ライフサイエンスコーパス: glyceraldehyde

1 ve synthetic route starting with protected d-glyceraldehyde.

2 or vitamin K1 and third for the substrate DL-glyceraldehyde.

3 ubated over time with glucose, galactose, or glyceraldehyde.

4 exhibited the highest rate of glycation with glyceraldehyde.

5 experiments performed with both NADPH and DL-glyceraldehyde.

6 ic nucleotide precursors, glycolaldehyde and glyceraldehyde.

7 e (ADH) catalysing oxidation of glycerol and glyceraldehyde.

8 dehyde, glyoxal, acetic acid, glycolic acid, glyceraldehyde, 2-hydroxypropanedialdehyde and lactic ac

9 Successful single cell analysis of the glyceraldehyde 3 phosphate dehydrogenase (GAPDH) gene in

10 ses confirmed localization of annexin A2 and glyceraldehyde 3-dehydrogenase (GAPDH), proteins identif

11 n of dihydroxyacetone phosphate (DHAP) and d-glyceraldehyde 3-phosphate (d-G3P) by an unresolved mech

12 s the formation of DXP via condensation of D-glyceraldehyde 3-phosphate (D-GAP) and pyruvate in a thi

13 diphosphate (ThDP) to convert pyruvate and d-glyceraldehyde 3-phosphate (d-GAP) into 1-deoxy-d-xylulo

14 se isomerization reactions of D-xylose and d-glyceraldehyde 3-phosphate (DGAP), respectively.

15 are alpha-d,l-glycerol phosphate (GP) and d-glyceraldehyde 3-phosphate (G3P), and examples of two ne

16 3-indole-d-glycerol 3'-phosphate (IGP) or d-glyceraldehyde 3-phosphate (G3P), for use in the investi

17 into dihydroxyacetone phosphate (DHAP) and d-glyceraldehyde 3-phosphate (G3P).

18 ally unfavorable isomerization reaction, (R)-glyceraldehyde 3-phosphate (GAP) and [2(R)-(2)H]-GAP (d-

19 y 50-fold increase in K(m) for the substrate glyceraldehyde 3-phosphate (GAP) and a 60-fold increase

20 n of dihydroxyacetone phosphate (DHAP) and d-glyceraldehyde 3-phosphate (GAP) bound to wild-type trio

21 is of the aldose-ketose isomerization of (R)-glyceraldehyde 3-phosphate (GAP) by triosephosphate isom

22 oduct distributions for the reactions of (R)-glyceraldehyde 3-phosphate (GAP) in D(2)O at pD 7.5-7.9

23 Product yields for the reactions of (R)-glyceraldehyde 3-phosphate (GAP) in D2O at pD 7.9 cataly

24 talysis of the reversible isomerization of R-glyceraldehyde 3-phosphate (GAP) to dihydroxyacetone pho

25 on of dihydroxyacetone phosphate (DHAP) to d-glyceraldehyde 3-phosphate (GAP), for which there is a w

26 the CB cycle with NADPH to produce the sugar glyceraldehyde 3-phosphate (GAP), which is used for rege

27 quent decarboxylation that is triggered by d-glyceraldehyde 3-phosphate (GAP).

28 substrates dihydroxyacetone phosphate and d-glyceraldehyde 3-phosphate [(k(cat)/K(m))(GAP) and (k(ca

29 ase (TIM) catalyzes the interconversion of d-glyceraldehyde 3-phosphate and dihydroxyacetone phosphat

30 dol condensation of the unstable catabolites glyceraldehyde 3-phosphate and dihydroxyacetone phosphat

31 enzymes of the pentose phosphate pathway to glyceraldehyde 3-phosphate and fructose 6-phosphate, thu

32 osphate isomerase-catalyzed reactions of (R)-glyceraldehyde 3-phosphate and k(cat)/K(HPi)K(GA) for re

33 DHAP as well as glyceraldehyde 3-phosphate and oxaloacetate inhibited ac

34 A structure was also obtained where glyceraldehyde 3-phosphate binds in the P(s) pocket in t

35 reatine kinase, aldolase A and an isoform of glyceraldehyde 3-phosphate dehydrogenase (G3PDH) showed

36 sp-Glu-Ala-Asp) box polypeptide, beta-actin, glyceraldehyde 3-phosphate dehydrogenase (G3PDH), annexi

