9GCA の概要
| エントリーDOI | 10.2210/pdb9gca/pdb |
| 分子名称 | 2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase, 6-methyl-5~{H}-pyrrolo[3,4-b]pyridin-7-one (3 entities in total) |
| 機能のキーワード | transferase, cytidylyltransferase, mep, isoprenoid biosynthesys, ispd, pseudomonas aeruginosa |
| 由来する生物種 | Pseudomonas aeruginosa |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 28207.05 |
| 構造登録者 | |
| 主引用文献 | Willocx, D.,D'Auria, L.,Walsh, D.,Scherer, H.,Alhayek, A.,Hamed, M.M.,Borel, F.,Diamanti, E.,Hirsch, A.K.H. Fragment Discovery by X-Ray Crystallographic Screening Targeting the CTP Binding Site of Pseudomonas Aeruginosa IspD. Angew.Chem.Int.Ed.Engl., 64:e202414615-e202414615, 2025 Cited by PubMed Abstract: With antimicrobial resistance (AMR) reaching alarming levels, new anti-infectives with unprecedented mechanisms of action are urgently needed. The 2-C-methylerythritol-D-erythritol-4-phosphate (MEP) pathway represents an attractive source of drug targets due to its essential role in numerous pathogenic Gram-negative bacteria and Mycobacterium tuberculosis (Mt), whilst being absent in human cells. Here, we solved the first crystal structure of Pseudomonas aeruginosa (Pa) IspD, the third enzyme in the MEP pathway and present the discovery of a fragment-based compound class identified through crystallographic screening of PaIspD. The initial fragment occupies the CTP binding cavity within the active site. Confirmation of fragment-protein interactions was achieved through H saturation-transfer difference nuclear magnetic resonance (H-STD NMR spectroscopy). Building upon these findings and insights from the co-crystal structures, we identified two growth vectors for fragment growing. We synthesized derivatives addressing both growth vectors, which showed improved affinities for PaIspD. Our new fragment class targets PaIspD, displays promising affinity and favorable growth vectors for further optimization. PubMed: 39676054DOI: 10.1002/anie.202414615 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.17 Å) |
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