{"context":{"query":">>uniprot>>pdb","source_dataset":"uniprot","target_dataset":"pdb"},"stats":{"queried":3,"total":108,"mapped":3},"pagination":{"has_next":true,"next_token":"-1[]P00734,1,P00734,49,1]["},"schema":"id|title|method|resolution|source_organism|chain_count|header","mappings":[{"input":"Q9UKV0","source":"Q9UKV0|Histone deacetylase 9","targets":["8Q9N|Crystal Structure of the MADS-box/MEF2 Domain of MEF2D bound to dsDNA and MITR deacetylase binding motif mutant L151V.|X-RAY DIFFRACTION|1.51|Homo sapiens; SYNTHETIC CONSTRUCT|0|TRANSCRIPTION","8Q9R|Crystal structure of MADS-box/MEF2D N-terminal domain bound to dsDNA and HDAC9 deacetylase binding motif|X-RAY DIFFRACTION|2.25|DNA molecule; Homo sapiens|0|TRANSCRIPTION"]},{"input":"Q9UM47","source":"Q9UM47|Neurogenic locus notch homolog protein 3","targets":["4ZLP|Crystal Structure of Notch3 Negative Regulatory Region|X-RAY DIFFRACTION|2.479|Homo sapiens|0|TRANSCRIPTION","5CZV|Crystal structure of Notch3 NRR in complex with 20350 Fab|X-RAY DIFFRACTION|3.19|Homo sapiens|0|IMMUNE SYSTEM","5CZX|Crystal structure of Notch3 NRR in complex with 20358 Fab|X-RAY DIFFRACTION|2.1|Homo sapiens|0|IMMUNE SYSTEM","6WQU|CSL (RBPJ) bound to Notch3 RAM and DNA|X-RAY DIFFRACTION|2.41|Homo sapiens; Mus musculus; SYNTHETIC CONSTRUCT|0|TRANSCRIPTION/SIGNALING PROTEIN/DNA","6XSW|Structure of the Notch3 NRR in complex with an antibody Fab Fragment|X-RAY DIFFRACTION|2.98|Homo sapiens; Rattus norvegicus|0|SIGNALING PROTEIN/Immune System","8OS0|Solution NMR structure of Notch3 WT TMD|SOLUTION NMR|||0|MEMBRANE PROTEIN"]},{"input":"P00734","source":"P00734|Prothrombin","targets":["1A2C|Structure of thrombin inhibited by AERUGINOSIN298-A from a BLUE-GREEN ALGA|X-RAY DIFFRACTION|2.1|Hirudo medicinalis; Homo sapiens; Microcystis aeruginosa|0|Hydrolase/Hydrolase Inhibitor","1A3B|COMPLEX OF HUMAN ALPHA-THROMBIN WITH THE BIFUNCTIONAL BORONATE INHIBITOR BOROLOG1|X-RAY DIFFRACTION|1.8|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1A3E|COMPLEX OF HUMAN ALPHA-THROMBIN WITH THE BIFUNCTIONAL BORONATE INHIBITOR BOROLOG2|X-RAY DIFFRACTION|1.85|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1A46|THROMBIN COMPLEXED WITH HIRUGEN AND A BETA-STRAND MIMETIC INHIBITOR|X-RAY DIFFRACTION|2.12|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1A4W|CRYSTAL STRUCTURES OF THROMBIN WITH THIAZOLE-CONTAINING INHIBITORS: PROBES OF THE S1' BINDING SITE|X-RAY DIFFRACTION|1.8|Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1A5G|HUMAN THROMBIN COMPLEXED WITH NOVEL SYNTHETIC PEPTIDE MIMETIC INHIBITOR AND HIRUGEN|X-RAY DIFFRACTION|2.06|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1A61|THROMBIN COMPLEXED WITH A BETA-MIMETIC THIAZOLE-CONTAINING INHIBITOR|X-RAY DIFFRACTION|2.2|Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1ABI|STRUCTURE OF THE HIRULOG 3-THROMBIN COMPLEX AND NATURE OF THE S' SUBSITES OF SUBSTRATES AND INHIBITORS|X-RAY DIFFRACTION|2.3|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1ABJ|STRUCTURE OF THE