37 argeted hAuNP exhibited high specificity for glyceraldehyde 3-phosphate dehydrogenase (GADPH) mRNA in

38 ity of two commonly used housekeeping genes, glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and 18S

39 lvin cycle by forming a ternary complex with glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and pho

40 Phosphoribulokinase (PRK) and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) are ess

41 e identified the mammalian glycolysis enzyme glyceraldehyde 3-phosphate dehydrogenase (GAPDH) as an N

42 These acyloxy nitroso compounds inhibit glyceraldehyde 3-phosphate dehydrogenase (GAPDH) by form

43 Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) has bee

44 Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) is a gl

45 elta12 desaturase, superoxide dismutase, and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) mRNA wi

46 hat the P39 peptide is a structural mimic of glyceraldehyde 3-phosphate dehydrogenase (GAPDH) on the

47 Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) plays a

48 ase 1, Lupus Ku autoantigen protein p70, and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) protein

49 Arginine kinase (AK) and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) were de

50 Here, we demonstrate that glyceraldehyde 3-phosphate dehydrogenase (GAPDH), a conv

51 Glyceraldehyde 3-phosphate dehydrogenase (GAPDH), a prot

52 ol) and measured for total protein quantity, glyceraldehyde 3-phosphate dehydrogenase (GAPDH), citrat

53 The glyceraldehyde 3-phosphate dehydrogenase (GAPDH)-normali

54 n, aggregation, and nuclear translocation of glyceraldehyde 3-phosphate dehydrogenase (GAPDH).

55 ive oxygen species accumulate and inactivate glyceraldehyde 3-phosphate dehydrogenase (GAPDH).

56 itated glucose transport into the cytoplasm; glyceraldehyde 3-phosphate dehydrogenase (GAPDH; a glyco

57 Tetrameric rabbit muscle glyceraldehyde 3-phosphate dehydrogenase (GAPDH; EC 1.2.

58 ere, we use RNA-seq to identify three genes (GLYCERALDEHYDE 3-PHOSPHATE DEHYDROGENASE (PvGAPC1), ORGA

59 -NSAID prodrug inhibited cylcooxgenase-2 and glyceraldehyde 3-phosphate dehydrogenase activity and tr

60 ve hippocampal content of glycolytic enzymes glyceraldehyde 3-phosphate dehydrogenase and pyruvate de

61 establish the blockade of glycolysis at the glyceraldehyde 3-phosphate dehydrogenase step as the cen

62 eads to the attenuation of glycolysis at the glyceraldehyde 3-phosphate dehydrogenase step due to the

63 f glycolytic intermediates before and at the glyceraldehyde 3-phosphate dehydrogenase step, promoting

64 decreased glycolytic intermediates after the glyceraldehyde 3-phosphate dehydrogenase step, thereby r

65 to attenuation of glycolysis by blocking the glyceraldehyde 3-phosphate dehydrogenase step.

66 re determined by (1)H NMR spectroscopy using glyceraldehyde 3-phosphate dehydrogenase to trap the fir

67 itution of malonylated lysine residue 184 in glyceraldehyde 3-phosphate dehydrogenase with glutamic a

68 ction of siRNA(GAPDH) [small interfering RNA(glyceraldehyde 3-phosphate dehydrogenase)] reduces PLCbe

69 dentified four points in central metabolism (Glyceraldehyde 3-phosphate dehydrogenase, transaldolase,

70 y untargeted glycolytic enzymes, aldolase A, glyceraldehyde 3-phosphate dehydrogenase, triose phospha

71 the intrinsic beta-actin, alpha-tubulin, and glyceraldehyde 3-phosphate dehydrogenase, which are usua

72 drogenase ExaC, arginine deiminase ArcA, and glyceraldehyde 3-phosphate dehydrogenase.

73 ersulfidation leads to decreased activity of glyceraldehyde 3-phosphate dehydrogenase.

