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Peptide thioester synthesis through N -> S acyl-transfer: application to the synthesis of a beta-defensin

Kang, J; Reynolds, NL; Tyrrell, C; Dorin, JR; Macmillan, D; (2009) Peptide thioester synthesis through N -> S acyl-transfer: application to the synthesis of a beta-defensin. ORG BIOMOL CHEM , 7 (23) 4918 - 4923. 10.1039/b913886b.

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Abstract

Peptide thioesters readily prepared through N -> S acyl transfer of a specific C-terminal motif provide access to biologically active mini-proteins using native chemical ligation.

Type:Article
Title:Peptide thioester synthesis through N -> S acyl-transfer: application to the synthesis of a beta-defensin
DOI:10.1039/b913886b
Keywords:CPE AUTOACTIVATING UNIT, LIGATION, BETA-DEFENSIN-3, GENERATION, PROTEINS, SHIFT
UCL classification:UCL > School of BEAMS > Faculty of Maths and Physical Sciences > Chemistry

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