Erythrose 4-phosphate

Erythrose 4-phosphate

Names
IUPAC name (2R,3R)-2,3-dihydroxy-4-oxobutyl phosphate
Other names E4P
Identifiers
CAS Number	585-18-2 Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:48153 N
ChemSpider	4573609 Y
MeSH	erythrose+4-phosphate
PubChem CID	5459862
UNII	2156QF7O8M Y
InChI InChI=1S/C4H9O7P/c5-1-3(6)4(7)2-11-12(8,9)10/h1,3-4,6-7H,2H2,(H2,8,9,10)/p-2/t3-,4+/m0/s1 Y Key: NGHMDNPXVRFFGS-IUYQGCFVSA-L Y InChI=1/C4H9O7P/c5-1-3(6)4(7)2-11-12(8,9)10/h1,3-4,6-7H,2H2,(H2,8,9,10)/p-2/t3-,4+/m0/s1 Key: NGHMDNPXVRFFGS-VVTNXMPSBK
SMILES [O-]P([O-])(=O)OC[C@@H](O)[C@@H](O)C=O
Properties
Chemical formula	C4H9O7P
Molar mass	200.084 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

Erythrose 4-phosphate is a phosphate of the simple sugar erythrose. It is an intermediate in the pentose phosphate pathway and the Calvin cycle.^[1]

The enzyme transaldolase catalyzes the formation of erythrose 4-phosphate and fructose 6-phosphate from sedoheptulose 7-phosphate and glyceraldehyde 3-phosphate.^[2] This reaction is a part of the non-oxidative phase of the pentose phosphate pathway.

In the Calvin cycle, the enzyme fructose-bisphosphate aldolase catalyzes the formation of sedoheptulose 1,7-bisphosphate from erythrose 4-phosphate and dihydroxyacetone phosphate.^[3]

In addition, it serves as a precursor in the biosynthesis of the aromatic amino acids tyrosine, phenylalanine, and tryptophan. It is used in the first step of the shikimate pathway. At this stage, phosphoenolpyruvate and erythrose-4-phosphate react to form 3-deoxy-D-arabinoheptulosonate-7-phosphate (DAHP), in a reaction catalyzed by the enzyme DAHP synthase.

It also used in 3-hydroxy-1-aminoacetone phosphate biosynthesis, which is a precursor of vitamin B6 in DXP-dependent pathway. Erythrose-4-phosphate dehydrogenase is used to produce erythronate-4-phosphate.