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EC Number
Substrates
Commentary Substrates
Organism
Products
Commentary (Products)
Reversibility
4.3.1.7
(2R)-2-aminopropanol
deamination with inversion of configuration
Clostridium sp.
?
-
?
4.3.1.7
(2S)-2-aminopropanol
deamination with retention of configuration
Clostridium sp.
propionaldehyde + ?
-
?
4.3.1.7
(R)-2-aminopropanol
-
Salmonella enterica subsp. enterica serovar Typhimurium
propanal + NH3
-
?
4.3.1.7
(S)-1-amino-2-propanol
inactive substrate analogue, which binds to the substrate binding site in EAL but does not form the cob(II)alamin-substrate radical pair state
Salmonella enterica subsp. enterica serovar Typhimurium
propanal + NH3
-
?
4.3.1.7
(S)-2-aminopropanol
-
Salmonella enterica subsp. enterica serovar Typhimurium
propanal + NH3
-
?
4.3.1.7
(S)-2-aminopropanol
building of a enzyme-coenzyme-substrate ternary complex, the steps are: radical pair separation, first hydrogen atom transfer, radical rearrangement, second hydrogen atom transfer, radical pair recombination, and product release/substrate binding
Homo sapiens
propanal + NH3
-
r
4.3.1.7
(S)-2-aminopropanol
-
Salmonella enterica subsp. enterica serovar Typhimurium
?
-
?
4.3.1.7
acetaldehyde + NH3
by selectively deuterating the substrate (ethanolamine) and/or the beta-carbon of the 5'-deoxyadenosyl moiety of the intrinsiccoenzyme B12, it is possible to experimentally probe both the forward and reverse hydrogen atom transfers between the 5'-deoxyadenosyl radical and substrate during single turnover stopped-flow measurements
Salmonella enterica
ethanolamine
-
r
4.3.1.7
ethanolamine
-
Salmonella enterica subsp. enterica serovar Typhimurium
acetaldehyde + NH3
-
?
4.3.1.7
ethanolamine
-
Escherichia coli
acetaldehyde + NH3
-
?
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