| PDB Identifier | Description | Ligand | Receptor | SCOP | pdb.org | |
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2QKH | Crystal structure of the extracellular domain of human GIP receptor in complex with the hormone GIP | B | A |
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2QOS | Crystal structure of complement protein C8 in complex with a peptide containing the C8 binding site on C8 | A | C |
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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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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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2VDR | INTEGRIN ALPHAIIBBETA3 HEADPIECE BOUND TO A CHIMERIC FIBRINOGEN GAMMA CHAIN PEPTIDE, LGGAKQRGDV | C | AB |
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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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3BU3 | Crystal structure of the insulin receptor kinase in complex with IRS2 KRLB peptide | B | A | Protein kinase-like (PK-like) |
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3BU5 | Crystal structure of the insulin receptor kinase in complex with IRS2 KRLB peptide and ATP | B | C |
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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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3C4M | Structure of human parathyroid hormone in complex with the extracellular domain of its G-protein-coupled receptor (PTH1R) | C | A |
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3C59 | Crystal structure of the ligand-bound glucagon-like peptide-1 receptor extracellular domain | B | A |
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3C5T | Crystal structure of the ligand-bound glucagon-like peptide-1 receptor extracellular domain | B | A |
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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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3DHK | Bisphenylic Thrombin Inhibitors | L | H |
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3DT0 | Understanding Thrombin Inhibition | L | H |
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3DUX | Understanding Thrombin Inhibition | L | H |
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3EGK | KNOBLE Inhibitor | L | H |
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3EHU | Crystal structure of the extracellular domain of human corticotropin releasing factor receptor type 1 (CRFR1) in complex with CRF | C | A |
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3EYF | Crystal structure of anti-human cytomegalovirus antibody 8f9 plus gB peptide | E | AB |
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3GIC | Structure of thrombin mutant delta(146-149e) in the free form | A | B |
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3H0T | Hepcidin-Fab complex | C | AB |
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3HK3 | Crystal structure of murine thrombin mutant W215A/E217A (one molecule in the asymmetric unit) | A | B |
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3HKI | Crystal structure of murine thrombin mutant W215A/E217A in complex with the extracellular fragment of human PAR1 | F | E |
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