2qtu

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(New page: 200px<br /> <applet load="2qtu" size="450" color="white" frame="true" align="right" spinBox="true" caption="2qtu, resolution 2.53&Aring;" /> '''Estrogen receptor b...)
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[[Image:2qtu.gif|left|200px]]<br />
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[[Image:2qtu.gif|left|200px]]<br /><applet load="2qtu" size="350" color="white" frame="true" align="right" spinBox="true"
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<applet load="2qtu" size="450" color="white" frame="true" align="right" spinBox="true"
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caption="2qtu, resolution 2.53&Aring;" />
caption="2qtu, resolution 2.53&Aring;" />
'''Estrogen receptor beta ligand-binding domain complexed to a benzopyran ligand'''<br />
'''Estrogen receptor beta ligand-binding domain complexed to a benzopyran ligand'''<br />
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==About this Structure==
==About this Structure==
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2QTU 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 3AS as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2QTU OCA].
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2QTU 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=3AS:'>3AS</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2QTU OCA].
==Reference==
==Reference==
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[[Category: zinc-finger]]
[[Category: zinc-finger]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 23:35:07 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 23 12:37:52 2008''

Revision as of 10:37, 23 January 2008


2qtu, resolution 2.53Å

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Estrogen receptor beta ligand-binding domain complexed to a benzopyran ligand

Overview

Benzopyrans are selective estrogen receptor (ER) beta agonists (SERBAs), which bind the ER subtypes alpha and beta in opposite orientations. Here, we describe the synthesis of a late stage intermediate that allowed us to, combine A-ring and C-ring modifications and carry out simultaneous SAR, studies at both positions. Modification of both positions proved additive, maintaining affinity and improving ERbeta selectivity up to 83-fold. An, X-ray cocrystal structure confirms the previously observed binding mode in, ERbeta.

About this Structure

2QTU is a Single protein structure of sequence from Homo sapiens with as ligand. Full crystallographic information is available from OCA.

Reference

Benzopyrans as selective estrogen receptor beta agonists (SERBAs). Part 5: Combined A- and C-ring structure-activity relationship studies., Richardson TI, Dodge JA, Wang Y, Durbin JD, Krishnan V, Norman BH, Bioorg Med Chem Lett. 2007 Oct 15;17(20):5563-6. Epub 2007 Aug 11. PMID:17804226

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