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Ligands
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CDO 2-((R)-1-((S)-2-(N-(6-carbamimidoylpyridin-3-yl)methylcarbamoyl)-2h-pyrrol-1(5h)-yl)-3-cyclohexyl-1-oxopropan-2-ylamino)acetic acid
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Code : 2ANM   PDBj   RCSB PDB   PDBe
Header : BLOOD CLOTTING
Title : Ternary complex of an orally active thrombin inhibitor with human thrombin and a C-terminal hirudin derived exo-sit inhibitor
Release Data : 2006-06-13
Compound :
mol_id molecule chains synonym
1 thrombin H Coagulation factor II
ec: 3.4.21.5
fragment: Thrombin heavy chain
mol_id molecule chains synonym
2 thrombin L Coagulation factor II
ec: 3.4.21.5
fragment: Thrombin light chain
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Escherichia coli  (taxid:562)
mol_id organism_scientific organism_common expression_system
2 Homo sapiens  (taxid:9606) Human Escherichia coli  (taxid:562)
Authors : Lange, U.E.W., Baucke, D., Hornberger, W., Mack, H., Seitz, W., Hoeffken, H.W.
Keywords : BLOOD CLOTTING
Exp. method : X-RAY DIFFRACTION ( 2.40 Å )
Citation :

Orally active thrombin inhibitors. Part 2: optimization of the P2-moiety

Lange, U.E.W.,Baucke, D.,Hornberger, W.  et al.
(2006)  Bioorg.Med.Chem.Lett.  16 : 2648 - 2653

PubMed: 16460939
DOI: 10.1016/j.bmcl.2006.01.046

Chain : L
UniProt : P00734 (THRB_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
Selective cleavage of Arg-|-Gly bonds in fibrinogen to form fibrin and release fibrinopeptides A and B. 3.4.21.5 -
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