Target type: biologicalprocess
The addition of a sulfate group to a molecule. [Wikipedia:Sulfation]
Sulfation is a critical biological process involving the covalent attachment of a sulfate group (SO4) to a variety of molecules, including proteins, lipids, carbohydrates, and steroids. This process is catalyzed by a family of enzymes known as sulfotransferases, which transfer the sulfate group from a donor molecule, 3'-phosphoadenosine 5'-phosphosulfate (PAPS), to the acceptor molecule.
Sulfation plays a diverse range of roles in cellular function and biological processes. It can:
* **Alter protein structure and function:** Sulfation can modify protein conformation and charge distribution, impacting their activity, stability, and interactions with other molecules.
* **Regulate protein trafficking and localization:** Sulfation can direct proteins to specific cellular compartments, such as the cell surface or lysosomes.
* **Modulate signaling pathways:** Sulfation can influence the activity of signaling molecules, such as growth factors and hormones, by affecting their binding to receptors or their downstream signaling cascades.
* **Protect against oxidative stress:** Sulfation can contribute to the detoxification of reactive oxygen species and protect against oxidative damage.
* **Influence immune responses:** Sulfation plays a role in the regulation of immune cell activation and cytokine production.
* **Modify carbohydrate structure:** Sulfation can alter the structure and properties of carbohydrates, impacting their function in cell adhesion, recognition, and signaling.
* **Influence drug metabolism:** Sulfation can contribute to the metabolism and elimination of drugs from the body.
The specific effects of sulfation depend on the nature of the acceptor molecule and the site of sulfation. For example, sulfation of tyrosine residues in proteins can modulate their binding to protein kinases, while sulfation of carbohydrates can influence their binding to lectins.
Sulfation dysregulation has been implicated in a variety of diseases, including cancer, inflammation, and neurological disorders. Aberrant sulfation patterns can lead to altered protein function, signaling defects, and cellular dysfunction.
In summary, sulfation is a highly versatile and essential biological process that plays a critical role in a wide range of cellular functions and biological processes.'
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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 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 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) |
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 |