHIBITOR K11002 | CYSTEINE PROTEASE, TRYPANOSOMA BRUCEI, NEGLECTED DISEASE, HYDROLASE
3s3r:A (GLY268) to (ARG321) STRUCTURE OF CATHEPSIN B1 FROM SCHISTOSOMA MANSONI IN COMPLEX WITH K11777 INHIBITOR | PEPTIDASE, DIGESTIVE TRACT, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3s3r:C (GLY268) to (ILE322) STRUCTURE OF CATHEPSIN B1 FROM SCHISTOSOMA MANSONI IN COMPLEX WITH K11777 INHIBITOR | PEPTIDASE, DIGESTIVE TRACT, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1bqi:A (HIS159) to (PRO209) USE OF PAPAIN AS A MODEL FOR THE STRUCTURE-BASED DESIGN OF CATHEPSIN K INHIBITORS. CRYSTAL STRUCTURES OF TWO PAPAIN INHIBITOR COMPLEXES DEMONSTRATE BINDING TO S'-SUBSITES. | HYDROLASE, SULFHYDRYL PROTEINASE, PAPAIN
3ff9:A (ASP129) to (VAL187) STRUCTURE OF NK CELL RECEPTOR KLRG1 | NATURAL KILLER CELL RECEPTOR KLTG1, GLYCOPROTEIN, LECTIN, MEMBRANE, PHOSPHOPROTEIN, RECEPTOR, SIGNAL-ANCHOR, TRANSMEMBRANE, IMMUNE SYSTEM
3ff9:B (ASP129) to (VAL187) STRUCTURE OF NK CELL RECEPTOR KLRG1 | NATURAL KILLER CELL RECEPTOR KLTG1, GLYCOPROTEIN, LECTIN, MEMBRANE, PHOSPHOPROTEIN, RECEPTOR, SIGNAL-ANCHOR, TRANSMEMBRANE, IMMUNE SYSTEM
3fjp:B (GLY197) to (ARG232) APO STRUCTURE OF BIOTIN PROTEIN LIGASE FROM AQUIFEX AEOLICUS | BPL, BIOTIN PROTEIN LIGASE, LIGASE
1cjl:A (HIS163) to (VAL220) CRYSTAL STRUCTURE OF A CYSTEINE PROTEASE PROFORM | PROPEPTIDE, INHIBITOR, CYSTEINE PROTEASE, HYDROLASE
1cte:B (GLY197) to (ILE250) CRYSTAL STRUCTURES OF RECOMBINANT RAT CATHEPSIN B AND A CATHEPSIN B-INHIBITOR COMPLEX: IMPLICATIONS FOR STRUCTURE- BASED INHIBITOR DESIGN | THIOL PROTEASE
2d98:A (ALA102) to (ALA153) STRUCTURE OF VIL (EXTRA KI/I2 ADDED)-XYLANASE | IODO-TYROSINE, VAPORIZING IODINE LABELING(VIL), HYDROLASE
2r6n:A (HIS162) to (MET215) CRYSTAL STRUCTURE OF A PYRROLOPYRIMIDINE INHIBITOR IN COMPLEX WITH HUMAN CATHEPSIN K | COVALENT BOND TO INHIBITOR, DISEASE MUTATION, GLYCOPROTEIN, HYDROLASE, LYSOSOME, PROTEASE, THIOL PROTEASE, ZYMOGEN
2r9o:B (HIS164) to (ILE217) CATHEPSIN S COMPLEXED WITH COMPOUND 8 | HYDROLASE, CATHEPSIN, PROTEASE, GLYCOPROTEIN, LYSOSOME, POLYMORPHISM, THIOL PROTEASE, ZYMOGEN
4jkr:C (TYR614) to (SER656) CRYSTAL STRUCTURE OF E. COLI RNA POLYMERASE IN COMPLEX WITH PPGPP | RNA POLYMERASE, TRANSCRIPTION REGULATION, TRANSCRIPTION, TRANSFERASE
4jkr:I (TYR614) to (SER656) CRYSTAL STRUCTURE OF E. COLI RNA POLYMERASE IN COMPLEX WITH PPGPP | RNA POLYMERASE, TRANSCRIPTION REGULATION, TRANSCRIPTION, TRANSFERASE
