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- Table of Contents
Facts about Kynurenine/alpha-aminoadipate aminotransferase, mitochondrial.
Shows activity also towards tryptophan, aspartate and hydroxykynurenine. Accepts a variety of oxo-acids as amino- group acceptors, with a preference for 2-oxoglutarate, 2- oxocaproic acid, phenylpyruvate and alpha-oxo-gamma-methiol butyric acid.
| Mouse | |
|---|---|
| Gene Name: | Aadat |
| Uniprot: | Q9WVM8 |
| Entrez: | 23923 |

| Belongs to: |
|---|
| class-I pyridoxal-phosphate-dependent aminotransferase family |

AADAT; alphaAminoadipate Aminotransferase; alpha-Aminoadipate Aminotransferase; aminoadipate aminotransferase; EC 2.6.1.39,2-aminoadipate aminotransferase; EC 2.6.1.7,2-aminoadipate transaminase; KAT/AadAT; KAT2; KAT2mitochondrial; Kynurenine aminotransferase II; Kynurenine--oxoglutarate aminotransferase II; Kynurenine--oxoglutarate transaminase II; L kynurenine/alpha aminoadipate aminotransferase
Mass (kDA):
47.598 kDA

| Mouse | |
|---|---|
| Location: | 8 B3.1|8 30.85 cM |
| Sequence: | 8; |
Expressed mainly in kidney and to a lesser amount in liver and brain.




PMID: 10441733 by Yu P., et al. Genomic organization and expression analysis of mouse kynurenine aminotransferase II, a possible factor in the pathophysiology of Huntington's disease.