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. 1974 Sep;141(3):725–728. doi: 10.1042/bj1410725

Properties of the phosphonomethyl isosteres of two phosphate ester glycolytic intermediates

Donald Stribling 1,*
PMCID: PMC1168178  PMID: 4377104

Abstract

The enzymic synthesis of the 1-phosphonomethyl isostere of fructose 1,6-diphosphate in which the 1-phosphate (–OPO3H2) is replaced by the phosphonomethyl group (–CH2PO3H2) is described. The kinetic properties of this fructose diphosphate isostere and of 4-hydroxy-3-oxobutylphosphonic acid, an isostere of dihydroxyacetone phosphate, with aldolase (EC 4.1.2.13), fructose diphosphatase (EC 3.1.3.11) and glycerol phosphate dehydrogenase (EC 1.1.1.8) are described (see Table 1).

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Selected References

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