3ibe: Difference between revisions

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


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===Crystal Structure of a Pyrazolopyrimidine Inhibitor Bound to PI3 Kinase Gamma===
===Crystal Structure of a Pyrazolopyrimidine Inhibitor Bound to PI3 Kinase Gamma===


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{{ABSTRACT_PUBMED_19645448}}
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==About this Structure==
==About this Structure==
3IBE 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=3IBE OCA].  
[[3ibe]] is a 1 chain structure of [[Phosphoinositide 3-Kinases]] 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=3IBE OCA].  
 
==See Also==
*[[Phosphoinositide 3-Kinases|Phosphoinositide 3-Kinases]]


==Reference==
==Reference==
<ref group="xtra">PMID:19645448</ref><references group="xtra"/>
<ref group="xtra">PMID:019645448</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Phosphatidylinositol-4,5-bisphosphate 3-kinase]]
[[Category: Phosphatidylinositol-4,5-bisphosphate 3-kinase]]
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[[Category: Pi3kinase inhibitor]]
[[Category: Pi3kinase inhibitor]]
[[Category: Transferase]]
[[Category: Transferase]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Sep  3 15:36:22 2009''

Revision as of 12:03, 26 July 2012

File:3ibe.png

Template:STRUCTURE 3ibe

Crystal Structure of a Pyrazolopyrimidine Inhibitor Bound to PI3 Kinase Gamma

Template:ABSTRACT PUBMED 19645448

About this Structure

3ibe is a 1 chain structure of Phosphoinositide 3-Kinases with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See Also

Reference

  1. Zask A, Verheijen JC, Curran K, Kaplan J, Richard DJ, Nowak P, Malwitz DJ, Brooijmans N, Bard J, Svenson K, Lucas J, Toral-Barza L, Zhang WG, Hollander I, Gibbons JJ, Abraham RT, Ayral-Kaloustian S, Mansour TS, Yu K. ATP-Competitive Inhibitors of the Mammalian Target of Rapamycin: Design and Synthesis of Highly Potent and Selective Pyrazolopyrimidines. J Med Chem. 2009 Jul 31. PMID:19645448 doi:10.1021/jm900851f

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