O-methyltransferase: Difference between revisions
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'''O-methyltransferase''' | {{Infobox enzyme | ||
| name = O-methyltransferase | |||
| image = <!-- Image removed --> | |||
| width = | |||
| caption = | |||
| EC_number = 2.1.1.6 | |||
| CAS_number = 9030-79-1 | |||
| IUBMB_EC_number = 2/1/1/6 | |||
| GO_code = 0008171 | |||
}} | |||
'''O-methyltransferase''' is an [[enzyme]] that catalyzes the transfer of a [[methyl group]] from [[S-adenosyl methionine]] (SAM) to a substrate, resulting in the methylation of the substrate. This enzyme is involved in various [[biochemical pathways]] and plays a crucial role in the [[metabolism]] of [[xenobiotics]], [[hormones]], and [[neurotransmitters]]. | |||
== Function == | == Function == | ||
O-methyltransferases are responsible for the [[methylation]] of [[hydroxyl]] groups on [[catecholamines]], [[phenols]], and other compounds. This process is essential for the [[inactivation]] and [[elimination]] of these compounds from the body. For example, the methylation of [[catecholamines]] such as [[dopamine]], [[epinephrine]], and [[norepinephrine]] is a key step in their [[metabolic degradation]]. | |||
O-methyltransferases | == Types == | ||
There are several types of O-methyltransferases, each with specific substrate preferences: | |||
* '''Catechol-O-methyltransferase''' (COMT) - involved in the methylation of catecholamines and catechol estrogens. | |||
* '''Phenol-O-methyltransferase''' (POMT) - involved in the methylation of phenolic compounds. | |||
== | == Clinical Significance == | ||
O-methyltransferases have significant clinical implications. For instance, variations in the [[COMT gene]] can affect the [[metabolism]] of [[neurotransmitters]] and influence [[neurological disorders]] such as [[schizophrenia]], [[bipolar disorder]], and [[Parkinson's disease]]. | |||
== See Also == | |||
* [[Methylation]] | |||
== | * [[Enzyme]] | ||
* [[ | |||
* [[S-adenosyl methionine]] | * [[S-adenosyl methionine]] | ||
* [[ | * [[Catecholamine]] | ||
== References == | == References == | ||
{{Reflist}} | |||
== External Links == | |||
* [https://www.wikimd.com/wiki/O-methyltransferase O-methyltransferase on WikiMD] | |||
[[Category:Enzymes]] | [[Category:Enzymes]] | ||
[[Category: | [[Category:Methylation]] | ||
[[Category: | [[Category:Metabolism]] | ||
[[Category:Biochemistry]] | [[Category:Biochemistry]] | ||
Latest revision as of 20:31, 30 December 2024
O-methyltransferase
O-methyltransferase is an enzyme that catalyzes the transfer of a methyl group from S-adenosyl methionine (SAM) to a substrate, resulting in the methylation of the substrate. This enzyme is involved in various biochemical pathways and plays a crucial role in the metabolism of xenobiotics, hormones, and neurotransmitters.
Function[edit]
O-methyltransferases are responsible for the methylation of hydroxyl groups on catecholamines, phenols, and other compounds. This process is essential for the inactivation and elimination of these compounds from the body. For example, the methylation of catecholamines such as dopamine, epinephrine, and norepinephrine is a key step in their metabolic degradation.
Types[edit]
There are several types of O-methyltransferases, each with specific substrate preferences:
- Catechol-O-methyltransferase (COMT) - involved in the methylation of catecholamines and catechol estrogens.
- Phenol-O-methyltransferase (POMT) - involved in the methylation of phenolic compounds.
Clinical Significance[edit]
O-methyltransferases have significant clinical implications. For instance, variations in the COMT gene can affect the metabolism of neurotransmitters and influence neurological disorders such as schizophrenia, bipolar disorder, and Parkinson's disease.
See Also[edit]
References[edit]
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