1c5r
From Proteopedia
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===STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR=== | ===STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR=== | ||
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==About this Structure== | ==About this Structure== | ||
- | + | [[1c5r]] is a 1 chain structure of [[Trypsin]] with sequence from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1C5R OCA]. | |
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+ | ==See Also== | ||
+ | *[[Trypsin|Trypsin]] | ||
==Reference== | ==Reference== | ||
- | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:010779411</ref><references group="xtra"/> |
[[Category: Bos taurus]] | [[Category: Bos taurus]] | ||
[[Category: Trypsin]] | [[Category: Trypsin]] | ||
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[[Category: Wang, J.]] | [[Category: Wang, J.]] | ||
[[Category: Wong, L.]] | [[Category: Wong, L.]] | ||
+ | [[Category: Hydrolase]] | ||
[[Category: S1 site inhibitor]] | [[Category: S1 site inhibitor]] | ||
[[Category: Selective]] | [[Category: Selective]] | ||
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[[Category: Trypsin]] | [[Category: Trypsin]] | ||
[[Category: Urokinase]] | [[Category: Urokinase]] | ||
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- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 13:34:46 2009'' |
Revision as of 18:36, 26 July 2012
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
1c5r is a 1 chain structure of Trypsin with sequence from Bos taurus. 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
Categories: Bos taurus | Trypsin | Chan, H. | Katz, B A. | Luong, C. | Mackman, R. | Martelli, A. | Radika, K. | Sprengeler, P A. | Wang, J. | Wong, L. | Hydrolase | S1 site inhibitor | Selective | Structure-based drug design | Thrombin | Urokinase