8hd3

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'''Unreleased structure'''
 
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The entry 8hd3 is ON HOLD
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==Farnesoid X Receptor Agonists_FXR fused with a HD3 peptide==
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<StructureSection load='8hd3' size='340' side='right'caption='[[8hd3]], [[Resolution|resolution]] 2.29&Aring;' scene=''>
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Authors: Lu, X., Zhang, H.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8hd3]] is a 2 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=8HD3 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8HD3 FirstGlance]. <br>
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Description: Farnesoid X Receptor Agonists_FXR fused with a HD3 peptide
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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]] 2.29&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=XAW:[(3s,5s,7s)-adamantan-1-yl][4-(2-amino-5-chlorophenyl)piperazin-1-yl]methanone'>XAW</scene></td></tr>
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[[Category: Zhang, H]]
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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=8hd3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8hd3 OCA], [https://pdbe.org/8hd3 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8hd3 RCSB], [https://www.ebi.ac.uk/pdbsum/8hd3 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8hd3 ProSAT]</span></td></tr>
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[[Category: Lu, X]]
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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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== References ==
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<references/>
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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: Lu X]]
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[[Category: Zhang H]]

Current revision

Farnesoid X Receptor Agonists_FXR fused with a HD3 peptide

PDB ID 8hd3

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