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Literature summary for 2.6.1.1 extracted from

  • Adams, B.; Lowpetch, K.; Thorndycroft, F.; Whyte, S.M.; Young, D.W.
    Stereochemistry of reactions of the inhibitor/substrates L- and D-beta-chloroalanine with beta-mercaptoethanol catalysed by L-aspartate aminotransferase and D-amino acid aminotransferase respectively (2005), Org. Biomol. Chem., 3, 3357-3364.
    View publication on PubMed
Search for more literature for 2.6.1.1

Organism

Organism UniProt Comment Textmining
Escherichia coli
-
-
-
Escherichia coli TY103
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
(2R,3R)-beta-chloroalanine + 2-mercaptoethanol beta-substitution, reaction occurs with retention of stereochemistry Escherichia coli 3-(2-hydroxyethyl)-cysteine + HCl
-
 ?
(2R,3R)-beta-chloroalanine + 2-mercaptoethanol beta-substitution, reaction occurs with retention of stereochemistry Escherichia coli TY103 3-(2-hydroxyethyl)-cysteine + HCl
-
 ?
(2R,3S)-beta-chloroalanine + 2-mercaptoethanol
-
 Escherichia coli (2R,3S)-3-(2-hydroxyethyl)-cysteine + HCl
-
 ?
(2R,3S)-beta-chloroalanine + 2-mercaptoethanol
-
 Escherichia coli TY103 (2R,3S)-3-(2-hydroxyethyl)-cysteine + HCl
-
 ?

Synonyms

Synonyms Comment Organism
L-aspartate aminotransferase
-
 Escherichia coli

Cofactor

Cofactor Comment Organism Structure
pyridoxal 5'-phosphate
-
 Escherichia coli