4YRQ
Crystal structure of T. cruzi Histidyl-tRNA synthetase in complex with 6-amino-2H-chromen-2-one (Chem 744)
Summary for 4YRQ
| Entry DOI | 10.2210/pdb4yrq/pdb |
| Related | 4YP0 4YPF 4YRC 4YRE 4YRF 4YRG 4YRI 4YRJ 4YRK 4YRL 4YRM 4YRN 4YRO 4YRP 4YRR 4YRS 4YRT |
| Descriptor | Histidyl-tRNA synthetase, HISTIDINE, 6-amino-2H-chromen-2-one, ... (7 entities in total) |
| Functional Keywords | ligase, aminoacyl-trna synthetase, aars, hisrs, trypanosoma cruzi, protein-inhibitor complex, ligase-ligase inhibitor complex, ligase/ligase inhibitor |
| Biological source | Trypanosoma cruzi (strain CL Brener) |
| Total number of polymer chains | 1 |
| Total formula weight | 51817.31 |
| Authors | Koh, C.-Y.,Hol, W.G.J. (deposition date: 2015-03-15, release date: 2015-08-12, Last modification date: 2023-09-27) |
| Primary citation | Koh, C.Y.,Siddaramaiah, L.K.,Ranade, R.M.,Nguyen, J.,Jian, T.,Zhang, Z.,Gillespie, J.R.,Buckner, F.S.,Verlinde, C.L.,Fan, E.,Hol, W.G. A binding hotspot in Trypanosoma cruzi histidyl-tRNA synthetase revealed by fragment-based crystallographic cocktail screens. Acta Crystallogr. D Biol. Crystallogr., 71:1684-1698, 2015 Cited by PubMed Abstract: American trypanosomiasis, commonly known as Chagas disease, is a neglected tropical disease caused by the protozoan parasite Trypanosoma cruzi. The chronic form of the infection often causes debilitating morbidity and mortality. However, the current treatment for the disease is typically inadequate owing to drug toxicity and poor efficacy, necessitating a continual effort to discover and develop new antiparasitic therapeutic agents. The structure of T. cruzi histidyl-tRNA synthetase (HisRS), a validated drug target, has previously been reported. Based on this structure and those of human cytosolic HisRS, opportunities for the development of specific inhibitors were identified. Here, efforts are reported to identify small molecules that bind to T. cruzi HisRS through fragment-based crystallographic screening in order to arrive at chemical starting points for the development of specific inhibitors. T. cruzi HisRS was soaked into 68 different cocktails from the Medical Structural Genomics of Pathogenic Protozoa (MSGPP) fragment library and diffraction data were collected to identify bound fragments after soaking. A total of 15 fragments were identified, all bound to the same site on the protein, revealing a fragment-binding hotspot adjacent to the ATP-binding pocket. On the basis of the initial hits, the design of reactive fragments targeting the hotspot which would be simultaneously covalently linked to a cysteine residue present only in trypanosomatid HisRS was initiated. Inhibition of T. cruzi HisRS was observed with the resultant reactive fragments and the anticipated binding mode was confirmed crystallographically. These results form a platform for the development of future generations of selective inhibitors for trypanosomatid HisRS. PubMed: 26249349DOI: 10.1107/S1399004715007683 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.05 Å) |
Structure validation
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