Q: Identify the N-terminal residue of a peptide that yields the
Identify the N-terminal residue of a peptide that yields the following PTH derivative upon Edman degradation:
See AnswerQ: Treatment of a tripeptide with phenyl isothiocyanate yields compound A and a
Treatment of a tripeptide with phenyl isothiocyanate yields compound A and a dipeptide. Treatment of the dipeptide with phenyl isothiocyanate yields compound B and glycine. Identify the structure of t...
See AnswerQ: Glucagon is a peptide hormone produced by the pancreas that, with
Glucagon is a peptide hormone produced by the pancreas that, with insulin, regulates blood glucose levels. Glucagon is comprised of 29 amino acid residues. Treatment with trypsin yields four fragments...
See AnswerQ: When the N terminus of a peptide is acetylated, the peptide
When the N terminus of a peptide is acetylated, the peptide derivative that is formed is unreactive toward phenyl isothiocyanate. Explain.
See AnswerQ: Predict the major product(s) of the reaction between L
Predict the major product(s) of the reaction between L-valine and: a. MeOH, H+ b. Di-tert-butyl-dicarbonate c. NaOH, H2O d. HCl
See AnswerQ: Draw the structure of the product with the molecular formula C10H10O that
Draw the structure of the product with the molecular formula C10H10O that is obtained when the compound below is heated with aqueous acid.
See AnswerQ: Show all steps necessary to make the dipeptide Phe-Ala from
Show all steps necessary to make the dipeptide Phe-Ala from L-phenylalanine and L-alanine.
See AnswerQ: Draw all four possible dipeptides that are obtained when a mixture of
Draw all four possible dipeptides that are obtained when a mixture of L-phenylalanine and L-alanine is treated with DCC.
See AnswerQ: Identify the steps you would use to combine Val-Leu and
Identify the steps you would use to combine Val-Leu and Phe-Ile to form the tetrapeptide Phe- Ile-Val-Leu.
See AnswerQ: Identify all of the steps necessary to prepare the tripeptide Leu-
Identify all of the steps necessary to prepare the tripeptide Leu-Val-Ala with a Merrifield synthesis.
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