1qhr

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Revision as of 19:46, 12 November 2007 by OCA (talk | contribs) (New page: left|200px<br /> <applet load="1qhr" size="450" color="white" frame="true" align="right" spinBox="true" caption="1qhr, resolution 2.2Å" /> '''NOVEL COVALENT ACTIV...)
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File:1qhr.gif


1qhr, resolution 2.2Å

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NOVEL COVALENT ACTIVE SITE THROMBIN INHIBITORS

OverviewOverview

The binding modes of four active site-directed, acylating inhibitors of, human alpha-thrombin have been determined using X-ray crystallography., These inhibitors (GR157368, GR166081, GR167088, and GR179849) are, representatives of a series utilizing a novel 5, 5-trans-lactone template, to specifically acylate Ser195 of thrombin, resulting in an acyl complex., In each case the crystal structure of the complex reveals a binding mode, which is consistent with the formation of a covalent bond between the, ring-opened lactone of the inhibitor and residue Ser195. Improvements in, potency and selectivity of these inhibitors for thrombin are rationalized, on the basis of the observed protein/inhibitor interactions identified in, these complexes. Occupation of the thrombin S2 and S3 pockets is shown to, be directly correlated with improved binding and a degree of selectivity., The binding mode of GR179849 to thrombin is compared with the, thrombin/PPACK complex [Bode, W., Turk, D., and Karshikov, A. (1992), Protein Sci. 1, 426-471] as this represents the archetypal binding mode, for a thrombin inhibitor. This series of crystal structures is the first, to be reported of synthetic, nonpeptidic acylating inhibitors bound to, thrombin and provides details of the molecular recognition features that, resulted in nanomolar potency.

DiseaseDisease

Known diseases associated with this structure: Dysprothrombinemia OMIM:[176930], Hyperprothrombinemia OMIM:[176930], Hypoprothrombinemia OMIM:[176930]

About this StructureAbout this Structure

1QHR is a Protein complex structure of sequences from Homo sapiens with 157 as ligand. Active as Thrombin, with EC number 3.4.21.5 Full crystallographic information is available from OCA.

ReferenceReference

Crystal structures of thrombin complexed to a novel series of synthetic inhibitors containing a 5,5-trans-lactone template., Jhoti H, Cleasby A, Reid S, Thomas PJ, Weir M, Wonacott A, Biochemistry. 1999 Jun 22;38(25):7969-77. PMID:10387040

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