Deck 21: Amino Acids, Peptides, and Proteins
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Deck 21: Amino Acids, Peptides, and Proteins
1
Which of the following amino acids has a hydroxy-containing R group?
A) asparagine
B) cysteine
C) proline
D) serine
E) valine
A) asparagine
B) cysteine
C) proline
D) serine
E) valine
serine
2
Which structure is naturally occurring isoleucine, which is(2S,3S)-2-amino-3-methylpentanoic acid?
A)
B)
C)
D)
E) B and C
A)

B)

C)

D)

E) B and C

3
Which L-amino acid has the R configuration at the ?-position?
A) tyrosine
B) cysteine
C) aspartate
D) leucine
E) methionine
A) tyrosine
B) cysteine
C) aspartate
D) leucine
E) methionine
cysteine
4
Which structure does tyrosine have at pH 7.3?
A)
B)
C)
D)
E)
A)

B)

C)

D)

E)

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5
What is the isoelectric point (pI) of arginine? 
A) 2.17
B) 7.90
C) 9.04
D) 10.76
E) 12.48

A) 2.17
B) 7.90
C) 9.04
D) 10.76
E) 12.48
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6
Which of the following amino acids will elute first during cation-exchange chromatography at pH 7?
A) aspartate
B) isoleucine
C) lysine
D) proline
E) threonine
A) aspartate
B) isoleucine
C) lysine
D) proline
E) threonine
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7
Which method forms leucine from 1-bromo-3-methylbutane?
A) HVZ
B) reductive amination
C) acetamidomalonic ester
D) Strecker
E) Kiliani-Fischer
A) HVZ
B) reductive amination
C) acetamidomalonic ester
D) Strecker
E) Kiliani-Fischer
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8
What is the name of this tripeptide?

A) Val-Asn-Thr
B) Leu-Asn-Ser
C) Val-Gln-Thr
D) Leu-Gln-Thr
E) Val-Asn-Thr valine threonine asparagine

A) Val-Asn-Thr
B) Leu-Asn-Ser
C) Val-Gln-Thr
D) Leu-Gln-Thr
E) Val-Asn-Thr valine threonine asparagine
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9
Regarding the strategy of peptide synthesis, which statement is true?
A) The N-terminal amino acid is protected using a t-BOC group.
B) The N-protected amino acid is activated using DCCD.
C) The reaction of the second amino acid with the first proceeds by way of nucleophilic acyl substitution.
D) Removing the protecting group drives the reaction to the completion.
E) all of the above
A) The N-terminal amino acid is protected using a t-BOC group.
B) The N-protected amino acid is activated using DCCD.
C) The reaction of the second amino acid with the first proceeds by way of nucleophilic acyl substitution.
D) Removing the protecting group drives the reaction to the completion.
E) all of the above
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10
Which of the following statements is not true about the Merrifield automated solid-phase peptide synthesis?
A) It provides a faster way of producing peptides.
B) It produces peptides in high yields.
C) It allows for synthesis of peptides containing up to 1000 amino acid residues.
D) It uses a solid support technique allowing easy purification after each step.
E) It allows synthesis of proteins that differ by one or a few
Amino acids.
The Merrifield method is practical for proteins
Of 100 amino acid residues or fewer.
A) It provides a faster way of producing peptides.
B) It produces peptides in high yields.
C) It allows for synthesis of peptides containing up to 1000 amino acid residues.
D) It uses a solid support technique allowing easy purification after each step.
E) It allows synthesis of proteins that differ by one or a few
Amino acids.
The Merrifield method is practical for proteins
Of 100 amino acid residues or fewer.
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11
The ____________ structure is the three-dimensional shape of the entire polypeptide.
A) Primary
B) secondary
C) tertiary
D) Quaternary
E) Molecular
A) Primary
B) secondary
C) tertiary
D) Quaternary
E) Molecular
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