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. 2016 Jul 12;291(35):18342–18352. doi: 10.1074/jbc.M116.737874

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© 2016 by The American Society for Biochemistry and Molecular Biology, Inc.

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FIGURE 1. — In vitro functional characterization of PgpB. A, chemical structure of lipid phosphate substrates and inhibitors of PgpB. B, each reaction of 100 μl contains 2 μg of PgpB protein and 5 μg of each substrate (30 mm for glycerol 3-phosphate) mixed for 40 min at room temperature and then characterized by colorimetric phosphatase assay. The activity was normalized with an individual background control. C and D, Michaelis-Menten kinetic assays using 6:0 LPA or 18:1 LPA as substrates plotted using GraphPad Prism^TM software. G-3-P, glycerol-3-phosphate.