EC Number | Activating Compound | Comment | Organism | Structure |
---|---|---|---|---|
2.7.1.153 | additional information | stimulation of almost every receptor that induces tyrosine kinase activity also leads to class IA phosphatidylinositol-4,5-bisphosphate 3-kinase activation | Drosophila melanogaster |
EC Number | Cloned (Comment) | Organism |
---|---|---|
2.7.1.153 | expression of P110delta in Sf9 insect cells | Homo sapiens |
EC Number | Crystallization (Comment) | Organism |
---|---|---|
2.7.1.153 | - |
Mammalia |
EC Number | Inhibitors | Comment | Organism | Structure |
---|---|---|---|---|
2.7.1.153 | LY294002 | - |
Homo sapiens | |
2.7.1.153 | LY294002 | - |
Mammalia | |
2.7.1.153 | Wortmannin | - |
Homo sapiens | |
2.7.1.153 | Wortmannin | - |
Mammalia |
EC Number | Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|---|
2.7.1.153 | cytosol | - |
Mammalia | 5829 | - |
EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
2.7.1.153 | additional information | Homo sapiens | - |
? | - |
? | |
2.7.1.153 | additional information | Drosophila melanogaster | enzyme can promote proliferation | ? | - |
? | |
2.7.1.153 | additional information | Mammalia | enzyme can promote proliferation | ? | - |
? | |
2.7.1.153 | additional information | Drosophila melanogaster | phosphoinositide 3-kinase and DNA synthesis | ? | - |
? | |
2.7.1.153 | additional information | Mammalia | phosphoinositide 3-kinase and DNA synthesis | ? | - |
? | |
2.7.1.153 | additional information | Dictyostelium discoideum | phosphoinositide 3-kinase and DNA synthesis | ? | - |
? | |
2.7.1.153 | additional information | Caenorhabditis elegans | phosphoinositide 3-kinase and DNA synthesis | ? | - |
? | |
2.7.1.153 | additional information | Drosophila melanogaster | enzyme is involved in the synthesis of 3-phosphoinositides. Class I phosphoinositide 3-kinases are further subdivided into class IA and IB enzymes, which signal downstream of tyrosine kinase and heterotrimeric G protein-coupled receptors, respectively. All class I phosphoinositide 3-kinase members also bind to Ras, but the role of this interaction in physiological phosphoinositide 3-kinase signalling is not entirely clear | ? | - |
? | |
2.7.1.153 | additional information | Mammalia | enzyme is involved in the synthesis of 3-phosphoinositides. Class I phosphoinositide 3-kinases are further subdivided into class IA and IB enzymes, which signal downstream of tyrosine kinase and heterotrimeric G protein-coupled receptors, respectively. All class I phosphoinositide 3-kinase members also bind to Ras, but the role of this interaction in physiological phosphoinositide 3-kinase signalling is not entirely clear | ? | - |
? | |
2.7.1.153 | additional information | Dictyostelium discoideum | enzyme is involved in the synthesis of 3-phosphoinositides. Class I phosphoinositide 3-kinases are further subdivided into class IA and IB enzymes, which signal downstream of tyrosine kinase and heterotrimeric G protein-coupled receptors, respectively. All class I phosphoinositide 3-kinase members also bind to Ras, but the role of this interaction in physiological phosphoinositide 3-kinase signalling is not entirely clear | ? | - |
? | |
2.7.1.153 | additional information | Caenorhabditis elegans | enzyme is involved in the synthesis of 3-phosphoinositides. Class I phosphoinositide 3-kinases are further subdivided into class IA and IB enzymes, which signal downstream of tyrosine kinase and heterotrimeric G protein-coupled receptors, respectively. All class I phosphoinositide 3-kinase members also bind to Ras, but the role of this interaction in physiological phosphoinositide 3-kinase signalling is not entirely clear | ? | - |
? | |
2.7.1.153 | additional information | Drosophila melanogaster | phosphoinositide 3-kinase and apoptosis | ? | - |
? | |
2.7.1.153 | additional information | Mammalia | phosphoinositide 3-kinase and apoptosis | ? | - |
? | |
2.7.1.153 | additional information | Dictyostelium discoideum | phosphoinositide 3-kinase and apoptosis | ? | - |
? | |
2.7.1.153 | additional information | Caenorhabditis elegans | phosphoinositide 3-kinase and apoptosis | ? | - |
? |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
2.7.1.137 | Caenorhabditis elegans | - |
- |
- |
2.7.1.137 | Dictyostelium discoideum | - |
- |
- |
2.7.1.137 | Drosophila melanogaster | - |
- |
- |
