The mammalian target of rapamycin (mTOR) partner, raptor, binds the mTOR substrates p70 S6 kinase and 4E-BP1 through their TOR signaling (TOS) motif
What this study shows
Raptor binds mTOR substrates via their TOS motifs, acting as the substrate-presenting scaffold of mTORC1.
At a glance
| Evidence type | M Molecular — cells, biochemistry, structure Marked M because it is molecular or in-vitro work (model: In vitro) rather than a whole-organism health-outcome study. That is often exactly where causal biology gets established -- the code says which system the finding was shown in, and nothing about how good the work is. |
| Study type | 5 - Mechanistic / In Vitro |
| Model system | In vitro |
| Journal | The Journal of biological chemistry |
| Year | 2003 |
| Peer reviewed | Yes |
| Record last updated | 2026-10-01 |
| Source | DOI 10.1074/jbc.C200665200 · PMID 12604610 |
Extracted findings
These fields were extracted from the paper with AI assistance and have not been checked against the source. Read them as a pointer into the paper, not as curated claims; where they disagree with the curated summary above, the curated summary stands.
| Intervention | Biochemical (TOS motif) |
| Target | mTOR / raptor / p70 S6K / 4E-BP1 |
| Model | In vitro |
| Effect | Raptor binds the mTOR substrates p70 S6K and 4E-BP1 through their TOR-signaling (TOS) motif |
In the Atlas
Related topics
Links in the pathway map
- Supports mTORC1 inhibits 4E-BP1
- Supports mTORC1 activates S6K1
- Supports Raptor required-for mTORC1
More studies on this topic
- Raptor, a binding partner of target of rapamycin (TOR), mediates TOR action (2002)
- mTOR interacts with raptor to form a nutrient-sensitive complex that signals to the cell growth machinery (2002)
- Mammalian cell size is controlled by mTOR and its downstream targets S6K1 and 4EBP1/eIF4E (2002)
- Amino acid sufficiency and mTOR regulate p70 S6 kinase and eIF-4E BP1 through a common effector mechanism (1998)
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