2zb0: Difference between revisions

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{{STRUCTURE_2zb0|  PDB=2zb0  |  SCENE=  }}  
{{STRUCTURE_2zb0|  PDB=2zb0  |  SCENE=  }}  


'''Crystal structure of P38 in complex with biphenyl amide inhibitor'''
===Crystal structure of P38 in complex with biphenyl amide inhibitor===




==Overview==
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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 line below this paragraph, {{ABSTRACT_PUBMED_18006306}}, adds the Publication Abstract to the page
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{{ABSTRACT_PUBMED_18006306}}


==About this Structure==
==About this Structure==
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==Reference==
==Reference==
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:[http://www.ncbi.nlm.nih.gov/pubmed/18006306 18006306]
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:[http://www.ncbi.nlm.nih.gov/pubmed/18006306 18006306]
Biphenyl amide p38 kinase inhibitors 2: Optimisation and SAR., Angell RM, Angell TD, Bamborough P, Brown D, Brown M, Buckton JB, Cockerill SG, Edwards CD, Jones KL, Longstaff T, Smee PA, Smith KJ, Somers DO, Walker AL, Willson M, Bioorg Med Chem Lett. 2008 Jan 1;18(1):324-8. Epub 2007 Oct 17. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/17981461 17981461]
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Mitogen-activated protein kinase]]
[[Category: Mitogen-activated protein kinase]]
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[[Category: Serine/threonine protein kinase]]
[[Category: Serine/threonine protein kinase]]
[[Category: Transferase]]
[[Category: Transferase]]
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