Gene Ontology annotation through association of InterPro records with GO terms

Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara

Combined Automated Annotation using Multiple IEA Methods

cDNA cloning, genomic structure, chromosomal mapping, and functional expression of a novel human alanine aminotransferase.

Quantitative high-confidence human mitochondrial proteome and its dynamics in cellular context.

PXLP-K341-GPT2 transaminates PYR to form L-Ala

PXLP-K341-GPT2 transaminates L-Ala to form PYR

Complete amino acid sequence of human liver cytosolic alanine aminotransferase (GPT) determined by a combination of conventional and mass spectral methods.

Detection of the mitochondrial and catalytically active alanine aminotransferase in human tissues and plasma.

Loss of function mutation in glutamic pyruvate transaminase 2 (GPT2) causes developmental encephalopathy.

Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features.

Normally fetched curated UniProt record for human GPT2