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Biochemistry Chapter 04 Assignment
Biochemistry Chapter 04 Assignment
1
At pH 5.0?
0
At pH 10.5?
-1
At pH 13.5?
Question 2
There are several amino acid side chains which are always charged at physiological pH. These
are:
Answer: D
Question 3
Which one of the following sequences of five amino acids would most likely be located in the
interior of a globular soluble protein?
a. Glu-Asn-Ser-Thr-Gln
b. Tyr-Phe-Glu-Asn-Leu
c. Val-Ala-Val-Glu-Val
d. Met-Cys-Pro-His-Tyr
e. Met-Phe-Pro-Ile-Leu
Answer: E
Question 4
Answer: D
Question 5
What would be the net charge for the peptide below at pH 7.0?
Asn-Asp-Cys-Tyr-Ser-Val-Lys
a. -2
b. +2
c. -1
d. 0
e. +1
Answer: 0
Question 6
Answer: E
Question 7
a. 0
b. 2
c. 1
d. 3
Answer: 2
Question 8
How many functional groups does the peptide MDFGRKCDE have that can be titrated?
a. 8
b. 7
c. 5
d. 6
Answer: 8
Question 9
Using the titration curve shown, identify the amino acid being titrated in this experiment.
a. Tyrosine
b. Arginine
c. Lysine
d. Cysteine
Answer: b
Question 10
Biological systems usually produce a single enantiomer, whereas chemical synthesis produces
a
Racemic mixture
.
Question 11
Glutamate
.
Question 12
Which of the following statements is true?
Answer: B
Question 13
The ionization of amino acids depends on the pH and the pKas of the ionizable groups. The
pK1 and pK2 for the amino acid shown below are 2.1 and 8.8, respectively. At what pH is the
amino acid ionized predominantly as shown?
a. pH 1.0
b. pH 2.1
c. pH 5.5
d. pH 8.8
e. pH 10.0
Answer: a
Question 14
The pK1, pK2, and pKR for the amino acid arginine are 1.8, 9.0, and 12.5, respectively. At pH
7.0 arginine would be charged predominantly as follows:
Answer: c
Question 15
The pK1, pK2, and pKR for the amino acid glutamate are 2.1, 9.5, and 4.1, respectively. At pH
11.0, glutamate would be charged predominantly as follows:
Answer: e
Question 16
The tripeptide glycylarginylglutamate contains four ionizable groups with pKas of 2.1, 4.1,
9.8, and 12.5. Calculate the pI for this molecule.
a. 3.1
b. 6.4
c. 7.0
d. 7.3
e. 8.3
Answer: c
Question 17
The side-chains of amino acids have
a. a positive charge in every situation.
b. pKas that assure the solubility of every protein.
c. constant pKas no matter what aqueous environment they are found in.
Answer: d
Question 18
Ribosomes use L amino acids to synthesize proteins.These amino acids are called “L” because
Answer: c
Question 19
All the standard amino acids except ____ are optically active.
a. Pro
b. Arg
c. Trp
d. Gly
e. Phe
Answer: D
Question 20
The __________ character of most standard amino acids causes solutions of amino acids to
rotate the plane of polarized light.
a. chiral
b. zwitterionic
c. polar
d. hydrophobic
e. none of the above
Answer: A
Question 21
What is the name of this molecule?
a. GABA
b. -carboxyglutamate
c. glutathione
d. epinephrine
e. thyroxine
Answer: c
Question 22
Glutamic acid has pK values of 2.10, 4.07, and 9.47 for its -carboxyl group, -carboxyl
group, and -amino group, respectively. What is its estimated pI?
a. 6.77
b. 4.07
c. 3.085
d. 5.785
Answer: c
Question 23
Why is the pK of the carboxyl group of glycine (2.35) so much lower than that of acetic acid
(4.76)?
a. because the positively-charged amino group of glycine stabilizes the carboxylate group
b. because the positively-charged amino group stabilizes the protonated carboxyl group
c. because the neutral amine of glycine stabilizes the carboxylate group
d. because the positively-charged amino group of glycine destabilizes the carboxylate
group
Answer: a
Question 24
bacterial
cell walls.
Question 25
glutathione
.