/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Problem 88 Draw the structures of the tripe... [FREE SOLUTION] | 91Ó°ÊÓ

91Ó°ÊÓ

Draw the structures of the tripeptides gly-ala-ser and ser-alagly. How many other tripeptides are possible using these three amino acids?

Short Answer

Expert verified
The tripeptide Gly-Ala-Ser has the structure: H2N-CH2-CO-NH-CH(CH3)-CO-NH-CH(OH)-CH2-COOH, and the tripeptide Ser-Ala-Gly has the structure: H2N-CH(OH)-CH2-CO-NH-CH(CH3)-CO-NH-CH2-COOH. There are 4 other possible tripeptides using the three amino acids Gly (glycine), Ala (alanine), and Ser (serine).

Step by step solution

01

Drawing the structure of Gly-Ala-Ser

First, we need to find the structure of each amino acid involved. Glycine (Gly) has the following structure: H2N-CH2-COOH, alanine (Ala) has the structure: H2N-CH(CH3)-COOH, and serine (Ser) has the structure: H2N-CH(OH)-CH2-COOH. To construct the tripeptide Gly-Ala-Ser, we need to connect amino acids through peptide bonds. A peptide bond forms by the reaction of the carboxyl group (-COOH) of one amino acid with the amino group (-NH2) of another amino acid, releasing a water molecule. The structure of Gly-Ala-Ser would be: H2N-CH2-CO-NH-CH(CH3)-CO-NH-CH(OH)-CH2-COOH
02

Drawing the structure of Ser-Ala-Gly

Similarly, we can construct the tripeptide Ser-Ala-Gly by connecting serine, alanine, and glycine through peptide bonds. The structure of Ser-Ala-Gly would be: H2N-CH(OH)-CH2-CO-NH-CH(CH3)-CO-NH-CH2-COOH
03

Calculate the number of other possible tripeptides

Now, we need to determine the number of other possible tripeptides using these three amino acids. To do this, we can use the permutation formula. We have three unique amino acids, and we want to arrange them in three positions, which will be calculated as 3 × 2 × 1. Number of other possible tripeptides = 3! = 3 × 2 × 1 = 6 However, we have already drawn two of these tripeptides (Gly-Ala-Ser and Ser-Ala-Gly), so the number of other possible tripeptides is: 6 - 2 = 4 So, there are 4 other possible tripeptides using the three amino acids Gly (glycine), Ala (alanine), and Ser (serine).

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with 91Ó°ÊÓ!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Write the sequence of all possible tetrapeptides composed of the following amino acids. a. two phenylalanines and two glycines b. two phenylalanines, glycine, and alanine

Using appropriate reactants, alcohols can be oxidized into aldehydes, ketones, and/or carboxylic acids. Primary alcohols can be oxidized into aldehydes, which can then be oxidized into carboxylic acids. Secondary alcohols can be oxidized into ketones, while tertiary alcohols do not undergo this type of oxidation. Give the structure of the product(s) resulting from the oxidation of each of the following alcohols. a. 3 -methyl-l-butanol b. 3 -methyl- 2 -butanol c. 2 -methyl-2-butanol

The base sequences in mRNA that code for certain amino acids are Glu: GAA, GAG Val: \(\quad\) GUU, GUC, GUA, GUG Met: AUG Trp: UGG Phe: UUU, UUC Asp: GAU, GAC These sequences are complementary to the sequences in DNA. a. Give the corresponding sequences in DNA for the amino acids listed above. b. Give a DNA sequence that would code for the peptide trp-glu-phe-met. c. How many different DNA sequences can code for the tetrapeptide in part b? d. What is the peptide that is produced from the DNA sequence T-A-C-C-T-G-A- A-G? e. What other DNA sequences would yield the same tripeptide as in part d?

Aspartame, the artificial sweetener marketed under the name NutraSweet, is a methyl ester of a dipeptide: a. What two amino acids are used to prepare aspartame? b. There is concern that methanol may be produced by the decomposition of aspartame. From what portion of the molecule can methanol be produced? Write an equation for this reaction.

Oxidation of an aldehyde yields a carboxylic acid: Draw the structures for the products of the following oxidation reactions. a. propanal \(\stackrel{\text { [ox] }}{\rightarrow}\) b. 2,3 -dimethylpentanal \(\stackrel{\text { [ox] }}{\longrightarrow}\) c. 3 -ethylbenzaldehyde \(\stackrel{\text { [ox] }}{\longrightarrow}\)

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.