Consecutive Ribosomal Incorporation of α-Aminoxy/α-Hydrazino Acids with <scp>l</scp>/<scp>d</scp>-Configurations into Nascent Peptide Chains
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- Takayuki Katoh
- Department of Chemistry, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan
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- Hiroaki Suga
- Department of Chemistry, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan
説明
α-Aminoxy and α-hydrazino acids are β-amino acid analogs with β-carbons replaced by oxygen and nitrogen, respectively. Such heteroatoms dictate the folding of peptides into specific secondary structures called pseudo-γ-turns. Achiral α-aminoxyacetic acid (
収録刊行物
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- Journal of the American Chemical Society
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Journal of the American Chemical Society 143 (45), 18844-18848, 2021-11-03
American Chemical Society (ACS)
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キーワード
- Chemical Sciences not elsewhere classified
- whether multiple
- l -< sup
- Immunology
- Biophysics
- ribosomal translation
- </ sup
- heteroatoms dictate
- carbons replaced
- Biochemistry
- Peptides, Cyclic
- 333
- possible remains unclear
- RNA, Transfer
- Genetics
- Escherichia coli
- Amino Acid Sequence
- RNA, Messenger
- various model peptides
- Amino Acids
- achiral α
- Molecular Biology
- ‑ configurations
- whether ribosomes tolerate
- Ecology
- consecutive incorporations
- first time
- Stereoisomerism
- consecutive ribosomal incorporation
- Hydrazines
- amino acid analogs
- nn </ sup
- single incorporation
- Physical Sciences not elsewhere classified
- α ‑ aminoxy
- Ribosomes
- Biological Sciences not elsewhere classified
- hydrazino acids
詳細情報 詳細情報について
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- CRID
- 1360013168750756480
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- ISSN
- 15205126
- 00027863
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- PubMed
- 34731572
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- 資料種別
- journal article
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- データソース種別
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- Crossref
- KAKEN
- OpenAIRE
