1c5l: Difference between revisions
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m Protected "1c5l" [edit=sysop:move=sysop] |
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==Reference== | ==Reference== | ||
<ref group="xtra">PMID: | <ref group="xtra">PMID:010779411</ref><references group="xtra"/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Thrombin]] | [[Category: Thrombin]] | ||
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[[Category: Wang, J.]] | [[Category: Wang, J.]] | ||
[[Category: Wong, L.]] | [[Category: Wong, L.]] | ||
[[Category: Blood clotting]] | [[Category: Blood clotting-hydrolase inhibitor complex]] | ||
[[Category: S1 site inhibitor]] | [[Category: S1 site inhibitor]] | ||
[[Category: Selective]] | [[Category: Selective]] | ||
Revision as of 05:24, 27 July 2011
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR
Template:ABSTRACT PUBMED 10779411
About this Structure
1c5l is a 3 chain structure of Hirudin with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Katz BA, Mackman R, Luong C, Radika K, Martelli A, Sprengeler PA, Wang J, Chan H, Wong L. Structural basis for selectivity of a small molecule, S1-binding, submicromolar inhibitor of urokinase-type plasminogen activator. Chem Biol. 2000 Apr;7(4):299-312. PMID:10779411
