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Literature summary for 3.1.3.18 extracted from

  • Segerer, G.; Hadamek, K.; Zundler, M.; Fekete, A.; Seifried, A.; Mueller, M.J.; Koentgen, F.; Gessler, M.; Jeanclos, E.; Gohla, A.
    An essential developmental function for murine phosphoglycolate phosphatase in safeguarding cell proliferation (2016), Sci. Rep., 6, 35160 .
    View publication on PubMedView publication on EuropePMC

Protein Variants

Protein Variants Comment Organism
D34N phosphatase-inactive mutant. Knockin replacement of murine Pgp with its D34N mutant is embryonically lethal Mus musculus

Organism

Organism UniProt Comment Textmining
Mus musculus Q8CHP8 cf. 3.1.3.48
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General Information

General Information Comment Organism
physiological function replacement of murine Pgp with its phosphatase-inactive PgpD34N mutant is embryonically lethal due to intrauterine growth arrest and developmental delay in midgestation. PGP inactivation attenuates triosephosphate isomerase activity, increases triglyceride levels at the expense of the cellular phosphatidylcholine content, and inhibits cell proliferation. These effects are prevented under hypoxic conditions or by blocking phosphoglycolate release from damaged DNA Mus musculus