<h2>Muscle contraction in cytoplasm </h2>
Explanation:
- Calcium stays in the sarcoplasmic reticulum until discharged by an improvement. Calcium at that point ties to troponin, causing the troponin to change shape and expel the tropomyosin from the coupling destinations. Cross-connect stick proceeds until the calcium particles and ATP are never again accessible.
- ATP is basic to get ready myosin for official and to "revive" the myosin.
- When the actin-restricting destinations are revealed, the high-vitality myosin head overcomes any issues, framing a cross-connect. When myosin ties to the actin, the Pi is discharged, and the myosin experiences a conformational change to a lower vitality state. As myosin consumes the vitality, it travels through the "power stroke," pulling the actin fiber toward the M-line.
We all have the same genetic makeup. DNA
Answer:
This question is incomplete
Explanation:
This question is incomplete because of the absence of the chart referred to in the question. However, what appears to be the case is that the three nitrogenous bases represent codons (and the missing chart is the codon chart). The mutation that has the potential to cause more damage will be the one that would change the amino acid formed from the codon change.
A. CAU to CAC: The codons CAU and CAC both form the amino acid histidine and thus is not expected to cause a major damage.
B. UGU to UGC: The codons UGU and UGC both form the amino acid cysteine and thus is not expected to cause a major damage.
C. UCU to UUU: <u>Codon UCU forms the amino acid serine while the codon UUU forms the amino acid phenylalanine</u>. Thus, this eventual change in the amino acid formed has the potential to cause a major damage and thus option C is the correct option.
NOTE that a codon is a sequence of three DNA/RNA nucleotides that corresponds to a single amino acid.
