5X22

Crystal structure of Thermus thermophilus transcription initiation complex with GpA and CMPcPP

5X22 の概要

• エントリーDOI: 10.2210/pdb5x22/pdb
• 関連するPDBエントリー: 5X21
• 分子名称: DNA-directed RNA polymerase subunit alpha, ZINC ION, 5'-O-[(S)-hydroxy{[(S)-hydroxy(phosphonooxy)phosphoryl]methyl}phosphoryl]cytidine, ... (11 entities in total)
• 機能のキーワード: transcription, rna polymerase, primer-dependent initiation, transferase-dna complex, transferase/dna
• 由来する生物種: Thermus thermophilus; 詳細
• タンパク質・核酸の鎖数: 18
• 化学式量合計: 890215.67

構造登録者

Zhang, Y.,Ebright, R. (登録日: 2017-01-29, 公開日: 2017-07-05, 最終更新日: 2024-11-20)

主引用文献

Maffioli, S.I.,Zhang, Y.,Degen, D.,Carzaniga, T.,Del Gatto, G.,Serina, S.,Monciardini, P.,Mazzetti, C.,Guglierame, P.,Candiani, G.,Chiriac, A.I.,Facchetti, G.,Kaltofen, P.,Sahl, H.G.,Deho, G.,Donadio, S.,Ebright, R.H.
Antibacterial Nucleoside-Analog Inhibitor of Bacterial RNA Polymerase.
Cell, 169:1240-1248.e23, 2017

PubMed Abstract: Drug-resistant bacterial pathogens pose an urgent public-health crisis. Here, we report the discovery, from microbial-extract screening, of a nucleoside-analog inhibitor that inhibits bacterial RNA polymerase (RNAP) and exhibits antibacterial activity against drug-resistant bacterial pathogens: pseudouridimycin (PUM). PUM is a natural product comprising a formamidinylated, N-hydroxylated Gly-Gln dipeptide conjugated to 6'-amino-pseudouridine. PUM potently and selectively inhibits bacterial RNAP in vitro, inhibits bacterial growth in culture, and clears infection in a mouse model of Streptococcus pyogenes peritonitis. PUM inhibits RNAP through a binding site on RNAP (the NTP addition site) and mechanism (competition with UTP for occupancy of the NTP addition site) that differ from those of the RNAP inhibitor and current antibacterial drug rifampin (Rif). PUM exhibits additive antibacterial activity when co-administered with Rif, exhibits no cross-resistance with Rif, and exhibits a spontaneous resistance rate an order-of-magnitude lower than that of Rif. PUM is a highly promising lead for antibacterial therapy.

PubMed: 28622509
DOI: 10.1016/j.cell.2017.05.042

実験手法

X-RAY DIFFRACTION (3.35 Å)