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dc.contributor.authorWang, Siyao
dc.contributor.authorCorcilius, Leo
dc.contributor.authorSharp, Phillip P.
dc.contributor.authorPayne, Richard J.
dc.date.accessioned2020-06-03
dc.date.available2020-06-03
dc.date.issued2017-06-01
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0968089617300482
dc.identifier.urihttps://hdl.handle.net/2123/22440
dc.description.abstractHerein we describe the synthesis of glycopeptide fragments from the death domains of TRADD and FADD bearing the recently discovered Nω-GlcNAc-β-arginine post-translational modification. TRADD and FADD glycopeptides were accessed through the use of a suitably protected synthetic glycosylamino acid ‘cassette’ that could be directly incorporated into conventional solid phase peptide synthesis (SPPS) protocols.en
dc.language.isoen_USen
dc.publisherElsevieren
dc.relationARC FT130100150en
dc.rightsOtheren
dc.subjectglycopeptidesen
dc.subjectGlycosylationen
dc.subjectGlcNAcylationen
dc.subjectArginineen
dc.subjectSPPSen
dc.subjectTRADDen
dc.subjectFADDen
dc.titleSynthesis of a GlcNAcylated arginine building block for the solid phase synthesis of death domain glycopeptide fragmentsen
dc.typeArticleen
dc.subject.asrcFoR::030599 - Organic Chemistry not elsewhere classifieden
dc.subject.asrcFoR::030499 - Medicinal and Biomolecular Chemistry not elsewhere classifieden
dc.identifier.doi10.1016/j.bmc.2017.03.012
dc.type.pubtypeAuthor accepted manuscripten
dc.relation.arcFT130100150
usyd.facultySeS faculties schools::Faculty of Scienceen


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