Exchange of valine-oxygen during the biosynthesis of δ-(L-α-aminoadipoyl)-L-cysteinyl-D-valine
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1991/C3/C39910001531
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2. δ -(L-α-Aminoadipyl)-L-cysteinyl-D-valine synthetase (ACV synthetase): a multifunctional enzyme with broad substrate specificity for the synthesis of penicillin and cephalosporin precursors
3. H. Kleinkauf and H.von Döhren, in Biochemistry of Peptide Antibiotics, eds. H. Kleinkauf and H. von Döhren, de Gruyter, Berlin, 1990.
4. Attempts to Map a Process Evolution of Peptide Biosynthesis
5. δ-(L-α-aminoadipyl)-L-cysteinyl-D-valine Synthetase from Aspergillus nidulans
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1. Biogenetic speculation and biosynthetic advances;Natural Product Reports;2004
2. The Mechanism of ACV Synthetase;Chemical Reviews;1997-11-01
3. l-δ-(α-Aminoadipoyl)-l-cysteinyl-d-valine Synthetase: Thioesterification of Valine Is Not Obligatory for Peptide Bond Formation;Biochemistry;1997-07-01
4. Some developments in the biosynthesis of antibiotics;Folia Microbiologica;1995-02
5. Regioselective ring opening of chiral N-Boc protected pyroglutamate and pyroaminoadipate ethyl esters with heteronucleophiles;Tetrahedron;1993-04
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