Deck 26: Amino Acids,peptides,proteins,and Nucleic Acids: Nitrogen-Containing Polymers in Nature

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سؤال
Which of the following is least likely to be found in nature?

A)
<strong>Which of the following is least likely to be found in nature?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Which of the following is least likely to be found in nature?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Which of the following is least likely to be found in nature?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Which of the following is least likely to be found in nature?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Which of the following is least likely to be found in nature?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
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سؤال
Which of the following amino acids would have the highest isoelectric point?

A) Lysine
B) Glutamine
C) Aspartic acid
D) Alanine
E) Tryptophan
سؤال
Why is the following not a good two step route for the preparation of pure L-alanine? <strong>Why is the following not a good two step route for the preparation of pure L-alanine?  </strong> A) The bromination is not selective (the CH<sub>3</sub> and CH<sub>2</sub> groups are both brominated). B) Ammonia is not sufficiently nucleophillic to react with a secondary bromide. C) Only the CH<sub>3</sub> group is brominated. D) The product will be racemic. E) Propanamide would be the major product. <div style=padding-top: 35px>

A) The bromination is not selective (the CH3 and CH2 groups are both brominated).
B) Ammonia is not sufficiently nucleophillic to react with a secondary bromide.
C) Only the CH3 group is brominated.
D) The product will be racemic.
E) Propanamide would be the major product.
سؤال
Disulfide bonds in proteins

A) result from oxidation of thiols (RSH).
B) function to help maintain the shape of proteins.
C) can be broken by reduction reactions.
D) link two cysteine amino acid residues.
E) All of these are true.
سؤال
Why is the additional (ring)nitrogen in tryptophan not very basic? <strong>Why is the additional (ring)nitrogen in tryptophan not very basic?  </strong> A) Cyclic amines are not basic. B) It is too far from the carboxyl group to be effected. C) Aromatic amines are weakly basic because of resonance. D) The additional amine group is offset by an additional carboxylic acid group. E) It is sp<sup>2</sup> hybridized as therefore not as basic. <div style=padding-top: 35px>

A) Cyclic amines are not basic.
B) It is too far from the carboxyl group to be effected.
C) Aromatic amines are weakly basic because of resonance.
D) The additional amine group is offset by an additional carboxylic acid group.
E) It is sp2 hybridized as therefore not as basic.
سؤال
The primary structure of a protein refers to the

A) sequence of amino acids.
B) overall 3-dimensional shape.
C) localized shape of the backbone.
D) degree of aggregation with other proteins.
E) structure of the active site.
سؤال
What material can be used repetitively (on a given sample)to sequence a polypeptide from the N-terminal end?

A) Chymotrypsin
B) Sanger reagent
C) Trypsin
D) Edman reagent
E) Carboxypeptidase
سؤال
Nearly all amino acids immediately release N2 gas upon diazotization (treatment with aqueous HCl and sodium nitrite).Which amino acid would not?

A) Lysine
B) Histidine
C) Tyrosine
D) Cysteine
E) Proline
سؤال
Which of the following amino acids is theoretically capable of existing in two diastereomeric forms?

A) Cysteine
B) Threonine
C) Leucine
D) Serine
E) Tryptophan
سؤال
What is dicyclohexylcarbodiimide (DCC)used for in peptide synthesis?

A) DCC protects the amino group of the intended N-terminal amino acid.
B) DCC activates the carboxyl group toward nucleophillic attack.
C) DCC cleaves the blocking groups from the final peptide.
D) DCC is the resin (solid support)used to anchor the growing polypeptide.
E) DCC removes the peptide from the resin at the conclusion of the synthesis.
سؤال
What is the name of the DNA base shown? <strong>What is the name of the DNA base shown?  </strong> A) Guanine B) Cytosine C) Adenine D) Uracil E) Thymine <div style=padding-top: 35px>

A) Guanine
B) Cytosine
C) Adenine
D) Uracil
E) Thymine
سؤال
What would be the abbreviated name of the following polypeptide? <strong>What would be the abbreviated name of the following polypeptide?  </strong> A) val-thr-glu-ala-gln B) ala-thr-glu-val-gln C) met-ser-asp-leu-pro-NH<sub>2</sub> D) ala-ser-asp-val-gln E) ala-ser-asp-val-pro-NH<sub>2</sub> <div style=padding-top: 35px>

A) val-thr-glu-ala-gln
B) ala-thr-glu-val-gln
C) met-ser-asp-leu-pro-NH2
D) ala-ser-asp-val-gln
E) ala-ser-asp-val-pro-NH2
سؤال
Which amino acid does not have an enantiomer?

