ライフサイエンスコーパス: glyceraldehyde

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

2 ve synthetic route starting with protected d-glyceraldehyde.

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

4 exhibited the highest rate of glycation with glyceraldehyde.

5 and 2) starting from 2,3-O-isopropylidene-d-glyceraldehyde.

6 competitive inhibition with respect to GAP/d-glyceraldehyde.

7 P synthase where pyruvate binds before GAP/d-glyceraldehyde.

8 ic nucleotide precursors, glycolaldehyde and glyceraldehyde.

9 ich was prepared from 2,3-O-isopropylidene-l-glyceraldehyde 1 in 13 steps, was condensed with various

10 l 6 was prepared from 2,3-O-isopropylidene-d-glyceraldehyde 1, which was converted to 5-O-benzoxy-d-2

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

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

13 ng the non-secreted proteins gamma-actin and glyceraldehyde 3'-phosphate dehydrogenase.

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

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

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

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

18 ate (DAH7-P) synthase was incubated with D,L-glyceraldehyde 3-phosphate (G3P) and [2,3-(13)C(2)]-PEP,

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

20 3-indole-d-glycerol 3'-phosphate (IGP) or d-glyceraldehyde 3-phosphate (G3P), for use in the investi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

41 complete recovery of oxidatively inactivated glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and glu

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

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

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

45 Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) has bee

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

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

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

49 Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) plays a

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

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

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

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

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

55 n 1 (Nramp1), ceruloplasmin, hephaestin, and glyceraldehyde 3-phosphate dehydrogenase (GAPDH), were m

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

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

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

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

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

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

62 gs indicate that the HMGB1-HMGB2-HSC70-ERp60-glyceraldehyde 3-phosphate dehydrogenase complex detects

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

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

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

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

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

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

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

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

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

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

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

74 Glyceraldehyde 3-phosphate dehydrogenase-S (GAPDS) is th

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

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

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

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

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

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

81 Glyceraldehyde 3-phosphate reacts with the second interm

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

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

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

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

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

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

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

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

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

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

92 derived from dihydroxyacetone phosphate and glyceraldehyde 3-phosphate.

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

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

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

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

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

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

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

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

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

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

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

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

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

108 ects and report association with SNPs in the glyceraldehyde-3-phosphate dehydrogenase (GAPD) gene.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

136 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) partici

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

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

139 malization of cDNA templates was achieved by glyceraldehyde-3-phosphate dehydrogenase (GAPDH) quantif

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

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

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

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

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

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

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

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

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

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

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

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

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

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

154 GSTP1, and GSTT1) and three reference gene [glyceraldehyde-3-phosphate dehydrogenase (GAPDH), beta-a

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

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

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

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

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

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

161 ent, pathways have been uncovered: (1) a p53-glyceraldehyde-3-phosphate dehydrogenase (GAPDH)-BAX pat

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

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

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

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

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

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

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

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

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

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

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

173 ipt [0.24 versus 0.008% relative to 100% for glyceraldehyde-3-phosphate dehydrogenase (GAPDH)], the r

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

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

176 6 arbitrary units, respectively, relative to glyceraldehyde-3-phosphate dehydrogenase (n = 5, p = non

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

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

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

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

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

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

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

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

185 ase, Akt kinase, phospho-BAD (inactive), and glyceraldehyde-3-phosphate dehydrogenase and increased t

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

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

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

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

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

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

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

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

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

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

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

197 Sperm glyceraldehyde-3-phosphate dehydrogenase has been shown

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

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

200 is inhibited by iodoacetate, an inhibitor of glyceraldehyde-3-phosphate dehydrogenase in glycolysis.

201 ucose, koningic acid (10 microM), a specific glyceraldehyde-3-phosphate dehydrogenase inhibitor, incr

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

203 Glyceraldehyde-3-phosphate dehydrogenase is a glycolytic

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

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

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

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

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

209 nces in amounts of WDNM1, epsilon-casein, or glyceraldehyde-3-phosphate dehydrogenase RNA were observ

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

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

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

213 A +142-Da delta(m) on glyceraldehyde-3-phosphate dehydrogenase was automatical

214 enhanced the rate of S-glutathionylation of glyceraldehyde-3-phosphate dehydrogenase with GSSG or S-

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

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

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

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

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

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

221 IGFBP-4, a structurally related protein, or glyceraldehyde-3-phosphate dehydrogenase, a housekeeping

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 rprisingly, p38 represents a nuclear form of glyceraldehyde-3-phosphate dehydrogenase, and binding to

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

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

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 r) had C-terminal lysine residues and three (glyceraldehyde-3-phosphate dehydrogenase, phosphoglycera

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

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 synthesis in vitro with substrates including glyceraldehyde-3-phosphate, fructose-6-phosphate, and gl

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

251 and GAP; k(cat) = 1.7 +/- 0.1 s(-1), K(m)(d-glyceraldehyde) = 33 +/- 3 mM, and K(m)(pyruvate) = 1.9

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

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

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

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

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

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

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

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

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

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

262 M, and K(m)(pyruvate) = 1.9 +/- 0.5 mM for d-glyceraldehyde and pyruvate.

263 rols when briefly stimulated with glucose or glyceraldehyde and when l-arginine was used to potentiat

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

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

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

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

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

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

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

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

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

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

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

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

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 nding of both substrates (pyruvate and GAP/d-glyceraldehyde) is required for the formation of a catal

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

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 FDPase-2, a glucokinase-binding protein, and glyceraldehyde phosphate dehydrogenase, which has been i

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

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

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

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

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

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

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

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

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

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

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

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

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

299 Glyceraldehyde treatment prevented expansion of the corn

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