2uzw
From Proteopedia
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==About this Structure== | ==About this Structure== | ||
- | 2UZW is a | + | 2UZW is a 2 chains structure of sequences from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2UZW OCA]. |
==Reference== | ==Reference== | ||
- | + | <ref group="xtra">PMID:17523610</ref><references group="xtra"/> | |
[[Category: Bos taurus]] | [[Category: Bos taurus]] | ||
- | [[Category: Protein complex]] | ||
[[Category: CAMP-dependent protein kinase]] | [[Category: CAMP-dependent protein kinase]] | ||
[[Category: Bouska, J.]] | [[Category: Bouska, J.]] | ||
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[[Category: Transferase]] | [[Category: Transferase]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 20:57:54 2009'' |
Revision as of 18:57, 16 February 2009
PKA STRUCTURES OF INDAZOLE-PYRIDINE SERIES OF AKT INHIBITORS
Template:ABSTRACT PUBMED 17523610
About this Structure
2UZW is a 2 chains structure of sequences from Bos taurus. Full crystallographic information is available from OCA.
Reference
- Zhu GD, Gandhi VB, Gong J, Thomas S, Woods KW, Song X, Li T, Diebold RB, Luo Y, Liu X, Guan R, Klinghofer V, Johnson EF, Bouska J, Olson A, Marsh KC, Stoll VS, Mamo M, Polakowski J, Campbell TJ, Martin RL, Gintant GA, Penning TD, Li Q, Rosenberg SH, Giranda VL. Syntheses of potent, selective, and orally bioavailable indazole-pyridine series of protein kinase b/akt inhibitors with reduced hypotension. J Med Chem. 2007 Jun 28;50(13):2990-3003. Epub 2007 May 25. PMID:17523610 doi:10.1021/jm0701019
Page seeded by OCA on Mon Feb 16 20:57:54 2009
Categories: Bos taurus | CAMP-dependent protein kinase | Bouska, J. | Campbell, T J. | Diebold, R B. | Gandhi, V B. | Giranda, V L. | Gong, J. | Guan, R. | Johnson, E F. | Klinghofer, V. | Li, Q. | Li, T. | Liu, X. | Luo, Y. | Mamo, M. | Marsh, K C. | Olson, A. | Penning, T D. | Polakowski, J. | Rosenberg, S H. | Song, X. | Stoll, V S. | Thomas, S. | Woods, K W. | Zhu, G D. | Akt inhibitor | Atp-binding | Camp | Kinase | Lipoprotein | Myristate | Nuclear protein | Nucleotide-binding | Phosphorylation | Protein kinase some | Serine/threonine-protein kinase | Transferase