TAF1A
TATA box-binding protein-associated factor RNA polymerase I subunit A
Also known as: SL1, TAF1A_HUMAN, TAFI48
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q15573
- Gene
- TAF1A
- Ensembl
- ENSG00000143498
- Chromosome
- 1
- Canonical length
- 450 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
This gene encodes a subunit of the RNA polymerase I complex, Selectivity Factor I (SLI). The encoded protein is a TATA box-binding protein-associated factor that plays a role in the assembly of the RNA polymerase I preinitiation complex. Alternate splicing results in multiple transcript variants encoding multiple isoforms.[provided by RefSeq, Jan 2011]
Canonical amino-acid sequenceUniProt
450 residues, UniProt reviewed canonical sequence.
>Q15573|TAF1A
1 MSDFSEELKG PVTDDEEVET SVLSGAGMHF PWLQTYVETV AIGGKRRKDF AQTTSACLSF
61 IQEALLKHQW QQAAEYMYSY FQTLEDSDSY KRQAAPEIIW KLGSEILFYH PKSNMESFNT
121 FANRMKNIGV MNYLKISLQH ALYLLHHGML KDAKRNLSEA ETWRHGENTS SREILINLIQ
181 AYKGLLQYYT WSEKKMELSK LDKDDYAYNA VAQDVFNHSW KTSANISALI KIPGVWDPFV
241 KSYVEMLEFY GDRDGAQEVL TNYAYDEKFP SNPNAHIYLY NFLKRQKAPR SKLISVLKIL
301 YQIVPSHKLM LEFHTLLRKS EKEEHRKLGL EVLFGVLDFA GCTKNITAWK YLAKYLKNIL
361 MGNHLAWVQE EWNSRKNWWP GFHFSYFWAK SDWKEDTALA CEKAFVAGLL LGKGCRYFRY
421 ILKQDHQILG KKIKRMKRSV KKYSIVNPRLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TAF1A 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)
- 0.31
- Highest tissue expression
- 6 nTPM
Expression across tissuesHPA
Tissue
- lymph node: 6 nTPM
- testis: 5.9 nTPM
- ovary: 5.2 nTPM
- tonsil: 5.2 nTPM
- urinary bladder: 4.9 nTPM
- thyroid gland: 4.7 nTPM
Single-cell type
- gastric progenitor cells: 23 nCPM
- lactotrophs: 20 nCPM
- oocytes: 18 nCPM
- somatotrophs: 18 nCPM
- foveolar cells: 17 nCPM
- microglia: 17 nCPM
Immune cell
- naive B-cell: 7.3 nTPM
- memory B-cell: 5.2 nTPM
- plasmacytoid DC: 5.2 nTPM
- MAIT T-cell: 4.7 nTPM
- naive CD8 T-cell: 4.1 nTPM
- naive CD4 T-cell: 3.3 nTPM
Brain region
- white matter: 6.6 nTPM
- hypothalamus: 6.4 nTPM
- medulla oblongata: 5.8 nTPM
- cerebellum: 5.3 nTPM
- pons: 5.3 nTPM
- basal ganglia: 4.9 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
- gnomAD pLI
- 0
- gnomAD missense Z
- 1
- DepMap mean gene effect
- -0.74
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 8% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- TATA box-binding protein-associated factor RNA polymerase I subunit A, chordata
- TATA box-binding protein-associated factor RNA polymerase I subunit A
- SL1/TIF-IB Complex Component
- TAF RNA Polymerase I subunit A
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TAF1A 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 TAF1A as an antibody target. Whether an autoantibody or antibody against TAF1A could matter depends on whether native TAF1A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TAF1A 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 TAF1A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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