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Literature summary for 2.5.1.18 extracted from

  • Shroads, A.L.; Coats, B.S.; Langaee, T.; Shuster, J.J.; Stacpoole, P.W.
    Chloral hydrate, through biotransformation to dichloroacetate, inhibits maleylacetoacetate isomerase and tyrosine catabolism in humans (2015), Drug Metab. Pers. Ther., 30, 49-55 .
    View publication on PubMedView publication on EuropePMC

Application

Application Comment Organism
medicine dichloroacetate, a degradation product of chloral hydrate, is further metabolized by glutathione transferase zeta 1, and inhibits its own metabolism through depletion/inactivation of GSTZ1/MAAI with repeated exposure, resulting in lower plasma clearance of the drug and the accumulation of the urinary biomarker maleylacetone. The amount of dichloroacetate produced from clinically relevant doses of chloral hydrate, although insufficient to alter dichloroacetate kinetics, is sufficient to inhibit MAAI and tyrosine catabolism Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens O43708 bifunctional enzyme, catalyzes reactions of maleylacetoacetate isomerase, EC 5.2.1.2 and of EC 2.5.1.18
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Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
dichloroacetate + glutathione
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Homo sapiens 2-(glutathion-S-yl)-chloroacetate + HCl
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Synonyms

Synonyms Comment Organism
glutathione transferase zeta 1
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Homo sapiens
Gstz1
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Homo sapiens
MAAI
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Homo sapiens
More maleylacetoacetate isomerase, EC 5.2.1.2, bifunctional enzyme Homo sapiens