1nrl: Difference between revisions

From Proteopedia
Jump to navigationJump to search
← Older editNewer edit →
OCA (talk | contribs)
Bots, Bureaucrats, journal, Administrators
3,332,843 edits
No edit summary
OCA (talk | contribs)
Bots, Bureaucrats, journal, Administrators
3,332,843 edits
No edit summary
Line 1: Line 1:
[[Image:1nrl.gif|left|200px]]
{{Seed}}
[[Image:1nrl.png|left|200px]]


<!--
<!--
Line 9: Line 10:
{{STRUCTURE_1nrl|  PDB=1nrl  |  SCENE=  }}  
{{STRUCTURE_1nrl|  PDB=1nrl  |  SCENE=  }}  


'''Crystal Structure of the human PXR-LBD in complex with an SRC-1 coactivator peptide and SR12813'''
===Crystal Structure of the human PXR-LBD in complex with an SRC-1 coactivator peptide and SR12813===




==Overview==
<!--
The pregnane X receptor (PXR) detects the presence of a wide variety of endogenous and xenobiotic compounds, and is a master regulator of the expression of genes central to drug metabolism and excretion. We present the 2.0A crystal structure of the human PXR ligand-binding domain (LBD) in complex with the cholesterol-lowering compound SR12813 and a 25 amino acid residue fragment of the human steroid receptor coactivator-1 (SRC-1) containing one LXXLL motif. PXR crystallizes as a homodimer in the asymmetric unit in this structure and possesses a novel alpha2 helix adjacent to its ligand-binding cavity. The SRC-1 peptide forms two distinct helices and binds adjacent to the ligand-dependent transactivation AF-2 helix on the surface of PXR. In contrast with previous PXR structures, in which SR12813 bound in multiple orientations, the small SR12813 agonist in this structure binds in a single, unique orientation within the receptor's ligand-binding pocket and contacts the AF-2 helix. Thermal denaturation studies reveal that the SR12813 ligand and SRC-1 coactivator peptide each stabilize the LBD of PXR, and that together they exert an additive effect on the stability of the receptor. These results indicate that the binding of coactivator to the surface of PXR limits the ability of this promiscuous receptor to "breathe" and helps to trap a single, active conformation of SR12813. They further reveal that specificity is required for PXR activation.
The line below this paragraph, {{ABSTRACT_PUBMED_12909012}}, adds the Publication Abstract to the page
(as it appears on PubMed at http://www.pubmed.gov), where 12909012 is the PubMed ID number.
-->
{{ABSTRACT_PUBMED_12909012}}


==About this Structure==
==About this Structure==
Line 32: Line 36:
[[Category: Src-1]]
[[Category: Src-1]]
[[Category: Xenobiotic]]
[[Category: Xenobiotic]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May  3 02:53:53 2008''
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 21:49:37 2008''

Revision as of 18:49, 28 July 2008

File:1nrl.png

Template:STRUCTURE 1nrl

Crystal Structure of the human PXR-LBD in complex with an SRC-1 coactivator peptide and SR12813

Template:ABSTRACT PUBMED 12909012

About this Structure

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

Reference

Coactivator binding promotes the specific interaction between ligand and the pregnane X receptor., Watkins RE, Davis-Searles PR, Lambert MH, Redinbo MR, J Mol Biol. 2003 Aug 22;331(4):815-28. PMID:12909012

Page seeded by OCA on Mon Jul 28 21:49:37 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "https://proteopedia.org/index.php?title=1nrl&oldid=716874"