WASF2 explained

Wiskott–Aldrich syndrome protein family member 2 is a protein that in humans is encoded by the WASF2 gene.[1]

This gene encodes a member of the Wiskott–Aldrich syndrome protein family. The gene product is a protein that forms a multiprotein complex that links receptor kinases and actin. Binding to actin occurs through a C-terminal verprolin homology domain in all family members. The multiprotein complex serves to tranduce signals that involve changes in cell shape, motility or function. The published map location[2] has been changed based on recent genomic sequence comparisons, which indicate that the expressed gene is located on chromosome 1, and a pseudogene may be located on chromosome X.[3]

Interactions

WASF2 has been shown to interact with BAIAP2.[4]

Further reading

Notes and References

  1. Suetsugu S, Miki H, Takenawa T . Identification of two human WAVE/SCAR homologues as general actin regulatory molecules which associate with the Arp2/3 complex . Biochem Biophys Res Commun . 260 . 1 . 296–302 . July 1999. 10381382 . 10.1006/bbrc.1999.0894 .
  2. 10381382 . 10.1006/bbrc.1999.0894 . 260 . Identification of two human WAVE/SCAR homologues as general actin regulatory molecules which associate with the Arp2/3 complex . June 1999 . Biochem. Biophys. Res. Commun. . 296–302 . Suetsugu S, Miki H, Takenawa T. 1 .
  3. Web site: Entrez Gene: WASF2 WAS protein family, member 2.
  4. Miki . H . Yamaguchi H . Suetsugu S . Takenawa T . December 2000. IRSp53 is an essential intermediate between Rac and WAVE in the regulation of membrane ruffling . . 408 . 6813 . 732–5 . 0028-0836. 11130076 . 10.1038/35047107 . 2000Natur.408..732M . 4426046 .