3fv8

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[[Image:3fv8.png|left|200px]]
[[Image:3fv8.png|left|200px]]
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{{STRUCTURE_3fv8| PDB=3fv8 | SCENE= }}
{{STRUCTURE_3fv8| PDB=3fv8 | SCENE= }}
===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==
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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].
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[[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].
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==See Also==
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*[[Mitogen-activated protein kinase|Mitogen-activated protein kinase]]
==Reference==
==Reference==
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<ref group="xtra">PMID:19433357</ref><references group="xtra"/>
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<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.]]
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[[Category: Alternative splicing]]
 
[[Category: Atp-binding]]
[[Category: Atp-binding]]
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[[Category: Chromosomal rearrangement]]
 
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[[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]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat Jul 4 18:15:07 2009''
 

Revision as of 00:13, 26 July 2012

Template:STRUCTURE 3fv8

Contents

JNK3 bound to piperazine amide inhibitor, SR2774.

Template:ABSTRACT PUBMED 19433357

About 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 Also

Reference

  • 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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