Data availabilityCryo-EM density maps and atomic coordinates generated in this study have been deposited in the Electron Microscopy Data Bank (EMDB; https://www.ebi.ac.uk/emdb/) and the Protein Data Bank (PDB; https://www.rcsb.org/) under the following accession numbers: apo CCHFV-L (EMD-66754, PDB 9XD4); 5′ vRNA bound CCHFV-L complex (EMD-66755, PDB 9XD5); 3′ vRNA bound CCHFV-L complex (EMD-66756, PDB 9XD6); CCHFV-L elongation complex containing a 9-bp RNA product (EMD-66787, PDB 9XEC); CCHFV-L elongation complex containing a 15-bp RNA product (EMD-66785, PDB 9XE9); CCHFV-L elongation complex containing a 10-bp RNA product and incorporated 2FC (EMD-66783, PDB 9XE6) and CCHFV-L elongation complex containing a 10-bp RNA product and incorporated cytidine (EMD-66784, PDB 9XE7). KASV endonuclease-WXSH0208 complex (PDB 9XF9). Previously published structures used in this study are available in the PDB under the following accession numbers: 1S76, 4WSB, 5AMP, 5UJ2, 6FS6, 6L42, 6Y6K, 6Z8K, 7BV2, 7KL3, 7OJL, 7OJN, 7ORL, 7ORM, 8AS7, 8ASD, 8C4T, 8KI7, 8KI9, 8P1L, 8PNQ, 8QGU, 8R6W, 8R6Y, 8Z9R, 9GJU. Uncropped gel images are included as Supplementary Fig. 13. Source data are provided with this paper.ReferencesErgönül, Ö. Crimean–Congo haemorrhagic fever. Lancet Infect. Dis. 6, 203–214 (2006).Article
Structures and inhibition of the Crimean–Congo haemorrhagic fever virus polymerase - Nature
Structural studies of Crimean–Congo haemorrhagic fever virus (CCHFV) polymerase reveal the structural basis of CCHFV RNA synthesis and highlight druggable sites for designing both nucleoside antivirals and non-nucleoside antivirals.













