ライフサイエンスコーパス: glyceraldehyde 3-phosphate

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

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

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

4 derived from dihydroxyacetone phosphate and glyceraldehyde 3-phosphate.

5 sphosphate to dihydroxyacetone phosphate and glyceraldehyde-3-phosphate.

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

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

8 ructose 1,6-bis(phosphate) (Fru-1,6-P(2)) to glyceraldehyde 3-phosphate and dihydroxyacetone phosphat

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

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

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

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

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

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

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

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

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

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

19 bolize intracellular glucose to pyruvate and glyceraldehyde 3-phosphate are coordinately regulated, c

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

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

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

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

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

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

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

27 s was identified by N-terminal sequencing as glyceraldehyde-3-phosphate dehy-drogenase (GAPDH).

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

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

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

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

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

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

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

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

36 olved in this DNA-protein complex identified glyceraldehyde 3-phosphate dehydrogenase (GAPDH) as a co

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

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

39 Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) has bee

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

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

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

43 Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) plays a

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

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

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

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

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

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

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

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

52 ose-1,6-bisphosphate aldolase (aldolase) and glyceraldehyde 3-phosphate dehydrogenase (GAPDH).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

70 SC70, protein disulfide isomerase ERp60, and glyceraldehyde 3-phosphate dehydrogenase.

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

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

73 phosphopeptide, including nitrate reductase, glyceraldehyde- 3-phosphate dehydrogenase, a calcium-dep

74 hat is, PML-RAR alpha mRNA copies divided by glyceraldehyde-3'-phosphate dehydrogenase (GAPDH) mRNA c

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

76 the activity of the oxidatively inactivated glyceraldehyde-3-phosphate dehydrogenase (G-3PD) in H2O2

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

78 ase (GR)-specific activity and a 24% loss in glyceraldehyde-3-phosphate dehydrogenase (G3PD)-specific

79 , which encodes the B subunit of chloroplast glyceraldehyde-3-phosphate dehydrogenase (GADPH) of Arab

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

81 t encode the A and B subunits of chloroplast glyceraldehyde-3-phosphate dehydrogenase (GAPA and GAPB)

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

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

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

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

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

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

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

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

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

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

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

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

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

95 quantitative reverse transcription-PCR using glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as cont

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

97 ix and Bcl-xL proteins decreased relative to glyceraldehyde-3-phosphate dehydrogenase (GAPDH) control

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

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

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

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

102 Recently, a surface-bound glyceraldehyde-3-phosphate dehydrogenase (GAPDH) has bee

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

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

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

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

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

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

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

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

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

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

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

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

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

116 bservations suggested that the length of the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mRNA 3'

117 All results were normalized according to glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mRNA in

118 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) partici

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

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

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

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

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

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

125 regulated telomere-binding proteins, nuclear glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was ide

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

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

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

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

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

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

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

133 ei glycosomal phosphoglycerate kinase (PGK), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and gl

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

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

136 otein kinase C iota/lambda (PKCiota/lambda), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and th

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

153 s (VTCs) where PKCiota/lambda phosphorylates glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

154 e identified as low micromolar inhibitors of glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

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

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

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

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

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

160 e [IA, an inhibitor of the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH)] on end

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

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

163 lytic domain of Trypanosoma cruzi glycosomal glyceraldehyde-3-phosphate dehydrogenase (gGAPDH) in whi

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

165 HeLa cell surface copurified with authentic glyceraldehyde-3-phosphate dehydrogenase (muscle form) (

166 6 arbitrary units, respectively, relative to glyceraldehyde-3-phosphate dehydrogenase (n = 5, p = non

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

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

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

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

171 Both decreased glyceraldehyde-3-phosphate dehydrogenase activity and in

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

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

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

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

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

177 h muscle actin protein or the mRNA levels of glyceraldehyde-3-phosphate dehydrogenase and interleukin

178 ion of proteins with a KFERQ motif including glyceraldehyde-3-phosphate dehydrogenase and Pax2.

