| Literature DB >> 1607358 |
T Abe1, T Fujino, R Fukuyama, S Minoshima, N Shimizu, H Toh, H Suzuki, T Yamamoto.
Abstract
A complementary DNA clone encoding the entire human long-chain acyl-CoA synthetase was isolated and the total 698-amino acid sequence was deduced. The amino acid sequence of human long-chain acyl-CoA synthetase shows 84.9% identity to that of rat long-chain acyl-CoA synthetase. The nucleotide sequences of the protein coding regions between human and rat long-chain acyl-CoA synthetase mRNAs are highly conserved (85.6%), whereas those of the 3' untranslated regions are less conserved (72%). The location of the human long-chain acyl-CoA synthetase gene was identified on chromosome 4 by spot hybridization of flow-sorted chromosomes. Computer-assisted homology search revealed a significant similarity of the enzyme with the enzymes of the luciferase family. Based on this similarity, the structure of human long-chain acyl-CoA synthetase can be divided into five domains: the N-terminus, two domains similar to those in enzymes of the luciferase family, a long gap region between the similar domains and the C-terminus.Entities:
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Year: 1992 PMID: 1607358 DOI: 10.1093/oxfordjournals.jbchem.a123707
Source DB: PubMed Journal: J Biochem ISSN: 0021-924X Impact factor: 3.387