ART3
Ecto-ADP-ribosyltransferase 3
Also known as: ARTC3, NAR3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q13508
- Gene
- ART3
- Ensembl
- ENSG00000156219
- Chromosome
- 4
- Canonical length
- 389 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Principal piece,End piece
- Secretome location
- Intracellular and membrane
OverviewNCBI Gene
This gene encodes an arginine-specific ADP-ribosyltransferase. The encoded protein catalyzes a reversible reaction which modifies proteins by the addition or removal of ADP-ribose to an arginine residue to regulate the function of the modified protein. An ADP-ribosyltransferase pseudogene is located on chromosome 11. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]
Canonical amino-acid sequenceUniProt
389 residues, UniProt reviewed canonical sequence.
>Q13508|ART3
1 MKTGHFEIVT MLLATMILVD IFQVKAEVLD MADNAFDDEY LKCTDRMEIK YVPQLLKEEK
61 ASHQQLDTVW ENAKAKWAAR KTQIFLPMNF KDNHGIALMA YISEAQEQTP FYHLFSEAVK
121 MAGQSREDYI YGFQFKAFHF YLTRALQLLR KPCEASSKTV VYRTSQGTSF TFGGLNQARF
181 GHFTLAYSAK PQAANDQLTV LSIYTCLGVD IENFLDKESE RITLIPLNEV FQVSQEGAGN
241 NLILQSINKT CSHYECAFLG GLKTENCIEN LEYFQPIYVY NPGEKNQKLE DHSEKNWKLE
301 DHGEKNQKLE DHGVKILEPT QIPGMKIPEP FPLPEDKSQG NINNPTPGPV PVPGPKSHPS
361 ASSGKLLLPQ FGMVIILISV SAINLFVALLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ART3 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.41
- Highest tissue expression
- 191 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 191 nTPM
- testis: 86 nTPM
- tongue: 71 nTPM
- heart muscle: 64 nTPM
- cerebellum: 10 nTPM
- blood vessel: 9.4 nTPM
Single-cell type
- myonuclei: 528 nCPM
- thymic myoid cells: 504 nCPM
- early primary spermatocytes: 267 nCPM
- late primary spermatocytes: 183 nCPM
- choroid plexus epithelial cells: 86 nCPM
- cardiomyocytes: 76 nCPM
Immune cell
- gdT-cell: 0.3 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- white matter: 8.4 nTPM
- cerebral cortex: 7.5 nTPM
- cerebellum: 5.1 nTPM
- hypothalamus: 4.2 nTPM
- basal ganglia: 2.5 nTPM
- choroid plexus: 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)
- 1.43
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.15
- DepMap mean gene effect
- -0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Molecular functions
- NAD+ poly-ADP-ribosyltransferase activity
- NAD+-protein-arginine ADP-ribosyltransferase activity
- nucleotidyltransferase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ART3 as an antibody target. Whether an autoantibody or antibody against ART3 could matter depends on whether native ART3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ART3 is annotated at the cell surface, where native ART3 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label ART3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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