Target intelligence / Profile preview

Pyruvate Kinase Liver and Red Blood Cell Isoform (None)

Target
None
Molecular classification
Enzyme
01

Overview

Pyruvate kinase is a key glycolytic enzyme that catalyzes the final step of glycolysis: the transfer of a phosphate group from phosphoenolpyruvate (PEP) to adenosine diphosphate (ADP), producing pyruvate and adenosine triphosphate (ATP). The liver and red blood cell isoforms—PKL and PKR—are both encoded by the PKLR gene. Mutations in the PKLR gene can cause pyruvate kinase deficiency—a common cause of hereditary nonspherocytic hemolytic anemia due to impaired ATP production in erythrocytes.

02

Mechanism of action

Catalyzes the transfer of a phosphate group from phosphoenolpyruvate (PEP) to adenosine diphosphate (ADP), producing pyruvate and adenosine triphosphate (ATP).

03

Biological functions

GlycolysisATP generationRegulation of glucose homeostasis
04

Disease associations

Pyruvate kinase deficiencyHereditary nonspherocytic hemolytic anemia
05

Safety considerations

Therapeutic interventions may disrupt glycolysis.

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