醯基輔酶A硫酯酶7
外觀
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醯基輔酶A硫酯酶7(英語:Acyl-CoA thioesterase 7)是一種在人類中由ACOT7基因編碼的酶。[5][6][7][8]
該基因編碼醯基輔酶家族的一個成員。編碼的蛋白質水解棕櫚醯輔酶A的輔酶A硫酯和其他長鏈脂肪酸。該基因表現的減少可能與內側顳葉癲癇有關。編碼具有不同亞細胞位置的不同異構物的選擇性剪接轉錄變體已經被表徵。[8]
參考資料
[編輯]- ^ 1.0 1.1 1.2 GRCh38: Ensembl release 89: ENSG00000097021 - Ensembl, May 2017
- ^ 2.0 2.1 2.2 GRCm38: Ensembl release 89: ENSMUSG00000028937 - Ensembl, May 2017
- ^ Human PubMed Reference:. National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ Mouse PubMed Reference:. National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ 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. Purification, molecular cloning, and genomic organization of human brain long-chain acyl-CoA hydrolase. J Biochem. Mar 2000, 126 (6): 1013–9. PMID 10578051. doi:10.1093/oxfordjournals.jbchem.a022544.
- ^ Hunt MC, Yamada J, Maltais LJ, Wright MW, Podesta EJ, Alexson SE. A revised nomenclature for mammalian acyl-CoA thioesterases/hydrolases. J Lipid Res. Aug 2005, 46 (9): 2029–32. PMID 16103133. doi:10.1194/jlr.E500003-JLR200
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- ^ Hunt MC, Rautanen A, Westin MA, Svensson LT, Alexson SE. 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. Aug 2006, 20 (11): 1855–64 [2023-03-07]. PMID 16940157. S2CID 501610. doi:10.1096/fj.06-6042com. (原始內容存檔於2017-11-03).
- ^ 8.0 8.1 Entrez Gene: ACOT7 acyl-CoA thioesterase 7.
外部連結
[編輯]- Human ACOT7 genome location and ACOT7 gene details page in the UCSC Genome Browser.
延申閱讀
[編輯]- Yamada J. Long-chain acyl-CoA hydrolase in the brain.. Amino Acids. 2006, 28 (3): 273–8. PMID 15731883. S2CID 10678899. doi:10.1007/s00726-005-0181-1.
- Yamada J, Kuramochi Y, Takagi M, et al. Human brain acyl-CoA hydrolase isoforms encoded by a single gene.. Biochem. Biophys. Res. Commun. 2003, 299 (1): 49–56. PMID 12435388. doi:10.1016/S0006-291X(02)02587-1.
- Strausberg RL, Feingold EA, Grouse LH, et al. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Proc. Natl. Acad. Sci. U.S.A. 2003, 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. PMC 139241
. PMID 12477932. doi:10.1073/pnas.242603899
.
- Ota T, Suzuki Y, Nishikawa T, et al. Complete sequencing and characterization of 21,243 full-length human cDNAs. Nat. Genet. 2004, 36 (1): 40–5. PMID 14702039. doi:10.1038/ng1285
.
- Gerhard DS, Wagner L, Feingold EA, et al. The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC). Genome Res. 2004, 14 (10B): 2121–7. PMC 528928
. PMID 15489334. doi:10.1101/gr.2596504.
- Yang JW, Czech T, Yamada J, et al. Aberrant cytosolic acyl-CoA thioester hydrolase in hippocampus of patients with mesial temporal lobe epilepsy. Amino Acids. 2005, 27 (3–4): 269–75. PMID 15592755. S2CID 2832201. doi:10.1007/s00726-004-0138-9.
- Gregory SG, Barlow KF, McLay KE, et al. The DNA sequence and biological annotation of human chromosome 1. Nature. 2006, 441 (7091): 315–21. Bibcode:2006Natur.441..315G. PMID 16710414. doi:10.1038/nature04727
.
- Lim J, Hao T, Shaw C, et al. A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration. Cell. 2006, 125 (4): 801–14. PMID 16713569. S2CID 13709685. doi:10.1016/j.cell.2006.03.032
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