4a9m
From Proteopedia
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- | + | [[Image:4a9m.jpg|left|200px]] | |
- | The | + | <!-- |
+ | The line below this paragraph, containing "STRUCTURE_4a9m", creates the "Structure Box" on the page. | ||
+ | You may change the PDB parameter (which sets the PDB file loaded into the applet) | ||
+ | or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | ||
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+ | {{STRUCTURE_4a9m| PDB=4a9m | SCENE= }} | ||
- | + | ===N-TERMINAL BROMODOMAIN OF HUMAN BRD2 WITH N-cyclopentyl-5-(3,5- dimethyl-1,2-oxazol-4-yl)-2-methylbenzene-1-sulfonamide=== | |
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+ | <!-- | ||
+ | The line below this paragraph, {{ABSTRACT_PUBMED_22136469}}, adds the Publication Abstract to the page | ||
+ | (as it appears on PubMed at http://www.pubmed.gov), where 22136469 is the PubMed ID number. | ||
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+ | {{ABSTRACT_PUBMED_22136469}} | ||
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+ | ==About this Structure== | ||
+ | [[4a9m]] 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=4A9M OCA]. | ||
+ | |||
+ | ==Reference== | ||
+ | <ref group="xtra">PMID:022136469</ref><references group="xtra"/> | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Bamborough, P.]] | ||
+ | [[Category: Chung, C.]] | ||
+ | [[Category: Epigenetic reader]] | ||
+ | [[Category: Histone]] | ||
+ | [[Category: Inhibitor]] | ||
+ | [[Category: Signaling protein]] |
Revision as of 06:26, 8 February 2012
N-TERMINAL BROMODOMAIN OF HUMAN BRD2 WITH N-cyclopentyl-5-(3,5- dimethyl-1,2-oxazol-4-yl)-2-methylbenzene-1-sulfonamide
Template:ABSTRACT PUBMED 22136469
About this Structure
4a9m is a 3 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- 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