3fv8: Difference between revisions

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[[Image:3fv8.png|left|200px]]
[[Image:3fv8.png|left|200px]]


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{{STRUCTURE_3fv8|  PDB=3fv8  |  SCENE=  }}  
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===JNK3 bound to piperazine amide inhibitor, SR2774.===
===JNK3 bound to piperazine amide inhibitor, SR2774.===


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{{ABSTRACT_PUBMED_19433357}}
{{ABSTRACT_PUBMED_19433357}}


==About this Structure==
==About this Structure==
3FV8 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=3FV8 OCA].  
[[3fv8]] is a 1 chain structure of [[Mitogen-activated protein kinase]] with 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=3FV8 OCA].  
 
==See Also==
*[[Mitogen-activated protein kinase|Mitogen-activated protein kinase]]


==Reference==
==Reference==
<ref group="xtra">PMID:19433357</ref><references group="xtra"/>
<ref group="xtra">PMID:019433357</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Mitogen-activated protein kinase]]
[[Category: Mitogen-activated protein kinase]]
[[Category: Habel, J E.]]
[[Category: Habel, J E.]]
[[Category: Alternative splicing]]
[[Category: Atp-binding]]
[[Category: Atp-binding]]
[[Category: Chromosomal rearrangement]]
[[Category: Cytoplasm]]
[[Category: Epilepsy]]
[[Category: Epilepsy]]
[[Category: Jnk3]]
[[Category: Jnk3]]
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[[Category: Serine/threonine-protein kinase]]
[[Category: Serine/threonine-protein kinase]]
[[Category: Transferase]]
[[Category: Transferase]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat Jul  4 18:15:07 2009''

Revision as of 03:13, 26 July 2012

File:3fv8.png

Template:STRUCTURE 3fv8

JNK3 bound to piperazine amide inhibitor, SR2774.JNK3 bound to piperazine amide inhibitor, SR2774.

Template:ABSTRACT PUBMED 19433357

About this StructureAbout this Structure

3fv8 is a 1 chain structure of Mitogen-activated protein kinase with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See AlsoSee Also

ReferenceReference

[xtra 1]

  1. Shin Y, Chen W, Habel J, Duckett D, Ling YY, Koenig M, He Y, Vojkovsky T, LoGrasso P, Kamenecka TM. Synthesis and SAR of piperazine amides as novel c-jun N-terminal kinase (JNK) inhibitors. Bioorg Med Chem Lett. 2009 Jun 15;19(12):3344-7. Epub 2009 Mar 26. PMID:19433357 doi:10.1016/j.bmcl.2009.03.086

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