2f7x: Difference between revisions

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{{Seed}}
[[Image:2f7x.png|left|200px]]
[[Image:2f7x.png|left|200px]]


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{{STRUCTURE_2f7x|  PDB=2f7x  |  SCENE=  }}  
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===Protein Kinase A bound to (S)-2-(1H-Indol-3-yl)-1-[5-((E)-2-pyridin-4-yl-vinyl)-pyridin-3-yloxymethyl]-ethylamine===
===Protein Kinase A bound to (S)-2-(1H-Indol-3-yl)-1-[5-((E)-2-pyridin-4-yl-vinyl)-pyridin-3-yloxymethyl]-ethylamine===


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{{ABSTRACT_PUBMED_16403626}}
{{ABSTRACT_PUBMED_16403626}}


==About this Structure==
==About this Structure==
2F7X 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=2F7X OCA].  
[[2f7x]] 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=2F7X OCA].  
 
==See Also==
*[[CAMP-dependent protein kinase|CAMP-dependent protein kinase]]


==Reference==
==Reference==
<ref group="xtra">PMID:16403626</ref><references group="xtra"/>
<ref group="xtra">PMID:016403626</ref><references group="xtra"/>
[[Category: Bos taurus]]
[[Category: Bos taurus]]
[[Category: Non-specific serine/threonine protein kinase]]
[[Category: Non-specific serine/threonine protein kinase]]
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[[Category: Akt inhibitor]]
[[Category: Akt inhibitor]]
[[Category: Protein kinase some]]
[[Category: Protein kinase some]]
 
[[Category: Transferase]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 21:55:33 2009''

Revision as of 15:13, 7 January 2013

File:2f7x.png

Template:STRUCTURE 2f7x

Protein Kinase A bound to (S)-2-(1H-Indol-3-yl)-1-[5-((E)-2-pyridin-4-yl-vinyl)-pyridin-3-yloxymethyl]-ethylamineProtein Kinase A bound to (S)-2-(1H-Indol-3-yl)-1-[5-((E)-2-pyridin-4-yl-vinyl)-pyridin-3-yloxymethyl]-ethylamine

Template:ABSTRACT PUBMED 16403626

About this StructureAbout this Structure

2f7x is a 2 chain structure with sequence from Bos taurus. Full crystallographic information is available from OCA.

See AlsoSee Also

ReferenceReference

[xtra 1]

  1. ↑ Li Q, Li T, Zhu GD, Gong J, Claibone A, Dalton C, Luo Y, Johnson EF, Shi Y, Liu X, Klinghofer V, Bauch JL, Marsh KC, Bouska JJ, Arries S, De Jong R, Oltersdorf T, Stoll VS, Jakob CG, Rosenberg SH, Giranda VL. Discovery of trans-3,4'-bispyridinylethylenes as potent and novel inhibitors of protein kinase B (PKB/Akt) for the treatment of cancer: Synthesis and biological evaluation. Bioorg Med Chem Lett. 2006 Mar 15;16(6):1679-85. Epub 2006 Jan 5. PMID:16403626 doi:10.1016/j.bmcl.2005.12.017

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