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Profilin 1


Profilin 1


Profilin-1 is a protein that in humans is encoded by the PFN1 gene.

Function

The protein encoded by this gene is a ubiquitous actin monomer-binding protein belonging to the profilin family. It is thought to regulate actin polymerization in response to extracellular signals. Deletion of this gene is associated with Miller-Dieker syndrome. Mutations in this gene may be a rare cause of amyotrophic lateral sclerosis, also called Lou Gehrig's disease.

Interactions

Profilin 1 has been shown to interact with:

  • FMNL1,
  • MLLT4
  • Vasodilator-stimulated phosphoprotein,
  • WASF1, and
  • WASL.

References

Further reading


Text submitted to CC-BY-SA license. Source: Profilin 1 by Wikipedia (Historical)