GPT
Alanine aminotransferase 1
Also known as: ALAT1_HUMAN, ALT, ALT1, GPT1, SGPT
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P24298
- Gene
- GPT
- Ensembl
- ENSG00000167701
- Chromosome
- 8
- Canonical length
- 496 aa
- Protein class
- Enzymes, Metabolic proteins, Plasma proteins, Predicted intracellular proteins
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes cytosolic alanine aminotransaminase 1 (ALT1); also known as glutamate-pyruvate transaminase 1. This enzyme catalyzes the reversible transamination between alanine and 2-oxoglutarate to generate pyruvate and glutamate and, therefore, plays a key role in the intermediary metabolism of glucose and amino acids. Serum activity levels of this enzyme are routinely used as a biomarker of liver injury caused by drug toxicity, infection, alcohol, and steatosis. A related gene on chromosome 16 encodes a putative mitochondrial alanine aminotransaminase.[provided by RefSeq, Nov 2009]
Canonical amino-acid sequenceUniProt
496 residues, UniProt reviewed canonical sequence.
>P24298|GPT
1 MASSTGDRSQ AVRHGLRAKV LTLDGMNPRV RRVEYAVRGP IVQRALELEQ ELRQGVKKPF
61 TEVIRANIGD AQAMGQRPIT FLRQVLALCV NPDLLSSPNF PDDAKKRAER ILQACGGHSL
121 GAYSVSSGIQ LIREDVARYI ERRDGGIPAD PNNVFLSTGA SDAIVTVLKL LVAGEGHTRT
181 GVLIPIPQYP LYSATLAELG AVQVDYYLDE ERAWALDVAE LHRALGQARD HCRPRALCVI
241 NPGNPTGQVQ TRECIEAVIR FAFEERLFLL ADEVYQDNVY AAGSQFHSFK KVLMEMGPPY
301 AGQQELASFH STSKGYMGEC GFRGGYVEVV NMDAAVQQQM LKLMSVRLCP PVPGQALLDL
361 VVSPPAPTDP SFAQFQAEKQ AVLAELAAKA KLTEQVFNEA PGISCNPVQG AMYSFPRVQL
421 PPRAVERAQE LGLAPDMFFC LRLLEETGIC VVPGSGFGQR EGTYHFRMTI LPPLEKLRLL
481 LEKLSRFHAK FTLEYSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GPT can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.24
- Highest tissue expression
- 183 nTPM
Expression across tissuesHPA
Tissue
- liver: 183 nTPM
- skeletal muscle: 47 nTPM
- heart muscle: 40 nTPM
- colon: 36 nTPM
- tongue: 23 nTPM
- adipose tissue: 23 nTPM
Single-cell type
- hepatocytes: 251 nCPM
- breast lactating cells: 164 nCPM
- colonocytes: 150 nCPM
- enterocytes: 131 nCPM
- late spermatids: 96 nCPM
- foveolar cells: 79 nCPM
Immune cell
- non-classical monocyte: 0.8 nTPM
- intermediate monocyte: 0.6 nTPM
- myeloid DC: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
Brain region
- choroid plexus: 13 nTPM
- cerebellum: 12 nTPM
- cerebral cortex: 11 nTPM
- amygdala: 9.5 nTPM
- hippocampal formation: 9.4 nTPM
- basal ganglia: 7.7 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.62
- gnomAD pLI
- 0
- gnomAD missense Z
- -1
- DepMap mean gene effect
- 0
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads GPT as an antibody target. Whether an autoantibody or antibody against GPT could matter depends on whether native GPT is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GPT is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label GPT as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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