"GTP-Binding Proteins" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Regulatory proteins that act as molecular switches. They control a wide range of biological processes including: receptor signaling, intracellular signal transduction pathways, and protein synthesis. Their activity is regulated by factors that control their ability to bind to and hydrolyze GTP to GDP. EC 3.6.1.-.
| Descriptor ID |
D019204
|
| MeSH Number(s) |
D08.811.277.040.330.300 D12.776.157.325
|
| Concept/Terms |
GTP-Binding Proteins- GTP-Binding Proteins
- GTP Binding Proteins
- Proteins, GTP-Binding
- G-Proteins
- G Proteins
- GTP-Binding Protein
- GTP Binding Protein
- Protein, GTP-Binding
- Guanine Nucleotide Regulatory Proteins
- GTP-Regulatory Protein
- GTP Regulatory Protein
- Protein, GTP-Regulatory
- GTP-Regulatory Proteins
- GTP Regulatory Proteins
- Proteins, GTP-Regulatory
- Guanine Nucleotide Coupling Protein
- G-Protein
- G Protein
|
Below are MeSH descriptors whose meaning is more general than "GTP-Binding Proteins".
Below are MeSH descriptors whose meaning is more specific than "GTP-Binding Proteins".
This graph shows the total number of publications written about "GTP-Binding Proteins" by people in this website by year, and whether "GTP-Binding Proteins" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2019 | 0 | 1 | 1 |
| 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "GTP-Binding Proteins" by people in Profiles.
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Biallelic variants in YRDC cause a developmental disorder with progeroid features. Hum Genet. 2021 Dec; 140(12):1679-1693.
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A disease causing ATLASTIN 3 mutation affects multiple endoplasmic reticulum-related pathways. Cell Mol Life Sci. 2019 Apr; 76(7):1433-1445.
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Do not trust the pedigree: reduced and sex-dependent penetrance at a novel mutation hotspot in ATL1 blurs autosomal dominant inheritance of spastic paraplegia. Hum Mutat. 2013 Jun; 34(6):860-3.
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Cloning and characterization of a dominant-negative vps1 allele of the yeast Saccharomyces cerevisiae. Biol Chem. 1997 Oct; 378(10):1187-91.
MeSH information
