Problem 166
Question
Assertion: The first amino acid in primary structure protein is called as N-terminal amino acid. Reason: \(\mathrm{NH}_{2}\) group of first amino acid is free, not bound to form peptide bond.
Step-by-Step Solution
Verified Answer
The first amino acid in a primary structure protein is indeed called the N-terminal amino acid because its amine (\(\mathrm{NH}_{2}\)) group is not bound to form a peptide bond.
1Step 1: Understanding the Terms
The primary structure of a protein is its sequence of amino acids. These amino acids are joined together by peptide bonds. Each amino acid has two functional groups: the amine group (\(\mathrm{NH}_{2}\)) and the carboxyl group (\(\mathrm{COOH}\)).
2Step 2: Confirming the Assertion
The first amino acid of a protein sequence is known as the 'N-terminal' amino acid because at this end of the protein, the amine (or nitrogen-terminus, hence the 'N' in 'N-terminal') group is free and not involved in forming a peptide bond.
3Step 3: Examining the Reason
The amine group (\(\mathrm{NH}_{2}\)) of the first amino acid is unbound, which is why it is known as the N-terminal amino acid. It does not form a peptide bond because peptide bonds are formed between the amine group of one amino acid and the carboxyl group of the next amino acid in the sequence. Therefore, as there would be no preceding amino acid for the first one, its amine group remains free.
Key Concepts
N-terminal amino acidPeptide bondsAmino acid functional groups
N-terminal amino acid
In the structure of a protein, the N-terminal amino acid holds a special position. It is the first amino acid in the protein chain and is characterized by its free amine group (\( \mathrm{NH}_2 \)). This amino group is not part of any peptide bond. Why is this significant? Because it helps give proteins directionality. Proteins have two ends: the N-terminal, starting end, and the C-terminal, ending end.
- The N-terminal end has a free amine group (\( \mathrm{NH}_2 \)).
- The C-terminal end has a free carboxyl group (\( \mathrm{COOH} \)).
Peptide bonds
Peptide bonds are the links that hold amino acids together in proteins. Each peptide bond forms when the amine group (\( \mathrm{NH}_2 \)) of one amino acid reacts with the carboxyl group (\( \mathrm{COOH} \)) of the next. This reaction results in a covalent bond between them, releasing a molecule of water—an example of a dehydration reaction.
- Peptide bonds are strong and not easily broken.
- They give proteins their primary structure.
Amino acid functional groups
Amino acids, the building blocks of proteins, contain two essential functional groups: the amine group (\( \mathrm{NH}_2 \)) and the carboxyl group (\( \mathrm{COOH} \)). Each plays a specific role in forming proteins:
- The amine group is a key component in forming peptide bonds, linking one amino acid to another.
- The carboxyl group also participates in creating peptide bonds, acting as the binding site for the subsequent amino acid.
Other exercises in this chapter
Problem 164
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Assertion: Oil containing PUFA are good for health. Reason: They reduce blood cholesterol level. Thus, decreases chance of heart diseases.
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Assertion: A B-DNA structure proposed by Watson and Crick is secondary structure. Reason: B- DNA contains hydrogen bond in addition to covalent bond.
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