HIRULOG 3-THROMBIN COMPLEX AND NATURE OF THE S' SUBSITES OF SUBSTRATES AND INHIBITORS|X-RAY DIFFRACTION|2.4|Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1AD8|COMPLEX OF THROMBIN WITH AND INHIBITOR CONTAINING A NOVEL P1 MOIETY|X-RAY DIFFRACTION|2|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1AE8|HUMAN ALPHA-THROMBIN INHIBITION BY EOC-D-PHE-PRO-AZALYS-ONP|X-RAY DIFFRACTION|2|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1AFE|HUMAN ALPHA-THROMBIN INHIBITION BY CBZ-PRO-AZALYS-ONP|X-RAY DIFFRACTION|2|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1AHT|CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN COMPLEXED WITH HIRUGEN AND P-AMIDINOPHENYLPYRUVATE AT 1.6 ANGSTROMS RESOLUTION|X-RAY DIFFRACTION|1.6|Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1AI8|HUMAN ALPHA-THROMBIN TERNARY COMPLEX WITH THE EXOSITE INHIBITOR HIRUGEN AND ACTIVE SITE INHIBITOR PHCH2OCO-D-DPA-PRO-BOROMPG|X-RAY DIFFRACTION|1.85|Hirudo medicinalis; Homo sapiens|0|BLOOD COAGULATION/HYDROLASE INHIBITOR","1AIX|HUMAN ALPHA-THROMBIN TERNARY COMPLEX WITH EXOSITE INHIBITOR HIRUGEN AND ACTIVE SITE INHIBITOR PHCH2OCO-D-DPA-PRO-BOROVAL|X-RAY DIFFRACTION|2.1|Hirudo medicinalis; Homo sapiens|0|BLOOD COAGULATION/HYDROLASE INHIBITOR","1AWF|NOVEL COVALENT THROMBIN INHIBITOR FROM PLANT EXTRACT|X-RAY DIFFRACTION|2.2|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1AWH|NOVEL COVALENT THROMBIN INHIBITOR FROM PLANT EXTRACT|X-RAY DIFFRACTION|3|Homo sapiens|0|COMPLEX (PROTEASE/INHIBITOR)","1AY6|THROMBIN INHIBITOR FROM THEONALLA, CYCLOTHEANAMIDE-BASED MACROCYCLIC TRIPEPTIDE MOTIF|X-RAY DIFFRACTION|1.8|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","1B5G|HUMAN THROMBIN COMPLEXED WITH NOVEL SYNTHETIC PEPTIDE MIMETIC INHIBITOR AND HIRUGEN|X-RAY DIFFRACTION|2.07|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1B7X|STRUCTURE OF HUMAN ALPHA-THROMBIN Y225I MUTANT BOUND TO D-PHE-PRO-ARG-CHLOROMETHYLKETONE|X-RAY DIFFRACTION|2.1|Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1BA8|THROMBIN INHIBITOR WITH A RIGID TRIPEPTIDYL ALDEHYDES|X-RAY DIFFRACTION|1.8|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1BB0|THROMBIN INHIBITORS WITH RIGID TRIPEPTIDYL ALDEHYDES|X-RAY DIFFRACTION|2.1|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1BCU|ALPHA-THROMBIN COMPLEXED WITH HIRUGEN AND PROFLAVIN|X-RAY DIFFRACTION|2|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1BHX|X-RAY STRUCTURE OF THE COMPLEX OF HUMAN ALPHA THROMBIN WITH THE INHIBITOR SDZ 229-357|X-RAY DIFFRACTION|2.3|Homo sapiens|0|SERINE PROTEASE","1BMM|HUMAN ALPHA-THROMBIN COMPLEXED WITH [S-(R*,R*)]-4-[(AMINOIMINOMETHYL)AMINO]-N-[[1-[3-HYDROXY-2-[(2-NAPHTHALENYLSULFONYL)AMINO]-1-OXOPROPYL]-2-PYRROLIDINYL] METHYL]BUTANAMIDE (BMS-186282)|X-RAY DIFFRACTION|2.6|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1BMN|HUMAN ALPHA-THROMBIN COMPLEXED WITH [S-(R*,R*)]-1-(AMINOIMINOMETHYL)-N-[[1-[N-[(2-NAPHTHALENYLSULFONYL)-L-SERYL]-PYRROLIDINYL]METHYL]-3-PIPERIDENECARBOXAMIDE (BMS-189090)|X-RAY