Target intelligence / Profile preview

Methionine metabolism pathway (null)

Target
null
Molecular classification
Other (biochemical pathway encompassing multiple enzymes), Enzyme (for individual components: e.g. Methionine adenosyltransferase, methionine synthase, S-adenosylhomocysteine hydrolase, methyltransferases)
01

Overview

The methionine metabolism pathway is an essential biochemical system responsible for the utilization, recycling, and transformation of methionine, a sulfur-containing amino acid critical for protein synthesis, methylation reactions, redox balance, and cellular signaling. The pathway comprises the methionine cycle (in which methionine is converted to S-adenosylmethionine, the universal methyl donor), transsulfuration (providing cysteine for glutathione and taurine synthesis), and various salvage and recycling steps. Key enzymes include methionine adenosyltransferase, methionine synthase, and S-adenosylhomocysteine hydrolase. Defects or dysregulation in methionine metabolism are implicated in cancer, cardiovascular disease, chronic liver disease, neurodegeneration, and aging. While not itself a classic drug target, the pathway is modulated by drugs and supplements that affect methionine, methylation, homocysteine, and related metabolites.

Other names
Methionine cycleOne-carbon metabolismTransmethylation pathwayMethionine salvage pathway
02

Mechanism of action

Inhibition of methyltransferases (block DNA/histone/protein methylation); Inhibition of methionine adenosyltransferase (affects SAM production); Promotion of homocysteine clearance (cardiovascular protective effects); Supplementation of methyl donors (restores methylation capacity, e.g., betaine or folate).

03

Biological functions

Methylation (DNA, protein, lipid methylation via S-adenosylmethionine)Protein synthesis initiation (methionine as initiator amino acid)Polyamine biosynthesisRedox balance (via glutathione synthesis through transsulfuration pathway)Epigenetic regulation (histone methylation, chromatin remodeling)Cell growth and proliferation (via mTOR sensing and translation regulation)
04

Disease associations

Cancer (altered methionine metabolism, methylation, homocystinuria, glutathione biosynthesis defects)Chronic liver disease (methionine cycle disruption, use in disease models)Cardiovascular disease (homocysteine accumulation)Neurodegenerative disease (homocysteine and methylation-related pathways)Other (aging, lifespan regulation, immune modulation)
05

Safety considerations

Risk of hypermethioninemia (excess methionine can be toxic)Hyperhomocysteinemia (risk factor for cardiovascular and neurodegenerative diseases)Liver toxicity (with impaired methionine metabolism, seen in certain genetic disorders and chronic liver diseases)Methylation imbalance (leading to unwarranted gene silencing or activation in cancer and other diseases)
06

Interacting drugs

Methotrexate (inhibits folate cycle, affecting methionine recycling)

3 more in the full profile.

07

Biomarkers

Homocysteine plasma levels (marker for cardiovascular and metabolic risk)S-adenosylmethionine (SAM) / S-adenosylhomocysteine (SAH) ratio (epigenetic and methylation status)Glutathione (GSH/GSSG ratio, redox status)

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