3bc5: Difference between revisions
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[[Image:3bc5.png|left|200px]] | [[Image:3bc5.png|left|200px]] | ||
{{STRUCTURE_3bc5| PDB=3bc5 | SCENE= }} | {{STRUCTURE_3bc5| PDB=3bc5 | SCENE= }} | ||
===X-ray crystal structure of human ppar gamma with 2-(5-(3-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)benzyl)-2-phenyl-2h-1,2,3-triazol-4-yl)acetic acid=== | ===X-ray crystal structure of human ppar gamma with 2-(5-(3-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)benzyl)-2-phenyl-2h-1,2,3-triazol-4-yl)acetic acid=== | ||
{{ABSTRACT_PUBMED_19201606}} | {{ABSTRACT_PUBMED_19201606}} | ||
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==See Also== | ==See Also== | ||
*[[Peroxisome Proliferator-Activated Receptors]] | *[[Peroxisome Proliferator-Activated Receptors|Peroxisome Proliferator-Activated Receptors]] | ||
==Reference== | ==Reference== | ||
<ref group="xtra">PMID: | <ref group="xtra">PMID:019201606</ref><references group="xtra"/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Muckelbauer, J K.]] | [[Category: Muckelbauer, J K.]] | ||
[[Category: Activator]] | [[Category: Activator]] | ||
[[Category: Diabetes mellitus]] | [[Category: Diabetes mellitus]] | ||
[[Category: Disease mutation]] | [[Category: Disease mutation]] | ||
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[[Category: Obesity]] | [[Category: Obesity]] | ||
[[Category: Phosphorylation]] | [[Category: Phosphorylation]] | ||
[[Category: | [[Category: Transcription]] | ||
[[Category: Transcription factor]] | [[Category: Transcription factor]] | ||
[[Category: Transcription regulation]] | [[Category: Transcription regulation]] | ||
[[Category: Zinc-finger]] | [[Category: Zinc-finger]] | ||
Revision as of 01:37, 26 July 2012
X-ray crystal structure of human ppar gamma with 2-(5-(3-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)benzyl)-2-phenyl-2h-1,2,3-triazol-4-yl)acetic acid
Template:ABSTRACT PUBMED 19201606
About this Structure
3bc5 is a 1 chain structure of Peroxisome Proliferator-Activated Receptors with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Zhang H, Ryono DE, Devasthale P, Wang W, O'Malley K, Farrelly D, Gu L, Harrity T, Cap M, Chu C, Locke K, Zhang L, Lippy J, Kunselman L, Morgan N, Flynn N, Moore L, Hosagrahara V, Zhang L, Kadiyala P, Xu C, Doweyko AM, Bell A, Chang C, Muckelbauer J, Zahler R, Hariharan N, Cheng PT. Design, synthesis and structure-activity relationships of azole acids as novel, potent dual PPAR alpha/gamma agonists. Bioorg Med Chem Lett. 2009 Mar 1;19(5):1451-6. Epub 2009 Jan 15. PMID:19201606 doi:10.1016/j.bmcl.2009.01.030
