ATP5H

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit d
Identifiers
Symbols ATP5H; ATP5JD; ATPQ
External IDs MGI1918929 HomoloGene81748 GeneCards: ATP5H Gene
EC number 3.6.1.14
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez 10476 71679
Ensembl ENSG00000167863 n/a
UniProt O75947 n/a
RefSeq (mRNA) NM_001003785.1 NM_027862
RefSeq (protein) NP_001003785.1 NP_082138
Location (UCSC) Chr 17:
73.03 – 73.04 Mb
n/a
PubMed search [1] [2]
ATP synthase D chain, mitochondrial
Identifiers
Symbol ATP5H
Pfam PF05873

ATP synthase subunit d, mitochondrial is an enzyme that in humans is encoded by the ATP5H gene.[1][2]

Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, F0, which comprises the proton channel. The F1 complex consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled in a ratio of 3 alpha, 3 beta, and a single representative of the other 3. The F0 seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the d subunit of the F0 complex. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. In addition, three pseudogenes are located on chromosomes 9, 12 and 15.[2]

References

Further reading