Ligand L-Val-OMe
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Basic Ligand Information
Molecular Structure
C6H13NO2
L-Val-OMe
CEMZBWPSKYISTN-YFKPBYRVSA-N
L-valine methyl ester, Val-OMe
Roles as Enzyme Ligand
Substrate in Enzyme-catalyzed Reactions (5 results)
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L-valine methyl ester + H2O = L-valine + methanol
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L-Val-OMe + beta-Ala-OBzl + beta-Ala-OBzl = (beta-Ala)2-L-Val-OMe + benzyl alcohol
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L-Val-OMe + beta-Ala-OBzl = beta-Ala-L-Val-OMe + benzyl alcohol
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L-Val-OMe + D-Pro-OBzl = D-Pro-L-Val-OMe + benzyl alcohol
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L-Val-OMe + L-Pro-OBzl = L-Pro-L-Val-OMe + benzyl alcohol
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Product in Enzyme-catalyzed Reactions (1 result)
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Arg-Val-OMe + H2O = Arg + Val-OMe
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3D Structure of Enzyme-Ligand-Complex (PDB) (1 result)
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Enzyme Kinetic Parameters
KM Value (1 result)
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References & Links
Literature References (4)
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Substrate specificity of an alpha-amino acid ester hydrolase produced by Acetobacter turbidans A.T.C.C. 9325
1974
Takahashi, T.; Yamazaki, Y.; Kato, K.
Biochem. J.
137
497-503
Aminopeptidase Y, a new aminopeptidase from Saccharomyces cerevisiae. Purification, properties, localization, and processing by protease B
1994
Yasuhara, T.; Nakai, T.; Ohashi, A.
J. Biol. Chem.
269
13644-13650
The aminolysis reaction of streptomyces S9 aminopeptidase promotes the synthesis of diverse prolyl dipeptides
2010
Arima, J.; Morimoto, M.; Usuki, H.; Mori, N.; Hatanaka, T.
Appl. Environ. Microbiol.
76
4109-4112
Beta-alanyl peptide synthesis by Streptomyces S9 aminopeptidase
2010
Arima, J.; Morimoto, M.; Usuki, H.; Mori, N.; Hatanaka, T.
J. Biotechnol.
147
52-58
Links to other databases for L-Val-OMe
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