1t73: Difference between revisions

Revision as of 08:57, 28 July 2008

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File:1t73.png

Template:STRUCTURE 1t73

Crystal structure of the androgen receptor ligand binding domain in complex with a FxxFF motifCrystal structure of the androgen receptor ligand binding domain in complex with a FxxFF motif

Template:ABSTRACT PUBMED 15328534

About this StructureAbout this Structure

1T73 is a Single protein structure of sequence from Pan troglodytes. Full crystallographic information is available from OCA.

ReferenceReference

Recognition and accommodation at the androgen receptor coactivator binding interface., Hur E, Pfaff SJ, Payne ES, Gron H, Buehrer BM, Fletterick RJ, PLoS Biol. 2004 Sep;2(9):E274. Epub 2004 Aug 24. PMID:15328534

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Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA

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-[[Image:1t73.gif|left|200px]]
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 {{STRUCTURE_1t73|  PDB=1t73  |  SCENE=  }}
-'''Crystal structure of the androgen receptor ligand binding domain in complex with a FxxFF motif'''
+===Crystal structure of the androgen receptor ligand binding domain in complex with a FxxFF motif===
-==Overview==
+<!--
-Prostate cancer is a leading killer of men in the industrialized world. Underlying this disease is the aberrant action of the androgen receptor (AR). AR is distinguished from other nuclear receptors in that after hormone binding, it preferentially responds to a specialized set of coactivators bearing aromatic-rich motifs, while responding poorly to coactivators bearing the leucine-rich "NR box" motifs favored by other nuclear receptors. Under normal conditions, interactions with these AR-specific coactivators through aromatic-rich motifs underlie targeted gene transcription. However, during prostate cancer, abnormal association with such coactivators, as well as with coactivators containing canonical leucine-rich motifs, promotes disease progression. To understand the paradox of this unusual selectivity, we have derived a complete set of peptide motifs that interact with AR using phage display. Binding affinities were measured for a selected set of these peptides and their interactions with AR determined by X-ray crystallography. Structures of AR in complex with FxxLF, LxxLL, FxxLW, WxxLF, WxxVW, FxxFF, and FxxYF motifs reveal a changing surface of the AR coactivator binding interface that permits accommodation of both AR-specific aromatic-rich motifs and canonical leucine-rich motifs. Induced fit provides perfect mating of the motifs representing the known family of AR coactivators and suggests a framework for the design of AR coactivator antagonists.
+The line below this paragraph, {{ABSTRACT_PUBMED_15328534}}, adds the Publication Abstract to the page
+(as it appears on PubMed at http://www.pubmed.gov), where 15328534 is the PubMed ID number.
+-->
+{{ABSTRACT_PUBMED_15328534}}
 ==About this Structure==
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 [[Category: Testosterone]]
 [[Category: Transcription factor]]
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