WASF2

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Template:Short description Template:Cs1 config An Error has occurred retrieving Wikidata item for infobox 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]

References

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  1. ^ Page Module:Citation/CS1/styles.css has no content.Suetsugu S, Miki H, Takenawa T (July 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. PMID 10381382.
  2. ^ Page Module:Citation/CS1/styles.css has no content.Suetsugu S, Miki H, Takenawa T (June 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. PMID 10381382.
  3. ^ Page Module:Citation/CS1/styles.css has no content."Entrez Gene: WASF2 WAS protein family, member 2".
  4. ^ Page Module:Citation/CS1/styles.css has no content.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". Nature. 408 (6813): 732–5. Bibcode:2000Natur.408..732M. doi:10.1038/35047107. ISSN 0028-0836. PMID 11130076. S2CID 4426046.

Further reading

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