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. 2012 Sep 4;2:255–259. doi: 10.1016/j.fob.2012.08.005

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© 2012 Published by Elsevier B.V. on behalf of Federation of European Biochemical Societies.

This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-No Derivative Works License, which permits non- commercial use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Fig. 4 — Critical region of Tespa1 for the association with IP₃R. (A) A schematic illustration of human Tespa1 (top) and HA-tagged Tespa1-deletion mutants used in this study (bottom). (B) Co-immunoprecipitations using full-length IP₃R1 and deletion mutants of Tespa1. (C) The critical region of Tespa1 required for the IP₃R interaction (top). Double or single amino acid substitutions from phenylalanine to alanine residue(s) within human Tespa1 (bottom). (D) Co-immunoprecipitations using full-length IP₃R and various mutants of Tespa1 (C). a.a., amino acids; IP, immunoprecipitations; total, total lysate.