Engineering β-sheets employing N-methylated heterochiral amino acids.
about
Toward accurately modeling N-methylated cyclic peptides.Crystal and NMR Structures of a Peptidomimetic β-Turn That Provides Facile Synthesis of 13-Membered Cyclic Tetrapeptides.Protein stabilization by tuning the steric restraint at the reverse turn† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c7sc05163h.
P2860
Engineering β-sheets employing N-methylated heterochiral amino acids.
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2016 nî lūn-bûn
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2016年の論文
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2016年学术文章
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name
Engineering β-sheets employing N-methylated heterochiral amino acids.
@en
Engineering β-sheets employing N-methylated heterochiral amino acids.
@nl
type
label
Engineering β-sheets employing N-methylated heterochiral amino acids.
@en
Engineering β-sheets employing N-methylated heterochiral amino acids.
@nl
prefLabel
Engineering β-sheets employing N-methylated heterochiral amino acids.
@en
Engineering β-sheets employing N-methylated heterochiral amino acids.
@nl
P2093
P2860
P356
P1433
P1476
Engineering β-sheets employing N-methylated heterochiral amino acids
@en
P2093
Dipan Ghosh
Jayanta Chatterjee
Priyanka Lahiri
Somnath Mukherjee
P2860
P304
P356
10.1039/C6SC00518G
P50
P577
2016-04-21T00:00:00Z