9I53
Crystal structure of the SARS-CoV-2 helicase NSP13 in complex with ATP
Summary for 9I53
| Entry DOI | 10.2210/pdb9i53/pdb |
| Related | 9I51 |
| Descriptor | SARS-CoV-2 helicase NSP13, ZINC ION, ADENOSINE-5'-TRIPHOSPHATE, ... (6 entities in total) |
| Functional Keywords | nsp13, helicase, sars-cov-2, hydrolase |
| Biological source | Severe acute respiratory syndrome coronavirus 2 |
| Total number of polymer chains | 2 |
| Total formula weight | 136915.05 |
| Authors | Kloskowski, P.,Neumann, P.,Ficner, R. (deposition date: 2025-01-27, release date: 2025-07-23, Last modification date: 2025-08-13) |
| Primary citation | Kloskowski, P.,Neumann, P.,Berndt, A.,Ficner, R. Nucleotide-bound crystal structures of the SARS-CoV-2 helicase NSP13. Acta Crystallogr.,Sect.F, 81:338-347, 2025 Cited by PubMed Abstract: Nucleotide-bound crystal structures of SARS-CoV-2 NSP13 in ADP- and ATP-bound states were resolved to 1.8 and 1.9 Å, respectively. The ADP-bound model captures a state immediately following ATP hydrolysis, with both ADP and orthophosphate still present in the active site. Further comparative analysis revealed that crystal packing influences NSP13 by stabilizing the nucleotide-binding site, underscoring the importance of accounting for these effects in structure-based drug design targeting NSP13. PubMed: 40638074DOI: 10.1107/S2053230X25005266 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.92 Å) |
Structure validation
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