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1 zation of glycolaldehyde to give threose and erythrose.
2 in a yield of 3.5% based on the ratio of His/erythrose.
3                                      A new d-erythrose 1,3-dioxane derivative was synthesized from d-
4 rom easily accessible 2,3-O-isopropylidene-d-erythrose (2b), and the combination of a strategic intra
5   We show that epd (gapB) mutants lacking an erythrose 4-phosphate (E4P) dehydrogenase are impaired f
6 value was inconsistent with the formation of erythrose 4-phosphate (E4P) exclusively by the carboxyla
7 densation of phosphoenolpyruvate (PEP) and D-erythrose 4-phosphate (E4P) with the formation of DAHP.
8 ding aldose: arabinose 5-phosphate (A5P) and erythrose 4-phosphate (E4P), respectively.
9 osphate (R5P) nor the four carbon analogue D-erythrose 4-phosphate (E4P).
10 vate (PEP), arabinose 5-phosphate (A5P), and erythrose 4-phosphate (E4P).
11 zes the isomerization of DXP to 2-C-methyl-D-erythrose 4-phosphate (MEsP) and subsequent NADPH-depend
12 hosphoenolpyruvate = 9.5-13 microm, Km for d-erythrose 4-phosphate = 57.3-350.1 microm, and kcat = 2.
13 s two natural substrates and two inhibitors, erythrose 4-phosphate and mannitol 1-phosphate, were inv
14 DAH 7-P synthase for its normal substrates D-erythrose 4-phosphate and PEP and provide direct evidenc
15 zyme does not catalyze the condensation of D-erythrose 4-phosphate and phosphoenolpyruvate to form 3-
16 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 how that Sad can substitute for the roles of erythrose 4-phosphate dehydrogenase in pyridoxal 5'-phos
20 e inferred intermediacy of 1-deoxy-1-imino-D-erythrose 4-phosphate in Amycolatopsis mediterranei cell
21                                              Erythrose 4-phosphate is epimerized and/or isomerized to
22 activation by phosphoenolpyruvate, whereas d-erythrose 4-phosphate offers only minimal protection.
23 he step(s) from either phosphoenolpyruvate/d-erythrose 4-phosphate or other precursors to 3,4-dideoxy
24 L-3-tetrulose-4-phosphate was converted to D-erythrose 4-phosphate through three previously unknown i
25 ldol condensation of phosphoenolpyruvate and erythrose 4-phosphate to form 3-deoxy-D-arabino-heptulos
26 the condensation of phosphoenolpyruvate, and erythrose 4-phosphate to form 3-deoxy-D-arabino-heptulos
27  in catalyzing the addition of pyruvate to d-erythrose 4-phosphate to form DAHP.
28 ments show that threitol is synthesized from erythrose 4-phosphate, a C(4) intermediate in the PPP.
29 ng carbohydrate metabolism exclusively via D-erythrose 4-phosphate, a pathway that may provide clues
30 ative form and in complex with the inhibitor erythrose 4-phosphate, and with the substrate glucose 6-
31 obtained label via the chorismate route from erythrose 4-phosphate, generated via the pentose phospha
32 nolpyruvate and d-arabinose 5-phosphate or d-erythrose 4-phosphate, respectively.
33 aves SBP into dihydroxyacetone phosphate and erythrose 4-phosphate.
34 diomyocytes by modulating PGI activity using erythrose 4-phosphate.
35 eavage of the ribityl tail to form DMB and D-erythrose 4-phosphate.
36 hat the product formed by KDOP synthase with erythrose-4-P as the substrate was 3-deoxy-D-ribo-heptul
37 f the ability of KDOP synthase to substitute erythrose-4-P for arabinose-5-P is (i) recognition of th
38 ability to replace arabinose-5-P with either erythrose-4-P or ribose-5-P as alternative substrates.
39              Based on the precedent of the d-erythrose-4-phosphate (E4P) modeled in the active site o
40 densation of phosphoenolpyruvate (PEP) and d-erythrose-4-phosphate (E4P) with the formation of DAHP.
