1d7p

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(New page: 200px<br /> <applet load="1d7p" size="450" color="white" frame="true" align="right" spinBox="true" caption="1d7p, resolution 1.5&Aring;" /> '''Crystal structure of...)
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Revision as of 14:23, 12 November 2007


1d7p, resolution 1.5Å

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Crystal structure of the c2 domain of human factor viii at 1.5 a resolution at 1.5 A

Contents

Overview

Human factor VIII is a plasma glycoprotein that has a critical role in, blood coagulation. Factor VIII circulates as a complex with von Willebrand, factor. After cleavage by thrombin, factor VIIIa associates with factor, IXa at the surface of activated platelets or endothelial cells. This, complex activates factor X (refs 6, 7), which in turn converts prothrombin, to thrombin in the presence of factor Va (refs 8, 9). The, carboxyl-terminal C2 domain of factor VIII contains sites that are, essential for its binding to von Willebrand factor and to negatively, charged phospholipid surfaces. Here we report the structure of human, factor VIII C2 domain at 1.5 A resolution. The structure reveals a, beta-sandwich core, from which two beta-turns and a loop display a group, of solvent-exposed hydrophobic residues. Behind the hydrophobic surface, lies a ring of positively charged residues. This motif suggests a, mechanism for membrane binding involving both hydrophobic and, electrostatic interactions. The structure explains, in part, mutations in, the C2 region of factor VIII that lead to bleeding disorders in, haemophilia A.

Disease

Known diseases associated with this structure: Hemophilia A OMIM:[306700]

About this Structure

1D7P is a Single protein structure of sequence from Homo sapiens with SO4, CYS and GOL as ligands. Full crystallographic information is available from OCA.

Reference

Structure of the C2 domain of human factor VIII at 1.5 A resolution., Pratt KP, Shen BW, Takeshima K, Davie EW, Fujikawa K, Stoddard BL, Nature. 1999 Nov 25;402(6760):439-42. PMID:10586887

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