The structural basis for 14-3-3:phosphopeptide binding specificity

Cell. 1997 Dec 26;91(7):961-71. doi: 10.1016/s0092-8674(00)80487-0.

Abstract

The 14-3-3 family of proteins mediates signal transduction by binding to phosphoserine-containing proteins. Using phosphoserine-oriented peptide libraries to probe all mammalian and yeast 14-3-3s, we identified two different binding motifs, RSXpSXP and RXY/FXpSXP, present in nearly all known 14-3-3 binding proteins. The crystal structure of 14-3-3zeta complexed with the phosphoserine motif in polyoma middle-T was determined to 2.6 A resolution. The bound peptide is in an extended conformation, with a tight turn created by the pS +2 Pro in a cis conformation. Sites of peptide-protein interaction in the complex rationalize the peptide library results. Finally, we show that the 14-3-3 dimer binds tightly to single molecules containing tandem repeats of phosphoserine motifs, implicating bidentate association as a signaling mechanism with molecules such as Raf, BAD, and Cbl.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 14-3-3 Proteins
  • Crystallography, X-Ray
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / metabolism*
  • Humans
  • Models, Molecular
  • Molecular Sequence Data
  • Peptide Library
  • Phosphopeptides / metabolism*
  • Phosphorylation
  • Phosphoserine / metabolism*
  • Protein Binding
  • Protein Conformation
  • Proteins / chemistry
  • Proteins / metabolism*
  • Substrate Specificity
  • Tyrosine 3-Monooxygenase*

Substances

  • 14-3-3 Proteins
  • Enzyme Inhibitors
  • Peptide Library
  • Phosphopeptides
  • Proteins
  • Phosphoserine
  • Tyrosine 3-Monooxygenase

Associated data

  • PDB/14PS