ATPAF1
ATP synthase mitochondrial F1 complex assembly factor 1
Also known as: ATP11, Atp11p, ATPF1_HUMAN, FLJ22351
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5TC12
- Gene
- ATPAF1
- Ensembl
- ENSG00000123472
- Chromosome
- 1
- Canonical length
- 328 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Mitochondria
OverviewNCBI Gene
This gene encodes an assembly factor for the F(1) component of the mitochondrial ATP synthase. This protein binds specifically to the F1 beta subunit and is thought to prevent this subunit from forming nonproductive homooligomers during enzyme assembly. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Aug 2011]
Canonical amino-acid sequenceUniProt
328 residues, UniProt reviewed canonical sequence.
>Q5TC12|ATPAF1
1 MAAVVVAAAG GAGPAVLQVA GLYRGLCAVR SRALGLGLVS PAQLRVFPVR PGSGRPEGGA
61 DSSGVGAEAE LQANPFYDRY RDKIQLLRRS DPAAFESRLE KRSEFRKQPV GHSRQGDFIK
121 CVEQKTDALG KQSVNRGFTK DKTLSSIFNI EMVKEKTAEE IKQIWQQYFA AKDTVYAVIP
181 AEKFDLIWNR AQSCPTFLCA LPRREGYEFF VGQWTGTELH FTALINIQTR GEAAASQLIL
241 YHYPELKEEK GIVLMTAEMD STFLNVAEAQ CIANQVQLFY ATDRKETYGL VETFNLRPNE
301 FKYMSVIAEL EQSGLGAELK CAQNQNKTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ATPAF1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Other membrane
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.4
- Highest tissue expression
- 296 nTPM
Expression across tissuesHPA
Tissue
- tongue: 296 nTPM
- skeletal muscle: 260 nTPM
- heart muscle: 249 nTPM
- choroid plexus: 168 nTPM
- parathyroid gland: 130 nTPM
- kidney: 107 nTPM
Single-cell type
- late spermatids: 647 nCPM
- early spermatids: 371 nCPM
- parietal cells: 126 nCPM
- choroid plexus epithelial cells: 94 nCPM
- cytotrophoblasts: 88 nCPM
- early primary spermatocytes: 82 nCPM
Immune cell
- NK-cell: 5.7 nTPM
- T-reg: 5 nTPM
- eosinophil: 4.8 nTPM
- naive CD4 T-cell: 3.6 nTPM
- intermediate monocyte: 3.4 nTPM
- MAIT T-cell: 3.2 nTPM
Brain region
- choroid plexus: 146 nTPM
- hypothalamus: 142 nTPM
- cerebellum: 121 nTPM
- thalamus: 115 nTPM
- basal ganglia: 114 nTPM
- amygdala: 102 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.72
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 1.18
- DepMap mean gene effect
- 0.02
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- ATP11
- ATP11 protein
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ATPAF1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ATPAF1 as an antibody target. Whether an autoantibody or antibody against ATPAF1 could matter depends on whether native ATPAF1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ATPAF1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label ATPAF1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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