3gbk
From Proteopedia
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[[Image:3gbk.png|left|200px]] | [[Image:3gbk.png|left|200px]] | ||
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{{STRUCTURE_3gbk| PDB=3gbk | SCENE= }} | {{STRUCTURE_3gbk| PDB=3gbk | SCENE= }} | ||
===Crystal Structure of Human PPAR-gamma Ligand Binding Domain Complexed with a Potent and Selective Agonist=== | ===Crystal Structure of Human PPAR-gamma Ligand Binding Domain Complexed with a Potent and Selective Agonist=== | ||
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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:019301897</ref><references group="xtra"/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Hsieh, H P.]] | [[Category: Hsieh, H P.]] | ||
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[[Category: Wu, S Y.]] | [[Category: Wu, S Y.]] | ||
[[Category: Activator]] | [[Category: Activator]] | ||
| - | [[Category: Alternative splicing]] | ||
[[Category: Diabetes mellitus]] | [[Category: Diabetes mellitus]] | ||
[[Category: Disease mutation]] | [[Category: Disease mutation]] | ||
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[[Category: Obesity]] | [[Category: Obesity]] | ||
[[Category: Phosphoprotein]] | [[Category: Phosphoprotein]] | ||
| - | [[Category: Polymorphism]] | ||
[[Category: Ppar aganist]] | [[Category: Ppar aganist]] | ||
[[Category: Receptor]] | [[Category: Receptor]] | ||
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[[Category: Type ii diabetes]] | [[Category: Type ii diabetes]] | ||
[[Category: X-ray co-crystal analysis]] | [[Category: X-ray co-crystal analysis]] | ||
| - | [[Category: Zinc]] | ||
[[Category: Zinc-finger]] | [[Category: Zinc-finger]] | ||
Revision as of 04:30, 26 July 2012
Contents |
Crystal Structure of Human PPAR-gamma Ligand Binding Domain Complexed with a Potent and Selective Agonist
Template:ABSTRACT PUBMED 19301897
About this Structure
3gbk is a 2 chain structure of Peroxisome Proliferator-Activated Receptors with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Lin CH, Peng YH, Coumar MS, Chittimalla SK, Liao CC, Lyn PC, Huang CC, Lien TW, Lin WH, Hsu JT, Cheng JH, Chen X, Wu JS, Chao YS, Lee HJ, Juo CG, Wu SY, Hsieh HP. Design and structural analysis of novel pharmacophores for potent and selective peroxisome proliferator-activated receptor gamma agonists. J Med Chem. 2009 Apr 23;52(8):2618-22. PMID:19301897 doi:10.1021/jm801594x
Categories: Homo sapiens | Hsieh, H P. | Lin, C H. | Peng, Y H. | Wu, S Y. | Activator | Diabetes mellitus | Disease mutation | Dna-binding | Ligand binding protein | Metal-binding | Nucleus | Obesity | Phosphoprotein | Ppar aganist | Receptor | Selective | Structure-based drug design | Transcription | Transcription regulation | Type ii diabetes | X-ray co-crystal analysis | Zinc-finger
