4.4.1.11: methionine gamma-lyase
This is an abbreviated version!
For detailed information about methionine gamma-lyase, go to the full flat file.
Word Map on EC 4.4.1.11
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4.4.1.11
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lipase
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monoacylglycerol
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endocannabinoids
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cannabinoids
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lectin
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putida
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c-type
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2-arachidonoylglycerol
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pyridoxal
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medicine
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monoglyceride
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orthotopic
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galactose-type
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galnac
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selenomethionine
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anandamide
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freundii
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2-arachidonoyl
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citrobacter
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alpha-ketobutyrate
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methylselenol
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meibomian
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methionine-dependent
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mercaptan
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beta-lyase
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5'-phosphate-dependent
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dc-sign
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s-substituted
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synthesis
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nutrition
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environmental protection
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analysis
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drug development
- 4.4.1.11
- lipase
- monoacylglycerol
-
endocannabinoids
- cannabinoids
- lectin
- putida
-
c-type
- 2-arachidonoylglycerol
- pyridoxal
- medicine
- monoglyceride
-
orthotopic
-
galactose-type
- galnac
- selenomethionine
- anandamide
- freundii
-
2-arachidonoyl
-
citrobacter
- alpha-ketobutyrate
- methylselenol
-
meibomian
-
methionine-dependent
- mercaptan
-
beta-lyase
-
5'-phosphate-dependent
-
dc-sign
-
s-substituted
- synthesis
- nutrition
- environmental protection
- analysis
- drug development
Reaction
Synonyms
CalE6, EhMGL1, EhMGL2, fer1MgL2, Fn1419, L-methionase, L-methioninase, L-methionine gamma-lyase, L-methionine gamma-lyase 1, L-methionine-alpha-deamino-gamma-mercaptomethane lyase, L-methionine-alpha-deamino-gamma-mercaptomethane-lyase, L-methionine-gamma-lyase, lyase, methionine, MdeA, MegL, METase, methioninase, methionine alpha,gamma-lyase, methionine dethiomethylase, methionine gamma-lyase, methionine lyase, methionine-gamma-lyase, MGL, MGL1, MGL2, rMETase, sav7062, TvMGL1, TvMGL2, YtjE
ECTree
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Inhibitors
Inhibitors on EC 4.4.1.11 - methionine gamma-lyase
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L-2-amino-4-chloro-4-pentenoate
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complete inhibition at 5 mol per mol of tetramer enzyme
DL-propargylglycine
inhibition profiles of wild-type and mutant enzymes, overview
glycine
competitive inhibitor, subtle conformational changes provide effective binding of the inhibitor and facilitate labilization of Calpha-protons of the external aldimine, binding structure, overview
L-Cycloserine
inactivation by L-cycloserine is completely reversed by dialysis against potassium phosphate buffer (pH 8.0), containing 0.5 mM PLP and 5 mM dithiothreitol
L-norleucine
Arg374 and Ser339 are involved in the binding of carboxyl groups of the inhibitor, the hydroxyl of Tyr113 is a potential acceptor of a proton from the amino groups of the amino acid
additional information
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recombinant METase alone inhibits the proliferation of 15/15 NB cell lines in vitro in a dose-dependent manner
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