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

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

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

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

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

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

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

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

187 In addition, we found that the chloroplast glyceraldehyde-3-phosphate dehydrogenase enzyme activity

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

189 of the light-activated pea leaf chloroplast glyceraldehyde-3-phosphate dehydrogenase form a disulfid

190 vailability of the structure of the extended glyceraldehyde-3-phosphate dehydrogenase from the archae

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

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

193 Sperm glyceraldehyde-3-phosphate dehydrogenase has been shown

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

195 Two crystal structures of L. mexicana glyceraldehyde-3-phosphate dehydrogenase in complex with

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

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

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

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

200 Glyceraldehyde-3-phosphate dehydrogenase is a glycolytic

201 ression levels, we found that beta-actin and glyceraldehyde-3-phosphate dehydrogenase levels fluctuat

202 hamtreated rats (kidney, densitometric value/glyceraldehyde-3-phosphate dehydrogenase mRNA value rati

203 us 0.58 +/- 0.04; liver, densitometric value/glyceraldehyde-3-phosphate dehydrogenase mRNA value rati

204 ERbeta mRNA steady-state levels (relative to glyceraldehyde-3-phosphate dehydrogenase mRNA) were sign

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

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

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

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

209 ted no significant effect of furosemide (NCC/glyceraldehyde-3-phosphate dehydrogenase ratios: group 1

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

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

212 c peptides independently confirmed actin and glyceraldehyde-3-phosphate dehydrogenase S-thiolation du

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 e, after which glutathione S-transferase and glyceraldehyde-3-phosphate dehydrogenase then ATPases un

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

218 he mRNA abundance for lipoprotein lipase and glyceraldehyde-3-phosphate dehydrogenase was elevated in

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

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

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

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

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

224 EGF or ammonia prolonged the half-life of glyceraldehyde-3-phosphate dehydrogenase, a classic subs

225 o 42 h circadian patterns in the activity of glyceraldehyde-3-phosphate dehydrogenase, a common clock

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

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

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

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

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

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

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

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

234 (ATP) synthase, alphaB-crystallin, galectin, glyceraldehyde-3-phosphate dehydrogenase, alpha-enolase,

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

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

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

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

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

240 inity-purified proteins we identified actin, glyceraldehyde-3-phosphate dehydrogenase, HSP27, protein

241 l respiratory chain enzymes, inactivation of glyceraldehyde-3-phosphate dehydrogenase, inhibition of

242 sin-beta4, alpha-tubulin, alphaB-crystallin, glyceraldehyde-3-phosphate dehydrogenase, metallothionei

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

244 eleton), protein 4.1, protein 4.2, aldolase, glyceraldehyde-3-phosphate dehydrogenase, phosphofructok

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

246 osphoglucose isomerase, phosphofructokinase, glyceraldehyde-3-phosphate dehydrogenase, phosphoglycera

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

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

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

250 Fluoride decreased expression of glyceraldehyde-3-phosphate dehydrogenase, which acts to

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

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

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

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

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

256 A 39-kDa species was identified as glyceraldehyde-3-phosphate dehydrogenase.

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

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

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

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

261 Glyceraldehyde-3-phosphate dehydrogenases (GAPDH) from t

262 of multifunctional, cell-surface-associated glyceraldehyde-3-phosphate dehydrogenases, which not onl

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

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

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

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

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

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

269 ion of dihydroxyacetone phosphate (DHAP) and glyceraldehyde 3-phosphate (G3P) to form fructose 1,6-bi

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

271 3-indole-d-glycerol 3'-phosphate (IGP) or d-glyceraldehyde 3-phosphate (G3P), for use in the investi

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

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

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

275 ion of dihydroxyacetone phosphate (DHAP) and glyceraldehyde 3-phosphate (GA3P), as well as a variety

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

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

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

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

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

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

282 PP)-dependent condensation of pyruvate and d-glyceraldehyde 3-phosphate (GAP) to yield DXP in the fir

283 ations test for channeling of the substrate, glyceraldehyde 3-phosphate (GAP), as it passes between t

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

285 ; TIM catalyzes the isomerization of DHAP to glyceraldehyde 3-phosphate (GAP), while MGS catalyzes th

286 The mevalonate pathway and the glyceraldehyde 3-phosphate (GAP)-pyruvate pathway are al

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

288 e reversible condensation of glycerone-P and glyceraldehyde 3-phosphate into fructose 1,6-bisphosphat

289 es an enzyme involved in the mobilization of glyceraldehyde-3-phosphate into the pentose phosphate pa

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

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

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

293 he expected NAD as the electron acceptor for glyceraldehyde 3-phosphate oxidation enables energy to b

294 onversion of dihydroxyacetone phosphate to D-glyceraldehyde 3-phosphate, probably because an active-s

295 Glyceraldehyde 3-phosphate reacts with the second interm

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

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

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

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

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