2p7a

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(New page: 200px<br /><applet load="2p7a" size="350" color="white" frame="true" align="right" spinBox="true" caption="2p7a, resolution 2.300&Aring;" /> '''Crystal Structure o...)
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[[Image:2p7a.jpg|left|200px]]<br /><applet load="2p7a" size="350" color="white" frame="true" align="right" spinBox="true"
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[[Image:2p7a.jpg|left|200px]]
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caption="2p7a, resolution 2.300&Aring;" />
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'''Crystal Structure of Estrogen Related Receptor g in complex with 3-methyl phenol'''<br />
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{{Structure
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|PDB= 2p7a |SIZE=350|CAPTION= <scene name='initialview01'>2p7a</scene>, resolution 2.300&Aring;
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|SITE= <scene name='pdbsite=AC1:43m+Binding+Site+For+Residue+A+1'>AC1</scene>
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|LIGAND= <scene name='pdbligand=43M:'>43M</scene>
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|ACTIVITY=
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|GENE= ESRRG, ERR3, ERRG2, KIAA0832, NR3B3 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
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}}
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'''Crystal Structure of Estrogen Related Receptor g in complex with 3-methyl phenol'''
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==Overview==
==Overview==
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==About this Structure==
==About this Structure==
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2P7A is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=43M:'>43M</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Known structural/functional Site: <scene name='pdbsite=AC1:43m+Binding+Site+For+Residue+A+1'>AC1</scene>. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2P7A OCA].
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2P7A is a [[Single protein]] structure of 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=2P7A OCA].
==Reference==
==Reference==
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Structural determination of estrogen-related receptor gamma in the presence of phenol derivative compounds., Abad MC, Askari H, O'Neill J, Klinger AL, Milligan C, Lewandowski F, Springer B, Spurlino J, Rentzeperis D, J Steroid Biochem Mol Biol. 2008 Jan;108(1-2):44-54. Epub 2007 Sep 14. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=17964775 17964775]
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Structural determination of estrogen-related receptor gamma in the presence of phenol derivative compounds., Abad MC, Askari H, O'Neill J, Klinger AL, Milligan C, Lewandowski F, Springer B, Spurlino J, Rentzeperis D, J Steroid Biochem Mol Biol. 2008 Jan;108(1-2):44-54. Epub 2007 Sep 14. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/17964775 17964775]
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: three layered alpha helical sandwich]]
[[Category: three layered alpha helical sandwich]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Feb 27 07:58:39 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 18:09:40 2008''

Revision as of 16:09, 20 March 2008


PDB ID 2p7a

Drag the structure with the mouse to rotate
, resolution 2.300Å
Sites:
Ligands:
Gene: ESRRG, ERR3, ERRG2, KIAA0832, NR3B3 (Homo sapiens)
Coordinates: save as pdb, mmCIF, xml



Crystal Structure of Estrogen Related Receptor g in complex with 3-methyl phenol


Overview

We screened the ligand-binding domain of estrogen-related receptor (ERR) gamma in ThermoFluor((R)), in an effort to develop chemical tools and decipher the biology of this orphan nuclear receptor. Several ligands were found to stabilize thermodynamically the protein. Amongst the ligands were bisphenol A (BPA) and 4-chloro-3-methyl phenol (ClCH(3)Ph). These ligands were further characterized and found to be competitive for 4-hydroxytamoxifen (4OHT) binding, a known reported antagonist ligand for ERRgamma, but functionally they did not enhance or disrupt affinity of the receptor for co-activator peptides. The preservation of the constitutive active conformation of the receptor in the presence of these two ligands was confirmed upon the determination of the co-crystal structures. The structures of BPA and ClCH(3)Ph were determined to a resolution of 2.1 and 2.3A, respectively, and the antagonist 4OHT was refined to 2.5A resolution. In the presence of BPA and ClCH(3)Ph the receptor maintained the transcriptional active conformation as reported previously for the apo-protein in the presence of a co-activator peptide fragment. In addition the ERRgamma-BPA structure identifies an interaction between the phenolic-OH and the side chain of N346. The preservation of the constitutive active conformation of the receptor in the presence of the small phenol compounds suggest that the biological activity of the receptor might be regulated by a natural occurring ligand.

About this Structure

2P7A is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Structural determination of estrogen-related receptor gamma in the presence of phenol derivative compounds., Abad MC, Askari H, O'Neill J, Klinger AL, Milligan C, Lewandowski F, Springer B, Spurlino J, Rentzeperis D, J Steroid Biochem Mol Biol. 2008 Jan;108(1-2):44-54. Epub 2007 Sep 14. PMID:17964775

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