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Literature summary for 3.5.2.6 extracted from

  • Ogawara, H.; Umezawa, H.
    Bacillus cereus beta-lactamase. Reaction with N-bromosuccinimide and the properties of the product (1975), Biochim. Biophys. Acta, 391, 435-447.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
2-Hydroxy-5-nitrobenzyl bromide
-
Bacillus cereus
N-bromosuccinimide 0.1 mM: 99% loss of activity within 30 min Bacillus cereus

Organism

Organism UniProt Comment Textmining
Bacillus cereus
-
-
-
Bacillus subtilis
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
ampicillin + H2O
-
Bacillus cereus (2R,4S)-2-[(R)-[[(2R)-2-amino-2-phenylacetyl]amino](carboxy)methyl]-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid
-
?
benzylpenicillin + H2O
-
Bacillus cereus (2R,4S)-2-[(R)-carboxy(2-phenylacetamido)methyl]-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid
-
?
carbenicillin + H2O
-
Bacillus cereus (2R,4S)-2-{(R)-carboxy[2-carboxy(phenyl)acetamido]methyl}-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid
-
?
ciclacillin + H2O
-
Bacillus cereus (2R,4S)-2-[(R)-[(1-aminocyclohexane-1-carbonyl)amino](carboxy)methyl]-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid
-
?
cloxacillin + H2O
-
Bacillus cereus (2R,4S)-2-[(R)-carboxy{[3-(2-chlorophenyl)-5-methyl-1,2-oxazole-4-carbonyl]amino}methyl]-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid
-
?
methicillin + H2O
-
Bacillus cereus (2R,4S)-2-[(R)-carboxy(2,6-dimethoxybenzamido)methyl]-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid
-
?