9H9L

Complex 3 (BODY) 30S-tRNA-GE81112

これはPDB形式変換不可エントリーです。

9H9L の概要

• エントリーDOI: 10.2210/pdb9h9l/pdb
• EMDBエントリー: 51968
• 分子名称: 16S RNA (1078-MER), Small ribosomal subunit protein uS17, Small ribosomal subunit protein bS18, ... (16 entities in total)
• 機能のキーワード: antibiotic, initiation factor, ge81112, 30s, ribosome
• 由来する生物種: Escherichia coli; 詳細
• タンパク質・核酸の鎖数: 13
• 化学式量合計: 657760.58

構造登録者

Schedlbauer, A.,Han, X.,van Bakel, W.,Kaminishi, T.,Ochoa-Lizarralde, B.,Iturrioz, I.,Capuni, R.,Parry, R.,Zegarra, R.,Gil-Carton, D.,Lopez-Alonso, J.P.,Barragan Sanz, K.,Brandi, L.,Gualerzi, C.O.,Fucini, P.,Connell, S.R. (登録日: 2024-10-31, 公開日: 2025-08-06)

主引用文献

Schedlbauer, A.,Han, X.,van Bakel, W.,Kaminishi, T.,Ochoa-Lizarralde, B.,Iturrioz, I.,Capuni, R.,Parry, R.,Zegarra, R.,Gil-Carton, D.,Lopez-Alonso, J.P.,Barragan Sanz, K.,Brandi, L.,Gualerzi, C.O.,Fucini, P.,Connell, S.R.
A binding site for the antibiotic GE81112 in the ribosomal mRNA channel.
bioRxiv, 2024

PubMed Abstract: The initiation phase is the rate-limiting step of protein synthesis (translation) and is finely regulated, making it an important drug target. In bacteria, initiation is guided by three initiation factors and involves positioning the start site on the messenger RNA within the P-site on the small ribosomal subunit (30S), where it is decoded by the initiator tRNA. This process can be efficiently inhibited by GE81112, a natural hydrophilic, noncyclic, nonribosomal tetrapeptide. It is found in nature in three structural variants (A, B and B1 with molecular masses of 643-658 Da). Previous biochemical and structural characterisation of GE81112 indicates that the primary mechanism of action of this antibiotic is to (1) prevent the initiator tRNA from binding correctly to the P-site and (2) block conformational rearrangements in initiation factor IF3, resulting in an 30S pre/C state. In this study, using cryoEM, we have determined the binding site of GE81112 in initiation complexes (3.2-3.7Å) and on empty ribosomes (2.09 Å). This binding site is within the mRNA channel (E-site) but remote from the binding site of the initiation factors and initiator tRNA. This suggests that it acts allosterically to prevent the initiator tRNA from being locked into place. The binding mode is consistent with previous biochemical studies and recent work identifying the key pharmacophores of GE81112.

PubMed: 39386670
DOI: 10.1101/2024.09.26.614503

実験手法

ELECTRON MICROSCOPY (3.2 Å)