A) Alanine
B) Glutamine
C) Histidine
D) Aspartic acid
E) Glycine
سؤال
How many tripeptides containing one residue each of L-alanine,L-valine,and glycine are possible?

A) 2
B) 3
C) 4
D) 6
E) 9
سؤال
In a DNA molecule,at which point would the base shown be attached to a deoxyribose fragment? <strong>In a DNA molecule,at which point would the base shown be attached to a deoxyribose fragment?  </strong> A) 1 B) 2 C) 3 D) 4 E) 5 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
E) 5
سؤال
Chymotrypsin catalyzes hydrolysis of peptide bonds where? <strong>Chymotrypsin catalyzes hydrolysis of peptide bonds where?  </strong> A) At the carboxy end of residues with basic side chains B) At the amino end of residues containing aliphatic residues C) At the carboxy end of residues with aromatic side chains D) At the amino end of residues with aromatic side chains E) At the carboxy end of methionine residues <div style=padding-top: 35px>

A) At the carboxy end of residues with basic side chains
B) At the amino end of residues containing aliphatic residues
C) At the carboxy end of residues with aromatic side chains
D) At the amino end of residues with aromatic side chains
E) At the carboxy end of methionine residues
سؤال
The artificial sweetener aspartame is a derivative of the dipeptide asp-phe.If aspartame (asp-phe)was prepared from racemic amino acids,how many stereoisomers (diastereomers + enantiomers)could be formed? <strong>The artificial sweetener aspartame is a derivative of the dipeptide asp-phe.If aspartame (asp-phe)was prepared from racemic amino acids,how many stereoisomers (diastereomers + enantiomers)could be formed?  </strong> A) 2 B) 3 C) 4 D) 6 E) 8 <div style=padding-top: 35px>

A) 2
B) 3
C) 4
D) 6
E) 8
سؤال
How many amino acid residues are present in the following polypeptide? <strong>How many amino acid residues are present in the following polypeptide?  </strong> A) 4 B) 5 C) 6 D) 7 E) 8 <div style=padding-top: 35px>

A) 4
B) 5
C) 6
D) 7
E) 8
سؤال
Which amino acid does not form a characteristic blue color with ninhydrin?

A) Cysteine
B) Lysine
C) Proline
D) Valine
E) Tryptophan
سؤال
It was not until 1974 that γ\gamma -carboxyglutamic acid (shown below)was discovered (by researchers at the University of Colorado)in polypeptides.Based on your knowledge of organic chemistry,what is the most likely reason that this particular amino acid escaped identification so long?  <strong>It was not until 1974 that  \gamma -carboxyglutamic acid (shown below)was discovered (by researchers at the University of Colorado)in polypeptides.Based on your knowledge of organic chemistry,what is the most likely reason that this particular amino acid escaped identification so long?  </strong> A) It tended to spontaneously form a cyclic anhydride:   B) It tended to spontaneously lose carbon dioxide:   C) It easily underwent a reverse-Knovenagle reaction:   D) It tended to spontaneously form a cyclic amide (lactam):   E) It was simply too polar to extract into non-polar organic solvents. <div style=padding-top: 35px>

