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Draw the structure of L-phenylalanine and L-valine in Fischer projection.

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A reagent that reacts with most amino acids to give an intense purple color is called ___________.

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C-terminal amino acids can be identified through the use of _____________.

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digestive ...

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The purple color of the anion formed in the ninhydrin test for α-amino acids is due to:


A) the attraction of the anion to a metal in a pi-complex.
B) intermolecular hydrogen bonding.
C) molecular vibrations.
D) the highly conjugated nature of the anion.
E) the color of the ninhydrin.

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

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Which of these natural amino acids contains an -OH group?


A) Serine
B) Threonine
C) Tyrosine
D) Two of these
E) All of these

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

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Which of the following amino acids is theoretically capable of existing in diastereomeric forms? Which of the following amino acids is theoretically capable of existing in diastereomeric forms?   A)  I B)  II C)  III D)  IV E)  V


A) I
B) II
C) III
D) IV
E) V

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

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Which of these amino acids is a D amino acid? Which of these amino acids is a D amino acid?   A)  I B)  II C)  III D)  IV E)  V


A) I
B) II
C) III
D) IV
E) V

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

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Which of these natural amino acids contains two carboxylic acid groups?


A) Cystine
B) Cysteine
C) Glutamic acid
D) A and B
E) A and C

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

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Which amino acid would have its isoelectric point near pH 10?


A) Glycine
B) Tryptophan
C) Serine
D) Proline
E) Lysine

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

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The secondary structure of proteins has three basic types of folding patterns.These are:

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blured image-helices,blured image-...

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Disulfide bonds in proteins:


A) result from an oxidation of thiols.
B) help to maintain the shape of proteins.
C) can be broken by reduction.
D) can link two cysteine amino acid residues.
E) All of the above

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

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Which attractive force is responsible for maintaining the tertiary structure of a protein?


A) Disulfide linkages
B) Hydrogen bonds
C) van der Waals forces
D) Hydrophobic interactions
E) All of these

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

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Draw the structure of the following tripeptide (starting with the N-terminal residue and ending with the C-terminal residue),showing stereochemical details: Gly-Phe-Met

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Which of these natural amino acids contains a phenolic group?


A) Phenylalanine
B) Tyrosine
C) Tryptophan
D) 4-Hydroxyproline
E) Serine

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

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Which of these natural amino acids,when present in a polypeptide,is likely to exhibit significant hydrogen bonding through its side chain?


A) Serine
B) Threonine
C) Tyrosine
D) Two of these
E) All of these

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

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Suggest a reasonable strategy for the synthesis of the dipeptide Leu-Phe,using established protocol for peptide synthesis.

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Which is an isolable intermediate in the Strecker synthesis of an amino acid? Which is an isolable intermediate in the Strecker synthesis of an amino acid?   A)  I B)  II C)  III D)  IV E)  V


A) I
B) II
C) III
D) IV
E) V

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

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What is the final product formed via the following reaction sequence? Give structural details of all significant intermediates. What is the final product formed via the following reaction sequence? Give structural details of all significant intermediates.

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A pentapeptide has the molecular formula: Asp,Glu,His,Phe,Val.Partial hydrolysis of the pentapeptide gives: Val·Asp,Glu·His,Phe·Val,and Asp·Glu.What is the amino acid sequence of the pentapeptide?


A) Phe·Val·Asp·Glu·His
B) His·Glu·Asp·Val·Phe
C) Asp·Glu·His·Phe·Val
D) Phe·Val·Glu·His·Asp
E) Glu·His·Phe·Val·Asp

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

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Draw the structures of the predominant forms of glycine at pH = 2.0,6.0,and 10.Indicate the direction of migration (toward anode or cathode)for each structure.

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