Towards biomolecular assembly employing extended native chemical ligation in combination with thioester synthesis using an N-->S acyl shift.
about
Expanding the chemical toolbox for the synthesis of large and uniquely modified proteins.Cysteine promoted C-terminal hydrazinolysis of native peptides and proteins.Synthesis of homogeneous MUC1 oligomers via a bi-directional ligation strategy.Shifting Native Chemical Ligation into Reverse through N→S Acyl Transfer.Tailored Synthesis of 162-Residue S-Monoglycosylated GM2-Activator Protein (GM2AP) Analogues that Allows Facile Access to a Protein Library.Intramolecular acyl transfer in peptide and protein ligation and synthesis.Chemical synthesis of biologically active monoglycosylated GM2-activator protein analogue using N-sulfanylethylanilide peptide.High-throughput synthesis of peptide α-thioesters: a safety catch linker approach enabling parallel hydrogen fluoride cleavage.
P2860
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P2860
Towards biomolecular assembly employing extended native chemical ligation in combination with thioester synthesis using an N-->S acyl shift.
description
2010 nî lūn-bûn
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2010年の論文
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2010年学术文章
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name
Towards biomolecular assembly ...... sis using an N-->S acyl shift.
@en
Towards biomolecular assembly ...... sis using an N-->S acyl shift.
@nl
type
label
Towards biomolecular assembly ...... sis using an N-->S acyl shift.
@en
Towards biomolecular assembly ...... sis using an N-->S acyl shift.
@nl
prefLabel
Towards biomolecular assembly ...... sis using an N-->S acyl shift.
@en
Towards biomolecular assembly ...... sis using an N-->S acyl shift.
@nl
P2093
P356
P1433
P1476
Towards biomolecular assembly ...... sis using an N-->S acyl shift.
@en
P2093
David W Anderson
Derek Macmillan
Tom Ackrill
P304
P356
10.1002/BIP.21473
P577
2010-01-01T00:00:00Z