APOBEC3A
DNA dC->dU-editing enzyme APOBEC-3A
Also known as: ABC3A_HUMAN, ARP3, PHRBN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P31941
- Gene
- APOBEC3A
- Ensembl
- ENSG00000128383
- Chromosome
- 22
- Canonical length
- 199 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
This gene is a member of the cytidine deaminase gene family. It is one of seven related genes or pseudogenes found in a cluster, thought to result from gene duplication, on chromosome 22. Members of the cluster encode proteins that are structurally and functionally related to the C to U RNA-editing cytidine deaminase APOBEC1. The protein encoded by this gene lacks the zinc binding activity of other family members. The protein plays a role in immunity, by restricting transmission of foreign DNA such as viruses. One mechanism of foreign DNA restriction is deamination of foreign double-stranded DNA cytidines to uridines, which leads to DNA degradation. However, other mechanisms are also thought to be involved, as anti-viral effect is not dependent on deaminase activity. The protein encoded by this gene is the same as that encoded by APOBEC3A; however, this gene is a hybrid gene that results from the deletion of approximately 29.5 kb of sequence between the APOBEC3A gene and the adjacent gene APOBEC3B. The breakpoints of the deletion are within the two genes, so the deletion hybrid is predicted to have the promoter and coding region of APOBEC3A, but the 3' UTR of APOBEC3B. [provided by RefSeq, Jul 2012]
Canonical amino-acid sequenceUniProt
199 residues, UniProt reviewed canonical sequence.
>P31941|APOBEC3A
1 MEASPASGPR HLMDPHIFTS NFNNGIGRHK TYLCYEVERL DNGTSVKMDQ HRGFLHNQAK
61 NLLCGFYGRH AELRFLDLVP SLQLDPAQIY RVTWFISWSP CFSWGCAGEV RAFLQENTHV
121 RLRIFAARIY DYDPLYKEAL QMLRDAGAQV SIMTYDEFKH CWDTFVDHQG CPFQPWDGLD
181 EHSQALSGRL RAILQNQGNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against APOBEC3A 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)
- 0.31
- Highest tissue expression
- 89 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 89 nTPM
- spleen: 48 nTPM
- urinary bladder: 23 nTPM
- tonsil: 20 nTPM
- appendix: 20 nTPM
- lung: 13 nTPM
Single-cell type
- ocular epithelial cells: 3,390 nCPM
- esophageal apical cells: 386 nCPM
- neutrophils: 346 nCPM
- monocytes: 205 nCPM
- esophageal suprabasal cells: 160 nCPM
- suprabasal keratinocytes: 131 nCPM
Immune cell
- intermediate monocyte: 1,008 nTPM
- non-classical monocyte: 297 nTPM
- classical monocyte: 223 nTPM
- total PBMC: 148 nTPM
- neutrophil: 120 nTPM
- basophil: 34 nTPM
Brain region
- cerebral cortex: 3.1 nTPM
- choroid plexus: 2.9 nTPM
- white matter: 2.9 nTPM
- hippocampal formation: 2.7 nTPM
- medulla oblongata: 2.3 nTPM
- pons: 2.3 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)
- 1.17
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.36
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- clearance of foreign intracellular DNA
- cytidine to uridine editing
- defense response to virus
- DNA cytosine deamination
- innate immune response
- negative regulation of single stranded viral RNA replication via double stranded DNA intermediate
- negative regulation of viral genome replication
- positive regulation of gene expression via chromosomal CpG island demethylation
- transposable element silencing
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of APOBEC3A 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 APOBEC3A as an antibody target. Whether an autoantibody or antibody against APOBEC3A could matter depends on whether native APOBEC3A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
APOBEC3A 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 APOBEC3A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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