| Autor: |
Natalya Pobigailo, Aleksei Babich, Mong-Lien Wang, Galina Ovcharenko, Valeriy Filonenko, Valeriy Naidenov, Ivan Nemazanyy, Oleksandr Kukharenko, Heike Rebholz, Genadiy Matsuka, M. I. Vudmaska, Frederique Verdier, Alexander Zhyvoloup, Ganna Panasyuk, Taras Valovka, Sergiy Palchevskii, Tim R. Fenton, Ivan Gout, L. O. Savinska, Peter R. Shepherd |
| Rok vydání: |
2002 |
| Předmět: |
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| Zdroj: |
Journal of Biological Chemistry. 277:22107-22110 |
| ISSN: |
0021-9258 |
| DOI: |
10.1074/jbc.c200195200 |
| Popis: |
Coenzyme A functions as a carrier of acetyl and acyl groups in living cells and is essential for numerous biosynthetic, energy-yielding, and degradative metabolic pathways. There are five enzymatic steps in CoA biosynthesis. To date, molecular cloning of enzymes involved in the CoA biosynthetic pathway in mammals has been only reported for pantothenate kinase. In this study, we present cDNA cloning and functional characterization of CoA synthase. It has an open reading frame of 563 aa and encodes a protein of ∼60 kDa. Sequence alignments suggested that the protein possesses both phosphopantetheine adenylyltransferase and dephospho-CoA kinase domains. Biochemical assays using wild type recombinant protein confirmed the gene product indeed contained both these enzymatic activities. The presence of intrinsic phosphopantetheine adenylyltransferase activity was further confirmed by site-directed mutagenesis. Therefore, this study describes the first cloning and characterization of a mammalian CoA synthase and confirms this is a bifunctional enzyme containing the last two components of CoA biosynthesis. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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