1id5

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(New page: 200px<br /><applet load="1id5" size="450" color="white" frame="true" align="right" spinBox="true" caption="1id5, resolution 2.50&Aring;" /> '''CRYSTAL STRUCTURE OF...)
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Revision as of 15:11, 20 November 2007


1id5, resolution 2.50Å

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CRYSTAL STRUCTURE OF BOVINE THROMBIN COMPLEX WITH PROTEASE INHIBITOR ECOTIN

Overview

The protease inhibitor ecotin fails to inhibit thrombin despite its broad, specificity against serine proteases. A point mutation (M84R) in ecotin, results in a 1.5 nM affinity for thrombin, 10(4) times stronger than that, of wild-type ecotin. The crystal structure of bovine thrombin is, determined in complex with ecotin M84R mutant at 2.5 A resolution. Surface, loops surrounding the active site cleft of thrombin have undergone, significant structural changes to permit inhibitor binding. Particularly, the insertion loops at residues 60 and 148 in thrombin, which likely, mediate the interactions with macromolecules, are displaced when the, complex forms. Thrombin and ecotin M84R interact in two distinct surfaces., The loop at residue 99 and the C-terminus of thrombin contact ecotin, through mixed polar and nonpolar interactions. The active site of thrombin, is filled with eight consecutive amino acids of ecotin and demonstrates, thrombin's preference for specific features that are compatible with the, thrombin cleavage site: negatively, charged-Pro-Val-X-Pro-Arg-hydrophobic-positively charged (P1 Arg is in, bold letters). The preference for a Val at P4 is clearly defined. The, insertion at residue 60 may further affect substrate binding by moving its, adjacent loops that are part of the substrate recognition sites.

About this Structure

1ID5 is a Protein complex structure of sequences from Bos taurus and Escherichia coli with CA and TRS as ligands. Active as Thrombin, with EC number 3.4.21.5 Full crystallographic information is available from OCA.

Reference

Crystal structure of thrombin-ecotin reveals conformational changes and extended interactions., Wang SX, Esmon CT, Fletterick RJ, Biochemistry. 2001 Aug 28;40(34):10038-46. PMID:11513582

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