 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
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| MeSH Number(s) |
D05.500.562.452.100 D08.811.600.391.100 D08.811.913.555.400.100
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| 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
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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 this website by year, and whether "Aminomethyltransferase" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2016 | 1 | 0 | 1 | | 2017 | 0 | 1 | 1 |
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Below are the most recent publications written about "Aminomethyltransferase" by people in Profiles.
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Swanson MA, Garcia SM, Spector E, Kronquist K, Creadon-Swindell G, Walter M, Christensen E, Van Hove JLK, Sass JO. d-Glyceric aciduria does not cause nonketotic hyperglycinemia: A historic co-occurrence. Mol Genet Metab. 2017 06; 121(2):80-82.
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Coughlin CR, Swanson MA, Kronquist K, Acquaviva C, Hutchin T, Rodr?guez-Pombo P, V?is?nen ML, Spector E, Creadon-Swindell G, Br?s-Goldberg AM, Rahikkala E, Moilanen JS, Mahieu V, Matthijs G, Bravo-Alonso I, P?rez-Cerd? C, Ugarte M, Vianey-Saban C, Scharer GH, Van Hove JL. The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT. Genet Med. 2017 01; 19(1):104-111.
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