2zb0: Difference between revisions

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New page: left|200px<br /><applet load="2zb0" size="350" color="white" frame="true" align="right" spinBox="true" caption="2zb0, resolution 2.100Å" /> '''Crystal structure o...
 
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==Overview==
==Overview==
The biphenyl amides (BPAs) are a novel series of p38 MAP kinase, inhibitors. The discovery of the series through structure-based focused, screening is described, and the binding mode of the compounds is explained, with reference to X-ray crystal structures.
The biphenyl amides (BPAs) are a novel series of p38 MAP kinase inhibitors. The discovery of the series through structure-based focused screening is described, and the binding mode of the compounds is explained with reference to X-ray crystal structures.


==About this Structure==
==About this Structure==
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[[Category: Mitogen-activated protein kinase]]
[[Category: Mitogen-activated protein kinase]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Somers, D.O.]]
[[Category: Somers, D O.]]
[[Category: GK3]]
[[Category: GK3]]
[[Category: GOL]]
[[Category: GOL]]
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[[Category: transferase]]
[[Category: transferase]]


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Revision as of 20:01, 21 February 2008

File:2zb0.jpg


2zb0, resolution 2.100Å

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Crystal structure of P38 in complex with biphenyl amide inhibitor

OverviewOverview

The biphenyl amides (BPAs) are a novel series of p38 MAP kinase inhibitors. The discovery of the series through structure-based focused screening is described, and the binding mode of the compounds is explained with reference to X-ray crystal structures.

About this StructureAbout this Structure

2ZB0 is a Single protein structure of sequence from Homo sapiens with and as ligands. Active as Mitogen-activated protein kinase, with EC number 2.7.11.24 Full crystallographic information is available from OCA.

ReferenceReference

Biphenyl amide p38 kinase inhibitors 1: Discovery and binding mode., Angell RM, Bamborough P, Cleasby A, Cockerill SG, Jones KL, Mooney CJ, Somers DO, Walker AL, Bioorg Med Chem Lett. 2008 Jan 1;18(1):318-23. Epub 2007 Nov 19. PMID:18006306

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