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Structure-function study of the N-terminal domain of exocyst subunit Sec3.

The exocyst is an evolutionarily conserved octameric complex involved in polarized exocytosis from yeast to humans. The Sec3 subunit of the exocyst acts as a spatial landmark for exocytosis through its ability to bind phospholipids and small GTPases. The structure of the N-terminal domain of Sec3 (Sec3N) was determined ab initio and defines a new subclass of pleckstrin homology (PH) domains along with a new family of proteins carrying this domain. Respectively, N- and C-terminal to the PH domain Sec3N presents an additional alpha-helix and two beta-strands that mediate dimerization through domain swapping. The structure identifies residues responsible for phospholipid binding, which when mutated in cells impair the localization of exocyst components at the plasma membrane and lead to defects in exocytosis. Through its ability to bind the small GTPase Cdc42 and phospholipids, the PH domain of Sec3 functions as a coincidence detector at the plasma membrane.

Pubmed ID: 20139078


  • Baek K
  • Kn√∂dler A
  • Lee SH
  • Zhang X
  • Orlando K
  • Zhang J
  • Foskett TJ
  • Guo W
  • Dominguez R


The Journal of biological chemistry

Publication Data

April 2, 2010

Associated Grants

  • Agency: NIGMS NIH HHS, Id: R01 GM073791
  • Agency: NIGMS NIH HHS, Id: R01-GM073791
  • Agency: NIGMS NIH HHS, Id: R01-GM64690

Mesh Terms

  • Amino Acid Sequence
  • Binding Sites
  • Cell Membrane
  • Crystallization
  • Crystallography, X-Ray
  • Dimerization
  • Exocytosis
  • Glucan Endo-1,3-beta-D-Glucosidase
  • Molecular Sequence Data
  • Mutation
  • Phospholipids
  • Protein Folding
  • Saccharomyces cerevisiae
  • Saccharomyces cerevisiae Proteins
  • Sequence Homology, Amino Acid
  • Structure-Activity Relationship