The Mechanism of Hsp90 regulation by the protein kinase-specific cochaperone p50(cdc37)

Cell. 2004 Jan 9;116(1):87-98. doi: 10.1016/s0092-8674(03)01027-4.


Recruitment of protein kinase clients to the Hsp90 chaperone involves the cochaperone p50(cdc37) acting as a scaffold, binding protein kinases via its N-terminal domain and Hsp90 via its C-terminal region. p50(cdc37) also has a regulatory activity, arresting Hsp90's ATPase cycle during client-protein loading. We have localized the binding site for p50(cdc37) to the N-terminal nucleotide binding domain of Hsp90 and determined the crystal structure of the Hsp90-p50(cdc37) core complex. Dimeric p50(cdc37) binds to surfaces of the Hsp90 N-domain implicated in ATP-dependent N-terminal dimerization and association with the middle segment of the chaperone. This interaction fixes the lid segment in an open conformation, inserts an arginine side chain into the ATP binding pocket to disable catalysis, and prevents trans-activating interaction of the N domains.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Arginine / metabolism
  • Binding Sites / physiology
  • Cell Cycle Proteins / metabolism*
  • Dimerization
  • Drosophila Proteins*
  • HSP90 Heat-Shock Proteins / metabolism*
  • Models, Molecular
  • Molecular Chaperones / metabolism*
  • Molecular Sequence Data
  • Molecular Structure
  • Protein Binding / physiology
  • Protein Conformation
  • Protein Kinases / metabolism*
  • Protein Structure, Tertiary / physiology
  • Sequence Homology, Amino Acid


  • Cell Cycle Proteins
  • Drosophila Proteins
  • HSP90 Heat-Shock Proteins
  • Molecular Chaperones
  • Adenosine Triphosphate
  • Arginine
  • Protein Kinases

Associated data

  • PDB/1US7