2.7.1.90	diphosphate + D-fructose 6-phosphate	-	
2.7.1.90	diphosphate + D-fructose 6-phosphate	physiological role of the enzyme	
2.7.1.90	diphosphate + D-fructose 6-phosphate	regulatory role in glucose metabolism	
2.7.1.90	diphosphate + D-fructose 6-phosphate	Prevotella copri is able to grow in minimal media containing xylose or hemicelluloses as the sole carbon source. The organism converts C5-sugars via the sedoheptulose-1,7-bisphosphate pathway (SBPP) to connect pentose metabolism with glycolysis. To circumvent the transaldolase reaction, Prevotella copri uses the combined catalysis of a pyrophosphate-dependent phosphofructokinase and a fructose-bisphosphate aldolase	
2.7.1.90	diphosphate + D-fructose 6-phosphate	the enzyme is required for efficient methanotrophic growth of Methylomicrobium alcaliphilum 20Z	
2.7.1.90	diphosphate + D-fructose 6-phosphate	the enzyme regulates sucrose metabolism	
2.7.1.90	diphosphate + sedoheptulose 7-phosphate	the pentose phosphate pathway of cellulolytic clostridia relies on pyrophosphate-dependent 6-phosphofructokinase instead of transaldolase	
2.7.1.90	additional information	enzyme is involved in maintaining a pH-gradient in tonoplast by regenerating diphosphate in reverse reaction	
2.7.1.90	additional information	involved in control of salt stress	
2.7.1.90	additional information	isolation of a 20-bp cis regulatory element from the AtPFPalpha2 5' upstream sequence. This sequence directs the normal expression of this gene in Arabidopsis. When fused to the -46 CaMV35S minimal promoter, this isolated cis element is sufficient to drive the strong expression of the GUS reporter gene in trichomes of Arabidopsis leaves in a manner that is characteristic of AtPFPalpha2 gene expression	
2.7.1.90	additional information	PFP influences the ability of young, biosynthetically active sugarcane culm tissue to accumulate sucrose but that the equilibrium of the glycolytic intermediates, including the stored sucrose, is restored when ATP-dependent phosphofructokinase and the residual PFP activity is sufficient to sustain the required glycolytic flux as the tissue matures. It suggests a role for PFP in glycolytic carbon flow, which could be rate limiting under conditions of high metabolic activity