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Ligand N-[(benzyloxy)carbonyl]-L-serine Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
Basic Ligand Information Molecular Structure
C1 1 H1 3 NO5
N-[(benzyloxy)carbonyl]-L-serine
GNIDSOFZAKMQAO-VIFPVBQESA-N
benzyloxycarbonyl-Ser, Nalpha-benzyloxycarbonyl-L-Ser, Nalpha-Benzyloxycarbonyl-Ser
Roles as Enzyme Ligand
Substrate in Enzyme-catalyzed Reactions (1 result)
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Nalpha-benzyloxycarbonyl-L-Ser + H2O = benzyl alcohol + CO2 + L-Ser
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Product in Enzyme-catalyzed Reactions (2 results)
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benzyloxycarbonyl-Ser-Leu + H2O = benzyloxycarbonyl-Ser + Leu
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benzyloxycarbonyl-Ser-Ala + H2O = benzyloxycarbonyl-Ser + Ala
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Inhibitor in Enzyme-catalyzed Reactions (1 result)
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Enzyme Kinetic Parameters
IC50 Value (1 result)
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0.1
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pH 5.0, 37°C, recombinant enzyme
References & Links Literature References (4)
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Bacterial peptidases. 3. An enzyme specific for N-acyl linkages to alanine
1969
Levy, C.C.; Goldman, P.
J. Biol. Chem.
244
4467-4472
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A novel enzyme, Nalpha-benzyloxycarbonyl amino acid urethane hydrolase IV
1985
Matsumura, E.; Shin, T.; Murao, S.; Sakaguchi, M.; Kawano, T.
Agric. Biol. Chem.
49
3643-3645
Pseudomonas aeruginosa amidase: aggregation in recombinant Escherichia coli
2011
Borges, P.; Pacheco, R.; Karmali, A.
Biotechnol. J.
6
888-897
N-(2-Oxo-3-oxetanyl)carbamic acid esters as N-acylethanolamine acid amidase inhibitors: synthesis and structure-activity and structure-property relationships
2012
Duranti, A.; Tontini, A.; Antonietti, F.; Vacondio, F.; Fioni, A.; Silva, C.; Lodola, A.; Rivara, S.; Solorzano, C.; Piomelli, D.; Tarzia, G.; Mor, M.
J. Med. Chem.
55
4824-4836
Links to other databases for N-[(benzyloxy)carbonyl]-L-serine
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