3sp6: Difference between revisions

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-[[Image:3sp6.png|left|200px]]
-{{STRUCTURE_3sp6|  PDB=3sp6  |  SCENE=  }}
+==Structural basis for iloprost as a dual PPARalpha/delta agonist==
+<StructureSection load='3sp6' size='340' side='right'caption='[[3sp6]], [[Resolution|resolution]] 2.21&Aring;' scene=''>
-===Structural basis for iloprost as a dual PPARalpha/delta agonist===
+== Structural highlights ==
+<table><tr><td colspan='2'>[[3sp6]] 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=3SP6 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3SP6 FirstGlance]. <br>
-{{ABSTRACT_PUBMED_21775429}}
+</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.21&#8491;</td></tr>
+<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=IL2:(5E)-5-[(3AS,4R,5R,6AS)-5-HYDROXY-4-[(1E,3S,4R)-3-HYDROXY-4-METHYLOCT-1-EN-6-YN-1-YL]HEXAHYDROPENTALEN-2(1H)-YLIDENE]PENTANOIC+ACID'>IL2</scene></td></tr>
-==About this Structure==
+<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=3sp6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3sp6 OCA], [https://pdbe.org/3sp6 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3sp6 RCSB], [https://www.ebi.ac.uk/pdbsum/3sp6 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3sp6 ProSAT]</span></td></tr>
-[[3sp6]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3SP6 OCA].
+</table>
+== Function ==
+[https://www.uniprot.org/uniprot/PPARA_HUMAN PPARA_HUMAN] Ligand-activated transcription factor. Key regulator of lipid metabolism. Activated by the endogenous ligand 1-palmitoyl-2-oleoyl-sn-glycerol-3-phosphocholine (16:0/18:1-GPC). Activated by oleylethanolamide, a naturally occurring lipid that regulates satiety (By similarity). Receptor for peroxisome proliferators such as hypolipidemic drugs and fatty acids. Regulates the peroxisomal beta-oxidation pathway of fatty acids. Functions as transcription activator for the ACOX1 and P450 genes. Transactivation activity requires heterodimerization with RXRA and is antagonized by NR2C2.<ref>PMID:7684926</ref> <ref>PMID:7629123</ref> <ref>PMID:9556573</ref> <ref>PMID:10195690</ref>
 ==See Also==
-*[[Peroxisome Proliferator-Activated Receptors|Peroxisome Proliferator-Activated Receptors]]
+*[[Peroxisome proliferator-activated receptor 3D structures|Peroxisome proliferator-activated receptor 3D structures]]
+== References ==
-==Reference==
+<references/>
-<ref group="xtra">PMID:021775429</ref><references group="xtra"/>
+__TOC__
+</StructureSection>
 [[Category: Homo sapiens]]
-[[Category: Li, Y.]]
+[[Category: Large Structures]]
-[[Category: Rong, H.]]
+[[Category: Li Y]]
-[[Category: Gene transcription]]
+[[Category: Rong H]]
-[[Category: Ligand binding]]
-[[Category: Nuclear receptor fold]]
-[[Category: Ppar lbd]]
-[[Category: Transcription]]