| PDB Identifier | Description | Ligand | Receptor | SCOP | pdb.org | |
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1EB1 | COMPLEX STRUCTURE OF HUMAN THROMBIN WITH N-METHYL-ARGININE INHIBITOR | L | H |
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1LHC | HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BOROARG-OH | I | H |
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1LHD | HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BOROLYS-OH | I | H |
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1LHE | HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BORO-N-BUTYL-AMIDINO-GLYCINE-OH | I | H |
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1LHF | HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BORO-HOMOLYS-OH | I | H |
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1LHG | HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BOROORNITHINE-OH | I | H |
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1TOM | ALPHA-THROMBIN COMPLEXED WITH HIRUGEN | L | H |
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1WAY | ACTIVE SITE THROMBIN INHIBITORS | A | B |
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1WBG | 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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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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2R0L | Short Form HGFA with Inhibitory Fab75 | B | A |
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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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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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2ZC9 | Thrombin in complex with Inhibitor | L | H |
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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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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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3BEF | Crystal structure of thrombin bound to the extracellular fragment of PAR1 | C | B |
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3BF6 | Thrombin:suramin complex | L | H |
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3BIU | Human thrombin-in complex with UB-THR10 | L | H |
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3BIV | Human thrombin-in complex with UB-THR11 | L | H |
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3BV9 | Structure of Thrombin Bound to the Inhibitor FM19 | A | B |
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3C27 | Cyanofluorophenylacetamides as Orally Efficacious Thrombin Inhibitors | H | B |
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3D49 | Thrombin Inhibition | L | H |
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3DA9 | Crystal structure of thrombin in complex with inhibitor | A | B |
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