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Literature summary extracted from

  • Montenegro, M.F.; Moral-Naranjo, M.T.; Munoz-Delgado, E.; Campoy, F.J.; Vidal, C.J.
    Hydrolysis of acetylthiocoline, o-nitroacetanilide and o-nitrotrifluoroacetanilide by fetal bovine serum acetylcholinesterase (2009), FEBS J., 276, 2074-2083.
    View publication on PubMed

Inhibitors

EC Number Inhibitors Comment Organism Structure
3.5.1.13 BW284c51
-
 Bos taurus
3.5.1.13 fasciculin-2
-
 Bos taurus

KM Value [mM]

EC Number KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
3.5.1.13 0.81
-
 N-(2-nitrophenyl)-trifluoroacetamide
-
 Bos taurus
3.5.1.13 15.22
-
 o-nitroacetanilide
-
 Bos taurus

Organism

EC Number Organism UniProt Comment Textmining
3.5.1.13 Bos taurus
-
-
-

Purification (Commentary)

EC Number Purification (Comment) Organism
3.5.1.13
-
 Bos taurus

Source Tissue

EC Number Source Tissue Comment Organism Textmining
3.5.1.13 fetal serum
-
 Bos taurus
-

Specific Activity [micromol/min/mg]

EC Number Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
3.5.1.13 0.319
-
 substrate: o-nitroacetanilide Bos taurus

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
3.5.1.13 N-(2-nitrophenyl)-trifluoroacetamide + H2O
-
 Bos taurus 2-nitroaniline + trifluoroacetic acid
-
 ?
3.5.1.13 o-nitroacetanilide + H2O
-
 Bos taurus 2-nitroaniline + acetic acid
-
 ?

Subunits

EC Number Subunits Comment Organism
3.5.1.13 tetramer sedimentation Bos taurus

Synonyms

EC Number Synonyms Comment Organism
3.5.1.13 aryl acylamidase aryl acylaminidase activity of acetylcholinesterase Bos taurus

Turnover Number [1/s]

EC Number Turnover Number Minimum [1/s] Turnover Number Maximum [1/s] Substrate Comment Organism Structure
3.5.1.13 208
-
 o-nitroacetanilide
-
 Bos taurus
3.5.1.13 237
-
 N-(2-nitrophenyl)-trifluoroacetamide
-
 Bos taurus