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  • 9.3.1: Peptide Bonds
    https://chem.libretexts.org/Courses/BridgeValley_Community_and_Technical_College/Consumer_Chemistry/09%3A_Biochemistry/9.03%3A_Amino_Acids/9.3.01%3A_Peptide_Bonds
    The formation of peptides is nothing more than the application of the amide synthesis reaction. By convention, the amide bond in the peptides should be made in the order that the amino acids are writt...The formation of peptides is nothing more than the application of the amide synthesis reaction. By convention, the amide bond in the peptides should be made in the order that the amino acids are written. The amine end (N terminal) of an amino acid is always on the left, while the acid end (C terminal) is on the right.
  • 18.2.2: Peptide Bonds
    https://chem.libretexts.org/Workbench/Chemistry_LHS_Bridge/18%3A_Proteins/18.02%3A_Peptides_and_Proteins/18.2.02%3A_Peptide_Bonds
    The formation of peptides is nothing more than the application of the amide synthesis reaction. By convention, the amide bond in the peptides should be made in the order that the amino acids are writt...The formation of peptides is nothing more than the application of the amide synthesis reaction. By convention, the amide bond in the peptides should be made in the order that the amino acids are written. The amine end (N terminal) of an amino acid is always on the left, while the acid end (C terminal) is on the right.

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