| PDB Identifier | Description | Ligand | Receptor | SCOP | pdb.org | |
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1G37 | CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN COMPLEXED WITH BCH-10556 AND EXOSITE-DIRECTED PEPTIDE | B | A | Trypsin-like serine proteases |
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1LQ8 | Crystal structure of cleaved protein C inhibitor | B | A | Serpins |
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1RIW | Thrombin in complex with natural product inhibitor Oscillarin | D | B |
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1SFI | HIGH RESOLUTION STRUCTURE OF A POTENT, CYCLIC PROTEASE INHIBITOR FROM SUNFLOWER SEEDS | I | A | Trypsin-like serine proteases |
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1SP5 | Crystal structure of HIV-1 protease complexed with a product of autoproteolysis | I | A |
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1TWB | SspB disulfide crosslinked to an ssrA degradation tag | C | A | SspB-like |
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1WAY | ACTIVE SITE THROMBIN INHIBITORS | A | B |
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2C8W | THROMBIN INHIBITORS | A | B |
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2C8X | THROMBIN INHIBITORS | A | B |
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2C8Y | THROMBIN INHIBITORS | A | B |
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2C8Z | THROMBIN INHIBITORS | A | B |
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2C90 | THROMBIN INHIBITORS | A | B |
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2C93 | THROMBIN INHIBITORS | A | B |
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2GVF | HCV NS3-4A protease domain complexed with a macrocyclic ketoamide inhibitor, SCH419021 | D | BCA |
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2JET | CRYSTAL STRUCTURE OF A TRYPSIN-LIKE MUTANT (S189D, A226G) CHYMOTRYPSIN. | A | CB |
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2JH0 | HUMAN THROMBIN HIRUGEN INHIBITOR COMPLEX. | C | D |
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2JH5 | HUMAN THROMBIN HIRUGEN INHIBITOR COMPLEX. | C | D |
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2JH6 | HUMAN THROMBIN HIRUGEN INHIBITOR COMPLEX. | C | D |
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2OIN | crystal structure of HCV NS3-4A R155K muntant | C | DAB |
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2QV1 | Crystal structure of HCV NS3-4A V36M mutant | C | DAB |
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2R2M | 2-(2-Chloro-6-Fluorophenyl)Acetamides as Potent Thrombin Inhibitors | H | B |
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2UUF | THROMBIN-HIRUGEN BINARY COMPLEX AT 1.26A RESOLUTION | A | B |
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2UUJ | THROMBIN-HIRUGEN-GW473178 TERNARY COMPLEX AT 1.32A RESOLUTION | A | B |
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2UUK | THROMBIN-HIRUGEN-GW420128 TERNARY COMPLEX AT 1.39A RESOLUTION | A | B |
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2V3H | THROMBIN WITH 3-CYCLE NO F | I | H |
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2V3O | THROMBIN WITH 3-CYCLE WITH F | I | H |
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2VU8 | CRYSTAL STRUCTURE OF AN INSECT INHIBITOR WITH A FUNGAL TRYPSIN | I | E |
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2ZDA | Exploring Thrombin S1 pocket | L | H |
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2ZDV | Exploring Thrombin S1 pocket | L | H |
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2ZF0 | Exploring Thrombin S1 Pocket | L | H |
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2ZFF | Exploring Thrombin S1-pocket | L | H |
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2ZFP | Thrombin Inibition | L | H |
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2ZFQ | Exploring thrombin S3 pocket | L | H |
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2ZFR | Exploring thrombin S3 pocket | L | H |
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2ZG0 | Exploring thrombin S3 pocket | L | H |
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2ZGB | Thrombin Inhibition | L | H |
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2ZGH | Crystal Structure of active granzyme M bound to its product | B | A |
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2ZGX | Thrombin Inhibition | L | H |
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2ZHE | Exploring thrombin S3 pocket | L | H |
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2ZHF | Exploring thrombin S3 pocket | L | H |
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2ZHQ | Thrombin Inhibition | L | H |
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2ZHW | Exploring thrombin S3 pocket | L | H |
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2ZI2 | Thrombin Inhibition | L | H |
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2ZIQ | Thrombin Inhibition | L | H |
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2ZNK | Thrombin Inhibition | L | H |
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2ZO3 | Bisphenylic Thrombin Inhibitors | L | H |
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3BF6 | Thrombin:suramin complex | L | H |
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3BG4 | The crystal structure of guamerin in complex with chymotrypsin and the development of an elastase-specific inhibitor | A | CB |
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3BP4 | The high resolution crystal structure of HLA-B*2705 in complex with a Cathepsin A signal sequence peptide pCatA | C | A |
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3BP7 | The high resolution crystal structure of HLA-B*2709 in complex with a Cathepsin A signal sequence peptide, pCatA | C | A |
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