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The E3 ligase adapter cereblon targets the C-terminal cyclic imide degron
C-terminal cyclic imides are physiological degrons that enable the ubiquitin E3 ligase adapter protein cereblon to target substrates for degradation.
- Saki Ichikawa
- , Hope A. Flaxman
- & Christina M. Woo
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Article
| Open AccessA prebiotically plausible scenario of an RNA–peptide world
Peptide synthesis can take place directly on RNA, which suggests how a nucleic acid–protein world might have originated on early Earth.
- Felix Müller
- , Luis Escobar
- & Thomas Carell
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Letter |
Asymmetric α-arylation of amino acids
This approach introduces an aryl substituent to the α-carbon of amino acids without a transition-metal catalyst, and uses the inherent chirality of the amino acid itself as the source of asymmetry.
- Daniel J. Leonard
- , John W. Ward
- & Jonathan Clayden
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Accurate de novo design of hyperstable constrained peptides
Computational methods for the de novo design of conformationally restricted peptides produce exceptionally stable short peptides stabilized by backbone cyclization and/or internal disulfide bonds that are promising starting points for a new generation of peptide-based drugs.
- Gaurav Bhardwaj
- , Vikram Khipple Mulligan
- & David Baker
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Human commensals producing a novel antibiotic impair pathogen colonization
The nasal commensal bacterium Staphylococcus lugdunensis produces a novel cyclic peptide antibiotic, lugdunin, that inhibits colonization by S. aureus in animal models and is associated with a significantly reduced S. aureus carriage rate in humans, suggesting that human commensal bacteria could be a valuable resource for the discovery of new antibiotics.
- Alexander Zipperer
- , Martin C. Konnerth
- & Bernhard Krismer
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Letter |
Atomic-resolution dynamics on the surface of amyloid-β protofibrils probed by solution NMR
- Nicolas L. Fawzi
- , Jinfa Ying
- & G. Marius Clore
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Article |
Umpolung reactivity in amide and peptide synthesis
The backbones of all natural peptides and proteins are composed of amide bonds. In the laboratory, the construction of such bonds generally relies on dehydrative approaches, although there are alternatives. It is now shown that the activation of amines and nitroalkanes with an electrophilic iodine source can lead directly to amide products.
- Bo Shen
- , Dawn M. Makley
- & Jeffrey N. Johnston