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Issue 18, 1984
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Penicillin biosynthesis: active site mapping with aminoadipoylcysteinylvaline variants

Abstract

A series of structural variants on the aminoadipoly 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 determined.

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Article information


J. Chem. Soc., Chem. Commun., 1984, 1225-1227
Article type
Paper

Penicillin biosynthesis: active site mapping with aminoadipoylcysteinylvaline variants

J. E. Baldwin, E. P. Abraham, R. M. Adlington, G. A. Bahadur, B. Chakravarti, B. P. Domayne-Hayman, L. D. Field, S. L. Flitsch, G. S. Jayatilake, A. Špakovaskis, H. Ting, N. J. Turner, R. L. White and J. J. Usher, J. Chem. Soc., Chem. Commun., 1984, 1225
DOI: 10.1039/C39840001225

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