Answer:
Aldehyde Dehydrogenase 2 (ALDH2) is an enzyme required to eliminate toxins such as acetaldehyde and alcohol, thereby mutations in this protein may be associated with the Alcohol flush syndrome (AFS)
Explanation:
ALDH2 is a protein required for ATP generation by catalyzing the oxidation of aldehydes to carboxylic acids (i.e., oxidation of NADH to NAD+). Mutations in the ALDH2 gene have been associated with the inactive form of this enzyme, and this specific mutation at position 487 alters its enzymatic activity associated with the metabolism of acetaldehyde and alcohol. This amino acid substitution may lead to the active site-directed inactivation of the enzyme.
Answer:
An acid is a substance that donates hydrogen ions. ... Now there are more hydrogen ions than hydroxide ions in the solution. This kind of solution is acidic
<span>The answer is c. Chromosomes carry the codes for hereditary traits. Chromosomes are thread-like structures made of proteins and DNA. Codes for hereditary traits are present in a molecule of DNA. Chromosomes can be found in the nucleus of each cell. Humans have 46 chromosomes in each cell (not 460) arranged in 23 pairs (not 230). Hope this helps. Let me know if you need additional help!</span>
Answer:
The digestion of dietary and blood protein.
Explanation:
Encephalopathy is a disease referring to brain damage or malfunction. This means that, a situation whereby the brain is not functioning very well.
This can be caused by drugs, toxins, trauma and infections among others.
In this case, the building up of ammonia in the blood will result to type of encephalopathy known as hepatic encephalopathy. This is when the consciousness level of the brain is being altered.
This happens when the the liver cannot remove toxic chemicals like ammonia from the body.
