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. 2013 Feb 19;8(2):e56292. doi: 10.1371/journal.pone.0056292

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© 2013 Pais et al

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.

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(A, B, and D) Y. enterocolitica ΔHOPEMT strains expressing the indicated proteins were grown in non-secreting conditions. The bacterial cells were lysed and proteins in the lysate supernatants (input) were immunoprecipitated with mouse monoclonal anti-Myc (A and D) or anti-HA (B) antibodies bound to Protein G agarose beads (output). The input (Inp.) and output (Outp.) fractions from the immunoprecipitations (IPs) were analyzed by immunoblotting with rabbit polyclonal anti-Myc and rat monoclonal anti-HA antibodies. (C) Scheme of the truncated Myc-tagged Tarp, CT694, and CT695 proteins analyzed to determine the binding regions of Slc1.