“…The cleavage of the P4a, P4b and P25K precursor proteins during VV morphogenesis is apparently an obligatory reaction, because drugs that inhibit cleavage, either directly or indirectly [e.g. rifampicin (Katz & Moss, 1970b;Moss & Rosenblum, 1973;Miner & Hruby, 1989), a-amanitin (Villarreal et al, 1984), nicotinamide (Child et al, 1988) or isatin-fl-thiosemicarbazone (Katz et al, 1973)], block virus replication, suggesting that proteolytic processing plays a key role in poxvirus development. Very little is known concerning the pathways, biochemistry or mechanisms by which the VV core protein precursors P4a, P4b and P25K undergo proteolytic maturation during infection.…”