Tyrosine Transaminase [tyrosinaminotransferasa]
- Terms
-
tyrosinaminotransferáza
tyrozinaminotransferáza
-
Tyrosine Aminotransferase
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.
- Annotation
- /defic: consider also TYROSINEMIAS
- DUI
- D014444 MeSH Browser
- CUI
- M0022204
- CAS
- L-Tyrosine:2-oxoglutarate aminotransferase
- History note
- 95; was TYROSINE AMINOTRANSFERASE 1964-94 (Prov 1964-68)
- Online note
- use TYROSINE TRANSAMINASE to search TYROSINE AMINOTRANSFERASE 1966-94 (as Prov 1966-68)
- Public note
- 95; was TYROSINE AMINOTRANSFERASE 1964-94
Allowable subheadings
- AD
- administration & dosage
- AE
- adverse effects
- AN
- analysis 3
- AI
- antagonists & inhibitors
- BI
- biosynthesis 2
- BL
- blood
- CF
- cerebrospinal fluid
- CS
- chemical synthesis
- CH
- chemistry
- CL
- classification
- DF
- deficiency
- DE
- drug effects 1
- EC
- economics
- GE
- genetics
- HI
- history
- IM
- immunology
- IP
- isolation & purification
- ME
- metabolism 3
- PK
- pharmacokinetics
- PD
- pharmacology
- PH
- physiology 1
- PO
- poisoning
- RE
- radiation effects 1
- ST
- standards
- SD
- supply & distribution
- TU
- therapeutic use
- TO
- toxicity
- UL
- ultrastructure
- UR
- urine
tatn-1 protein, C elegans Chemical MeSH Browser