4.3.1.2: methylaspartate ammonia-lyase
This is an abbreviated version!
For detailed information about methylaspartate ammonia-lyase, go to the full flat file.
Word Map on EC 4.3.1.2
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4.3.1.2
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seizure
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grand
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epilepsy
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petit
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children
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convulsion
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pain
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discharge
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anticonvulsant
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photodynamic
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myoclonic
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woman
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electroencephalograph
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allergen
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aminolevulinate
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antiepileptic
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wave
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awaken
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palmoplantar
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diazepam
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phenytoin
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tonic-clonic
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arcuate
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celiac
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cream
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rehabilitation
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hemiparesis
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consciousness
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carbamazepine
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ligament
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paroxysm
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birch
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epilepticus
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seizure-free
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electroshock
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clonazepam
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jerk
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psychogenic
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analysis
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reoviridae
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ictal
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keratoses
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trif
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maackia
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amurensis
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interictal
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clonic
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synthesis
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biotechnology
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diphenylhydantoin
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sway
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daylight
-
wolf
- 4.3.1.2
- seizure
-
grand
- epilepsy
-
petit
- children
- convulsion
- pain
- discharge
-
anticonvulsant
-
photodynamic
-
myoclonic
- woman
-
electroencephalograph
- allergen
-
aminolevulinate
-
antiepileptic
-
wave
-
awaken
-
palmoplantar
- diazepam
- phenytoin
-
tonic-clonic
-
arcuate
-
celiac
-
cream
-
rehabilitation
- hemiparesis
- consciousness
- carbamazepine
-
ligament
-
paroxysm
- birch
- epilepticus
-
seizure-free
-
electroshock
- clonazepam
- jerk
-
psychogenic
- analysis
- reoviridae
-
ictal
- keratoses
- trif
-
maackia
- amurensis
-
interictal
-
clonic
- synthesis
- biotechnology
- diphenylhydantoin
-
sway
-
daylight
- wolf
Reaction
Synonyms
3-methyl-L-aspartic acid ammonia-lyase, 3-methylaspartase, 3-methylaspartate ammonia lyase, 3-methylaspartate ammonia-lyase, ammonia-lyase, methylaspartate, beta-methylaspartase, Ch-MAL, MAL, methylaspartate ammonia lyase, methylaspartate ammonia-lyase, threo-3-methyl-L-aspartate ammonia-lyase, threo-3-methylaspartase ammonia-lyase
ECTree
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Application
Application on EC 4.3.1.2 - methylaspartate ammonia-lyase
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analysis
biotechnology
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Fusobacterium varium can simultaneously utilize both glucose and L-glutamate as energy sources, intracellular concentrations of methylaspartate ammonia-lyase is elevated when the bacterium is cultured in media supplemented with excess L-glutamate
synthesis
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a marker enzyme of the mesaconate pathway for (S)-glutamate fermentation in Enterobacteriaceae
analysis
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a marker enzyme of the mesaconate pathway for (S)-glutamate fermentation in Enterobacteriaceae
analysis
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a marker enzyme of the mesaconate pathway for (S)-glutamate fermentation in Enterobacteriaceae
analysis
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a marker enzyme of the mesaconate pathway for (S)-glutamate fermentation in Enterobacteriaceae
analysis
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a marker enzyme of the mesaconate pathway for (S)-glutamate fermentation in Enterobacteriaceae
analysis
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procedure for the synthesis of mesaconic acids that are specifically mono- or di-deuterated in the methyl group in order to investigate the mechanisms of enzyme-catalyzed reactions
analysis
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a marker enzyme of the mesaconate pathway for (S)-glutamate fermentation in Enterobacteriaceae
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analysis
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a marker enzyme of the mesaconate pathway for (S)-glutamate fermentation in Enterobacteriaceae
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analysis
-
a marker enzyme of the mesaconate pathway for (S)-glutamate fermentation in Enterobacteriaceae
-
analysis
-
a marker enzyme of the mesaconate pathway for (S)-glutamate fermentation in Enterobacteriaceae
-
analysis
-
a marker enzyme of the mesaconate pathway for (S)-glutamate fermentation in Enterobacteriaceae
-
analysis
-
a marker enzyme of the mesaconate pathway for (S)-glutamate fermentation in Enterobacteriaceae
-
analysis
-
a marker enzyme of the mesaconate pathway for (S)-glutamate fermentation in Enterobacteriaceae
-
analysis
-
a marker enzyme of the mesaconate pathway for (S)-glutamate fermentation in Enterobacteriaceae
-
analysis
-
a marker enzyme of the mesaconate pathway for (S)-glutamate fermentation in Enterobacteriaceae
-
analysis
-
a marker enzyme of the mesaconate pathway for (S)-glutamate fermentation in Enterobacteriaceae
-
analysis
-
a marker enzyme of the mesaconate pathway for (S)-glutamate fermentation in Enterobacteriaceae
-
synthesis
starting from simple non-chiral dicarboxylic acids (either fumaric acid or mesaconic acid), vitamin B5 and both diastereoisomers of alpha-methyl-substituted vitamin B5, which are valuable precursors for promising antimicrobials against Plasmodium falciparum and multidrug-resistant Staphylococcus aureus, can be generated in good yields (up to 70%) and excellent enantiopurity (>99% ee). Access to vitamin B5 ((R)-pantothenic acid) and both diastereoisomers of alpha-methyl-substituted vitamin B5 ((R)- and (S)-3-((R)-2,4-dihydroxy-3,3-dimethylbutanamido)-2-methylpropanoic acid) is achieved using a modular three-step biocatalytic cascade involving 3-methylaspartate ammonia lyase (MAL), aspartate-a-decarboxylase (ADC), beta-methylaspartate-alpha-decarboxylase (CrpG) or glutamate decarboxylase (GAD), and pantothenate synthetase (PS) enzymes