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Valine 181 is critical for the nucleotide exchange activity of human mitochondrial ADP/ATP carriers in yeast.
- Source :
-
Biochemistry [Biochemistry] 2005 Mar 22; Vol. 44 (11), pp. 4342-8. - Publication Year :
- 2005
-
Abstract
- We isolated yeast Saccharomyces cerevisiae cells transformed with one of the three human adenine nucleotide carrier genes (HANC) that exhibited higher growth capacity than previously observed. The HANC genes were isolated from these clones, and we identified two independent mutations of HANC that led to replacement of valine 181 located in the fourth transmembrane segment by methionine or phenylalanine. Tolerance of this position toward substitution with various amino acids was systematically investigated, and since HANC/V181M was among the most efficient in growth complementation, it was more extensively studied. Here we show that increased growth capacities were associated with higher ADP/ATP exchange activities and not with higher human carrier amount in yeast mitochondria. These results are discussed in the light of the bovine Ancp structure, that shares more than 90% amino acid identity with Hancps, and its interaction with the lipid environment.
- Subjects :
- Adenine Nucleotide Translocator 1 genetics
Adenine Nucleotide Translocator 2 genetics
Adenine Nucleotide Translocator 3 genetics
Amino Acid Substitution genetics
Animals
Cattle
Genetic Complementation Test
Humans
Methionine genetics
Mitochondria enzymology
Mitochondria genetics
Mitochondria metabolism
Mutagenesis, Site-Directed
Saccharomyces cerevisiae enzymology
Saccharomyces cerevisiae genetics
Ultraviolet Rays
Adenine Nucleotide Translocator 1 metabolism
Adenine Nucleotide Translocator 2 metabolism
Adenine Nucleotide Translocator 3 metabolism
Guanine Nucleotide Exchange Factors metabolism
Mitochondrial ADP, ATP Translocases metabolism
Saccharomyces cerevisiae metabolism
Saccharomyces cerevisiae Proteins metabolism
Valine genetics
Subjects
Details
- Language :
- English
- ISSN :
- 0006-2960
- Volume :
- 44
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 15766263
- Full Text :
- https://doi.org/10.1021/bi0475370