2.7.1.153 | Caenorhabditis elegans | - |
- |
- |
2.7.1.153 | Dictyostelium discoideum | - |
- |
- |
2.7.1.153 | Drosophila melanogaster | - |
- |
- |
2.7.1.153 | Homo sapiens | - |
- |
- |
2.7.1.153 | Mammalia | - |
- |
- |
EC Number | Source Tissue | Comment | Organism | Textmining |
---|---|---|---|---|
2.7.1.153 | leukocyte | - |
Mammalia | - |
2.7.1.153 | leukocyte | - |
Homo sapiens | - |
2.7.1.153 | MCF-7 cell | - |
Homo sapiens | - |
2.7.1.153 | MOLT-4 cell | - |
Homo sapiens | - |
2.7.1.153 | additional information | all mammalian cell types investigated express at least one class IA isoform, class IB isoform is present only in mammals, where it shows a restricted tissue distribution, being abundant only in white blood cells | Mammalia | - |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
2.7.1.137 | ATP + 1-phosphatidylinositol | - |
Drosophila melanogaster | ADP + phosphatidylinositol 3-phosphate | - |
? | |
2.7.1.137 | ATP + 1-phosphatidylinositol | - |
Dictyostelium discoideum | ADP + phosphatidylinositol 3-phosphate | - |
? | |
2.7.1.137 | ATP + 1-phosphatidylinositol | - |
Caenorhabditis elegans | ADP + phosphatidylinositol 3-phosphate | - |
? | |
2.7.1.153 | ATP + 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate | - |
Drosophila melanogaster | ADP + 1-phosphatidyl-1D-myo-inositol 3,4,5-trisphosphate | - |
? | |
2.7.1.153 | ATP + 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate | - |
Mammalia | ADP + 1-phosphatidyl-1D-myo-inositol 3,4,5-trisphosphate | - |
? | |
2.7.1.153 | ATP + 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate | - |
Homo sapiens | ADP + 1-phosphatidyl-1D-myo-inositol 3,4,5-trisphosphate | - |
? | |
2.7.1.153 | ATP + 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate | - |
Dictyostelium discoideum | ADP + 1-phosphatidyl-1D-myo-inositol 3,4,5-trisphosphate | - |
? | |
2.7.1.153 | ATP + 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate | - |
Caenorhabditis elegans | ADP + 1-phosphatidyl-1D-myo-inositol 3,4,5-trisphosphate | - |
? | |
2.7.1.153 | ATP + phosphatidylinositol | - |
Drosophila melanogaster | ADP + phosphatidylinositol 3-phosphate | - |
? | |
2.7.1.153 | ATP + phosphatidylinositol | - |
Mammalia | ADP + phosphatidylinositol 3-phosphate | - |
? | |
2.7.1.153 | ATP + phosphatidylinositol | - |
Homo sapiens | ADP + phosphatidylinositol 3-phosphate | - |
? | |
2.7.1.153 | ATP + phosphatidylinositol | - |
Dictyostelium discoideum | ADP + phosphatidylinositol 3-phosphate | - |
? | |
2.7.1.153 | ATP + phosphatidylinositol | - |
Caenorhabditis elegans | ADP + phosphatidylinositol 3-phosphate | - |
? | |
2.7.1.153 | ATP + phosphatidylinositol 4-phosphate | - |
Drosophila melanogaster | ADP + phosphatidylinositol 4,5-diphosphate | - |
? | |
2.7.1.153 | ATP + phosphatidylinositol 4-phosphate | - |
Mammalia | ADP + phosphatidylinositol 4,5-diphosphate | - |
? | |
2.7.1.153 | ATP + phosphatidylinositol 4-phosphate | - |
Homo sapiens | ADP + phosphatidylinositol 4,5-diphosphate | - |
? | |
2.7.1.153 | ATP + phosphatidylinositol 4-phosphate | - |
Dictyostelium discoideum | ADP + phosphatidylinositol 4,5-diphosphate | - |
? | |
2.7.1.153 | ATP + phosphatidylinositol 4-phosphate | - |
Caenorhabditis elegans | ADP + phosphatidylinositol 4,5-diphosphate | - |
? | |
2.7.1.153 | additional information | - |
Homo sapiens | ? | - |
? | |
2.7.1.153 | additional information | enzyme can promote proliferation | Drosophila melanogaster | ? | - |
? | |
2.7.1.153 | additional information | enzyme can promote proliferation | Mammalia | ? | - |
? | |
2.7.1.153 | additional information | phosphoinositide 3-kinase and DNA synthesis | Drosophila melanogaster | ? | - |
? | |
2.7.1.153 | additional information | phosphoinositide 3-kinase and DNA synthesis | Mammalia | ? | - |
? | |
2.7.1.153 | additional information | phosphoinositide 3-kinase and DNA synthesis | Dictyostelium discoideum | ? | - |
? | |
2.7.1.153 | additional information | phosphoinositide 3-kinase and DNA synthesis | Caenorhabditis elegans | ? | - |
? | |
2.7.1.153 | additional information | enzyme is involved in the synthesis of 3-phosphoinositides. Class I phosphoinositide 3-kinases are further subdivided into class IA and IB enzymes, which signal downstream of tyrosine kinase and heterotrimeric G protein-coupled receptors, respectively. All class I phosphoinositide 3-kinase members also bind to Ras, but the role of this interaction in physiological phosphoinositide 3-kinase signalling is not entirely clear | Drosophila melanogaster | ? | - |
