JavaScript is disabled in your browser. Please enable JavaScript to view this website.

GPT

GeneName

GPT

Summary

GPT, also known as ALT, Gpp, or glutamate pyruvate transaminase, is a 55 kDa enzyme primarily located in the cytosol and cytoplasm, with some presence in extracellular exosomes. It catalyses the transamination reaction between L-alanine and 2-oxoglutarate, producing pyruvate and glutamate, thus playing a vital role in amino acid metabolism and the biosynthesis of various biomolecules. This enzyme is crucial for the catabolism of L-alanine, contributing to energy production and metabolic homeostasis.

Importance

GPT is relevant to: - Metabolic disorders, as it is involved in amino acid metabolism and energy production - Liver function assessments, since elevated levels of GPT are often indicative of liver damage or disease - Research into metabolic pathways, particularly those involving amino acid catabolism and biosynthesis - Understanding the role of transaminases in various physiological and pathological processes

Top Products

For researchers studying GPT, we recommend the well-cited polyclonal antibody, Anti-Alanine Transaminase antibody (ab231715). This antibody is particularly effective for Western blotting (WB) and immunohistochemistry (IHC), making it a reliable choice for various applications in your research. With its citation count of 1, it demonstrates a growing recognition in the scientific community. The ALT Assay Kit (384 well, Colorimetric/Fluorometric) (ab241035) is a reliable option for researchers looking to measure GPT levels, supported by 8 citations.

Abcam Product Citation Summary

The use of the Abcam antibody ab234578 in a humanized liver mouse model highlights its relevance in studying GPT in the context of HBV infection. This suggests a potential role for GPT in liver-related diseases and viral infections.

Abcam Product Citation Table

Product Code
Species
Application
Study Context
PMID
ab234578
Mouse
HBV infection
31097716

Function

Catalyzes the reversible transamination between alanine and 2-oxoglutarate to form pyruvate and glutamate. Participates in cellular nitrogen metabolism and also in liver gluconeogenesis starting with precursors transported from skeletal muscles (By similarity).

Pathway

Amino-acid degradation; L-alanine degradation via transaminase pathway; pyruvate from L-alanine: step 1/1.

Sequence Similarities

Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family. Alanine aminotransferase subfamily.

Tissue Specificity

Liver, kidney, heart, and skeletal muscles. Expressed at moderate levels in the adipose tissue.

Cellular localization

Alternative names

AAT1, GPT1, GPT, Alanine aminotransferase 1, ALT1, Glutamate pyruvate transaminase 1, Glutamic--alanine transaminase 1, Glutamic--pyruvic transaminase 1, GPT 1

swissprot:P24298 entrezGene:2875 omim:138200