3of8

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[[Image:3of8.png|left|200px]]
[[Image:3of8.png|left|200px]]
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{{STRUCTURE_3of8| PDB=3of8 | SCENE= }}
{{STRUCTURE_3of8| PDB=3of8 | SCENE= }}
===Structural Basis for Reversible and Irreversible Inhibition of Human Cathepsin L by their Respective Dipeptidyl Glyoxal and Diazomethylketone Inhibitors===
===Structural Basis for Reversible and Irreversible Inhibition of Human Cathepsin L by their Respective Dipeptidyl Glyoxal and Diazomethylketone Inhibitors===
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{{ABSTRACT_PUBMED_20850545}}
{{ABSTRACT_PUBMED_20850545}}
==About this Structure==
==About this Structure==
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[[3of8]] 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=3OF8 OCA].
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[[3of8]] 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=3OF8 OCA].
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==See Also==
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*[[Cathepsin|Cathepsin]]
==Reference==
==Reference==
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<ref group="xtra">PMID:20850545</ref><references group="xtra"/>
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<ref group="xtra">PMID:020850545</ref><references group="xtra"/>
[[Category: Cathepsin L]]
[[Category: Cathepsin L]]
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Shenoy, R T.]]
[[Category: Shenoy, R T.]]
[[Category: Sivaraman, J.]]
[[Category: Sivaraman, J.]]
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[[Category: Hydrolase-hydrolase inhibitor complex]]

Revision as of 11:49, 26 July 2012

Template:STRUCTURE 3of8

Contents

Structural Basis for Reversible and Irreversible Inhibition of Human Cathepsin L by their Respective Dipeptidyl Glyoxal and Diazomethylketone Inhibitors

Template:ABSTRACT PUBMED 20850545

About this Structure

3of8 is a 1 chain structure of Cathepsin with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See Also

Reference

  • Shenoy RT, Sivaraman J. Structural basis for reversible and irreversible inhibition of human cathepsin L by their respective dipeptidyl glyoxal and diazomethylketone inhibitors. J Struct Biol. 2010 Sep 17. PMID:20850545 doi:10.1016/j.jsb.2010.09.007

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