A) It tended to spontaneously form a cyclic anhydride:
 <strong>It was not until 1974 that  \gamma -carboxyglutamic acid (shown below)was discovered (by researchers at the University of Colorado)in polypeptides.Based on your knowledge of organic chemistry,what is the most likely reason that this particular amino acid escaped identification so long?  </strong> A) It tended to spontaneously form a cyclic anhydride:   B) It tended to spontaneously lose carbon dioxide:   C) It easily underwent a reverse-Knovenagle reaction:   D) It tended to spontaneously form a cyclic amide (lactam):   E) It was simply too polar to extract into non-polar organic solvents. <div style=padding-top: 35px>
B) It tended to spontaneously lose carbon dioxide:
 <strong>It was not until 1974 that  \gamma -carboxyglutamic acid (shown below)was discovered (by researchers at the University of Colorado)in polypeptides.Based on your knowledge of organic chemistry,what is the most likely reason that this particular amino acid escaped identification so long?  </strong> A) It tended to spontaneously form a cyclic anhydride:   B) It tended to spontaneously lose carbon dioxide:   C) It easily underwent a reverse-Knovenagle reaction:   D) It tended to spontaneously form a cyclic amide (lactam):   E) It was simply too polar to extract into non-polar organic solvents. <div style=padding-top: 35px>
C) It easily underwent a reverse-Knovenagle reaction:
 <strong>It was not until 1974 that  \gamma -carboxyglutamic acid (shown below)was discovered (by researchers at the University of Colorado)in polypeptides.Based on your knowledge of organic chemistry,what is the most likely reason that this particular amino acid escaped identification so long?  </strong> A) It tended to spontaneously form a cyclic anhydride:   B) It tended to spontaneously lose carbon dioxide:   C) It easily underwent a reverse-Knovenagle reaction:   D) It tended to spontaneously form a cyclic amide (lactam):   E) It was simply too polar to extract into non-polar organic solvents. <div style=padding-top: 35px>
D) It tended to spontaneously form a cyclic amide (lactam):
 <strong>It was not until 1974 that  \gamma -carboxyglutamic acid (shown below)was discovered (by researchers at the University of Colorado)in polypeptides.Based on your knowledge of organic chemistry,what is the most likely reason that this particular amino acid escaped identification so long?  </strong> A) It tended to spontaneously form a cyclic anhydride:   B) It tended to spontaneously lose carbon dioxide:   C) It easily underwent a reverse-Knovenagle reaction:   D) It tended to spontaneously form a cyclic amide (lactam):   E) It was simply too polar to extract into non-polar organic solvents. <div style=padding-top: 35px>
E) It was simply too polar to extract into non-polar organic solvents.
سؤال
The secondary structure of proteins is held together by hydrogen bonds between which protein sub-structures?

A) The C=O and N-H on amino acid side chains
B) The C=O on the protein backbone and the N-H on the amino acid side chains
C) The C=O on the amino acid side chains and the N-H on the protein backbone
D) The C=O and the N-H on the protein backbone
E) There are no hydrogen bonds involved with secondary structure.
سؤال
Which amino acid is shown? <strong>Which amino acid is shown?  </strong> A) Alanine B) Glycine C) Tyrosine D) Lysine E) Arginine <div style=padding-top: 35px>

A) Alanine
B) Glycine
C) Tyrosine
D) Lysine
E) Arginine
سؤال
Which of the following DNA base pairs can participate in Watson and Crick type hydrogen bonding?

A) A-T
B) G-T
C) G-C
D) Both A and B
E) Both A and C
سؤال
Which attractive force is responsible for maintaining the tertiary structure of proteins?

A) Disulfide linkages
B) Hydrogen bonds
C) Salt bridges
D) Hydrophobic interactions
E) All of these
سؤال
The difference(s)between DNA and RNA is (are):

A) DNA incorporates 2-deoxyribose sugars rather than ribose.
B) RNA is smaller than DNA.
C) DNA uses thymine,RNA uses uracil.
D) Two of the above are true.
E) All of the above are true.
سؤال
At the isoelectric point,the amino acid alanine will exist as what structure?

A) A positive ion
B) A negative ion
C) An uncharged molecule
D) A zwitterion
E) A carbocation
سؤال
Which of the following amino acids contains an aromatic ring?

