5hjp: Difference between revisions

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New page: '''Unreleased structure''' The entry 5hjp is ON HOLD Authors: Gopal Parthasarathy, Daniel Klein Description: Identification of LXRbeta selective agonists for the treatment of Alzheimer...
 
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'''Unreleased structure'''


The entry 5hjp is ON HOLD
==Identification of LXRbeta selective agonists for the treatment of Alzheimer's Disease==
<StructureSection load='5hjp' size='340' side='right'caption='[[5hjp]], [[Resolution|resolution]] 2.60&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[5hjp]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5HJP OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5HJP FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.6&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=668:2-CHLORO-4-{1-[(2R)-2-HYDROXY-3-METHYL-2-(TRIFLUOROMETHYL)BUTANOYL]-4,4-BIPIPERIDIN-1-YL}-N,N-DIMETHYLBENZAMIDE'>668</scene>, <scene name='pdbligand=PEG:DI(HYDROXYETHYL)ETHER'>PEG</scene></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=5hjp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5hjp OCA], [https://pdbe.org/5hjp PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5hjp RCSB], [https://www.ebi.ac.uk/pdbsum/5hjp PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5hjp ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/RXRB_HUMAN RXRB_HUMAN] Receptor for retinoic acid. Retinoic acid receptors bind as heterodimers to their target response elements in response to their ligands, all-trans or 9-cis retinoic acid, and regulate gene expression in various biological processes. The RAR/RXR heterodimers bind to the retinoic acid response elements (RARE) composed of tandem 5'-AGGTCA-3' sites known as DR1-DR5 (By similarity). Specifically binds 9-cis retinoic acid (9C-RA).


Authors: Gopal Parthasarathy, Daniel Klein
==See Also==
 
*[[Liver X receptor|Liver X receptor]]
Description: Identification of LXRbeta selective agonists for the treatment of Alzheimer's Disease
*[[Retinoid X receptor 3D structures|Retinoid X receptor 3D structures]]
[[Category: Unreleased Structures]]
__TOC__
[[Category: Gopal Parthasarathy, Daniel Klein]]
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Klein D]]
[[Category: Parthasarathy G]]