3o0u
From Proteopedia
(Difference between revisions)
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- | + | [[Image:3o0u.jpg|left|200px]] | |
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+ | The line below this paragraph, containing "STRUCTURE_3o0u", creates the "Structure Box" on the page. | ||
+ | You may change the PDB parameter (which sets the PDB file loaded into the applet) | ||
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+ | {{STRUCTURE_3o0u| PDB=3o0u | SCENE= }} | ||
- | + | ===Cathepsin K covalently bound to a cyano-pyrimidine inhibitor with improved selectivity over hERG=== | |
- | Description: Cathepsin K covalently bound to a cyano-pyrimidine inhibitor with improved selectivity over hERG | ||
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+ | The line below this paragraph, {{ABSTRACT_PUBMED_20843687}}, adds the Publication Abstract to the page | ||
+ | (as it appears on PubMed at http://www.pubmed.gov), where 20843687 is the PubMed ID number. | ||
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+ | {{ABSTRACT_PUBMED_20843687}} | ||
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+ | ==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]. | ||
+ | |||
+ | ==Reference== | ||
+ | <ref group="xtra">PMID:20843687</ref><references group="xtra"/> | ||
+ | [[Category: Cathepsin K]] | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Fradera, X.]] | ||
+ | [[Category: Uitdehaag, J C.M.]] | ||
+ | [[Category: Zeeland, M van.]] |
Revision as of 08:04, 30 March 2011
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 with sequence from Homo sapiens. Full crystallographic information is available from OCA.
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