74 onstituted by the combined activities of the glyceraldehyde 3-phosphate dehydrogenases GapA/GapB and

75 )]dihydroxyacetone phosphate and [U-(13)C(3)]glyceraldehyde 3-phosphate followed by rearrangements in

76 his block in metabolism could be overcome if glyceraldehyde 3-phosphate is exported to the cytosol, w

77 eaction from dihydroxyacetone phosphate to D-glyceraldehyde 3-phosphate is significantly slower than

78 reduced k(cat) relative to WT with either d-glyceraldehyde 3-phosphate or dihyrdroxyacetone phosphat

79 Glyceraldehyde 3-phosphate reacts with the second interm

80 yme in the Calvin-Benson cycle that converts glyceraldehyde 3-phosphate to dihydroxyacetone phosphate

81 reversible enzyme-catalyzed isomerization of glyceraldehyde 3-phosphate to give dihydroxyacetone phos

82 Triose glycolysis (generation of ATP from glyceraldehyde 3-phosphate via phosphoenol pyruvate) is

83 e labeling ratios C-4/C-3 of glucose versus (glyceraldehyde 3-phosphate)/(dihydroxyacetone phosphate)

84 f MtFBA bound to dihydroxyacetone phosphate, glyceraldehyde 3-phosphate, and fructose 1,6-bisphosphat

85 decrease in k(cat)/K(m) for isomerization of glyceraldehyde 3-phosphate, and the activity of this mut

86 ontents revealed dihydroxyacetone phosphate, glyceraldehyde 3-phosphate, ribulose, erythrose, and suc

87 ereospecific, NADPH-dependent reduction of l-glyceraldehyde 3-phosphate, the enantiomer of the TIM su

88 with the behavior of the natural product, d-glyceraldehyde 3-phosphate.

89 ion of dihydroxyacetone phosphate (DHAP) and glyceraldehyde 3-phosphate.

90 PLP) from glutamine, ribose 5-phosphate, and glyceraldehyde 3-phosphate.

91 derived from dihydroxyacetone phosphate and glyceraldehyde 3-phosphate.

92 ulin), elongation factor 1 alpha (EF1alpha), glyceraldehyde-3 phosphate dehydrogenase (GAPDH), 40 S r

93 metastases and on normalization to 5 x 10(6) glyceraldehyde-3'-phosphate dehydrogenase mRNA copies, n

94 ctose-6-P and fructose-1,6-bisP convert into glyceraldehyde-3-P (Ga-P-3), which converts into methylg

95 rveys and subsequent genetic analysis of the glyceraldehyde-3-phosate dehydrogenase (G3PDH), heat-sho

96 of pyruvate as a 2-hydroxyethyl donor with d-glyceraldehyde-3-phosphate (d-GAP) as acceptor forming D

97 bunit, Pdx1, where ribose-5-phosphate (R5P), glyceraldehyde-3-phosphate (G3P), and ammonia are conden

98 tion of dihydroxyacetone phosphate (DHAP) to glyceraldehyde-3-phosphate (G3P); however, little is kno

99 We show that it is a heterodimeric glyceraldehyde-3-phosphate (GAP) ferredoxin oxidoreducta

100 nversion of indole-3-glycerol phosphate to d-glyceraldehyde-3-phosphate and indole.

101 quently cleaved by the aldolase DgaF to form glyceraldehyde-3-phosphate and pyruvate.

102 However, pretreatment of glyceraldehyde-3-phosphate and ribonuclease A with BOH i

103 (HB) as donor substrates, in each case using glyceraldehyde-3-phosphate as acceptor substrate.

104 Pyrophosphate, polyphosphate, and glyceraldehyde-3-phosphate could support growth as sole

105 uctase (GR), thioredoxin reductase (TR), and glyceraldehyde-3-phosphate dehydrogenase (G3PD) activiti

106 yphal wall protein-1 (Hwp1); enolase (Enol); glyceraldehyde-3-phosphate dehydrogenase (Gap1); and pho

107 The cytosolic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPC) catalyze

108 A cytosolic glyceraldehyde-3-phosphate dehydrogenase (GAPC) was iden

109 nduce the nuclear translocation of cytosolic glyceraldehyde-3-phosphate dehydrogenase (GAPC), but its

110 thaliana) plastidial glycolytic isoforms of glyceraldehyde-3-phosphate dehydrogenase (GAPCp) in phot

111 etoxification via synergistic interaction of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and a m

112 Rab2 requires glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and aty

113 orms an inactive supramolecular complex with glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and pho

114 identified as possibly acetylated, including glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and Rpa

115 hat are regulated by S-nitrosylation such as glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and the

116 pathway initiated by the interaction between glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and the

117 cting proteins to be the glycolytic enzymes, glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and tri

118 y experimental approaches, we identified the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as a C1

119 us and processed for RT-PCR and qrtPCR using glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as an e

