3l1b
From Proteopedia
(Difference between revisions)
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+ | [[Image:3l1b.jpg|left|200px]] | ||
- | The | + | <!-- |
+ | The line below this paragraph, containing "STRUCTURE_3l1b", creates the "Structure Box" on the page. | ||
+ | You may change the PDB parameter (which sets the PDB file loaded into the applet) | ||
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+ | {{STRUCTURE_3l1b| PDB=3l1b | SCENE= }} | ||
- | + | ===Complex Structure of FXR Ligand-binding domain with a tetrahydroazepinoindole compound=== | |
- | Description: Complex Structure of FXR Ligand-binding domain with a tetrahydroazepinoindole compound | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | <!-- |
+ | The line below this paragraph, {{ABSTRACT_PUBMED_20095622}}, adds the Publication Abstract to the page | ||
+ | (as it appears on PubMed at http://www.pubmed.gov), where 20095622 is the PubMed ID number. | ||
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+ | {{ABSTRACT_PUBMED_20095622}} | ||
+ | |||
+ | ==About this Structure== | ||
+ | 3L1B is a 1 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=3L1B OCA]. | ||
+ | |||
+ | ==Reference== | ||
+ | <ref group="xtra">PMID:20095622</ref><references group="xtra"/> | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Lundquist, J T.]] | ||
+ | [[Category: Xu, W.]] | ||
+ | [[Category: Fxr agonist]] | ||
+ | [[Category: Fxr ligand-binding domain]] | ||
+ | [[Category: Nuclear receptor]] | ||
+ | [[Category: Nucleus]] | ||
+ | [[Category: Receptor]] | ||
+ | [[Category: Transcription]] | ||
+ | [[Category: Transcription regulation]] | ||
+ | |||
+ | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Mar 3 16:23:11 2010'' |
Revision as of 14:23, 3 March 2010
Complex Structure of FXR Ligand-binding domain with a tetrahydroazepinoindole compound
Template:ABSTRACT PUBMED 20095622
About this Structure
3L1B is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Lundquist JT, Harnish DC, Kim CY, Mehlmann JF, Unwalla RJ, Phipps KM, Crawley ML, Commons T, Green DM, Xu W, Hum WT, Eta JE, Feingold I, Patel V, Evans MJ, Lai K, Borges-Marcucci L, Mahaney PE, Wrobel JE. Improvement of physiochemical properties of the tetrahydroazepinoindole series of farnesoid X receptor (FXR) agonists: beneficial modulation of lipids in primates. J Med Chem. 2010 Feb 25;53(4):1774-87. PMID:20095622 doi:10.1021/jm901650u
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