Poly-L-leucine in an organic solvent such as dioxane is a helical, whereas poly-L-isoleucine is not. Why do these amino acids with the same number and kinds of atoms have different helix-forming tendencies? L-isoleucine's methyl group sterically interferes with α-helix formation, whereas L-leucine's methyl group does not interfere. L-isoleucine lacks an NH group that can donate a hydrogen bond to stabilize an a helix, whereas L-leucine has an NH group. L-isoleucine contains a hydrogen-bond acceptor in close proximity to the main chain, whereas L-leucine lacks this group. L-isoleucine's ring structure prevents it from assuming the op value to fit into an a helix, whereas L-isoleucine does not have a ring structure.
Poly-L-leucine in an organic solvent such as dioxane is a helical, whereas poly-L-isoleucine is not. Why do these amino acids with the same number and kinds of atoms have different helix-forming tendencies? L-isoleucine's methyl group sterically interferes with α-helix formation, whereas L-leucine's methyl group does not interfere. L-isoleucine lacks an NH group that can donate a hydrogen bond to stabilize an a helix, whereas L-leucine has an NH group. L-isoleucine contains a hydrogen-bond acceptor in close proximity to the main chain, whereas L-leucine lacks this group. L-isoleucine's ring structure prevents it from assuming the op value to fit into an a helix, whereas L-isoleucine does not have a ring structure.
Human Heredity: Principles and Issues (MindTap Course List)
11th Edition
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Author:Michael Cummings
Publisher:Michael Cummings
Chapter9: Gene Expression And Gene Regulation
Section: Chapter Questions
Problem 19QP: Below is the structure of glycine. Draw a tripeptide composed exclusively of glycine. Label the...
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Transcribed Image Text:Poly-L-leucine in an organic solvent such as dioxane is a helical, whereas poly-L-isoleucine is not.
Why do these amino acids with the same number and kinds of atoms have different helix-forming tendencies?
L-isoleucine's methyl group sterically interferes with α-helix formation, whereas L-leucine's methyl group does
not interfere.
L-isoleucine lacks an NH group that can donate a hydrogen bond to stabilize an a helix, whereas L-leucine has an
NH group.
L-isoleucine contains a hydrogen-bond acceptor in close proximity to the main chain, whereas L-leucine lacks
this group.
L-isoleucine's ring structure prevents it from assuming the op value to fit into an a helix, whereas L-isoleucine does
not have a ring structure.
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