Aminomethyltransferase
"Aminomethyltransferase" 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.
A one-carbon group transferase that transfers lipoamide-linked methylamine groups to tetrahydrofolate (TETRAHYDROFOLATES) to form methylenetetrahydrofolate and AMMONIA. It is one of four components of the glycine decarboxylase complex.
| Descriptor ID |
D050960
|
| MeSH Number(s) |
D05.500.562.452.100 D08.811.600.391.100 D08.811.913.555.400.100
|
| Concept/Terms |
Aminomethyltransferase- Aminomethyltransferase
- Tetrahydrofolate Aminomethyltransferase
- Aminomethyltransferase, Tetrahydrofolate
- T-Protein, Glycine Cleavage System
- T Protein, Glycine Cleavage System
- Glycine Decarboxylase Complex T-Protein
- Glycine Decarboxylase Complex T Protein
- Glycine Synthase
- Synthase, Glycine
|
Below are MeSH descriptors whose meaning is more general than "Aminomethyltransferase".
Below are MeSH descriptors whose meaning is more specific than "Aminomethyltransferase".
This graph shows the total number of publications written about "Aminomethyltransferase" by people in UAMS Profiles by year, and whether "Aminomethyltransferase" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Aminomethyltransferase" by people in Profiles over the past ten years.
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Silverstein S, Veerapandiyan A, Hayes-Rosen C, Ming X, Kornitzer J. A novel intronic homozygous mutation in the AMT gene of a patient with nonketotic hyperglycinemia and hyperammonemia. Metab Brain Dis. 2019 02; 34(1):373-376.