3g9l: Difference between revisions

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New page: '''Unreleased structure''' The entry 3g9l is ON HOLD until Paper Publication Authors: Jacobs, M.D. Description: JNK3 bound to (Z)-1-((6-fluoro-4H-benzo[d][1,3]dioxin-8-yl)methyl)-3-(hy...
 
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'''Unreleased structure'''
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[[Image:3g9l.jpg|left|200px]]


The entry 3g9l is ON HOLD until Paper Publication
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{{STRUCTURE_3g9l|  PDB=3g9l  |  SCENE=  }}


Authors: Jacobs, M.D.
===JNK3 bound to (Z)-1-((6-fluoro-4H-benzo[d][1,3]dioxin-8-yl)methyl)-3-(hydroxyimino)-4-styrylindolin-2-one===


Description: JNK3 bound to (Z)-1-((6-fluoro-4H-benzo[d][1,3]dioxin-8-yl)methyl)-3-(hydroxyimino)-4-styrylindolin-2-one


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Mar  4 14:45:34 2009''
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{{ABSTRACT_PUBMED_19361991}}
 
==About this Structure==
3G9L 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=3G9L OCA].
 
==Reference==
<ref group="xtra">PMID:19361991</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Mitogen-activated protein kinase]]
[[Category: Jacobs, M D.]]
[[Category: Alternative splicing]]
[[Category: Atp-binding]]
[[Category: Chromosomal rearrangement]]
[[Category: Cytoplasm]]
[[Category: Epilepsy]]
[[Category: Inhibitor]]
[[Category: Kinase]]
[[Category: Nucleotide-binding]]
[[Category: Phosphoprotein]]
[[Category: Phosphorylation]]
[[Category: Serine/threonine-protein kinase]]
[[Category: Transferase]]
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Apr 30 09:39:00 2009''

Revision as of 06:39, 30 April 2009

File:3g9l.jpg

Template:STRUCTURE 3g9l

JNK3 bound to (Z)-1-((6-fluoro-4H-benzo[d][1,3]dioxin-8-yl)methyl)-3-(hydroxyimino)-4-styrylindolin-2-one

Template:ABSTRACT PUBMED 19361991

About this Structure

3G9L is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  1. Cao J, Gao H, Bemis G, Salituro F, Ledeboer M, Harrington E, Wilke S, Taslimi P, Pazhanisamy S, Xie X, Jacobs M, Green J. Structure-based design and parallel synthesis of N-benzyl isatin oximes as JNK3 MAP kinase inhibitors. Bioorg Med Chem Lett. 2009 May 15;19(10):2891-5. Epub 2009 Mar 17. PMID:19361991 doi:10.1016/j.bmcl.2009.03.043

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