Biochemistry : Amino Acids and Proteins

Study concepts, example questions & explanations for Biochemistry

varsity tutors app store varsity tutors android store

Example Questions

1 2 3 4 5 7 Next →

Example Question #61 : Amino Acids And Proteins

If a certain functional group on a peptide has a pKa of , then what percentage of it would be expected to be protonated if it were in a solution with a pH of ?

Possible Answers:

Correct answer:

Explanation:

In this question, we're given the pKa of a peptide's functional group and we're told that the peptide is in a solution at a certain pH. We're asked to estimate the proportion of the functional group that we would expect to be protonated.

The first thing we can realize about this problem is that the peptide is in a solution that is far more acidic than the pKa of the functional group. Therefore, we would certainly expect a lot of it to be protonated. The question is, by how much?

We can make use of the Henderson-Hasselbalch equation to quantify the degree to which the functional group will become protonated.

In the equation above, we can take base to mean the deprotonated functional group, while acid we can take as the protonated functional group.

We can also rearrange the above expression in order to isolate the base to acid ratio.

Next, we can plug in the values given to us in the question stem.

We can rewrite this expression alternatively to make it more intuitive.

In other words, for every one equivalent of base, there are  equivalents of acid. To find the proportion of acid, we can take the number of acidic equivalents and divide that by the total number of acidic plus basic equivalents.

Thus,  of the functional group is expected to be in the protonated form. This makes sense, considering that the solution is significantly more acidic than this particular functional group's pKa.

Example Question #61 : Macromolecule Fundamentals

Which amino acid is the primary source of ammonia?

Possible Answers:

Serine

Glycine

Glutamate

Tyrosine

Glutamine

Correct answer:

Glutamate

Explanation:

Glutamate is the primary source of ammonia. Glutamine is similar however it is the amide free form of ammonia. Glutamate plays an important role in the urea cycle. The urea cycle serves to rid the body of ammonia, which can be toxic in high amounts.

Example Question #62 : Macromolecule Fundamentals

What is true concerning charged hydrophilic amino acids?

Possible Answers:

The side chains form hydrogen bonds

The side chains are insoluble in water

The side chains carry at net charge at or near neutral pH

They are nonpolar

They can traverse the plasma membrane via simple diffusion

Correct answer:

The side chains carry at net charge at or near neutral pH

Explanation:

Charged hydrophilic amino acids are polar and their side chains carry a net charge at or near a neutral pH. For instance, lysine has a positive charge at a pH of 7. Examples of essential amino acids that are in this group include arginine, histidine, and lysine.

1 2 3 4 5 7 Next →
Learning Tools by Varsity Tutors