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4aac

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[[Image:4aac.jpg|left|200px]]
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===P38ALPHA MAP KINASE BOUND TO CMPD 29===
===P38ALPHA MAP KINASE BOUND TO CMPD 29===
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(as it appears on PubMed at http://www.pubmed.gov), where 22608965 is the PubMed ID number.
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{{ABSTRACT_PUBMED_22608965}}
==About this Structure==
==About this Structure==
[[4aac]] 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=4AAC OCA].
[[4aac]] 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=4AAC OCA].
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==Reference==
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<ref group="xtra">PMID:022608965</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Mitogen-activated protein kinase]]
[[Category: Mitogen-activated protein kinase]]

Revision as of 06:39, 6 June 2012

Template:STRUCTURE 4aac

P38ALPHA MAP KINASE BOUND TO CMPD 29

Template:ABSTRACT PUBMED 22608965

About this Structure

4aac is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  • Brown DS, Cumming JG, Bethel P, Finlayson J, Gerhardt S, Nash I, Pauptit RA, Pike KG, Reid A, Snelson W, Swallow S, Thompson C. The discovery of N-cyclopropyl-4-methyl-3-[6-(4-methylpiperazin-1-yl)-4-oxoquinazolin-3(4H)-yl]ben zamide (AZD6703), a clinical p38alpha MAP kinase inhibitor for the treatment of inflammatory diseases. Bioorg Med Chem Lett. 2012 Jun 15;22(12):3879-83. Epub 2012 May 2. PMID:22608965 doi:10.1016/j.bmcl.2012.04.116

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