A) Alanine
B) Serine
C) Tyrosine
D) Asparagine
E) Glycine
سؤال
Which amino acid is responsible for the condition known as phenylketonuria (PKU)which occurs in a small fraction of the population?

A) Tryptophan
B) Histidine
C) Phenylalanine
D) Proline
E) Valine
سؤال
What process would one use to make multiple copies of a fragment of DNA?

A) Polymerase chain reaction
B) Electrophoresis
C) Transcription
D) Translation
E) Merrifield solid-phase synthesis
سؤال
Amino acids are covalently bonded to each other through_______.

A) hydrogen bonding
B) disulfide bridges
C) peptide bonds
D) ( α\alpha and β\beta folds)
E) None of the above.
سؤال
The organic portion of which of the following biological materials does not consist mainly of polypeptides and/or proteins?

A) Enzymes
B) Hair
C) Hemoglobin
D) Membranes
E) Insulin
سؤال
Although traces of racemic amino acids have been found in meteorites,nearly all naturally occurring amino acids on Earth have the stereochemistry shown.What is true of this stereochemistry? (Assume R = alkyl) <strong>Although traces of racemic amino acids have been found in meteorites,nearly all naturally occurring amino acids on Earth have the stereochemistry shown.What is true of this stereochemistry? (Assume R = alkyl)  </strong> A) Amino acids are of the (R)configuration. B) Amino acids are of the (S)configuration. C) Amino acids are not chiral. D) Amino acids are meso compounds. E) Amino acids easily change configuration. <div style=padding-top: 35px>

A) Amino acids are of the (R)configuration.
B) Amino acids are of the (S)configuration.
C) Amino acids are not chiral.
D) Amino acids are meso compounds.
E) Amino acids easily change configuration.
سؤال
Folding of polypeptides influenced by distant residues is an example of what protein structure?

A) Primary
B) Secondary
C) Tertiary
D) Quaternary
E) None of the above.
سؤال
Which of the following represents how a typical amino acid would mainly exist in basic solution (pH > 7)?

A)
<strong>Which of the following represents how a typical amino acid would mainly exist in basic solution (pH > 7)?</strong> A)   B)   C)   D)   E) None of the above. <div style=padding-top: 35px>
B)
<strong>Which of the following represents how a typical amino acid would mainly exist in basic solution (pH > 7)?</strong> A)   B)   C)   D)   E) None of the above. <div style=padding-top: 35px>
C)
<strong>Which of the following represents how a typical amino acid would mainly exist in basic solution (pH > 7)?</strong> A)   B)   C)   D)   E) None of the above. <div style=padding-top: 35px>
D)
<strong>Which of the following represents how a typical amino acid would mainly exist in basic solution (pH > 7)?</strong> A)   B)   C)   D)   E) None of the above. <div style=padding-top: 35px>
E) None of the above.
سؤال
How many polypeptides would be present if the following was treated with trypsin? <strong>How many polypeptides would be present if the following was treated with trypsin?  </strong> A) 1 B) 2 C) 3 D) 4 E) 5 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
E) 5
سؤال
Which nitrogen in the imidazole ring of histidine is the more basic? <strong>Which nitrogen in the imidazole ring of histidine is the more basic?  </strong> A) #1 B) #2 C) both have same basicity D) neither is basic E) the histidine N-H is actually acidic <div style=padding-top: 35px>

A) #1
B) #2
C) both have same basicity
D) neither is basic
E) the histidine N-H is actually acidic
سؤال
Which of the following statements is not true of amino acids?

A) They are less acidic than carboxylic acids.
B) In acid solution (pH ~ 2)they would show an IR absorption near 1720 cm-1.
C) They are soluble in water but not in non-polar organic solvents.
D) They are more basic than amines.
E) In basic solution (pH ~ 12)they would show an IR absorption near 3300 cm-1.
سؤال
What would result from the following reactions? <strong>What would result from the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>

A)
<strong>What would result from the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>What would result from the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>What would result from the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>What would result from the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>What would result from the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
سؤال
Given that the pKa of the acidic form of proline is 2.0,and the pKa of the basic form of proline is 10.6,what is the isoelectric point?