2e3x:C (PRO64) to (LYS122) CRYSTAL STRUCTURE OF RUSSELL'S VIPER VENOM METALLOPROTEINASE | DISINTEGRIN, METALLOPROTEINASE, C-TYPE LECTIN, HYDROLASE, BLOOD CLOTTING, TOXIN
1f29:A (HIS159) to (GLY212) CRYSTAL STRUCTURE ANALYSIS OF CRUZAIN BOUND TO A VINYL SULFONE DERIVED INHIBITOR (I) | CYSTEINE PROTEASE, COVALENT INHIBITOR, VINYL SULFONE DERIVED, P1' POCKET, HYDROLASE
1f29:B (HIS159) to (GLY212) CRYSTAL STRUCTURE ANALYSIS OF CRUZAIN BOUND TO A VINYL SULFONE DERIVED INHIBITOR (I) | CYSTEINE PROTEASE, COVALENT INHIBITOR, VINYL SULFONE DERIVED, P1' POCKET, HYDROLASE
1f29:C (HIS159) to (GLY212) CRYSTAL STRUCTURE ANALYSIS OF CRUZAIN BOUND TO A VINYL SULFONE DERIVED INHIBITOR (I) | CYSTEINE PROTEASE, COVALENT INHIBITOR, VINYL SULFONE DERIVED, P1' POCKET, HYDROLASE
2eko:A (LEU31) to (LYS76) SOLUTION STRUCTURE OF RUH-073, A PSEUDO CHROMO DOMAIN FROM HUMAN CDNA | CHROMO DOMAIN, HISTONE TAIL, CHROMATIN ORGANIZATION MODIFIER, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, TRANSFERASE
1r5o:A (PHE560) to (LYS601) CRYSTAL STRUCTURE ANALYSIS OF SUP35 COMPLEXED WITH GMPPNP | TRANSLATION TERMINATION, PEPTIDE RELEASE, GTPASE
3ubu:B (SER64) to (LYS125) CRYSTAL STRUCTURE OF AGKISACUCETIN, A GPIB-BINDING SNACLEC (SNAKE C- TYPE LECTIN) THAT INHIBITS PLATELET | PLATELET INHIBITING, AGKISACUCETIN, DIMER, TOXIN, C-TYPE LECTIN-LIKE, GPIB INHIBITOR, GPIB BINDING
1fvu:B (ASP462) to (GLN524) CRYSTAL STRUCTURE OF BOTROCETIN | VON WILLBRAND FACTOR MODULATOR, C-TYPE LECTIN, METAL- BINDING, LOOP EXCHANGED DIMER, TOXIN
1fvu:D (ASP662) to (GLN724) CRYSTAL STRUCTURE OF BOTROCETIN | VON WILLBRAND FACTOR MODULATOR, C-TYPE LECTIN, METAL- BINDING, LOOP EXCHANGED DIMER, TOXIN
4yyq:B (HIS160) to (PRO214) FICIN A | CYSTEIN PROTEASE, HYDROLASE
2fo5:A (HIS167) to (TYR226) CRYSTAL STRUCTURE OF RECOMBINANT BARLEY CYSTEINE ENDOPROTEASE B ISOFORM 2 (EP-B2) IN COMPLEX WITH LEUPEPTIN | EP-B2, EPB2, EPB, CYSTEINE ENDOPROTEASE, ENDOPEPTIDASE, LEUPEPTIN, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2fo5:B (HIS167) to (TYR226) CRYSTAL STRUCTURE OF RECOMBINANT BARLEY CYSTEINE ENDOPROTEASE B ISOFORM 2 (EP-B2) IN COMPLEX WITH LEUPEPTIN | EP-B2, EPB2, EPB, CYSTEINE ENDOPROTEASE, ENDOPEPTIDASE, LEUPEPTIN, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2fo5:C (HIS167) to (PRO222) CRYSTAL STRUCTURE OF RECOMBINANT BARLEY CYSTEINE ENDOPROTEASE B ISOFORM 2 (EP-B2) IN COMPLEX WITH LEUPEPTIN | EP-B2, EPB2, EPB, CYSTEINE ENDOPROTEASE, ENDOPEPTIDASE, LEUPEPTIN, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2fo5:D (HIS167) to (TYR226) CRYSTAL STRUCTURE OF RECOMBINANT BARLEY CYSTEINE ENDOPROTEASE B ISOFORM 2 (EP-B2) IN COMPLEX WITH LEUPEPTIN | EP-B2, EPB2, EPB, CYSTEINE ENDOPROTEASE, ENDOPEPTIDASE, LEUPEPTIN, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1s4v:B (GLY163) to (PRO217) THE 2.0 A CRYSTAL STRUCTURE OF THE KDEL-TAILED CYSTEINE ENDOPEPTIDASE FUNCTIONING IN PROGRAMMED CELL DEATH OF RICINUS COMMUNIS ENDOSPERM | KDEL ER RETENTION SIGNAL, ENDOSPERM, RICINOSOMES, SEED GERMINATION, SENESCENCE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1s5j:A (LYS49) to (ASP93) INSIGHT IN DNA REPLICATION: THE CRYSTAL STRUCTURE OF DNA POLYMERASE B1 FROM THE ARCHAEON SULFOLOBUS SOLFATARICUS | DNA POLYMERASE, REPLICATION, DISULFIDE BONDS, TRANSFERASE
2vrp:A (ASP68) to (LEU134) STRUCTURE OF RHODOCYTIN | C-TYPE LECTIN-LIKE, SUGAR-BINDING PROTEIN, LECTIN, CLEC-2, VENOM, AGGRETIN
2vrp:B (ASN62) to (LYS122) STRUCTURE OF RHODOCYTIN | C-TYPE LECTIN-LIKE, SUGAR-BINDING PROTEIN, LECTIN, CLEC-2, VENOM, AGGRETIN
1snk:A (HIS162) to (MET215) CATHEPSIN K COMPLEXED WITH CARBAMATE DERIVATIZED NORLEUCINE ALDEHYDE | CATK, HYDROLASE
4zi8:A (GLU55) to (PRO106) STRUCTURE OF MOUSE CLUSTERED PCDHGC3 EC1-3 | PROTOCADHERIN, COMPLEX, CELL ADHESION
3iej:B (HIS164) to (ILE217) PYRAZOLE-BASED CATHEPSIN S INHIBITORS WITH ARYLALKYNES AS P1 BINDING ELEMENTS | CATHEPSIN S, DISULFIDE BOND, GLYCOPROTEIN, HYDROLASE, LYSOSOME, POLYMORPHISM, PROTEASE, THIOL PROTEASE, ZYMOGEN
2h7j:B (HIS164) to (ILE217) CRYSTAL STRUCTURE OF CATHEPSIN S IN COMPLEX WITH A NONPEPTIDIC INHIBITOR. | CATHEPSIN S, NONPEPTIDIC, CHLOROMETHYLKETONE, SUBSTRATE ACTIVITY SCREENING, HYDROLASE
1tu6:A (HIS276) to (MET329) CATHEPSIN K COMPLEXED WITH A KETOAMIDE INHIBITOR | CATK, CYSTEINE PROTEASE, HYDROLASE
1u0n:C (GLY2061) to (GLN2124) THE TERNARY VON WILLEBRAND FACTOR A1-GLYCOPROTEIN IBALPHA- BOTROCETIN COMPLEX | ROSSMANN FOLD, LRR MOTIF, C-TYPE LECTIN FOLD, PROTEIN- PROTEIN COMPLEX, BLOOD CLOTTING
1u0o:A (LEU65) to (PRO131) THE MOUSE VON WILLEBRAND FACTOR A1-BOTROCETIN COMPLEX | ROSSMANN FOLD, C-TYPE LECTIN FOLD, PROTEIN-PROTEIN COMPLEX, BLOOD CLOTTING
1u0o:B (ASP262) to (GLN324) THE MOUSE VON WILLEBRAND FACTOR A1-BOTROCETIN COMPLEX | ROSSMANN FOLD, C-TYPE LECTIN FOLD, PROTEIN-PROTEIN COMPLEX, BLOOD CLOTTING
2hxz:B (HIS164) to (ILE217) CRYSTAL STRUCTURE OF CATHEPSIN S IN COMPLEX WITH A NONPEPTIDIC INHIBITOR (HEXAGONAL SPACEGROUP) | CATHEPSIN S, NONPEPTIDIC, CHLOROMETHYLKETONE, SUBSTRATE ACTIVITY SCREENING, HYDROLASE
