EC Number | Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|---|
2.7.1.137 | endosome | - |
Saccharomyces cerevisiae | 5768 | - |
2.7.1.137 | multivesicular body | - |
Saccharomyces cerevisiae | 5771 | - |
2.7.1.137 | peroxisome | - |
Saccharomyces cerevisiae | 5777 | - |
2.7.1.137 | phagosome | - |
Saccharomyces cerevisiae | - |
- |
EC Number | Metals/Ions | Comment | Organism | Structure |
---|---|---|---|---|
2.7.1.137 | Mg2+ | required | Saccharomyces cerevisiae |
EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
2.7.1.137 | ATP + 1-phosphatidyl-1D-myo-inositol | Saccharomyces cerevisiae | - |
ADP + 1-phosphatidyl-1D-myo-inositol 3-phosphate | - |
? |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
2.7.1.137 | Saccharomyces cerevisiae | P22543 | - |
- |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
2.7.1.137 | ATP + 1-phosphatidyl-1D-myo-inositol | - |
Saccharomyces cerevisiae | ADP + 1-phosphatidyl-1D-myo-inositol 3-phosphate | - |
? |
EC Number | Subunits | Comment | Organism |
---|---|---|---|
2.7.1.137 | More | domain organization of phosphatidylinositol 3-kinase class III (PIK3C3) complex subunits in Saccharomyces cerevisiae, overview | Saccharomyces cerevisiae |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
2.7.1.137 | class III phosphatidylinositol 3-kinase | - |
Saccharomyces cerevisiae |
2.7.1.137 | lipid kinase Vps34 | - |
Saccharomyces cerevisiae |
2.7.1.137 | vacuolar protein sorting 34 | - |
Saccharomyces cerevisiae |
2.7.1.137 | VPS34 | - |
Saccharomyces cerevisiae |
EC Number | Cofactor | Comment | Organism | Structure |
---|---|---|---|---|
2.7.1.137 | ATP | - |
Saccharomyces cerevisiae |
EC Number | General Information | Comment | Organism |
---|---|---|---|
2.7.1.137 | malfunction | the deletion of Vps34, Vps15 or Vps30 affects both autophagy and vacuolar protein sorting. The deletion of Vps34 or Vps15 results in a reduced mRNA production from G + C-rich coding sequences (CDS). Vps34 and Vps15 can enhance the efficiency of transcription elongation based on their physical proximity to nuclear pores and transcribed chromatin | Saccharomyces cerevisiae |
2.7.1.137 | metabolism | together with Vps34, Vps15 and Vps30 it forms the PIK3C3-Complex II, which is mainly found at endosomal membranes, modulation of PIK3C3 complex function through different subunit compositions, overview. The Vps15 kinase domain intercts with the Vps34 activation loop, which might regulate the activity of Vps34 | Saccharomyces cerevisiae |
2.7.1.137 | physiological function | PI3K-III (or PIK3C3) represents the most conserved PI3K class. It is the sole PI3K in yeast and plants. The catalytic subunit of the PI3K complex is Vps34, which exclusively utilizes PtdIns as substrate. It phosphorylates PtdIns at the 3-hydoxyl group of the inositol ring in order to generate PtdIns3P. Class III phosphatidylinositol 3-kinase Vps34 (vacuolar protein sorting 34) catalyzes for the formation of the signaling lipid phosphatidylinositol-3-phopsphate, which is a central factor in the regulation of autophagy, endocytic trafficking and vesicular transport. The Vps15 kinase domain interacts with the Vps34 activation loop, which might regulate the activity of Vps34. Regulation of Vps34 function by G-protein signaling. Vps34 and Vps15 act as suppressors of Gpa1 (Galpha)-mediated transcriptional responses involved in pheromone signaling. Direct link between trimeric G-proteins and Vps34p function in yeast | Saccharomyces cerevisiae |