A) 2.0
B) 6.3
C) 4.4
D) 10.6
E) 7.0
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ملء الشاشة (f)
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Deck 26: Amino Acids,peptides,proteins,and Nucleic Acids: Nitrogen-Containing Polymers in Nature
1
Which of the following is least likely to be found in nature?

A)
<strong>Which of the following is least likely to be found in nature?</strong> A)   B)   C)   D)   E)
B)
<strong>Which of the following is least likely to be found in nature?</strong> A)   B)   C)   D)   E)
C)
<strong>Which of the following is least likely to be found in nature?</strong> A)   B)   C)   D)   E)
D)
<strong>Which of the following is least likely to be found in nature?</strong> A)   B)   C)   D)   E)
E)
<strong>Which of the following is least likely to be found in nature?</strong> A)   B)   C)   D)   E)
2
Which of the following amino acids would have the highest isoelectric point?

A) Lysine
B) Glutamine
C) Aspartic acid
D) Alanine
E) Tryptophan
Lysine
3
Why is the following not a good two step route for the preparation of pure L-alanine? <strong>Why is the following not a good two step route for the preparation of pure L-alanine?  </strong> A) The bromination is not selective (the CH<sub>3</sub> and CH<sub>2</sub> groups are both brominated). B) Ammonia is not sufficiently nucleophillic to react with a secondary bromide. C) Only the CH<sub>3</sub> group is brominated. D) The product will be racemic. E) Propanamide would be the major product.

A) The bromination is not selective (the CH3 and CH2 groups are both brominated).
B) Ammonia is not sufficiently nucleophillic to react with a secondary bromide.
C) Only the CH3 group is brominated.
D) The product will be racemic.
E) Propanamide would be the major product.
The product will be racemic.
4
Disulfide bonds in proteins

A) result from oxidation of thiols (RSH).
B) function to help maintain the shape of proteins.
C) can be broken by reduction reactions.
D) link two cysteine amino acid residues.
E) All of these are true.
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5
Why is the additional (ring)nitrogen in tryptophan not very basic? <strong>Why is the additional (ring)nitrogen in tryptophan not very basic?  </strong> A) Cyclic amines are not basic. B) It is too far from the carboxyl group to be effected. C) Aromatic amines are weakly basic because of resonance. D) The additional amine group is offset by an additional carboxylic acid group. E) It is sp<sup>2</sup> hybridized as therefore not as basic.

A) Cyclic amines are not basic.
B) It is too far from the carboxyl group to be effected.
C) Aromatic amines are weakly basic because of resonance.
D) The additional amine group is offset by an additional carboxylic acid group.
E) It is sp2 hybridized as therefore not as basic.
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6
The primary structure of a protein refers to the

A) sequence of amino acids.
B) overall 3-dimensional shape.
C) localized shape of the backbone.
D) degree of aggregation with other proteins.
E) structure of the active site.
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7
What material can be used repetitively (on a given sample)to sequence a polypeptide from the N-terminal end?

A) Chymotrypsin
B) Sanger reagent
C) Trypsin
D) Edman reagent
E) Carboxypeptidase
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8
Nearly all amino acids immediately release N2 gas upon diazotization (treatment with aqueous HCl and sodium nitrite).Which amino acid would not?

A) Lysine
B) Histidine
C) Tyrosine
D) Cysteine
E) Proline
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9
Which of the following amino acids is theoretically capable of existing in two diastereomeric forms?

A) Cysteine
B) Threonine
C) Leucine
D) Serine
E) Tryptophan
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10
What is dicyclohexylcarbodiimide (DCC)used for in peptide synthesis?

