ATP synthase F(0) complex subunit C3, mitochondrial

Summary
UniProt ID
P48201
Gene Symbol
  • ATP5MC3
  • ATP5G3
Organism
Homo sapiens (human)
External Links
GlyGen
P48201
PubChem
P48201
The Human Metabolome Database
HMDBP03102
The O-GlcNAc Database
P48201
RaftProt
P48201
Annotation
Keyword
  • CF(0)
  • Disease variant
  • Dystonia
  • Hereditary spastic paraplegia
  • Lipid-binding
  • Methylation
  • Mitochondrion
  • Reference proteome
  • Transit peptide
  • Transmembrane helix
Gene Ontology (GO)
Sequence
MFACAKLACTPSLIRAGSRVAYRPISASVLSRPEASRTGEGSTVFNGAQNGVSQLIQREFQTSAISRDIDTAAKFIGAGAATVGVAGSGAGIGTVFGSLIIGYARNPSLKQQLFSYAILGFALSEAMGLFCLMVAFLILFAM
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 2 entries
Pathway Name Organism
Cristae formation Homo sapiens
Formation of ATP by chemiosmotic coupling Homo sapiens

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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