Wiskott–Aldrich syndrome protein family member 3 is a protein that in humans is encoded by the WASF3gene.[5][6]
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 transduce signals that involve changes in cell shape, motility or function.[6]
^"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^Suetsugu S, Miki H, Takenawa T (Jul 1999). "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. doi:10.1006/bbrc.1999.0894. PMID10381382.
Sossey-Alaoui K, Head K, Nowak N, Cowell JK (2003). "Genomic organization and expression profile of the human and mouse WAVE gene family". Mamm. Genome. 14 (5): 314–22. doi:10.1007/s00335-002-2247-7. PMID12856283. S2CID1042966.
Sossey-Alaoui K, Ranalli TA, Li X, et al. (2005). "WAVE3 promotes cell motility and invasion through the regulation of MMP-1, MMP-3, and MMP-9 expression". Exp. Cell Res. 308 (1): 135–45. doi:10.1016/j.yexcr.2005.04.011. PMID15907837.
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