A) DCC protects the amino group of the intended N-terminal amino acid.
B) DCC activates the carboxyl group toward nucleophillic attack.
C) DCC cleaves the blocking groups from the final peptide.
D) DCC is the resin (solid support)used to anchor the growing polypeptide.
E) DCC removes the peptide from the resin at the conclusion of the synthesis.
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11
What is the name of the DNA base shown? <strong>What is the name of the DNA base shown?  </strong> A) Guanine B) Cytosine C) Adenine D) Uracil E) Thymine

A) Guanine
B) Cytosine
C) Adenine
D) Uracil
E) Thymine
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12
What would be the abbreviated name of the following polypeptide? <strong>What would be the abbreviated name of the following polypeptide?  </strong> A) val-thr-glu-ala-gln B) ala-thr-glu-val-gln C) met-ser-asp-leu-pro-NH<sub>2</sub> D) ala-ser-asp-val-gln E) ala-ser-asp-val-pro-NH<sub>2</sub>

A) val-thr-glu-ala-gln
B) ala-thr-glu-val-gln
C) met-ser-asp-leu-pro-NH2
D) ala-ser-asp-val-gln
E) ala-ser-asp-val-pro-NH2
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13
Which amino acid does not have an enantiomer?

A) Alanine
B) Glutamine
C) Histidine
D) Aspartic acid
E) Glycine
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14
How many tripeptides containing one residue each of L-alanine,L-valine,and glycine are possible?

A) 2
B) 3
C) 4
D) 6
E) 9
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15
In a DNA molecule,at which point would the base shown be attached to a deoxyribose fragment? <strong>In a DNA molecule,at which point would the base shown be attached to a deoxyribose fragment?  </strong> A) 1 B) 2 C) 3 D) 4 E) 5

A) 1
B) 2
C) 3
D) 4
E) 5
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16
Chymotrypsin catalyzes hydrolysis of peptide bonds where? <strong>Chymotrypsin catalyzes hydrolysis of peptide bonds where?  </strong> A) At the carboxy end of residues with basic side chains B) At the amino end of residues containing aliphatic residues C) At the carboxy end of residues with aromatic side chains D) At the amino end of residues with aromatic side chains E) At the carboxy end of methionine residues

A) At the carboxy end of residues with basic side chains
B) At the amino end of residues containing aliphatic residues
C) At the carboxy end of residues with aromatic side chains
D) At the amino end of residues with aromatic side chains
E) At the carboxy end of methionine residues
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17
The artificial sweetener aspartame is a derivative of the dipeptide asp-phe.If aspartame (asp-phe)was prepared from racemic amino acids,how many stereoisomers (diastereomers + enantiomers)could be formed? <strong>The artificial sweetener aspartame is a derivative of the dipeptide asp-phe.If aspartame (asp-phe)was prepared from racemic amino acids,how many stereoisomers (diastereomers + enantiomers)could be formed?  </strong> A) 2 B) 3 C) 4 D) 6 E) 8

A) 2
B) 3
C) 4
D) 6
E) 8
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18
How many amino acid residues are present in the following polypeptide? <strong>How many amino acid residues are present in the following polypeptide?  </strong> A) 4 B) 5 C) 6 D) 7 E) 8

A) 4
B) 5
C) 6
D) 7
E) 8
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19
Which amino acid does not form a characteristic blue color with ninhydrin?

A) Cysteine
B) Lysine
C) Proline
D) Valine
E) Tryptophan
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20
It was not until 1974 that γ\gamma -carboxyglutamic acid (shown below)was discovered (by researchers at the University of Colorado)in polypeptides.Based on your knowledge of organic chemistry,what is the most likely reason that this particular amino acid escaped identification so long?  <strong>It was not until 1974 that  \gamma -carboxyglutamic acid (shown below)was discovered (by researchers at the University of Colorado)in polypeptides.Based on your knowledge of organic chemistry,what is the most likely reason that this particular amino acid escaped identification so long?  </strong> A) It tended to spontaneously form a cyclic anhydride:   B) It tended to spontaneously lose carbon dioxide:   C) It easily underwent a reverse-Knovenagle reaction:   D) It tended to spontaneously form a cyclic amide (lactam):   E) It was simply too polar to extract into non-polar organic solvents.

