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Showing 1-50 of 56 results
PDB Identifier Description Ligand Receptor SCOP pdb.org
1C5W STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR A B
1C5X STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR A B
1C5Y STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR A B
1C5Z STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR A B
1D3P CRYSTAL STRUCTURE OF HUMAN APLHA-THROMBIN IN COMPLEX WITH BENZO[B]THIOPHENE INHIBITOR 3 A B
1G37 CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN COMPLEXED WITH BCH-10556 AND EXOSITE-DIRECTED PEPTIDE B A Trypsin-like serine proteases
1GI7 A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE A B
1GI8 A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE A B
1GI9 A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE A B
1GJ4 SELECTIVITY AT S1, H2O DISPLACEMENT, UPA, TPA, SER190/ALA190 PROTEASE, STRUCTURE-BASED DRUG DESIGN L H
1ID5 CRYSTAL STRUCTURE OF BOVINE THROMBIN COMPLEX WITH PROTEASE INHIBITOR ECOTIN L H
1MKW THE CO-CRYSTAL STRUCTURE OF UNLIGANDED BOVINE ALPHA-THROMBIN AND PRETHROMBIN-2: MOVEMENT OF THE YPPW SEGMENT AND ACTIVE SITE RESIDUES UPON LIGAND BINDING L H
1MKX THE CO-CRYSTAL STRUCTURE OF UNLIGANDED BOVINE ALPHA-THROMBIN AND PRETHROMBIN-2: MOVEMENT OF THE YPPW SEGMENT AND ACTIVE SITE RESIDUES UPON LIGAND BINDING L H
1NZQ D-Phe-Pro-Arg-Type Thrombin Inhibitor L H
1O3P Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors A B
1O5A Dissecting and Designing Inhibitor Selectivity Determinants at the S1 site Using an Artificial Ala190 Protease (Ala190 uPA) A B
1O5B Dissecting and Designing Inhibitor Selectivity Determinants at the S1 site Using an Artificial Ala190 Protease (Ala190 uPA) A B
1O5C Dissecting and Designing Inhibitor Selectivity Determinants at the S1 site Using an Artificial Ala190 Protease (Ala190 uPA) A B
1O5G Dissecting and Designing Inhibitor Selectivity Determinants at the S1 site Using an Artificial Ala190 Protease (Ala190 uPA) L H
1QBV CRYSTAL STRUCTURE OF THROMBIN COMPLEXED WITH AN GUANIDINE-MIMETIC INHIBITOR L H
1RIW Thrombin in complex with natural product inhibitor Oscillarin D B
1SG8 Crystal structure of the procoagulant fast form of thrombin A B
1SGI Crystal structure of the anticoagulant slow form of thrombin D E
1TWX Crystal structure of the thrombin mutant D221A/D222K A B
1UVT BOVINE THROMBIN--BM14.1248 COMPLEX L H
1VR1 Specifity for Plasminogen Activator Inhibitor-1 L H
1W7G ALPHA-THROMBIN COMPLEX WITH SULFATED HIRUDIN (RESIDUES 54-65) AND L-ARGININE TEMPLATE INHIBITOR CS107 L H
1YCP THE CRYSTAL STRUCTURE OF FIBRINOGEN-AA PEPTIDE 1-23 (F8Y) BOUND TO BOVINE THROMBIN EXPLAINS WHY THE MUTATION OF PHE-8 TO TYROSINE STRONGLY INHIBITS NORMAL CLEAVAGE AT ARGININE-16 L H
1YPE Thrombin Inhibitor Complex L H
1YPG Thrombin Inhibitor Complex L H
1YPJ Thrombin Inhibitor Complex L H
1YPK Thrombin Inhibitor Complex L H
1YPL X-ray crystal structure of thrombin inhibited by synthetic cyanopeptide analogue RA-1008 L H
1YPM X-ray crystal structure of thrombin inhibited by synthetic cyanopeptide analogue RA-1014 L H
2C8W THROMBIN INHIBITORS A B
2C8X THROMBIN INHIBITORS A B
2C8Y THROMBIN INHIBITORS A B
2C8Z THROMBIN INHIBITORS A B
2C90 THROMBIN INHIBITORS A B
2C93 THROMBIN INHIBITORS A B
2GDE Thrombin in complex with inhibitor L H
2H9T Crystal structure of human alpha-thrombin in complex with suramin L H
2HWL Crystal structure of thrombin in complex with fibrinogen gamma\' peptide A B
2JH0 HUMAN THROMBIN HIRUGEN INHIBITOR COMPLEX. C D
2JH5 HUMAN THROMBIN HIRUGEN INHIBITOR COMPLEX. C D
2JH6 HUMAN THROMBIN HIRUGEN INHIBITOR COMPLEX. C D
2PW8 Crystal structure of sulfo-hirudin complexed to thrombin L H
2R2M 2-(2-Chloro-6-Fluorophenyl)Acetamides as Potent Thrombin Inhibitors H B
2UUF THROMBIN-HIRUGEN BINARY COMPLEX AT 1.26A RESOLUTION A B
2UUJ THROMBIN-HIRUGEN-GW473178 TERNARY COMPLEX AT 1.32A RESOLUTION A B