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1  of glyceraldeyde-3 phosphate dehydrogenase (G3PDH).
2 ne glyceraldehyde 3-phosphate dehydrogenase (G3pdh).
3 droxyacetone phosphate by G3P dehydrogenase (G3PDH).
4 hich is annotated GpsA, a G3P dehydrogenase (G3PDH).
5 evels of mRNA of all 3 collagenases, but not G3PDH.
6 nsistent with B3P binding the active site of G3PDH.
7                         Since the amounts of G3PDH activity in INS-1 and hepatocyte extracts are simi
8 er in trans) and were required for the total G3PDH activity of cell lysates.
9 wazekii purified from hen egg yolk sacs, and G3PDH activity was assayable in R. prowazekii lysed-cell
10 ed loci, including the low copy nuclear gene G3pdh and 5 SSR loci.
11 a tight association between activities of nr-G3PDH and mannose-6-P reductase and mRNA expression leve
12 of glyceraldehyde-3-phosphate dehydrogenase (G3PDH) and aldolase to the N-terminus of human erythrocy
13 opmental, and environmental regulation of nr-G3PDH, and also suggest that the supply of NADPH necessa
14  1, betaS-crystallin, betaB2-crystallin, and G3PDH, and UV-absorbing contact lenses significantly pre
15 n, glyceraldehyde 3-phosphate dehydrogenase (G3PDH), annexin A2, triose phosphate isomerase, and ubiq
16                                          The G3PDH-bound B3P structure was found to be very similar t
17     The stoichiometry of binding for the B3P-G3PDH complex was determined from Sephadex G-50 displace
18 stabilizing the loop, in the case of the B3P-G3PDH complex, is a hydrogen bond between the side chain
19 LY1 gene, which encodes a G3P dehydrogenase (G3Pdh), conferred enhanced resistance.
20 e gly1, a mutation in a cytosolic isoform of G3Pdh did not alter basal resistance to C. higginsianum.
21 ersible glyceraldehyde-3-P dehydrogenase (nr-G3PDH, EC 1.2.1.9), the apparent key contributor of the
22 enealogical context, relationships among the G3pdh haplotypes are incongruent with taxonomic boundari
23 es of band 3 (MEELQDDYEDMMEEN-NH2), bound to G3PDH has been determined using the exchange-transferred
24 proteins identified including, LDH (Ra, Ch), G3PDH (Hu, Ch), pyruvate kinase (Ch), Annexin II (Ch), a
25                   Specific binding of B3P to G3PDH is demonstrated by reversion of the NMR spectral p
26                                          The G3pdh locus provides high levels of noncoding sequence v
27 nhibit activity in vitro, suggesting that nr-G3PDH may be regulated through feedback inhibition by on
28             H. volcanii harbors two putative G3PDH operons: (i) glpA1B1C1, located on the chromosome
29 ecause the abundance of mRNA encoding actin, G3PDH or interphotoreceptor retinoid-binding protein did
30 s (glyceraldehyde-3-phosphate dehydrogenase [G3PDH]) or exogenous sequence (PCR mimic for TGF-beta 1)
31 yacrylamide gel electrophoresis, purified nr-G3PDH showed a molecular mass of 53 kD.
32 of glyceraldehyde 3-phosphate dehydrogenase (G3PDH) showed elevated oxidation in chilled non-suppleme
33 tabolize glycolytic intermediates beyond the G3PDH step.
34 he glyceraldehyde-3-phosphate dehydrogenase (G3PDH) step in the former cells.
35 A clone (accession no. AF196292) encoding nr-G3PDH was identified using polymerase chain reaction and
36                K(m) values for the celery nr-G3PDH were low (6.8 microM for NADP(+) and 29 microM for

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