
We have isolated a full-length cDNA clone specifying the nuclear-encoded subunit Va of the human mitochondrial respiratory enzyme cytochrome c oxidase (COX; EC 1.9.3.1.). The deduced sequence of the polypeptide is 95% identical to that of the corresponding subunit of bovine COX, which makes it the most conserved polypeptide among the known bovine/human pairs of COX subunits. This polypeptide contains an N-terminal presequence which is rich in basic and hydroxylated residues, but differs from the deduced presequences of all other previously isolated COX subunits in that it also contains a negatively charged residue. We find no evidence of tissue-specific isoforms of subunit Va, as Northern analysis showed a single, identically-sized transcript in RNA from human muscle, liver, and brain, while coxVa cDNAs isolated from both endothelial and fetal muscle cDNA libraries had identical nucleotide sequences.
Base Sequence, Transcription, Genetic, Macromolecular Substances, Protein Conformation, Molecular Sequence Data, Restriction Mapping, Biological Evolution, Electron Transport Complex IV, Genes, Species Specificity, Animals, Humans, Cattle, Amino Acid Sequence, Cloning, Molecular
Base Sequence, Transcription, Genetic, Macromolecular Substances, Protein Conformation, Molecular Sequence Data, Restriction Mapping, Biological Evolution, Electron Transport Complex IV, Genes, Species Specificity, Animals, Humans, Cattle, Amino Acid Sequence, Cloning, Molecular
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