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3v9v
From Proteopedia
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| - | + | [[Image:3v9v.jpg|left|200px]] | |
| - | The | + | <!-- |
| + | The line below this paragraph, containing "STRUCTURE_3v9v", 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_3v9v| PDB=3v9v | SCENE= }} | ||
| - | + | ===Crystal structure of the PPARgamma-LBD complexed with a cercosporamide derivative modulator=== | |
| - | + | ||
| + | <!-- | ||
| + | The line below this paragraph, {{ABSTRACT_PUBMED_22225641}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 22225641 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_22225641}} | ||
| + | |||
| + | ==About this Structure== | ||
| + | [[3v9v]] is a 2 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=3V9V OCA]. | ||
| + | |||
| + | ==Reference== | ||
| + | <ref group="xtra">PMID:022225641</ref><references group="xtra"/> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Hanzawa, H.]] | ||
| + | [[Category: Matsui, Y.]] | ||
| + | [[Category: Three-layered alpha-helical sandwich]] | ||
| + | [[Category: Transcription regulation]] | ||
| + | [[Category: Transcription-transcription regulator complex]] | ||
Revision as of 07:19, 1 February 2012
Crystal structure of the PPARgamma-LBD complexed with a cercosporamide derivative modulator
Template:ABSTRACT PUBMED 22225641
About this Structure
3v9v is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Furukawa A, Arita T, Fukuzaki T, Satoh S, Mori M, Honda T, Matsui Y, Wakabayashi K, Hayashi S, Araki K, Ohsumi J. Substituents at the naphthalene C3 position of (-)-Cercosporamide derivatives significantly affect the maximal efficacy as PPARgamma partial agonists. Bioorg Med Chem Lett. 2012 Feb 1;22(3):1348-51. Epub 2011 Dec 16. PMID:22225641 doi:10.1016/j.bmcl.2011.12.066
