 |
|
| PROSITE documentation PDOC00710 [for PROSITE entry PS00915] |
Phosphatidylinositol 3- and 4-kinases signatures and profile
Phosphatidylinositol 3-kinase (PI3-kinase) (EC 2.7.1.137) [1] is an enzyme that phosphorylates phosphoinositides on the 3-hydroxyl group of the inositol ring. The exact function of the three products of PI3-kinase - PI-3-P, PI-3,4-P(2) and PI-3,4,5-P(3) - is not yet known, although it is proposed that they function as second messengers in cell signalling. Currently, three forms of PI3-kinase are known:
- The mammalian enzyme which is a heterodimer of a 110 Kd catalytic chain (p110) and an 85 Kd subunit (p85) which allows it to bind to activated tyrosine protein kinases. There are at least two different types of p100 subunits (α and β).
- Yeast TOR1/DRR1 and TOR2/DRR2 [2], PI3-kinases required for cell cycle activation. Both are proteins of about 280 Kd.
- Yeast VPS34 [3], a PI3-kinase involved in vacuolar sorting and segregation. VPS34 is a protein of about 100 Kd.
- Arabidopsis thaliana and soybean VPS34 homologs.
Phosphatidylinositol 4-kinase (PI4-kinase) (EC 2.7.1.67) [4] is an enzyme that acts on phosphatidylinositol (PI) in the first committed step in the production of the second messenger inositol-1,4,5,-trisphosphate. Currently the following forms of PI4-kinases are known:
- Human PI4-kinase α.
- Yeast PIK1, a nuclear protein of 120 Kd.
- Yeast STT4, a protein of 214 Kd.
The PI3- and PI4-kinases share a well conserved domain at their C-terminal section; this domain seems to be distantly related to the catalytic domain of protein kinases [2]. We developed two signature patterns from the best conserved parts of this domain.
Four additional proteins belong to this family:
- Mammalian FKBP-rapamycin associated protein (FRAP) [5], which acts as the target for the cell-cycle arrest and immunosuppressive effects of the FKBP12-rapamycin complex.
- Yeast protein ESR1 [6] which is required for cell growth, DNA repair and meiotic recombination.
- Yeast protein TEL1 which is involved in controlling telomere length.
- Yeast hypothetical protein YHR099w, a distantly related member of this family.
- Fission yeast hypothetical protein SpAC22E12.16C.
A profile was also developed that spans the complete C-terminal domain.
Last update:December 2004 / Patterns and text revised.
PROSITE methods (with tools and information) covered by this documentation:
| 1 | Authors | Hiles I.D., Otsu M., Volinia S., Fry M.J., Gout I., Dhand R., Panayotou G., Ruiz-Larrea F., Thompson A., Totty N.F. |
| Title | Phosphatidylinositol 3-kinase: structure and expression of the 110 kd catalytic subunit. | |
| Source | Cell 70:419-429(1992). | |
| PubMed ID | 1322797 |
| 2 | Authors | Kunz J., Henriquez R., Schneider U., Deuter-Reinhard M., Movva N.R., Hall M.N. |
| Title | Target of rapamycin in yeast, TOR2, is an essential phosphatidylinositol kinase homolog required for G1 progression. | |
| Source | Cell 73:585-596(1993). | |
| PubMed ID | 8387896 |
| 3 | Authors | Schu P.V., Takegawa K., Fry M.J., Stack J.H., Waterfield M.D., Emr S.D. |
| Title | Phosphatidylinositol 3-kinase encoded by yeast VPS34 gene essential for protein sorting. | |
| Source | Science 260:88-91(1993). | |
| PubMed ID | 8385367 |
| 4 | Authors | Garcia-Bustos J.F., Marini F., Stevenson I., Frei C., Hall M.N. |
| Source | EMBO J. 13:2352-2361(1994). |
| 5 | Authors | Brown E.J., Albers M.W., Shin T.B., Ichikawa K., Keith C.T., Lane W.S., Schreiber S.L. |
| Title | A mammalian protein targeted by G1-arresting rapamycin-receptor complex. | |
| Source | Nature 369:756-758(1994). | |
| PubMed ID | 8008069 | |
| DOI | 10.1038/369756a0 |
| 6 | Authors | Kato R., Ogawa H. |
| Title | An essential gene, ESR1, is required for mitotic cell growth, DNA repair and meiotic recombination in Saccharomyces cerevisiae. | |
| Source | Nucleic Acids Res. 22:3104-3112(1994). | |
| PubMed ID | 8065923 |
PROSITE is copyright. It is produced by the SIB Swiss Institute Bioinformatics. There are no restrictions on its use by non-profit institutions as long as its content is in no way modified. Usage by and for commercial entities requires a license agreement. For information about the licensing scheme send an email to Prosite License or see: prosite_license.html.
View entry in original PROSITE document format
View entry in raw text format (no links)