Pathway link AKT-PRAS40
Akt/PKB PRAS40
Akt/PKB inhibits PRAS40.
Akt tags PRAS40, which then gets pulled away from mTORC1 – a second way insulin releases a brake.
The conditions it holds under
Three 2007 studies in cultured mammalian cells. Not tested in whole animals or in people, and how much this branch adds beside Akt's route through TSC2 is not measured.
- Time it takes
- seconds
- Step
- direct (one molecule acts on the other)
- Measured in
- mammalian cells
- Where in the cell
- cytosol
- Reaches people?
- plausible in people, not shown directly
- How settled
- settled in the literature
Studies behind it
| Year | Evidence | Study |
|---|---|---|
| 2007 | M | PRAS40 is an insulin-regulated inhibitor of the mTORC1 protein kinaseSAN2007 Identified PRAS40 as the missing insulin-controlled brake INSIDE mTORC1. When insulin is absent PRAS40 clamps the complex shut; insulin makes Akt phosphorylate PRAS40, releasing the brake so Rheb can fully switch mTORC1 on. Explained how hormone signals set the exact strength of mTORC1 activity. |
| 2007 | M | Insulin signalling to mTOR mediated by the Akt/PKB substrate PRAS40VAN2007 Insulin signals to mTORC1 through Akt phosphorylation of the inhibitor PRAS40. |
| 2007 | M | The proline-rich Akt substrate of 40 kDa (PRAS40) is a physiological substrate of mammalian target of rapamycin complex 1OSH2007 PRAS40 is a physiological raptor-bound substrate and inhibitor of mTORC1. |
Points the other way
No study in the Atlas contradicts this link. That means none in this curated set, not none in the literature.
Who has checked this
- Checked by
- No researcher outside the project has checked this link yet.
- Curator sign-off
- Not signed off yet. This link was drafted with AI help and has not been reviewed link by link; treat it as a proposal until it is.
- Curated by
- Oliver Barton, with AI help for drafting; see how links are checked.
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