ACOT7

Cytosolic acyl coenzyme A thioester hydrolase is an enzyme that in humans is encoded by the ACOT7 gene.[5][6][7][8]

ACOT7
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 2QQ2
Identifiers
Aliases	ACOT7, ACH1, ACT, BACH, CTE-II, LACH, LACH1, hBACH, acyl-CoA thioesterase 7
External IDs	OMIM: 602587 MGI: 1917275 HomoloGene: 15780 GeneCards: ACOT7
Gene location (Human) Chr. Chromosome 1 (human)[1] Band 1p36.31 Start 6,264,269 bp[1] End 6,394,391 bp[1]
Gene location (Mouse) Chr. Chromosome 4 (mouse)[2] Band 4|4 E2 Start 152,178,134 bp[2] End 152,271,855 bp[2]
RNA expression pattern More reference expression data
Gene ontology Molecular function • palmitoyl-CoA hydrolase activity • fatty-acyl-CoA binding • protein homodimerization activity • GO:0004091 carboxylic ester hydrolase activity • long-chain fatty acyl-CoA binding • GO:0001948 protein binding • hydrolase activity • acyl-CoA hydrolase activity • myristoyl-CoA hydrolase activity • thiolester hydrolase activity Cellular component • cytosol • nucleoplasm • mitochondrion • extracellular exosome • cytoplasm Biological process • medium-chain fatty acid biosynthetic process • medium-chain fatty-acyl-CoA catabolic process • long-chain fatty-acyl-CoA catabolic process • coenzyme A biosynthetic process • palmitic acid biosynthetic process • acyl-CoA metabolic process • lipid metabolism • fatty acid metabolic process Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	11332	70025
Ensembl	ENSG00000097021	ENSMUSG00000028937
UniProt	O00154	Q91V12
RefSeq (mRNA)	NM_181866 NM_007274 NM_181862 NM_181863 NM_181864 NM_181865	NM_001146057 NM_001146058 NM_133348 NM_001369273 NM_001369274 NM_001369275 NM_001369276
RefSeq (protein)	NP_009205 NP_863654 NP_863655 NP_863656	NP_001139529 NP_001139530 NP_579926 NP_001356202 NP_001356203 NP_001356204 NP_001356205
Location (UCSC)	Chr 1: 6.26 – 6.39 Mb	Chr 4: 152.18 – 152.27 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

This gene encodes a member of the acyl coenzyme family. The encoded protein hydrolyzes the CoA thioester of palmitoyl-CoA and other long-chain fatty acids. Decreased expression of this gene may be associated with mesial temporal lobe epilepsy. Alternatively spliced transcript variants encoding distinct isoforms with different subcellular locations have been characterized.[8]

References

1. GRCh38: Ensembl release 89: ENSG00000097021 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000028937 - Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. Yamada J, Kurata A, Hirata M, Taniguchi T, Takama H, Furihata T, Shiratori K, Iida N, Takagi-Sakuma M, Watanabe T, Kurosaki K, Endo T, Suga T (Mar 2000). "Purification, molecular cloning, and genomic organization of human brain long-chain acyl-CoA hydrolase". J Biochem. 126 (6): 1013–9. doi:10.1093/oxfordjournals.jbchem.a022544. PMID 10578051.
6. Hunt MC, Yamada J, Maltais LJ, Wright MW, Podesta EJ, Alexson SE (Aug 2005). "A revised nomenclature for mammalian acyl-CoA thioesterases/hydrolases". J Lipid Res. 46 (9): 2029–32. doi:10.1194/jlr.E500003-JLR200. PMID 16103133.
7. Hunt MC, Rautanen A, Westin MA, Svensson LT, Alexson SE (Aug 2006). "Analysis of the mouse and human acyl-CoA thioesterase (ACOT) gene clusters shows that convergent, functional evolution results in a reduced number of human peroxisomal ACOTs". FASEB J. 20 (11): 1855–64. doi:10.1096/fj.06-6042com. PMID 16940157. S2CID 501610.
8. "Entrez Gene: ACOT7 acyl-CoA thioesterase 7".

External links

• Human ACOT7 genome location and ACOT7 gene details page in the UCSC Genome Browser.

Further reading

• Yamada J (2006). "Long-chain acyl-CoA hydrolase in the brain". Amino Acids. 28 (3): 273–8. doi:10.1007/s00726-005-0181-1. PMID 15731883. S2CID 10678899.
• Yamada J, Kuramochi Y, Takagi M, et al. (2003). "Human brain acyl-CoA hydrolase isoforms encoded by a single gene". Biochem. Biophys. Res. Commun. 299 (1): 49–56. doi:10.1016/S0006-291X(02)02587-1. PMID 12435388.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
• Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
• Yang JW, Czech T, Yamada J, et al. (2005). "Aberrant cytosolic acyl-CoA thioester hydrolase in hippocampus of patients with mesial temporal lobe epilepsy". Amino Acids. 27 (3–4): 269–75. doi:10.1007/s00726-004-0138-9. PMID 15592755. S2CID 2832201.
• Gregory SG, Barlow KF, McLay KE, et al. (2006). "The DNA sequence and biological annotation of human chromosome 1". Nature. 441 (7091): 315–21. Bibcode:2006Natur.441..315G. doi:10.1038/nature04727. PMID 16710414.
• Lim J, Hao T, Shaw C, et al. (2006). "A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration". Cell. 125 (4): 801–14. doi:10.1016/j.cell.2006.03.032. PMID 16713569. S2CID 13709685.