8yt6: Difference between revisions
From Proteopedia
Jump to navigationJump to search
No edit summary |
No edit summary |
||
| Line 1: | Line 1: | ||
==Human PPAR alpha ligand binding domain in complex with a 1H-pyrazolo[3,4-b]pyridine-derived compound== | |||
<StructureSection load='8yt6' size='340' side='right'caption='[[8yt6]], [[Resolution|resolution]] 1.85Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[8yt6]] 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=8YT6 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8YT6 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]] 1.85Å</td></tr> | |||
[[Category: | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=A1LZX:6-(2-ethoxyethyl)-1-(4-fluorophenyl)-3-pentan-3-yl-pyrazolo[3,4-b]pyridine-4-carboxylic+acid'>A1LZX</scene></td></tr> | ||
[[Category: | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8yt6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8yt6 OCA], [https://pdbe.org/8yt6 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8yt6 RCSB], [https://www.ebi.ac.uk/pdbsum/8yt6 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8yt6 ProSAT]</span></td></tr> | ||
[[Category: | </table> | ||
[[Category: | == Function == | ||
[[Category: | [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> | ||
[[Category: | == References == | ||
[[Category: | <references/> | ||
[[Category: | __TOC__ | ||
[[Category: | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: | [[Category: Large Structures]] | ||
[[Category: | [[Category: Akai S]] | ||
[[Category: | [[Category: Doi T]] | ||
[[Category: | [[Category: Fukuda S]] | ||
[[Category: | [[Category: Ishimoto K]] | ||
[[Category: | [[Category: Kawahara K]] | ||
[[Category: | [[Category: Lin B]] | ||
[[Category: Meguro K]] | |||
[[Category: Miyachi H]] | |||
[[Category: Morie T]] | |||
[[Category: Nakagawa S]] | |||
[[Category: Nunomura K]] | |||
[[Category: Oki H]] | |||
[[Category: Tachibana K]] | |||
[[Category: Tsujikawa K]] | |||
[[Category: Yoshida T]] | |||
[[Category: Yuzuriha T]] | |||