3o0u
From Proteopedia
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- | [[Image:3o0u. | + | [[Image:3o0u.png|left|200px]] |
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{{STRUCTURE_3o0u| PDB=3o0u | SCENE= }} | {{STRUCTURE_3o0u| PDB=3o0u | SCENE= }} | ||
===Cathepsin K covalently bound to a cyano-pyrimidine inhibitor with improved selectivity over hERG=== | ===Cathepsin K covalently bound to a cyano-pyrimidine inhibitor with improved selectivity over hERG=== | ||
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{{ABSTRACT_PUBMED_20843687}} | {{ABSTRACT_PUBMED_20843687}} | ||
==About this Structure== | ==About this Structure== | ||
- | [[3o0u]] is a 1 chain structure 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=3O0U OCA]. | + | [[3o0u]] is a 1 chain structure of [[Cathepsin]] 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=3O0U OCA]. |
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+ | ==See Also== | ||
+ | *[[Cathepsin|Cathepsin]] | ||
==Reference== | ==Reference== | ||
- | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:020843687</ref><references group="xtra"/> |
[[Category: Cathepsin K]] | [[Category: Cathepsin K]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
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[[Category: Uitdehaag, J C.M.]] | [[Category: Uitdehaag, J C.M.]] | ||
[[Category: Zeeland, M van.]] | [[Category: Zeeland, M van.]] | ||
+ | [[Category: Bone]] | ||
+ | [[Category: Covalent 2-cyano-pyrimidine inhibitor]] | ||
+ | [[Category: Hydrolase]] | ||
+ | [[Category: Hydrolase-hydrolase inhibitor complex]] | ||
+ | [[Category: Reversible covalent bond between cys25 and ligand]] |
Revision as of 10:05, 25 July 2012
Contents |
Cathepsin K covalently bound to a cyano-pyrimidine inhibitor with improved selectivity over hERG
Template:ABSTRACT PUBMED 20843687
About this Structure
3o0u is a 1 chain structure of Cathepsin with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Rankovic Z, Cai J, Kerr J, Fradera X, Robinson J, Mistry A, Finlay W, McGarry G, Andrews F, Caulfield W, Cumming I, Dempster M, Waller J, Arbuckle W, Anderson M, Martin I, Mitchell A, Long C, Baugh M, Westwood P, Kinghorn E, Jones P, Uitdehaag JC, van Zeeland M, Potin D, Saniere L, Fouquet A, Chevallier F, Deronzier H, Dorleans C, Nicolai E. Optimisation of 2-cyano-pyrimidine inhibitors of cathepsin K: Improving selectivity over hERG. Bioorg Med Chem Lett. 2010 Aug 24. PMID:20843687 doi:10.1016/j.bmcl.2010.08.101