Ligand Nalpha-carbobenzoxy-Val
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Basic Ligand Information
Molecular Structure

C13H17NO4
Nalpha-carbobenzoxy-Val
CANZBRDGRHNSGZ-NSHDSACASA-N
alpha-N-carbobenzoxy-Val, benzyloxycarbonyl-Val, Carboxybenzoyl-Val, N-alpha-Carbobenzoxy-Val, N-benzyloxycarbonyl-L-Val, N-benzyloxycarbonyl-L-valine, Nalpha-benzyloxycarbonyl-L-Val, Nalpha-Benzyloxycarbonyl-Val
Roles as Enzyme Ligand
Substrate in Enzyme-catalyzed Reactions (2 results)
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N-benzyloxycarbonyl-L-valine + H2O = benzyl hydrogencarbonate + L-valine
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Nalpha-benzyloxycarbonyl-L-Val + H2O = benzyl alcohol + CO2 + L-Val
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Product in Enzyme-catalyzed Reactions (4 results)
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benzyloxycarbonyl-Val-Leu + H2O = benzyloxycarbonyl-Val + Leu
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benzyloxycarbonyl-Val-Phe + H2O = benzyloxycarbonyl-Val + L-Phe
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Nalpha-carbobenzoxy-Val 4-nitrophenyl ester + H2O = Nalpha-carbobenzoxy-Val + 4-nitrophenol
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Nalpha-carbobenzoxy-Val p-nitrophenyl ester + H2O = Nalpha-carbobenzoxy-Val + 4-nitrophenyl
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Enzyme Kinetic Parameters
References & Links
Literature References (2)
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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
A thermostable L-aminoacylase from Thermococcus litoralis: cloning, overexpression, characterization, and applications in biotransformations
2002
Toogood, H.S.; Hollingsworth, E.J.; Brown, R.C.; Taylor, I.N.; Taylor, S.J.; McCague, R.; Littlechild, J.A.
Extremophiles
6
111-122
Links to other databases for Nalpha-carbobenzoxy-Val