Deck 25: Amino Acids, Peptides, and Proteins
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Deck 25: Amino Acids, Peptides, and Proteins
1
How many different amino acids are found abundantly in proteins?
A) 10
B) 16
C) 20
D) 40
E) none of these
A) 10
B) 16
C) 20
D) 40
E) none of these
40
2
Which of the following amino acids is achiral?
A) alanine
B) leucine
C) glycine
D) phenylalanine
E) none of these
A) alanine
B) leucine
C) glycine
D) phenylalanine
E) none of these
glycine
3
Amino acids are connected to each other by____________.
A) an ether linkage
B) a peptide linkage
C) an ester linkage
D) an amide linkage
E) both B & D
A) an ether linkage
B) a peptide linkage
C) an ester linkage
D) an amide linkage
E) both B & D
both B & D
4
Which of the following statements is(are) true about -amino acids?
A) the amino and carboxylic acid groups are separated by one carbon atom
B) the amino group is connected to a carbon atom that is to the carboxylic acid group
C) the carbon can be a chirality center
D) all of these
A) the amino and carboxylic acid groups are separated by one carbon atom
B) the amino group is connected to a carbon atom that is to the carboxylic acid group
C) the carbon can be a chirality center
D) all of these
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5
Which of the following is a correct structure for L-valine? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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6
Proteins found in humans have all amino acids with ____configuration.
A) D
B) L
C) meso
D) A & B
E) none of these
A) D
B) L
C) meso
D) A & B
E) none of these
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7
In -amino acids the amino and carboxylic acid groups are separated by ____,
A) two carbon atoms
B) one carbon atom
C) peptide linkage
D) amide linkage
E) none of these
A) two carbon atoms
B) one carbon atom
C) peptide linkage
D) amide linkage
E) none of these
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8
Which of the following amino acids have an acidic side chain? 
A) I & III
B) I, II & III
C) IV & V
D) II, IV & V
E) all of these

A) I & III
B) I, II & III
C) IV & V
D) II, IV & V
E) all of these
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9
Which of the following naturally occurring amino acids does not have the S configuration? 
A) I
B) II
C) III
D) IV
E) none of these

A) I
B) II
C) III
D) IV
E) none of these
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10
Which of the following is a correct structure for D-leucine? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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11
Which one of the following amino acid does not have an L-isomer?
A) valine
B) alanine
C) leucine
D) glycine
E) none of these
A) valine
B) alanine
C) leucine
D) glycine
E) none of these
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12
When more than fifty amino acids are connected to each other, they form _________.
A) a tripeptide
B) a protein
C) a polypeptide
D) a tetrapeptide
E) none of these
A) a tripeptide
B) a protein
C) a polypeptide
D) a tetrapeptide
E) none of these
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13
Draw the Fischer projection for L-aspartic acid and assign the configuration (R/S) at the chirality center.
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14
When four amino acids are connected to each other, they form ____________.
A) a tripeptide
B) a protein
C) a polypeptide
D) a tetrapeptide
E) none of these
A) a tripeptide
B) a protein
C) a polypeptide
D) a tetrapeptide
E) none of these
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15
When thirty amino acids are connected to each other, they form ____________.
A) a tripeptide
B) a protein
C) a polypeptide
D) a tetrapeptide
E) none of these
A) a tripeptide
B) a protein
C) a polypeptide
D) a tetrapeptide
E) none of these
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16
Which of the following amino acids have a basic side chain? 
A) I & II
B) I, II & IV
C) III & V
D) I, II, III & IV
E) all of these

