8etm

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m (Protected "8etm" [edit=sysop:move=sysop])
Current revision (06:38, 19 June 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 8etm is ON HOLD
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==Human triacylglycerol synthesizing enzyme DGAT1 in complex with DGAT1IN1 inhibitor==
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<StructureSection load='8etm' size='340' side='right'caption='[[8etm]], [[Resolution|resolution]] 3.20&Aring;' scene=''>
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Authors:
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8etm]] 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=8ETM OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8ETM FirstGlance]. <br>
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Description:
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.2&#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=WTT:[(1S,4r)-4-{4-[(4S)-2-({[4-(trifluoromethoxy)phenyl]methyl}carbamoyl)imidazo[1,2-a]pyridin-6-yl]phenyl}cyclohexyl]acetic+acid'>WTT</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=8etm FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8etm OCA], [https://pdbe.org/8etm PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8etm RCSB], [https://www.ebi.ac.uk/pdbsum/8etm PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8etm ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/DGAT1_HUMAN DGAT1_HUMAN] Congenital chronic diarrhea with protein-losing enteropathy. The disease is caused by mutations affecting the gene represented in this entry.
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== Function ==
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[https://www.uniprot.org/uniprot/DGAT1_HUMAN DGAT1_HUMAN] Catalyzes the terminal and only committed step in triacylglycerol synthesis by using diacylglycerol and fatty acyl CoA as substrates. In contrast to DGAT2 it is not essential for survival. May be involved in VLDL (very low density lipoprotein) assembly. In liver, plays a role in esterifying exogenous fatty acids to glycerol. Functions as the major acyl-CoA retinol acyltransferase (ARAT) in the skin, where it acts to maintain retinoid homeostasis and prevent retinoid toxicity leading to skin and hair disorders.<ref>PMID:16214399</ref> <ref>PMID:9756920</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: Farese R]]
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[[Category: Kun W]]
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[[Category: Liao M]]
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[[Category: Sui X]]
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[[Category: Walther T]]

Current revision

Human triacylglycerol synthesizing enzyme DGAT1 in complex with DGAT1IN1 inhibitor

PDB ID 8etm

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OCA

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