1tfc

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[[Image:1tfc.gif|left|200px]]
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{{Seed}}
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[[Image:1tfc.png|left|200px]]
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{{STRUCTURE_1tfc| PDB=1tfc | SCENE= }}
{{STRUCTURE_1tfc| PDB=1tfc | SCENE= }}
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'''CRYSTAL STRUCTURE OF THE LIGAND-BINDING DOMAIN OF THE ESTROGEN-RELATED RECEPTOR GAMMA IN COMPLEX WITH A STEROID RECEPTOR COACTIVATOR-1 PEPTIDE'''
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===CRYSTAL STRUCTURE OF THE LIGAND-BINDING DOMAIN OF THE ESTROGEN-RELATED RECEPTOR GAMMA IN COMPLEX WITH A STEROID RECEPTOR COACTIVATOR-1 PEPTIDE===
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==Overview==
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The estrogen-related receptor (ERR) gamma behaves as a constitutive activator of transcription. Although no natural ligand is known, ERRgamma is deactivated by the estrogen receptor (ER) agonist diethylstilbestrol and the selective ER modulator 4-hydroxytamoxifen but does not significantly respond to estradiol or raloxifene. Here we report the crystal structures of the ERRgamma ligand binding domain (LBD) complexed with diethylstilbestrol or 4-hydroxytamoxifen. Antagonist binding to ERRgamma results in a rotation of the side chain of Phe-435 that partially fills the cavity of the apoLBD. The new rotamer of Phe-435 displaces the "activation helix" (helix 12) from the agonist position observed in the absence of ligand. In contrast to the complexes of the ERalpha LBD with 4-hydroxytamoxifen or raloxifene, helix 12 of antagonist-bound ERRgamma does not occupy the coactivator groove but appears to be completely dissociated from the LBD body. Comparison of the ligand-bound LBDs of ERRgamma and ERalpha reveals small but significant differences in the architecture of the ligand binding pockets that result in a slightly shifted binding position of diethylstilbestrol and a small rotation of 4-hydroxytamoxifen in the cavity of ERRgamma relative to ERalpha. Our results provide detailed molecular insight into the conformational changes occurring upon binding of synthetic antagonists to the constitutive orphan receptor ERRgamma and reveal structural differences with ERs that explain why ERRgamma does not bind estradiol or raloxifene and will help to design new selective antagonists.
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(as it appears on PubMed at http://www.pubmed.gov), where 15161930 is the PubMed ID number.
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{{ABSTRACT_PUBMED_15161930}}
==About this Structure==
==About this Structure==
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==Reference==
==Reference==
Structural basis for the deactivation of the estrogen-related receptor gamma by diethylstilbestrol or 4-hydroxytamoxifen and determinants of selectivity., Greschik H, Flaig R, Renaud JP, Moras D, J Biol Chem. 2004 Aug 6;279(32):33639-46. Epub 2004 May 24. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15161930 15161930]
Structural basis for the deactivation of the estrogen-related receptor gamma by diethylstilbestrol or 4-hydroxytamoxifen and determinants of selectivity., Greschik H, Flaig R, Renaud JP, Moras D, J Biol Chem. 2004 Aug 6;279(32):33639-46. Epub 2004 May 24. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15161930 15161930]
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Structural and functional evidence for ligand-independent transcriptional activation by the estrogen-related receptor 3., Greschik H, Wurtz JM, Sanglier S, Bourguet W, van Dorsselaer A, Moras D, Renaud JP, Mol Cell. 2002 Feb;9(2):303-13. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/11864604 11864604]
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Renaud, J P.]]
[[Category: Renaud, J P.]]
[[Category: Transcriptionally active conformation in absence of ligand]]
[[Category: Transcriptionally active conformation in absence of ligand]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 09:53:09 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 12:00:41 2008''

Revision as of 09:00, 28 July 2008

Image:1tfc.png

Template:STRUCTURE 1tfc

CRYSTAL STRUCTURE OF THE LIGAND-BINDING DOMAIN OF THE ESTROGEN-RELATED RECEPTOR GAMMA IN COMPLEX WITH A STEROID RECEPTOR COACTIVATOR-1 PEPTIDE

Template:ABSTRACT PUBMED 15161930

About this Structure

1TFC is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Structural basis for the deactivation of the estrogen-related receptor gamma by diethylstilbestrol or 4-hydroxytamoxifen and determinants of selectivity., Greschik H, Flaig R, Renaud JP, Moras D, J Biol Chem. 2004 Aug 6;279(32):33639-46. Epub 2004 May 24. PMID:15161930

Structural and functional evidence for ligand-independent transcriptional activation by the estrogen-related receptor 3., Greschik H, Wurtz JM, Sanglier S, Bourguet W, van Dorsselaer A, Moras D, Renaud JP, Mol Cell. 2002 Feb;9(2):303-13. PMID:11864604

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