4J75
Crystal Structure of a parasite tRNA synthetase, product-bound
Summary for 4J75
| Entry DOI | 10.2210/pdb4j75/pdb |
| Related | 4J75 |
| Descriptor | Tryptophanyl-tRNA synthetase, TRYPTOPHANYL-5'AMP, GLYCEROL, ... (4 entities in total) |
| Functional Keywords | aminoacyl-trna synthetase, aars, trprs, parasite, protein-substrate complex, rossmann fold, translation, nucleotide binding, ligase |
| Biological source | Plasmodium falciparum |
| Total number of polymer chains | 2 |
| Total formula weight | 95684.52 |
| Authors | Koh, C.Y.,Kim, J.E.,Verlinde, C.L.M.J.,Hol, W.G.J. (deposition date: 2013-02-12, release date: 2013-05-22, Last modification date: 2023-09-20) |
| Primary citation | Koh, C.Y.,Kim, J.E.,Napoli, A.J.,Verlinde, C.L.,Fan, E.,Buckner, F.S.,Van Voorhis, W.C.,Hol, W.G. Crystal structures of Plasmodium falciparum cytosolic tryptophanyl-tRNA synthetase and its potential as a target for structure-guided drug design. Mol.Biochem.Parasitol., 189:26-32, 2013 Cited by PubMed Abstract: Malaria, most commonly caused by the parasite Plasmodium falciparum, is a devastating disease that remains a large global health burden. Lack of vaccines and drug resistance necessitate the continual development of new drugs and exploration of new drug targets. Due to their essential role in protein synthesis, aminoacyl-tRNA synthetases are potential anti-malaria drug targets. Here we report the crystal structures of P. falciparum cytosolic tryptophanyl-tRNA synthetase (Pf-cTrpRS) in its ligand-free state and tryptophanyl-adenylate (WAMP)-bound state at 2.34 Å and 2.40 Å resolutions, respectively. Large conformational changes are observed when the ligand-free protein is bound to WAMP. Multiple residues, completely surrounding the active site pocket, collapse onto WAMP. Comparison of the structures to those of human cytosolic TrpRS (Hs-cTrpRS) provides information about the possibility of targeting Pf-cTrpRS for inhibitor development. There is a high degree of similarity between Pf-cTrpRS and Hs-cTrpRS within the active site. However, the large motion that Pf-cTrpRS undergoes during transitions between different functional states avails an opportunity to arrive at compounds which selectively perturb the motion, and may provide a starting point for the development of new anti-malaria therapeutics. PubMed: 23665145DOI: 10.1016/j.molbiopara.2013.04.007 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.4 Å) |
Structure validation
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