Target type: molecularfunction
Catalysis of the transfer of a sulfate group from 3'-phosphoadenosine 5'-phosphosulfate to the hydroxyl group of an acceptor, producing the sulfated derivative and 3'-phosphoadenosine 5'-phosphate. [GOC:curators]
Sulfotransferase activity is a crucial biochemical process that involves the transfer of a sulfonate group (SO3-) from a donor molecule, typically 3'-phosphoadenosine 5'-phosphosulfate (PAPS), to an acceptor molecule. This process is catalyzed by a family of enzymes known as sulfotransferases.
Sulfotransferases play a vital role in various cellular processes, including detoxification, signal transduction, and the biosynthesis of bioactive compounds.
**Detoxification:** Sulfotransferases contribute to detoxification by converting harmful substances, such as xenobiotics (foreign chemicals), into more water-soluble forms, facilitating their excretion.
**Signal Transduction:** Sulfotransferases modify signaling molecules, such as hormones and neurotransmitters, influencing their activity and duration of action. For instance, sulfotransferases regulate the activity of steroid hormones, influencing their signaling pathways.
**Biosynthesis of Bioactive Compounds:** Sulfotransferases are involved in the synthesis of various bioactive compounds, including bile acids, heparin, and chondroitin sulfate. These compounds play essential roles in digestion, blood coagulation, and connective tissue structure, respectively.
The molecular mechanism of sulfotransferase activity involves a two-step reaction:
1. **Binding of both PAPS and the acceptor molecule to the enzyme's active site.** This binding event brings the donor and acceptor molecules into close proximity, facilitating the transfer reaction.
2. **Transfer of the sulfonate group from PAPS to the acceptor molecule.** This transfer is a nucleophilic attack, where the acceptor molecule's nucleophile attacks the sulfonate group on PAPS, resulting in the formation of a sulfoconjugate and adenosine 3',5'-bisphosphate (PAP).
The specificity of sulfotransferases for their substrates is determined by the amino acid residues lining their active sites. These residues interact with the substrate molecules, facilitating their binding and promoting the transfer reaction.
Sulfotransferases are essential enzymes involved in various biological processes, making them key players in maintaining cellular homeostasis and organismal health. Their activity is tightly regulated by factors such as substrate concentration, pH, and cofactor availability.'
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Protein | Definition | Taxonomy |
---|---|---|
Sulfotransferase 2A1 | A sulfotransferase 2A1 that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q06520] | Homo sapiens (human) |
Sulfotransferase 1A1 | A sulfotransferase 1A1 that is encoded in the genome of human. [PRO:DNx, UniProtKB:P50225] | Homo sapiens (human) |
Sulfotransferase 1E1 | A sulfotransferase 1E1 that is encoded in the genome of human. [PRO:DNx, UniProtKB:P49888] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
amoxapine | amoxapine : A dibenzooxazepine compound having a chloro substituent at the 2-position and a piperazin-1-yl group at the 11-position. Amoxapine: The N-demethylated derivative of the antipsychotic agent LOXAPINE that works by blocking the reuptake of norepinephrine, serotonin, or both; it also blocks dopamine receptors. Amoxapine is used for the treatment of depression. | dibenzooxazepine | adrenergic uptake inhibitor; antidepressant; dopaminergic antagonist; geroprotector; serotonin uptake inhibitor |
protriptyline | Protriptyline: Tricyclic antidepressant similar in action and side effects to IMIPRAMINE. It may produce excitation. | carbotricyclic compound | antidepressant |
ethinyl estradiol | 17alpha-ethynylestradiol : A 3-hydroxy steroid that is estradiol substituted by a ethynyl group at position 17. It is a xenoestrogen synthesized from estradiol and has been shown to exhibit high estrogenic potency on oral administration. Ethinyl Estradiol: A semisynthetic alkylated ESTRADIOL with a 17-alpha-ethinyl substitution. It has high estrogenic potency when administered orally, and is often used as the estrogenic component in ORAL CONTRACEPTIVES. | 17-hydroxy steroid; 3-hydroxy steroid; terminal acetylenic compound | xenoestrogen |
2-naphthol | 2-naphthol : A naphthol carrying a hydroxy group at position 2. 2-naphthol: RN given refers to parent cpd naphthols : Any hydroxynaphthalene derivative that has a single hydroxy substituent. | naphthol | antinematodal drug; genotoxin; human urinary metabolite; human xenobiotic metabolite; mouse metabolite; radical scavenger |
5-hydroxyindole | hydroxyindoles | human metabolite | |
6-hydroxybenzothiazole | |||
6-hydroxyindole | 6-hydroxyindole: structure in first source | ||
4-hydroxytoremifene | 4-hydroxytoremifene: metabolite of toremifene; RN refers to (Z)-isomer; structure in first source | ||
5-hydroxybenzimidazole | 5-hydroxybenzimidazole : A member of the class of benzimidazoles that is 1H-benzimidazole carrying a single hydroxy substituent at position 5. 5-hydroxybenzimidazole: only base detected in cobamide cpds from methanol-grown Methanosarcina barkeri | benzimidazoles; phenols | bacterial metabolite; human metabolite; rat metabolite |
2-(4'-(methylamino)phenyl)-6-hydroxybenzothiazole |