1ijk:B (LEU65) to (PRO131) THE VON WILLEBRAND FACTOR MUTANT (I546V) A1 DOMAIN- BOTROCETIN COMPLEX | DINUCLEOTIDE-BINDING FOLD, C-TYPE LECTIN FOLD, BLOOD CLOTTING/TOXIN COMPLEX
1ijk:C (ASP262) to (GLN324) THE VON WILLEBRAND FACTOR MUTANT (I546V) A1 DOMAIN- BOTROCETIN COMPLEX | DINUCLEOTIDE-BINDING FOLD, C-TYPE LECTIN FOLD, BLOOD CLOTTING/TOXIN COMPLEX
1iod:B (GLY262) to (GLN322) CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN THE COAGULATION FACTOR X BINDING PROTEIN FROM SNAKE VENOM AND THE GLA DOMAIN OF FACTOR X | CALCIUM BRIDGING, DOMAIN SWAPPING, HYDROLASE/HYDROLASE INHIBITOR COMPLEX
1umr:B (SER66) to (PRO132) CRYSTAL STRUCTURE OF THE PLATELET ACTIVATOR CONVULXIN, A DISULFIDE LINKED A4B4 CYCLIC TETRAMER FROM THE VENOM OF CROTALUS DURISSUS TERRIFICUS | LECTIN, C-TYPE LECTIN, PLATELET, SUGAR-BINDING PROTEIN, ACTIVATOR, SNAKE VENOM
1uos:A (SER64) to (PRO130) THE CRYSTAL STRUCTURE OF THE SNAKE VENOM TOXIN CONVULXIN | SUGAR-BINDING PROTEIN, LECTIN, CONVULXIN, C-TYPE LECTIN, SNAKE TOXIN, GPVI, STRUCTURAL PROTEOMICS IN EUROPE, SPINE, STRUCTURAL GENOMICS
1uos:C (SER64) to (PRO130) THE CRYSTAL STRUCTURE OF THE SNAKE VENOM TOXIN CONVULXIN | SUGAR-BINDING PROTEIN, LECTIN, CONVULXIN, C-TYPE LECTIN, SNAKE TOXIN, GPVI, STRUCTURAL PROTEOMICS IN EUROPE, SPINE, STRUCTURAL GENOMICS
1ixx:F (SER62) to (GLN122) CRYSTAL STRUCTURE OF COAGULATION FACTORS IX/X-BINDING PROTEIN (IX/X- BP) FROM VENOM OF HABU SNAKE WITH A HETERODIMER OF C-TYPE LECTIN DOMAINS | COAGULATION FACTOR BINDING, C-TYPE LECTIN, GLA-DOMAIN BINDING, C-TYPE CRD MOTIF, LOOP EXCHANGED DIMER
1j34:B (SER262) to (GLN322) CRYSTAL STRUCTURE OF MG(II)-AND CA(II)-BOUND GLA DOMAIN OF FACTOR IX COMPLEXED WITH BINDING PROTEIN | MAGNESIUM ION, CALCIUM ION, GLA DOMAIN, PROTEIN BINDING/BLOOD CLOTTING COMPLEX
1v7p:B (THR61) to (LEU123) STRUCTURE OF EMS16-ALPHA2-I DOMAIN COMPLEX | SNAKE VENOM, C-TYPE LECTIN, ANTAGONIST, INTEGRIN, CELL ADHESION, GLYCOPROTEIN, TOXIN-CELL ADHESION COMPLEX
3woj:A (ASN183) to (GLY271) CRYSTAL STRUCTURE OF THE DAP BII | CHYMOTRYPSIN FOLD, S46 PEPTIDASE, HYDROLASE
3wwk:A (ASP68) to (LEU134) CRYSTAL STRUCTURE OF CLEC-2 IN COMPLEX WITH RHODOCYTIN | C-TYPE LECTIN FOLD, CARBOHYDRATE BINDING, PODOPLANIN, RHODOCYTIN, SUGAR BINDING PROTEIN
3wwk:D (ASP68) to (LEU134) CRYSTAL STRUCTURE OF CLEC-2 IN COMPLEX WITH RHODOCYTIN | C-TYPE LECTIN FOLD, CARBOHYDRATE BINDING, PODOPLANIN, RHODOCYTIN, SUGAR BINDING PROTEIN
