EC Number |
Title |
Organism |
---|
2.7.1.150 | Fluconazole-induced actin cytoskeleton remodeling requires phosphatidylinositol 3-phosphate 5-kinase in the pathogenic yeast Candida glabrata |
[Candida] glabrata |
2.7.1.150 | Inhibition of PIKfyve kinase prevents infection by Zaire ebolavirus and SARS-CoV-2 |
Homo sapiens |
2.7.1.150 | Ste12/Fab1 phosphatidylinositol-3-phosphate 5-kinase is required for nitrogen-regulated mitotic commitment and cell size control |
Schizosaccharomyces pombe |
2.7.1.150 | Ste12/Fab1 phosphatidylinositol-3-phosphate 5-kinase is required for nitrogen-regulated mitotic commitment and cell size control |
Schizosaccharomyces pombe ATCC 24843 |
2.7.1.150 | Ste12/Fab1 phosphatidylinositol-3-phosphate 5-kinase is required for nitrogen-regulated mitotic commitment and cell size control |
Schizosaccharomyces pombe 972 |
2.7.1.150 | The amino acid transporter SLC-36.1 cooperates with PtdIns3P 5-kinase to control phagocytic lysosome reformation |
Caenorhabditis elegans |
2.7.1.150 | Cloning and subcellular localization of a human phosphatidylinositol 3-phosphate 5-kinase, PIKfyve/Fab1 |
Homo sapiens |
2.7.1.150 | Distinct requirements for vacuolar protein sorting 34 downstream effector phosphatidylinositol 3-phosphate 5-kinase in podocytes versus proximal tubular cells |
Mus musculus |
2.7.1.150 | Fab1 phosphatidylinositol 3-phosphate 5-kinase controls trafficking but not silencing of endocytosed receptors |
Drosophila sp. (in: flies) |
2.7.1.150 | Fab1p and AP-1 are required for trafficking of endogenously ubiquitylated cargoes to the vacuole lumen in S. cerevisiae |
Saccharomyces cerevisiae |