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Literature summary for 3.5.1.13 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
Search for more literature for 3.5.1.13

Inhibitors

Inhibitors Comment Organism Structure
BW284c51
-
 Bos taurus
fasciculin-2
-
 Bos taurus

KM Value [mM]

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

Organism

Organism UniProt Comment Textmining
Bos taurus
-
-
-

Purification (Commentary)

Purification (Comment) Organism
-
 Bos taurus

Source Tissue

Source Tissue Comment Organism Textmining
fetal serum
-
 Bos taurus
-

Specific Activity [micromol/min/mg]

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

Substrates and Products (Substrate)

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

Subunits

Subunits Comment Organism
tetramer sedimentation Bos taurus

Synonyms

Synonyms Comment Organism
aryl acylamidase aryl acylaminidase activity of acetylcholinesterase Bos taurus

Turnover Number [1/s]

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