DIFFRACTION|2.8|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1BTH|STRUCTURE OF THROMBIN COMPLEXED WITH BOVINE PANCREATIC TRYPSIN INHIBITOR|X-RAY DIFFRACTION|2.3|Bos taurus|0|COMPLEX (SERINE PROTEASE/INHIBITOR)","1C1U|RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES|X-RAY DIFFRACTION|1.75|Homo sapiens; SYNTHETIC CONSTRUCT|0|BLOOD CLOTTING/HYDROLASE INHIBITOR","1C1V|RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES|X-RAY DIFFRACTION|1.98|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1C1W|RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES|X-RAY DIFFRACTION|1.9|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1C4U|SELECTIVE NON ELECTROPHILIC THROMBIN INHIBITORS WITH CYCLOHEXYL MOIETIES.|X-RAY DIFFRACTION|2.1|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","1C4V|SELECTIVE NON ELECTROPHILIC THROMBIN INHIBITORS WITH CYCLOHEXYL MOIETIES.|X-RAY DIFFRACTION|2.1|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","1C4Y|SELECTIVE NON-ELECTROPHILIC THROMBIN INHIBITORS|X-RAY DIFFRACTION|2.7|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","1C5L|STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR|X-RAY DIFFRACTION|1.47|Homo sapiens; SYNTHETIC CONSTRUCT|0|BLOOD CLOTTING/HYDROLASE INHIBITOR","1C5N|STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR|X-RAY DIFFRACTION|1.5|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1C5O|STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR|X-RAY DIFFRACTION|1.9|Hirudo medicinalis; Homo sapiens|0|BLOOD CLOTTING/HYDROLASE INHIBITOR","1CA8|Thrombin inhibitors with rigid tripeptidyl aldehydes|X-RAY DIFFRACTION|2.1|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1D3D|CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH BENZOTHIOPHENE INHIBITOR 4|X-RAY DIFFRACTION|2.04|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1D3P|CRYSTAL STRUCTURE OF HUMAN APLHA-THROMBIN IN COMPLEX WITH BENZO[B]THIOPHENE INHIBITOR 3|X-RAY DIFFRACTION|2.1|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1D3Q|CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH BENZO[B]THIOPHENE INHIBITOR 2|X-RAY DIFFRACTION|2.9|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1D3T|CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH BENZO[B]THIOPHENE INHIBITOR 1|X-RAY DIFFRACTION|3|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1D4P|CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH 5-AMIDINOINDOLE-4-BENZYLPIPERIDINE INHIBITOR|X-RAY DIFFRACTION|2.07|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1D6W|STRUCTURE OF THROMBIN COMPLEXED WITH SELECTIVE NON-ELECTROPHILIC INHIBITORS HAVING CYCLOHEXYL MOIETIES AT P1|X-RAY DIFFRACTION|2|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","1D9I|STRUCTURE OF THROMBIN COMPLEXED WITH SELECTIVE NON-ELECTOPHILIC INHIBITORS HAVING CYCLOHEXYL MOIETIES AT P1|X-RAY DIFFRACTION|2.3|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","1DE7|INTERACTION OF FACTOR XIII ACTIVATION PEPTIDE WITH ALPHA-THROMBIN: CRYSTAL STRUCTURE OF THE ENZYME-SUBSTRATE