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Literature summary for 3.1.3.95 extracted from

  • Oppelt, A.; Lobert, V.H.; Haglund, K.; Mackey, A.M.; Rameh, L.E.; Liest?l, K.; Schink, K.O.; Pedersen, N.M.; Wenzel, E.M.; Haugsten, E.M.; Brech, A.; Rusten, T.E.; Stenmark, H.; Wesche, J.
    Production of phosphatidylinositol 5-phosphate via PIKfyve and MTMR3 regulates cell migration (2013), EMBO Rep., 14, 57-64.
    View publication on PubMedView publication on EuropePMC

Protein Variants

Protein Variants Comment Organism
C413S mutant without catalytic activity, mutant is unable to rescue the RNAi-knockdown phenotype, indicating that isoform MTMR3 acts enzymatically on phosphoinositides during cell migration Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining
fibroblast
-
Homo sapiens
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1-phosphatidyl-1D-myo-inositol 3,5-bisphosphate + H2O
-
Homo sapiens 1-phosphatidyl-1D-myo-inositol 5-phosphate + phosphate product stimulates cell migration ?
1-phosphatidyl-1D-myo-inositol 3-phosphate + H2O
-
Homo sapiens 1-phosphatidyl-1D-myo-inositol + phosphate
-
?

Synonyms

Synonyms Comment Organism
MTMR3
-
Homo sapiens

General Information

General Information Comment Organism
physiological function on depletion of isoform MTMR3 by RNAi, BJ cells are unable to migrate into the wound and show a significant decrease in velocity of about 60% and a decrease in persistence. While 80% of control cells present actin fibres perpendicular to the wound, only 52% of the cells show this on MTMR3 depletion Homo sapiens