Essentials of Genetics (9th Edition) - Standalone book
9th Edition
ISBN: 9780134047799
Author: William S. Klug, Michael R. Cummings, Charlotte A. Spencer, Michael A. Palladino
Publisher: PEARSON
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Textbook Question
Chapter 13, Problem 18PDQ
Shown in the following table are several amino acid substitutions in the α and β chains of human hemoglobin. Use the genetic code table in Figure 12–7 to determine how many of them can occur as a result of a single
Hb Type | Normal Amino Acid | Substituted Amino Acid |
HbJ 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) |
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Which of the following mutations would most likely keep the transitions of T state to R state in hemoglobin unchanged, or similar to the
transitions that occur in the native molecule? The three-letter codes for amino acids are used, and the numbers following the amino
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O A. Asp94→Ile94
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O C. Asp94 Glu94
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Which amino acid pair constitutes the hydrophobic patch on sickle cell
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acid pair constituting a hydrophobic patch?
Phe 85 / Leu 88; no
Phe 85 / Leu 88; yes
Trp 85 / Leu 88; yes
Olle 85 / Leu 88; yes
Pro 85 / Lys 88; no
Sickle cell anemia is caused by a point mutation in the β-globin chain of hemoglobin. Glutamic acid is replaced by Valine.
HBB sequence in normal adult hemoglobin (Hb A): Leu-Thr-Pro-Glu-Glu-Lys-Ser
HBB sequence in mutant adult hemoglobin (Hb S): Leu-Thr-Pro-Val-Glu-Lys-Ser
What effect does this mutation have on the structure and function of the protein?
Predict what would happen to the RBC if the glutamic acid was replaced with asparagine instead of valine.
Chapter 13 Solutions
Essentials of Genetics (9th Edition) - Standalone book
Ch. 13 - CASE STUDY | Crippled ribosomes Diamond Blackfan...Ch. 13 - CASE STUDY | Crippled ribosomes Diamond Blackfan...Ch. 13 - Prob. 3CSCh. 13 -
HOW DO WE KNOW?
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