COMPLEX|X-RAY DIFFRACTION|2|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE SUBSTRATE","1DIT|COMPLEX OF A DIVALENT INHIBITOR WITH THROMBIN|X-RAY DIFFRACTION|2.3|Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1DM4|SER195ALA MUTANT OF HUMAN THROMBIN COMPLEXED WITH FIBRINOPEPTIDE A (7-16)|X-RAY DIFFRACTION|2.5|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE","1DOJ|Crystal structure of human alpha-thrombin*RWJ-51438 complex at 1.7 A|X-RAY DIFFRACTION|1.7|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","1DWB|CRYSTALLOGRAPHIC ANALYSIS AT 3.0-ANGSTROMS RESOLUTION OF THE BINDING TO HUMAN THROMBIN OF FOUR ACTIVE SITE-DIRECTED INHIBITORS|X-RAY DIFFRACTION|3.16|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","1DWC|CRYSTALLOGRAPHIC ANALYSIS AT 3.0-ANGSTROMS RESOLUTION OF THE BINDING TO HUMAN THROMBIN OF FOUR ACTIVE SITE-DIRECTED INHIBITORS|X-RAY DIFFRACTION|3|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYROLASE INHIBITOR","1DWD|CRYSTALLOGRAPHIC ANALYSIS AT 3.0-ANGSTROMS RESOLUTION OF THE BINDING TO HUMAN THROMBIN OF FOUR ACTIVE SITE-DIRECTED INHIBITORS|X-RAY DIFFRACTION|3|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYROLASE INHIBITOR","1DWE|Crystallographic analysis at 3.0-Angstroms resolution of the binding to human thrombin of four active site-directed inhibitors|X-RAY DIFFRACTION|3|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1DX5|Crystal structure of the thrombin-thrombomodulin complex|X-RAY DIFFRACTION|2.3|Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1E0F|Crystal structure of the human alpha-thrombin-haemadin complex: an exosite II-binding inhibitor|X-RAY DIFFRACTION|3.1|HAEMADIPSA SYLVESTRIS; HOMO SAPIENS|0|HYDROLASE","1EB1|Complex structure of human thrombin with N-methyl-arginine inhibitor|X-RAY DIFFRACTION|1.8|HOMO SAPIENS; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","1EOJ|Design of P1' and P3' residues of trivalent thrombin inhibitors and their crystal structures|X-RAY DIFFRACTION|2.1|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","1EOL|Design of P1' and P3' residues of trivalent thrombin inhibitors and their crystal structures|X-RAY DIFFRACTION|2.1|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","1FPC|ACTIVE SITE MIMETIC INHIBITION OF THROMBIN|X-RAY DIFFRACTION|2.3|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1FPH|THE INTERACTION OF THROMBIN WITH FIBRINOGEN: A STRUCTURAL BASIS FOR ITS SPECIFICITY|X-RAY DIFFRACTION|2.5|Hirudo medicinalis; Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","1G30|THROMBIN INHIBITOR COMPLEX|X-RAY DIFFRACTION|2|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1G32|THROMBIN INHIBITOR COMPLEX|X-RAY DIFFRACTION|1.9|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1G37|CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN COMPLEXED WITH BCH-10556 AND EXOSITE-DIRECTED PEPTIDE|X-RAY DIFFRACTION|2|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","1GHV|A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE|X-RAY