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10.15252/embj.201797469

http://scihub22266oqcxt.onion/10.15252/embj.201797469
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C5502876!5502876 !28623241
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suck abstract from ncbi


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pmid28623241
      EMBO+J 2017 ; 36 (13 ): 1809-1810
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  • Suppressing mTORC1 on the lysosome #MMPMID28623241
  • Raiborg C ; Schink KO ; Stenmark H
  • EMBO J 2017[Jul]; 36 (13 ): 1809-1810 PMID28623241 show ga
  • The mechanistic target of rapamycin, mTOR, is a protein kinase that integrates environmental and nutritional inputs into regulation of cell growth and metabolism. Key outputs of mTOR signalling occur from the lysosome membrane in the form of the multi?subunit mTOR complex 1 (mTORC1), which phosphorylates multiple targets. While class I phosphoinositide kinase (PI3K?I) is a well?known activator of mTORC1, a recent paper (Marat et al, 2017) shows that a class II PI3K with a different substrate specificity, PI3K?C2?, serves to inhibit mTORC1 on lysosomes under conditions of growth factor deprivation.
  • |*Lysosomes [MESH]
  • |*Mechanistic Target of Rapamycin Complex 1 [MESH]
  • |Multiprotein Complexes [MESH]


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