Figure 2
Comparison of consensus secondary structures of entire nucleocapsid (N) proteins of DKGV VN2913B72 (large top panel) and other representative hantaviruses (smaller panels), predicted using several methods at the NPS@ structure server14. N protein structures are shown for bat-borne mobatviruses (DKGV VN2913B72, LAIV BT20 and XSV VN1982B4), rodent borne orthohantaviruses (HTNV 76-118, SEOV HR80-39, SOOV SOO-1, DOBV/BGDV Greece, PUUV Sotkamo, MUJV 11-1, PHV PH-1, SNV NMH10 and ANDV Chile9719869) and shrew-borne thottimviruses (TPMV VRC66412 and MJNV Cl05-11), shrew-borne orthohantaviruses (JJUV SH42, BOWV VN1512, ASIV Drahany, ARTV MukawaAH301, CBNV CBN-3 and YKSV Si-210), and mole-borne orthohantaviruses (RKPV MSB57412, OXBV Ng1453 and ASAV N10) and mole-borne mobatvirus (NVAV MSB95703). Blue bars represent α-helices, red bars β-strands, and purple indicate random coil and unclassified structures, respectively. Abbreviations: ANDV, Andes virus; ARTV, Artybash virus; ASAV, Asama virus; ASIV, Asikkala virus; BOWV, Bowé virus; CBNV, Cao Bằng virus; DKGV, Đakrông virus; DOBV/BGDV, Dobrava-Belgrade virus; HTNV, Hantaan virus; JJUV, Jeju virus; LAIV, Láibīn virus; MJNV, Imjin virus; MUJV, Muju virus; NVAV, Nova virus; OXBV, Oxbow virus; PHV, Prospect Hill virus; PUUV, Puumala virus; RKPV, Rockport virus; SEOV, Seoul virus; SNV, Sin Nombre virus; SOOV, Soochong virus; TPMV, Thottapalayam virus; XSV, Xuân Sơn virus; YKSV, Yákèshí virus.
