Shown below is an internal fragment of a polypeptide. If this polypeptide were growing, onto which end would the next amino acid be added? a) Onto the right b) Onto the left
Shown below is an internal fragment of a polypeptide. If this polypeptide were growing, onto which end would the next amino acid be added? a) Onto the right b) Onto the left
Biochemistry
9th Edition
ISBN:9781319114671
Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Publisher:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Chapter1: Biochemistry: An Evolving Science
Section: Chapter Questions
Problem 1P
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Question
Shown below is an internal fragment of a polypeptide. If this polypeptide were growing, onto which end would the next amino acid be added?
a) Onto the right
b) Onto the left

Transcribed Image Text:The image depicts the chemical structure of the tripeptide glutathione. It is composed of three amino acids linked by peptide bonds:
1. **N-terminal Cysteine**:
- The structure starts with a cysteine residue. The amino group (NH2) is bonded to an α-carbon, which also carries a methyl group (CH2) attached to a thiol group (SH).
2. **Central Glycine**:
- Connected to cysteine via a peptide bond (CO-NH), the second amino acid is glycine. It has a simpler structure with an amino group, an α-carbon bonded to a hydrogen atom, and a carboxyl group (COOH).
3. **C-terminal Glutamic Acid**:
- The final amino acid is glutamic acid. It links to glycine through another peptide bond. Glutamic acid features an α-carbon with a side chain containing a carboxyl group (COOH), in addition to the terminal carboxyl group.
The structure illustrates these amino acids forming glutathione, a tripeptide known for its role in cellular defense and detoxification.
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