Search results for REACT_2071

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Identifier: R-HSA-70268
Species: Homo sapiens
Compartment: cytosol, mitochondrial intermembrane space, mitochondrial matrix
Pyruvate sits at an intersection of key pathways of energy metabolism. It is the end product of glycolysis and the starting point for gluconeogenesis and can be generated by the transamination of alanine. The pyruvate dehydrogenase complex can convert it to acetyl CoA (Reed and Hackert 1990), which can enter the TCA cycle or serve as the starting point for the syntheses of long-chain fatty acids, steroids, and ketone bodies depending on the tissue and metabolic state in which it is formed. It also plays a central role in balancing the energy needs of various tissues in the body. Under conditions in which oxygen supply is limiting, e.g., in exercising muscle, or in the absence of mitochondria, e.g., in red blood cells, re-oxidation of NADH produced by glycolysis cannot be coupled to the generation of ATP. Instead, re-oxidation is coupled to the reduction of pyruvate to lactate. This lactate is released into the blood and taken up primarily by the liver, where it is oxidized to pyruvate and can be used for gluconeogenesis (Cori 1981). For a recent review, see Prochownik & Wang, 2021.
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