Chapter 4: Q6CP (page 91)
Explain why all the amino acids except for glycine are chiral.
Short Answer
All the standard amino acids except for glycine are chiral because they all have four different substituents attached to their carbon (Cα) atom.
/*! 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}
Learning Materials
Features
Discover
Chapter 4: Q6CP (page 91)
Explain why all the amino acids except for glycine are chiral.
All the standard amino acids except for glycine are chiral because they all have four different substituents attached to their carbon (Cα) atom.
All the tools & learning materials you need for study success - in one app.
Get started for free
Calculate the number of possible pentapeptides that contain one residue each of and .
Some bacteria produce poly-γ-glutamic acid, a polymer in which the amino group of each glutamate residue is condensed with the γ-carboxylate group of the adjacent residue. Draw the repeating structure of this polymer.
The 20 standard amino acids are calledα-amino acids. Certainβ-amino acids are found in nature. Draw the structure ofβ-alanine(3-amino-n-propionate).
Draw the four stereoisomers of threonine as Fischer projections.
In some proteins, the side chain of serine appears to undergo ionization. Explain why ionization would be facilitated by the presence of an aspartate residue nearby.
What do you think about this solution?
We value your feedback to improve our textbook solutions.