3J25

Structural basis for TetM-mediated tetracycline resistance

3J25 の概要

• エントリーDOI: 10.2210/pdb3j25/pdb
• EMDBエントリー: 2183
• 分子名称: Tetracycline resistance protein tetM, PHOSPHOMETHYLPHOSPHONIC ACID GUANYLATE ESTER (2 entities in total)
• 機能のキーワード: antibiotic resistance, translation
• 由来する生物種: Enterococcus faecalis
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 72960.97

構造登録者

Doenhoefer, A.,Franckenberg, S.,Wickles, S.,Berninghausen, O.,Beckmann, R.,Wilson, D.N. (登録日: 2012-08-22, 公開日: 2012-10-17, 最終更新日: 2024-02-21)

主引用文献

Donhofer, A.,Franckenberg, S.,Wickles, S.,Berninghausen, O.,Beckmann, R.,Wilson, D.N.
Structural basis for TetM-mediated tetracycline resistance.
Proc.Natl.Acad.Sci.USA, 109:16900-16905, 2012

PubMed Abstract: Ribosome protection proteins (RPPs) confer tetracycline resistance by binding to the ribosome and chasing the drug from its binding site. The current model for the mechanism of action of RPPs proposes that drug release is indirect and achieved via conformational changes within the drug-binding site induced upon binding of the RPP to the ribosome. Here we report a cryo-EM structure of the RPP TetM in complex with the 70S ribosome at 7.2-Å resolution. The structure reveals the contacts of TetM with the ribosome, including interaction between the conserved and functionally critical C-terminal extension of TetM and the decoding center of the small subunit. Moreover, we observe direct interaction between domain IV of TetM and the tetracycline binding site and identify residues critical for conferring tetracycline resistance. A model is presented whereby TetM directly dislodges tetracycline to confer resistance.

PubMed: 23027944
DOI: 10.1073/pnas.1208037109

実験手法

ELECTRON MICROSCOPY (7.2 Å)