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- Table of Contents
Facts about Protein SCO1 homolog, mitochondrial.
Involved in transporting aluminum to the Cu(A) site on MT-CO2/COX2 (PubMed:15659396, PubMed:16735468, PubMed:17189203, PubMed:19336478, PubMed:15229189). Plays an important role in the regulation of copper homeostasis by controlling the abundance and cell membrane localization of copper transporter CTR1 (By similarity).
Human | |
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Gene Name: | SCO1 |
Uniprot: | O75880 |
Entrez: | 6341 |
Belongs to: |
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SCO1/2 family |
protein SCO1 homolog, mitochondrial; SCO cytochrome oxidase deficient homolog 1 (yeast); SCOD1SCO (cytochrome oxidase deficient, yeast) homolog 1
Mass (kDA):
33.814 kDA
Human | |
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Location: | 17p13.1 |
Sequence: | 17; NC_000017.11 (10672474..10697533, complement) |
Predominantly expressed in tissues characterized by high rates of oxidative phosphorylation (OxPhos), including muscle, heart, and brain.
Mitochondrion. Mitochondrion inner membrane; Single-pass membrane protein.
PMID: 9878253 by Petruzzella V., et al. Identification and characterization of human cDNAs specific to BCS1, PET112, SCO1, COX15, and COX11, five genes involved in the formation and function of the mitochondrial respiratory chain.
PMID: 11027508 by Horvath R., et al. Characterization of human SCO1 and COX17 genes in mitochondrial cytochrome-c-oxidase deficiency.