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1 phoribulokinase), and part of cbbT (encoding transketolase).
2 tion by ribokinase and further metabolism by transketolase.
3 or substrate binding were examined for human transketolase.
4 vered a mechanism by which null mutations in transketolase A (tktA) and glycerol-3-phosphate (G3P) de
5 ate cyclase two-hybrid system, we found that transketolase A (TktA) interacts with MarR.
6 ldtype strain by the presence of an isozyme, transketolase A (TktA).
7 crease in the fraction of ribose derived via transketolase, a thiamine-dependent enzyme in the pentos
8   Finally, we propose a two-species model of transketolase activation that describes the interconvers
9 utcome measure was 15% change in erythrocyte transketolase activity (ETKA) in group 3.
10 serum and erythrocyte magnesium, erythrocyte transketolase activity (ETKA), lactate dehydrogenase (LD
11                                              Transketolase activity is required in cells to make eryt
12 eveal the crucial importance of the level of transketolase activity to provide the precursor for synt
13 atic testing confirmed significantly reduced transketolase activity.
14 m microtubules by washing with salt included transketolase, alpha-enolase, and betaB2-crystallin.
15 ypyruvate (HPA) donor substrate to wild-type transketolase and a variant, S385Y/D469T/R520Q, that is
16 ns with synthesis, by the combined action of transketolase and aldolase, of the seven-carbon bisphosp
17 , three- to fivefold increased expression of transketolase and glutathione reductase.
18 de in genes encoding phosphoribulokinase and transketolase and in the gene encoding the LysR-type tra
19 ethyl thiamine pyrophosphate intermediate of transketolase and inactivating this enzyme.
20 PAGE (-DTT) resolved mouse serum albumin and transketolase and indicated that serum albumin was 13% o
21  bears homology to the equivalent domains in transketolase and the E1 subunit of pyruvate dehydrogena
22 abel in the glucose moiety was scrambled via transketolase and transaldolase activities of the pentos
23                                     Separate transketolase and transaldolase fluxes could be distingu
24 n assumptions about the reversibility of the transketolase and transaldolase reactions in the nonoxid
25  represent a novel class of highly conserved transketolases and likely plays a key role in the biosyn
26 etion increased expression of hexokinase II, transketolase, and ribose-5-phosphate isomerase genes in
27 tion factor 2, glucose-regulated protein 78, transketolase, and succinyl-CoA transferase were primari
28 ity again revealed the two distinct forms of transketolase at a TK(high):TK(low) ratio that matched t
29 ent functional pathway that operates through transketolase B (TktB), and which is 'buffered' in wildt
30 Serum albumin from cornea was separated from transketolase by SDS-PAGE (+/-dithiothreitol [DTT]) and
31 ional protein domains was examined using the transketolase C-terminal (TKC)-domain as an example.
32 ced nucleic acid production through impaired transketolase catalysis is the underlying biochemical di
33 mposed of a full-length Arabidopsis thaliana transketolase cDNA under the control of the cauliflower
34 ase multienzyme complex E1 subunit and yeast transketolase crystal structures indicates a general str
35                                              Transketolase deficiency is one of a growing list of inb
36                                              Transketolase deficiency reduces NADPH synthesis and nuc
37  also known as DHTKD1, dehydrogenase E1, and transketolase domain-containing protein 1) is a thiamin
38 utosomal-recessively inherited deficiency of transketolase, encoded by TKT, on chromosome 3p21.
39  thiamine and benfotiamine therapy increased transketolase expression in renal glomeruli, increased t
40 s increased further by knockdown of nrf2 and transketolase expression.
41 ng mediation by nrf2 and related increase of transketolase expression.
42 ulate the three individual transaldolase and transketolase extents of reversibility.
43 glucose, fructose induces thiamine-dependent transketolase flux and is preferentially metabolized via
44 or the in vitro determination of activity of transketolase from Escherichia coli (TKec) using commerc
45      Moreover, the up-regulation of specific transketolase genes (tktAB) suggests the importance of t
46 perglycemia in which increased expression of transketolase has a pivotal role.
47                                   The enzyme transketolase has been employed as a catalyst for asymme
48                                              Transketolase HPA affinity again revealed the two distin
49 systems, scale-up of the reaction and use of transketolase in multi-enzyme experiments.
50 histidine is distinct from its role in yeast transketolase in which it aids in binding donor substrat
51 a brief overview of the use of aldolases and transketolases in the synthesis of sugars, sugar analogs
52 t activation of the nonoxidative PPP enzyme, transketolase, in imatinib-resistant CML cells.
