Fig. 4 NDR2 interacts with RIG-I and promotes RIG-I K63-linked polyubiquitination. NDR2 interacts with RIG-I and promotes RIG-I K63-linked polyubiquitination.

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Volume 21, Issue 6, Pages (November 2017)
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Fig. 2 Transport properties of a BP transistor at low temperature.
Fig. 2 Global production, use, and fate of polymer resins, synthetic fibers, and additives (1950 to 2015; in million metric tons). Global production, use,
Vibrational spectra of medieval human bones (Leopoli-Cencelle, Italy)
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Fig. 1 Map of water stress and shale plays.
Fig. 1 Examples of experimental stimuli and behavioral performance.
Fig. 3 Electron PSD in various regions.
Fig. 4 Resynthesized complex boronic acid derivatives based on different scaffolds on a millimole scale and corresponding yields. Resynthesized complex.
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Fig. 2 Reference-fixing experiment, results.
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Fig. 3 Rotation experiment, setup.
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Fig. 5 NDR2 enhances TRIM25-mediated RIG-I K63-linked ubiquitination via facilitating recruitment of TRIM25 to RIG-I. NDR2 enhances TRIM25-mediated RIG-I.
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Fig. 1 Histograms of the number of first messages received by men and women in each of our four cities. Histograms of the number of first messages received.
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Fig. 4 Spatial mapping of the distribution and intensity of industrial fishing catch. Spatial mapping of the distribution and intensity of industrial fishing.
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Fig. 4 NDR2 interacts with RIG-I and promotes RIG-I K63-linked polyubiquitination. NDR2 interacts with RIG-I and promotes RIG-I K63-linked polyubiquitination. (A) Immunoblot analysis of extracts of RAW264.7 macrophages stably overexpressing Flag-NDR2 and infected with VSV for the indicated times was performed, and then, whole-cell lysates were immunoprecipitated with anti-Flag mouse magnetic (M2) beads, followed by immunoblotting with the indicated antibodies. (B) Flag-tagged RIG-I, MAVS, TBK1, or IKKi was coexpressed with Myc-NDR2 in HEK293 cells, followed by IP with anti-Flag M2 beads, followed by immunoblotting with anti-Flag or anti-Myc antibodies. (C) Lysates from murine PMs infected with VSV for the indicated time periods were subjected to IP with anti–RIG-I antibody, followed by Western blot analysis with the indicated antibodies. GAPDH, glyceraldehyde-3-phosphate dehydrogenase. (D) Flag-tagged full-length NDR2(1–464), dN(90–464), dC(1–383), dNC(90–383), or dS-TKc truncation mutants were coexpressed with Myc–RIG-I in HEK293 cells, and whole-cell lysates were immunoprecipitated with anti-Flag M2 beads, followed by immunoblotting with anti-Flag or anti-Myc antibodies. (E) Flag-tagged full-length RIG-I(1–926), 2CARD(1–233), Heli(234–734), CTD(735–926), or dCARD(234–926) truncation mutants were coexpressed with Myc-NDR2 in HEK293 cells, and whole-cell lysates were immunoprecipitated with anti-Flag M2 beads, followed by immunoblotting with anti-Flag or anti-Myc antibodies. (F) Immunoblot analysis of the polyubiquitination of RIG-I in HEK293 cells cotransfected with Flag–RIG-I, hemagglutinin (HA)–ubiquitin (HA-ub), and increasing concentrations (wedge) of vectors for the Myc-NDR2 constructs, followed by denaturation-IP with anti-Flag M2 beads and immunoblot analysis with an anti-HA antibody. (G) Immunoblot analysis of the polyubiquitination of RIG-I in HEK293 cells cotransfected with Flag–RIG-I, HA-ubiquitin, and Myc-NDR2 or its kinase-inactive mutant constructs, followed by denaturation-IP with anti-Flag M2 beads and immunoblot analysis with anti-HA antibodies. (H) Immunoblot analysis of the ubiquitination of RIG-I in HEK293 cells cotransfected with Flag–RIG-I, Myc-NDR2, and HA-ub or the mutant ubiquitin constructs, followed by denaturation-IP with anti-Flag M2 beads and immunoblot analysis with anti-HA antibodies. (I) NDR2f/f and Lysm+NDR2f/f BMDMs were infected with or without VSV for the indicated periods. Cell lysates were immunoprecipitated with anti–RIG-I, and the immunoprecipitates were analyzed by immunoblots with the indicated antibodies. Zhiyong Liu et al. Sci Adv 2019;5:eaav0163 Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).