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What is the predominant form of the amino acid abbreviated val at pH 7?


A) positive
B) neutral
C) negative

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B

 Exhibit 3A (for this chapter)   Amino acid α-carboxyl group pK a α-amino group pK a  R-group pK  Ala 2.39.7 Arg 2.29.012.5 Asn or Gln 2.19.04.0 Asp or Glu 2.29.88.3 Cys 1.710.86.0 His 1.89.2 Ser 2.29.210.1\begin{array}{l}\text { Exhibit } \mathbf { 3 A } \text { (for this chapter) }\\\begin{array} { l l l l } \text { Amino acid } & \boldsymbol { \alpha } \text {-carboxyl group pK a } & \boldsymbol { \alpha } \text {-amino group pK a } & \text { R-group pK } \\\hline \text { Ala } & 2.3 & 9.7 & \\\text { Arg } & 2.2 & 9.0 & 12.5 \\\text { Asn or Gln } & 2.1 & 9.0 & 4.0 \\\text { Asp or Glu } & 2.2 & 9.8 & 8.3 \\\text { Cys } & 1.7 & 10.8 & 6.0 \\\text { His } & 1.8 & 9.2 & \\\text { Ser } & 2.2 & 9.2 & 10.1\end{array}\end{array} -Refer to Exhibit 3A. Which one has the R-group with the highest pK?


A) Alanine
B) Arginine
C) Histidine
D) Cysteine
E) Aspartic Acid

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How many possible tetrapeptides can be made using all four of the amino acids D, W, F, and R?


A) 4
B) 6
C) 12
D) 24
E) none of the choices

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The side chain groups of amino acids are bonded to which carbon?


A) The α-carbon.
B) The β-carbon.
C) The carbonyl carbon.
D) Different amino acids have their side chains attached to different carbons.

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 Exhibit 3A (for this chapter)   Amino acid α-carboxyl group pK a α-amino group pK a  R-group pK  Ala 2.39.7 Arg 2.29.012.5 Asn or Gln 2.19.04.0 Asp or Glu 2.29.88.3 Cys 1.710.86.0 His 1.89.2 Ser 2.29.210.1\begin{array}{l}\text { Exhibit } \mathbf { 3 A } \text { (for this chapter) }\\\begin{array} { l l l l } \text { Amino acid } & \boldsymbol { \alpha } \text {-carboxyl group pK a } & \boldsymbol { \alpha } \text {-amino group pK a } & \text { R-group pK } \\\hline \text { Ala } & 2.3 & 9.7 & \\\text { Arg } & 2.2 & 9.0 & 12.5 \\\text { Asn or Gln } & 2.1 & 9.0 & 4.0 \\\text { Asp or Glu } & 2.2 & 9.8 & 8.3 \\\text { Cys } & 1.7 & 10.8 & 6.0 \\\text { His } & 1.8 & 9.2 & \\\text { Ser } & 2.2 & 9.2 & 10.1\end{array}\end{array} -Refer to Exhibit 3A. Calculate the pI of ASN:


A) 2.5
B) 5.0
C) 5.5
D) 6.0
E) 10.7

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Which amino acid has a polar, non-ionic R-group


A) Glutamic Acid
B) Histidine
C) Isoleucine
D) Serine
E) Tyrosine

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Which group consists only of amino acids with polar side chains?


A) serine, threonine, and leucine
B) serine, threonine, and cysteine
C) serine, threonine, and valine
D) serine, threonine, and isoleucine

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Which of the following correctly describes peptide bonds?


A) They are special type of amide bond.
B) They are a very stable bonds.
C) They are formed when water is split out from an amino group and a carboxylic acid.
D) They are a bond which displays resonance.
E) All of these

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The isoelectric pH of glycine is closest to


A) pH 4
B) pH 6
C) pH 8
D) pH 10

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Which amino acid has the one-letter symbol E?


A) lysine
B) phenylalanine
C) histidine
D) glutamic acid

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Which statement is true about the classification of amino acids?


A) Alanine and valine are basic amino acids.
B) Lysine and arginine are acidic amino acids.
C) Glutamic acid and asparagine are hydrophobic amino acids.
D) Tryptophan and phenylalanine are aromatic amino acids.
E) Methionine and cysteine are hydroxyl-containing amino acids.

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 Exhibit 3A (for this chapter)   Amino acid α-carboxyl group pK a α-amino group pK a  R-group pK  Ala 2.39.7 Arg 2.29.012.5 Asn or Gln 2.19.04.0 Asp or Glu 2.29.88.3 Cys 1.710.86.0 His 1.89.2 Ser 2.29.210.1\begin{array}{l}\text { Exhibit } \mathbf { 3 A } \text { (for this chapter) }\\\begin{array} { l l l l } \text { Amino acid } & \boldsymbol { \alpha } \text {-carboxyl group pK a } & \boldsymbol { \alpha } \text {-amino group pK a } & \text { R-group pK } \\\hline \text { Ala } & 2.3 & 9.7 & \\\text { Arg } & 2.2 & 9.0 & 12.5 \\\text { Asn or Gln } & 2.1 & 9.0 & 4.0 \\\text { Asp or Glu } & 2.2 & 9.8 & 8.3 \\\text { Cys } & 1.7 & 10.8 & 6.0 \\\text { His } & 1.8 & 9.2 & \\\text { Ser } & 2.2 & 9.2 & 10.1\end{array}\end{array} -Refer to Exhibit 3A. The pI of an amino acid is the pH at which it has a zero net charge. What is the increasing order of isoelectric points (low pH to high) for these three amino acids?


A) ALA, HIS, ASP
B) ASP, ALA, HIS
C) HIS, ALA, ASP
D) ALA, ASL, HIS
E) ASP, HIS, ALA

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The pKa values of the amino groups of common amino acids


A) occur at very low pH values
B) occur in a range from pH 9 to pH 11
C) all occur at pH 8
D) all occur above pH 12

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Which of the following is NOT a correct combination of an amino acid, its three-letter designation, and its one-letter designation?


A) Lysine, lys, L
B) Glycine, gly, G
C) Histidine, his, H
D) Tryptophan, Trp, W
E) Arginine, arg, R

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Exhibit 3B A titration curve. Exhibit 3B A titration curve.    -Refer to Exhibit 3B. The amino acid depicted by the titration curve is A)  aspartic acid B)  histidine C)  lysine D)  tyrosine E)  lysine or tyrosine -Refer to Exhibit 3B. The amino acid depicted by the titration curve is


A) aspartic acid
B) histidine
C) lysine
D) tyrosine
E) lysine or tyrosine

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Which is the correct one-letter designation for tryptophan?


A) E
B) T
C) W
D) Q
E) none of the choices

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What is the predominant form of the amino acid abbreviated E at pH 7?


A) positive
B) neutral
C) negative

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C

At its isolectric pH, glycine will have


A) both of its ionizable functional groups dissociated.
B) neither of its ionizable functional groups dissociated.
C) only its carboxyl group dissociated.
D) only its amino group dissociated.

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A

Which of the following is true about oxytocin?


A) it is a peptide hormone
B) during pregnancy the number of receptors for oxytocin increases
C) it is involved in stimulating the flow of milk during nursing
D) all of the choices

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Which amino acid would likely be least water-soluble at pH 7.0


A) Histidine
B) Isoleucine
C) Isoleucine or Tyrosine, you cannot tell
D) Serine
E) Tyrosine

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