TOR complex 1 (TORC1) is an evolutionarily conserved protein kinase complex that promotes cellular macromolecular synthesis and suppresses autophagy. Amino-acid-induced activation of mammalian TORC1 is initiated by its recruitment to the RagA/B-RagC/D GTPase heterodimer, which is anchored to lysosomal membranes through the Ragulator complex. We have identified in the model organism Schizosaccharomyces pombe a Ragulator-like complex that tethers the Gtr1-Gtr2 Rag heterodimer to the membranes of vacuoles, the lysosome equivalent in yeasts. Unexpectedly, the Ragulator-Rag complex is not required for the vacuolar targeting of TORC1, but the complex plays a crucial role in attenuating TORC1 activity independently of the Tsc1-Tsc2 complex, a know...
Target of rapamycin (TOR) is an evolutionarily conserved protein kinase that controls multiple cellu...
Background The protein kinase Target Of Rapamycin (TOR) is a nexus for the regulation of eukaryotic ...
Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biology, 2010.This electronic versi...
TOR complex 1 (TORC1) is an evolutionarily conserved protein kinase complex that promotes cellular m...
The target of rapamycin kinase complex 1 (TORC1) regulates cell growth and metabolism in eukaryotes....
Target of rapamycin complex 1 (TORC1), a serine/threonine-protein kinase complex highly conserved am...
The Target of Rapamycin Complex 1 (TORC1) is a critical coordinator of eukaryotic growth. A large am...
Target of rapamycin complex 1 (TORC1) is an evolutionarily conserved protein kinase complex, whose a...
2018 dissertation for MRes. The Target of Rapamycin (TOR) pathway is responsible for the growth and ...
Funding: The APC was funded by the Biotechnology and Biological Sciences Research Council (BB/V01633...
SummaryRag GTPases assemble into heterodimeric complexes consisting of RagA or RagB and RagC or RagD...
AbstractThe Target of Rapamycin (TOR) proteins function in signaling pathways that promote protein s...
The target of rapamycin (TOR) kinase is a central controller of cell growth. In yeast, the TOR prote...
The Rag guanosine triphosphatases (GTPases) recruit the master kinase mTORC1 to lysosomes to regulat...
<div><p>In mammalian cells, mTORC1 activity is regulated by Rag GTPases. It is thought that the Ragu...
Target of rapamycin (TOR) is an evolutionarily conserved protein kinase that controls multiple cellu...
Background The protein kinase Target Of Rapamycin (TOR) is a nexus for the regulation of eukaryotic ...
Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biology, 2010.This electronic versi...
TOR complex 1 (TORC1) is an evolutionarily conserved protein kinase complex that promotes cellular m...
The target of rapamycin kinase complex 1 (TORC1) regulates cell growth and metabolism in eukaryotes....
Target of rapamycin complex 1 (TORC1), a serine/threonine-protein kinase complex highly conserved am...
The Target of Rapamycin Complex 1 (TORC1) is a critical coordinator of eukaryotic growth. A large am...
Target of rapamycin complex 1 (TORC1) is an evolutionarily conserved protein kinase complex, whose a...
2018 dissertation for MRes. The Target of Rapamycin (TOR) pathway is responsible for the growth and ...
Funding: The APC was funded by the Biotechnology and Biological Sciences Research Council (BB/V01633...
SummaryRag GTPases assemble into heterodimeric complexes consisting of RagA or RagB and RagC or RagD...
AbstractThe Target of Rapamycin (TOR) proteins function in signaling pathways that promote protein s...
The target of rapamycin (TOR) kinase is a central controller of cell growth. In yeast, the TOR prote...
The Rag guanosine triphosphatases (GTPases) recruit the master kinase mTORC1 to lysosomes to regulat...
<div><p>In mammalian cells, mTORC1 activity is regulated by Rag GTPases. It is thought that the Ragu...
Target of rapamycin (TOR) is an evolutionarily conserved protein kinase that controls multiple cellu...
Background The protein kinase Target Of Rapamycin (TOR) is a nexus for the regulation of eukaryotic ...
Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biology, 2010.This electronic versi...