A) I & II
B) I, II & IV
C) III & V
D) I, II, III & IV
E) all of these
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17
The _______form of amino acid is a dipolar ion that carries both positive and negative charge.
A) cationic
B) anionic
C) zwitterionic
D) none of these
A) cationic
B) anionic
C) zwitterionic
D) none of these
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18
Draw the Fischer projection for D-serine and assign the configuration (R/S) at the chirality center.
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19
Which of the following naturally occurring amino acids does not have the S configuration?
A) alanine
B) cysteine
C) tyrosine
D) isoleucine
E) none of these
A) alanine
B) cysteine
C) tyrosine
D) isoleucine
E) none of these
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20
Draw the Fischer projection for L-cysteine and assign the configuration (R/S) at the chirality center.
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21
Which of the following is the predominant form of aspartic acid at pH 1? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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22
Which of the following is the predominant form of arginine at pH 2? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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23
Amino acids are considered amphoteric because _____________.
A) they only react with acids
B) they only react with bases
C) they react with both acids and bases
D) they do not react with acids or bases
E) none of these
A) they only react with acids
B) they only react with bases
C) they react with both acids and bases
D) they do not react with acids or bases
E) none of these
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24
The pH at which the concentration of the zwitterionic form of an amino acid is at a maximum value is called the _______.
A) dipolar point
B) electric point
C) neutral point
D) isoelectric point
E) none of these
A) dipolar point
B) electric point
C) neutral point
D) isoelectric point
E) none of these
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25
Provide the structure of the predominant form of alanine at pH 2?
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26
Which of the following is used to detect the presence of amino acids using chromatography?
A) 2,4-DNP
B) methyl orange
C) phenolphthalein
D) ninhydrin
E) none of these
A) 2,4-DNP
B) methyl orange
C) phenolphthalein
D) ninhydrin
E) none of these
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27
Which of the following is the predominant form of asparagine at physiological pH? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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28
Which of the following amino acids have a pI around pH 3? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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29
Which of the following is the predominant form of serine at physiological pH? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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30
Which of the following is true about the amino acids with isoelectric point around
PH 10?
A) The side chain must be acidic.
B) The side chain must be basic.
C) The side chain must be polar.
D) The side chain must be non polar.
E) none of these
PH 10?
A) The side chain must be acidic.
B) The side chain must be basic.
C) The side chain must be polar.
D) The side chain must be non polar.
E) none of these
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31
Which of the following amino acids will migrate towards the anode at pH 7?
Glycine: pI=6.0
Lysine: pI=9.7
Glycine: pI=6.0
Lysine: pI=9.7
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32
Which of the following amino acids will migrate towards the anode at pH 6?
Phenylalanine: pI = 5.5
Leucine: pI = 6
Phenylalanine: pI = 5.5
Leucine: pI = 6
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33
Which of the following amino acids will migrate towards the cathode at pH 7?
Glycine: pI=6.0
Lysine: pI=9.7
Glycine: pI=6.0
Lysine: pI=9.7
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34
Which of the following is the predominant form of lysine at pH 14? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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35
Separation of amino acids using electrophoresis is mainly based on ______.
A) differences in the pI values
B) concentration
C) differences in pH values
D) none of these
A) differences in the pI values
B) concentration
C) differences in pH values
D) none of these
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36
Which of the following amino acids have a pI around pH 10? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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37
Which of the following is a zwitterionic form for alanine? 
A) I
B) II
C) III
D) IV
E) both I & IV

A) I
B) II
C) III
D) IV
E) both I & IV
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38
Which of the following amino acids will not migrate towards the cathode/anode at pH 6?
Phenylalanine: pI = 5.5
Leucine: pI = 6
Phenylalanine: pI = 5.5
Leucine: pI = 6
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39
Provide the structure of the predominant form of valine at pH 10?
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40
Which of the following is true about the amino acids with isoelectric point around
PH 3?
A) The side chain must be acidic.
B) The side chain must be basic.
C) The side chain must be polar.
D) The side chain must be non polar.
E) none of these
PH 3?
A) The side chain must be acidic.
B) The side chain must be basic.
C) The side chain must be polar.
D) The side chain must be non polar.
E) none of these
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41
Provide the reagents necessary to prepare phenylalanine using a Strecker synthesis.
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42
How will you prepare phenylalanine using a Hell-Volhard-Zelinski reaction?
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43
Which amino acid is produced from the following reaction sequence? 
A) alanine
B) valine
C) leucine
D) isoleucine
E) none of these

A) alanine
B) valine
C) leucine
D) isoleucine
E) none of these
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44
Which amino acid is produced from the following reaction? 
A) methionine
B) serine
C) cysteine
D) lysine
E) none of these

A) methionine
B) serine
C) cysteine
D) lysine
E) none of these
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45
Provide the reagents necessary to synthesize the following amino acid via the amidomalonate synthesis. 

