Target of Rapamycin (TOR) is an atypical Ser/Thr protein kinase that is evolutionally conserved among yeasts, plants, and mammals. In plants, TOR signaling functions as a central hub to integrate different kinds of nutrient, energy, hormone, and environmental signals. TOR thereby orchestrates every stage of plant life, from embryogenesis, meristem activation, root, and leaf growth to flowering


Gene name - Target of rapamycin. Synonyms - dTOR, mechanistic target of rapamycin (mTOR), TORC1, FRAP/TOR Cytological map position - 34A4 Function - signaling. Keywords - Tor pathway, growth, nutrient sensing Symbol - Tor. FlyBase ID: FBgn0021796. Genetic map position - 2L Classification - Phosphatidylinositol 3- and 4-kinase

Target of Rapamycin (TOR) is a major nutrition and energy sensor that regulates growth and life span in yeast and animals. In plants, growth and life span are intertwined not only with nutrient acquisition from the soil and nutrition generation via Rapamycin is a member of a family of macrolide immunosuppressants that bind to and inhibit the FK506 binding protein (FKBP) proline rotamase. Format/Formulation: Lyophilized 2001-06-01 · Part of the mammalian target of rapamycin complex 2 (mTORC2) which contains MTOR, MLST8, PRR5, RICTOR, MAPKAP1 and DEPTOR. Contrary to mTORC1, mTORC2 does not bind to and is not sensitive to FKBP12-rapamycin. Interacts directly with MTOR and RPTOR.

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In fundamental biology, TOR is a nutrient-sensitive, central controller of cell growth and aging. In clinical biology, TOR is implicated in many diseases and is the target of the drug rapamycin used in three different 2004-04-19 TOR, the Target of Rapamycin, is now known to be a central controller of cell, tissue and organism growth and an important molecule in many human diseases including cancer, cardiac hypertrophy, diabetes and obesity. The mechanistic target of rapamycin (mTOR), previously referred to as the mammalian target of rapamycin, and sometimes called FK506-binding protein 12-rapamycin-associated protein 1 (FRAP1), is a kinase that in humans is encoded by the MTOR gene. mTOR is a member of the phosphatidylinositol 3-kinase-related kinase family of protein kinases.

Mechanistic Target of Rapamycin. mTOR is a downstream substrate in the insulin signaling pathway, which has been demonstrated by the observation that the lifespan extension in insulin signaling mutant could not be further extended by 

Rapamycin potently inhibits downstream signaling from the target of rapamycin (TOR) proteins. These evolutionarily conserved protein kinases coordinate the balance between protein synthesis and protein degradation in response to nutrient quality and quantity. Mechanistic Target of Rapamycin mTOR.

2004-04-19 · Target of rapamycin (TOR): an integrator of nutrient and growth factor signals and coordinator of cell growth and cell cycle progression Abstract. Cell growth (an increase in cell mass and size through macromolecular biosynthesis) and cell cycle progression Introduction. Tumorigenesis is a

Mechanistic Target of Rapamycin. mTOR is a downstream substrate in the insulin signaling pathway, which has been demonstrated by the observation that the lifespan extension in insulin signaling mutant could not be further extended by  Mechanistic target of rapamycin (mTOR), a serine/threonine protein kinase of the phosphatidylinositol kinase-related kinase family, assembles into two functionally distinct complexes, namely mTORC1 (Raptor) and mTORC2 (Rictor),  The IUPHAR/BPS Guide to Pharmacology. mechanistic target of rapamycin kinase - FRAP subfamily. Detailed annotation on the structure, function, physiology, pharmacology and clinical relevance of drug targets. 12 Nov 2018 Target of Rapamycin Inhibition in Chlamydomonas reinhardtii Triggers de Novo Amino Acid Synthesis by Enhancing Nitrogen Assimilation. Umarah Mubeen, Jessica Jüppner, Jessica Alpers, Dirk K. Hincha, Patrick Giavalisco.

The target of rapamycin (known as mTOR or the mechanistic target of rapamycin) is a protein that tells cells when to grow, divide, and survive.
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mTORC1 The immunosuppressive agents target of rapamycin inhibitors (TOR‐I) (sirolimus, and everolimus) have been widely used in kidney transplantation for >10 years.

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Chondrocyte hypertrophy contributes to 80% of bone growth. Activation of mammalian Target of Rapamycin (mTOR) pathway promotes chondrocyte hypertrophy 

The Target of Rapamycin (TOR) signaling pathway is conserved in all eukaryotes and acts as a central regulatory hub between growth and extrinsic factors, such as nutrients or stress. However, relatively little is known about the regulations and roles of this pathway in plants and algae. Mechanistic target of rapamycin (mTOR) is a threonine and serine protein kinase that is a great target for immunosuppressive drug rapamycin. There are two distinct complexes of mTOR: mTOR complex 1 (mTORC1) and mTOR complex 2 (mTORC2). mTORC1 is a growth regulator that senses and integrates energy levels, growth factors, amino acids, and cellular stress, whereas mTORC2 promotes cellular Target of rapamycin (TOR) acts as a master regulator in coordination of cell growth with energy and nutrient availability. Despite the increased appreciation of the essential role of the TOR complex in interaction with phytohormone signaling, little is known about its function on ethylene signaling.