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9G06

Structure of 30S-IF1-IF3-mRNA-fMet-tRNA-GE81112A complex

これはPDB形式変換不可エントリーです。
9G06 の概要
エントリーDOI10.2210/pdb9g06/pdb
EMDBエントリー50912
分子名称Small ribosomal subunit protein uS3, Small ribosomal subunit protein uS13, Small ribosomal subunit protein uS14, ... (28 entities in total)
機能のキーワードantibiotics, 30s initiation, translational inhibitor, translation
由来する生物種Escherichia coli
詳細
タンパク質・核酸の鎖数24
化学式量合計835762.97
構造登録者
Safdari, H.A.,Morici, M.,Wilson, D.N. (登録日: 2024-07-07, 公開日: 2025-03-19)
主引用文献Safdari, H.A.,Morici, M.,Sanchez-Castro, A.,Dallape, A.,Paternoga, H.,Giuliodori, A.M.,Fabbretti, A.,Milon, P.,Wilson, D.N.
The translation inhibitors kasugamycin, edeine and GE81112 target distinct steps during 30S initiation complex formation.
Nat Commun, 16:2470-2470, 2025
Cited by
PubMed Abstract: During bacterial translation initiation, the 30S ribosomal subunit, initiation factors, and initiator tRNA define the reading frame of the mRNA. This process is inhibited by kasugamycin, edeine and GE81112, however, their mechanisms of action have not been fully elucidated. Here we present cryo-electron microscopy structures of 30S initiation intermediate complexes formed in the presence of kasugamycin, edeine and GE81112 at resolutions of 2.0-2.9 Å. The structures reveal that all three antibiotics bind within the E-site of the 30S and preclude 30S initiation complex formation. While kasugamycin and edeine affect early steps of 30S pre-initiation complex formation, GE81112 stalls pre-initiation complex formation at a further step by allowing start codon recognition, but impeding IF3 departure. Collectively, our work highlights how chemically distinct compounds binding at a conserved site on the 30S can interfere with translation initiation in a unique manner.
PubMed: 40075065
DOI: 10.1038/s41467-025-57731-8
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (2.85 Å)
構造検証レポート
Validation report summary of 9g06
検証レポート(詳細版)ダウンロードをダウンロード

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件を2025-07-30に公開中

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