3wwk:E (ASN62) to (LYS122) CRYSTAL STRUCTURE OF CLEC-2 IN COMPLEX WITH RHODOCYTIN | C-TYPE LECTIN FOLD, CARBOHYDRATE BINDING, PODOPLANIN, RHODOCYTIN, SUGAR BINDING PROTEIN
3wwk:G (ASP68) to (LEU134) CRYSTAL STRUCTURE OF CLEC-2 IN COMPLEX WITH RHODOCYTIN | C-TYPE LECTIN FOLD, CARBOHYDRATE BINDING, PODOPLANIN, RHODOCYTIN, SUGAR BINDING PROTEIN
3wwk:H (ASN62) to (LYS122) CRYSTAL STRUCTURE OF CLEC-2 IN COMPLEX WITH RHODOCYTIN | C-TYPE LECTIN FOLD, CARBOHYDRATE BINDING, PODOPLANIN, RHODOCYTIN, SUGAR BINDING PROTEIN
3wwk:J (ASP68) to (LEU134) CRYSTAL STRUCTURE OF CLEC-2 IN COMPLEX WITH RHODOCYTIN | C-TYPE LECTIN FOLD, CARBOHYDRATE BINDING, PODOPLANIN, RHODOCYTIN, SUGAR BINDING PROTEIN
3wwk:K (ASN62) to (LYS122) CRYSTAL STRUCTURE OF CLEC-2 IN COMPLEX WITH RHODOCYTIN | C-TYPE LECTIN FOLD, CARBOHYDRATE BINDING, PODOPLANIN, RHODOCYTIN, SUGAR BINDING PROTEIN
2xu5:A (HIS163) to (VAL220) CATHEPSIN L WITH A NITRILE INHIBITOR | HYDROLASE, DRUG DESIGN, THIOL PROTEASE
1jzn:B (GLU64) to (LYS134) CRYSTAL STRUCTURE OF A GALACTOSE-SPECIFIC C-TYPE LECTIN | C-TYPE LECTIN, PROTEIN-DISACCHARIDE COMPLEX, SUGAR BINDING PROTEIN
1jzn:D (GLU64) to (LYS134) CRYSTAL STRUCTURE OF A GALACTOSE-SPECIFIC C-TYPE LECTIN | C-TYPE LECTIN, PROTEIN-DISACCHARIDE COMPLEX, SUGAR BINDING PROTEIN
2jic:A (ALA102) to (ALA153) HIGH RESOLUTION STRUCTURE OF XYLANASE-II FROM ONE MICRON BEAM EXPERIMENT | HYDROLASE, ENDONUCLEASE, XYLAN DEGRADATION, FUNGI, XYLAN, MICROBEAM, GLYCOSIDASE
1x2w:B (SER62) to (GLN122) CRYSTAL STRUCTURE OF APO-HABU IX-BP AT PH 4.6 | HETERODIMER, DOMAIN SWAPPING, C-TYPE LECTIN-LIKE PROTEIN, PROTEIN BINDING
1m6d:B (HIS159) to (ASP212) CRYSTAL STRUCTURE OF HUMAN CATHEPSIN F | PAPAIN FAMILY CYSTEINE PROTEASE, HYDROLASE
4p6g:A (HIS164) to (ILE217) CRYSTAL STRUCTURE OF HUMAN CATHEPSIN S BOUND TO A NON-COVALENT INHIBITOR. | CATHESPSIN S, NON-COVALENT INHIBITOR, CYSTEINE PROTEASE
4p6g:B (HIS164) to (ILE217) CRYSTAL STRUCTURE OF HUMAN CATHEPSIN S BOUND TO A NON-COVALENT INHIBITOR. | CATHESPSIN S, NON-COVALENT INHIBITOR, CYSTEINE PROTEASE
4p6g:D (HIS164) to (ILE217) CRYSTAL STRUCTURE OF HUMAN CATHEPSIN S BOUND TO A NON-COVALENT INHIBITOR. | CATHESPSIN S, NON-COVALENT INHIBITOR, CYSTEINE PROTEASE
5d74:A (PHE199) to (LYS245) THE CRYSTAL STRUCTURE OF LY7917 | ENDOLYSIN, PROPHAGE, LYTIC ACTIVITY, HYDROLASE
1muq:B (GLU64) to (LYS134) X-RAY CRYSTAL STRUCTURE OF RATTLESNAKE VENOM COMPLEXED WITH THIODIGALACTOSIDE | C-TYPE LECTIN, PROTEIN-CARBOHYDRATE COMPLEX, DECAMER, CALCIUM BINDING, SUGAR BINDING PROTEIN