120 We found that I/R induces glyceraldehyde-3-phosphate dehydrogenase (GAPDH) associa

121 ose-1,6-bisphosphate aldolase (aldolase) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) followe

122 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) from hu

123 Translocation of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) from th

124 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) has bee

125 ir ability to perform molecular targeting of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) in huma

126 The translocation and accumulation of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) in the

127 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a cl

128 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a gl

129 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a ke

130 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a mu

131 NAD-dependent glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a ub

132 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a ub

133 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is an a

134 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is an e

135 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is ofte

136 ling cascade involving nitric oxide (NO) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mediate

137 In a second pathway, the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mediate

138 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) partici

139 ow that, unexpectedly, the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH) physica

140 METH also increases glyceraldehyde-3-phosphate dehydrogenase (GAPDH) protein

141 n kinase C iota/lambda (aPKCiota/lambda) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) recruit

142 Using glyceraldehyde-3-phosphate dehydrogenase (GAPDH) silenci

143 yzed the mechanism of NADH-channeling from D-glyceraldehyde-3-phosphate dehydrogenase (GAPDH) to L-la

144 mide gel electrophoresis, and phosphorylated glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was ide

145 protein of 362 amino acids with identity to glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was obt

146 dual photooxidizable residues in the protein glyceraldehyde-3-phosphate dehydrogenase (GAPDH) were ex

147 ar SMCs that involves interaction of nuclear glyceraldehyde-3-phosphate dehydrogenase (GAPDH) with ap

148 id (KA) is a selective covalent inhibitor of glyceraldehyde-3-phosphate dehydrogenase (GAPDH), a crit

149 nown to serve as receptors for Plg including glyceraldehyde-3-phosphate dehydrogenase (GAPDH), a cyto

150 P-ribosyl)ation of the key glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH), a modi

151 a natural product that specifically inhibits glyceraldehyde-3-phosphate dehydrogenase (GAPDH), a rate

152 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH), an imp

153 s adenylate kinase, phosphoglycerate kinase, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and en

154 g transcription of the cyclophilin A (PPIA), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and se

155 Its ability to protect citrate synthase, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and th

156 lity, some common housekeeping genes such as glyceraldehyde-3-phosphate dehydrogenase (GAPDH), beta-a

157 Commonly used glyceraldehyde-3-phosphate dehydrogenase (Gapdh), beta-a

158 two major proteins, creatine kinase (CK) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH), confor

159 yotic translation elongation factor 2 (EF2), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), hypoxa

160 ion and inhibition of the sulfhydryl enzyme, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), in vit

161 dy, we have discovered that Escherichia coli glyceraldehyde-3-phosphate dehydrogenase (GAPDH), which

162 Superoxide inhibits glyceraldehyde-3-phosphate dehydrogenase (GAPDH), which

163 gical concentrations, nitroalkenes inhibited glyceraldehyde-3-phosphate dehydrogenase (GAPDH), which

164 ssion and the involvement in this process of glyceraldehyde-3-phosphate dehydrogenase (GAPDH), which

165 ar localization of the key glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

166 bind directly to the L1 interaction partner glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

167 otein 1 (NSAP1), ribosomal protein L13a, and glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

168 cycle enzymes phosphoribulokinase (PRK) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

169 es fructose bisphosphate aldolase (FBPA) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

170 o oxidative stress: creatine kinase (CK) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

171 nown association with NFTs; one of these was glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

172 We focused on one of these, glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

173 esicles also contained the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

174 forms of all six mammalian Prx isoforms and glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

175 n of nitric oxide (NO), which S-nitrosylates glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

176 keeping genes beta-2 microglobulin (B2M) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

177 lated a 37-kDa AUBP, which was identified as glyceraldehyde-3-phosphate dehydrogenase (GAPDH).To summ

178 olar concentrations of palmitoyl-CoA inhibit glyceraldehyde-3-phosphate dehydrogenase (GAPDH; EC 1.2.

