APOBEC3H
DNA dC->dU-editing enzyme APOBEC-3H
Also known as: ABC3H_HUMAN, ARP10
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6NTF7
- Gene
- APOBEC3H
- Ensembl
- ENSG00000100298
- Chromosome
- 22
- Canonical length
- 200 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a member of the apolipoprotein B mRNA-editing enzyme catalytic polypeptide 3 family of proteins. The encoded protein is a cytidine deaminase that has antiretroviral activity by generating lethal hypermutations in viral genomes. Polymorphisms and alternative splicing in this gene influence its antiretroviral activity and are associated with increased resistence to human immunodeficiency virus type 1 infection in certain populations. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Oct 2009]
Canonical amino-acid sequenceUniProt
200 residues, UniProt reviewed canonical sequence.
>Q6NTF7|APOBEC3H
1 MALLTAETFR LQFNNKRRLR RPYYPRKALL CYQLTPQNGS TPTRGYFENK KKCHAEICFI
61 NEIKSMGLDE TQCYQVTCYL TWSPCSSCAW ELVDFIKAHD HLNLGIFASR LYYHWCKPQQ
121 KGLRLLCGSQ VPVEVMGFPE FADCWENFVD HEKPLSFNPY KMLEELDKNS RAIKRRLERI
181 KIPGVRAQGR YMDILCDAEVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against APOBEC3H 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)
- 0.32
- Highest tissue expression
- 3.6 nTPM
Expression across tissuesHPA
Tissue
- lymph node: 3.6 nTPM
- bone marrow: 3.4 nTPM
- epididymis: 3.4 nTPM
- rectum: 3.1 nTPM
- spleen: 2.8 nTPM
- thymus: 2.7 nTPM
Single-cell type
- t-cells: 15 nCPM
- nk-cells: 13 nCPM
- hofbauer cells: 9.8 nCPM
- cytotrophoblasts: 7.9 nCPM
- migrating cytotrophoblasts: 6.5 nCPM
- thymocytes: 5.1 nCPM
Immune cell
- gdT-cell: 23 nTPM
- NK-cell: 20 nTPM
- memory CD8 T-cell: 19 nTPM
- memory CD4 T-cell: 12 nTPM
- T-reg: 12 nTPM
- MAIT T-cell: 9.4 nTPM
Brain region
- cerebellum: 3.2 nTPM
- medulla oblongata: 2.6 nTPM
- cerebral cortex: 2.5 nTPM
- basal ganglia: 2.2 nTPM
- white matter: 2.2 nTPM
- midbrain: 2.1 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)
- 1.02
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.02
- DepMap mean gene effect
- -0.02
- 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
- host-mediated suppression of viral genome replication
- 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 APOBEC3H 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 APOBEC3H as an antibody target. Whether an autoantibody or antibody against APOBEC3H could matter depends on whether native APOBEC3H is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
APOBEC3H 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 APOBEC3H as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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