2p15

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[[Image:2p15.gif|left|200px]]
[[Image:2p15.gif|left|200px]]
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{{Structure
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|PDB= 2p15 |SIZE=350|CAPTION= <scene name='initialview01'>2p15</scene>, resolution 1.940&Aring;
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The line below this paragraph, containing "STRUCTURE_2p15", creates the "Structure Box" on the page.
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|SITE=
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|LIGAND= <scene name='pdbligand=EZT:(17BETA)-17-{(E)-2-[2-(TRIFLUOROMETHYL)PHENYL]VINYL}ESTRA-1(10),2,4-TRIENE-3,17-DIOL'>EZT</scene>
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|GENE= ESR1, ESR, NR3A1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
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|DOMAIN=
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{{STRUCTURE_2p15| PDB=2p15 | SCENE= }}
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|RELATEDENTRY=
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2p15 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2p15 OCA], [http://www.ebi.ac.uk/pdbsum/2p15 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2p15 RCSB]</span>
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'''Crystal structure of the ER alpha ligand binding domain with the agonist ortho-trifluoromethylphenylvinyl estradiol'''
'''Crystal structure of the ER alpha ligand binding domain with the agonist ortho-trifluoromethylphenylvinyl estradiol'''
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[[Category: Kim, Y.]]
[[Category: Kim, Y.]]
[[Category: Nettles, K W.]]
[[Category: Nettles, K W.]]
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[[Category: helix 12]]
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[[Category: Helix 12]]
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[[Category: ligand binding domain]]
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[[Category: Ligand binding domain]]
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[[Category: nulear receptor]]
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[[Category: Nulear receptor]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 12:07:01 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 04:26:42 2008''
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Revision as of 09:07, 4 May 2008

Template:STRUCTURE 2p15

Crystal structure of the ER alpha ligand binding domain with the agonist ortho-trifluoromethylphenylvinyl estradiol


Overview

The steroid hormone receptors are characterized by binding to relatively rigid, inflexible endogenous steroid ligands. Other members of the nuclear receptor superfamily bind to conformationally flexible lipids and show a corresponding degree of elasticity in the ligand-binding pocket. Here, we report the X-ray crystal structure of the oestrogen receptor alpha (ERalpha) bound to an oestradiol derivative with a prosthetic group, ortho- trifluoromethlyphenylvinyl, which binds in a novel extended pocket in the ligand-binding domain. Unlike ER antagonists with bulky side groups, this derivative is enclosed in the ligand-binding pocket, and acts as a potent agonist. This work shows that steroid hormone receptors can interact with a wider array of pharmacophores than previously thought through structural plasticity in the ligand-binding pocket.

About this Structure

2P15 is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Structural plasticity in the oestrogen receptor ligand-binding domain., Nettles KW, Bruning JB, Gil G, O'Neill EE, Nowak J, Guo Y, Kim Y, DeSombre ER, Dilis R, Hanson RN, Joachimiak A, Greene GL, EMBO Rep. 2007 Jun;8(6):563-8. Epub 2007 Apr 27. PMID:17468738 Page seeded by OCA on Sun May 4 12:07:01 2008

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