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1 host PPP, augmenting production of NADPH and ribose 5-phosphate.
2 )G degrees for D-ribose and two species of D-ribose 5-phosphate.
3 ees for two protonation states of 2'-deoxy-D-ribose 5-phosphate.
4 ependent hydrolysis of ADP-ribose to AMP and ribose 5-phosphate.
5 ze the negative charge of the leaving group, ribose 5-phosphate.
6 d more information as compared to those from ribose 5-phosphate.
7 6PGD), nor prevented by supplementation with ribose 5-phosphate.
8 eficiency rescues age-associated declines in ribose 5-phosphate.
9            The first intermediate forms with ribose 5-phosphate.
10 ssed in isolation, cleaves ADPR into AMP and ribose-5-phosphate.
11 NADPH and the essential nucleotide component ribose-5-phosphate.
12 he nonoxidative pentose phosphate pathway to ribose-5-phosphate.
13 thesis from 4,5-dimethylphenylenediamine and ribose-5-phosphate.
14  to the equation: ADP-ribose + H2O --> AMP + ribose-5-phosphate.
15 lucose was mainly converted into lactate and ribose-5-phosphate.
16 e and in the absence of the reaction product ribose 5'-phosphate.
17 zyme hydrolyzes ADP-ribose (ADPR) to AMP and ribose 5'-phosphate.
18 ed OAADPr to the products AMP and acetylated ribose 5'-phosphate.
19 his shows that Delta(f)G degrees (2'-deoxy-D-ribose 5-phosphate(2)(-)) - Delta(f)G degrees (D-ribose
20 se 5-phosphate(2)(-)) - Delta(f)G degrees (D-ribose 5-phosphate(2)(-)) = 147.86 kJ mol(-1) at 298.15
21 cted evolution of Escherichia coli 2-deoxy-d-ribose-5-phosphate aldolase (EcDERA), we developed an ef
22 at SAICAR (succinylaminoimidazolecarboxamide ribose-5'-phosphate, an intermediate of the de novo puri
23 glycosomal ribokinase to regenerate ATP from ribose 5-phosphate and ADP.
24 onstruction of the C-glycosidic bond between ribose 5-phosphate and an oxygen-labile pyridine heteroc
25 lmonella enterica) that synthesizes PRA from ribose 5-phosphate and glutamine/asparagine.
26 . mediterranei cell-free lysate along with D-ribose 5-phosphate and phosphoenolpyruvate.
27 osphate isomerases (EC 5.3.1.6) interconvert ribose 5-phosphate and ribulose 5-phosphate.
28 , identified binding sites for the substrate ribose 5-phosphate and the activator alpha-D-glucose 1,6
29 nceivably through Michael-type addition of d-ribose-5-phosphate and dephosphorylation.
30  and then this intermediate is hydrolyzed to ribose-5-phosphate and inorganic phosphate.
31 hat interconvert alpha-D-ribose 5-phosphate (ribose 5-phosphate) and alpha-D-ribose 1-phosphate (ribo
32 haride analogues, D-arabinose 5-phosphate, D-ribose 5-phosphate, and 2-deoxy-D-ribose 5-phosphate, we
33 pyridoxal 5'-phosphate (PLP) from glutamine, ribose 5-phosphate, and glyceraldehyde 3-phosphate.
34 rapid hydrolysis of p-nitrophenyl phosphate, ribose-5-phosphate, and phosphotyrosine.
35 reased the conversion of triosephosphates to ribose-5-phosphate, and strongly inhibited the developme
36 eptulose 7-phosphate as the C(3) donor and D-ribose 5-phosphate as the C(5) acceptor.
37 lyze the conversion of ribose-1-phosphate to ribose-5-phosphate, enabling the Pi mop to remove large
38 edoheptulose 7-phosphate, failure to recycle ribose 5-phosphate for the oxidative PPP, depleted NADPH
39 o produce NADPH for antioxidant function and ribose-5-phosphate for nucleotide synthesis.
40 dditive effects on the reaction rate so that ribose-5-phosphate forms at high specificity under mild,
41 ltransferases, and catalyzes the transfer of ribose 5-phosphate from alpha-d-5-phosphoribosyl-1-pyrop
42 ed the formation of RNA nucleoside precursor ribose-5-phosphate from 6-phosphogluconate.
