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. 2013 Oct 15;24(20):3177–3186. doi: 10.1091/mbc.E13-04-0182

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© 2013 Henry and Crosson. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0).

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FIGURE 4: — Catalysis and a C-terminal tail are required for normal Venus-Ppk1 localization. (A) Representative micrographs of venus-ppk1(H434A)++ expressed in the WT or ∆ppk1 background. For merged images in A and C, Venus is depicted in the red channel and DAPI (polyP) in the green channel. (B) Positions of Venus-Ppk1 or Venus-Ppk1(H434A) expressed from the native locus in populations of cells 120 min postsynchrony. For A and B, N = 299 cells with detected foci. (C) Representative micrographs of venus-ppk1(∆CT16)++ expressed in the WT or ∆ppk1 background. (D) Positions of Venus-Ppk1(∆CT16) in populations of cells grown in M2G. Cells were imaged at 120 min postsynchrony. For C and D, N = 352 cells with detected foci.