4ae8
From Proteopedia
(Difference between revisions)
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== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[4ae8]] is a 4 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=4AE8 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4AE8 FirstGlance]. <br> | <table><tr><td colspan='2'>[[4ae8]] is a 4 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=4AE8 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4AE8 FirstGlance]. <br> | ||
| - | </td></tr><tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4ae8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4ae8 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4ae8 RCSB], [http://www.ebi.ac.uk/pdbsum/4ae8 PDBsum]</span></td></tr> | + | </td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4ae8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4ae8 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4ae8 RCSB], [http://www.ebi.ac.uk/pdbsum/4ae8 PDBsum]</span></td></tr> |
| - | <table> | + | </table> |
| + | == Function == | ||
| + | [[http://www.uniprot.org/uniprot/THEM4_HUMAN THEM4_HUMAN]] Has acyl-CoA thioesterase activity towards medium and long-chain (C14 to C18) fatty acyl-CoA substrates, and probably plays an role in mitochondrial fatty acid metabolism. Plays a role in the apoptotic process, possibly via its regulation of AKT1 activity. According to PubMed:11598301, inhibits AKT1 phosphorylation and activity. According to PubMed:17615157, enhances AKT1 activity by favoring its phosphorylation and translocation to plasma membrane.<ref>PMID:11598301</ref> <ref>PMID:17615157</ref> <ref>PMID:19453107</ref> <ref>PMID:19168129</ref> <ref>PMID:19421406</ref> <ref>PMID:22871024</ref> | ||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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</StructureSection> | </StructureSection> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
| - | [[Category: Bleck, C K.E | + | [[Category: Bleck, C K.E]] |
| - | [[Category: Cron, P | + | [[Category: Cron, P]] |
| - | [[Category: Dummler, B | + | [[Category: Dummler, B]] |
| - | [[Category: Esposti, M Degli | + | [[Category: Esposti, M Degli]] |
| - | [[Category: Genoud, C | + | [[Category: Genoud, C]] |
| - | [[Category: Gut, H | + | [[Category: Gut, H]] |
| - | [[Category: Hemmings, B A | + | [[Category: Hemmings, B A]] |
| - | [[Category: Hynx, D | + | [[Category: Hynx, D]] |
| - | [[Category: Keusch, J J | + | [[Category: Keusch, J J]] |
| - | [[Category: Marcellin, D | + | [[Category: Marcellin, D]] |
| - | [[Category: Zhuravleva, E | + | [[Category: Zhuravleva, E]] |
[[Category: Hotdog-fold]] | [[Category: Hotdog-fold]] | ||
[[Category: Hydrolase]] | [[Category: Hydrolase]] | ||
Revision as of 19:13, 25 December 2014
Crystal structure of human THEM4
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Categories: Homo sapiens | Bleck, C K.E | Cron, P | Dummler, B | Esposti, M Degli | Genoud, C | Gut, H | Hemmings, B A | Hynx, D | Keusch, J J | Marcellin, D | Zhuravleva, E | Hotdog-fold | Hydrolase
