Definition of optimal substrate recognition motifs of Ca2+- calmodulin-dependent protein kinases IV and II reveals shared and distinctive features

Ronald R. White, Young-Guen Kwon, Meng Taing, David S. Lawrence, Arthur M. Edelman

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Abstract

The substrate recognition determinants of Ca2+ -calmodulin-dependent protein kinase (CaMK) IV and CaMKIIα were investigated using peptide substrates modeled on the amino acid sequence encompassing Set-9 of synapsin I. For both kinases, hydrophobic residues (Leu or Phe) at the -5 position, are well tolerated, whereas non-hydrophobic residues (Arg, Ala, or Asp) decrease V(max)/K(m) by 55- to >4000-fold. At the -3 position, substitution of Ala for Arg leads to decreases of 99-and 343- fold in V(max)/K(m) for CaMKIV and CaMKIIα, respectively. For both kinases, the nature of the residues occupying the -4, -1, and +4 positions exerts relatively little influence on phosphorylation kinetics. CaMKIV and CaMKIIα respond differently to substitutions at the -2 and +1 positions. Substitution of Arg at the -2 position with non-basic residues (Gln or Ala) leads to 6-fold decreases in V(max)/K(m) for CaMKIV, but 17-28-fold increases for CaMKIIα. Additionally, peptides containing Leu, Asp, or Ala at the +1 position are phosphorylated with similar efficiencies by CaMKIV, whereas the Leu- substituted peptide is preferred by CaMKIIα (by a factor of 5.8-9.7-fold). Thus, CaMKIV and CaMKHα preferentially phosphorylate substrates with the motifs: Hyd-X-Arg-X-X-Ser*/Thr*, and Hyd-X-Arg-NB-X-Ser*/Thr*-Hyd, respectively, where Hyd represents a hydrophobic, X any, and NB a non-basic amino acid residue. The different specificities of the two kinases may contribute to their targeting to distinct physiological substrates during Ca2+ -dependent cellular events.

Original languageEnglish
Pages (from-to)3166-3172
Number of pages7
JournalJournal of Biological Chemistry
Volume273
Issue number6
DOIs
Publication statusPublished - 1998 Feb 6

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Calcium-Calmodulin-Dependent Protein Kinase Type 4
Calcium-Calmodulin-Dependent Protein Kinase Type 2
Substrates
Substitution reactions
Phosphotransferases
Peptides
Synapsins
Amino Acids
Phosphorylation
Viperidae
Amino Acid Sequence
Kinetics

All Science Journal Classification (ASJC) codes

  • Biochemistry

Cite this

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title = "Definition of optimal substrate recognition motifs of Ca2+- calmodulin-dependent protein kinases IV and II reveals shared and distinctive features",
abstract = "The substrate recognition determinants of Ca2+ -calmodulin-dependent protein kinase (CaMK) IV and CaMKIIα were investigated using peptide substrates modeled on the amino acid sequence encompassing Set-9 of synapsin I. For both kinases, hydrophobic residues (Leu or Phe) at the -5 position, are well tolerated, whereas non-hydrophobic residues (Arg, Ala, or Asp) decrease V(max)/K(m) by 55- to >4000-fold. At the -3 position, substitution of Ala for Arg leads to decreases of 99-and 343- fold in V(max)/K(m) for CaMKIV and CaMKIIα, respectively. For both kinases, the nature of the residues occupying the -4, -1, and +4 positions exerts relatively little influence on phosphorylation kinetics. CaMKIV and CaMKIIα respond differently to substitutions at the -2 and +1 positions. Substitution of Arg at the -2 position with non-basic residues (Gln or Ala) leads to 6-fold decreases in V(max)/K(m) for CaMKIV, but 17-28-fold increases for CaMKIIα. Additionally, peptides containing Leu, Asp, or Ala at the +1 position are phosphorylated with similar efficiencies by CaMKIV, whereas the Leu- substituted peptide is preferred by CaMKIIα (by a factor of 5.8-9.7-fold). Thus, CaMKIV and CaMKHα preferentially phosphorylate substrates with the motifs: Hyd-X-Arg-X-X-Ser*/Thr*, and Hyd-X-Arg-NB-X-Ser*/Thr*-Hyd, respectively, where Hyd represents a hydrophobic, X any, and NB a non-basic amino acid residue. The different specificities of the two kinases may contribute to their targeting to distinct physiological substrates during Ca2+ -dependent cellular events.",
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Definition of optimal substrate recognition motifs of Ca2+- calmodulin-dependent protein kinases IV and II reveals shared and distinctive features. / White, Ronald R.; Kwon, Young-Guen; Taing, Meng; Lawrence, David S.; Edelman, Arthur M.

In: Journal of Biological Chemistry, Vol. 273, No. 6, 06.02.1998, p. 3166-3172.

Research output: Contribution to journalArticle

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