Homo sapiens Gene: GOT2
Summary
InnateDB Gene IDBG-34707.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol GOT2
Gene Name glutamic-oxaloacetic transaminase 2, mitochondrial (aspartate aminotransferase 2)
Synonyms KAT4; KATIV; mitAAT
Species Homo sapiens
Ensembl Gene ENSG00000125166
Encoded Proteins
glutamic-oxaloacetic transaminase 2, mitochondrial (aspartate aminotransferase 2)
glutamic-oxaloacetic transaminase 2, mitochondrial (aspartate aminotransferase 2)
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary Glutamic-oxaloacetic transaminase is a pyridoxal phosphate-dependent enzyme which exists in cytoplasmic and inner-membrane mitochondrial forms, GOT1 and GOT2, respectively. GOT plays a role in amino acid metabolism and the urea and tricarboxylic acid cycles. The two enzymes are homodimeric and show close homology. [provided by RefSeq, Jul 2008]
Glutamic-oxaloacetic transaminase is a pyridoxal phosphate-dependent enzyme which exists in cytoplasmic and inner-membrane mitochondrial forms, GOT1 and GOT2, respectively. GOT plays a role in amino acid metabolism and the urea and tricarboxylic acid cycles. The two enzymes are homodimeric and show close homology. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2013]
Gene Information
Type Protein coding
Genomic Location Chromosome 16:58707131-58734357
Strand Reverse strand
Band q21
Transcripts
ENST00000245206 ENSP00000245206
ENST00000434819 ENSP00000394100
ENST00000494627
ENST00000496461
ENST00000492378
ENST00000564400
ENST00000568368 ENSP00000456205
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 20 experimentally validated interaction(s) in this database.
Experimentally validated
Total 20 [view]
Protein-Protein 20 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0004069 L-aspartate:2-oxoglutarate aminotransferase activity
GO:0016212 kynurenine-oxoglutarate transaminase activity
GO:0030170 pyridoxal phosphate binding
GO:0044822 poly(A) RNA binding
GO:0080130 L-phenylalanine:2-oxoglutarate aminotransferase activity
Biological Process
GO:0005975 carbohydrate metabolic process
GO:0006006 glucose metabolic process
GO:0006094 gluconeogenesis
GO:0006103 2-oxoglutarate metabolic process
GO:0006107 oxaloacetate metabolic process
GO:0006531 aspartate metabolic process
GO:0006532 aspartate biosynthetic process
GO:0006533 aspartate catabolic process
GO:0006536 glutamate metabolic process
GO:0008652 cellular amino acid biosynthetic process
GO:0009058 biosynthetic process
GO:0015908 fatty acid transport
GO:0019470 4-hydroxyproline catabolic process
GO:0019550 glutamate catabolic process to aspartate
GO:0019551 glutamate catabolic process to 2-oxoglutarate
GO:0034641 cellular nitrogen compound metabolic process
GO:0044281 small molecule metabolic process
GO:0045471 response to ethanol
GO:0097052 L-kynurenine metabolic process
Cellular Component
GO:0005739 mitochondrion
GO:0005743 mitochondrial inner membrane
GO:0005759 mitochondrial matrix
GO:0005886 plasma membrane
GO:0070062 extracellular vesicular exosome
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Gluconeogenesis pathway
Amino acid synthesis and interconversion (transamination) pathway
Myoclonic epilepsy of Lafora pathway
Metabolism of carbohydrates pathway
Metabolism of amino acids and derivatives pathway
Metabolism pathway
Disease pathway
Glucose metabolism pathway
Glycogen storage diseases pathway
KEGG
Phenylalanine metabolism pathway
Arginine and proline metabolism pathway
Phenylalanine, tyrosine and tryptophan biosynthesis pathway
Tyrosine metabolism pathway
Cysteine and methionine metabolism pathway
Alanine, aspartate and glutamate metabolism pathway
Fat digestion and absorption pathway
INOH
Phenylalanine degradation pathway
Arginine Proline metabolism pathway
Methionine Cysteine metabolism pathway
Alanine Aspartate Asparagine metabolism pathway
Glycine Serine metabolism pathway
PID NCI
Cross-References
SwissProt
TrEMBL H3BRE7
UniProt Splice Variant
Entrez Gene 2806
UniGene Hs.599470 Hs.657304
RefSeq NM_001286220 NM_002080
HUGO HGNC:4433
OMIM 138150
CCDS CCDS10801 CCDS67045
HPRD 00684
IMGT
EMBL AC012183
GenPept
RNA Seq Atlas 2806