? | |
2.7.1.153 | additional information | enzyme is involved in the synthesis of 3-phosphoinositides. Class I phosphoinositide 3-kinases are further subdivided into class IA and IB enzymes, which signal downstream of tyrosine kinase and heterotrimeric G protein-coupled receptors, respectively. All class I phosphoinositide 3-kinase members also bind to Ras, but the role of this interaction in physiological phosphoinositide 3-kinase signalling is not entirely clear | Mammalia | ? | - |
? | |
2.7.1.153 | additional information | enzyme is involved in the synthesis of 3-phosphoinositides. Class I phosphoinositide 3-kinases are further subdivided into class IA and IB enzymes, which signal downstream of tyrosine kinase and heterotrimeric G protein-coupled receptors, respectively. All class I phosphoinositide 3-kinase members also bind to Ras, but the role of this interaction in physiological phosphoinositide 3-kinase signalling is not entirely clear | Dictyostelium discoideum | ? | - |
? | |
2.7.1.153 | additional information | enzyme is involved in the synthesis of 3-phosphoinositides. Class I phosphoinositide 3-kinases are further subdivided into class IA and IB enzymes, which signal downstream of tyrosine kinase and heterotrimeric G protein-coupled receptors, respectively. All class I phosphoinositide 3-kinase members also bind to Ras, but the role of this interaction in physiological phosphoinositide 3-kinase signalling is not entirely clear | Caenorhabditis elegans | ? | - |
? | |
2.7.1.153 | additional information | phosphoinositide 3-kinase and apoptosis | Drosophila melanogaster | ? | - |
? | |
2.7.1.153 | additional information | phosphoinositide 3-kinase and apoptosis | Mammalia | ? | - |
? | |
2.7.1.153 | additional information | phosphoinositide 3-kinase and apoptosis | Dictyostelium discoideum | ? | - |
? | |
2.7.1.153 | additional information | phosphoinositide 3-kinase and apoptosis | Caenorhabditis elegans | ? | - |
? |
EC Number | Subunits | Comment | Organism |
---|---|---|---|
2.7.1.153 | More | class I phosphoinositide 3-kinases are heterodimers made up of an catalytic subunit, called p110, of about 110000 Da and an adaptor/regulatory subunit. Class I phosphoinositide 3-kinases are further subdivided into class Ia and IB enzymes, which signal downstream of tyrosine kinase and heterotrimeric G protein-coupled receptors, respectively | Drosophila melanogaster |
2.7.1.153 | More | class I phosphoinositide 3-kinases are heterodimers made up of an catalytic subunit, called p110, of about 110000 Da and an adaptor/regulatory subunit. Class I phosphoinositide 3-kinases are further subdivided into class Ia and IB enzymes, which signal downstream of tyrosine kinase and heterotrimeric G protein-coupled receptors, respectively | Mammalia |
2.7.1.153 | More | class I phosphoinositide 3-kinases are heterodimers made up of an catalytic subunit, called p110, of about 110000 Da and an adaptor/regulatory subunit. Class I phosphoinositide 3-kinases are further subdivided into class Ia and IB enzymes, which signal downstream of tyrosine kinase and heterotrimeric G protein-coupled receptors, respectively | Dictyostelium discoideum |
2.7.1.153 | More | class I phosphoinositide 3-kinases are heterodimers made up of an catalytic subunit, called p110, of about 110000 Da and an adaptor/regulatory subunit. Class I phosphoinositide 3-kinases are further subdivided into class Ia and IB enzymes, which signal downstream of tyrosine kinase and heterotrimeric G protein-coupled receptors, respectively | Caenorhabditis elegans |
2.7.1.153 | More | a single type of catalytic/adaptor heterodimer: AGE-1/AAP-1 | Caenorhabditis elegans |
2.7.1.153 | More | a single type of catalytic/adaptor heterodimer: Dp110/p60 | Drosophila melanogaster |
2.7.1.153 | More | three class IA p110 isoforms, p110alpha, beta and delta, which are encoded by three separate genes, at least seven adaptor proteins, which are generated by expression and alternative splicing of three different genes, namely p85alpha, p85beta and p55gamma. All these splice variants make functional complexes with p110 subunits | Mammalia |
2.7.1.153 | More | three catalytic subunits: PIK1, PIK2 or PIK3 | Dictyostelium discoideum |