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Identification
HMDB Protein ID HMDBP11550
Secondary Accession Numbers
  • 20994
Name Putative acyl-coenzyme A thioesterase 6
Synonyms
  1. Acyl-CoA thioesterase 6
Gene Name ACOT6
Protein Type Enzyme
Biological Properties
General Function Involved in carboxylesterase activity
Specific Function Not Available
Pathways Not Available
Reactions Not Available
GO Classification Not Available
Cellular Location
  1. Cytoplasm
Gene Properties
Chromosome Location Chromosome:1
Locus 14q24.3
SNPs ACOT6
Gene Sequence
>624 bp
ATGCTGCAGCATCCAAAGGTGAAAGGTCCTAGTATTGCGCTTCTTGGATTTTCCAAAGGA
GGTGACCTGTGTCTCTCAATGGCTTCTTTCTTGAAGGGCATCACAGCCACTGTACTTATC
AATGCCTGTGTAGCCAACACAGTAGCTCCTCTACATTACAAGGATATGATTATTCCTAAA
CTTGTCGATGATCTAGGAAAAGTAAAAATCACTAAGTCAGGATTTCTCACTTTTATGGAC
ACTTGGAGCAATCCACTGGAGGAACACAATCACCAAAGTCTTGTTCCATTGGAAAAGGCG
CAGGTGCCCTTCTTGTTTATTGTTGGCATGGATGATCAAAGCTGGAAGAGTGAATTCTAT
GCTCAGATAGCCTCTGAAAGGCTACAAGCTCATGGGAAAGAAAGACCCCAGATAATCTGT
TACCCAGAAACTGGTCACTGTATTGACCCACCTTATTTTCCTCCTTCTAGAGCTTCTGTG
CACGCTGTTTTGGGTGAGGCAATATTCTATGGAGGTGAGCCAAAGGCTCACTCAAAGGCA
CAGGTAGATGCCTGGCAGCAAATTCAAACTTTCTTCCATAAACATCTCAATGGTAAAAAA
TCTGTCAAGCACAGCAAAATATAA
Protein Properties
Number of Residues 207
Molecular Weight 22990.5
Theoretical pI 8.9
Pfam Domain Function
Signals
  • None
Transmembrane Regions
  • None
Protein Sequence
>Putative acyl-coenzyme A thioesterase 6
MLQHPKVKGPSIALLGFSKGGDLCLSMASFLKGITATVLINACVANTVAPLHYKDMIIPK
LVDDLGKVKITKSGFLTFMDTWSNPLEEHNHQSLVPLEKAQVPFLFIVGMDDQSWKSEFY
AQIASERLQAHGKERPQIICYPETGHCIDPPYFPPSRASVHAVLGEAIFYGGEPKAHSKA
QVDAWQQIQTFFHKHLNGKKSVKHSKI
GenBank ID Protein 118835784
UniProtKB/Swiss-Prot ID Q3I5F7
UniProtKB/Swiss-Prot Entry Name ACOT6_HUMAN
PDB IDs Not Available
GenBank Gene ID BC126378
GeneCard ID ACOT6
GenAtlas ID ACOT6
HGNC ID HGNC:33159
References
General References
  1. Gerhard DS, Wagner L, Feingold EA, Shenmen CM, Grouse LH, Schuler G, Klein SL, Old S, Rasooly R, Good P, Guyer M, Peck AM, Derge JG, Lipman D, Collins FS, Jang W, Sherry S, Feolo M, Misquitta L, Lee E, Rotmistrovsky K, Greenhut SF, Schaefer CF, Buetow K, Bonner TI, Haussler D, Kent J, Kiekhaus M, Furey T, Brent M, Prange C, Schreiber K, Shapiro N, Bhat NK, Hopkins RF, Hsie F, Driscoll T, Soares MB, Casavant TL, Scheetz TE, Brown-stein MJ, Usdin TB, Toshiyuki S, Carninci P, Piao Y, Dudekula DB, Ko MS, Kawakami K, Suzuki Y, Sugano S, Gruber CE, Smith MR, Simmons B, Moore T, Waterman R, Johnson SL, Ruan Y, Wei CL, Mathavan S, Gunaratne PH, Wu J, Garcia AM, Hulyk SW, Fuh E, Yuan Y, Sneed A, Kowis C, Hodgson A, Muzny DM, McPherson J, Gibbs RA, Fahey J, Helton E, Ketteman M, Madan A, Rodrigues S, Sanchez A, Whiting M, Madari A, Young AC, Wetherby KD, Granite SJ, Kwong PN, Brinkley CP, Pearson RL, Bouffard GG, Blakesly RW, Green ED, Dickson MC, Rodriguez AC, Grimwood J, Schmutz J, Myers RM, Butterfield YS, Griffith M, Griffith OL, Krzywinski MI, Liao N, Morin R, Palmquist D, Petrescu AS, Skalska U, Smailus DE, Stott JM, Schnerch A, Schein JE, Jones SJ, Holt RA, Baross A, Marra MA, Clifton S, Makowski KA, Bosak S, Malek J: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). Genome Res. 2004 Oct;14(10B):2121-7. [PubMed:15489334 ]
  2. 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. 2006 Sep;20(11):1855-64. [PubMed:16940157 ]