2012Angewandte Chemie International EditionRequires access

Induction of Unexpected Left‐Handed Helicity by an N‐Terminal L ‐Amino Acid in an Otherwise Achiral Peptide Chain

Robert A. Brown, Tommaso Marcelli, Matteo De Poli, Jordi Solà, Jonathan Clayden

Open publisher page 87 citations

Abstract

Peptide helices containing L-amino acids are typically right-handed. Exceptions are peptide helices containing the achiral amino acids 2-aminoisobutyric acid and glycine with a single chiral amino acid at the N terminus. These helices are left-handed when the N-terminal residue is a common tertiary proteinogenic amino acid, such as L-valine (see picture, left), but right-handed when the N-terminal residue is the quaternary amino acid L-α-methylvaline (right).

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What this paper is about

Peptide helices containing L-amino acids are typically right-handed. Exceptions are peptide helices containing the achiral amino acids 2-aminoisobutyric acid and glycine with a single chiral amino acid at the N terminus. These helices are left-handed when the N-terminal residue is a common tertiary proteinogenic amino acid, such as L-valine (see picture, left), but right-handed when the N-terminal residue is the quaternary amino acid L-α-methylvaline (right).

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Available abstract

Peptide helices containing L-amino acids are typically right-handed. Exceptions are peptide helices containing the achiral amino acids 2-aminoisobutyric acid and glycine with a single chiral amino acid at the N terminus. These helices are left-handed when the N-terminal residue is a common tertiary proteinogenic amino acid, such as L-valine (see picture, left), but right-handed when the N-terminal residue is the quaternary amino acid L-α-methylvaline (right).

Key concepts: Peptide, Amino acid, Valine, Glycine, Stereochemistry, Residue (chemistry), Amino acid residue, Chemistry

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