1ykr

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[[Image:1ykr.png|left|200px]]
[[Image:1ykr.png|left|200px]]
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{{STRUCTURE_1ykr| PDB=1ykr | SCENE= }}
{{STRUCTURE_1ykr| PDB=1ykr | SCENE= }}
===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==
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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].
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[[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].
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==See Also==
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*[[Cell Division Protein Kinase 2|Cell Division Protein Kinase 2]]
==Reference==
==Reference==
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<ref group="xtra">PMID:15780638</ref><references group="xtra"/>
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<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]]
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[[Category: Transferase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 14:12:48 2009''
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Revision as of 14:23, 25 July 2012

Template:STRUCTURE 1ykr

Contents

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

  • 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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