Chapter 29: 19P (page 1170)
Draw the structure of the N-phenylthiohydantoin formed by initial Edman degradation of each peptide: (a) Ala-Gly-Phe-Phe; (b) Val-Ile-Tyr.
Chapter 29: 19P (page 1170)
Draw the structure of the N-phenylthiohydantoin formed by initial Edman degradation of each peptide: (a) Ala-Gly-Phe-Phe; (b) Val-Ile-Tyr.
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Get started for freeThe anti-obesity drug orlistat works by irreversibly inhibiting pancreatic lipase, an enzyme responsible for the hydrolysis of triacylglycerols in the intestines, so they are excreted without metabolism, inhibition occurs by reaction of orlistat with a serine residue of the enzyme, forming a covalently bound, inactive enzyme product. Draw the structure of the product formed during inhibition.
Draw the organic products formed in the following reaction.
Consider two molecules of a tetrapeptide composed of only alanine residues. Draw the hydrogen bonding interactions that result when these two peptides adopt a parallel ฮฒ-pleated sheet arrangement. Answer this same question for the antiparallel ฮฒ-pleated sheet arrangement.
L-thyroxine, a thyroid hormone and oral medication used to treat thyroid hormone deficiency, is an amino acid that does not exist in proteins. Draw the zwitterionic form of L-thyroxine.
Explain why the pKaof the -NH3+group of an -amino acid is lower than the pKaof the ammonium ion derived from a amine . For example, pKaof the group of alanine is 9.87 but the pKaof is 10.63.
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