AIP1 mediates TNF-α–induced ASK1 activation by facilitating dissociation of ASK1 from its inhibitor 14-3-3
J. Clin. Invest. Rong Zhang, et al. 111:1933 doi:10.1172/JCI17790 [Go to this article.]

Figure 2
A lysine-rich cluster within the C2 domain of AIP1 is critical for ASK1 binding. (a) Sequence alignment of C2 domains in AIP1 and a conserved C2 domain of PKC. The amino acid residues in b are Ca²⁺-binding sites. The K clusters in AIP1 are underlined and are mutated to A to generate KA1, KA2, and KA1/2 (mutations at both K clusters). (b) Mutations at the second K cluster significantly reduce ASK1 binding. FLAG-tagged AIP1-N, KA1, KA2, or KA1/2 ASK1-ΔN was cotransfected with ASK1 in ECs, and interaction of ASK1 with AIP1-N or mutants was examined by immunoprecipitation with anti-ASK1, followed by Western blot with anti-FLAG.