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6BFB

Crystal structure of a F. nucleatum FMN riboswitch bound to WG-3

6BFB の概要
エントリーDOI10.2210/pdb6bfb/pdb
分子名称RNA (54-MER), RNA (56-MER), 5-[(3S,4S)-3-(dimethylamino)-4-hydroxypyrrolidin-1-yl]-6-fluoro-4-methyl-8-oxo-3,4-dihydro-8H-1-thia-4,9b-diazacyclopenta[cd]phenalene-9-carboxylic acid, ... (5 entities in total)
機能のキーワードrna, translation, rna-inhibitor complex
由来する生物種Fusobacterium nucleatum
詳細
タンパク質・核酸の鎖数2
化学式量合計36004.93
構造登録者
Rizvi, N.F.,Fischmann, T.O. (登録日: 2017-10-26, 公開日: 2018-02-21, 最終更新日: 2024-03-06)
主引用文献Rizvi, N.F.,Howe, J.A.,Nahvi, A.,Klein, D.J.,Fischmann, T.O.,Kim, H.Y.,McCoy, M.A.,Walker, S.S.,Hruza, A.,Richards, M.P.,Chamberlin, C.,Saradjian, P.,Butko, M.T.,Mercado, G.,Burchard, J.,Strickland, C.,Dandliker, P.J.,Smith, G.F.,Nickbarg, E.B.
Discovery of Selective RNA-Binding Small Molecules by Affinity-Selection Mass Spectrometry.
ACS Chem. Biol., 13:820-831, 2018
Cited by
PubMed Abstract: Recent advances in understanding the relevance of noncoding RNA (ncRNA) to disease have increased interest in drugging ncRNA with small molecules. The recent discovery of ribocil, a structurally distinct synthetic mimic of the natural ligand of the flavin mononucleotide (FMN) riboswitch, has revealed the potential chemical diversity of small molecules that target ncRNA. Affinity-selection mass spectrometry (AS-MS) is theoretically applicable to high-throughput screening (HTS) of small molecules binding to ncRNA. Here, we report the first application of the Automated Ligand Detection System (ALIS), an indirect AS-MS technique, for the selective detection of small molecule-ncRNA interactions, high-throughput screening against large unbiased small-molecule libraries, and identification and characterization of novel compounds (structurally distinct from both FMN and ribocil) that target the FMN riboswitch. Crystal structures reveal that different compounds induce various conformations of the FMN riboswitch, leading to different activity profiles. Our findings validate the ALIS platform for HTS screening for RNA-binding small molecules and further demonstrate that ncRNA can be broadly targeted by chemically diverse yet selective small molecules as therapeutics.
PubMed: 29412640
DOI: 10.1021/acschembio.7b01013
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.82 Å)
構造検証レポート
Validation report summary of 6bfb
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2026-02-04に公開中

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