DIFFRACTION|1.85|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","1GHW|A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE|X-RAY DIFFRACTION|1.75|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","1GHX|A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE|X-RAY DIFFRACTION|1.65|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","1GHY|A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE|X-RAY DIFFRACTION|1.85|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","1GJ4|SELECTIVITY AT S1, H2O DISPLACEMENT, UPA, TPA, SER190/ALA190 PROTEASE, STRUCTURE-BASED DRUG DESIGN|X-RAY DIFFRACTION|1.81|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","1GJ5|SELECTIVITY AT S1, H2O DISPLACEMENT, UPA, TPA, SER190/ALA190 PROTEASE, STRUCTURE-BASED DRUG DESIGN|X-RAY DIFFRACTION|1.73|Homo sapiens; SYNTHETIC CONSTRUCT|0|BLOOD CLOTTING,HYDROLASE/INHIBITOR","1H8D|X-ray structure of the human alpha-thrombin complex with a tripeptide phosphonate inhibitor.|X-RAY DIFFRACTION|1.4|HIRUDO MEDICINALIS; HOMO SAPIENS|0|HYDROLASE/HYDROLASE INHIBITOR","1H8I|X-ray crystal structure of human alpha-thrombin with a tripeptide phosphonate inhibitor.|X-RAY DIFFRACTION|1.75|HIRUDO MEDICINALIS; HOMO SAPIENS|0|HYDROLASE/HYDROLASE INHIBITOR","1HAG|THE ISOMORPHOUS STRUCTURES OF PRETHROMBIN2, HIRUGEN-AND PPACK-THROMBIN: CHANGES ACCOMPANYING ACTIVATION AND EXOSITE BINDING TO THROMBIN|X-RAY DIFFRACTION|2|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1HAH|THE ISOMORPHOUS STRUCTURES OF PRETHROMBIN2, HIRUGEN-AND PPACK-THROMBIN: CHANGES ACCOMPANYING ACTIVATION AND EXOSITE BINDING TO THROMBIN|X-RAY DIFFRACTION|2.3|Hirudo medicinalis; Homo sapiens|0|COMPLEX(SERINE PROTEINASE/INHIBITOR)","1HAI|THE ISOMORPHOUS STRUCTURES OF PRETHROMBIN2, HIRUGEN-AND PPACK-THROMBIN: CHANGES ACCOMPANYING ACTIVATION AND EXOSITE BINDING TO THROMBIN|X-RAY DIFFRACTION|2.4|Homo sapiens|0|HYDROLASE/hydrolase inhibitor","1HAO|COMPLEX OF HUMAN ALPHA-THROMBIN WITH A 15MER OLIGONUCLEOTIDE GGTTGGTGTGGTTGG (BASED ON NMR MODEL OF DNA)|X-RAY DIFFRACTION|2.8|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR/DNA","1HAP|COMPLEX OF HUMAN ALPHA-THROMBIN WITH A 15MER OLIGONUCLEOTIDE GGTTGGTGTGGTTGG (BASED ON X-RAY MODEL OF DNA)|X-RAY DIFFRACTION|2.8|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR/DNA","1HBT|Human alpha-thrombin complexed with a peptidyl pyridinium methyl ketone containing bivalent inhibitor|X-RAY DIFFRACTION|2|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","1HDT|STRUCTURE OF A RETRO-BINDING PEPTIDE INHIBITOR COMPLEXED WITH HUMAN ALPHA-THROMBIN|X-RAY DIFFRACTION|2.6|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1HGT|STRUCTURE OF THE HIRUGEN AND HIRULOG 1 COMPLEXES OF ALPHA-THROMBIN|X-RAY DIFFRACTION|2.2|Hirudo medicinalis; Homo sapiens|0|HYDROLASE(SERINE PROTEASE)","1HLT|THE STRUCTURE OF A NONADECAPEPTIDE OF THE FIFTH EGF DOMAIN OF THROMBOMODULIN COMPLEXED WITH THROMBIN|X-RAY DIFFRACTION|3|Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1HUT|THE STRUCTURE OF