Answer:
ok sike i lied you thought i tried
Explanation:
Answer:
(A). Result in different amino acids to be read due to frame shifts
Explanation:
Insertion or deletion mutations (or Indel mutations) can be defined as mutations in DNA due to insertion (addition) or deletion of nucleotide bases in DNA.
These mutations lead to change in reading frames (sequence of codons), which leads to formation of protein having completely different amino acid sequence. Hence, these mutations are also cause frameshift mutations.
This is due due to triplet nature of genetic codes as insertion or deletion of one or more bases (but not three) would change change in codon sequence and mutated sequence can form a non-functional or truncated protein.
Thus, the correct answer is option (A).
Answer:
Amino acid sequence is directly related to the differences in the DNA of the species.
Explanation:
Above situation is related to the evolutionary research in which scientists are in search of common characteristics between species and from those species they will examine the amino acid sequence of proteins because amino acids sequence is directly related to the sequence of DNA and DNA is the main thing among all other variables by which differences in species can be identified effectively.
Answer:Curare molecules have a chemical structure like the neurotransmitter ACh. Curare can bind to the ACh receptor site on the chemically gated ion channels in the motor end plate. Even though curare will bind to the receptor site it will not open the ion channel and no ions will pass through. hope this helps ! :)
