AADAT (aminoadipate aminotransferase)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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51166 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Aminoadipate aminotransferase |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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AADAT |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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KAT2, KATII, KYAT2 |
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Chromosome
Chromosome number
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4 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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4q33 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a protein that is highly similar to mouse and rat kynurenine aminotransferase II. The rat protein is a homodimer with two transaminase activities. One activity is the transamination of alpha-aminoadipic acid, a final step in the saccarop |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | |||||||||||
| UniProt ID | Q8N5Z0 | ||||||||||
| Protein name | Kynurenine/alpha-aminoadipate aminotransferase, mitochondrial (KAT/AadAT) (2-aminoadipate aminotransferase) (2-aminoadipate transaminase) (EC 2.6.1.39) (Alpha-aminoadipate aminotransferase) (AadAT) (Glycine transaminase AADAT) (EC 2.6.1.4) (Kynurenine ami | ||||||||||
| Protein function | Transaminase with broad substrate specificity. Has transaminase activity towards aminoadipate, kynurenine, methionine and glutamate. Shows activity also towards tryptophan, aspartate and hydroxykynurenine. Accepts a variety of oxo-acids as amino | ||||||||||
| PDB | 2QLR , 2R2N , 2VGZ , 2XH1 , 3DC1 , 3UE8 , 4GDY , 4GE4 , 4GE7 , 4GE9 , 4GEB , 5EFS , 5EUN , 5TF5 , 6D0A , 6T8P , 6T8Q | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Higher expression in the liver. Also found in heart, brain, kidney, pancreas, prostate, testis and ovary. | ||||||||||
| Sequence | |||||||||||
| Sequence length | 425 | ||||||||||
| Interactions | View interactions | ||||||||||
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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