A reversible protection strategy to improve Fmoc-SPPS of peptide thioesters by the N-Acylurea approach.
about
New insights into nucleosome and chromatin structure: an ordered state or a disordered affair?Chemical and biological tools for the preparation of modified histone proteinsHemi-methylated DNA regulates DNA methylation inheritance through allosteric activation of H3 ubiquitylation by UHRF1Fmoc-based peptide thioester synthesis with self-purifying effect: heading to native chemical ligation in parallel formats.Expanding the chemical toolbox for the synthesis of large and uniquely modified proteins.Synthesis of thioester peptides for the incorporation of thioamides into proteins by native chemical ligation.Histone core phosphorylation regulates DNA accessibility.Linker histone H1 and H3K56 acetylation are antagonistic regulators of nucleosome dynamicsHybrid phase ligation for efficient synthesis of histone proteins.Chemical Synthesis of Phosphorylated Histone H2A at Tyr57 Reveals Insight into the Inhibition Mode of the SAGA Deubiquitinating Module.Modern tools for the chemical ligation and synthesis of modified peptides and proteins.Self-assembled artificial viral capsids bearing coiled-coils at the surface.Chemical Synthesis of Ubiquitin Chains.Making Ends Meet: Microwave-Accelerated Synthesis of Cyclic and Disulfide Rich Proteins Via In Situ Thioesterification and Native Chemical Ligation.Serine promoted synthesis of peptide thioester-precursor on solid support for native chemical ligation.Preparing semisynthetic and fully synthetic histones h3 and h4 to modify the nucleosome core.One-pot total chemical synthesis of human α-synuclein.Sequence Diversification by Divergent C-Terminal Elongation of Peptides.Exploiting the MeDbz Linker To Generate Protected or Unprotected C-Terminally Modified Peptides.Epimerization-free access to C-terminal cysteine peptide acids, carboxamides, secondary amides, and esters via complimentary strategies.A straightforward method for automated Fmoc-based synthesis of bio-inspired peptide crypto-thioesters.One-pot native chemical ligation of peptide hydrazides enables total synthesis of modified histones
P2860
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P2860
A reversible protection strategy to improve Fmoc-SPPS of peptide thioesters by the N-Acylurea approach.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
A reversible protection strate ...... rs by the N-Acylurea approach.
@ast
A reversible protection strate ...... rs by the N-Acylurea approach.
@en
type
label
A reversible protection strate ...... rs by the N-Acylurea approach.
@ast
A reversible protection strate ...... rs by the N-Acylurea approach.
@en
prefLabel
A reversible protection strate ...... rs by the N-Acylurea approach.
@ast
A reversible protection strate ...... rs by the N-Acylurea approach.
@en
P2860
P356
P1433
P1476
A reversible protection strate ...... ers by the N-Acylurea approach
@en
P2093
John C Shimko
Santosh K Mahto
P2860
P304
P356
10.1002/CBIC.201100472
P577
2011-09-12T00:00:00Z