Target intelligence / Profile preview

Methionine biosynthesis enzyme

Molecular classification
Enzyme, Methyltransferase, Lyase, Synthase, Transferase
01

Overview

Methionine biosynthesis enzymes catalyze the sequential transformation of metabolic precursors (starting from aspartate in bacteria and plants) to ultimately produce methionine, a crucial amino acid for protein synthesis and as a methyl group donor through the S-adenosylmethionine cycle[1][3][5][7]. Key enzymes in the pathway include aspartokinase, homoserine dehydrogenase, homoserine O-transsuccinylase, cystathionine γ-synthase, cystathionine β-lyase, and methionine synthase. Methionine synthase exists in cobalamin-dependent and cobalamin-independent forms, further differentiating the pathway in different organisms[1][3]. As vertebrates lack the full *de novo* biosynthesis pathway, these enzymes are attractive targets for antimicrobials—disruption impairs pathogen growth and virulence by preventing methionine synthesis[7]. The pathway is highly conserved in microbes, and its critical role in metabolism underpins broad impacts on growth, translation, and epigenetic regulation through methylation[2][4]. *Note*: For structured data, it is recommended to use specific enzyme names (e.g., "Methionine synthase") rather than the generic pathway name[3][7].

Other names
Methionine biosynthetic pathway enzymesMet biosynthesis enzymesMethionine synthaseCystathionine γ-synthaseAspartokinase
02

Mechanism of action

Inhibition of enzyme activity leading to depletion of methionine, impaired protein synthesis and methylation Disruption of S-adenosylmethionine (SAM)–dependent pathways

03

Biological functions

Amino acid biosynthesis (methionine)Methyl group transfer/S-adenosylmethionine (SAM) cycleRegulation of cellular metabolism and anabolic signalingInitiation of protein synthesis (methionine as start codon)
04

Disease associations

Infection (antimicrobial target in bacteria)Disruption may affect bacterial virulenceNot directly relevant to cancer, inflammation, etc., but pathway has epigenetic impact through SAM cycle
05

Safety considerations

Human safety challenges limited—humans do not have *de novo* methionine biosynthesis enzymesSpecificity against bacterial targets is important to avoid microbiome disruption and resistancePossible off-target effects in non-pathogenic microbes in the human gut
06

Interacting drugs

No widely used approved drugs directly target these enzymes in clinical medicine

2 more in the full profile.

07

Biomarkers

None specifically established for human therapeuticsMethionine or SAM levels may be used in research as biomarkers for metabolic activity

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