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. 2007 Oct 12;189(24):8961–8972. doi: 10.1128/JB.01365-07

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FIG. 5. — Membrane insertion of −3M-PC-Lep, F_oC, and CyoA-N-P2 is strongly inhibited in the CS YidC(P431L) mutant. (A) Signal peptide processing of PC-Lep in the YidC(P431L) mutant. JS7131 bearing both pACYC184-YidC(P431L) and pMS119-Pf3 P2 was grown and analyzed as described in Materials and Methods. (B) Signal peptide processing of −3M-PC-Lep in the YidC(P431L) strain. (C) Protease accessibility of Pf3 P2 in the CS YidC(P431L) mutant. (D) Protease accessibility of the F_oC in YidC(P431L) mutant. (E) Signal peptide processing of preCyoA-N-P2 in the YidC(P431L) mutant. The control in panel A was prepared in strain JS7131 grown under YidC depletion conditions. The control in panel B was prepared in strain JS7131 grown under yidC-expressing conditions. The Pf3 P2 and CyoA-N-P2 controls in panels C and E, respectively, were produced in the JS7131 strain grown with or without glucose (Glu; YidC depletion) or arabinose (Ara; YidC expression).