Table of contents
- 1. Introduction to Genetics51m
- 2. Mendel's Laws of Inheritance3h 37m
- 3. Extensions to Mendelian Inheritance2h 41m
- 4. Genetic Mapping and Linkage2h 28m
- 5. Genetics of Bacteria and Viruses1h 21m
- 6. Chromosomal Variation1h 48m
- 7. DNA and Chromosome Structure56m
- 8. DNA Replication1h 10m
- 9. Mitosis and Meiosis1h 34m
- 10. Transcription1h 0m
- 11. Translation58m
- 12. Gene Regulation in Prokaryotes1h 19m
- 13. Gene Regulation in Eukaryotes44m
- 14. Genetic Control of Development44m
- 15. Genomes and Genomics1h 50m
- 16. Transposable Elements47m
- 17. Mutation, Repair, and Recombination1h 6m
- 18. Molecular Genetic Tools19m
- 19. Cancer Genetics29m
- 20. Quantitative Genetics1h 26m
- 21. Population Genetics50m
- 22. Evolutionary Genetics29m
11. Translation
Proteins
4:04 minutes
Problem 23
Textbook Question
Textbook QuestionSeveral amino acid substitutions in the α and β chains of human hemoglobin are shown in the following table. Hb Type Normal Amino Acid Substituted Amino Acid Hb Toronto Ala Asp (α-5) HbJ Oxford Gly Asp (α-15) Hb Mexico Gln Glu (α-54) Hb Bethesda Tyr His (β-145) Hb Sydney Val Ala (β-67) HbM Saskatoon His Tyr (β-63) Using the code table (Figure 13.7), determine how many of them can occur as a result of a single-nucleotide change.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Amino Acids and Their Properties
Amino acids are the building blocks of proteins, each with distinct properties determined by their side chains. Understanding the nature of these side chains—whether they are polar, nonpolar, acidic, or basic—is crucial for predicting how substitutions can affect protein structure and function. For instance, substituting a polar amino acid for a nonpolar one can significantly alter the protein's behavior.
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Single Nucleotide Polymorphism (SNP)
A single nucleotide polymorphism (SNP) is a variation at a single position in a DNA sequence among individuals. SNPs can lead to amino acid substitutions in proteins if they occur in coding regions of genes. Recognizing which amino acid changes can arise from a single nucleotide change is essential for analyzing the hemoglobin variants listed in the question.
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Genetic Code and Codon Translation
The genetic code consists of codons, which are sequences of three nucleotides that correspond to specific amino acids. Understanding how codons translate into amino acids allows for the identification of potential substitutions resulting from nucleotide changes. For example, a change in one nucleotide can alter a codon, leading to a different amino acid being incorporated into the protein.
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