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PDB Identifier Description Ligand Receptor SCOP pdb.org
1G37 CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN COMPLEXED WITH BCH-10556 AND EXOSITE-DIRECTED PEPTIDE B A Trypsin-like serine proteases
1LQ8 Crystal structure of cleaved protein C inhibitor B A Serpins
1RIW Thrombin in complex with natural product inhibitor Oscillarin D B
1SFI HIGH RESOLUTION STRUCTURE OF A POTENT, CYCLIC PROTEASE INHIBITOR FROM SUNFLOWER SEEDS I A Trypsin-like serine proteases
1SP5 Crystal structure of HIV-1 protease complexed with a product of autoproteolysis I A
1TWB SspB disulfide crosslinked to an ssrA degradation tag C A SspB-like
1WAY ACTIVE SITE THROMBIN INHIBITORS A B
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
2GVF HCV NS3-4A protease domain complexed with a macrocyclic ketoamide inhibitor, SCH419021 D BCA
2JET CRYSTAL STRUCTURE OF A TRYPSIN-LIKE MUTANT (S189D, A226G) CHYMOTRYPSIN. A CB
2JH0 HUMAN THROMBIN HIRUGEN INHIBITOR COMPLEX. C D
2JH5 HUMAN THROMBIN HIRUGEN INHIBITOR COMPLEX. C D
2JH6 HUMAN THROMBIN HIRUGEN INHIBITOR COMPLEX. C D
2OIN crystal structure of HCV NS3-4A R155K muntant C DAB
2QV1 Crystal structure of HCV NS3-4A V36M mutant C DAB
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
2UUK THROMBIN-HIRUGEN-GW420128 TERNARY COMPLEX AT 1.39A RESOLUTION A B
2V3H THROMBIN WITH 3-CYCLE NO F I H
2V3O THROMBIN WITH 3-CYCLE WITH F I H
2VU8 CRYSTAL STRUCTURE OF AN INSECT INHIBITOR WITH A FUNGAL TRYPSIN I E
2ZDA Exploring Thrombin S1 pocket L H
2ZDV Exploring Thrombin S1 pocket L H
2ZF0 Exploring Thrombin S1 Pocket L H
2ZFF Exploring Thrombin S1-pocket L H
2ZFP Thrombin Inibition L H
2ZFQ Exploring thrombin S3 pocket L H
2ZFR Exploring thrombin S3 pocket L H
2ZG0 Exploring thrombin S3 pocket L H
2ZGB Thrombin Inhibition L H
2ZGH Crystal Structure of active granzyme M bound to its product B A
2ZGX Thrombin Inhibition L H
2ZHE Exploring thrombin S3 pocket L H
2ZHF Exploring thrombin S3 pocket L H
2ZHQ Thrombin Inhibition L H
2ZHW Exploring thrombin S3 pocket L H
2ZI2 Thrombin Inhibition L H
2ZIQ Thrombin Inhibition L H
2ZNK Thrombin Inhibition L H
2ZO3 Bisphenylic Thrombin Inhibitors L H
3BF6 Thrombin:suramin complex L H
3BG4 The crystal structure of guamerin in complex with chymotrypsin and the development of an elastase-specific inhibitor A CB
3BP4 The high resolution crystal structure of HLA-B*2705 in complex with a Cathepsin A signal sequence peptide pCatA C A
3BP7 The high resolution crystal structure of HLA-B*2709 in complex with a Cathepsin A signal sequence peptide, pCatA C A