3g9l

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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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{{Seed}}
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[[Image:3g9l.jpg|left|200px]]
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The entry 3g9l is ON HOLD until Paper Publication
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{{STRUCTURE_3g9l| PDB=3g9l | SCENE= }}
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Authors: Jacobs, M.D.
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===JNK3 bound to (Z)-1-((6-fluoro-4H-benzo[d][1,3]dioxin-8-yl)methyl)-3-(hydroxyimino)-4-styrylindolin-2-one===
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Description: JNK3 bound to (Z)-1-((6-fluoro-4H-benzo[d][1,3]dioxin-8-yl)methyl)-3-(hydroxyimino)-4-styrylindolin-2-one
 
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''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}}
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==About this Structure==
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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].
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==Reference==
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<ref group="xtra">PMID:19361991</ref><references group="xtra"/>
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[[Category: Homo sapiens]]
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[[Category: Mitogen-activated protein kinase]]
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[[Category: Jacobs, M D.]]
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[[Category: Alternative splicing]]
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[[Category: Atp-binding]]
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[[Category: Chromosomal rearrangement]]
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[[Category: Cytoplasm]]
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[[Category: Epilepsy]]
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[[Category: Inhibitor]]
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[[Category: Kinase]]
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[[Category: Nucleotide-binding]]
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[[Category: Phosphoprotein]]
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[[Category: Phosphorylation]]
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[[Category: Serine/threonine-protein kinase]]
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[[Category: Transferase]]
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''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

Image: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

  • 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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