6WRU
Structure of the 50S subunit of the ribosome from Methicillin Resistant Staphylococcus aureus in complex with an isomer of the tedizolid
6WRU の概要
エントリーDOI | 10.2210/pdb6wru/pdb |
関連するPDBエントリー | 6WQN 6WQQ 6WRS |
EMDBエントリー | 21888 |
分子名称 | 50S ribosomal protein L19, 50S ribosomal protein L29, 50S ribosomal protein L3, ... (29 entities in total) |
機能のキーワード | antibiotic, tedizolid, oxazolidinone, ribosome |
由来する生物種 | Staphylococcus aureus 詳細 |
タンパク質・核酸の鎖数 | 28 |
化学式量合計 | 1315436.25 |
構造登録者 | |
主引用文献 | Wright, A.,Deane-Alder, K.,Marschall, E.,Bamert, R.,Venugopal, H.,Lithgow, T.,Lupton, D.W.,Belousoff, M.J. Characterization of the Core Ribosomal Binding Region for the Oxazolidone Family of Antibiotics Using Cryo-EM. Acs Pharmacol Transl Sci, 3:425-432, 2020 Cited by PubMed Abstract: Linezolid and tedizolid are oxazolidinones with established clinical utility for the treatment of Gram-positive pathogens. Over time it has become apparent that even modest structural changes to the core phenyl oxazolidinone leads to drastic changes in biological activity. Consequently, the structure-activity relationship around the core oxazolidinone is constantly evolving, often reflected with new structural motifs present in nascent oxazolidinones. Herein we describe the use of cryo-electron microscopy to examine the differences in binding of several functionally different oxazolidinones in the hopes of enhanced understanding of their SAR. Tedizolid, radezolid, T145, and contezolid have been examined within the peptidyl transferase center (PTC) of the 50S ribosomal subunit from methicillin resistant . The ribosome-antibiotic complexes were resolved to a resolution of around 3 Å enabling unambiguous assignment of how each antibiotic interacts with the PTC. PubMed: 32566908DOI: 10.1021/acsptsci.0c00041 主引用文献が同じPDBエントリー |
実験手法 | ELECTRON MICROSCOPY (3.1 Å) |
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