3pa4: Difference between revisions

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[[Image:3pa4.png|left|200px]]
[[Image:3pa4.jpg|left|200px]]


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{{STRUCTURE_3pa4|  PDB=3pa4  |  SCENE=  }}  
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===X-ray crystal structure of compound 2a bound to human CHK1 kinase domain===
===X-ray crystal structure of compound 2a bound to human CHK1 kinase domain===


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{{ABSTRACT_PUBMED_21074424}}


==About this Structure==
==About this Structure==
3PA4 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=3PA4 OCA].  
[[3pa4]] is a 1 chain structure of [[Serine/threonine 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=3PA4 OCA].  
 
==See Also==
*[[Serine/threonine protein kinase|Serine/threonine protein kinase]]


==Reference==
==Reference==
<ref group="xtra">PMID:21074424</ref><references group="xtra"/>
<ref group="xtra">PMID:021074424</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Non-specific serine/threonine protein kinase]]
[[Category: Non-specific serine/threonine protein kinase]]
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[[Category: Transferase]]
[[Category: Transferase]]
[[Category: Transferase-transferase inhibitor complex]]
[[Category: Transferase-transferase inhibitor complex]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Dec  8 11:54:10 2010''

Revision as of 17:56, 27 July 2012

File:3pa4.png

Template:STRUCTURE 3pa4

X-ray crystal structure of compound 2a bound to human CHK1 kinase domainX-ray crystal structure of compound 2a bound to human CHK1 kinase domain

Template:ABSTRACT PUBMED 21074424

About this StructureAbout this Structure

3pa4 is a 1 chain structure of Serine/threonine protein kinase with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See AlsoSee Also

ReferenceReference

[xtra 1]

  1. ↑ Zhao L, Zhang Y, Dai C, Guzi T, Wiswell D, Seghezzi W, Parry D, Fischmann T, Siddiqui MA. Design, synthesis and SAR of thienopyridines as potent CHK1 inhibitors. Bioorg Med Chem Lett. 2010 Dec 15;20(24):7216-21. Epub 2010 Oct 26. PMID:21074424 doi:10.1016/j.bmcl.2010.10.105

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