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. 2006 Jul;188(14):5066–5076. doi: 10.1128/JB.00368-06

FIG. 3.

FIG. 3.

Verification of the function of DsbDTH. (A) Scheme showing DsbDTH, DsbD containing the thrombin cleavage site between the domains, and the c-Myc epitope after the thrombin cleavage site between the α and β domains. (B) The in vivo redox states of DsbC were assessed in the strains expressing wild-type DsbD, wild-type DsbDTH, and P284A DsbDTH using AMS alkylation. In lane 1, SEN45 (the dsbD mutant) containing only the vector (pAM238) was used. In the other lanes, the cells express wild-type DsbD (pSC01, lanes 2 to 4), wild-type DsbDTH (pSC49, lanes 5 to 7), and P284A DsbDTH (pSC49-10, lanes 8 to 10).