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EC Number Cloned (Commentary)
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.B14-
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.B14cloned into plasmids under T7 promoter control and cotransfected into HeLa-MHVR cells infected with recombinant vaccinia virus
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.B14expressed in Escherichia coli
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.B14expressed in Escherichia coli Rosetta (DE3)pLysS cells
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.B14expression in Escherichia coli
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.B14expression in Escherichia coli by using a T7 RNA polymerase promoter system or as a maltose-binding protein fusion protein. With both overexpression systems the recombinant PLP-1 exhibits trans cleavage activity. When PLP-1 is expressed as a polypeptide that includes additional viral sequences at the carboxyl terminus of the predicted PLP-1 domain, a fivefold increase in proteolytic activity is observed
Results 1 - 6 of 6
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