2i0h

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[[Image:2i0h.png|left|200px]]
[[Image:2i0h.png|left|200px]]
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{{STRUCTURE_2i0h| PDB=2i0h | SCENE= }}
{{STRUCTURE_2i0h| PDB=2i0h | SCENE= }}
===The structure of p38alpha in complex with an arylpyridazinone===
===The structure of p38alpha in complex with an arylpyridazinone===
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{{ABSTRACT_PUBMED_16945533}}
{{ABSTRACT_PUBMED_16945533}}
==About this Structure==
==About this Structure==
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2I0H 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=2I0H OCA].
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[[2i0h]] 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=2I0H 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:16945533</ref><references group="xtra"/>
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<ref group="xtra">PMID:016945533</ref><ref group="xtra">PMID:017070898</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: Inhibitor design]]
[[Category: Inhibitor design]]
[[Category: Serine/threonine kinase]]
[[Category: Serine/threonine kinase]]
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[[Category: Transferase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Feb 18 04:56:33 2009''
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Revision as of 11:19, 27 July 2012

Template:STRUCTURE 2i0h

Contents

The structure of p38alpha in complex with an arylpyridazinone

Template:ABSTRACT PUBMED 16945533

About this Structure

2i0h 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

  • Natarajan SR, Heller ST, Nam K, Singh SB, Scapin G, Patel S, Thompson JE, Fitzgerald CE, O'Keefe SJ. p38 MAP kinase inhibitors. Part 6: 2-arylpyridazin-3-ones as templates for inhibitor design. Bioorg Med Chem Lett. 2006 Nov 15;16(22):5809-13. Epub 2006 Aug 30. PMID:16945533 doi:10.1016/j.bmcl.2006.08.074
  • Lahiri SD, Zhang G, Dunaway-Mariano D, Allen KN. Diversification of function in the haloacid dehalogenase enzyme superfamily: The role of the cap domain in hydrolytic phosphoruscarbon bond cleavage. Bioorg Chem. 2006 Dec;34(6):394-409. Epub 2006 Oct 27. PMID:17070898 doi:10.1016/j.bioorg.2006.09.007

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