SULT1A3 - sulfotransferase family 1A member 3 Gene
Also Known as STM; HAST; HAST3; M-PST; ST1A3; ST1A4; ST1A5; TL-PST; ST1A3/ST1A4
Species: Homo sapiens
About SULT1A3
This gene has 10 transcripts (splice variants), 759 orthologues and 12 paralogues. Broad expression in duodenum (RPKM 134.6), small intestine (RPKM 93.8) and 23 other tissues.
Summary
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 a phenol sulfotransferase with thermolabile enzyme activity. Four sulfotransferase genes are located on the p arm of chromosome 16; this gene and SULT1A4 arose from a segmental duplication. This gene is the most centromeric of the four sulfotransferase genes. Read-through transcription exists between this gene and the upstream SLX1A (SLX1 structure-specific Endonuclease subunit homolog A) gene that encodes a protein containing GIY-YIG domains. [provided by RefSeq, Nov 2010]
SULT1A3 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_177552.4 | NP_808220.1 | sulfotransferase 1A3 |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables amine sulfotransferase activity |
IDA
IDA: Inferred from direct assay
|
23207770 | GOA |
| enables aryl sulfotransferase activity |
IMP
IMP: Inferred from mutant phenotype
|
9855620 | GOA |
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
25416956 | GOA |
| enables sulfate binding |
IDA
IDA: Inferred from direct assay
|
10543947 | GOA |
| enables sulfotransferase activity |
IDA
IDA: Inferred from direct assay
|
20056724 | GOA |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| involved in 3'-phosphoadenosine 5'-phosphosulfate metabolic process |
IDA
IDA: Inferred from direct assay
|
23207770 | GOA |
| involved in cellular response to dopamine |
IMP
IMP: Inferred from mutant phenotype
|
24136195 | GOA |
| involved in dopamine catabolic process |
IDA
IDA: Inferred from direct assay
|
23207770 | GOA |
| involved in dopamine metabolic process |
IMP
IMP: Inferred from mutant phenotype
|
24136195 | GOA |
| involved in ethanol catabolic process |
IDA
IDA: Inferred from direct assay
|
23207770 | GOA |
| involved in flavonoid metabolic process |
IDA
IDA: Inferred from direct assay
|
20056724 | GOA |
| involved in sulfation |
IDA
IDA: Inferred from direct assay
|
20056724 | GOA |
| involved in xenobiotic metabolic process |
IDA
IDA: Inferred from direct assay
|
20056724 | GOA |
SULT1A3 Protein Structure
Sulfotransfer_1: Sulfotransferase domain (38 - 287)
- 0
- 100
- 200
- 295 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
sulfotransferase 1A3 |
|
SULT1A3 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
SULT1A3 | P0DMM9 | SHMT1 | Homo sapiens | P34896 | 25416956 | |
|
Intra
|
SULT1A3 | P0DMM9 | SHMT1 | Homo sapiens | P34896 | 25416956 | |
|
Intra
|
SULT1A3 | P0DMM9 | NIF3L1 | Homo sapiens | Q9GZT8 | 25416956 | |
|
Intra
|
SULT1A3 | P0DMM9 | NIF3L1 | Homo sapiens | Q9GZT8 | 25416956 | |
|
Intra
|
SULT1A3 | P0DMM9 | NIF3L1 | Homo sapiens | Q9GZT8 | 25416956 | |
|
Intra
|
SULT1A3 | P0DMM9 | KHDRBS2 | Homo sapiens | Q5VWX1 | 25416956 |
Recombinant SULT1A3 Proteins
| Cat. No. | Product Name | Accession | Purity |
|---|---|---|---|
| HY-P71341 | SULT1A3 Protein, Human (His, solution) | P0DMM9-1 (M1-L295) | ≥ 95%, as determined by reducing SDS-PAGE. |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Dengue Shock Syndrome |
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| Epilepsy, Idiopathic Generalized 2 |
|
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| Antiphospholipid Syndrome |
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| Pyometritis |
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| Stroke, Ischemic |
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| Vasculitis |
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| Hepatic Veno-Occlusive Disease |
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| Dengue Disease |
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| Median Neuropathy |
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| Ceroid Lipofuscinosis, Neuronal, 3 |
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| Cardiovascular System Disease |
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| Pulmonary Hypertension |
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| Systemic Lupus Erythematosus |
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| Malaria |
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| Myocardial Infarction |
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| Type 2 Diabetes Mellitus |
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| Hypertension, Essential |
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