4xao: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
No edit summary
OCA (talk | contribs)
No edit summary
Line 1: Line 1:
'''Unreleased structure'''
==Crystal structure of the hPXR-LBD obtained in presence of the pesticide trans-nonachlor==
 
<StructureSection load='4xao' size='340' side='right' caption='[[4xao]], [[Resolution|resolution]] 2.58&Aring;' scene=''>
The entry 4xao is ON HOLD  until Paper Publication
== Structural highlights ==
 
<table><tr><td colspan='2'>[[4xao]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4XAO OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4XAO FirstGlance]. <br>
Authors: DELFOSSE, V., HUET, T., BOURGUET, W.
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=IPA:ISOPROPYL+ALCOHOL'>IPA</scene>, <scene name='pdbligand=MPD:(4S)-2-METHYL-2,4-PENTANEDIOL'>MPD</scene></td></tr>
 
<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4x1f|4x1f]], [[4x1g|4x1g]]</td></tr>
Description: Crystal structure of the hPXR-LBD obtained in presence of the pesticide trans-nonachlor
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4xao FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4xao OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4xao RCSB], [http://www.ebi.ac.uk/pdbsum/4xao PDBsum]</span></td></tr>
[[Category: Unreleased Structures]]
</table>
[[Category: Delfosse, V]]
== Function ==
[[Category: Bourguet, W]]
[[http://www.uniprot.org/uniprot/NR1I2_HUMAN NR1I2_HUMAN]] Nuclear receptor that binds and is activated by variety of endogenous and xenobiotic compounds. Transcription factor that activates the transcription of multiple genes involved in the metabolism and secretion of potentially harmful xenobiotics, drugs and endogenous compounds. Activated by the antibiotic rifampicin and various plant metabolites, such as hyperforin, guggulipid, colupulone, and isoflavones. Response to specific ligands is species-specific. Activated by naturally occurring steroids, such as pregnenolone and progesterone. Binds to a response element in the promoters of the CYP3A4 and ABCB1/MDR1 genes.<ref>PMID:9727070</ref> <ref>PMID:11668216</ref> <ref>PMID:11297522</ref> <ref>PMID:19297428</ref> <ref>PMID:12578355</ref> <ref>PMID:18768384</ref> 
[[Category: Huet, T]]
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: BOURGUET, W]]
[[Category: DELFOSSE, V]]
[[Category: HUET, T]]
[[Category: Gene regulation]]
[[Category: Hormone receptor]]
[[Category: Pesticide]]

Revision as of 11:20, 9 September 2015

Crystal structure of the hPXR-LBD obtained in presence of the pesticide trans-nonachlor

4xao, resolution 2.58Å

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA