Deck 17: Amino Acids, Peptides, and Proteins
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Deck 17: Amino Acids, Peptides, and Proteins
1
Under what condition would phenylalanine exist as follows? 
A) at a low pH
B) at a high pH
C) at the pI
D) when pH = pKa
E) none of these

A) at a low pH
B) at a high pH
C) at the pI
D) when pH = pKa
E) none of these
at a high pH
2
In the dipeptide shown the following segment of the molecule is likely to lie in a single plane: 
A)
B)
C)
D)
E)

A)

B)

C)

D)

E)


3
What is the only -amino acid that does not have a stereogenic carbon?
A) glycine
B) alanine
C) phenylalanine
D) valine
E) leucine
A) glycine
B) alanine
C) phenylalanine
D) valine
E) leucine
glycine
4
Hydrogen bonds, -helices, and pleated sheets are structural properties of proteins.
A) primary
B) secondary
C) tertiary
D) quaternary
E) sole
A) primary
B) secondary
C) tertiary
D) quaternary
E) sole
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5
Which of the following -amino acids contains a hydroxyl group?
A) asparagine
B) threonine
C) cysteine
D) isoleucine
E) phenylalanine
A) asparagine
B) threonine
C) cysteine
D) isoleucine
E) phenylalanine
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6
Which of the following molecules is -aminopropanoic acid?
A)
B)
C)
D)
E)
A)

B)

C)

D)

E)

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7
What is the correct relationship between valylalanine and alanylvaline?
A) enantiomeric pair
B) meso compounds
C) structural isomers
D) geometric isomers
E) racemic mixture
A) enantiomeric pair
B) meso compounds
C) structural isomers
D) geometric isomers
E) racemic mixture
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8
What is the name of the following molecule? 
A) 3-amino-3-phenylvaleric acid
B) 4-amino-4-methyl-4-phenylbutanoic acid
C) 4-amino-4-phenylpentanoic acid
D) 4-amino-4-phenyl-4-methylbutanoic acid
E) 2-amino-2-phenylbutanoic acid

A) 3-amino-3-phenylvaleric acid
B) 4-amino-4-methyl-4-phenylbutanoic acid
C) 4-amino-4-phenylpentanoic acid
D) 4-amino-4-phenyl-4-methylbutanoic acid
E) 2-amino-2-phenylbutanoic acid
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9
The dipeptides
are
A) constitutional isomers.
B) stereoisomers.
C) diastereoisomers.
D) enantiomers.
E) identical.
areA) constitutional isomers.
B) stereoisomers.
C) diastereoisomers.
D) enantiomers.
E) identical.
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10
What is the name of the amide bond linking two amino acids?
A) ionic
B) hydrogen
C) glycosidic
D) nonpolar
E) peptide
A) ionic
B) hydrogen
C) glycosidic
D) nonpolar
E) peptide
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11
How many different combinations are possible for a tripeptide containing one of each of the following amino acids: Phe, Val, Asp?
A) 2
B) 6
C) 8
D) 10
E) greater than 10
A) 2
B) 6
C) 8
D) 10
E) greater than 10
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12
Which one of the following represents a tetrapeptide?
A) Val-Ile-Asp-Asp
B) Ala-Ala-Ala-Ala-Val-Val
C) Ala-Ser-Val-Val-Ile
D) Ser-Ser-Ala-Ala-Gly-Gly-Glu-Glu
E) Ser-Ala-Thr-Pro-Leu
A) Val-Ile-Asp-Asp
B) Ala-Ala-Ala-Ala-Val-Val
C) Ala-Ser-Val-Val-Ile
D) Ser-Ser-Ala-Ala-Gly-Gly-Glu-Glu
E) Ser-Ala-Thr-Pro-Leu
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13
Which molecule is an -amino acid?
A)
B)
C)
D)
E)
A)

B)

C)

D)

E)

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14
Which of the following -amino acids contains an imidazole?
A) arginine
B) asparagine
C) aspartic acid
D) histidine
E) tyrosine
A) arginine
B) asparagine
C) aspartic acid
D) histidine
E) tyrosine
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15
What is the net charge of isoleucine at its isoelectric point?
A) 0
B) +1
C) +2
D) -1
E) -2
A) 0
B) +1
C) +2
D) -1
E) -2
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16
In the octapeptide, Cys-Ile-Ser-Asp-Gly-His-Gly-Gly, which is the N-terminal amino acid?
A) Ser
B) Ile
C) Asp
D) Cys
E) Gly
A) Ser
B) Ile
C) Asp
D) Cys
E) Gly
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17
To what family of polymers do proteins belong?
A) polyesters
B) polyacids
C) polyamines
D) polyurethanes
E) polyamides
A) polyesters
B) polyacids
C) polyamines
D) polyurethanes
E) polyamides
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18
How many different combinations are possible for a tetrapeptide containing two glycines (Gly,) one alanine (Ala,) and one phenylalanine (Phe)?
A) 3
B) 6
C) 12
D) 24
E) 36
A) 3
B) 6
C) 12
D) 24
E) 36
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19
In the octapeptide, Phe-Ile-Ser-Asp-Gly-His-Gly-Tyr, which is the C-terminal amino acid?
A) Ser
B) Phe
C) Tyr
D) His
E) Gly
A) Ser
B) Phe
C) Tyr
D) His
E) Gly
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20
Which of the following amino acids can form disulfide bonds?
A) Gly
B) His
C) Cys
D) Asp
E) Glu
A) Gly
B) His
C) Cys
D) Asp
E) Glu
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21
Which of the following is Sanger's reagent?
A)
B)
C)
D)
E)
A)

B)

C)

D)

E)

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22
The structure of
at the isoelectric point is:
A)
B)
C)
D)
E)
at the isoelectric point is:A)

B)

C)

D)

E)

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23
Based on the pKa's of aspartic acid shown below, what is its approximate isoelectric point?
A) 2
B) 3
C) 5
D) 7
E) 10
A) 2
B) 3
C) 5
D) 7
E) 10
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24
A useful reagent for detecting amino acids is
A) hydrogen peroxide.
B) Tollens' reagent.
C) ninhydrin.
D) Benedict's reagent.
E) Merrifield's reagent.
A) hydrogen peroxide.
B) Tollens' reagent.
C) ninhydrin.
D) Benedict's reagent.
E) Merrifield's reagent.
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25
Bradykinin is a nonapeptide, Arg-Pro-Pro-Gly-Phe-Ser-Pro-Phe-Arg.In addition to one mole of Arg, what peptides are present after hydrolysis of bradykinin with chymotrypsin?
A) Arg-Pro-Pro and Gly-Phe and Ser-Pro-Phe
B) Pro-Pro-Gly and Phe-Ser-Pro-Phe-Arg
C) Arg-Pro-Pro-Gly-Phe and Ser-Pro-Phe
D) Arg-Pro-Pro-Gly-Phe-Ser and Pro-Phe
A) Arg-Pro-Pro and Gly-Phe and Ser-Pro-Phe
B) Pro-Pro-Gly and Phe-Ser-Pro-Phe-Arg
C) Arg-Pro-Pro-Gly-Phe and Ser-Pro-Phe
D) Arg-Pro-Pro-Gly-Phe-Ser and Pro-Phe
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26
At the isoelectric point, the structure of methionine (2-amino-4-methylthiobutanoic acid) is:
A)
B)
C)
D)
E)
A)

B)

C)

D)

E)

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27
What class of compound is produced when leucine reacts with acetyl chloride?
A) ester
B) amide
C) ether
D) phenol
E) alcohol
A) ester
B) amide
C) ether
D) phenol
E) alcohol
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28
Which reagent is used to determine the N-terminal amino acid of a peptide?
A) Jones'
B) Fehling's
C) Ninhydrin
D) Sanger's
E) Tollens'
A) Jones'
B) Fehling's
C) Ninhydrin
D) Sanger's
E) Tollens'
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29
What fragments will be obtained by a trypsin hydrolysis of the following octapeptide? Ala-Val-Trp-Lys-Phe-Gly-Arg-Met
A) Ala-Val-Trp-Lys-Phe and Gly-Arg-Met
B) Ala-Val-Trp-Lys-Phe -Gly and Arg-Met
C) Ala-Val-Trp-Lys and Phe-Gly-Arg and Met
D) Ala-Val-Trp-Lys and Phe and Gly-Arg and Met
E) Ala-Val-Trp and Lys-Phe-Gly and Arg-Met
A) Ala-Val-Trp-Lys-Phe and Gly-Arg-Met
B) Ala-Val-Trp-Lys-Phe -Gly and Arg-Met
C) Ala-Val-Trp-Lys and Phe-Gly-Arg and Met
D) Ala-Val-Trp-Lys and Phe and Gly-Arg and Met
E) Ala-Val-Trp and Lys-Phe-Gly and Arg-Met
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30
Which of the following will migrate toward the positive electrode in an electrophoresis experiment? 
A) I
B) II
C) III
D) I and III
E) none will migrate

A) I
B) II
C) III
D) I and III
E) none will migrate
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31
If an amino acid has one carboxyl group and one amino group, and the pKa's are 2.4 and 9.8 respectively, what is its isoelectric point?
A) 3.7
B) 6.1
C) 7.0
D) 7.9
E) 12.2
A) 3.7
B) 6.1
C) 7.0
D) 7.9
E) 12.2
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32
Sanger's reagent is used
A) to determine the amino acid sequence of a peptide.
B) to determine the C-terminal amino acid of a peptide.
C) to determine the isoelectric point of a peptide.
D) to determine the number of amino acids in a peptide.
E) to determine the N-terminal amino acid of a peptide.
A) to determine the amino acid sequence of a peptide.
B) to determine the C-terminal amino acid of a peptide.
C) to determine the isoelectric point of a peptide.
D) to determine the number of amino acids in a peptide.
E) to determine the N-terminal amino acid of a peptide.
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33
Based on the equilibria shown below, what is the net charge on structure IV?
A) -2
B) -1
C) 0
D) +1
E) +2
A) -2
B) -1
C) 0
D) +1
E) +2
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34
Which reagent is used specifically to cleave the C-terminal amino acid of a peptide?
A) trypsin
B) carboxypeptidase
C) cyanogen bromide
D) chymotrypsin
E) HCl/H2O
A) trypsin
B) carboxypeptidase
C) cyanogen bromide
D) chymotrypsin
E) HCl/H2O
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35
The Edman degradation is used
A) to identify the C-terminal amino acid of a peptide.
B) to determine the tertiary structure of peptides.
C) to synthesize peptides.
D) to cleave polypeptides on the carboxyl side of Phe, Tyr, and Trp residues.
E) to identify the N-terminal amino acid of a peptide.
A) to identify the C-terminal amino acid of a peptide.
B) to determine the tertiary structure of peptides.
C) to synthesize peptides.
D) to cleave polypeptides on the carboxyl side of Phe, Tyr, and Trp residues.
E) to identify the N-terminal amino acid of a peptide.
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36
Ninhydrin is used
A) to determine the N-terminal amino acid of a peptide.
B) to sequence amino acids in a peptide.
C) to detect amino acids derived from hydrolysis of a peptide.
D) to couple amino acids during solid-phase peptide synthesis.
E) to hydrolyze peptides on the carboxyl side of aromatic amino acid residues.
A) to determine the N-terminal amino acid of a peptide.
B) to sequence amino acids in a peptide.
C) to detect amino acids derived from hydrolysis of a peptide.
D) to couple amino acids during solid-phase peptide synthesis.
E) to hydrolyze peptides on the carboxyl side of aromatic amino acid residues.
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37
The isoelectric pH (pI) of
is likely to be at a pH that is
A) below pK1.
B) at pK1.
C) between pK1 and pK2.
D) at pK2.
E) above pK2.
is likely to be at a pH that isA) below pK1.
B) at pK1.
C) between pK1 and pK2.
D) at pK2.
E) above pK2.
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38
What is the structure of the phenylhydantoin derived from the first cycle of the Edman degradation of Phe-Ala-Ser?
A)
B)
C)
D)
E)
A)

