UCL logo

UCL Discovery

UCL home » Library Services » Electronic resources » UCL Discovery

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.

Full text not available from this repository.

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
URI: http://discovery.ucl.ac.uk/id/eprint/154739
Downloads since deposit
0Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item