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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'

F) B) and D)
G) B) and C)

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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

F) A) and C)
G) None of the above

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Which molecule is an α\alpha -amino acid?


A)  Which molecule is an  \alpha -amino acid? A)    B)    C)    D)    E)
B)  Which molecule is an  \alpha -amino acid? A)    B)    C)    D)    E)
C)  Which molecule is an  \alpha -amino acid? A)    B)    C)    D)    E)
D)  Which molecule is an  \alpha -amino acid? A)    B)    C)    D)    E)
E)  Which molecule is an  \alpha -amino acid? A)    B)    C)    D)    E)

F) B) and C)
G) C) and D)

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Which of the following α\alpha -amino acids contains an imidazole?


A) arginine
B) asparagine
C) aspartic acid
D) histidine
E) tyrosine

F) All of the above
G) A) and D)

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D

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.

F) A) and B)
G) B) and C)

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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.

F) B) and D)
G) A) and B)

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A

Which of the following molecules is α\alpha -aminopropanoic acid?


A)  Which of the following molecules is  \alpha -aminopropanoic acid? A)    B)    C)    D)    E)
B)  Which of the following molecules is  \alpha -aminopropanoic acid? A)    B)    C)    D)    E)
C)  Which of the following molecules is  \alpha -aminopropanoic acid? A)    B)    C)    D)    E)
D)  Which of the following molecules is  \alpha -aminopropanoic acid? A)    B)    C)    D)    E)
E)  Which of the following molecules is  \alpha -aminopropanoic acid? A)    B)    C)    D)    E)

F) All of the above
G) B) and E)

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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.

F) A) and C)
G) All of the above

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In the dipeptide shown the following segment of the molecule is likely to lie in a single plane: In the dipeptide shown the following segment of the molecule is likely to lie in a single plane:   A)    B)    C)    D)    E)


A) In the dipeptide shown the following segment of the molecule is likely to lie in a single plane:   A)    B)    C)    D)    E)
B) In the dipeptide shown the following segment of the molecule is likely to lie in a single plane:   A)    B)    C)    D)    E)
C) In the dipeptide shown the following segment of the molecule is likely to lie in a single plane:   A)    B)    C)    D)    E)
D) In the dipeptide shown the following segment of the molecule is likely to lie in a single plane:   A)    B)    C)    D)    E)
E) In the dipeptide shown the following segment of the molecule is likely to lie in a single plane:   A)    B)    C)    D)    E)

F) B) and E)
G) A) and D)

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Which of the following reagents is used to protect the N-terminal amino acid in a solid phase peptide synthesis?


A) 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)
B) 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)
C) 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)
D) 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)
E) 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)

F) All of the above
G) A) and B)

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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

F) None of the above
G) A) and C)

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The reaction of The reaction of   with bromine water is likely to give: A)    B)    C)    D)    E)   with bromine water is likely to give:


A) The reaction of   with bromine water is likely to give: A)    B)    C)    D)    E)
B) The reaction of   with bromine water is likely to give: A)    B)    C)    D)    E)
C) The reaction of   with bromine water is likely to give: A)    B)    C)    D)    E)
D) The reaction of   with bromine water is likely to give: A)    B)    C)    D)    E)
E) The reaction of   with bromine water is likely to give: A)    B)    C)    D)    E)

F) C) and D)
G) D) and E)

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Based on the equilibria shown below, what is the net charge on structure IV? Based on the equilibria shown below, what is the net charge on structure IV?   <sub> </sub> A)  -2 B)  -1 C)  0 D)  +1 E)  +2


A) -2
B) -1
C) 0
D) +1
E) +2

F) A) and B)
G) A) and C)

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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

F) A) and B)
G) A) and C)

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What is the name of the amide bond linking two amino acids?


A) ionic
B) hydrogen
C) glycosidic
D) nonpolar
E) peptide

F) A) and E)
G) C) and D)

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What is the net charge of isoleucine at its isoelectric point?


A) 0
B) +1
C) +2
D) -1
E) -2

F) D) and E)
G) A) and E)

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At the isoelectric point, the structure of methionine (2-amino-4-methylthiobutanoic acid) is:


A) At the isoelectric point, the structure of methionine (2-amino-4-methylthiobutanoic acid)  is: A)    B)    C)    D)    E)
B) At the isoelectric point, the structure of methionine (2-amino-4-methylthiobutanoic acid)  is: A)    B)    C)    D)    E)
C) At the isoelectric point, the structure of methionine (2-amino-4-methylthiobutanoic acid)  is: A)    B)    C)    D)    E)
D) At the isoelectric point, the structure of methionine (2-amino-4-methylthiobutanoic acid)  is: A)    B)    C)    D)    E)
E) At the isoelectric point, the structure of methionine (2-amino-4-methylthiobutanoic acid)  is: A)    B)    C)    D)    E)

F) C) and D)
G) A) and C)

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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

F) B) and C)
G) A) and E)

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Which of the following will migrate toward the positive electrode in an electrophoresis experiment? 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

F) A) and C)
G) A) and B)

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B

The dipeptides The dipeptides   are A)  constitutional isomers. B)  stereoisomers. C)  diastereoisomers. D)  enantiomers. E)  identical. are


A) constitutional isomers.
B) stereoisomers.
C) diastereoisomers.
D) enantiomers.
E) identical.

F) B) and C)
G) B) and E)

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