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 (*).
21.4
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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 .

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