4.2.3.3: methylglyoxal synthase
This is an abbreviated version!
For detailed information about methylglyoxal synthase, go to the full flat file.
Word Map on EC 4.2.3.3
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4.2.3.3
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meibomian
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glass
-
film
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tear
-
ocular
-
eyelid
-
gather
-
grading
-
grimace
-
saccade
-
dihydroxyacetone
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mongolian
-
gerbil
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glory
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microgels
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monoglycerides
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dropout
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break-up
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1,2-propanediol
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ductility
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schirmer
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sire
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dhap
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polydactyly
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alloy
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phantom
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corrosion
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microtia
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orifice
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encephalocele
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cdt1
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orc6
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pre-replication
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synthesis
- 4.2.3.3
-
meibomian
-
glass
-
film
- tear
-
ocular
-
eyelid
-
gather
-
grading
-
grimace
-
saccade
- dihydroxyacetone
-
mongolian
- gerbil
-
glory
-
microgels
- monoglycerides
-
dropout
-
break-up
- 1,2-propanediol
-
ductility
-
schirmer
-
sire
- dhap
- polydactyly
-
alloy
-
phantom
-
corrosion
- microtia
-
orifice
- encephalocele
- cdt1
- orc6
-
pre-replication
- synthesis
Reaction
Synonyms
EC 4.2.99.11, methylglyoxal synthase, methylglyoxal synthetase, MGS, MgsA, msgA, synthase, methylglyoxal
ECTree
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Inhibitors
Inhibitors on EC 4.2.3.3 - methylglyoxal synthase
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3-bromoacetol phosphate
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irreversible inactivation by reacting with a nucleophilic group located in the active center, dihydroxyacetone phosphate or phosphate protects
3-iodoacetol phosphate
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irreversible inactivation by reacting with a nucleophilic group located in the active center, dihydroxyacetone phosphate or phosphate protects
Crh protein
in the absence of preferred carbon sources, the phosphoprotein Crh is present in the nonphosphorylated state and binds to and thereby inhibits the enzyme
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Phosphoglycolate
inhibits wild-type enzyme and activates H98Q variant
phosphoglycolohydroxamic acid
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tight binding inhibitor, neither a strictly competitive, non-competitive, nor uncompetitive mechanism
additional information
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no inactivation by iodoacetate or p-mercuribenzoate
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phosphate
acts as competitive inhibitor on the H98Q variant and as an allosteric-type inhibitor on the wild-type enzyme