Inositol monophosphatase 2 explained

Inositol monophosphatase 2 is a 32 kDa enzyme that in humans is encoded by the IMPA2 gene.[1] [2] IMPA2 dephosphorylates myo-inositol monophosphate to myo-inositol.

The function of IMPA2 appears to be similar to IMPA1 within tissues; however, the genes are expressed differently in various tissues with IMPA2 expressed at the highest level in certain tissues of the brain and the lumen of the kidney. IMPA2 exists as a homodimer within cells and cannot form heterodimers with IMPA1.[3]

Further reading

Notes and References

  1. Yoshikawa T, Turner G, Esterling LE, Sanders AR, Detera-Wadleigh SD . A novel human myo-inositol monophosphatase gene, IMP.18p, maps to a susceptibility region for bipolar disorder . Mol Psychiatry . 2 . 5 . 393–97 . Nov 1997 . 9322233 . 10.1038/sj.mp.4000325 . 24336959 .
  2. Web site: Entrez Gene: IMPA2 inositol(myo)-1(or 4)-monophosphatase 2.
  3. Ohnishi T, Ohba H, Seo KC, Im J, Sato Y, Iwayama Y, Furuichi T, Chung SK, Yoshikawa T . Spatial expression patterns and biochemical properties distinguish a second myo-inositol monophosphatase IMPA2 from IMPA1 . J. Biol. Chem. . 282 . 1 . 637–46 . January 2007 . 17068342 . 10.1074/jbc.M604474200 . free .