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. 2020 Dec 3;16(12):e1008449. doi: 10.1371/journal.pcbi.1008449

Fig 4. Interface differences between human and SARS-CoV-2neg models.

Fig 4

The top panels show key residue-residue interactions at the interface between hACE2 (white) and the viral RBD (teal), which are conserved in nearly all SARS-CoV-2pos species: salt-bridge between D30 and K417 (left); three-body interaction between K31, E35, and RBD Q493 (middle); and the interactions of K353, an intramolecular salt-bridge with D38 and an intermolecular hydrogen bonds with G496 and G502 (right). The bottom panels highlight equivalent regions in three SARS-CoV-2neg species: D30N mutation in mice (left) disrupts the intermolecular salt-bridge; D31K/D35R in ducks stabilizes an intramolecular salt-bridge and weakens the intermolecular hydrogen bond (middle); K353H in mice disrupts the intramolecular salt-bridge (right).