TADA1
Transcriptional adapter 1
Also known as: ADA1, hADA1, HFI1, STAF42, TADA1_HUMAN, TADA1L
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96BN2
- Gene
- TADA1
- Ensembl
- ENSG00000152382
- Chromosome
- 1
- Canonical length
- 335 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Focal adhesion sites,Cytosol
OverviewNCBI Gene
TADA1L is a protein subunit of the human STAGA complex (SPT3; (MIM 602947)/TAF9 (MIM 600822)/GCN5 (MIM 602301) acetyltransferase complex), which is a chromatin-modifying multiprotein complex (Martinez et al., 2001 [PubMed 11564863]).[supplied by OMIM, Apr 2009]
Canonical amino-acid sequenceUniProt
335 residues, UniProt reviewed canonical sequence.
>Q96BN2|TADA1
1 MATFVSELEA AKKNLSEALG DNVKQYWANL KLWFKQKISK EEFDLEAHRL LTQDNVHSHN
61 DFLLAILTRC QILVSTPDGA GSLPWPGGSA AKPGKPKGKK KLSSVRQKFD HRFQPQNPLS
121 GAQQFVAKDP QDDDDLKLCS HTMMLPTRGQ LEGRMIVTAY EHGLDNVTEE AVSAVVYAVE
181 NHLKDILTSV VSRRKAYRLR DGHFKYAFGS NVTPQPYLKN SVVAYNNLIE SPPAFTAPCA
241 GQNPASHPPP DDAEQQAALL LACSGDTLPA SLPPVNMYDL FEALQVHREV IPTHTVYALN
301 IERIITKLWH PNHEELQQDK VHRQRLAAKE GLLLCLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TADA1 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)
- 0.46
- Highest tissue expression
- 25 nTPM
Expression across tissuesHPA
Tissue
- liver: 25 nTPM
- bone marrow: 18 nTPM
- retina: 16 nTPM
- cerebral cortex: 14 nTPM
- thymus: 12 nTPM
- cerebellum: 12 nTPM
Single-cell type
- oocytes: 46 nCPM
- cone photoreceptor cells: 35 nCPM
- hepatocytes: 33 nCPM
- myonuclei: 27 nCPM
- gonadotrophs: 25 nCPM
- epicardial cells: 25 nCPM
Immune cell
- naive CD4 T-cell: 28 nTPM
- NK-cell: 28 nTPM
- total PBMC: 25 nTPM
- memory CD8 T-cell: 24 nTPM
- T-reg: 24 nTPM
- MAIT T-cell: 23 nTPM
Brain region
- white matter: 17 nTPM
- basal ganglia: 15 nTPM
- cerebral cortex: 14 nTPM
- cerebellum: 14 nTPM
- hypothalamus: 13 nTPM
- spinal cord: 13 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)
- 0.6
- gnomAD pLI
- 0.09
- gnomAD missense Z
- 0.8
- DepMap mean gene effect
- -0.12
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 14% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- positive regulation of DNA-templated transcription
- regulation of DNA repair
- regulation of RNA splicing
- regulation of transcription by RNA polymerase II
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Transcriptional coactivator Hfi1/Transcriptional adapter 1
- Transcriptional regulator of RNA polII, SAGA, subunit
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TADA1 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 TADA1 as an antibody target. Whether an autoantibody or antibody against TADA1 could matter depends on whether native TADA1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TADA1 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 TADA1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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