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46
How will you prepare glycine staring with ethanol and using a Hell-Volhard-Zelinski reaction?
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47
Which amino acid is produced from the following reaction sequence? 
A) alanine
B) valine
C) leucine
D) isoleucine
E) none of these

A) alanine
B) valine
C) leucine
D) isoleucine
E) none of these
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48
Which amino acid is produced from the following reaction? 
A) methionine
B) serine
C) cysteine
D) lysine
E) none of these

A) methionine
B) serine
C) cysteine
D) lysine
E) none of these
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49
Which amino acid is produced from the following reaction sequence? 
A) alanine
B) valine
C) leucine
D) isoleucine
E) none of these

A) alanine
B) valine
C) leucine
D) isoleucine
E) none of these
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50
Provide the structure of the predominant form of the following amino acids at pH 7 and predict the migration towards anode or cathode during electrophoresis. 

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51
Which amino acid is produced from the following reaction sequence? 
A) alanine
B) valine
C) leucine
D) isoleucine
E) none of these

A) alanine
B) valine
C) leucine
D) isoleucine
E) none of these
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52
Provide the structure of the amino acid produced from the following reaction sequence. 

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53
Which of the following aldehydes would produce isoleucine using a Strecker synthesis?
A) 3-methylbutanal
B) 2-methylbutanal
C) 2-methylpropanal
D) propanal
E) none of these
A) 3-methylbutanal
B) 2-methylbutanal
C) 2-methylpropanal
D) propanal
E) none of these
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54
Provide the structure of the amino acid produced from the following reaction sequence. 

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55
Provide the reagents necessary to synthesize the following amino acid via the amidomalonate synthesis. 

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56
Which of the following amino acids will move the farthest when subjected to electrophoresis at pH 7? 
A) I
B) II
C) III
D) II & III
E) none of these

A) I
B) II
C) III
D) II & III
E) none of these
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57
Which amino acid is produced from the following reaction sequence? 
A) alanine
B) valine
C) leucine
D) isoleucine
E) none of these

A) alanine
B) valine
C) leucine
D) isoleucine
E) none of these
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58
Which of the following aldehydes would produce glycine using a Strecker synthesis?
A) methanal
B) ethanal
C) propanal
D) none of these
A) methanal
B) ethanal
C) propanal
D) none of these
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59
Which amino acid is produced from the following reaction sequence? 
A) alanine
B) valine
C) leucine
D) isoleucine
E) none of these

A) alanine
B) valine
C) leucine
D) isoleucine
E) none of these
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60
Provide the structure of the predominant form of the following amino acids at pH 6 and predict the migration towards anode or cathode during electrophoresis. 

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61
Which of the following alkenes is used to prepare isoleucine using an asymmetric catalytic hydrogenation?

A) I
B) II
C) III
D) IV
E) none of these

A) I
B) II
C) III
D) IV
E) none of these
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62
Provide the structure of the amino acid produced from the following reaction sequence. 

