3ovx

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[[Image:3ovx.png|left|200px]]
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{{STRUCTURE_3ovx| PDB=3ovx | SCENE= }}
{{STRUCTURE_3ovx| PDB=3ovx | SCENE= }}
===Cathepsin S in complex with a covalent inhibitor with an aldehyde warhead===
===Cathepsin S in complex with a covalent inhibitor with an aldehyde warhead===
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{{ABSTRACT_PUBMED_21030256}}
{{ABSTRACT_PUBMED_21030256}}
==About this Structure==
==About this Structure==
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3OVX is a 2 chains structure with sequences 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=3OVX OCA].
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[[3ovx]] is a 2 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=3OVX OCA].
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==See Also==
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*[[Cathepsin|Cathepsin]]
==Reference==
==Reference==
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<ref group="xtra">PMID:21030256</ref><references group="xtra"/>
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<ref group="xtra">PMID:021030256</ref><references group="xtra"/>
[[Category: Cathepsin S]]
[[Category: Cathepsin S]]
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Ligand is covalently bound to cys25]]
[[Category: Ligand is covalently bound to cys25]]
[[Category: Lysosomeal protein]]
[[Category: Lysosomeal protein]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Dec 22 09:57:42 2010''
 

Revision as of 02:52, 27 July 2012

Template:STRUCTURE 3ovx

Contents

Cathepsin S in complex with a covalent inhibitor with an aldehyde warhead

Template:ABSTRACT PUBMED 21030256

About this Structure

3ovx is a 2 chain structure of Cathepsin with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See Also

Reference

  • Cai J, Robinson J, Belshaw S, Everett K, Fradera X, van Zeeland M, van Berkom L, van Rijnsbergen P, Popplestone L, Baugh M, Dempster M, Bruin J, Hamilton W, Kinghorn E, Westwood P, Kerr J, Rankovic Z, Arbuckle W, Bennett DJ, Jones PS, Long C, Martin I, Uitdehaag JC, Meulemans T. Trifluoromethylphenyl as P2 for ketoamide-based cathepsin S inhibitors. Bioorg Med Chem Lett. 2010 Dec 1;20(23):6890-4. Epub 2010 Oct 26. PMID:21030256 doi:10.1016/j.bmcl.2010.10.012

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