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Literature summary extracted from

  • Adediran, S.A.; Pratt, R.F.
    Penicillin acylase and O-aryloxycarbonyl hydroxamates Two acyl-enzymes, one leading to hydrolysis, the other to inactivation (2017), Arch. Biochem. Biophys., 614, 65-71 .
    View publication on PubMed

Inhibitors

EC Number Inhibitors Comment Organism Structure
3.5.1.11 benzothiophene-2-boronic acid fast reversible competitive inhibitor Escherichia coli

KM Value [mM]

EC Number KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
3.5.1.11 0.081
-
2-nitro-5-phenylacetamidobenzoic acid pH 7.5, 25°C Escherichia coli

Organism

EC Number Organism UniProt Comment Textmining
3.5.1.11 Escherichia coli
-
-
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
3.5.1.11 2-nitro-5-phenylacetamidobenzoic acid + H2O
-
Escherichia coli phenylacetate + 2-aminobenzoic acid
-
?

Synonyms

EC Number Synonyms Comment Organism
3.5.1.11 penicillin acylase
-
Escherichia coli

Ki Value [mM]

EC Number Ki Value [mM] Ki Value maximum [mM] Inhibitor Comment Organism Structure
3.5.1.11 0.0086
-
benzothiophene-2-boronic acid pH 7.5, 25°C Escherichia coli