2zdu: Difference between revisions
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[[Image:2zdu.png|left|200px]] | [[Image:2zdu.png|left|200px]] | ||
{{STRUCTURE_2zdu| PDB=2zdu | SCENE= }} | {{STRUCTURE_2zdu| PDB=2zdu | SCENE= }} | ||
===Crystal Structure of human JNK3 complexed with an isoquinolone inhibitor=== | ===Crystal Structure of human JNK3 complexed with an isoquinolone inhibitor=== | ||
{{ABSTRACT_PUBMED_18313304}} | {{ABSTRACT_PUBMED_18313304}} | ||
==About this Structure== | ==About this Structure== | ||
[[2zdu]] 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=2ZDU OCA]. | |||
==See Also== | |||
*[[Mitogen-activated protein kinase|Mitogen-activated protein kinase]] | |||
==Reference== | ==Reference== | ||
<ref group="xtra">PMID: | <ref group="xtra">PMID:018313304</ref><references group="xtra"/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Mitogen-activated protein kinase]] | [[Category: Mitogen-activated protein kinase]] | ||
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[[Category: Ohra, T.]] | [[Category: Ohra, T.]] | ||
[[Category: Sogabe, S.]] | [[Category: Sogabe, S.]] | ||
[[Category: Atp-binding]] | [[Category: Atp-binding]] | ||
[[Category: Epilepsy]] | [[Category: Epilepsy]] | ||
[[Category: Nucleotide-binding]] | [[Category: Nucleotide-binding]] | ||
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[[Category: Serine/threonine-protein kinase]] | [[Category: Serine/threonine-protein kinase]] | ||
[[Category: Transferase]] | [[Category: Transferase]] | ||
Revision as of 20:24, 25 July 2012
Crystal Structure of human JNK3 complexed with an isoquinolone inhibitor
Template:ABSTRACT PUBMED 18313304
About this Structure
2zdu 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
- Asano Y, Kitamura S, Ohra T, Aso K, Igata H, Tamura T, Kawamoto T, Tanaka T, Sogabe S, Matsumoto S, Yamaguchi M, Kimura H, Itoh F. Discovery, synthesis and biological evaluation of isoquinolones as novel and highly selective JNK inhibitors (1). Bioorg Med Chem. 2008 Apr 15;16(8):4715-32. Epub 2008 Feb 13. PMID:18313304 doi:10.1016/j.bmc.2008.02.027
