I think this is an theory changing because a new scientific method was developed. They used what Mendel had learned to test the hypothesis themselves and discovered that he was right.
Answer:
The correct answer is - proteins.
Explanation:
Enzymes are made up of the long chains of amino acids that are linked by the peptide bonds that make a polypeptide chain known as proteins. Proteins are the building block of the enzyme and the building of thevarious structures in the body.
Enzymes are made up of two protein that also plays as the role of a biological catalyst whereas protein only plays role in forming different structure and performing functions.
Answer:
The cell membrane is semi-permeable. It allows some molecules to enter easily inside the cell whereas some molecules are blocked from entering the cell.
Small, polar molecules and hydrophobic molecules enter easily through the cell membrane. But large molecules and ions cannot easily move inside the cell membrane.
A hydrophilic substance like the substance L mentioned in the question enters the cell membrane through the help of carrier proteins. The substance attached to the large protein might enter through active or passive diffusion but it can only enter the cell by attaching to carrier proteins.
Answer:
It would most likely render the protein nonfunctional or mis-functional.
The mutation could result in three outcomes:
- Silent mutation, which changes the codon to the same amino acid. (AAA->AAG, both are lysine). But since the problem specified that it has a "slightly different amino acid sequence," we can assume this doesn't happen.
- Nonsense mutation, which changes a codon to a stop codon. This would end the chain of amino acids, making the protein potentially nonfunctional.
- Missense mutation, which changes a codon to another completely different codon. This can be harmful, as in sickle-cell disease, where just one amino acid, glutamic acid, is changed to valine.
