2. Information about the structure of an octapeptide is given below.
a. Hydrolysis of the peptide gives the following amino acids in equal amounts: Ala, Asp, Glu, Met, Lys, Phe, Tyr, and Val.
b. Treatment of the peptide with 2,4-dinitrofluorobenzene followed by hydrolysis yields Asp labeled with a 2,4-DNP group.
c. When the peptide is treated with carboxypeptidase, the concentration of Val increases rapidly.
d. Hydrolysis of the peptide with trypsin gives a tripeptide (A) and a pentapeptide (B).
e. The tripeptide (A) is cleaved by chymotrypsin to give Phe and a dipeptide with a pI of about 5.6.
f. The pentapeptide (B) is cleaved by chymotrypsin to give a dipeptide and a tripeptide. Reaction of the tripeptide with cyanogen bromide gives Tyr.
Write the sequence of amino acids in the octapeptide and explain how this sequence was determined.