Aliases for ATP5O Gene
External Ids for ATP5O Gene
The protein encoded by this gene is a component of the F-type ATPase found in the mitochondrial matrix. F-type ATPases are composed of a catalytic core and a membrane proton channel. The encoded protein appears to be part of the connector linking these two components and may be involved in transmission of conformational changes or proton conductance. [provided by RefSeq, Jul 2008]
GeneCards Summary for ATP5O Gene
ATP5O (ATP Synthase, H+ Transporting, Mitochondrial F1 Complex, O Subunit) is a Protein Coding gene. Diseases associated with ATP5O include autoimmune polyglandular syndrome type 2 and 2-hydroxyglutaric aciduria. Among its related pathways are Metabolism and Metabolism. GO annotations related to this gene include transporter activity and drug binding. An important paralog of this gene is ENSG00000249209.
UniProtKB/Swiss-Prot for ATP5O Gene
Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation. Part of the complex F(0) domain and the peripheric stalk, which acts as a stator to hold the catalytic alpha(3)beta(3) subcomplex and subunit a/ATP6 static relative to the rotary elements