Structured Summary
Abstract
An intracellular signaling and tumor suppressor protein that forms a complex with TUBEROUS SCLEROSIS COMPLEX 2 PROTEIN (TSC2) and other signaling factors to negatively regulate MTORC1 signaling and affect cell growth and proliferation. Structurally, it interacts with TSC2 through its N-terminal, which also contains GSK-3BETA phosphorylation sites and a RHO-KINASE activation domain. It also contains a C-terminal coiled-coil domain and ezrin-radixin-moesin (ERM) domain. Mutations in the TSC1 gene are associated with TUBEROUS SCLEROSIS.
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- Hamartin
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30 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, agonists, analysis, antagonists & inhibitors, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, deficiency, drug effects, economics, genetics, history, immunology, isolation & purification, metabolism, pharmacokinetics, pharmacology, physiology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, ultrastructure, urine.
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History Note
2019 (1997)
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References
- National Library of Medicine. Tuberous Sclerosis Complex 1 Protein. Medical Subject Headings (MeSH). 2026. Unique ID D000077004. http://id.nlm.nih.gov/mesh/2026/D000077004
- Tuberous Sclerosis Complex 1 Protein. In: Wikipedia. https://en.wikipedia.org/wiki/TSC1
- Tuberous Sclerosis Complex 1 Protein. In: Wikidata. https://www.wikidata.org/wiki/Q898669