4J3F
Crystal Structure of FabI from F. tularensis in complex with novel inhibitors based on the benzimidazole scaffold.
4J3F の概要
| エントリーDOI | 10.2210/pdb4j3f/pdb |
| 関連するPDBエントリー | 3UIC 4J1N 4J4T |
| 分子名称 | Enoyl-[acyl-carrier-protein] reductase [NADH], 1-(4-methoxy-3-methylbenzyl)-5,6,7,8-tetrahydro-1H-naphtho[2,3-d]imidazole, NICOTINAMIDE-ADENINE-DINUCLEOTIDE, ... (7 entities in total) |
| 機能のキーワード | rossmann fold, reductase, nadh, reduction, oxidoreductase-oxidoreductase inhibitor complex, oxidoreductase/oxidoreductase inhibitor |
| 由来する生物種 | Francisella tularensis subsp. tularensis |
| タンパク質・核酸の鎖数 | 8 |
| 化学式量合計 | 248891.92 |
| 構造登録者 | Mehboob, S.,Boci, T.,Brubaker, L.,Santarsiero, B.D.,Johnson, M.E. (登録日: 2013-02-05, 公開日: 2014-07-23, 最終更新日: 2023-09-20) |
| 主引用文献 | Mehboob, S.,Song, J.,Hevener, K.E.,Su, P.C.,Boci, T.,Brubaker, L.,Truong, L.,Mistry, T.,Deng, J.,Cook, J.L.,Santarsiero, B.D.,Ghosh, A.K.,Johnson, M.E. Structural and biological evaluation of a novel series of benzimidazole inhibitors of Francisella tularensis enoyl-ACP reductase (FabI). Bioorg.Med.Chem.Lett., 25:1292-1296, 2015 Cited by PubMed Abstract: Francisella tularensis, the causative agent of tularemia, presents a significant biological threat and is a Category A priority pathogen due to its potential for weaponization. The bacterial FASII pathway is a viable target for the development of novel antibacterial agents treating Gram-negative infections. Here we report the advancement of a promising series of benzimidazole FabI (enoyl-ACP reductase) inhibitors to a second-generation using a systematic, structure-guided lead optimization strategy, and the determination of several co-crystal structures that confirm the binding mode of designed inhibitors. These compounds display an improved low nanomolar enzymatic activity as well as promising low microgram/mL antibacterial activity against both F. tularensis and Staphylococcus aureus and its methicillin-resistant strain (MRSA). The improvements in activity accompanying structural modifications lead to a better understanding of the relationship between the chemical structure and biological activity that encompasses both enzymatic and whole-cell activity. PubMed: 25677657DOI: 10.1016/j.bmcl.2015.01.048 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.85 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