3kwn:A (HIS164) to (ILE217) CATHEPSIN S IN COMPLEX WITH THIOETHER ACETAMIDE P3 INHIBITOR | GLYCOPROTEIN, HYDROLASE, LYSOSOME, PROTEASE, THIOL PROTEASE, ZYMOGEN
3kwz:A (HIS162) to (MET215) CATHEPSIN K IN COMPLEX WITH A NON-SELECTIVE 2-CYANO-PYRIMIDINE INHIBITOR | CATHEPSIN K, ENZYME INHIBITOR, COVALENT REVERSIBLE INHIBITOR, DISEASE MUTATION, DISULFIDE BOND, GLYCOPROTEIN, HYDROLASE, LYSOSOME, PROTEASE, THIOL PROTEASE, ZYMOGEN
4qh6:A (HIS162) to (ALA212) CRYSTAL STRUCTURE OF CRUZAIN WITH NITRILE INHIBITOR N-(2-AMINOETHYL)- NALPHA-BENZOYL-L-PHENYLALANINAMIDE | THIOL PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3mpe:B (HIS164) to (ILE217) CRYSTAL STRUCTURE OF HUMAN CATHEPSIN-S C25S MUTANT WITH BOUND DRUG | CATS, CATHEPSIN S, DIAZINONES, PYRAZOLE, P3, HYDROLASE
3mpf:B (HIS164) to (ILE217) CRYSTAL STRUCTURE OF HUMAN CATHEPSIN-S C25S MUTANT WITH BOUND DRUG | CATS, CATHEPSIN S, PYRAZOLE, DIAZINONES, P3, HYDROLASE
4bqv:C (HIS287) to (ILE340) MOUSE CATHEPSIN S WITH COVALENT LIGAND | HYDROLASE, CYSTEINE PROTEASE
4bs5:A (HIS287) to (ILE340) MOUSE CATHEPSIN S WITH COVALENT LIGAND | HYDROLASE, CYSTEINE PROTEASE, COVALENT LIGAND
4bs6:B (HIS287) to (ILE340) MOUSE CATHEPSIN S WITH COVALENT LIGAND | HYDROLASE, CYSTEINE PROTEASE, COVALENT LIGAND
3bx4:A (VAL70) to (LEU134) CRYSTAL STRUCTURE OF THE SNAKE VENOM TOXIN AGGRETIN | TOXIN
3bx4:B (ASN62) to (LYS122) CRYSTAL STRUCTURE OF THE SNAKE VENOM TOXIN AGGRETIN | TOXIN
3bx4:C (ASP68) to (LEU134) CRYSTAL STRUCTURE OF THE SNAKE VENOM TOXIN AGGRETIN | TOXIN
3bx4:D (ASN62) to (LYS122) CRYSTAL STRUCTURE OF THE SNAKE VENOM TOXIN AGGRETIN | TOXIN
5fg3:A (PRO476) to (ASP512) CRYSTAL STRUCTURE OF GDP-BOUND AIF5B FROM AEROPYRUM PERNIX | TRANSLATION INITIATON FACTOR, GTPASE, RIBOSOMAL SUBUNIT JOINING, CRENARCHAEA, TRANSLATION
3c4s:B (ARG19) to (LYS56) CRYSTAL STRUCTURE OF THE SSL0352 PROTEIN FROM SYNECHOCYSTIS SP. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET SGR42 | P74795_SYNY3, SSL0352, NESG, SGR42, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, UNKNOWN FUNCTION
3o0u:A (HIS162) to (MET215) CATHEPSIN K COVALENTLY BOUND TO A CYANO-PYRIMIDINE INHIBITOR WITH IMPROVED SELECTIVITY OVER HERG | HYDROLASE, COVALENT 2-CYANO-PYRIMIDINE INHIBITOR, REVERSIBLE COVALENT BOND BETWEEN CYS25 AND LIGAND, BONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3o1g:A (HIS162) to (MET215) CATHEPSIN K COVALENTLY BOUND TO A 2-CYANO PYRIMIDINE INHIBITOR WITH A BENZYL P3 GROUP. | HYDROLASE, REVERSIBLE COVALENT INHIBITOR, LIGAND COVALENTLY BOUND TO CYS25, BONE, K PROTEIN FROM COMP
