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  • The EMBO Journal (2002) 21, 5396 - 5407
  • doi:10.1093/emboj/cdf551

A phosphoserine/threonine-binding pocket in AGC kinases and PDK1 mediates activation by hydrophobic motif phosphorylation

Morten Frödin1, Torben L. Antal1, Bettina A. Dümmler1, Claus J. Jensen1, Maria Deak2, Steen Gammeltoft1 and Ricardo M. Biondi3,4

  1. Department of Clinical Biochemistry, Glostrup Hospital, DK-2600 Glostrup, Denmark
  2. MRC Protein Phosphorylation Unit, MSI/WTB complex, University of Dundee, Dow Street, Dundee DD1 5EH, UK
  3. Division of Signal Transduction Therapy, MSI/WTB complex, University of Dundee, Dow Street, Dundee DD1 5EH, UK
  4. Present address: PhosphoSites GmbH, Starterzentrum 3, D-66421 Homburg, Germany

Correspondence to:

Morten Frödin, E-mail: mf@dcb-glostrup.dk

Received 24 May 2002; Accepted 28 August 2002; Revised 26 August 2002

The growth factor-activated AGC protein kinases RSK, S6K, PKB, MSK and SGK are activated by serine/threonine phosphorylation in the activation loop and in the hydrophobic motif, C-terminal to the kinase domain. In some of these kinases, phosphorylation of the hydrophobic motif creates a specific docking site that recruits and activates PDK1, which then phosphorylates the activation loop. Here, we discover a pocket in the kinase domain of PDK1 that recognizes the phosphoserine/phosphothreonine in the hydrophobic motif by identifying two oppositely positioned arginine and lysine residues that bind the phosphate. Moreover, we demonstrate that RSK2, S6K1, PKBalpha, MSK1 and SGK1 contain a similar phosphate-binding pocket, which they use for intramolecular interaction with their own phosphorylated hydrophobic motif. Molecular modelling and experimental data provide evidence for a common activation mechanism in which the phosphorylated hydrophobic motif and activation loop act on the alphaC-helix of the kinase structure to induce synergistic stimulation of catalytic activity. Sequence conservation suggests that this mechanism is a key feature in activation of >40 human AGC kinases.

  • Keywords:

    • AGC kinase,
    • docking site,
    • PDK1,
    • PKB,
    • RSK