ライフサイエンスコーパス: erythrose 4-phosphate

1 aves SBP into dihydroxyacetone phosphate and erythrose 4-phosphate.

2 diomyocytes by modulating PGI activity using erythrose 4-phosphate.

3 eavage of the ribityl tail to form DMB and D-erythrose 4-phosphate.

4 ically requires synthesis of R5P rather than erythrose-4-phosphate.

5 ation of DAHP from phosphoenolpyruvate and D-erythrose-4-phosphate.

6 ctivated the enzyme at low concentrations of erythrose-4-phosphate.

7 hosphoenolpyruvate = 9.5-13 microm, Km for d-erythrose 4-phosphate = 57.3-350.1 microm, and kcat = 2.

8 ments show that threitol is synthesized from erythrose 4-phosphate, a C(4) intermediate in the PPP.

9 ng carbohydrate metabolism exclusively via D-erythrose 4-phosphate, a pathway that may provide clues

10 tolase activity is required in cells to make erythrose-4-phosphate, a precursor of aromatic amino aci

11 In eukaryotes, adventitious oxidation of erythrose-4-phosphate, an intermediate of the pentose ph

12 s two natural substrates and two inhibitors, erythrose 4-phosphate and mannitol 1-phosphate, were inv

13 DAH 7-P synthase for its normal substrates D-erythrose 4-phosphate and PEP and provide direct evidenc

14 zyme does not catalyze the condensation of D-erythrose 4-phosphate and phosphoenolpyruvate to form 3-

15 The S0.5 was 35 microM for erythrose-4-phosphate and 5.3 microM for phosphoenolpyru

16 Phe, the enzyme loses the ability to bind D-erythrose-4-phosphate and binds phosphoenolpyruvate in a

17 rbolic mixed-type inhibition with respect to erythrose-4-phosphate and partial noncompetitive inhibit

18 ative form and in complex with the inhibitor erythrose 4-phosphate, and with the substrate glucose 6-

19 of DAH7P synthase the two substrates PEP and erythrose 4-phosphate appear to bind in a configuration

20 ,4-DHB (1) involved phosphoenol pyruvate and erythrose-4-phosphate as ultimate precursors.

21 cation with transketolase, which increases d-erythrose 4-phosphate availability, afforded 16 g/L 3-de

22 icular, [6-13C]hexose 6-phosphate and [4-13C]erythrose 4-phosphate carbon enrichment values resulting

23 how that Sad can substitute for the roles of erythrose 4-phosphate dehydrogenase in pyridoxal 5'-phos

24 ne in Vibrio cholerae (epd) which encodes an erythrose-4-phosphate dehydrogenase activity and is loca

25 tent with the isotopomer distribution of the erythrose-4-phosphate-derived amino acids phenylalanine

26 We show that epd (gapB) mutants lacking an erythrose 4-phosphate (E4P) dehydrogenase are impaired f

27 value was inconsistent with the formation of erythrose 4-phosphate (E4P) exclusively by the carboxyla

28 densation of phosphoenolpyruvate (PEP) and D-erythrose 4-phosphate (E4P) with the formation of DAHP.

29 ding aldose: arabinose 5-phosphate (A5P) and erythrose 4-phosphate (E4P), respectively.

30 osphate (R5P) nor the four carbon analogue D-erythrose 4-phosphate (E4P).

31 vate (PEP), arabinose 5-phosphate (A5P), and erythrose 4-phosphate (E4P).

32 Based on the precedent of the d-erythrose-4-phosphate (E4P) modeled in the active site o

33 densation of phosphoenolpyruvate (PEP) and d-erythrose-4-phosphate (E4P) with the formation of DAHP.

34 obtained label via the chorismate route from erythrose 4-phosphate, generated via the pentose phospha

35 e inferred intermediacy of 1-deoxy-1-imino-D-erythrose 4-phosphate in Amycolatopsis mediterranei cell

36 eration of the tricarboxylic acid cycle, and erythrose-4-phosphate inhibits 6-phosphogluconate dehydr

37 Erythrose 4-phosphate is epimerized and/or isomerized to

38 D-erythrose-4-phosphate is then converted by enzymes of th

39 sphate isomerase; renamed EryH), and RpiB (D-erythrose-4-phosphate isomerase; renamed EryI), a pathwa

40 zes the isomerization of DXP to 2-C-methyl-D-erythrose 4-phosphate (MEsP) and subsequent NADPH-depend

41 activation by phosphoenolpyruvate, whereas d-erythrose 4-phosphate offers only minimal protection.

42 he step(s) from either phosphoenolpyruvate/d-erythrose 4-phosphate or other precursors to 3,4-dideoxy

43 nolpyruvate and d-arabinose 5-phosphate or d-erythrose 4-phosphate, respectively.

44 L-3-tetrulose-4-phosphate was converted to D-erythrose 4-phosphate through three previously unknown i

45 ldol condensation of phosphoenolpyruvate and erythrose 4-phosphate to form 3-deoxy-D-arabino-heptulos

46 the condensation of phosphoenolpyruvate, and erythrose 4-phosphate to form 3-deoxy-D-arabino-heptulos

47 in catalyzing the addition of pyruvate to d-erythrose 4-phosphate to form DAHP.

48 the condensation of phosphoenolpyruvate and erythrose-4-phosphate to form 3-deoxy-D-arabino-heptulos

49 is shown to interfere with the production of erythrose-4-phosphate, which is essential for the first

50 and histidine synthesis-and subsequently to erythrose-4-phosphate, which is required for synthesis o

51 ke condensation of phosphoenolpyruvate and D-erythrose-4-phosphate with the formation of 3-deoxy-D-ar