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