Chapter 29: Q5. (page 1157)
What - halo carbonyl compoundis needed to synthesize each amino acid?
(a) Glycine
(b) Isoleucine
(c) Phenylalanine
Short Answer
(a)
(b)
(c)
Chapter 29: Q5. (page 1157)
What - halo carbonyl compoundis needed to synthesize each amino acid?
(a) Glycine
(b) Isoleucine
(c) Phenylalanine
(a)
(b)
(c)
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Get started for freea.(S)-Penicillamine, an amino acid that does not occur in proteins, is used as a copper chelating agent to treat Wilson’s disease, an inherited defect in copper metabolism.
(R)-Penicillamine is toxic, sometimes causing blindness. Draw the structures of (R) and (S)-penicillamine.
b. What disulfide is formed from oxidation of L-penicillamine?
Draw the mechanism for the reaction that removes an Fmoc group from an amino acid under the following conditions:
Write out the steps for the synthesis of each peptide using the Merrifield method:
Draw the structure of the N-phenylthiohydantoin formed by initial Edman degradation of each peptide: (a) Ala-Gly-Phe-Phe; (b) Val-Ile-Tyr.
Name each peptide using both the three-letter and one-letter abbreviations of the component amino acids.
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