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Literature summary for 3.5.2.6 extracted from

  • Guo, F.; Huynh, J.; Dmitrienko, G.I.; Viswanatha, T.; Clarke, A.J.
    The role of the non-conserved residue at position 104 of class A beta-lactamases in susceptibility to mechanism-based inhibitors (1999), Biochim. Biophys. Acta, 1431, 132-147.
    View publication on PubMed

Cloned(Commentary)

Cloned (Comment) Organism
expressed in Escherichia coli Bacillus cereus

Protein Variants

Protein Variants Comment Organism
D104A km for benzylpenicillin and methicillin increased 2 fold, no change in catalytic activity Bacillus cereus

Inhibitors

Inhibitors Comment Organism Structure
6-beta-trifluoromethanesulfonamidopenicillanic acid
-
Bacillus cereus
6-bromopenicillanic acid
-
Bacillus cereus
clavulanic acid
-
Staphylococcus aureus

Localization

Localization Comment Organism GeneOntology No. Textmining
extracellular
-
Staphylococcus aureus
-
-
extracellular
-
Bacillus cereus
-
-

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) 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
-
?
ampicillin + H2O Bacillus cereus 569/H/9
-
(2R,4S)-2-[(R)-[[(2R)-2-amino-2-phenylacetyl]amino](carboxy)methyl]-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid
-
?

Organism

Organism UniProt Comment Textmining
Bacillus cereus
-
-
-
Bacillus cereus 569/H/9
-
-
-
Staphylococcus aureus
-
-
-
Staphylococcus aureus PC1
-
-
-

Purification (Commentary)

Purification (Comment) Organism
-
Staphylococcus aureus
-
Bacillus cereus

Storage Stability

Storage Stability Organism
-20°C, 50 mM sodium phosphate buffer, pH 6.8, 50% glycerol Staphylococcus aureus
-20°C, 50 mM sodium phosphate buffer, pH 6.8, 50% glycerol Bacillus cereus

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
ampicillin + H2O
-
Staphylococcus aureus (2R,4S)-2-[(R)-[[(2R)-2-amino-2-phenylacetyl]amino](carboxy)methyl]-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid
-
?
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
-
?
ampicillin + H2O
-
Bacillus cereus 569/H/9 (2R,4S)-2-[(R)-[[(2R)-2-amino-2-phenylacetyl]amino](carboxy)methyl]-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid
-
?
ampicillin + H2O
-
Staphylococcus aureus PC1 (2R,4S)-2-[(R)-[[(2R)-2-amino-2-phenylacetyl]amino](carboxy)methyl]-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid
-
?
benzylpenicillin + H2O
-
Staphylococcus aureus (2R,4S)-2-[(R)-carboxy(2-phenylacetamido)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
-
?
benzylpenicillin + H2O
-
Bacillus cereus 569/H/9 (2R,4S)-2-[(R)-carboxy(2-phenylacetamido)methyl]-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid
-
?
benzylpenicillin + H2O
-
Staphylococcus aureus PC1 (2R,4S)-2-[(R)-carboxy(2-phenylacetamido)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
-
?
methicillin + H2O
-
Bacillus cereus 569/H/9 (2R,4S)-2-[(R)-carboxy(2,6-dimethoxybenzamido)methyl]-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid
-
?
oxacillin + H2O
-
Staphylococcus aureus (2R,4S)-2-{(R)-carboxy[(5-methyl-3-phenyl-1,2-oxazole-4-carbonyl)amino]methyl}-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid
-
?
oxacillin + H2O
-
Bacillus cereus (2R,4S)-2-{(R)-carboxy[(5-methyl-3-phenyl-1,2-oxazole-4-carbonyl)amino]methyl}-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid
-
?
oxacillin + H2O
-
Bacillus cereus 569/H/9 (2R,4S)-2-{(R)-carboxy[(5-methyl-3-phenyl-1,2-oxazole-4-carbonyl)amino]methyl}-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid
-
?
oxacillin + H2O
-
Staphylococcus aureus PC1 (2R,4S)-2-{(R)-carboxy[(5-methyl-3-phenyl-1,2-oxazole-4-carbonyl)amino]methyl}-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid
-
?

Synonyms

Synonyms Comment Organism
beta-lactamse A-D A,C and D enzymes utilize a nucleophilic serine at the active center which becomes acylated by substrate, B enzymes are metalloenzymes requiring Zn2+ for activity Staphylococcus aureus
beta-lactamse A-D A,C and D enzymes utilize a nucleophilic serine at the active center which becomes acylated by substrate, B enzymes are metalloenzymes requiring Zn2+ for activity Bacillus cereus

Turnover Number [1/s]

Turnover Number Minimum [1/s] Turnover Number Maximum [1/s] Substrate Comment Organism Structure
8
-
Oxacillin
-
Staphylococcus aureus
135
-
benzylpenicillin
-
Staphylococcus aureus
145
-
Methicillin
-
Bacillus cereus
261
-
Oxacillin
-
Bacillus cereus
550
-
ampicillin
-
Staphylococcus aureus
1350
-
benzylpenicillin
-
Bacillus cereus
5400
-
ampicillin
-
Bacillus cereus