2q6j

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[[Image:2q6j.gif|left|200px]]
[[Image:2q6j.gif|left|200px]]
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{{Structure
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|LIGAND= <scene name='pdbligand=A48:4-[(DIMESITYLBORYL)(2,2,2-TRIFLUOROETHYL)AMINO]PHENOL'>A48</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]), Ncoa2 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=10090 Mus musculus])
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{{STRUCTURE_2q6j| PDB=2q6j | SCENE= }}
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2q6j FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2q6j OCA], [http://www.ebi.ac.uk/pdbsum/2q6j PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2q6j RCSB]</span>
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'''Crystal Structure of Estrogen Receptor alpha Complexed to a B-N Substituted Ligand'''
'''Crystal Structure of Estrogen Receptor alpha Complexed to a B-N Substituted Ligand'''
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[[Category: Stossi, F.]]
[[Category: Stossi, F.]]
[[Category: Zhou, H.]]
[[Category: Zhou, H.]]
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[[Category: protein-ligand complex]]
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[[Category: Protein-ligand complex]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 14:26:39 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 04:45:27 2008''
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Revision as of 11:26, 4 May 2008

Template:STRUCTURE 2q6j

Crystal Structure of Estrogen Receptor alpha Complexed to a B-N Substituted Ligand


Overview

To increase the chemical diversity of bioactive molecules by incorporating unusual elements, we have examined the replacement of a C=C double bond with the isoelectronic, isostructural B-N bond in the context of nonsteroidal estrogen receptor (ER) ligands. While the B-N bond was hydrolytically labile in the unhindered cyclofenil system, the more hindered anilino dimesitylboranes, analogs of triarylethylene estrogens, were easily prepared, hydrolytically stable, and demonstrated substantial affinity for ERs. X-ray analysis of one ERalpha-ligand complex revealed steric clashes with the para methyl groups distorting the receptor; removal of these groups resulted in an increase in affinity, potency, and transcriptional efficacy. These studies define the structural determinants of stability and cellular bioactivity of a B-N for C=C substitution in nonsteroidal estrogens and provide a framework for further exploration of "elemental isomerism" for diversification of drug-like molecules.

About this Structure

2Q6J is a Protein complex structure of sequences from Homo sapiens and Mus musculus. Full crystallographic information is available from OCA.

Reference

Elemental isomerism: a boron-nitrogen surrogate for a carbon-carbon double bond increases the chemical diversity of estrogen receptor ligands., Zhou HB, Nettles KW, Bruning JB, Kim Y, Joachimiak A, Sharma S, Carlson KE, Stossi F, Katzenellenbogen BS, Greene GL, Katzenellenbogen JA, Chem Biol. 2007 Jun;14(6):659-69. PMID:17584613 Page seeded by OCA on Sun May 4 14:26:39 2008

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