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63
What is the correct sequence of amino acids for the following tripeptide? 
A) Ser-Met-Ile
B) Ser-Cys-Ile
C) Thr-Met-Leu
D) Thr-Cys-Leu
E) none of these

A) Ser-Met-Ile
B) Ser-Cys-Ile
C) Thr-Met-Leu
D) Thr-Cys-Leu
E) none of these
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64
Which of the following peptides results after a single Edman degradation of the tetrapeptide Gly-Phe-Tyr-Ser?
A) Gly-Phe-Tyr
B) Tyr-Ser
C) Phe-Tyr-Ser
D) Gly-Phe
E) none of these
A) Gly-Phe-Tyr
B) Tyr-Ser
C) Phe-Tyr-Ser
D) Gly-Phe
E) none of these
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65
Which of the following is a correct bond-line structure for the tripeptide Ser-Lys-Cys? 
A) I
B) II
C) III
D) IV
E) none of these

A) I
B) II
C) III
D) IV
E) none of these
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66
Which of the following reagent(s) is(are) used to remove the N-terminus amino acid residue using Edman degradation? 
A) I
B) II
C) III
D) IV
E) none of these

A) I
B) II
C) III
D) IV
E) none of these
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67
Draw a bond-line structure for the tetrapetide Ile-Ser-Leu-Gly.
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68
What is the correct sequence of amino acids for the following tripeptide? 
A) Leu-Phe-Ala
B) Val-Phe-Ala
C) Ile-Tyr-Leu
D) Leu-Tyr-Val
E) none of these

A) Leu-Phe-Ala
B) Val-Phe-Ala
C) Ile-Tyr-Leu
D) Leu-Tyr-Val
E) none of these
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69
Which of the following results after three steps of Edman degradation of the heptapeptide Lys-His-Gly-Phe-Tyr-Ser-Ala?
A) Lys-His-Gly
B) Phe-Tyr-Ser-Ala
C) Tyr-Ser-Ala
D) Lys-His-Gly-Phe
E) none of these
A) Lys-His-Gly
B) Phe-Tyr-Ser-Ala
C) Tyr-Ser-Ala
D) Lys-His-Gly-Phe
E) none of these
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70
Provide the structure of the amino acid produced from the following reaction. 

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71
Disulfide bridges are formed by:
A) oxidation of thiol groups
B) joining cysteine residues within a peptide
C) joining cysteine residues between two strands of a peptide
D) all of these
A) oxidation of thiol groups
B) joining cysteine residues within a peptide
C) joining cysteine residues between two strands of a peptide
D) all of these
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72
Chymotrypsin, a digestive enzyme, catalyzes the hydrolysis of the peptide bond at the carboxyl end of which of the following amino acids? 
A) phenylalanine
B) tyrosine
C) tryptophan
D) histidine
E) A, B & C

A) phenylalanine
B) tyrosine
C) tryptophan
D) histidine
E) A, B & C
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73
What is the three letter abbreviation for the amino acid sequence of the following peptide? 

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74
Which of the following is a correct bond-line structure for the tripeptide Val-Asp-Ala? 
A) I
B) II
C) III
D) IV
E) none of these

A) I
B) II
C) III
D) IV
E) none of these
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75
Edman degradation removes the amino acid residue from the _______ of the peptide.
A) C-terminus
B) N-terminus
C) middle
D) none of these
A) C-terminus
B) N-terminus
C) middle
D) none of these
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76
Draw a bond-line structure for the tetrapetide Ala-Ser-Cys-Phe.
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77
Provide the reagents necessary to prepare cysteine using a Strecker synthesis.
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78
Trypsin, a digestive enzyme, catalyzes the hydrolysis of the peptide bond at the carboxyl end of which of the following amino acids? 
A) arginine
B) lysine
C) histidine
D) tryptophan
E) A & B

A) arginine
B) lysine
C) histidine
D) tryptophan
E) A & B
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79
The s-trans conformation of a peptide bond is more stable than the s-cis conformation because:
A) there is a restricted rotation around the peptide bond
B) rotation is allowed around the peptide bond
C) it has reduced steric hindrance
D) none of these
A) there is a restricted rotation around the peptide bond
B) rotation is allowed around the peptide bond
C) it has reduced steric hindrance
D) none of these
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80
Provide the structure of the amino acid produced from the following reaction. 

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