NDLI: Cloning of the yeast FAS3 gene and primary structure of yeast acetyl-CoA carboxylase.

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Cloning of the yeast FAS3 gene and primary structure of yeast acetyl-CoA carboxylase.

Content Provider	World Health Organization (WHO)-Global Index Medicus
Author	Wakil, S. J. Al-feel, W. Chirala, S. S.
Description	Author Affiliation: Al-Feel W ( Verna and Marrs McLean Department of Biochemistry, Baylor College of Medicine, Houston, TX 77030.);
Abstract	We have isolated and determined the nucleotide sequence of the yeast FAS3 gene, which encodes acetyl-CoA carboxylase (EC 6.4.1.2). The sequence has an open reading frame of 6711 bases coding for a protein of 2237 amino acids with a calculated molecular weight of 250,593. The presence of the unique biotin-binding site, Met-Lys-Met, and the known CNBr peptide and COOH-terminal sequences confirmed the nucleotide-derived amino acid sequence. The yeast, chicken, and rat carboxylases have an overall sequence identity of 34%, suggesting that the eukaryotic carboxylase evolved from a single ancestral gene. The amino acid sequences of yeast fatty acid synthase subunits are least homologous with the animal synthase sequences, whereas carboxylase sequences are highly conserved. The sequences of the ATP, HCO3-, and CoA binding sites of the carboxylases are also well conserved (approximately 50% identical). The sequences surrounding the biotin binding site are poorly conserved, suggesting that this sequence may not be critical as long as the biotin is available for carboxylase reactions. On the basis of this sequence identity, we have defined the putative biotin carboxylase and transcarboxylase domains.
ISSN	00278424
e-ISSN	10916490
Journal	Proceedings of the National Academy of Sciences of the United States of America
Issue Number	10
Volume Number	89
Language	English
Publisher	National Academy of Sciences
Publisher Date	1992-06-01
Publisher Place	United States
Access Restriction	Open
Subject Keyword	Acetyl-CoA Carboxylase Genetics Saccharomyces Cerevisiae Isolation & Purification Amino Acid Sequence Animals Binding Sites Cloning, Molecular Electrophoresis, Polyacrylamide Gel Macromolecular Substances Molecular Sequence Data Molecular Weight Recombinant Fusion Proteins Restriction Mapping Enzymology Sequence Homology, Nucleic Acid Comparative Study Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S. Multidisciplinary
Content Type	Text
Resource Type	Article
Subject	Multidisciplinary

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