Chapter 3: Problem 30
REFLECT AND APPLY What are the sequences of all the possible tripeptides that contain the amino acids aspartic acid, leucine, and phenylalanine? Use the three-letter abbreviations to express your answer.
Short Answer
Expert verified
Asp-Leu-Phe, Asp-Phe-Leu, Leu-Asp-Phe, Leu-Phe-Asp, Phe-Asp-Leu, Phe-Leu-Asp.
Step by step solution
01
- Identify amino acids and their abbreviations
First, identify the three amino acids given in the problem and their three-letter abbreviations. Aspartic Acid is abbreviated as Asp, Leucine as Leu, and Phenylalanine as Phe.
02
- Determine number of tripeptides
Calculate the number of possible tripeptide sequences. As there are 3 amino acids and each position in the tripeptide can be any of the 3 amino acids, there are a total of 3! (3 factorial) sequences possible.
03
- List all possible permutations
List all permutations of the three amino acids (Asp, Leu, and Phe). There are 6 permutations in total:
04
Step 3.1 - Permutation 1
Asp-Leu-Phe
05
Step 3.2 - Permutation 2
Asp-Phe-Leu
06
Step 3.3 - Permutation 3
Leu-Asp-Phe
07
Step 3.4 - Permutation 4
Leu-Phe-Asp
08
Step 3.5 - Permutation 5
Phe-Asp-Leu
09
Step 3.6 - Permutation 6
Phe-Leu-Asp
Unlock Step-by-Step Solutions & Ace Your Exams!
-
Full Textbook Solutions
Get detailed explanations and key concepts
-
Unlimited Al creation
Al flashcards, explanations, exams and more...
-
Ads-free access
To over 500 millions flashcards
-
Money-back guarantee
We refund you if you fail your exam.
Over 30 million students worldwide already upgrade their learning with Vaia!
Key Concepts
These are the key concepts you need to understand to accurately answer the question.
Amino Acids
Amino acids are the building blocks of proteins. Each amino acid has a specific structure that includes an amino group, a carboxyl group, a hydrogen atom, and a distinctive side chain or R group. The unique properties of the side chain determine the role of each amino acid in a protein.
There are 20 standard amino acids in nature. Each one plays a different role in protein folding and function. For example, aspartic acid (Asp) is typically found in the active sites of proteins because of its acidic properties.
Understanding amino acids is foundational to learning about biochemistry and molecular biology. They join together in specific sequences to form peptides and proteins, which perform countless functions in the body.
There are 20 standard amino acids in nature. Each one plays a different role in protein folding and function. For example, aspartic acid (Asp) is typically found in the active sites of proteins because of its acidic properties.
Understanding amino acids is foundational to learning about biochemistry and molecular biology. They join together in specific sequences to form peptides and proteins, which perform countless functions in the body.
Permutations
Permutations refer to all the possible arrangements of a given set of elements. In this exercise, we are working with three amino acids: Aspartic Acid (Asp), Leucine (Leu), and Phenylalanine (Phe).
To find all possible tripeptide sequences, we calculate the permutations of these three amino acids. The formula for permutations of n elements is n!, which stands for 'n factorial.'
For three amino acids, we have 3!, which equals 3 x 2 x 1 = 6.
So, there are 6 different ways to arrange Asp, Leu, and Phe to form tripeptides:
To find all possible tripeptide sequences, we calculate the permutations of these three amino acids. The formula for permutations of n elements is n!, which stands for 'n factorial.'
For three amino acids, we have 3!, which equals 3 x 2 x 1 = 6.
So, there are 6 different ways to arrange Asp, Leu, and Phe to form tripeptides:
- Permutation 1: Asp-Leu-Phe
- Permutation 2: Asp-Phe-Leu
- Permutation 3: Leu-Asp-Phe
- Permutation 4: Leu-Phe-Asp
- Permutation 5: Phe-Asp-Leu
- Permutation 6: Phe-Leu-Asp
Peptide Synthesis
Peptide synthesis is the process of creating peptides, which are short chains of amino acids. In biological systems, peptides are synthesized through a process called translation, which occurs in the ribosome. However, in a laboratory setting, peptides can be synthesized chemically.
Each amino acid in the chain is linked by a peptide bond, formed between the carboxyl group of one amino acid and the amino group of another. The sequence in which amino acids are linked is crucial, as it determines the peptide's properties and function.
In our exercise, we looked at the tripeptide sequence. Synthesizing tripeptides like Asp-Leu-Phe involves adding each amino acid step-by-step in a specific order to ensure the correct sequence.
Each amino acid in the chain is linked by a peptide bond, formed between the carboxyl group of one amino acid and the amino group of another. The sequence in which amino acids are linked is crucial, as it determines the peptide's properties and function.
In our exercise, we looked at the tripeptide sequence. Synthesizing tripeptides like Asp-Leu-Phe involves adding each amino acid step-by-step in a specific order to ensure the correct sequence.
Abbreviations of Amino Acids
Amino acids are commonly represented by both three-letter and single-letter abbreviations in scientific literature to save space and simplify communication.
In this exercise, we used three-letter abbreviations for Aspartic Acid (Asp), Leucine (Leu), and Phenylalanine (Phe). These abbreviations help quickly identify the amino acids involved without writing out their full names.
Knowing these abbreviations is essential for reading and understanding biochemical texts and databases, as well as for labeling and communicating sequences in peptide synthesis and protein studies.
Here are some examples of common amino acid abbreviations:
In this exercise, we used three-letter abbreviations for Aspartic Acid (Asp), Leucine (Leu), and Phenylalanine (Phe). These abbreviations help quickly identify the amino acids involved without writing out their full names.
Knowing these abbreviations is essential for reading and understanding biochemical texts and databases, as well as for labeling and communicating sequences in peptide synthesis and protein studies.
Here are some examples of common amino acid abbreviations:
- Glycine - Gly (G)
- Alanine - Ala (A)
- Valine - Val (V)
- Tyrosine - Tyr (Y)
- Threonine - Thr (T)