ADAT1
tRNA-specific adenosine deaminase 1
Also known as: ADAT1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BUB4
- Gene
- ADAT1
- Ensembl
- ENSG00000065457
- Chromosome
- 16
- Canonical length
- 502 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
This gene is a member of the ADAR (adenosine deaminase acting on RNA) family. Using site-specific adenosine modification, proteins encoded by these genes participate in the pre-mRNA editing of nuclear transcripts. The protein encoded by this gene, tRNA-specific adenosine deaminase 1, is responsible for the deamination of adenosine 37 to inosine in eukaryotic tRNA. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jul 2010]
Canonical amino-acid sequenceUniProt
502 residues, UniProt reviewed canonical sequence.
>Q9BUB4|ADAT1
1 MWTADEIAQL CYEHYGIRLP KKGKPEPNHE WTLLAAVVKI QSPADKACDT PDKPVQVTKE
61 VVSMGTGTKC IGQSKMRKNG DILNDSHAEV IARRSFQRYL LHQLQLAATL KEDSIFVPGT
121 QKGVWKLRRD LIFVFFSSHT PCGDASIIPM LEFEDQPCCP VFRNWAHNSS VEASSNLEAP
181 GNERKCEDPD SPVTKKMRLE PGTAAREVTN GAAHHQSFGK QKSGPISPGI HSCDLTVEGL
241 ATVTRIAPGS AKVIDVYRTG AKCVPGEAGD SGKPGAAFHQ VGLLRVKPGR GDRTRSMSCS
301 DKMARWNVLG CQGALLMHLL EEPIYLSAVV IGKCPYSQEA MQRALIGRCQ NVSALPKGFG
361 VQELKILQSD LLFEQSRSAV QAKRADSPGR LVPCGAAISW SAVPEQPLDV TANGFPQGTT
421 KKTIGSLQAR SQISKVELFR SFQKLLSRIA RDKWPHSLRV QKLDTYQEYK EAASSYQEAW
481 STLRKQVFGS WIRNPPDYHQ FKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ADAT1 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.34
- Highest tissue expression
- 21 nTPM
Expression across tissuesHPA
Tissue
- testis: 21 nTPM
- kidney: 18 nTPM
- liver: 17 nTPM
- spleen: 16 nTPM
- parathyroid gland: 14 nTPM
- adrenal gland: 13 nTPM
Single-cell type
- late spermatids: 161 nCPM
- early spermatids: 55 nCPM
- late primary spermatocytes: 25 nCPM
- neutrophils: 18 nCPM
- platelets: 18 nCPM
- renal collecting duct intercalated cells: 18 nCPM
Immune cell
- eosinophil: 12 nTPM
- MAIT T-cell: 11 nTPM
- memory CD8 T-cell: 11 nTPM
- NK-cell: 11 nTPM
- non-classical monocyte: 10 nTPM
- T-reg: 9.1 nTPM
Brain region
- white matter: 22 nTPM
- cerebral cortex: 20 nTPM
- medulla oblongata: 20 nTPM
- pons: 20 nTPM
- thalamus: 20 nTPM
- midbrain: 20 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)
- 1.19
- gnomAD pLI
- 0
- gnomAD missense Z
- -1.47
- DepMap mean gene effect
- -0.03
- DepMap dependency class
- none
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
Molecular functions
- metal ion binding
- RNA binding
- tRNA-specific adenosine deaminase activity
- tRNA-specific adenosine-37 deaminase activity
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ADAT1 as an antibody target. Whether an autoantibody or antibody against ADAT1 could matter depends on whether native ADAT1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ADAT1 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 ADAT1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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