3hec: Difference between revisions

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[[Image:3hec.png|left|200px]]
[[Image:3hec.png|left|200px]]


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{{STRUCTURE_3hec|  PDB=3hec  |  SCENE=  }}  
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===P38 in complex with Imatinib===
===P38 in complex with Imatinib===


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{{ABSTRACT_PUBMED_20337484}}
{{ABSTRACT_PUBMED_20337484}}


==About this Structure==
==About this Structure==
3HEC 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=3HEC OCA].  
[[3hec]] is a 1 chain structure of [[Mitogen-activated protein kinase]] 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=3HEC OCA].  
 
==See Also==
*[[Mitogen-activated protein kinase|Mitogen-activated protein kinase]]


==Reference==
==Reference==
<ref group="xtra">PMID:20337484</ref><references group="xtra"/>
<ref group="xtra">PMID:020337484</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Mitogen-activated protein kinase]]
[[Category: Mitogen-activated protein kinase]]
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[[Category: Serine/threonine-protein kinase]]
[[Category: Serine/threonine-protein kinase]]
[[Category: Transferase]]
[[Category: Transferase]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Aug 18 11:04:28 2010''

Revision as of 17:39, 26 July 2012

File:3hec.png

Template:STRUCTURE 3hec

P38 in complex with ImatinibP38 in complex with Imatinib

Template:ABSTRACT PUBMED 20337484

About this StructureAbout this Structure

3hec is a 1 chain structure of Mitogen-activated protein kinase with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See AlsoSee Also

ReferenceReference

[xtra 1]

  1. Namboodiri HV, Bukhtiyarova M, Ramcharan J, Karpusas M, Lee Y, Springman EB. Analysis of imatinib and sorafenib binding to p38alpha compared with c-Abl and b-Raf provides structural insights for understanding the selectivity of inhibitors targeting the DFG-out form of protein kinases. Biochemistry. 2010 May 4;49(17):3611-8. PMID:20337484 doi:10.1021/bi100070r

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