APOBEC3B
DNA dC->dU-editing enzyme APOBEC-3B
Also known as: ABC3B_HUMAN, FLJ21201, PHRBNL
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UH17
- Gene
- APOBEC3B
- Ensembl
- ENSG00000179750
- Chromosome
- 22
- Canonical length
- 382 aa
- Protein class
- Cancer-related genes, Enzymes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
- Quaternary structure
- Homodimer
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. It is thought that the proteins may be RNA editing enzymes and have roles in growth or cell cycle control. A hybrid gene results from the deletion of approximately 29.5 kb of sequence between this gene, APOBEC3B, and the adjacent gene APOBEC3A. The breakpoints of the deletion are within the two genes, so the deletion allele is predicted to have the promoter and coding region of APOBEC3A, but the 3' UTR of APOBEC3B. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2012]
Canonical amino-acid sequenceUniProt
382 residues, UniProt reviewed canonical sequence.
>Q9UH17|APOBEC3B
1 MNPQIRNPME RMYRDTFYDN FENEPILYGR SYTWLCYEVK IKRGRSNLLW DTGVFRGQVY
61 FKPQYHAEMC FLSWFCGNQL PAYKCFQITW FVSWTPCPDC VAKLAEFLSE HPNVTLTISA
121 ARLYYYWERD YRRALCRLSQ AGARVTIMDY EEFAYCWENF VYNEGQQFMP WYKFDENYAF
181 LHRTLKEILR YLMDPDTFTF NFNNDPLVLR RRQTYLCYEV ERLDNGTWVL MDQHMGFLCN
241 EAKNLLCGFY GRHAELRFLD LVPSLQLDPA QIYRVTWFIS WSPCFSWGCA GEVRAFLQEN
301 THVRLRIFAA RIYDYDPLYK EALQMLRDAG AQVSIMTYDE FEYCWDTFVY RQGCPFQPWD
361 GLEEHSQALS GRLRAILQNQ GNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against APOBEC3B 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)
- 0.27
- Highest tissue expression
- 27 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 27 nTPM
- colon: 11 nTPM
- rectum: 11 nTPM
- tonsil: 8.1 nTPM
- urinary bladder: 7.1 nTPM
- duodenum: 6.9 nTPM
Single-cell type
- endometrial secretory cells: 8.4 nCPM
- erythrocyte progenitors: 5.9 nCPM
- epididymal basal cells: 5 nCPM
- ocular epithelial cells: 4.9 nCPM
- plasma cells: 4.9 nCPM
- monocyte progenitors: 4.7 nCPM
Immune cell
- memory B-cell: 7.2 nTPM
- intermediate monocyte: 4.9 nTPM
- total PBMC: 3.5 nTPM
- naive B-cell: 3.1 nTPM
- T-reg: 2.8 nTPM
- NK-cell: 1.7 nTPM
Brain region
- thalamus: 0.5 nTPM
- cerebral cortex: 0.4 nTPM
- white matter: 0.4 nTPM
- pons: 0.3 nTPM
- spinal cord: 0.3 nTPM
- amygdala: 0.2 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)
- 1.36
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.52
- DepMap mean gene effect
- 0.01
- 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
- 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
- transposable element silencing
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of APOBEC3B 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 APOBEC3B as an antibody target. Whether an autoantibody or antibody against APOBEC3B could matter depends on whether native APOBEC3B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
APOBEC3B 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 APOBEC3B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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