2vnw
From Proteopedia
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{{STRUCTURE_2vnw| PDB=2vnw | SCENE= }} | {{STRUCTURE_2vnw| PDB=2vnw | SCENE= }} | ||
===STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH (1-(9H-PURIN-6-YL)PIPERIDIN-4-YL)METHANAMINE=== | ===STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH (1-(9H-PURIN-6-YL)PIPERIDIN-4-YL)METHANAMINE=== | ||
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{{ABSTRACT_PUBMED_18345609}} | {{ABSTRACT_PUBMED_18345609}} | ||
==About this Structure== | ==About this Structure== | ||
| - | + | [[2vnw]] is a 2 chain structure with sequence 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=2VNW OCA]. | |
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| + | ==See Also== | ||
| + | *[[CAMP-dependent protein kinase|CAMP-dependent protein kinase]] | ||
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:018345609</ref><references group="xtra"/> |
[[Category: Bos taurus]] | [[Category: Bos taurus]] | ||
[[Category: CAMP-dependent protein kinase]] | [[Category: CAMP-dependent protein kinase]] | ||
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[[Category: Atp-binding]] | [[Category: Atp-binding]] | ||
[[Category: Camp]] | [[Category: Camp]] | ||
| - | [[Category: Cytoplasm]] | ||
[[Category: Kinase]] | [[Category: Kinase]] | ||
[[Category: Lipoprotein]] | [[Category: Lipoprotein]] | ||
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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 00:46:02 2009'' | ||
Revision as of 21:37, 7 January 2013
Contents |
STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH (1-(9H-PURIN-6-YL)PIPERIDIN-4-YL)METHANAMINE
Template:ABSTRACT PUBMED 18345609
About this Structure
2vnw is a 2 chain structure with sequence from Bos taurus. Full crystallographic information is available from OCA.
See Also
Reference
- Caldwell JJ, Davies TG, Donald A, McHardy T, Rowlands MG, Aherne GW, Hunter LK, Taylor K, Ruddle R, Raynaud FI, Verdonk M, Workman P, Garrett MD, Collins I. Identification of 4-(4-Aminopiperidin-1-yl)-7H-pyrrolo[2,3-d]pyrimidines as Selective Inhibitors of Protein Kinase B through Fragment Elaboration. J Med Chem. 2008 Apr 10;51(7):2147-57. Epub 2008 Mar 18. PMID:18345609 doi:10.1021/jm701437d
Categories: Bos taurus | CAMP-dependent protein kinase | Aherne, G W. | Caldwell, J J. | Collins, I. | Davies, T G. | Donald, A. | Garrett, M D. | Hunter, L K. | Mchardy, T. | Raynaud, F I. | Rowlands, M G. | Ruddle, R. | Taylor, K. | Verdonk, M. | Workman, P. | Atp-binding | Camp | Kinase | Lipoprotein | Myristate | Nucleotide-binding | Nucleus | Phosphoprotein | Protein kinase inhibitor | Serine/threonine-protein kinase | Transferase
