9D89
E. coli 50S ribosomal subunit in complex with PrAMP rumicidin-2 (focused refinement)
9D89 の概要
エントリーDOI | 10.2210/pdb9d89/pdb |
EMDBエントリー | 46632 |
分子名称 | 50S ribosomal protein L33, 50S ribosomal protein L15, 50S ribosomal protein L17, ... (36 entities in total) |
機能のキーワード | proline-rich antimicrobial peptides, pramp, ribosome, cryo-em |
由来する生物種 | Escherichia coli 詳細 |
タンパク質・核酸の鎖数 | 31 |
化学式量合計 | 1280904.67 |
構造登録者 | |
主引用文献 | Panteleev, P.V.,Pichkur, E.B.,Kruglikov, R.N.,Paleskava, A.,Shulenina, O.V.,Bolosov, I.A.,Bogdanov, I.V.,Safronova, V.N.,Balandin, S.V.,Marina, V.I.,Kombarova, T.I.,Korobova, O.V.,Shamova, O.V.,Myasnikov, A.G.,Borzilov, A.I.,Osterman, I.A.,Sergiev, P.V.,Bogdanov, A.A.,Dontsova, O.A.,Konevega, A.L.,Ovchinnikova, T.V. Rumicidins are a family of mammalian host-defense peptides plugging the 70S ribosome exit tunnel. Nat Commun, 15:8925-8925, 2024 Cited by PubMed Abstract: The antimicrobial resistance crisis along with challenges of antimicrobial discovery revealed the vital necessity to develop new antibiotics. Many of the animal proline-rich antimicrobial peptides (PrAMPs) inhibit the process of bacterial translation. Genome projects allowed to identify immune-related genes encoding animal host defense peptides. Here, using genome mining approach, we discovered a family of proline-rich cathelicidins, named rumicidins. The genes encoding these peptides are widespread among ruminant mammals. Biochemical studies indicated that rumicidins effectively inhibited the elongation stage of bacterial translation. The cryo-EM structure of the Escherichia coli 70S ribosome in complex with one of the representatives of the family revealed that the binding site of rumicidins span the ribosomal A-site cleft and the nascent peptide exit tunnel interacting with its constriction point by the conservative Trp23-Phe24 dyad. Bacterial resistance to rumicidins is mediated by knockout of the SbmA transporter or modification of the MacAB-TolC efflux pump. A wide spectrum of antibacterial activity, a high efficacy in the animal infection model, and lack of adverse effects towards human cells in vitro make rumicidins promising molecular scaffolds for development of ribosome-targeting antibiotics. PubMed: 39414793DOI: 10.1038/s41467-024-53309-y 主引用文献が同じPDBエントリー |
実験手法 | ELECTRON MICROSCOPY (1.95 Å) |
構造検証レポート
検証レポート(詳細版)
をダウンロード
