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.
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Chapter9: Gene Expression And Gene Regulation
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Problem 19QP: Below is the structure of glycine. Draw a tripeptide composed exclusively of glycine. Label the...
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![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.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fd2659b4c-30a6-48d4-90ed-e5c7a02f7b8e%2Fa00d9d75-9796-43c3-9745-1066d1faa588%2Fk2layhk_processed.png&w=3840&q=75)
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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