Answer:
Lysosomes.
Explanation:
HEXA (Hexosaminidase A) is the functional enzyme and encoded by the HEXA gene. The main function of this enzyme is the hydroxylation of the gangliosides.
The mutation in this gene leads to the lysosomal storage disease. The GM2 starts accumulating in the lysosomes and causes Tay Sach's disease. This is a genetic disorder that leads to the breakdown of the cells of the spinal cord and the brain.
Thus, the answer is lysosomes.
Answer:
The lysosome and vacuole are similar to the excretory system. They both store waste and removes waste. The nucleus is similar to the nervous system. The both provide instructions for the functioning of the system. Summary. Cells are highly organized which allows for specialization of each cellular process.
Explanation:
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Answer:
non-covalent hydrogen bonding between paired bases :)
Explanation:
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Eukaryotic cells rely on the molecular energy of ATP to sustain all of the reactions necessary to maintain life, in the absence of ATP, these reactions would come to a halt, and the cell would inevitably die.
ATP is a molecular compound that provides the energy needed by most cells to survive. ATP represents Adenosine triphosphate, which is an organic compound that provides energy to drive the essential metabolic reactions of living cells, such as:
- Muscle contractions
- Nerve impulses
- Chemical synthesis
- Nutrient absorbtion
In the situation in which a cell was to run out of ATP, these reactions would stop, given that they require ATP to function. This means that the cell would not be able to send or receive nerve signals, absorb the nutrients it needs, or even create necessary compounds such as proteins. The stoppage of these functions would lead to the death of the cell.
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