"Tyrosine Transaminase" 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.
An enzyme that catalyzes the conversion of L-TYROSINE and 2-oxoglutarate to 4-hydroxyphenylpyruvate and L-GLUTAMATE. It is a pyridoxal-phosphate protein. L-PHENYLALANINE is hydroxylated to L-tyrosine. The mitochondrial enzyme may be identical with ASPARTATE AMINOTRANSFERASES (EC 2.6.1.1.). Deficiency of this enzyme may cause type II Tyrosinemia (see TYROSINEMIAS). EC 2.6.1.5.
| Descriptor ID |
D014444
|
| MeSH Number(s) |
D08.811.913.477.700.900
|
| Concept/Terms |
Tyrosine Transaminase- Tyrosine Transaminase
- Transaminase, Tyrosine
- Tyrosine Aminotransferase
- Aminotransferase, Tyrosine
|
Below are MeSH descriptors whose meaning is more general than "Tyrosine Transaminase".
Below are MeSH descriptors whose meaning is more specific than "Tyrosine Transaminase".
This graph shows the total number of publications written about "Tyrosine Transaminase" by people in this website by year, and whether "Tyrosine Transaminase" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2008 | 1 | 1 | 2 |
| 2010 | 1 | 0 | 1 |
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Below are the most recent publications written about "Tyrosine Transaminase" by people in Profiles.
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Tyrosinemia type II (Richner-Hanhart syndrome): a new mutation in the TAT gene. Eur J Med Genet. 2011 May-Jun; 54(3):205-8.
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Identification of two new mutations in the TAT gene in a Danish family with tyrosinaemia type II. Br J Dermatol. 2009 Mar; 160(3):704-6.
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Richner-Hanhart syndrome detected by expanded newborn screening. Pediatr Dermatol. 2008 May-Jun; 25(3):378-80.
MeSH information
