A1CF
APOBEC1 complementation factor
Also known as: A1CF_HUMAN, ACF, ACF64, ACF65, APOBEC1CF, ASP
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NQ94
- Gene
- A1CF
- Ensembl
- ENSG00000148584
- Chromosome
- 10
- Canonical length
- 594 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Mammalian apolipoprotein B mRNA undergoes site-specific C to U deamination, which is mediated by a multi-component enzyme complex containing a minimal core composed of APOBEC-1 and a complementation factor encoded by this gene. The gene product has three non-identical RNA recognition motifs and belongs to the hnRNP R family of RNA-binding proteins. It has been proposed that this complementation factor functions as an RNA-binding subunit and docks APOBEC-1 to deaminate the upstream cytidine. Studies suggest that the protein may also be involved in other RNA editing or RNA processing events. Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]
Canonical amino-acid sequenceUniProt
594 residues, UniProt reviewed canonical sequence.
>Q9NQ94|A1CF
1 MESNHKSGDG LSGTQKEAAL RALVQRTGYS LVQENGQRKY GGPPPGWDAA PPERGCEIFI
61 GKLPRDLFED ELIPLCEKIG KIYEMRMMMD FNGNNRGYAF VTFSNKVEAK NAIKQLNNYE
121 IRNGRLLGVC ASVDNCRLFV GGIPKTKKRE EILSEMKKVT EGVVDVIVYP SAADKTKNRG
181 FAFVEYESHR AAAMARRKLL PGRIQLWGHG IAVDWAEPEV EVDEDTMSSV KILYVRNLML
241 STSEEMIEKE FNNIKPGAVE RVKKIRDYAF VHFSNREDAV EAMKALNGKV LDGSPIEVTL
301 AKPVDKDSYV RYTRGTGGRG TMLQGEYTYS LGQVYDPTTT YLGAPVFYAP QTYAAIPSLH
361 FPATKGHLSN RAIIRAPSVR EIYMNVPVGA AGVRGLGGRG YLAYTGLGRG YQVKGDKRED
421 KLYDILPGME LTPMNPVTLK PQGIKLAPQI LEEICQKNNW GQPVYQLHSA IGQDQRQLFL
481 YKITIPALAS QNPAIHPFTP PKLSAFVDEA KTYAAEYTLQ TLGIPTDGGD GTMATAAAAA
541 TAFPGYAVPN ATAPVSAAQL KQAVTLGQDL AAYTTYEVYP TFAVTARGDG YGTFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against A1CF 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.44
- Highest tissue expression
- 143 nTPM
Expression across tissuesHPA
Tissue
- liver: 143 nTPM
- small intestine: 24 nTPM
- duodenum: 21 nTPM
- kidney: 12 nTPM
- colon: 10 nTPM
- rectum: 9.7 nTPM
Single-cell type
- hepatocytes: 815 nCPM
- neuroendocrine cells: 262 nCPM
- enterocytes: 259 nCPM
- cholangiocytes: 254 nCPM
- pancreatic islet cells: 160 nCPM
- colonocytes: 142 nCPM
Immune cell
- basophil: 0.2 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebral cortex: 0.7 nTPM
- basal ganglia: 0.6 nTPM
- cerebellum: 0.6 nTPM
- white matter: 0.6 nTPM
- amygdala: 0.5 nTPM
- hippocampal formation: 0.5 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)
- 0.88
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.99
- DepMap mean gene effect
- -0.08
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- chromosomal 5-methylcytosine DNA demethylation pathway
- cytidine to uridine editing
- embryo implantation
- mRNA localization resulting in post-transcriptional regulation of gene expression
- mRNA modification
- mRNA processing
- negative regulation of nuclear-transcribed mRNA catabolic process, nonsense-mediated decay
- protein stabilization
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- RNA recognition motif domain
- HnRNP R/Q splicing factor
- Nucleotide-binding alpha-beta plait domain superfamily
- RNA-binding domain superfamily
- RNA recognition motif
- double strand RNA binding domain from DEAD END PROTEIN 1
- ACF, RNA recognition motif 1
- A1CF, double-stranded RNA binding domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of A1CF 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 A1CF as an antibody target. Whether an autoantibody or antibody against A1CF could matter depends on whether native A1CF is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
A1CF 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 A1CF as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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