B)

C)

D)

E)

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39
A tetrapeptide contains the amino acids Phe, Ala, Gly, and Leu.Partial hydrolysis affords the dipeptides Phe-Ala, Ala-Gly, and Leu-Phe.The structure of the tetrapeptide is
A) Ala-Gly-Leu-Phe.
B) Leu-Phe-Ala-Gly.
C) Gly-Ala-Phe-Leu.
D) Leu-Phe-Gly-Ala.
E) Phe-Leu-Gly-Ala.
A) Ala-Gly-Leu-Phe.
B) Leu-Phe-Ala-Gly.
C) Gly-Ala-Phe-Leu.
D) Leu-Phe-Gly-Ala.
E) Phe-Leu-Gly-Ala.
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40
The mechanism by which Sanger's reagent reacts with an amine is
A) nucleophilic aromatic substitution.
B) electrophilic aromatic substitution.
C) hydrolysis.
D) nucleophilic acyl substitution.
E) electrophilic addition.
A) nucleophilic aromatic substitution.
B) electrophilic aromatic substitution.
C) hydrolysis.
D) nucleophilic acyl substitution.
E) electrophilic addition.
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41
The reaction of
with bromine water is likely to give:
A)
B)
C)
D)
E)
with bromine water is likely to give:A)

B)

C)

D)

E)

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42
Sanger's reagent (2,4-dinitrofluorobenzene) reacts with the following to give, after complete hydrolysis, 
A) no labeled amino acids.
B) one labeled and two unlabeled amino acids.
C) one labeled and three unlabeled amino acids.
D) two labeled and one unlabeled amino acids.
E) two labeled and two unlabeled amino acids.

A) no labeled amino acids.
B) one labeled and two unlabeled amino acids.
C) one labeled and three unlabeled amino acids.
D) two labeled and one unlabeled amino acids.
E) two labeled and two unlabeled amino acids.
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43
The product from the following is: 
A)
B)
C)
D)
E)

A)

B)

C)

D)

E)

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44
Treatment of
with HF (Merrifield method) gives:
A)
B)
C)
D)
E)
with HF (Merrifield method) gives:A)

B)

C)

D)

E)

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45
Which of the following reagents is used to protect the N-terminal amino acid in a solid phase peptide synthesis?
A)
B)
C)
D)
E)
A)

B)

C)

D)

E)

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46
Dicyclohexylcarbodiimide (DCC) is used
A) to determine the N-terminal amino acid of a peptide.
B) to sequence amino acids in a peptide.
C) to detect amino acids derived from hydrolysis of a peptide.
D) to couple amino acids during solid-phase peptide synthesis.
E) to hydrolyze peptides on the carboxyl side of aromatic amino acid residues.
A) to determine the N-terminal amino acid of a peptide.
B) to sequence amino acids in a peptide.
C) to detect amino acids derived from hydrolysis of a peptide.
D) to couple amino acids during solid-phase peptide synthesis.
E) to hydrolyze peptides on the carboxyl side of aromatic amino acid residues.
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47
An aniline derivative that is suitable for use in the Merrifield peptide synthesis is: 
A) 1
B) 2
C) 3
D) 4
E) none of the above

A) 1
B) 2
C) 3
D) 4
E) none of the above
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