201. Multiple Ca2+-Calmodulin-dependent Protein Kinase Kinases from Rat Brain
- Author
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Sara S. Hook, Arthur M. Edelman, Elaine G. Goldstein, David Stapleton, Bruce E. Kemp, Ken I. Mitchelhill, Anthony R. Means, Kristin A. Anderson, and Michele A. Selbert
- Subjects
animal structures ,biology ,MAP kinase kinase kinase ,Cyclin-dependent kinase 4 ,Cyclin-dependent kinase 2 ,Cell Biology ,Mitogen-activated protein kinase kinase ,Biochemistry ,Cell biology ,MAP2K7 ,Calmodulin dependent protein kinase ,biology.protein ,ASK1 ,Cyclin-dependent kinase 9 ,Molecular Biology - Abstract
We have purified to near homogeneity from rat brain two Ca-calmodulin-dependent protein kinase I (CaM kinase I) activating kinases, termed here CaM kinase I kinase-α and CaM kinase I kinase-β (CaMKIKα and CaMKIKβ, respectively). Both CaMKIKα and CaMKIKβ are also capable of activating CaM kinase IV. Activation of CaM kinase I and CaM kinase IV occurs via phosphorylation of an equivalent Thr residue within the “activation loop” region of both kinases, Thr-177 and Thr-196, respectively. The activities of CaMKIKα and CaMKIKβ are themselves strongly stimulated by the presence of Ca-CaM, and both appear to be capable of Ca-CaM-dependent autophosphorylation. Automated microsequence analysis of the purified enzymes established that CaMKIKα and -β are the products of distinct genes. In addition to rat, homologous nucleic acids corresponding to these CaM kinase kinases are present in humans and the nematode, Caenorhabditis elegans. CaMKIKα and CaMKIKβ are thus representatives of a family of enzymes, which may function as key intermediaries in Ca-CaM-driven signal transduction cascades in a wide variety of eukaryotic organisms.
- Published
- 1996
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