APOBEC1
C->U-editing enzyme APOBEC-1
Also known as: ABEC1_HUMAN, APOBEC-1, BEDP, CDAR1, HEPR
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P41238
- Gene
- APOBEC1
- Ensembl
- ENSG00000111701
- Chromosome
- 12
- Canonical length
- 236 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a member of the cytidine deaminase enzyme family. The encoded protein forms a multiple-protein editing holoenzyme with APOBEC1 complementation factor (ACF) and APOBEC1 stimulating protein (ASP). This holoenzyme is involved in the editing of C-to-U nucleotide bases in apolipoprotein B and neurofibromatosis-1 mRNAs. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2015]
Canonical amino-acid sequenceUniProt
236 residues, UniProt reviewed canonical sequence.
>P41238|APOBEC1
1 MTSEKGPSTG DPTLRRRIEP WEFDVFYDPR ELRKEACLLY EIKWGMSRKI WRSSGKNTTN
61 HVEVNFIKKF TSERDFHPSM SCSITWFLSW SPCWECSQAI REFLSRHPGV TLVIYVARLF
121 WHMDQQNRQG LRDLVNSGVT IQIMRASEYY HCWRNFVNYP PGDEAHWPQY PPLWMMLYAL
181 ELHCIILSLP PCLKISRRWQ NHLTFFRLHL QNCHYQTIPP HILLATGLIH PSVAWRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against APOBEC1 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)
- 0.28
- Highest tissue expression
- 27 nTPM
Expression across tissuesHPA
Tissue
- duodenum: 27 nTPM
- small intestine: 25 nTPM
- stomach: 1 nTPM
- colon: 0.9 nTPM
- rectum: 0.2 nTPM
- appendix: 0.1 nTPM
Single-cell type
- enterocytes: 162 nCPM
- tuft cells: 23 nCPM
- foveolar cells: 23 nCPM
- goblet cells: 14 nCPM
- colonocytes: 11 nCPM
- enteric transient amplifying cells: 8.2 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- amygdala: 0 nTPM
- basal ganglia: 0 nTPM
- cerebellum: 0 nTPM
- cerebral cortex: 0 nTPM
- choroid plexus: 0 nTPM
- hippocampal formation: 0 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)
- 1.59
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.77
- DepMap mean gene effect
- 0
- DepMap dependency class
- none
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
- establishment of localization in cell
- lipid metabolic process
- lipoprotein biosynthetic process
- lipoprotein transport
- mRNA modification
- mRNA processing
- mRNA stabilization
- negative regulation of nuclear-transcribed mRNA catabolic process, nonsense-mediated decay
- negative regulation of triglyceride metabolic process
- positive regulation of gene expression via chromosomal CpG island demethylation
- regulation of cell population proliferation
- response to gamma radiation
- triglyceride metabolic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Cytidine and deoxycytidylate deaminase domain
- APOBEC/CMP deaminase, zinc-binding
- Cytidine deaminase-like
- APOBEC Cytidine Deaminase
- C->U-editing enzyme APOBEC-1
- APOBEC4-like -AID/APOBEC-deaminase
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of APOBEC1 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 APOBEC1 as an antibody target. Whether an autoantibody or antibody against APOBEC1 could matter depends on whether native APOBEC1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
APOBEC1 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 APOBEC1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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