A) It tended to spontaneously form a cyclic anhydride:
 <strong>It was not until 1974 that  \gamma -carboxyglutamic acid (shown below)was discovered (by researchers at the University of Colorado)in polypeptides.Based on your knowledge of organic chemistry,what is the most likely reason that this particular amino acid escaped identification so long?  </strong> A) It tended to spontaneously form a cyclic anhydride:   B) It tended to spontaneously lose carbon dioxide:   C) It easily underwent a reverse-Knovenagle reaction:   D) It tended to spontaneously form a cyclic amide (lactam):   E) It was simply too polar to extract into non-polar organic solvents.
B) It tended to spontaneously lose carbon dioxide:
 <strong>It was not until 1974 that  \gamma -carboxyglutamic acid (shown below)was discovered (by researchers at the University of Colorado)in polypeptides.Based on your knowledge of organic chemistry,what is the most likely reason that this particular amino acid escaped identification so long?  </strong> A) It tended to spontaneously form a cyclic anhydride:   B) It tended to spontaneously lose carbon dioxide:   C) It easily underwent a reverse-Knovenagle reaction:   D) It tended to spontaneously form a cyclic amide (lactam):   E) It was simply too polar to extract into non-polar organic solvents.
C) It easily underwent a reverse-Knovenagle reaction:
 <strong>It was not until 1974 that  \gamma -carboxyglutamic acid (shown below)was discovered (by researchers at the University of Colorado)in polypeptides.Based on your knowledge of organic chemistry,what is the most likely reason that this particular amino acid escaped identification so long?  </strong> A) It tended to spontaneously form a cyclic anhydride:   B) It tended to spontaneously lose carbon dioxide:   C) It easily underwent a reverse-Knovenagle reaction:   D) It tended to spontaneously form a cyclic amide (lactam):   E) It was simply too polar to extract into non-polar organic solvents.
D) It tended to spontaneously form a cyclic amide (lactam):
 <strong>It was not until 1974 that  \gamma -carboxyglutamic acid (shown below)was discovered (by researchers at the University of Colorado)in polypeptides.Based on your knowledge of organic chemistry,what is the most likely reason that this particular amino acid escaped identification so long?  </strong> A) It tended to spontaneously form a cyclic anhydride:   B) It tended to spontaneously lose carbon dioxide:   C) It easily underwent a reverse-Knovenagle reaction:   D) It tended to spontaneously form a cyclic amide (lactam):   E) It was simply too polar to extract into non-polar organic solvents.
E) It was simply too polar to extract into non-polar organic solvents.
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21
The secondary structure of proteins is held together by hydrogen bonds between which protein sub-structures?

A) The C=O and N-H on amino acid side chains
B) The C=O on the protein backbone and the N-H on the amino acid side chains
C) The C=O on the amino acid side chains and the N-H on the protein backbone
D) The C=O and the N-H on the protein backbone
E) There are no hydrogen bonds involved with secondary structure.
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22
Which amino acid is shown? <strong>Which amino acid is shown?  </strong> A) Alanine B) Glycine C) Tyrosine D) Lysine E) Arginine

A) Alanine
B) Glycine
C) Tyrosine
D) Lysine
E) Arginine
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23
Which of the following DNA base pairs can participate in Watson and Crick type hydrogen bonding?

A) A-T
B) G-T
C) G-C
D) Both A and B
E) Both A and C
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24
Which attractive force is responsible for maintaining the tertiary structure of proteins?

A) Disulfide linkages
B) Hydrogen bonds
C) Salt bridges
D) Hydrophobic interactions
E) All of these
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25
The difference(s)between DNA and RNA is (are):

A) DNA incorporates 2-deoxyribose sugars rather than ribose.
B) RNA is smaller than DNA.
C) DNA uses thymine,RNA uses uracil.
D) Two of the above are true.
E) All of the above are true.
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26
At the isoelectric point,the amino acid alanine will exist as what structure?

A) A positive ion
B) A negative ion
C) An uncharged molecule
D) A zwitterion
E) A carbocation
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27
Which of the following amino acids contains an aromatic ring?

