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Ditlev E. Brodersen

Researcher at Aarhus University

Publications -  88
Citations -  9982

Ditlev E. Brodersen is an academic researcher from Aarhus University. The author has contributed to research in topics: RNA & Antitoxin. The author has an hindex of 33, co-authored 82 publications receiving 9277 citations. Previous affiliations of Ditlev E. Brodersen include La Trobe University & Laboratory of Molecular Biology.

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Structure of the 30S ribosomal subunit.

TL;DR: The crystal structure of the 30S subunit from Thermus thermophilus, refined to 3 Å resolution, is reported, which will facilitate the interpretation in molecular terms of lower resolution structural data on several functional states of the ribosome from electron microscopy and crystallography.
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Functional insights from the structure of the 30S ribosomal subunit and its interactions with antibiotics

TL;DR: The functional implications of the high-resolution 30S crystal structure are described, and details of the interactions between the 30S subunit and its tRNA and mRNA ligands are inferred, which lead to a model for the role of the universally conserved 16S RNA residues A1492 and A1493 in the decoding process.
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Recognition of Cognate Transfer RNA by the 30S Ribosomal Subunit

TL;DR: Crystal structures of the 30S ribosomal subunit in complex with messenger RNA and cognate transfer RNA in the A site, both in the presence and absence of the antibiotic paromomycin, have been solved at between 3.1 and 3.3 angstroms resolution.
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The structural basis for the action of the antibiotics tetracycline, pactamycin, and hygromycin B on the 30S ribosomal subunit

TL;DR: The recently determined atomic structure of the 30S ribosomal subunit is used to determine the structures of its complexes with the antibiotics tetracycline, pactamycin, and hygromycin B to suggest a mechanism for its effects on ribosome function.
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Toxins, Targets, and Triggers: An Overview of Toxin-Antitoxin Biology

TL;DR: How multiple levels of regulation shape the conditions of toxin activation to achieve the different biological functions of TA modules is highlighted.