41                   The S0.5 was 35 microM for erythrose-4-phosphate and 5.3 microM for phosphoenolpyru
42  Phe, the enzyme loses the ability to bind D-erythrose-4-phosphate and binds phosphoenolpyruvate in a
43 rbolic mixed-type inhibition with respect to erythrose-4-phosphate and partial noncompetitive inhibit
44 ,4-DHB (1) involved phosphoenol pyruvate and erythrose-4-phosphate as ultimate precursors.
45 ne in Vibrio cholerae (epd) which encodes an erythrose-4-phosphate dehydrogenase activity and is loca
46 eration of the tricarboxylic acid cycle, and erythrose-4-phosphate inhibits 6-phosphogluconate dehydr
47                                            D-erythrose-4-phosphate is then converted by enzymes of th
48 sphate isomerase; renamed EryH), and RpiB (D-erythrose-4-phosphate isomerase; renamed EryI), a pathwa
49  the condensation of phosphoenolpyruvate and erythrose-4-phosphate to form 3-deoxy-D-arabino-heptulos
50 ke condensation of phosphoenolpyruvate and D-erythrose-4-phosphate with the formation of 3-deoxy-D-ar
51 tolase activity is required in cells to make erythrose-4-phosphate, a precursor of aromatic amino aci
52     In eukaryotes, adventitious oxidation of erythrose-4-phosphate, an intermediate of the pentose ph
53 is shown to interfere with the production of erythrose-4-phosphate, which is essential for the first
54  and histidine synthesis-and subsequently to erythrose-4-phosphate, which is required for synthesis o
55 tent with the isotopomer distribution of the erythrose-4-phosphate-derived amino acids phenylalanine
56 ically requires synthesis of R5P rather than erythrose-4-phosphate.
57 ation of DAHP from phosphoenolpyruvate and D-erythrose-4-phosphate.
58 ctivated the enzyme at low concentrations of erythrose-4-phosphate.
59 nversions of glycolaldehyde, glyceraldehyde, erythrose, a heptose, and glucosamine are also demonstra
60            Mode of action studies with the D-erythrose analogues established that 8b acted by inhibit
61 o measured with the alternative substrates D-erythrose and D-ribose, making SalM the first reported s
62 round by employing a combination of [4-(13)C]erythrose and deuterated pyruvate during growth on deute
63 etaldehyde took place by the condensation of erythrose and formamidine, two compounds that are known
64 nts vary markedly in both their affinity for erythrose and their catalytic capacity (turnover number)
65 phate, glyceraldehyde 3-phosphate, ribulose, erythrose, and sucrose as potential precursors of plant
66 the sodA sodB strain against the toxicity of erythrose as did the carbonyl-blocking reagents hydrazin
67                                              Erythrose inhibited the growth of a sodA sodB strain of
68                   Third, glyceraldehyde- and erythrose-labeling studies showed increased incorporatio
69 hibition led to increased glyceraldehyde and erythrose levels in the cell.
70 on converted fructose plus glyceraldehyde to erythrose plus xylulose, the same products as are formed
71 l step of erythritol synthesis (reduction of erythrose to erythritol), is not characterized.
72 man ADH1 and SORD catalyze the conversion of erythrose to erythritol, pointing to novel roles for two
73  Both recombinant human ADH1 and SORD reduce erythrose to erythritol, using NADPH as a co-factor, and
74 iver capable of catalyzing the conversion of erythrose to erythritol: alcohol dehydrogenase 1 (ADH1)
75  derived from dihydroxyacetone phosphate and erythrose via an aldolase reaction.
76         The asymmetric effect is largest for erythrose, which may reach a D-enantiomeric excess of >8
77 complished experimentally by the reaction of erythrose with formamidine followed by a Strecker synthe
78 increased activity for the aldol reaction of erythrose with pyruvate compared with the wild-type enzy