Structured Summary
Abstract
An intracellular signaling and tumor suppressor protein that forms a complex with TUBEROUS SCLEROSIS COMPLEX 1 PROTEIN (TSC1) and other signaling factors to negatively regulate MTORC1 and affect cell growth and proliferation. It can also function as GTPASE-ACTIVATING PROTEIN (GAP) for RHEB GTPASE to activate mTORC1 independent of its role in the complex. Structurally, it interacts with TSC1 through its N-terminus, which also contains a leucine zipper and coiled-coil region. It also has multiple phosphorylation sites for different cell signaling kinases, a central coiled-coil region, a C-terminal GAP domain and CALMODULIN binding domain. Mutations in the TSC2 gene are associated with TUBEROUS SCLEROSIS.
MeSH Record
Classification
Related Concepts
Knowledge Graph
Drag nodes to rearrange; hover to trace links; click a node to open its page.
MeSH Record
Synonyms
2 entry terms
- Tuberin
- Tuberous Sclerosis 2 Protein
MeSH Record
Aspects Covered
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.
MeSH Record
History Note
2019 (1994)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Tuberous Sclerosis Complex 2 Protein. Medical Subject Headings (MeSH). 2026. Unique ID D000077005. http://id.nlm.nih.gov/mesh/2026/D000077005
- Tuberous Sclerosis Complex 2 Protein. In: Wikipedia. https://en.wikipedia.org/wiki/TSC2
- Tuberous Sclerosis Complex 2 Protein. In: Wikidata. https://www.wikidata.org/wiki/Q21109261