SULT1A2
Sulfotransferase 1A2
Also known as: HAST4, ST1A2_HUMAN, STP2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P50226
- Gene
- SULT1A2
- Ensembl
- ENSG00000197165
- Chromosome
- 16
- Canonical length
- 295 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. These cytosolic enzymes are different in their tissue distributions and substrate specificities. The gene structure (number and length of exons) is similar among family members. This gene encodes one of two phenol sulfotransferases with thermostable enzyme activity. Two alternatively spliced variants that encode the same protein have been described. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
295 residues, UniProt reviewed canonical sequence.
>P50226|SULT1A2
1 MELIQDISRP PLEYVKGVPL IKYFAEALGP LQSFQARPDD LLISTYPKSG TTWVSQILDM
61 IYQGGDLEKC HRAPIFMRVP FLEFKVPGIP SGMETLKNTP APRLLKTHLP LALLPQTLLD
121 QKVKVVYVAR NAKDVAVSYY HFYHMAKVYP HPGTWESFLE KFMAGEVSYG SWYQHVQEWW
181 ELSRTHPVLY LFYEDMKENP KREIQKILEF VGRSLPEETV DLMVEHTSFK EMKKNPMTNY
241 TTVRREFMDH SISPFMRKGM AGDWKTTFTV AQNERFDADY AKKMAGCSLS FRSELLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SULT1A2 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)
- 0.23
- Highest tissue expression
- 49 nTPM
Expression across tissuesHPA
Tissue
- duodenum: 49 nTPM
- liver: 48 nTPM
- small intestine: 45 nTPM
- colon: 13 nTPM
- rectum: 13 nTPM
- lung: 7.2 nTPM
Single-cell type
- enterocytes: 240 nCPM
- colonocytes: 52 nCPM
- epididymal efferent duct absorptive cells: 27 nCPM
- podocytes: 13 nCPM
- hepatocytes: 9.8 nCPM
- enteric transient amplifying cells: 6.9 nCPM
Immune cell
- neutrophil: 15 nTPM
- classical monocyte: 11 nTPM
- intermediate monocyte: 8.7 nTPM
- total PBMC: 5.4 nTPM
- non-classical monocyte: 4.7 nTPM
- myeloid DC: 4.1 nTPM
Brain region
- cerebellum: 6.1 nTPM
- cerebral cortex: 4.8 nTPM
- amygdala: 4.2 nTPM
- hippocampal formation: 4.1 nTPM
- pons: 3.9 nTPM
- basal ganglia: 3.6 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)
- 1.59
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.85
- DepMap mean gene effect
- 0.09
- 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
- 3'-phosphoadenosine 5'-phosphosulfate metabolic process
- catecholamine metabolic process
- ethanol catabolic process
- phenol-containing compound metabolic process
- steroid metabolic process
- sulfation
- xenobiotic metabolic process
- amine biosynthetic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SULT1A2 as an antibody target. Whether an autoantibody or antibody against SULT1A2 could matter depends on whether native SULT1A2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SULT1A2 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 SULT1A2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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