1g37

Revision as of 17:53, 12 November 2007 by OCA (talk | contribs) (New page: left|200px<br /> <applet load="1g37" size="450" color="white" frame="true" align="right" spinBox="true" caption="1g37, resolution 2.0Å" /> '''CRYSTAL STRUCTURE OF...)
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CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN COMPLEXED WITH BCH-10556 AND EXOSITE-DIRECTED PEPTIDE

File:1g37.gif


1g37, resolution 2.0Å

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OverviewOverview

Bicyclic piperazinone based thrombin inhibitors of general structure 2, were prepared and evaluated in vitro and in vivo. These inhibitors, having, in common an electrophilic basic trans-cyclohexylamine P1 residue, displayed high thrombin affinity, high selectivity against trypsin and, good in vivo efficacy in the rat arterial thrombosis model.

DiseaseDisease

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

About this StructureAbout this Structure

1G37 is a Single protein structure of sequence from Homo sapiens with 110 as ligand. Active as Thrombin, with EC number 3.4.21.5 Full crystallographic information is available from OCA.

ReferenceReference

Potent and selective bicyclic lactam inhibitors of thrombin. Part 4: transition state inhibitors., Bachand B, Tarazi M, St-Denis Y, Edmunds JJ, Winocour PD, Leblond L, Siddiqui MA, Bioorg Med Chem Lett. 2001 Feb 12;11(3):287-90. PMID:11212093

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