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3ibe
From Proteopedia
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| + | [[Image:3ibe.jpg|left|200px]] | ||
| - | The | + | <!-- |
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| + | {{STRUCTURE_3ibe| PDB=3ibe | SCENE= }} | ||
| - | + | ===Crystal Structure of a Pyrazolopyrimidine Inhibitor Bound to PI3 Kinase Gamma=== | |
| - | Description: Crystal Structure of a Pyrazolopyrimidine Inhibitor Bound to PI3 Kinase Gamma | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | <!-- |
| + | The line below this paragraph, {{ABSTRACT_PUBMED_19645448}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 19645448 is the PubMed ID number. | ||
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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 12:36, 3 September 2009
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 sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- 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
Page seeded by OCA on Thu Sep 3 15:36:22 2009
