1bhx
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(New page: 200px<br /> <applet load="1bhx" size="450" color="white" frame="true" align="right" spinBox="true" caption="1bhx, resolution 2.30Å" /> '''X-RAY STRUCTURE OF ...)
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Revision as of 14:03, 12 November 2007
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X-RAY STRUCTURE OF THE COMPLEX OF HUMAN ALPHA THROMBIN WITH THE INHIBITOR SDZ 229-357
Contents |
Overview
We have designed, synthesized, and tested in vitro a novel class of, noncovalent thrombin inhibitors. The main feature of these inhibitors is a, 6,5-fused bicyclic core structure that fills the S2 pocket of the active, site of thrombin. The bicycle introduces conformational constraint into, the ligand and locks the Xaa-Pro amide bond into the desired trans, configuration. Among the known ring systems, we selected by molecular, modeling the 7-thiaindolizidinones (BTD) as our basic template. The, influence of several structural features was analyzed: the length of the, argininal side chain, the stereochemistry at C6, and the importance of, making optimal use of the S3 pocket. Finally, an X-ray crystal structure, of inhibitor 15 bound to thrombin was obtained at a resolution of 2.3 A., These designed thrombin inhibitors, which were prepared by an efficient, synthesis, showed high selectivity over trypsin and other serine, proteases. Further derivation based on the information obtained by X-ray, crystallography should certainly allow to improve the potency.
Disease
Known diseases associated with this structure: Dysprothrombinemia OMIM:[176930], Hyperprothrombinemia OMIM:[176930], Hypoprothrombinemia OMIM:[176930]
About this Structure
1BHX is a Protein complex structure of sequences from Homo sapiens with R56 as ligand. Active as Thrombin, with EC number 3.4.21.5 Full crystallographic information is available from OCA.
Reference
Rational design, synthesis, and X-ray structure of selective noncovalent thrombin inhibitors., Wagner J, Kallen J, Ehrhardt C, Evenou JP, Wagner D, J Med Chem. 1998 Sep 10;41(19):3664-74. PMID:9733491
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