3ibe: Difference between revisions
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{{STRUCTURE_3ibe| PDB=3ibe | SCENE= }} | |||
===Crystal Structure of a Pyrazolopyrimidine Inhibitor Bound to PI3 Kinase Gamma=== | |||
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{{ABSTRACT_PUBMED_19645448}} | |||
==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]. | |||
==Reference== | |||
<ref group="xtra">PMID:19645448</ref><references group="xtra"/> | |||
[[Category: Homo sapiens]] | |||
[[Category: Phosphatidylinositol-4,5-bisphosphate 3-kinase]] | |||
[[Category: Bard, J.]] | |||
[[Category: Svenson, K.]] | |||
[[Category: Atp-binding]] | |||
[[Category: Kinase]] | |||
[[Category: Nucleotide-binding]] | |||
[[Category: Pi3kinase inhibitor]] | |||
[[Category: Transferase]] | |||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Sep 3 15:36:22 2009'' |
Revision as of 15:36, 3 September 2009
Crystal Structure of a Pyrazolopyrimidine Inhibitor Bound to PI3 Kinase GammaCrystal Structure of a Pyrazolopyrimidine Inhibitor Bound to PI3 Kinase Gamma
Template:ABSTRACT PUBMED 19645448
About this StructureAbout this Structure
3IBE is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
ReferenceReference
- ↑ 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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