1e0f

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[[Image:1e0f.gif|left|200px]]
[[Image:1e0f.gif|left|200px]]
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{{Structure
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|PDB= 1e0f |SIZE=350|CAPTION= <scene name='initialview01'>1e0f</scene>, resolution 3.1&Aring;
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The line below this paragraph, containing "STRUCTURE_1e0f", creates the "Structure Box" on the page.
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|SITE= <scene name='pdbsite=ATE:Catalytic+Site+Triad'>ATE</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Thrombin Thrombin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.5 3.4.21.5] </span>
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{{STRUCTURE_1e0f| PDB=1e0f | SCENE= }}
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1e0f FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1e0f OCA], [http://www.ebi.ac.uk/pdbsum/1e0f PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1e0f RCSB]</span>
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'''CRYSTAL STRUCTURE OF THE HUMAN ALPHA-THROMBIN-HAEMADIN COMPLEX: AN EXOSITE II-BINDING INHIBITOR'''
'''CRYSTAL STRUCTURE OF THE HUMAN ALPHA-THROMBIN-HAEMADIN COMPLEX: AN EXOSITE II-BINDING INHIBITOR'''
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[[Category: Pereira, P.]]
[[Category: Pereira, P.]]
[[Category: Richardson, J.]]
[[Category: Richardson, J.]]
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[[Category: coagulation/crystal structure/heparin-binding site/ hirudin/thrombin inhibitor]]
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[[Category: Coagulation/crystal structure/heparin-binding site/ hirudin/thrombin inhibitor]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 14:30:21 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 19:52:29 2008''
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Revision as of 11:30, 2 May 2008

Template:STRUCTURE 1e0f

CRYSTAL STRUCTURE OF THE HUMAN ALPHA-THROMBIN-HAEMADIN COMPLEX: AN EXOSITE II-BINDING INHIBITOR


Overview

The serine proteinase alpha-thrombin plays a pivotal role in the regulation of blood fluidity, and therefore constitutes a primary target in the treatment of various haemostatic disorders. Haemadin is a slow tight- binding thrombin inhibitor from the land-living leech Haemadipsa sylvestris. Here we present the 3.1 A crystal structure of the human alpha-thrombin- haemadin complex. The N-terminal segment of haemadin binds to the active site of thrombin, forming a parallel beta-strand with residues Ser214-Gly216 of the proteinase. This mode of binding is similar to that observed in another leech-derived inhibitor, hirudin. In contrast to hirudin, however, the markedly acidic C-terminal peptide of haemadin does not bind the fibrinogen-recognition exosite, but interacts with the heparin-binding exosite of thrombin. Thus, haemadin binds to thrombin according to a novel mechanism, despite an overall structural similarity with hirudin. Haemadin inhibits both free and thrombomodulin-bound alpha-thrombin, but not intermediate activation forms such as meizothrombin. This specific anticoagulant ability of haemadin makes it an ideal candidate for an antithrombotic agent, as well as a starting point for the design of novel antithrombotics.

About this Structure

1E0F is a Protein complex structure of sequences from Haemadipsa sylvestris and Homo sapiens. Full crystallographic information is available from OCA.

Reference

Crystal structure of the human alpha-thrombin-haemadin complex: an exosite II-binding inhibitor., Richardson JL, Kroger B, Hoeffken W, Sadler JE, Pereira P, Huber R, Bode W, Fuentes-Prior P, EMBO J. 2000 Nov 1;19(21):5650-60. PMID:11060016 Page seeded by OCA on Fri May 2 14:30:21 2008

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