A) Alanine
B) Serine
C) Tyrosine
D) Asparagine
E) Glycine
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28
Which amino acid is responsible for the condition known as phenylketonuria (PKU)which occurs in a small fraction of the population?

A) Tryptophan
B) Histidine
C) Phenylalanine
D) Proline
E) Valine
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29
What process would one use to make multiple copies of a fragment of DNA?

A) Polymerase chain reaction
B) Electrophoresis
C) Transcription
D) Translation
E) Merrifield solid-phase synthesis
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30
Amino acids are covalently bonded to each other through_______.

A) hydrogen bonding
B) disulfide bridges
C) peptide bonds
D) ( α\alpha and β\beta folds)
E) None of the above.
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31
The organic portion of which of the following biological materials does not consist mainly of polypeptides and/or proteins?

A) Enzymes
B) Hair
C) Hemoglobin
D) Membranes
E) Insulin
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32
Although traces of racemic amino acids have been found in meteorites,nearly all naturally occurring amino acids on Earth have the stereochemistry shown.What is true of this stereochemistry? (Assume R = alkyl) <strong>Although traces of racemic amino acids have been found in meteorites,nearly all naturally occurring amino acids on Earth have the stereochemistry shown.What is true of this stereochemistry? (Assume R = alkyl)  </strong> A) Amino acids are of the (R)configuration. B) Amino acids are of the (S)configuration. C) Amino acids are not chiral. D) Amino acids are meso compounds. E) Amino acids easily change configuration.

A) Amino acids are of the (R)configuration.
B) Amino acids are of the (S)configuration.
C) Amino acids are not chiral.
D) Amino acids are meso compounds.
E) Amino acids easily change configuration.
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33
Folding of polypeptides influenced by distant residues is an example of what protein structure?

A) Primary
B) Secondary
C) Tertiary
D) Quaternary
E) None of the above.
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34
Which of the following represents how a typical amino acid would mainly exist in basic solution (pH > 7)?

A)
<strong>Which of the following represents how a typical amino acid would mainly exist in basic solution (pH > 7)?</strong> A)   B)   C)   D)   E) None of the above.
B)
<strong>Which of the following represents how a typical amino acid would mainly exist in basic solution (pH > 7)?</strong> A)   B)   C)   D)   E) None of the above.
C)
<strong>Which of the following represents how a typical amino acid would mainly exist in basic solution (pH > 7)?</strong> A)   B)   C)   D)   E) None of the above.
D)
<strong>Which of the following represents how a typical amino acid would mainly exist in basic solution (pH > 7)?</strong> A)   B)   C)   D)   E) None of the above.
E) None of the above.
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35
How many polypeptides would be present if the following was treated with trypsin? <strong>How many polypeptides would be present if the following was treated with trypsin?  </strong> A) 1 B) 2 C) 3 D) 4 E) 5

A) 1
B) 2
C) 3
D) 4
E) 5
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36
Which nitrogen in the imidazole ring of histidine is the more basic? <strong>Which nitrogen in the imidazole ring of histidine is the more basic?  </strong> A) #1 B) #2 C) both have same basicity D) neither is basic E) the histidine N-H is actually acidic

A) #1
B) #2
C) both have same basicity
D) neither is basic
E) the histidine N-H is actually acidic
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37
Which of the following statements is not true of amino acids?

A) They are less acidic than carboxylic acids.
B) In acid solution (pH ~ 2)they would show an IR absorption near 1720 cm-1.
C) They are soluble in water but not in non-polar organic solvents.
D) They are more basic than amines.
E) In basic solution (pH ~ 12)they would show an IR absorption near 3300 cm-1.
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38
What would result from the following reactions? <strong>What would result from the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)

A)
<strong>What would result from the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)
B)
<strong>What would result from the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)
C)
<strong>What would result from the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)
D)
<strong>What would result from the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)
E)
<strong>What would result from the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)
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39
Given that the pKa of the acidic form of proline is 2.0,and the pKa of the basic form of proline is 10.6,what is the isoelectric point?

A) 2.0
B) 6.3
C) 4.4
D) 10.6
E) 7.0
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