Target intelligence / Profile preview

Glutamate oxaloacetate transaminase 1 (GOT1)

Target
GOT1
Molecular classification
Enzyme, Aminotransferase, Pyridoxal phosphate-dependent enzyme
01

Overview

Glutamate oxaloacetate transaminase 1 is a cytoplasmic pyridoxal phosphate-dependent enzyme that catalyzes the reversible transamination between L-aspartate and α-ketoglutarate to form oxaloacetate and L-glutamate. It plays a central role in amino acid metabolism, the urea cycle, TCA cycle anaplerosis/cataplerosis via the malate-aspartate shuttle system for NADH transport into mitochondria. In cancer cells—especially those with KRAS mutations—GOT1 supports anabolic growth by maintaining NADPH/NADP+ balance critical for reactive oxygen species detoxification. Its upregulation is linked to tumor progression and poor prognosis; thus it is considered a promising target for anticancer drug development despite potential safety challenges due to its ubiquitous metabolic functions.

Other names
Aspartate aminotransferase, cytoplasmicGlutamic-oxaloacetic transaminase 1AATC (less common)Cytosolic aspartate aminotransferase
02

Mechanism of action

Drugs or inhibitors targeting GOT1 typically act by blocking its enzymatic activity, thereby disrupting the malate-aspartate shuttle, impairing redox homeostasis, and sensitizing cancer cells to metabolic stress such as glucose deprivation.

03

Biological functions

Amino acid metabolism (transamination between aspartate and glutamate)Urea cycle participationTricarboxylic acid (TCA) cycle involvementRegulation of cellular redox state and NADPH productionMalate-aspartate shuttle component for transferring reducing equivalents
04

Disease associations

Cancer (notably in KRAS-mutated cancers)Metabolic syndrome/obesity
05

Safety considerations

Potential safety concerns include disruption of normal amino acid metabolism and redox balance.Since GOT1 is involved in fundamental metabolic pathways across many tissues—including the brain—systemic inhibition could lead to off-target effects or toxicity related to impaired energy metabolism or neurotransmitter imbalance. These challenges are discussed when considering therapeutic targeting of this enzyme.
06

Interacting drugs

There are no widely approved drugs specifically targeting GOT1 in clinical use, but several experimental inhibitors are under investigation for cancer therapy. Examples include small-molecule GOT1 inhibitors used in preclinical studies.
07

Biomarkers

Elevated expression of GOT1 has been associated with poor prognosis in certain cancers such as lung adenocarcinoma, thyroid carcinoma, breast carcinoma, and metastatic melanoma; thus it may serve as a prognostic biomarker in these contexts.

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