ATP synthase subunit a

Summary
UniProt ID
P00846
Gene Symbol
  • MT-ATP6
  • ATP6
  • ATPASE6
  • MTATP6
Organism
Homo sapiens (human)
External Links
GlyGen
P00846
PubChem
P00846
The O-GlcNAc Database
P00846
Annotation
Keyword
  • 3D-structure
  • ATP synthesis
  • CF(0)
  • Cardiomyopathy
  • Disease variant
  • Leber hereditary optic neuropathy
  • Leigh syndrome
  • Mitochondrion inner membrane
  • Neuropathy
  • Reference proteome
  • Retinitis pigmentosa
  • Transmembrane helix
Gene Ontology (GO)
Sequence
MNENLFASFIAPTILGLPAAVLIILFPPLLIPTSKYLINNRLITTQQWLIKLTSKQMMTMHNTKGRTWSLMLVSLIIFIATTNLLGLLPHSFTPTTQLSMNLAMAIPLWAGTVIMGFRSKIKNALAHFLPQGTPTPLIPMLVIIETISLLIQPMALAVRLTANITAGHLLMHLIGSATLAMSTINLPSTLIIFTILILLTILEIAVALIQAYVFTLLVSLYLHDNT
Glycosylation Sites
Displaying 1 entry
Position Description PubMed ID GlyTouCan ID Source
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying all 3 entries
Pathway Name Organism
Cristae formation Homo sapiens
Formation of ATP by chemiosmotic coupling Homo sapiens
Mitochondrial protein degradation Homo sapiens

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024