The development of anti‐hepatitis C virus agents
Kunitada Shimotohno – 1 March 1995 – We have built a model of the specificity pocket of the protease of hepatitis C virus on the basis of the known structures of trypsin‐like serine proteases and of the conservation pattern of the protease sequences among various hepatitis C strains. The model allowed us to predict that the substrate of this protease should have a cysteine residue in position P1. This hypothesis was subsequently proved by N‐terminal sequencing of two products of the protease.