| PDB ID | Description | |
|---|---|---|
![]() |
1G37 | CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN COMPLEXED WITH BCH-10556 AND EXOSITE-DIRECTED PEPTIDE |
![]() |
1HXE | SERINE PROTEASE |
![]() |
1THR | STRUCTURES OF THROMBIN COMPLEXES WITH A DESIGNED AND A NATURAL EXOSITE INHIBITOR |
![]() |
1HXF | HUMAN THROMBIN COMPLEX WITH HIRUDIN VARIANT |
![]() |
2PUX | Crystal structure of murine thrombin in complex with the extracellular fragment of murine PAR3 |
![]() |
1RIW | Thrombin in complex with natural product inhibitor Oscillarin |
![]() |
2R2M | 2-(2-Chloro-6-Fluorophenyl)Acetamides as Potent Thrombin Inhibitors |
![]() |
3C27 | Cyanofluorophenylacetamides as Orally Efficacious Thrombin Inhibitors |
![]() |
1A3B | COMPLEX OF HUMAN ALPHA-THROMBIN WITH THE BIFUNCTIONAL BORONATE INHIBITOR BOROLOG1 |
![]() |
1TMT | CHANGES IN INTERACTIONS IN COMPLEXES OF HIRUDIN DERIVATIVES AND HUMAN ALPHA-THROMBIN DUE TO DIFFERENT CRYSTAL FORMS |