Glycolysis Enzymes

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'''Phosphofructokinase'''
'''Phosphofructokinase'''
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[[Phosphofructokinase_(PFK)|Phosphofructokinase]] catalyzes the second phosphorylation reaction, and is the most highly regulated step of the pathway. '''Phosphofructokinase-1''' (PFK-1) is a glycolytic enzyme that catalyzes the transfer of a phosphoryl group from <scene name='Phosphofructokinase_(PFK)/Cv/21'>ATP</scene> to <scene name='Phosphofructokinase_(PFK)/Cv/22'>fructose-6-phosphate (F6P)</scene> to yield <scene name='Phosphofructokinase_(PFK)/Cv/16'>ADP</scene> and <scene name='Phosphofructokinase_(PFK)/Cv/23'>fructose-1,6-bisphosphate (FBP)</scene>. See [[Glycolysis Enzymes]]. Mg2+ is also important in this reaction (<scene name='Phosphofructokinase_(PFK)/Cv/24'>click here to see animation of reaction</scene>). '''Phosphofructokinase-2''' (PFK-2) acts on the same substrates to yield ADP and <scene name='Phosphofructokinase_(PFK)/Cv1/3'>fructose-2,6-bisphosphate (F2,6P)</scene>. <scene name='Phosphofructokinase_(PFK)/Cv1/4'>Click here to see the difference between FBP and F2,6P</scene>. PFK reaction is strongly exergonic (irreversible) under physiological conditions and hence is one of the glycolytic pathway's rate-determining steps. In most organisms/tissues, PFK is the glycolytic pathway's major flux-regulating enzyme; its activity is controlled by the concentrations of an unusually large number of metabolites including ATP, ADP, AMP, PEP and fructose-2,6-bisphosphate.
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[[Phosphofructokinase_(PFK)|Phosphofructokinase]] catalyzes the second phosphorylation reaction, and is the most highly regulated step of the pathway. '''Phosphofructokinase-1''' (PFK-1) is a glycolytic enzyme that catalyzes the transfer of a phosphoryl group from <scene name='Phosphofructokinase_(PFK)/Cv/21'>ATP</scene> to <scene name='Phosphofructokinase_(PFK)/Cv/22'>fructose-6-phosphate (F6P)</scene> to yield <scene name='Phosphofructokinase_(PFK)/Cv/16'>ADP</scene> and <scene name='Phosphofructokinase_(PFK)/Cv/23'>fructose-1,6-bisphosphate (FBP)</scene>. Mg2+ is also important in this reaction (<scene name='Phosphofructokinase_(PFK)/Cv/24'>click here to see animation of reaction</scene>). '''Phosphofructokinase-2''' (PFK-2) acts on the same substrates to yield ADP and <scene name='Phosphofructokinase_(PFK)/Cv1/3'>fructose-2,6-bisphosphate (F2,6P)</scene>. <scene name='Phosphofructokinase_(PFK)/Cv1/4'>Click here to see the difference between FBP and F2,6P</scene>. PFK reaction is strongly exergonic (irreversible) under physiological conditions and hence is one of the glycolytic pathway's rate-determining steps. In most organisms/tissues, PFK is the glycolytic pathway's major flux-regulating enzyme; its activity is controlled by the concentrations of an unusually large number of metabolites including ATP, ADP, AMP, PEP and fructose-2,6-bisphosphate.
[[Austin_Drake_Sandbox|Aldolase]] catalyzes the retro-aldol cleavage of fructose 1,6-bisphosphate into two three carbon phosphosugars, dihydroxyacetone phosphate and glyceraldehyde-3-phosphate. The interconversion of these two sugars is catalyzed by [[Christian_Krenk_Sandbox|triose phosphate isomerase]], also referred to as TIM.
[[Austin_Drake_Sandbox|Aldolase]] catalyzes the retro-aldol cleavage of fructose 1,6-bisphosphate into two three carbon phosphosugars, dihydroxyacetone phosphate and glyceraldehyde-3-phosphate. The interconversion of these two sugars is catalyzed by [[Christian_Krenk_Sandbox|triose phosphate isomerase]], also referred to as TIM.

Revision as of 12:03, 18 July 2022

Hexokinase I complex with ATP analog, glucose, glucose-phosphate and Mg+2 ion (PDB code 1qha)

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References

  1. Lee JH, Chang KZ, Patel V, Jeffery CJ. Crystal structure of rabbit phosphoglucose isomerase complexed with its substrate D-fructose 6-phosphate. Biochemistry. 2001 Jul 3;40(26):7799-805. PMID:11425306

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