3ovz:A (HIS162) to (MET215) CATHEPSIN K IN COMPLEX WITH A COVALENT INHIBITOR WITH A KETOAMIDE WARHEAD | CATHEPSIN K, HYDROLASE, COVALENT INHIBITOR, KETOAMIDE WARHEAD, LIGAND FORMS COVALENT BOND TO CYS25, LYSOSOMES, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5jaj:A (TYR585) to (PRO641) STRUCTURE OF CHICKEN LGP2 WITHA 5'P 10-MER DSRNA AND ADP-ALF4-MG. | INNATE IMMUNE PATTERN RECOGNITION RECEPTOR, RIG-I LIKE HELCASE, DSRNA BINDING, DSRNA-DEPENDENT ATPASE, RNA BINDING PROTEIN
1nqc:A (HIS164) to (ILE217) CRYSTAL STRUCTURES OF CATHEPSIN S INHIBITOR COMPLEXES | ANTIGEN PRESENTATION, BINDING SPECIFICITY, CYSTEINE PROTEASES, INHIBITOR COMPLEXES, STRUCTURE-BASED DESIGN, STRUCTURAL PLASTICITY, HYDROLASE
1c3a:A (GLN66) to (THR132) CRYSTAL STRUCTURE OF FLAVOCETIN-A FROM THE HABU SNAKE VENOM, A NOVEL CYCLIC TETRAMER OF C-TYPE LECTIN-LIKE HETERODIMERS | C-TYPE LECTIN-LIKE DOMAINS, MEMBRANE PROTEIN
1c3a:B (ASP264) to (GLN324) CRYSTAL STRUCTURE OF FLAVOCETIN-A FROM THE HABU SNAKE VENOM, A NOVEL CYCLIC TETRAMER OF C-TYPE LECTIN-LIKE HETERODIMERS | C-TYPE LECTIN-LIKE DOMAINS, MEMBRANE PROTEIN
1ewl:A (HIS159) to (ALA209) CRYSTAL STRUCTURE OF CRUZAIN BOUND TO WRR-99 | PAPAIN-LIKE CYSTEINE PROTEASE, DRUG DESIGN, COVALENT INHIBITOR, CRUZIPAIN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1ree:A (ALA102) to (ALA153) ENDO-1,4-BETA-XYLANASE II COMPLEX WITH 3,4-EPOXYBUTYL-BETA- D-XYLOSIDE | XYLANASE, XYLAN DEGRADATION, HYDROLASE
1v4l:A (GLN66) to (THR132) CRYSTAL STRUCTURE OF A PLATELET AGGLUTINATION FACTOR ISOLATED FROM THE VENOM OF TAIWAN HABU (TRIMERESURUS MUCROSQUAMATUS) | LECTIN-LIKE, SQUARE-SHAPED RING, BLOOD CLOTTING
1v4l:B (ASP264) to (GLN324) CRYSTAL STRUCTURE OF A PLATELET AGGLUTINATION FACTOR ISOLATED FROM THE VENOM OF TAIWAN HABU (TRIMERESURUS MUCROSQUAMATUS) | LECTIN-LIKE, SQUARE-SHAPED RING, BLOOD CLOTTING
1v4l:C (GLN66) to (THR132) CRYSTAL STRUCTURE OF A PLATELET AGGLUTINATION FACTOR ISOLATED FROM THE VENOM OF TAIWAN HABU (TRIMERESURUS MUCROSQUAMATUS) | LECTIN-LIKE, SQUARE-SHAPED RING, BLOOD CLOTTING
1v4l:D (ASP264) to (GLN324) CRYSTAL STRUCTURE OF A PLATELET AGGLUTINATION FACTOR ISOLATED FROM THE VENOM OF TAIWAN HABU (TRIMERESURUS MUCROSQUAMATUS) | LECTIN-LIKE, SQUARE-SHAPED RING, BLOOD CLOTTING
