6a5y

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'''Unreleased structure'''
 
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The entry 6a5y is ON HOLD until Paper Publication
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==Crystal structure of human FXR/RXR-LBD heterodimer bound to HNC143 and 9cRA and SRC1==
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<StructureSection load='6a5y' size='340' side='right'caption='[[6a5y]], [[Resolution|resolution]] 2.10&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6a5y]] 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=6A5Y OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6A5Y FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.1&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=9CR:(9CIS)-RETINOIC+ACID'>9CR</scene>, <scene name='pdbligand=9R0:2-[2-[[3-[2,6-bis(chloranyl)phenyl]-5-cyclopropyl-1,2-oxazol-4-yl]methoxy]-6-azaspiro[3.4]octan-6-yl]-1,3-benzothiazole-6-carboxylic+acid'>9R0</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6a5y FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6a5y OCA], [https://pdbe.org/6a5y PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6a5y RCSB], [https://www.ebi.ac.uk/pdbsum/6a5y PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6a5y ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/NR1H4_HUMAN NR1H4_HUMAN] Ligand-activated transcription factor. Receptor for bile acids such as chenodeoxycholic acid, lithocholic acid and deoxycholic acid. Represses the transcription of the cholesterol 7-alpha-hydroxylase gene (CYP7A1) through the induction of NR0B2 or FGF19 expression, via two distinct mechanisms. Activates the intestinal bile acid-binding protein (IBABP). Activates the transcription of bile salt export pump ABCB11 by directly recruiting histone methyltransferase CARM1 to this locus.<ref>PMID:10334992</ref> <ref>PMID:10334993</ref> <ref>PMID:12815072</ref> <ref>PMID:15471871</ref> <ref>PMID:12718892</ref> <ref>PMID:18621523</ref> <ref>PMID:19410460</ref> <ref>PMID:19586769</ref>
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Authors: Wang, N., Liu, J.
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==See Also==
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*[[Bile acid receptor 3D structures|Bile acid receptor 3D structures]]
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Description: Crystal structure of human FXR/RXR-LBD heterodimer bound to HNC143 and 9cRA and SRC1
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*[[Retinoid X receptor 3D structures|Retinoid X receptor 3D structures]]
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[[Category: Unreleased Structures]]
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== References ==
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[[Category: Liu, J]]
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<references/>
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[[Category: Wang, N]]
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__TOC__
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Liu J]]
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[[Category: Wang N]]

Current revision

Crystal structure of human FXR/RXR-LBD heterodimer bound to HNC143 and 9cRA and SRC1

PDB ID 6a5y

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