SH3BP4 is a negative regulator of amino acid-Rag GTPase-mTORC1 signaling
What this study shows
SH3BP4 negatively regulates amino-acid-Rag-GTPase-mTORC1 signalling.
At a glance
| Evidence type | M Molecular — cells, biochemistry, structure Marked M because it is molecular or in-vitro work (model: Mammalian cells) 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 | Mammalian cells |
| Journal | Molecular cell |
| Year | 2012 |
| Peer reviewed | Yes |
| Record last updated | 2026-10-01 |
| Source | DOI 10.1016/j.molcel.2012.04.007 · PMID 22575674 · Free full text (PMC3389276) |
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/genetic (SH3BP4) |
| Target | SH3BP4 / Rag GTPase / mTORC1 |
| Model | Mammalian cells |
| Effect | SH3BP4 is a negative regulator of amino-acid-Rag-GTPase-mTORC1 signaling |
In the Atlas
Related topics
Links in the pathway map
- Supports Rag GTPases recruits mTORC1
More studies on this topic
- Regulation of TORC1 in response to amino acid starvation via lysosomal recruitment of TSC2 (2014)
- A Rag GTPase dimer code defines the regulation of mTORC1 by amino acids (2022)
- The molecular basis of nutrient sensing and signalling by mTORC1 in metabolism regulation and disease (2023)
- Rag GTPases mediate amino acid-dependent recruitment of TFEB and MITF to lysosomes (2013)
Was this page useful?
Thank you. Your answer was counted anonymously.