ライフサイエンスコーパス: G3PDH

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1 ecause the abundance of mRNA encoding actin, G3PDH or interphotoreceptor retinoid-binding protein did

2 1, betaS-crystallin, betaB2-crystallin, and G3PDH, and UV-absorbing contact lenses significantly pre

3 wazekii purified from hen egg yolk sacs, and G3PDH activity was assayable in R. prowazekii lysed-cell

4 The stoichiometry of binding for the B3P-G3PDH complex was determined from Sephadex G-50 displace

5 stabilizing the loop, in the case of the B3P-G3PDH complex, is a hydrogen bond between the side chain

6 proteins identified including, LDH (Ra, Ch), G3PDH (Hu, Ch), pyruvate kinase (Ch), Annexin II (Ch), a

7 droxyacetone phosphate by G3P dehydrogenase (G3PDH).

8 hich is annotated GpsA, a G3P dehydrogenase (G3PDH).

9 of glyceraldehyde-3-phosphate dehydrogenase (G3PDH) and aldolase to the N-terminus of human erythrocy

10 of glyceraldehyde 3-phosphate dehydrogenase (G3PDH) showed elevated oxidation in chilled non-suppleme

11 he glyceraldehyde-3-phosphate dehydrogenase (G3PDH) step in the former cells.

12 n, glyceraldehyde 3-phosphate dehydrogenase (G3PDH), annexin A2, triose phosphate isomerase, and ubiq

13 of glyceraldeyde-3 phosphate dehydrogenase (G3PDH).

14 s (glyceraldehyde-3-phosphate dehydrogenase [G3PDH]) or exogenous sequence (PCR mimic for TGF-beta 1)

15 evels of mRNA of all 3 collagenases, but not G3PDH.

16 K(m) values for the celery nr-G3PDH were low (6.8 microM for NADP(+) and 29 microM for

17 ersible glyceraldehyde-3-P dehydrogenase (nr-G3PDH, EC 1.2.1.9), the apparent key contributor of the

18 A clone (accession no. AF196292) encoding nr-G3PDH was identified using polymerase chain reaction and

19 a tight association between activities of nr-G3PDH and mannose-6-P reductase and mRNA expression leve

20 opmental, and environmental regulation of nr-G3PDH, and also suggest that the supply of NADPH necessa

21 yacrylamide gel electrophoresis, purified nr-G3PDH showed a molecular mass of 53 kD.

22 nhibit activity in vitro, suggesting that nr-G3PDH may be regulated through feedback inhibition by on

23 Since the amounts of G3PDH activity in INS-1 and hepatocyte extracts are simi

24 nsistent with B3P binding the active site of G3PDH.

25 H. volcanii harbors two putative G3PDH operons: (i) glpA1B1C1, located on the chromosome

26 The G3PDH-bound B3P structure was found to be very similar t

27 tabolize glycolytic intermediates beyond the G3PDH step.

28 Specific binding of B3P to G3PDH is demonstrated by reversion of the NMR spectral p

29 es of band 3 (MEELQDDYEDMMEEN-NH2), bound to G3PDH has been determined using the exchange-transferred

30 er in trans) and were required for the total G3PDH activity of cell lysates.

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