1c1v
From Proteopedia
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{{STRUCTURE_1c1v| PDB=1c1v | SCENE= }} | {{STRUCTURE_1c1v| PDB=1c1v | SCENE= }} | ||
===RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES=== | ===RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES=== | ||
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{{ABSTRACT_PUBMED_9468142}} | {{ABSTRACT_PUBMED_9468142}} | ||
==About this Structure== | ==About this Structure== | ||
- | [[1c1v]] is a 3 chain structure of [[Hirudin]] with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1C1V OCA]. | + | [[1c1v]] is a 3 chain structure of [[Cytochrome c peroxidase]], [[Hirudin]] and [[Thrombin]] with sequence from [http://en.wikipedia.org/wiki/Hirudo_medicinalis Hirudo medicinalis] and [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1C1V OCA]. |
==See Also== | ==See Also== | ||
- | *[[Hirudin]] | + | *[[Cytochrome c peroxidase|Cytochrome c peroxidase]] |
+ | *[[Hirudin|Hirudin]] | ||
+ | *[[Thrombin|Thrombin]] | ||
==Reference== | ==Reference== | ||
- | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:009468142</ref><references group="xtra"/> |
+ | [[Category: Hirudo medicinalis]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Thrombin]] | [[Category: Thrombin]] | ||
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[[Category: Luong, C.]] | [[Category: Luong, C.]] | ||
[[Category: Blood clotting]] | [[Category: Blood clotting]] | ||
+ | [[Category: Hydrolase-hydrolase inhibitor complex]] | ||
[[Category: Ph dependence]] | [[Category: Ph dependence]] | ||
[[Category: Serine protease/inhibitor]] | [[Category: Serine protease/inhibitor]] |
Revision as of 12:04, 27 July 2012
Contents |
RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES
Template:ABSTRACT PUBMED 9468142
About this Structure
1c1v is a 3 chain structure of Cytochrome c peroxidase, Hirudin and Thrombin with sequence from Hirudo medicinalis and Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Katz BA, Clark JM, Finer-Moore JS, Jenkins TE, Johnson CR, Ross MJ, Luong C, Moore WR, Stroud RM. Design of potent selective zinc-mediated serine protease inhibitors. Nature. 1998 Feb 5;391(6667):608-12. PMID:9468142 doi:http://dx.doi.org/10.1038/35422