Enclosed is a peptide sequence: Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Glx -Tyr-Glu-Val-His-His-Gln-Lys Draw a reasonable structure for this sequence using PXMOL and explain your choice of structure. You may use whatever tools you can find (PYMOL and online help).

Answer is attached.

Explanation:

Because the N-terminus of a peptide chain is distinct from the C-terminus, a small peptide composed of different aminoacids may have a several constitutional isomers. For example, a dipeptide made from two different amino acids may have two different structures. Thus, aspartic acid (Asp) and phenylalanine (Phe) may be combined to make Asp-Phe or Phe-Asp, remember that the amino acid on the left is the N-terminus. The methyl ester of the first dipeptide (structure on the right) is the artificial sweetener aspartame, which is nearly 200 times sweeter than sucrose. Neither of the component amino acids is sweet (Phe is actually bitter), and derivatives of the other dipeptide (Phe-Asp) are not sweet.

A tripeptide composed of three different amino acids can be made in 6 different constitutions, and the tetrapeptide shown above (composed of four different amino acids) would have 24 constitutional isomers. When all twenty of the natural amino acids are possible components of a peptide, the possible combinations are enormous. Simple statistical probability indicates that the decapeptides made up from all possible combinations of these amino acids would total 2010!

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