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Provide the structure of the predominant form of L-phenylalanine present in an aqueous solution at biological pH.

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Provide a structure of the dipeptide Ala-Ser at biological pH.

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Which of the following amino acids has its isoelectric point at the lowest pH?


A) arginine
B) aspartic acid
C) valine
D) glycine
E) methionine

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Nearly all naturally occurring amino acids:


A) are racemic mixtures.
B) are achiral.
C) have the (R) configuration at the α-carbon.
D) have the (S) configuration at the α-carbon.
E) have basic side chains.

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Show the step-wise synthesis of glutamic acid starting with α-ketoglutarate and ammonia.

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Provide a reasonable synthesis of racemic alanine from ethanol.

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1. PCC
2. ...

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Show where chymotrypsin would cleave the peptide shown below. Show where chymotrypsin would cleave the peptide shown below.

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Peptide bonds are:


A) ester linkages.
B) imido linkages.
C) ether linkages.
D) amide linkages.
E) disulfide linkages.

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Draw the form of L-tryptophan which is present at biological pH.

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Which of the following amino acids has its isoelectric point at the highest pH?


A) glycine
B) aspartic acid
C) valine
D) lysine
E) methionine

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Provide the structure of L-arginine at pH 2.0.

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What compound is also known as Sanger reagent, and how is it used in peptide structure determination?

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2,4-dinitrofluoroben...

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Which type of protein, globular or fibrous, tends to function primarily as structural parts of an organism?

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A protein bonded to a sugar residue would be classified as a:


A) simple protein.
B) glycoprotein.
C) lipoprotein.
D) metalloprotein.
E) nucleoprotein.

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What is the practical limit on the use of carboxypeptidase in providing sequence information?


A) two residues on the C-terminal end
B) two residues on the N-terminal end
C) three residues on the N-terminal end
D) three residues on the C-terminal end
E) six residues on the N-terminal end

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The nonprotein part of a conjugated protein is called a ________ group.

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Which of the following reagents is used to protect the amino group of the N-terminal residue in solution-phase peptide synthesis?


A) lithium diisopropyl amide
B) benzyl chloroformate
C) phenyl isothiocyanate
D) dicyclohexylcarbodiimide
E) trifluoroacetic acid

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Which of the following amino acids has its isoelectric point at the highest pH?


A) glycine
B) aspartic acid
C) valine
D) arginine
E) methionine

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The isoelectric point is important in:


A) the enzymatic resolution of amino acids.
B) electrophoresis.
C) determination of the C-terminal amino acid.
D) determination of the N-terminal amino acid.
E) the ninhydrin test.

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Given the following pKa values, what is the major ionization state of histidine at pH 11? (α-COOH = 2.0, α-NH3+ = 9.0 and R-group imine = 6.5)


A)
Given the following pKa values, what is the major ionization state of histidine at pH 11? (α-COOH = 2.0, α-NH<sub>3</sub><sup>+</sup> = 9.0 and R-group imine = 6.5)  A)    B)    C)    D)    E)
B)
Given the following pKa values, what is the major ionization state of histidine at pH 11? (α-COOH = 2.0, α-NH<sub>3</sub><sup>+</sup> = 9.0 and R-group imine = 6.5)  A)    B)    C)    D)    E)
C)
Given the following pKa values, what is the major ionization state of histidine at pH 11? (α-COOH = 2.0, α-NH<sub>3</sub><sup>+</sup> = 9.0 and R-group imine = 6.5)  A)    B)    C)    D)    E)
D)
Given the following pKa values, what is the major ionization state of histidine at pH 11? (α-COOH = 2.0, α-NH<sub>3</sub><sup>+</sup> = 9.0 and R-group imine = 6.5)  A)    B)    C)    D)    E)
E)
Given the following pKa values, what is the major ionization state of histidine at pH 11? (α-COOH = 2.0, α-NH<sub>3</sub><sup>+</sup> = 9.0 and R-group imine = 6.5)  A)    B)    C)    D)    E)

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