Lawrence O. answered 03/09/22
A Physiology writer for more than 3 years.
In the given question, the mutation of the gene causes the substitution of serine by phenylalanine amino acid, which causes a decrease in the activity of the enzyme. Serine is polar, hence it will be involved in the formation of bonds with the substrate. Hence, the substitution changed the enzyme's secondary and tertiary structures, causing the mutant enzyme to fold in a different way than the normal enzyme.