ALPHA-THROMBIN INHIBITED BY A 15-MER SINGLE-STRANDED DNA APTAMER|X-RAY DIFFRACTION|2.9|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR/DNA","1HXE|SERINE PROTEASE|X-RAY DIFFRACTION|2.1|Homo sapiens|0|HYDROLASEE/HYDROLASE INHIBITOR","1HXF|HUMAN THROMBIN COMPLEX WITH HIRUDIN VARIANT|X-RAY DIFFRACTION|2.1|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1IHS|CRYSTAL STRUCTURE OF THE COMPLEX OF HUMAN ALPHA-THROMBIN AND NON-HYDROLYZABLE BIFUNCTIONAL INHIBITORS, HIRUTONIN-2 AND HIRUTONIN-6|X-RAY DIFFRACTION|2|Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1IHT|CRYSTAL STRUCTURE OF THE COMPLEX OF HUMAN ALPHA-THROMBIN AND NON-HYDROLYZABLE BIFUNCTIONAL INHIBITORS, HIRUTONIN-2 AND HIRUTONIN-6|X-RAY DIFFRACTION|2.1|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","1JMO|Crystal Structure of the Heparin Cofactor II-S195A Thrombin Complex|X-RAY DIFFRACTION|2.2|Homo sapiens|0|BLOOD CLOTTING","1JOU|Crystal Structure of Native S195A Thrombin with an Unoccupied Active Site|X-RAY DIFFRACTION|1.8|Homo sapiens|0|BLOOD CLOTTING","1JWT|CRYSTAL STRUCTURE OF THROMBIN IN COMPLEX WITH A NOVEL BICYCLIC LACTAM INHIBITOR|X-RAY DIFFRACTION|2.5|Homo sapiens|0|HYDROLASE","1K21|HUMAN THROMBIN-INHIBITOR COMPLEX|X-RAY DIFFRACTION|1.86|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1K22|HUMAN THROMBIN-INHIBITOR COMPLEX|X-RAY DIFFRACTION|1.93|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1KTS|Thrombin Inhibitor Complex|X-RAY DIFFRACTION|2.4|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1KTT|Thrombin inhibitor complex|X-RAY DIFFRACTION|2.1|Hirudo medicinalis; Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","1LHC|HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BOROARG-OH|X-RAY DIFFRACTION|1.95|Hirudo medicinalis; Homo sapiens|0|COMPLEX (SERINE PROTEASE/INHIBITOR)","1LHD|HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BOROLYS-OH|X-RAY DIFFRACTION|2.35|Hirudo medicinalis; Homo sapiens|0|COMPLEX (SERINE PROTEASE/INHIBITOR)","1LHE|HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BORO-N-BUTYL-AMIDINO-GLYCINE-OH|X-RAY DIFFRACTION|2.25|Hirudo medicinalis; Homo sapiens|0|COMPLEX (SERINE PROTEASE/INHIBITOR)","1LHF|HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BORO-HOMOLYS-OH|X-RAY DIFFRACTION|2.4|Hirudo medicinalis; Homo sapiens|0|COMPLEX (SERINE PROTEASE/INHIBITOR)","1LHG|HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BOROORNITHINE-OH|X-RAY DIFFRACTION|2.25|Hirudo medicinalis; Homo sapiens|0|COMPLEX (SERINE PROTEASE/INHIBITOR)","1MH0|Crystal structure of the anticoagulant slow form of thrombin|X-RAY DIFFRACTION|2.8|Homo sapiens|0|BLOOD CLOTTING","1MU6|Crystal Structure of Thrombin in Complex with L-378,622|X-RAY DIFFRACTION|1.99|Homo sapiens; SYNTHETIC CONSTRUCT|0|BLOOD CLOTTING,HYDROLASE/INHIBITOR","1MU8|thrombin-hirugen_l-378,650|X-RAY DIFFRACTION|2|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","1MUE|Thrombin-Hirugen-L405,426|X-RAY DIFFRACTION|2|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE INHIBITOR"]}]}