EC Number   |
Title   |
Organism   |
|---|
 3.1.3.56 | 3-hydroxybenzene 1,2,4-trisphosphate, a novel second messenger mimic and unusual substrate for type-I myo-inositol 1,4,5-trisphosphate 5-phosphatase: Synthesis and physicochemistry |
Homo sapiens |
 3.1.3.56 | A distinct and replicable variant of the squamous cell carcinoma gene inositol polyphosphate-5-phosphatase modifies the susceptibility of arsenic-associated skin lesions in Bangladesh |
Homo sapiens |
 3.1.3.56 | A molecular basis for inositol polyphosphate synthesis in Drosophila melanogaster |
Drosophila melanogaster |
 3.1.3.56 | A phosphatidylinositol phosphate-specific myo-inositol polyphosphate 5-phosphatase required for seedling growth |
Arabidopsis thaliana |
 3.1.3.56 | A putative tomato inositol polyphosphate 5-phosphatase, Le5PT1, is involved in plant growth and abiotic stress responses |
Solanum lycopersicum |
 3.1.3.56 | A putative tomato inositol polyphosphate 5-phosphatase, Le5PT1, is involved in plant growth and abiotic stress responses |
Solanum lycopersicum Ohio 8245 |
 3.1.3.56 | A universal role for inositol 1,4,5-trisphosphate-mediated signaling in plant gravitropism |
Homo sapiens |
 3.1.3.56 | An Arabidopsis inositol 5-phosphatase gain-of-function alters abscisic acid signaling |
Arabidopsis sp. |
 3.1.3.56 | Arginine 343 and 350 are two active site residues involved in substrate binding by human type I D-myo-inositol 1,4,5-trisphosphate 5-phosphatase |
Homo sapiens |
 3.1.3.56 | Benzene polyphosphates as tools for cell signalling: inhibition of inositol 1,4,5-trisphosphate 5-phosphatase and interaction with the pH domain of protein kinase Balpha |
Homo sapiens |