5.2.1.2: maleylacetoacetate isomerase
This is an abbreviated version!
For detailed information about maleylacetoacetate isomerase, go to the full flat file.
Word Map on EC 5.2.1.2
-
5.2.1.2
-
dichloroacetate
-
fumarylacetoacetate
-
dca-induced
-
succinylacetone
-
chlorofluoroacetic
-
homogentisate
-
tyrosinemia
-
medicine
- 5.2.1.2
- dichloroacetate
- fumarylacetoacetate
-
dca-induced
- succinylacetone
-
chlorofluoroacetic
- homogentisate
- tyrosinemia
- medicine
Reaction
Synonyms
AtGSTZ1, AtMAAI, glutathione S-transferase Zeta 1-1, glutathione S-transferase zeta-class 1, glutathione S-transferase zeta/maleylacetoacetate isomerase, glutathione transferase zeta, glutathione transferase zeta 1/maleylacetoacetate isomerase, Gstz1, GSTZ1-1, GSTz1/MAAI, GSTzeta/MAAI, Isomerase, maleylacetoacetate, MAAI, MAc-tI, maleylacetoacetate isomerase, Maleylacetoacetic isomerase, Maleylacetone cis-trans-isomerase, Maleylacetone isomerase, More
ECTree
Advanced search results
Application
Application on EC 5.2.1.2 - maleylacetoacetate isomerase
Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
medicine
additional information
-
knowledge of the GSTz1/MAAI haplotype can be used prospectively to identify individuals at potential risk of dichloroacetates adverse side effects from environmental or clinical exposure or who may exhibit aberrant amino acid metabolism in response to dietary protein
cis and/or trans isomers of 2,4-dioxohept-2-enoic acid might be diagnostic for human deficiency of maleylacetoacetate isomerase
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