Not available outside of the UK & Ireland.

Application

Pyruvate Kinase (PK) has been used as a sample in ATPase Assays.

Pyruvate Kinase (PK) has been used in the kinase assay.

Biochem/physiol Actions

Pyruvate kinase catalyzes the irreversible conversion of P-enolpyruvate and ADP to pyruvate and ATP with the utilization of a proton. The first step is the transfer of phosphate group from P-enolpyruvate to ADP with the formation of bound enolate of pyruvate and ATP. In the second step, a proton is added to enolate to generate the keto form of pyruvate. The enzyme also exhibits other activities, such as ATP- and bicarbonate-dependent ATPase, phosphorylation of fluoride and hydroxylamine, ATP-dependent phosphorylation of glycolate, and decarboxylation of oxaloacetate.

General description

Pyruvate kinase has a molar mass of 237,000 and exists as a tetramer. Each polypeptide chain of this tetramer has a molar mass of 57,200. The enzyme contains two identical catalytic particles called protomers. Each of these protomers contains two polypeptide chains. Each protomer contains one site each for Mn²⁺ and phosphoenolpyruvate.

Other Notes

For life science research only. Not for use in diagnostic procedures.

Physical form

Solution in 50% glycerol (v/v), pH approximately 6

Preparation Note

Activator: PK requires Mg²⁺ (or Mn²⁺, Co²⁺) and K⁺ (or NH⁴⁺, Rb⁺) for full activity.

Quality

Contaminants: ﹤0.001% GK, ﹤0.002% HK, “NADH oxidase”, and ATPase, each, ﹤0.01% enolase, LDH, and myokinase, each.

Specificity

Specific activity: Approximately 200 U/mg at +25°C with PEP as the substrate.