Structural versatility of peptides from Cα, α-disubstituted glycines: Crystal-state conformational analysis of homopeptides from Cα-methyl, Cα-benzylglycine [(αMe)Phe]n-Reference-Cited by-同舟云学术

Structural versatility of peptides from Cα, α-disubstituted glycines: Crystal-state conformational analysis of homopeptides from Cα-methyl, Cα-benzylglycine [(αMe)Phe]n

Published:1993-10 Issue:10 Volume:33 Page:1617-1625
ISSN:0006-3525
Container-title:Biopolymers
language:en
Short-container-title:Biopolymers

Author:

Valle Giovanni,Pantano Monica,Formaggio Fernando,Crisma Marco,Toniolo Claudio,Précigoux Gilles,Sulzenbacher Gerlind,Boesten Wilhelmus H. J.,Broxterman Quirinus B.,Schoemaker Hans E.,Kamphuis Johan

Publisher

Wiley

Subject

Organic Chemistry,Biomaterials,Biochemistry,General Medicine,Biophysics

Reference72 articles.

1. Linear oligopeptides. 273. Structural versatility of peptides from C.alpha.,.alpha.-disubstituted glycines. Synthesis, characterization, and solution conformational analysis of homopeptides from C.alpha.-methyl-C.alpha.-benzylglycine, and [(.alpha.-Me)Phe]n1

2. Structural characteristics of .alpha.-helical peptide molecules containing Aib residues

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