Questions
Single choice
If a protein is slightly misfolded, it could be because of
Options
A.a mutation causing a change to an amino acid.
B.the mRNA was accidentally read backwards by the ribosome.
C.a deletion mutation causing one nucleotide to be lost.
D.processing occurring in the cytoplasm instead of the endoplasmic reticulum.
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Step-by-Step Analysis
When evaluating why a protein might be slightly misfolded, consider how sequence changes or cellular handling could influence structure.
Option 1: a mutation causing a change to an amino acid. A missense mutation alters one amino acid in the polypeptide, which can disrupt local interactions (hydrogen bonds, hydrophobic packing, charge interactions) and subtly shift folding, potentially leading to a slight misfold. This is a common and plausible cause of near-norma......Login to view full explanationLog in for full answers
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Genetic Code Consider a gene that is mutated, generating the change in the mRNA shown below. (Assume that this is a piece of mRNA from within the middle of the protein-coding sequence.) mRNA from original gene: 5’-CCUGGCUAUUGC-3’ mRNA from mutated gene: 5’-CCUGCGCUAUUGC-3’ What type of mutation is this?
Sickle cell disease is caused by which type of mutation?
Sickle-cell anemia is associated with a mutation in the gene encoding the beta subunit of hemoglobin that results in a change from glutamic acid to valine at position 6. All other amino acids are identical to a normal hemoglobin molecule. Based on the information above, which of the following mutations is the most likely cause of sickle-cell anemia?
Sickle-cell anemia is an inherited blood disorder in which one of the hemoglobin subunits is replaced with a different form of hemoglobin. Partial DNA sequences of the HBB gene for normal hemoglobin and for sickle-cell hemoglobin are shown in Figure 1. Partial sequence for normal hemoglobin: Partial sequence for sickle-cell hemoglobin: Figure 1. Comparison of partial DNA sequences for normal hemoglobin and hemoglobin with a sickle-cell mutation Which of the following best describes the type of mutation shown in Figure 1 that leads to sickle-cell anemia?
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