COMT


Summary: Catechol-O-methyltransferase catalyzes the transfer of a methyl group from S-adenosylmethionine to catecholamines, including the neurotransmitters dopamine, epinephrine, and norepinephrine. This O-methylation results in one of the major degradative pathways of the catecholamine transmitters. In addition to its role in the metabolism of endogenous substances, COMT is important in the metabolism of catechol drugs used in the treatment of hypertension, asthma, and Parkinson disease. COMT is found in two forms in tissues, a soluble form (S-COMT) and a membrane-bound form (MB-COMT). The differences between S-COMT and MB-COMT reside within the N-termini. Several transcript variants are formed through the use of alternative translation initiation sites and promoters. [provided by RefSeq, Sep 2008].

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Name
OMIM ID
Ensembl ID
HGNC ID
PHARMGKB ID
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GO terms in COMT


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Term Type
Evidence Type
GO Term ID
GO Des.
MF IEA GO:0000287 magnesium ion binding
MF IPI GO:0005515 protein binding
MF TAS GO:0008168 methyltransferase activity
MF IBA GO:0008171 O-methyltransferase activity
MF TAS GO:0008171 O-methyltransferase activity
MF IBA GO:0016206 catechol O-methyltransferase activity
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Gene expression in normal tissue: COMT

Gene-model tissue-cancer distribution: Bubble Plot

undefinetissue: undefine cancer: undefined model num: 0undefinedtissue: undefined cancer: PANCAN model num: 2

Gene-drug pathway distribution

ERK MAPK signaling1Metabolism1

Pathways in COMT


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Database
Pathway ID
Pathway Des.
reactome R-HSA-112311 Neurotransmitter clearance
reactome R-HSA-112315 Transmission across Chemical Synapses
reactome R-HSA-112316 Neuronal System
reactome R-HSA-1430728 Metabolism
reactome R-HSA-156580 Phase II - Conjugation of compounds
reactome R-HSA-156581 Methylation
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Gene-Drug: Aster Plot


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Drug ID
Drug Name
Model Num.
iGMDRD185 DMOG 1
iGMDRD353 PD0325901 1
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in COMT

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Model
Level
Reference ID
Tissue
Cancer
Drug
Clinical Response
Source
No matching records found

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