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Answer:
It would most likely render the protein nonfunctional or mis-functional.
The mutation could result in three outcomes:
- Silent mutation, which changes the codon to the same amino acid. (AAA->AAG, both are lysine). But since the problem specified that it has a "slightly different amino acid sequence," we can assume this doesn't happen.
- Nonsense mutation, which changes a codon to a stop codon. This would end the chain of amino acids, making the protein potentially nonfunctional.
- Missense mutation, which changes a codon to another completely different codon. This can be harmful, as in sickle-cell disease, where just one amino acid, glutamic acid, is changed to valine.
Because without it you would have no support to stand
Cell wall and chloraplast!
THAT IS THE ONLY TWO!
hope this helps
xoxo-
Jojo