53  and II in the same monomer, whereas that of transketolase is located at the interface of the dimer.
54 i pyruvate dehydrogenase and His263 in yeast transketolase, is on a largely ordered phosphorylation l
55                      Finally, inhibiting the transketolase isoenzyme transketolase-like 1 (TKTL1) by
56 se) or leucine (the corresponding residue in transketolase) led to greatly diminished kcat values, sh
57 ally, inhibiting the transketolase isoenzyme transketolase-like 1 (TKTL1) by siRNA reversed theses ef
58 e from a YAC in Xp22, the recently described transketolase-like gene in a YAC from Xq28 and a putativ
59 s been associated with overexpression of the transketolase-like-1-gene (TKTL1), which encodes an esse
60 and metabolic enzymes such as transaldolase, transketolase, malate dehydrogenase, asparagine syntheta
61  in M. jannaschii as endoglucanase (MJ0555), transketolase (MJ0681), thiamine biosynthetic protein th
62 tabolic enzymes, including transaldolase and transketolase of the nonoxidative pentose pathway, malat
63 evated expression of the TKL1 gene, encoding transketolase of the pentose phosphate pathway.
64  investigate the effect of increased plastid transketolase on photosynthetic capacity and growth, tob
65 active centers of the E. coli E1 subunit and transketolase on the basis of the parallels in the ligat
66 ere complemented by germinating the seeds of transketolase-overexpressing lines in media containing e
67 ls in the seeds and cotyledons were lower in transketolase-overexpressing lines than in wild-type pla
68                                         When transketolase-overexpressing plants were supplemented wi
69 led a major and unexpected effect of plastid transketolase overexpression as the transgenic tobacco p
70                    The mechanism determining transketolase protein levels remains to be elucidated, b
71 ana tabacum) plants with increased levels of transketolase protein were produced.
72  versus untreated mice: fatty acid synthase, transketolase, pulmonary surfactant-associated protein C
73                                            A transketolase reaction was catalyzed by cyanide ion unde
74                          Since the analogous transketolase reaction, being involved in the carbohydra
75 ing regions of the color pigment genes and a transketolase-related gene.
76  both the pyruvate dehydrogenase complex and transketolase, resulted in enhanced imatinib sensitivity
77 ted to another enzymatic reaction with yeast transketolase that changes the mass of the products to b
78 s is suppressed by overexpression of TKL1, a transketolase that generates NADPH, which balances redox
79 , as we have previously observed for E. coli transketolase, the mutations that improved activity towa
80 drogenase (G6PD) catalyzed oxidative and the transketolase (TK) catalyzed nonoxidative pentose cycle
81                                              Transketolase (TK) cofactor binding has been studied ext
82        We have previously engineered E. coli transketolase (TK) enzyme variants that accept new subst
83 volution of the mechanism and specificity of transketolase (TK) has been minor, and that the smallest
84                                              Transketolase (TK) has been previously engineered, using
85 d on thiamine pyrophosphate (ThDP)-dependent transketolase (TK)-catalyzed reaction, followed by the o
86 ithin the flexible loops of Escherichia coli transketolase (TK).
87 characterised a low-activity form of E. coli transketolase, TK(low), which also binds the cofactor th
88 incident with a more than 90% loss of tissue transketolase (TKT) and aldehyde dehydrogenase (ALDH) cl
89 undantly express two water-soluble proteins, transketolase (TKT) and aldehyde dehydrogenase class 1A1
90                                          The transketolase (TKT) gene is expressed 30-50 times more h
91                                              Transketolase (TKT) is a ubiquitous enzyme used in multi
92 y and Akt association and phosphorylation of transketolase (TKT), a key enzyme of the nonoxidative pe
93 nase 2 (GLUD2), adenylate kinase 2 (AK2) and transketolase (TKT).
94 tors inducing loss of the corneal crystallin transketolase (TKT).
95 ent study, we focused on one key PPP enzyme, transketolase (TKT).
96    Here, we demonstrate that this protein is transketolase (TKT; EC 2.2.1.1), an enzyme in the nonoxi
97 r two proteins, phosphoglucomutase (Pgm) and transketolase (TktA), are enzymes involved in carbohydra
98 hosphate and triose phosphate and reversible transketolase velocity were similar to net glycolytic fl
99     The S385Y/D469T/R520Q variant of E. coli transketolase was evolved previously with three successi
100                           Heat-activation of transketolase was similarly investigated and found to co
101                         Coamplification with transketolase, which increases d-erythrose 4-phosphate a

 
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