1ykr: Difference between revisions

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{{Seed}}
[[Image:1ykr.png|left|200px]]
[[Image:1ykr.png|left|200px]]


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{{STRUCTURE_1ykr|  PDB=1ykr  |  SCENE=  }}  
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===Crystal structure of cdk2 with an aminoimidazo pyridine inhibitor===
===Crystal structure of cdk2 with an aminoimidazo pyridine inhibitor===


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{{ABSTRACT_PUBMED_15780638}}
{{ABSTRACT_PUBMED_15780638}}


==About this Structure==
==About this Structure==
1YKR is a 1 chain structure of 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=1YKR OCA].  
[[1ykr]] is a 1 chain structure of [[Cell Division Protein Kinase 2]] 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=1YKR OCA].  
 
==See Also==
*[[Cell Division Protein Kinase 2|Cell Division Protein Kinase 2]]


==Reference==
==Reference==
<ref group="xtra">PMID:15780638</ref><references group="xtra"/>
<ref group="xtra">PMID:015780638</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: Cdk2]]
[[Category: Cdk2]]
[[Category: Cell cycle division protein kinase 2]]
[[Category: Cell cycle division protein kinase 2]]
 
[[Category: Transferase]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 14:12:48 2009''

Revision as of 14:23, 25 July 2012

File:1ykr.png

Template:STRUCTURE 1ykr

Crystal structure of cdk2 with an aminoimidazo pyridine inhibitor

Template:ABSTRACT PUBMED 15780638

About this Structure

1ykr is a 1 chain structure of Cell Division Protein Kinase 2 with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See Also

Reference

  1. Hamdouchi C, Zhong B, Mendoza J, Collins E, Jaramillo C, De Diego JE, Robertson D, Spencer CD, Anderson BD, Watkins SA, Zhang F, Brooks HB. Structure-based design of a new class of highly selective aminoimidazo[1,2-a]pyridine-based inhibitors of cyclin dependent kinases. Bioorg Med Chem Lett. 2005 Apr 1;15(7):1943-7. PMID:15780638 doi:10.1016/j.bmcl.2005.01.052

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