1pxl

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[[Image:1pxl.png|left|200px]]
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{{STRUCTURE_1pxl| PDB=1pxl | SCENE= }}
{{STRUCTURE_1pxl| PDB=1pxl | SCENE= }}
===HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR [4-(2,4-Dimethyl-thiazol-5-yl)-pyrimidin-2-yl]-(4-trifluoromethyl-phenyl)-amine===
===HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR [4-(2,4-Dimethyl-thiazol-5-yl)-pyrimidin-2-yl]-(4-trifluoromethyl-phenyl)-amine===
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{{ABSTRACT_PUBMED_12679018}}
{{ABSTRACT_PUBMED_12679018}}
==About this Structure==
==About this Structure==
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1PXL 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=1PXL OCA].
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[[1pxl]] 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=1PXL 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:12679018</ref><references group="xtra"/>
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<ref group="xtra">PMID:012679018</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Fischer, P M.]]
[[Category: Fischer, P M.]]
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[[Category: Serine/threonine-protein kinase]]
[[Category: Serine/threonine-protein kinase]]
[[Category: Transferase]]
[[Category: Transferase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Feb 18 03:36:10 2009''
 

Revision as of 09:49, 27 July 2012

Image:1pxl.png

Template:STRUCTURE 1pxl

Contents

HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR [4-(2,4-Dimethyl-thiazol-5-yl)-pyrimidin-2-yl]-(4-trifluoromethyl-phenyl)-amine

Template:ABSTRACT PUBMED 12679018

About this Structure

1pxl 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

  • Wu SY, McNae I, Kontopidis G, McClue SJ, McInnes C, Stewart KJ, Wang S, Zheleva DI, Marriage H, Lane DP, Taylor P, Fischer PM, Walkinshaw MD. Discovery of a novel family of CDK inhibitors with the program LIDAEUS: structural basis for ligand-induced disordering of the activation loop. Structure. 2003 Apr;11(4):399-410. PMID:12679018

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