14-3-3 Proteins directly regulate Ca(2+)/calmodulin-dependent protein kinase kinase alpha through phosphorylation-dependent multisite binding |
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Authors: | Ichimura Tohru Taoka Masato Hozumi Yasukazu Goto Kaoru Tokumitsu Hiroshi |
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Affiliation: | Department of Chemistry, Graduate School of Science, Tokyo Metropolitan University, Tokyo, Japan. ichimura@nda.ac.jp |
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Abstract: | ![]() Ca(2+)/calmodulin-dependent protein kinase kinase alpha (CaMKKalpha) plays critical roles in the modulation of neuronal cell survival as well as many other cellular activities. Here we show that 14-3-3 proteins directly regulate CaMKKalpha when the enzyme is phosphorylated by protein kinase A on either Ser74 or Ser475. Mutational analysis revealed that these two serines are both functional: the CaMKKalpha mutant with a mutation at either of these residues, but not the double mutant, was inhibited significantly by 14-3-3. The mode of regulation described herein differs the recently described mode of 14-3-3 regulation of CaMKKalpha. |
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Keywords: | CaMKKα, Ca2+/calmodulin-dependent protein kinase kinase α CaMKI, Ca2+/calmodulin-dependent protein kinase I CaMKIV, Ca2+/calmodulin-dependent protein kinase IV PKA, cAMP-dependent protein kinase A MAPK, mitogen-activated protein kinase PKB, protein kinase B CaM, calmodulin GST, glutathione S-transferase WT, wild-type |
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