Glucokinase, phosphofructokinase-1, pyruvate kinase
PKD is caused by a deficiency in the enzyme, pyruvate kinase.
Pyruvate kinase deficiency (PKD) is part of a group of disorders called hereditary nonspherocytic hemolytic anemias.
pyruvate
Yes, Mg2+ is a cofactor for the enzymes phosphofructo kinase-1, phosphoglycerate kinase, enolase, and pyruvate kinase in glycolysis.
pyruvate carboxylase and phosphoenolpyruvate carboxykinase (PEPCK)
There are very many enzymes involved. A few from glycolysis are: hexokinase and glucokinase, phosphohexose isomerase, phosphofructokinase, pyruvate kinase; from pyruvate decarboxylation are pyruvate dehydrogenase phosphatase and pyruvate dehydrogenase kinase; and a few from the Kreb's cycle are: aconitase, alpha-ketoglutamate dehydrogenase, succinate thiokinase, and fumarase.
A diagnosis of PKD can be made by measuring the amount of pyruvate kinase in red blood cells.
The lactate is taken to the liver and converted back to pyruvate.
Caucasians of northern and central European decent are more likely to have the 1529A mutations, individuals of southern European descent usually have the 1456T mutation,
Philip Dykshoorn has written: 'Identification of an upstream activating sequence of the yeast pyruvate kinase gene (PYK)'
this is shamefully vague question. In glycolysis, glucose and (hexokinase, phosphogluco-mutase, aldolase, triose-phosphate isomerase, glyceraldehyde-phosphate dehydrogenase, phosphoglycerate-kinase, phosphoglycerate mutase, enolase and pyruvate kinase) enzymes are used.