1v4l:E (GLN66) to (THR132) CRYSTAL STRUCTURE OF A PLATELET AGGLUTINATION FACTOR ISOLATED FROM THE VENOM OF TAIWAN HABU (TRIMERESURUS MUCROSQUAMATUS) | LECTIN-LIKE, SQUARE-SHAPED RING, BLOOD CLOTTING
1v4l:F (ASP264) to (GLN324) CRYSTAL STRUCTURE OF A PLATELET AGGLUTINATION FACTOR ISOLATED FROM THE VENOM OF TAIWAN HABU (TRIMERESURUS MUCROSQUAMATUS) | LECTIN-LIKE, SQUARE-SHAPED RING, BLOOD CLOTTING
1x2t:B (SER62) to (GLN122) CRYSTAL STRUCTURE OF HABU IX-BP AT PH 6.5 | HETERODIMER, DOMAIN SWAPPING, C-TYPE LECTIN-LIKE PROTEIN, PROTEIN BINDING
1x2t:D (SER62) to (GLN122) CRYSTAL STRUCTURE OF HABU IX-BP AT PH 6.5 | HETERODIMER, DOMAIN SWAPPING, C-TYPE LECTIN-LIKE PROTEIN, PROTEIN BINDING
1mem:A (HIS159) to (MET211) CRYSTAL STRUCTURE OF CATHEPSIN K COMPLEXED WITH A POTENT VINYL SULFONE INHIBITOR | OSTEOPOROSIS, PROTEASE, DRUG DESIGN, CYSTEINE, OSTEOCLAST, DISEASE MUTATION, DISULFIDE BOND, GLYCOPROTEIN, LYSOSOME, THIOL PROTEASE, ZYMOGEN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qki:B (PRO142) to (SER187) DIMERIC FORM OF HUMAN LLT1, A LIGAND FOR NKR-P1 | C-TYPE LECTIN LIKE FOLD, LIGAND FOR HUMAN RECEPTOR NKR-P1, GLYCOSYLATION; DEGLYCOSYLATED AFTER THE FIRST GLCNAC UNIT, ANCHORED IN MEMBRANE ON CELL SURFACE, IMMUNE SYSTEM
3bdw:B (PRO171) to (HIS231) HUMAN CD94/NKG2A | NK CELLS, RECEPTOR, GLYCOPROTEIN, LECTIN, MEMBRANE, SIGNAL-ANCHOR, TRANSMEMBRANE, IMMUNE SYSTEM RECEPTOR
3c9e:A (HIS162) to (MET215) CRYSTAL STRUCTURE OF THE CATHEPSIN K : CHONDROITIN SULFATE COMPLEX. | N:1 CATHEPSIN K : CHONDROITIN SULFATE COMPLEX, "BEADS-ON-A-STRING" ORGANIZATION, HYDROLASE, LYSOSOME, PROTEASE, THIOL PROTEASE
4c5e:A (SER702) to (ALA752) CRYSTAL STRUCTURE OF THE MINIMAL PHO-SFMBT COMPLEX (P21 SPACEGROUP) | TRANSCRIPTION
4w5c:A (HIS162) to (GLY215) CRYSTAL STRUCTURE ANALYSIS OF CRUZAIN WITH THREE FRAGMENTS: 1 (N-(1H- BENZIMIDAZOL-2-YL)-1,3-DIMETHYL-PYRAZOLE-4-CARBOXAMIDE), 6 (2-AMINO- 4,6-DIFLUOROBENZOTHIAZOLE) AND 9 (N-(1H-BENZIMIDAZOL-2-YL)-3-(4- FLUOROPHENYL)-1H-PYRAZOLE-4-CARBOXAMIDE). | CYSTEINE PROTEASE, CRUZAIN, FRAGMENTS-BASED DRUG DISCOVERY, MUTAGENESIS, SPR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4w5c:B (HIS162) to (GLY215) CRYSTAL STRUCTURE ANALYSIS OF CRUZAIN WITH THREE FRAGMENTS: 1 (N-(1H- BENZIMIDAZOL-2-YL)-1,3-DIMETHYL-PYRAZOLE-4-CARBOXAMIDE), 6 (2-AMINO- 4,6-DIFLUOROBENZOTHIAZOLE) AND 9 (N-(1H-BENZIMIDAZOL-2-YL)-3-(4- FLUOROPHENYL)-1H-PYRAZOLE-4-CARBOXAMIDE). | CYSTEINE PROTEASE, CRUZAIN, FRAGMENTS-BASED DRUG DISCOVERY, MUTAGENESIS, SPR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX