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PDB Identifier Description Ligand Receptor SCOP pdb.org
1LHC HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BOROARG-OH I H
1LHD HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BOROLYS-OH I H
1LHE HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BORO-N-BUTYL-AMIDINO-GLYCINE-OH I H
1LHF HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BORO-HOMOLYS-OH I H
1LHG HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BOROORNITHINE-OH I H
1WAY ACTIVE SITE THROMBIN INHIBITORS A B
1WBG ACTIVE SITE THROMBIN INHIBITORS A B
2C8W THROMBIN INHIBITORS A B
2C8Y THROMBIN INHIBITORS A B
2C90 THROMBIN INHIBITORS A B
2CF8 COMPLEX OF RECOMBINANT HUMAN THROMBIN WITH A INHIBITOR I H
2CF9 COMPLEX OF RECOMBINANT HUMAN THROMBIN WITH A INHIBITOR I H
2CN0 COMPLEX OF RECOMBINANT HUMAN THROMBIN WITH A DESIGNED INHIBITOR I H
2JH0 HUMAN THROMBIN HIRUGEN INHIBITOR COMPLEX. C D
2JH5 HUMAN THROMBIN HIRUGEN INHIBITOR COMPLEX. C D
2JH6 HUMAN THROMBIN HIRUGEN INHIBITOR COMPLEX. C D
2R2M 2-(2-Chloro-6-Fluorophenyl)Acetamides as Potent Thrombin Inhibitors H B
2RKY Crystal structure of the fourth and fifth fibronectin F1 modules in complex with a fragment of staphylococcus aureus fnbpa-1 D BAC FnI-like domain
2UUF THROMBIN-HIRUGEN BINARY COMPLEX AT 1.26A RESOLUTION A B
2V3H THROMBIN WITH 3-CYCLE NO F I H
2V3O THROMBIN WITH 3-CYCLE WITH F I H
2ZC9 Thrombin in complex with Inhibitor L H
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
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
3BEF Crystal structure of thrombin bound to the extracellular fragment of PAR1 C B
3BF6 Thrombin:suramin complex L H
3BIU Human thrombin-in complex with UB-THR10 L H
3BIV Human thrombin-in complex with UB-THR11 L H
3BV9 Structure of Thrombin Bound to the Inhibitor FM19 A B
3C27 Cyanofluorophenylacetamides as Orally Efficacious Thrombin Inhibitors H B
3CAL Crystal structure of the second and third fibronectin F1 modules in complex with a fragment of staphylococcus aureus fnbpa-5 B A FnI-like domain
3D49 Thrombin Inhibition L H
3DA9 Crystal structure of thrombin in complex with inhibitor A B
3DHK Bisphenylic Thrombin Inhibitors L H