Ligand N-methylpropionamide
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Basic Ligand Information
Molecular Structure

C4H9NO
N-methylpropionamide
QJQAMHYHNCADNR-UHFFFAOYSA-N
Roles as Enzyme Ligand
In Vivo Substrate in Enzyme-catalyzed Reactions (1 result)
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N-methylpropionamide + H2O = methylamine + propionate
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Substrate in Enzyme-catalyzed Reactions (2 results)
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N-methylpropionamide + H2O = methylamine + propionate
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N-methyl-propionamide + H2O = ?
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Inhibitor in Enzyme-catalyzed Reactions (1 result)
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amide analogue, inhibits the biosynthesis of acetamidase, strain R312
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Enzyme Kinetic Parameters
kcat Value (Turnover Number) (1 result)
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References & Links
Literature References (3)
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Kinetic mechanismen of the aliphatic amidase from Pseudomonas aeruginosa
1979
Woods, M.J.; Findlater, J.D.; Orsi, B.A.
Biochim. Biophys. Acta
567
225-237
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Activity and regulation of an amidase, acylamide amidohydrolase EC 3.5.1.4, with a wide substrate spectrum from a Brevibacterium sp.
1984
Maestracci, M.; Thiery, A.; Bui, K.; Arnaud, A.; Galzy, P.
Arch. Microbiol.
138
315-320
Production and characterization of a nitrilase from Pseudomonas aeruginosa RZ44 and its potential for nitrile biotransformation
2016
Badoei-Dalfard, A.; Ramezani-Pour, N.; Karami, Z.
Iran. J. Biotechnol.
14
142-153
Links to other databases for N-methylpropionamide