8JE5
Crystal Structure of Anopheles culicifacies Prolyl-tRNA Synthetase (AcPRS) in complex with Halofuginone
Summary for 8JE5
| Entry DOI | 10.2210/pdb8je5/pdb |
| Descriptor | PROLYL-TRNA SYNTHETASE, 7-bromo-6-chloro-3-{3-[(2R,3S)-3-hydroxypiperidin-2-yl]-2-oxopropyl}quinazolin-4(3H)-one, ZINC ION, ... (6 entities in total) |
| Functional Keywords | malaria, vector, anopheles, mosquito, larvicidal, aminoacyl-trna synthetase, ligase, ligase-inhibitor complex, ligase/inhibitor |
| Biological source | Anopheles culicifacies |
| Total number of polymer chains | 2 |
| Total formula weight | 117544.83 |
| Authors | Goswami, R.,Manickam, Y.,Chhibber-Goel, J.,Harlos, K.,Sharma, A. (deposition date: 2023-05-15, release date: 2024-11-27, Last modification date: 2025-06-11) |
| Primary citation | Goswami, R.,Manickam, Y.,Goel, J.C.,Gupta, S.,B M, S.,Sharma, A. Chemical targeting of prolyl-tRNA synthetase stalls ovarian development and kills malaria vectors. J.Infect.Dis., 2025 Cited by PubMed Abstract: Along with rising resistance to antimalarials, the emergence of insecticide resistance in Anopheles mosquito species also remains a serious concern. Here, we reveal two potent compounds that show larvicidal and endectocidal activity against malaria vectors, Anopheles culicifacies and Anopheles stephensi, respectively. PubMed: 40048639DOI: 10.1093/infdis/jiaf095 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.57 Å) |
Structure validation
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