Question 21.4: Locate the peptide bond in the dipeptide shown in the ball-a...
Locate the peptide bond in the dipeptide shown in the ball-and-stick model, and identify the amino acids that form the dipeptide. Name the dipeptide using the three-letter abbreviations for the amino acids.
Analysis
• Convert the ball-and-stick model to a structural formula. The peptide bond is the amide bond that joins the two amino acids together.
• Identify the side chains of the amino acids and use Table 21.2 to determine the names.
• Name the dipeptide by writing the three-letter abbreviations for the amino acids with the N-terminal amino acid first, followed by the C-terminal amino acid.
Table 21.2 The 20 Common Naturally Occurring Amino Acids | |||||
Neutral Amino Acids | |||||
Name | Structure | Abbreviations | Name | Structure | Abbreviations |
Alanine | ![]() |
Ala A | Phenylalanine* | ![]() |
Phe F |
Asparagine | ![]() |
Asn N | Proline | ![]() |
Pro P |
Cysteine | ![]() |
Cys C | Serine | ![]() |
Ser S |
Glutamine | ![]() |
Gln Q | Threonine* | ![]() |
Thr T |
Glycine | ![]() |
Gly G | Tryptophan* | ![]() |
Trp W |
Isoleucine* | ![]() |
Ile I | Tyrosine | ![]() |
Tyr Y |
Leucine* | ![]() |
Leu L | Valine* | ![]() |
Val V |
Methionine* | ![]() |
Met M | Arginine* | ![]() |
Arg R |
Aspartic acid | ![]() |
Asp D | Histidine* | ![]() |
His H |
Glutamic acid | ![]() |
Glu E | Lysine* | ![]() |
Lys K |
Essential amino acids are labeled with an asterisk (*). |

Learn more on how we answer questions.
The peptide bond is the amide bond that contains a carbon atom doubly bonded to oxygen and singly bonded to nitrogen.
The side chains of the two amino acids, the R groups that extend from the peptide backbone, identify them as alanine and cysteine ( Table 21.2 ). The dipeptide is named with the N-terminal amino acid (alanine) first, followed by the C-terminal amino acid (cysteine), using the three-letter abbreviations: Ala–Cys .
