Homo sapiens Protein: ATP5S
Summary
InnateDB Protein IDBP-367940.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ATP5S
Protein Name ATP synthase, H+ transporting, mitochondrial Fo complex, subunit s (factor B)
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000389246
InnateDB Gene IDBG-5967 (ATP5S)
Protein Structure
UniProt Annotation
Function Involved in regulation of mitochondrial membrane ATP synthase. Necessary for H(+) conduction of ATP synthase. Facilitates energy-driven catalysis of ATP synthesis by blocking a proton leak through an alternative proton exit pathway (By similarity). {ECO:0000250}.
Subcellular Localization Mitochondrion {ECO:0000250}. Mitochondrion inner membrane {ECO:0000250}.
Disease Associations
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 0
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0015078 hydrogen ion transmembrane transporter activity
GO:0046872 metal ion binding
Biological Process
GO:0006754 ATP biosynthetic process
GO:0015992 proton transport
GO:1902600 hydrogen ion transmembrane transport
Cellular Component
GO:0005743 mitochondrial inner membrane
GO:0045263 proton-transporting ATP synthase complex, coupling factor F(o)
Protein Structure and Domains
PDB ID
InterPro
PFAM
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q99766
PhosphoSite PhosphoSite-Q99766
TrEMBL
UniProt Splice Variant
Entrez Gene 27109
UniGene Hs.656689
RefSeq NP_056499
HUGO HGNC:18799
OMIM
CCDS CCDS45102
HPRD 12503
IMGT
EMBL AK290008 AL359397 AY052377 BC011549 CH471078 U79253
GenPept AAB50202 AAH11549 AAL13058 BAF82697 EAW65718 EAW65722