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1 eavage of the ribityl tail to form DMB and D-erythrose 4-phosphate.
2 ation of DAHP from phosphoenolpyruvate and D-erythrose-4-phosphate.
3 ctivated the enzyme at low concentrations of erythrose-4-phosphate.
4 hosphoenolpyruvate = 9.5-13 microm, Km for d-erythrose 4-phosphate = 57.3-350.1 microm, and kcat = 2.
5 ments show that threitol is synthesized from erythrose 4-phosphate, a C(4) intermediate in the PPP.
6 ng carbohydrate metabolism exclusively via D-erythrose 4-phosphate, a pathway that may provide clues
7 tolase activity is required in cells to make erythrose-4-phosphate, a precursor of aromatic amino aci
8 s two natural substrates and two inhibitors, erythrose 4-phosphate and mannitol 1-phosphate, were inv
9 DAH 7-P synthase for its normal substrates D-erythrose 4-phosphate and PEP and provide direct evidenc
10 zyme does not catalyze the condensation of D-erythrose 4-phosphate and phosphoenolpyruvate to form 3-
12 Phe, the enzyme loses the ability to bind D-erythrose-4-phosphate and binds phosphoenolpyruvate in a
13 rbolic mixed-type inhibition with respect to erythrose-4-phosphate and partial noncompetitive inhibit
14 ative form and in complex with the inhibitor erythrose 4-phosphate, and with the substrate glucose 6-
15 of DAH7P synthase the two substrates PEP and erythrose 4-phosphate appear to bind in a configuration
17 cation with transketolase, which increases d-erythrose 4-phosphate availability, afforded 16 g/L 3-de
18 icular, [6-13C]hexose 6-phosphate and [4-13C]erythrose 4-phosphate carbon enrichment values resulting
19 ne in Vibrio cholerae (epd) which encodes an erythrose-4-phosphate dehydrogenase activity and is loca
20 tent with the isotopomer distribution of the erythrose-4-phosphate-derived amino acids phenylalanine
21 We show that epd (gapB) mutants lacking an erythrose 4-phosphate (E4P) dehydrogenase are impaired f
22 value was inconsistent with the formation of erythrose 4-phosphate (E4P) exclusively by the carboxyla
23 densation of phosphoenolpyruvate (PEP) and D-erythrose 4-phosphate (E4P) with the formation of DAHP.
28 densation of phosphoenolpyruvate (PEP) and d-erythrose-4-phosphate (E4P) with the formation of DAHP.
29 obtained label via the chorismate route from erythrose 4-phosphate, generated via the pentose phospha
30 e inferred intermediacy of 1-deoxy-1-imino-D-erythrose 4-phosphate in Amycolatopsis mediterranei cell
33 sphate isomerase; renamed EryH), and RpiB (D-erythrose-4-phosphate isomerase; renamed EryI), a pathwa
34 zes the isomerization of DXP to 2-C-methyl-D-erythrose 4-phosphate (MEsP) and subsequent NADPH-depend
35 activation by phosphoenolpyruvate, whereas d-erythrose 4-phosphate offers only minimal protection.
36 he step(s) from either phosphoenolpyruvate/d-erythrose 4-phosphate or other precursors to 3,4-dideoxy
38 L-3-tetrulose-4-phosphate was converted to D-erythrose 4-phosphate through three previously unknown i
39 ldol condensation of phosphoenolpyruvate and erythrose 4-phosphate to form 3-deoxy-D-arabino-heptulos
40 the condensation of phosphoenolpyruvate, and erythrose 4-phosphate to form 3-deoxy-D-arabino-heptulos
42 the condensation of phosphoenolpyruvate and erythrose-4-phosphate to form 3-deoxy-D-arabino-heptulos
43 is shown to interfere with the production of erythrose-4-phosphate, which is essential for the first
44 ke condensation of phosphoenolpyruvate and D-erythrose-4-phosphate with the formation of 3-deoxy-D-ar
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