1c5l
From Proteopedia
(Difference between revisions)
m (Protected "1c5l" [edit=sysop:move=sysop]) |
|||
Line 25: | Line 25: | ||
==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]] | ||
Line 37: | Line 37: | ||
[[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
Contents |
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