1fph
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THE INTERACTION OF THROMBIN WITH FIBRINOGEN: A STRUCTURAL BASIS FOR ITS SPECIFICITY
OverviewOverview
The structure of the ternary complex of human alpha-thrombin with a, covalently bound analogue of fibrinopeptide A and a C-terminal hirudin, peptide has been determined by X-ray diffraction methods at 0.25 nm, resolution. Fibrinopeptide A folds in a compact manner, bringing together, hydrophobic residues that slot into the apolar binding site of human, alpha-thrombin. Fibrinogen residue Phe8 occupies the aryl-binding site of, thrombin, adjacent to fibrinogen residues Leu9 and Val15 in the S2, subsite. The species diversity of fibrinopeptide A is analysed with, respect to its conformation and its interaction with thrombin. The, non-covalently attached peptide fragment hirudin(54-65) exhibits an, identical conformation to that observed in the hirudin-thrombin complex., The occupancy of the secondary fibrinogen-recognition exosite by this, peptide imposes restrictions on the manner of fibrinogen binding. The, surface topology of the thrombin molecule indicates positions P1'-P3', differ from those of the canonical serine-proteinase inhibitors, suggesting a mechanical model for the switching of thrombin activity from, fibrinogen cleavage to protein-C activation on thrombomodulin complex, formation. The multiple interactions between thrombin and fibrinogen, provide an explanation for the narrow specificity of thrombin. Structural, grounds can be put forward for certain congenital clotting disorders.
DiseaseDisease
Known diseases associated with this structure: Dysprothrombinemia OMIM:[176930], Hyperprothrombinemia OMIM:[176930], Hypoprothrombinemia OMIM:[176930]
About this StructureAbout this Structure
1FPH is a Single protein structure of sequence from Homo sapiens with and as ligands. Active as Thrombin, with EC number 3.4.21.5 Full crystallographic information is available from OCA.
ReferenceReference
The interaction of thrombin with fibrinogen. A structural basis for its specificity., Stubbs MT, Oschkinat H, Mayr I, Huber R, Angliker H, Stone SR, Bode W, Eur J Biochem. 1992 May 15;206(1):187-95. PMID:1587268
Page seeded by OCA on Fri Feb 15 15:48:39 2008