2x6e: Difference between revisions

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m Protected "2x6e" [edit=sysop:move=sysop]
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[[Image:2x6e.png|left|200px]]
[[Image:2x6e.png|left|200px]]


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{{STRUCTURE_2x6e|  PDB=2x6e  |  SCENE=  }}  
{{STRUCTURE_2x6e|  PDB=2x6e  |  SCENE=  }}  


===AURORA-A BOUND TO AN INHIBITOR===
===AURORA-A BOUND TO AN INHIBITOR===


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{{ABSTRACT_PUBMED_20565112}}


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==Reference==
==Reference==
<ref group="xtra">PMID:20565112</ref><references group="xtra"/>
<ref group="xtra">PMID:020565112</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Non-specific serine/threonine protein kinase]]
[[Category: Non-specific serine/threonine protein kinase]]
[[Category: Bayliss, R.]]
[[Category: Bayliss, R.]]
[[Category: Kosmopoulou, M.]]
[[Category: Kosmopoulou, M.]]
[[Category: Cell cycle]]
[[Category: Mitosis]]
[[Category: Transferase]]

Revision as of 18:16, 27 February 2013

File:2x6e.png

Template:STRUCTURE 2x6e

AURORA-A BOUND TO AN INHIBITORAURORA-A BOUND TO AN INHIBITOR

Template:ABSTRACT PUBMED 20565112

About this StructureAbout this Structure

2x6e is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

ReferenceReference

[xtra 1]

  1. Bavetsias V, Large JM, Sun C, Bouloc N, Kosmopoulou M, Matteucci M, Wilsher NE, Martins V, Reynisson J, Atrash B, Faisal A, Urban F, Valenti M, de Haven Brandon A, Box G, Raynaud FI, Workman P, Eccles SA, Bayliss R, Blagg J, Linardopoulos S, McDonald E. Imidazo[4,5-b]pyridine Derivatives As Inhibitors of Aurora Kinases: Lead Optimization Studies toward the Identification of an Orally Bioavailable Preclinical Development Candidate. J Med Chem. 2010 Jun 21. PMID:20565112 doi:10.1021/jm100262j

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OCA