2zb0: Difference between revisions
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'''Crystal structure of P38 in complex with biphenyl amide inhibitor''' | '''Crystal structure of P38 in complex with biphenyl amide inhibitor''' | ||
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[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Somers, D O.]] | [[Category: Somers, D O.]] | ||
[[Category: | [[Category: Alternative splicing]] | ||
[[Category: | [[Category: Atp-binding]] | ||
[[Category: | [[Category: Cytoplasm]] | ||
[[Category: | [[Category: Map kinase]] | ||
[[Category: | [[Category: Nucleotide-binding]] | ||
[[Category: | [[Category: Nucleus]] | ||
[[Category: | [[Category: P38]] | ||
[[Category: | [[Category: Phosphorylation]] | ||
[[Category: | [[Category: Serine/threonine protein kinase]] | ||
[[Category: | [[Category: Transferase]] | ||
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Revision as of 20:06, 4 May 2008
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. 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 Page seeded by OCA on Sun May 4 20:06:14 2008