179 of tropomyosin, arginine or creatine kinase, glyceraldehyde-3-phosphate dehydrogenase (GPDH), calcium

180 6 arbitrary units, respectively, relative to glyceraldehyde-3-phosphate dehydrogenase (n = 5, p = non

181 Cytosolic Oryza sativa glyceraldehyde-3-phosphate dehydrogenase (OsGAPDH), the

182 1), penicillin-binding protein 2b (SAG0765), glyceraldehyde-3-phosphate dehydrogenase (SAG0823), and

183 xoplasma gondii egresses from the host cell, glyceraldehyde-3-phosphate dehydrogenase 1 (GAPDH1), whi

184 s the abundance of glycolytic enzymes (e.g., glyceraldehyde-3-phosphate dehydrogenase [GAPDH]) and tr

185 e maintenance of NAD(+) pools sufficient for glyceraldehyde-3-phosphate dehydrogenase activity and Wa

186 Heparan sulfate was also capable of inducing glyceraldehyde-3-phosphate dehydrogenase aggregation, bu

187 Overexpression of the secretory protein glyceraldehyde-3-phosphate dehydrogenase and ATP synthas

188 abolic enzymes, including nonphosphorylating glyceraldehyde-3-phosphate dehydrogenase and beta-glucos

189 Nuclear complex of glyceraldehyde-3-phosphate dehydrogenase and DNA repair

190 demonstrated an increased ability to degrade glyceraldehyde-3-phosphate dehydrogenase and ribonucleas

191 splayed an increased ability to degrade both glyceraldehyde-3-phosphate dehydrogenase and ribonucleas

192 lic enzymes that are sensitive to oxidation, glyceraldehyde-3-phosphate dehydrogenase and the sodium-

193 le expression level such actin, tubulin, and glyceraldehyde-3-phosphate dehydrogenase are frequently

194 We have obtained soluble recombinant sperm glyceraldehyde-3-phosphate dehydrogenase as a heterotetr

195 Of the latter, we confirmed glyceraldehyde-3-phosphate dehydrogenase as a key target

196 Colell et al. identify the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase as a potent inh

197 ocytes, and identified glucose transport and glyceraldehyde-3-phosphate dehydrogenase as the most sel

198 in prefibrillar species, the heparin-induced glyceraldehyde-3-phosphate dehydrogenase early oligomers

199 in vitro the early oligomers present in the glyceraldehyde-3-phosphate dehydrogenase fibrillation pa

200 designed to target the histidine kinase and glyceraldehyde-3-phosphate dehydrogenase genes of B. der

201 s on several genes including c-myc, p21, and glyceraldehyde-3-phosphate dehydrogenase genes, indicati

202 Sperm glyceraldehyde-3-phosphate dehydrogenase has been shown

203 s a heterotetramer with the Escherichia coli glyceraldehyde-3-phosphate dehydrogenase in a ratio of 1

204 b proteins, alpha-synuclein, synapsin-I, and glyceraldehyde-3-phosphate dehydrogenase in cultured hip

205 ent of glucose metabolism via iodoacetate, a glyceraldehyde-3-phosphate dehydrogenase inhibitor, is s

206 Glyceraldehyde-3-phosphate dehydrogenase is a glycolytic

207 re we report a mechanism by which glycolytic glyceraldehyde-3-phosphate dehydrogenase of Arabidopsis

208 nin, and Tmod) but did not affect endogenous glyceraldehyde-3-phosphate dehydrogenase or expression f

209 g reduced levels of the Calvin cycle enzymes glyceraldehyde-3-phosphate dehydrogenase or ribulose-1,5

210 chromosome 4 (heterochromatic) and the human glyceraldehyde-3-phosphate dehydrogenase promoter (euchr

211 e with hyperplastic polyps (median IFN-gamma/glyceraldehyde-3-phosphate dehydrogenase ratio x 100,000

212 ructures of human somatic and sperm-specific glyceraldehyde-3-phosphate dehydrogenase revealed few di

213 of cocaine are mediated by the nitric oxide-glyceraldehyde-3-phosphate dehydrogenase signaling pathw

214 ever, further detailed analysis of the sperm glyceraldehyde-3-phosphate dehydrogenase structure revea

215 t difference compared with published somatic glyceraldehyde-3-phosphate dehydrogenase structures that

216 rase, glucose-6-phosphate dehydrogenase, and glyceraldehyde-3-phosphate dehydrogenase) and their resp

217 -C but had no effect on beta-actin or GAPDH (glyceraldehyde-3-phosphate dehydrogenase).

218 and an internal manufacturer control, GAPDH (glyceraldehyde-3-phosphate dehydrogenase).

