NRP1 and viral infectious disease: Docking of solo and inhibitor-bound NRP1 with the CendR motif of S1 showed that the CendR motif of S1 and inhibitor share the same binding site on the b1 domain of NRP1 and inhibitors identified in the present study could block the CendR binding motif and diminish the binding of S1 and thus could be an attractive strategy to stop viral infection.