43 bose, glucose, glycerylaldehyde-3-phosphate, ribose-5-phosphate, glucose-6-phosphate, and mannose-6-p
44 id, form glycosidic linkages with ribose and ribose-5-phosphate in water to produce nucleosides and n
45 olite analysis identified acylcarnitines and ribose-5-phosphate increasing in the BMI > 32 group and
46  The crystal structure of the complex with D-ribose-5-phosphate indicated that the phosphosugar is bo
47                         p-Nitrophenyl beta-D-ribose 5'-phosphate is a poor substrate of PfOPRT and Hs
48 y enriched [(14)C]orotic acid show that when ribose 5'-phosphate is deleted from substrate orotidine
49 s on CAIR and N5-CAIR analogues in which the ribose 5'-phosphate is replaced with a methyl group.
50 ventions suggested by this algorithm, genes (ribose 5-phosphate isomerase and ribulose 5-phosphate 3-
51 t homologs of triose phosphate isomerase and ribose 5-phosphate isomerase B, were necessary, as previ
52 reas other targets, such as glyoxalase I and ribose 5-phosphate isomerase, detoxify byproducts from g
53 ression of hexokinase II, transketolase, and ribose-5-phosphate isomerase genes involved in glycolysi
54 tions to an exonic insertion of ONSEN in the ribose-5-phosphate-isomerase 2 gene.
55                                              Ribose-5-phosphate isomerases (EC 5.3.1.6) interconvert
56 ences steady-state concentrations of 5'-GMP, ribose-5-phosphate, ketone bodies, and purines.
57 inder of the cavity binds the nicotinate and ribose-5'-phosphate moieties, which are nestled within t
58           Recently, we have identified the D-ribose-5-phosphate origin of the dioxane unit and demons
59 dent apoptosis through controlling NADPH and ribose 5-phosphate production via the pentose phosphate
60 vage of pseudouridine 5'-phosphate, yielding ribose 5-phosphate (R5P) and uracil via a Schiff base in
61 2dR5P), as an alternate substrate, but not D-ribose 5-phosphate (R5P) nor the four carbon analogue D-
62 n complex with phosphoenolpyruvate (PEP) and ribose 5-phosphate (R5P), and with a bisubstrate inhibit
63  of a crystal structure of MtbPYK with bound ribose 5-phosphate (R5P), combined with biochemical anal
64                 Here we use TEM to show that ribose-5-phosphate (R5P) glycation of collagen fibrils -
65 ite of the PLP synthase subunit, Pdx1, where ribose-5-phosphate (R5P), glyceraldehyde-3-phosphate (G3
66 e OPPP, ribulose-5-phosphate is converted to ribose-5-phosphate (R5P)-required for purine nucleotide
67                            The K(i) value of ribose 5'-phosphate, representing the part of the natura
68 uperfamily members that interconvert alpha-D-ribose 5-phosphate (ribose 5-phosphate) and alpha-D-ribo
69 of succinyl-5-aminoimidazole-4-carboxamide-1-ribose-5'-phosphate (SAICAR), a metabolite abundant in p
70                          After coupling with ribose 5-phosphate, the resulting C-nucleoside undergoes
71 anges that occur upon binding of purines and ribose 5'-phosphate to HGPRT.
72 ynthase, which catalyzes the attachment of D-ribose-5-phosphate to prealnumycin by formation of the C
73 is derived from D-fructose 6-phosphate and D-ribose 5-phosphate via a transaldol reaction catalyzed b
74 -phosphate) and nucleotide metabolism (via D-ribose 5-phosphate) was associated with perturbations in
75 ribose 5-[(18)O(3)]phosphate and [U-(13)C(5)]ribose 5-phosphate were analyzed by mass spectrometry.
76 osphate, D-ribose 5-phosphate, and 2-deoxy-D-ribose 5-phosphate, were separately condensed with (Z)-
77 nd therefore activates the PPP for NADPH and ribose-5-phosphate, which consequently detoxifies intrac
78 y of 6-PG for oxidative decarboxylation to D-ribose-5-phosphate, which is essential for the utilizati
79  that converts glycolytic intermediates into ribose-5-phosphate without production of NADPH.