FUNDAMENTALS OF BIOCHEMISTRY - LL FD
FUNDAMENTALS OF BIOCHEMISTRY - LL FD
5th Edition
ISBN: 9781119598022
Author: Voet
Publisher: WILEY
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Chapter 6, Problem 3E
Summary Introduction

To identify: The reason why α helix structure does not contain the following amino acids: Arg, Lys, Met, Phe, Trp, Tyr, and Val.

Concept introduction: α helix is one of the secondary structures of proteins. There are 3.6 residues per turn in the right-handed helical conformation. The peptide bond (C=O) of the nth residue points toward the peptide N-H group of the (n+4)th residue along the helical axis. This forms strong backbone hydrogen bonds.

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H₂N NH peptide_0e60 A dipeptide is made up of two (2) amino acids. The figure above shows one such dipeptide with an unknown sequence. Your task is to find out the two (2) letter sequence of this dipeptide.
carbons in each of the structures below. For instance, the central carbon of chloromethylbutane (pictured 3. A chiral carbon is a carbon that is single-bonded to four different types of groups. Identify the chiral above) is a chiral carbon. (Can you see how the groups attached to it are all chemically different?) In each of the chiral molecules below, identify all the carbons that are chiral carbons by drawing a circle around each one of them. (a) the carbohydrate glucose H O (b) the carbohydrate fructose CH₂OH 1C H-C-OH 3 HO-C-H 4 H-C-OH 5 H-C-OH 6CH₂OH D-Glucose (linear form) (c) the amino acid leucine O O H3C. HO H H- -OH CH 3 NH2 H- -OH CH₂OH OH

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FUNDAMENTALS OF BIOCHEMISTRY - LL FD

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