ATP5B

Protein-coding gene in humans From Wikipedia, the free encyclopedia

ATP synthase F1 subunit beta, mitochondrial is an enzyme that in humans is encoded by the ATP5F1B gene.[5][6]

AliasesATP5F1B, ATPMB, ATPSB, HEL-S-271, ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide, ATP synthase F1 subunit beta, ATP5B
End56,645,984 bp[1]
Quick facts ATP5F1B, Identifiers ...
ATP5F1B
Identifiers
AliasesATP5F1B, ATPMB, ATPSB, HEL-S-271, ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide, ATP synthase F1 subunit beta, ATP5B
External IDsOMIM: 102910; MGI: 107801; HomoloGene: 1273; GeneCards: ATP5F1B; OMA:ATP5F1B - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001686

NM_016774

RefSeq (protein)

NP_001677

NP_058054

Location (UCSC)Chr 12: 56.64 – 56.65 MbChr 10: 127.92 – 127.93 Mb
PubMed search[3][4]
Wikidata
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Function

This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel consists of three main subunits (a, b, c). This gene encodes the beta subunit of the catalytic core.[6]

References

Further reading

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