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Issue 21, 1987
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Penicillin biosynthesis: active site mapping with L-α-aminoadipoyl-(C-methyl-L-cysteinyl)-D-valine variants

Abstract

A series of structural variants of the cysteinyl moiety of the natural precursor of penicillins, δ(L-α-aminoadipoyl)-L-cysteinyl-D-valine, have been synthesised and their effectiveness as substrates for the enzyme isopenicillin N synthetase has been evaluated.

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Article information


J. Chem. Soc., Chem. Commun., 1987, 1664-1667
Article type
Paper

Penicillin biosynthesis: active site mapping with L-α-aminoadipoyl-(C-methyl-L-cysteinyl)-D-valine variants

J. E. Baldwin, R. M. Adlington, N. Moss and N. G. Robinson, J. Chem. Soc., Chem. Commun., 1987, 1664
DOI: 10.1039/C39870001664

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