Human RPTOR protein (Recombinant) (N-His) (STJP007479)

SPECIFICATIONS
HostE.coli
ImmunogenHomo sapiens (Human)
STJP007479
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General Information

Short DescriptionRecombinant-Human RPTOR-N-His protein was developed from e.coli for the region N-His. For use in research applications.
ApplicationsELISA/Immunogen/SDS-PAGE/WB
HostE.coli
NoteSTRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.

Product Properties

Dilution RangeReconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.
FormulationLyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.
Storage InstructionUse a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at-20 to-80°C for twelve months from the date of receipt.

Target Information

Gene SymbolRPTOR
Gene ID57521
Uniprot IDRPTOR_HUMAN
ImmunogenHomo sapiens (Human)
Immunogen RegionArg1012-Arg1335

Additional Info

Post Translational Modifications Insulin-stimulated phosphorylation at Ser-863 by MTOR and MAPK8 regulates mTORC1 activity. Phosphorylated at Ser-863 by NLK in response to stress, disrupting the interaction with small GTPases Rag (RagA/RRAGA, RagB/RRAGB, RagC/RRAGC and/or RagD/RRAGD), thereby preventing lysosome recruitment and activation of the mTORC1 complex. Osmotic stress also induces phosphorylation at Ser-696, Thr-706 and Ser-863 by MAPK8. Ser-863 phosphorylation is required for phosphorylation at Ser-855 and Ser-859. In response to nutrient limitation, phosphorylated at Ser-722 and Ser-792 by AMPK.phosphorylation promotes interaction with 14-3-3 proteins, leading to negative regulation of the mTORC1 complex. Phosphorylation at Ser-722 and Ser-792 by AMPK in response to glucose starvation inhibits O-GlcNAcylation by OGT and subsequent activation of mTORC1. In response to growth factors, phosphorylated at Ser-719, Ser-721 and Ser-722 by RPS6KA1, which stimulates mTORC1 activity. Phosphorylation at Ser-791 by PKA downstream of cAMP inhibits the mTORC1 complex. Phosphorylated at Ser-877 by TBK1, leading to negative regulation of the mTORC1 complex. O-GlcNAcylated by OGT upon glucose sufficiency, promoting interaction with small GTPases Rag (RagA/RRAGA, RagB/RRAGB, RagC/RRAGC and/or RagD/RRAGD) and subsequent recruitment of mTORC1 to lysosomal membranes, leading to activation of the mTORC1 complex. Phosphorylation at Ser-722 and Ser-792 by AMPK in response to glucose starvation inhibits O-GlcNAcylation. Acetylation at Lys-1097 by EP300/p300 in response to leucine metabolite acetyl-coA promotes its activity, leading to activation of the mTORC1 complex. Acetylation is decreased in response to fasting. Ubiquitinated, leading to its degradation by the proteasome. Deubiquitinated by OTUB1 via a non-catalytic mechanism. Ubiquitinated by an E3 ubiquitin ligase complex containing VHL.
Function Component of the mechanistic target of rapamycin complex 1 (mTORC1), an evolutionarily conserved central nutrient sensor that stimulates anabolic reactions and macromolecule biosynthesis to promote cellular biomass generation and growth. In response to nutrients, growth factors or amino acids, mTORC1 is recruited to the lysosome membrane and promotes protein, lipid and nucleotide synthesis by phosphorylating several substrates, such as ribosomal protein S6 kinase (RPS6KB1 and RPS6KB2) and EIF4EBP1 (4E-BP1). In the same time, it inhibits catabolic pathways by phosphorylating the autophagy initiation components ULK1 and ATG13, as well as transcription factor TFEB, a master regulators of lysosomal biogenesis and autophagy. The mTORC1 complex is inhibited in response to starvation and amino acid depletion. Within the mTORC1 complex, RPTOR acts both as a molecular adapter, which (1) mediates recruitment of mTORC1 to lysosomal membranes via interaction with small GTPases Rag (RagA/RRAGA, RagB/RRAGB, RagC/RRAGC and/or RagD/RRAGD), and a (2) substrate-specific adapter, which promotes substrate specificity by binding to TOS motif-containing proteins and direct them towards the active site of the MTOR kinase domain for phosphorylation. mTORC1 complex regulates many cellular processes, such as odontoblast and osteoclast differentiation or neuronal transmission. mTORC1 complex in excitatory neuronal transmission is required for the prosocial behavior induced by the psychoactive substance lysergic acid diethylamide (LSD).
Protein Name Regulatory-Associated Protein Of Mtor
Raptor
P150 Target Of Rapamycin
Tor-Scaffold Protein
Database Links Reactome: R-HSA-1632852
Reactome: R-HSA-165159
Reactome: R-HSA-166208
Reactome: R-HSA-3371571
Reactome: R-HSA-380972
Reactome: R-HSA-5628897
Reactome: R-HSA-8943724
Reactome: R-HSA-9639288
Cellular Localisation Lysosome Membrane
Cytoplasm
Cytoplasmic Granule
Targeting To Lysosomes Depends On Amino Acid Availability: Recruited To Lysosome Membranes Via Interaction With Gtp-Bound Form Of Raga/Rraga (Or Ragb/Rragb) In Complex With The Gdp-Bound Form Of Ragc/Rragc (Or Ragd/Rragd)
Promoting Recruitment Of Mtorc1 To The Lysosomes
In Arsenite-Stressed Cells
Accumulates In Stress Granules When Associated With Spag5 And Association With Lysosomes Is Drastically Decreased
Alternative Protein Names Regulatory-Associated Protein Of Mtor protein
Raptor protein
P150 Target Of Rapamycin protein
Tor-Scaffold Protein protein
RPTOR protein
KIAA1303 protein
RAPTOR protein

Information sourced from Uniprot.org

Citations

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