SULT1B1
Sulfotransferase 1B1
Also known as: ST1B1_HUMAN, ST1B2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O43704
- Gene
- SULT1B1
- Ensembl
- ENSG00000173597
- Chromosome
- 4
- Canonical length
- 296 aa
- Protein class
- Enzymes, Metabolic proteins, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Golgi apparatus
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. However, the total genomic length of this gene is greater than that of other SULT1 genes. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
296 residues, UniProt reviewed canonical sequence.
>O43704|SULT1B1
1 MLSPKDILRK DLKLVHGYPM TCAFASNWEK IEQFHSRPDD IVIATYPKSG TTWVSEIIDM
61 ILNDGDIEKC KRGFITEKVP MLEMTLPGLR TSGIEQLEKN PSPRIVKTHL PTDLLPKSFW
121 ENNCKMIYLA RNAKDVSVSY YHFDLMNNLQ PFPGTWEEYL EKFLTGKVAY GSWFTHVKNW
181 WKKKEEHPIL FLYYEDMKEN PKEEIKKIIR FLEKNLNDEI LDRIIHHTSF EVMKDNPLVN
241 YTHLPTTVMD HSKSPFMRKG TAGDWKNYFT VAQNEKFDAI YETEMSKTAL QFRTEILocalizationUniProt · AlphaFold · HPA
Whether an antibody against SULT1B1 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)
- 0.22
- Highest tissue expression
- 93 nTPM
Expression across tissuesHPA
Tissue
- duodenum: 93 nTPM
- small intestine: 89 nTPM
- colon: 65 nTPM
- rectum: 58 nTPM
- stomach: 42 nTPM
- liver: 22 nTPM
Single-cell type
- neutrophils: 509 nCPM
- colonocytes: 285 nCPM
- enterocytes: 258 nCPM
- foveolar cells: 163 nCPM
- parietal cells: 113 nCPM
- enteric transient amplifying cells: 94 nCPM
Immune cell
- neutrophil: 32 nTPM
- basophil: 11 nTPM
- naive CD4 T-cell: 4.9 nTPM
- classical monocyte: 4.8 nTPM
- non-classical monocyte: 3.4 nTPM
- NK-cell: 2.9 nTPM
Brain region
- cerebellum: 38 nTPM
- cerebral cortex: 35 nTPM
- white matter: 33 nTPM
- choroid plexus: 30 nTPM
- basal ganglia: 28 nTPM
- hippocampal formation: 28 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)
- 1.31
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.45
- DepMap mean gene effect
- -0.01
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% 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
- biogenic amine metabolic process
- epithelial cell differentiation
- ethanol catabolic process
- flavonoid metabolic process
- phenol-containing compound metabolic process
- sulfation
- thyroid hormone metabolic process
- xenobiotic metabolic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SULT1B1 as an antibody target. Whether an autoantibody or antibody against SULT1B1 could matter depends on whether native SULT1B1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SULT1B1 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 SULT1B1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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