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  2. Glutathione—homocystine transhydrogenase - Wikipedia

    en.wikipedia.org/wiki/Glutathione—homocystine...

    In enzymology, a glutathione—homocystine transhydrogenase (EC 1.8.4.1) is an enzyme that catalyzes the chemical reaction 2 glutathione + homocystine ⇌ {\displaystyle \rightleftharpoons } glutathione disulfide + 2 homocysteine

  3. Homocysteine - Wikipedia

    en.wikipedia.org/wiki/Homocysteine

    In the body, homocysteine can be recycled into methionine or converted into cysteine with the aid of vitamin B 6, B 9, and B 12. [3] High levels of homocysteine in the blood (hyperhomocysteinemia) is regarded as a marker of cardiovascular disease, likely working through atherogenesis, which can result in ischemic injury.

  4. Glutathione peroxidase 3 - Wikipedia

    en.wikipedia.org/wiki/Glutathione_peroxidase_3

    Glutathione peroxidase 3 (GPx-3), also known as plasma glutathione peroxidase (GPx-P) or extracellular glutathione peroxidase is an enzyme that in humans is encoded by the GPX3 gene. [5] [6] [7] GPx-3 belongs to the glutathione peroxidase family, which functions in the detoxification of

  5. Transsulfuration pathway - Wikipedia

    en.wikipedia.org/wiki/Transsulfuration_pathway

    The reverse transsulfuration pathway depicting the conversion of homocysteine to cysteine in reactions 5 and 6. Reaction 5 is catalyzed by cystathionine beta-synthase while reaction 6 is catalyzed by cystathionine gamma-lyase. The required homocysteine is synthesized from methionine in reactions 1, 2, and 3.

  6. Why Is Everyone Talking About Glutathione? - AOL

    www.aol.com/why-everyone-talking-glutathione...

    Glutathione is also linked to the newly popular NAC, or N-acetyl cysteine supplements. As of late, NAC supplements have become the elixir du jour. Of course, no one supplement is a cure-all, but ...

  7. Homocystinuria - Wikipedia

    en.wikipedia.org/wiki/Homocystinuria

    Homocystinuria (HCU) [2] is an inherited disorder of the metabolism of the amino acid methionine due to a deficiency of cystathionine beta synthase or methionine synthase. [3] It is an inherited autosomal recessive trait, which means a child needs to inherit a copy of the defective gene from both parents to be affected.

  8. S-Adenosyl methionine - Wikipedia

    en.wikipedia.org/wiki/S-Adenosyl_methionine

    This is hydrolysed to homocysteine and adenosine by S-adenosylhomocysteine hydrolase EC 3.3.1.1 and the homocysteine recycled back to methionine through transfer of a methyl group from 5-methyltetrahydrofolate, by one of the two classes of methionine synthases (i.e. cobalamin-dependent (EC 2.1.1.13) or cobalamin-independent (EC 2.1.1.14)).

  9. Cystathionine beta synthase - Wikipedia

    en.wikipedia.org/wiki/Cystathionine_beta_synthase

    Cystathionine-β-synthase, also known as CBS, is an enzyme (EC 4.2.1.22) that in humans is encoded by the CBS gene.It catalyzes the first step of the transsulfuration pathway, from homocysteine to cystathionine: [5]

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