219 tose phosphate pathway by ADPr inhibition of glyceraldehyde-3-phosphate dehydrogenase, a central enzy

220 influential role for the nonphosphorylating glyceraldehyde-3-phosphate dehydrogenase, a cytosolic en

221 ngerprinting and peptide sequencing included glyceraldehyde-3-phosphate dehydrogenase, a glycolytic e

222 covalent inhibitors of Plasmodium falciparum glyceraldehyde-3-phosphate dehydrogenase, a validated ta

223 or catalysis or FeS cluster binding, such as glyceraldehyde-3-phosphate dehydrogenase, aldehyde dehyd

224 ajor glycated amino acids) of serum albumin, glyceraldehyde-3-phosphate dehydrogenase, aldolase, and

225 erythrocytes were stained with antibodies to glyceraldehyde-3-phosphate dehydrogenase, aldolase, phos

226 exin A1/A3/A4/A5/A6, clathrin heavy chain 1, glyceraldehyde-3-phosphate dehydrogenase, alpha-enolase,

227 east homologues of Hsp70 proteins), Tdh2/3p (glyceraldehyde-3-phosphate dehydrogenase, an RNA-binding

228 her macromolecules including Tau, ubiquitin, glyceraldehyde-3-phosphate dehydrogenase, and glycosamin

229 We found that the HKGs glyceraldehyde-3-phosphate dehydrogenase, beta actin and

230 e, while spermadhesin-1, gelsolin, tubulins, glyceraldehyde-3-phosphate dehydrogenase, calmodulin, AT

231 or bovine serum albumin, choriogonadotropin, glyceraldehyde-3-phosphate dehydrogenase, Herceptin, and

232 ng cytosolic creatine kinase, tropomyosin 1, glyceraldehyde-3-phosphate dehydrogenase, myosin light c

233 cle pyruvate kinase, malate dehydrogenase 1, glyceraldehyde-3-phosphate dehydrogenase, proteoglycan 4

234 Catfish L-lactate dehydrogenase, glyceraldehyde-3-phosphate dehydrogenase, pyruvate kinas

235 E. coli and demonstration that the resulting glyceraldehyde-3-phosphate dehydrogenase, the normal tar

236 o observed on binding of a metabolic enzyme, glyceraldehyde-3-phosphate dehydrogenase, to cdAE1.

237 ed with an siRNA for the housekeeping enzyme glyceraldehyde-3-phosphate dehydrogenase, wild-type HSV

238 our system: alpha-synuclein, synapsin-I, and glyceraldehyde-3-phosphate dehydrogenase.

239 itrosylation of the major apoptotic effector glyceraldehyde-3-phosphate dehydrogenase.

240 an operon that encode the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase.

241 One, gapdh, encodes the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase.

242 calcium channels; DC, dendritic cell; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; IFN-gamma, int

243 Preexisting stable mRNAs (e.g., GAPDH [glyceraldehyde-3-phosphate dehydrogenase]) are rapidly d

244 e show that the cytosolic glycolytic enzymes glyceraldehyde-3-phosphate dehydrogenases (GAPCs) intera

245 ltered the surface expression of enolase and glyceraldehyde-3-phosphate dehydrogenease, two glycolyti

246 , catalyzes the oxidative phosphorylation of glyceraldehyde-3-phosphate to 1,3-biphosphoglycerate (BP

247 es the condensation of ribulose 5-phosphate, glyceraldehyde-3-phosphate, and ammonia, and YaaE cataly

248 sphoenolpyruvate, glyceric acid 2-phosphate, glyceraldehyde-3-phosphate, and product, dihydroxyaceton

249 mportant conformational states: ligand-free, glyceraldehyde-3-phosphate-bound(like), and the active s

250 The Cu(I)-catalyzed reactions of (R)-glyceraldehyde acetonide and dibenzylamine with terminal

251 Using glyceraldehyde acetonide as a chiral-pool precursor, an

252 D-Glyceraldehyde acetonide has been used as the starting p

253 ed magnetization transfer in cornea, whereas glyceraldehyde also increased magnetization transfer in

254 oro-2,3-endo-methylene-pentofuranoses from d-glyceraldehyde and 2,3-dideoxy-2-fluoro-3-C-hydroxymethy

255 ted acidity are able to convert the trioses, glyceraldehyde and dihydroxyacetone, quantitatively into

256 Fourth, NAMPT inhibition led to increased glyceraldehyde and erythrose levels in the cell.

257 ldol reaction between optically pure d- or l-glyceraldehyde and hydroxyacetylfuran is demonstrated as

