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14-3-3 Proteins directly regulate Ca(2+)/calmodulin-dependent protein kinase kinase alpha through phosphorylation-dependent multisite binding
Authors:Ichimura Tohru  Taoka Masato  Hozumi Yasukazu  Goto Kaoru  Tokumitsu Hiroshi
Affiliation:Department of Chemistry, Graduate School of Science, Tokyo Metropolitan University, Tokyo, Japan. ichimura@nda.ac.jp
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.
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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