3o2f: Difference between revisions

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==About this Structure==
==About this Structure==
[[3o2f]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Canis_lupus_familiaris Canis lupus familiaris]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3O2F OCA].  
[[3o2f]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Canfa Canfa]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3O2F OCA].  


==See Also==
==See Also==
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==Reference==
==Reference==
<ref group="xtra">PMID:023995768</ref><references group="xtra"/><references/>
<ref group="xtra">PMID:023995768</ref><references group="xtra"/><references/>
[[Category: Canis lupus familiaris]]
[[Category: Canfa]]
[[Category: Gewirth, D T.]]
[[Category: Gewirth, D T.]]
[[Category: Seidler, P M.]]
[[Category: Seidler, P M.]]
[[Category: Chaperone-inhibitor complex]]
[[Category: Chaperone-inhibitor complex]]
[[Category: Hsp90 heat-shock protein]]
[[Category: Hsp90 heat-shock protein]]

Revision as of 15:22, 20 November 2013

Template:STRUCTURE 3o2f

Structure of the N-domain of GRP94 bound to the HSP90 inhibitor PU-H54Structure of the N-domain of GRP94 bound to the HSP90 inhibitor PU-H54

Template:ABSTRACT PUBMED 23995768

FunctionFunction

[ENPL_CANFA] Molecular chaperone that functions in the processing and transport of secreted proteins. When associated with CNPY3, required for proper folding of Toll-like receptors. Functions in endoplasmic reticulum associated degradation (ERAD). Has ATPase activity (By similarity).

About this StructureAbout this Structure

3o2f is a 2 chain structure with sequence from Canfa. Full crystallographic information is available from OCA.

See AlsoSee Also

ReferenceReference

[xtra 1]

  1. Patel PD, Yan P, Seidler PM, Patel HJ, Sun W, Yang C, Que NS, Taldone T, Finotti P, Stephani RA, Gewirth DT, Chiosis G. Paralog-selective Hsp90 inhibitors define tumor-specific regulation of HER2. Nat Chem Biol. 2013 Sep 1. doi: 10.1038/nchembio.1335. PMID:23995768 doi:10.1038/nchembio.1335

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