The answer is; B
This type of inhibitors does not bind the active site of the enzyme hence does not compete with the substrate (hence its name non-competitive inhibitors). They bind the enzyme at another site and change its conformation. The substrate may still be able to bind the active site but the efficiency of catalysis can be drastically reduced threatening life. This type of inhibition cannot be cured by increasing substrate levels.
This represents the anaerobic part of cellular respiration, this specifically would represent the Krebs cycle. I highly doubt that they want you to be that specific, so Cellular respiration
ATP stores and transports energy in the cells, usually in the mitochondria. Energy is released by hydrolysis (carbohydrates being broken down into sugar molecules), which eventually results in forming ADP (adenosine diphosphate) that absorbs the energy and recharges the phosphate group and ATP
Answer:
1.The pleural cavity aids optimal functioning of the lugs during breathing. It transmits movements of the chest wall to the lungs, particularly during heavy breathing. The closely approved chest wall transmits pressures to the visceral pleural surface and hence to the lung (10-19.
2.The diaphragm, located below the lungs, is the major muscle of respiration. It is a large, dome-shaped muscle that contracts rhythmically and continually, and most of the time, involuntarily. Upon inhalation, the diaphragm contracts and flattens and the chest cavity enlarge.
Explanation:
Enzymes are regulated by more than the binding of small molecules. A second method that is used all the time by eucaryotic cells to regulate a protein's function is the covalent addition of a phosphate group to one of its amino acid side chains. These phosphorylation events can affect the protein in two important ways.