258 s-cyanamide, cyanoacetylene, glycolaldehyde, glyceraldehyde and inorganic phosphate-are plausible pre

259 ytidine exhibited comparable reactivity with glyceraldehyde and no appreciable reactivity with galact

260 uch as proline transporter 2, NADP-dependent glyceraldehyde and superoxide dismutase were found signi

261 With D-glucose, D-galactose, D/L-glyceraldehyde, and D-glucosamine serving as the model g

262 derived from dihydroxyacetone phosphate and glyceraldehyde, and sedoheptulose 1-phosphate was derive

263 Third, glyceraldehyde- and erythrose-labeling studies showed in

264 Stool metabolomic studies identified glyceraldehyde as significantly elevated in IC.

265 is primarily mediated by the blockage of DL-glyceraldehyde binding to ALR2.

266 We find that the synthesis of glyceraldehyde by reaction of formaldehyde with glycolal

267 blocks for the synthesis--glycolaldehyde and glyceraldehyde--could be shown to derive from one carbon

268 ened tissue and evaluated riboflavin/UVA and glyceraldehyde cross-linking treatments.

269 D-Glyceraldehyde (D-GLYC) is usually considered to be a st

270 D-Glyceraldehyde (DGA) is the triose fragment common to th

271 The fructose-specific metabolite glyceraldehyde did not increase GLUT5 expression.

272 Efficient conversions of glycolaldehyde, glyceraldehyde, erythrose, a heptose, and glucosamine ar

273 the in vitro Maillard reaction of GlcN with glyceraldehyde (GA), glucose (Glc), and fructose (Fru) a

274 rylates to chiral iminoesters derived from D-glyceraldehyde have been investigated.

275 limine derived from conveniently protected d-glyceraldehyde, (ii) ring-closing metathesis, (iii) debe

276 ant nucleotide precursors glycolaldehyde and glyceraldehyde in a stable, crystalline form.

277 lyoxylate, formaldehyde, glycolaldehyde, and glyceraldehyde) in water were investigated and shown to

278 d three-carbon molecules (glycolaldehyde and glyceraldehyde), in the presence of aqueous sodium silic

279 genous dihydroxyacetone and fructose-derived glyceraldehyde, is neither molecularly identified nor fi

280 involved in fructose metabolism through its glyceraldehyde kinase activity and in the generation of

281 Lastly, treatments with increasing glyceraldehyde (mimicking crosslinking conditions) and c

282 on of dihydroxyacetone phosphate (DHAP) to d-glyceraldehyde phosphate (GAP), via general base catalys

283 protists, and plant chloroplasts, converts D-glyceraldehyde phosphate and pyruvate to isopentenyl dip

284 We also find that the glycolytic enzyme glyceraldehyde phosphate dehydrogenase constitutes a maj

285 ss to unnatural L-carbohydrates from the (S)-glyceraldehyde precursor.

286 er, metabolites entering downstream of PFK1 (glyceraldehyde, pyruvate, and ketoisocaproate) failed to

287 The D/L glyceraldehyde ratio in water solution is amplified to 9

288 lets with glucose, alpha-ketoisocaproate, or glyceraldehyde resulted in the appearance of cytochrome

289 detected compounds, accurate quantitation of glyceraldehyde, ribose, glucose, glycerylaldehyde-3-phos

290 A di-O-TBS protected glyceraldehyde synthon was condensed with Ellman's reage

291 s phosphate-truncated analogue, 2-C-methyl-D-glyceraldehyde, the current study revealed a loss of 6.1

292 D-glyceraldehyde, the simplest sugar with a D center, is t

293 ed from readily available (R)-isopropylidene glyceraldehyde through a route featuring 1,2-addition, c

294 catalysed the oxidation of both glycerol and glyceraldehyde thus demonstrating a consecutive two-step

295 Cyanide ion converted fructose plus glyceraldehyde to erythrose plus xylulose, the same prod

296 ydrogen transfer during the isomerization of glyceraldehyde to the corresponding dihydroxyacetone.

297 riboflavin/UVA treatment of the cornea, and glyceraldehyde treatment of the entire globe) were teste

298 Glyceraldehyde treatment prevented expansion of the corn

299 cluding the sugar-related glycolaldehyde and glyceraldehyde--two species considered as key prebiotic

300 rolysis, glycerol is selectively oxidized to glyceraldehyde with a turnover number (TON) of ~1000 and