1ykr

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==About this Structure==
==About this Structure==
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1YKR is a [[Single protein]] 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].
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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].
==Reference==
==Reference==
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Structure-based design of a new class of highly selective aminoimidazo[1,2-a]pyridine-based inhibitors of cyclin dependent kinases., 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, Bioorg Med Chem Lett. 2005 Apr 1;15(7):1943-7. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15780638 15780638]
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<ref group="xtra">PMID:15780638</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: Single protein]]
 
[[Category: Brooks, H B.]]
[[Category: Brooks, H B.]]
[[Category: Hamdouchi, C.]]
[[Category: Hamdouchi, C.]]
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[[Category: Cell cycle division protein kinase 2]]
[[Category: Cell cycle division protein kinase 2]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 16:48:14 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 14:12:48 2009''

Revision as of 12:12, 16 February 2009

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 sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  • 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

Page seeded by OCA on Mon Feb 16 14:12:48 2009

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