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l-DOPA, also known as l-3,4-dihydroxyphenylalanine and used medically as levodopa, is made and used as part of the normal biology of some plants [2] and animals, including humans. Humans, as well as a portion of the other animals that utilize l -DOPA, make it via biosynthesis from the amino acid l -tyrosine .
The long term use of levodopa increases oxidative stress through monoamine oxidase led enzymatic degradation of synthesized dopamine causing neuronal damage and cytotoxicity. The oxidative stress is caused by the formation of reactive oxygen species (H 2 O 2 ) during the monoamine oxidase led metabolism of dopamine.
3,4-dihydroxyphenylalanine oxidative deaminase (EC 1.13.12.15, 3,4-dihydroxy-L-phenylalanine: oxidative deaminase, oxidative deaminase, DOPA oxidative deaminase, DOPAODA) is an enzyme with systematic name 3,4-dihydroxy-L-phenylalanine:oxygen oxidoreductase (deaminating). [1] This enzyme catalyses the following chemical reaction
Dihydroxyphenylalanine may refer to either of two chemical compounds: D -DOPA (R), 3,4-dihydroxyphenylalanine L -DOPA (S), 3,4-dihydroxyphenylalanine, a precursor of a neurotransmitter
Droxidopa, also known as (–)-threo-3-(3,4-dihydroxyphenyl)-L-serine (L-DOPS), is a substituted phenethylamine and is chemically analogous to levodopa (L-3,4-dihydroxyphenylalanine; L-DOPA). Whereas levodopa functions as a precursor and prodrug to dopamine , droxidopa is a precursor and prodrug of norepinephrine .
In enzymology, a dihydroxyphenylalanine transaminase (EC 2.6.1.49) is an enzyme that catalyzes the chemical reaction 3,4-dihydroxy-L-phenylalanine + 2-oxoglutarate ⇌ {\displaystyle \rightleftharpoons } 3,4-dihydroxyphenylpyruvate + L-glutamate
3-O-methyldopa is a major metabolite of L-3,4-dihydroxyphenylalanine (L-DOPA) and is formed by catechol-O-methyltransferase (COMT). One of the L-DOPA's metabolic pathways is the decarboxylation and the other is the O-methylation. L-DOPA has the main role in the metabolic pathway as a metabolite in the biosynthesis of dopamine.
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