1c5l

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==Reference==
==Reference==
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<ref group="xtra">PMID:10779411</ref><references group="xtra"/>
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<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.]]
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[[Category: Blood clotting]]
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[[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

Template:STRUCTURE 1c5l

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

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