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6P24

Escherichia coli tRNA synthetase

6P24 の概要
エントリーDOI10.2210/pdb6p24/pdb
分子名称Phenylalanine--tRNA ligase alpha subunit, Phenylalanine--tRNA ligase beta subunit, MAGNESIUM ION, ... (10 entities in total)
機能のキーワードinhibitor, aminoacyl-trna synthetase, phers, antibacterial, ligase
由来する生物種Escherichia coli (strain K12)
詳細
タンパク質・核酸の鎖数4
化学式量合計253449.95
構造登録者
Kahne, D.,Baidin, V.,Owens, T.W. (登録日: 2019-05-20, 公開日: 2020-11-18, 最終更新日: 2023-10-11)
主引用文献Baidin, V.,Owens, T.W.,Lazarus, M.B.,Kahne, D.
Simple Secondary Amines Inhibit Growth of Gram-Negative Bacteria through Highly Selective Binding to Phenylalanyl-tRNA Synthetase.
J.Am.Chem.Soc., 143:623-627, 2021
Cited by
PubMed Abstract: Antibiotics to treat drug-resistant Gram-negative infections are urgently needed but challenging to discover. Using a cell-based screen, we identified a simple secondary amine that inhibited the growth of wild-type and but not the growth of the Gram-positive organism . Resistance mutations in and mapped exclusively to the aminoacyl-tRNA synthetase PheRS. We confirmed biochemically that the compound inhibited PheRS from these organisms and showed that it did not inhibit PheRS from or humans. To understand the basis for the compound's high selectivity for only some PheRS enzymes, we solved crystal structures of and PheRS complexed with the inhibitor. The structures showed that the compound's benzyl group mimics the benzyl of phenylalanine. The other amine substituent, a 2-(cyclohexen-1-yl)ethyl group, induces a hydrophobic pocket in which it binds. Through bioinformatic analysis and mutagenesis, we show that the ability to induce a complementary hydrophobic pocket that can accommodate the second substituent explains the high selectivity of this remarkably simple molecular scaffold for Gram-negative PheRS. Because this secondary amine scaffold is active against wild-type Gram-negative pathogens but is not cytotoxic to mammalian cells, we suggest that it may be possible to develop it for use in combination antibiotic therapy to treat Gram-negative infections.
PubMed: 33411531
DOI: 10.1021/jacs.0c11113
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.12 Å)
構造検証レポート
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件を2026-04-15に公開中

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