4a9n: Difference between revisions
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{{STRUCTURE_4a9n| PDB=4a9n | SCENE= }} | |||
===N-TERMINAL BROMODOMAIN OF HUMAN BRD2 WITH N-cyclopropyl-5-(3,5- dimethyl-1,2-oxazol-4-yl)-2-methylbenzene-1-sulfonamide=== | |||
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{{ABSTRACT_PUBMED_22136469}} | |||
==About this Structure== | |||
[[4a9n]] is a 3 chain structure 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=4A9N OCA]. | |||
==Reference== | |||
<ref group="xtra">PMID:022136469</ref><references group="xtra"/> | |||
[[Category: Homo sapiens]] | |||
[[Category: Bamborough, P.]] | |||
[[Category: Chung, C.]] | |||
[[Category: Signaling protein-inhibitor complex]] |
Revision as of 09:28, 8 February 2012
N-TERMINAL BROMODOMAIN OF HUMAN BRD2 WITH N-cyclopropyl-5-(3,5- dimethyl-1,2-oxazol-4-yl)-2-methylbenzene-1-sulfonamideN-TERMINAL BROMODOMAIN OF HUMAN BRD2 WITH N-cyclopropyl-5-(3,5- dimethyl-1,2-oxazol-4-yl)-2-methylbenzene-1-sulfonamide
Template:ABSTRACT PUBMED 22136469
About this StructureAbout this Structure
4a9n is a 3 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
ReferenceReference
- ↑ Bamborough P, Diallo H, Goodacre JD, Gordon L, Lewis A, Seal JT, Wilson DM, Woodrow MD, Chung CW. Fragment-based discovery of bromodomain inhibitors part 2: optimization of phenylisoxazole sulfonamides. J Med Chem. 2012 Jan 26;55(2):587-96. Epub 2012 Jan 11. PMID:22136469 doi:10.1021/jm201283q