ライフサイエンスコーパス: ribulose 5-phosphate

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1 generated by promiscuous phosphatases from d-ribulose 5-phosphate.

2 5.3.1.6) interconvert ribose 5-phosphate and ribulose 5-phosphate.

3 ic kinetics relative to the concentration of ribulose 5-phosphate.

4 me demonstrated Michaelis constant values of ribulose-5-phosphate (226 microM) and ATP (208 microM),

5 orted functional and structural studies of d-ribulose 5-phosphate 3-epimerase (RPE) from Streptococcu

6 The superfamily includes d-ribulose 5-phosphate 3-epimerase (RPE), orotidine 5'-mon

7 thm, genes (ribose 5-phosphate isomerase and ribulose 5-phosphate 3-epimerase) in the pentose phospha

8 Assays determined that ribulose-5-phosphate 3-epimerase (Rpe) was specifically

9 terologous expression of the gene encoding D-ribulose-5-phosphate 3-epimerase from any source, thereb

10 nate 6-phosphate decarboxylase (SgbH), and L-ribulose 5-phosphate 4-epimerase (SgbE).

11 lulose 5-phosphate 3-epimerase (UlaE), and L-ribulose 5-phosphate 4-epimerase (UlaF).

12 is of (13)C and deuterium isotope effects, L-ribulose-5-phosphate 4-epimerase catalyzes the epimeriza

13 H97N, H95N, and Y229F mutants of L-ribulose-5-phosphate 4-epimerase had 10, 1, and 0.1%, re

14 ryotes, that mediates the interconversion of ribulose 5-phosphate and arabinose 5-phosphate.

15 The CD spectra of L-ribulose 5-phosphate and D-xylulose 5-phosphate differ s

16 quilibration of the pentulose 5-phosphates d-ribulose 5-phosphate and d-xylulose 5-phosphate in the p

17 ses (APIs) catalyze the interconversion of d-ribulose-5-phosphate and D-arabinose-5-phosphate, the fi

18 e in part to reduced levels of 6PGD products ribulose-5-phosphate and NADPH, which led to reduced RNA

19 entanediol, were used to model the substrate ribulose 5-phosphate, and to propose catalytic roles for

20 crystal structure suggests the location of a ribulose 5-phosphate binding site and suggests a role fo

21 at connects the active site of YaaE with the ribulose 5-phosphate binding site was identified.

22 observations implicate new components of the ribulose 5-phosphate binding site.

23 miting tautomerization of the 1,2-enediol of ribulose 5-phosphate consistent with the proposed role o

24 ssibility of a catalytic role of Asp186 of D-ribulose 5-phosphate epimerase by site-directed mutagene

25 subunits: YaaD catalyzes the condensation of ribulose 5-phosphate, glyceraldehyde-3-phosphate, and am

26 ldol condensation between formaldehyde and d-ribulose 5-phosphate in formaldehyde-fixing methylotroph

27 structures were used to model the substrate ribulose 5-phosphate in the active site with the phospha

28 Y. pestis yrbH, catalyses the conversion of ribulose 5-phosphate into arabinose 5-phosphate (A5P), t

29 The pH profile of V/K for L-ribulose 5-phosphate is bell-shaped with pK values of 5.

30 A ribulose 5-phosphate is bound to YaaD via an imine with

31 lative to the wild-type enzyme, the Km for D-ribulose 5-phosphate is essentially unaltered with D186N

32 r each, the promiscuity is altered so that d-ribulose 5-phosphate is the preferred substrate.

33 rophosphate or ethanol and destabilized by D-ribulose-5-phosphate or 2-mercaptoethanol.

34 decarboxylation of 6PG to the 1,2-enediol of ribulose 5-phosphate proceeds via a stepwise mechanism w

35 versible aldol-ketol isomerization between D-ribulose 5-phosphate (Ru5P) and D-arabinose 5-phosphate

36 I), which catalyzes the interconversion of d-ribulose 5-phosphate (Ru5P) and d-arabinose 5-phosphate

37 eps in the riboflavin pathway and converts d-ribulose 5-phosphate (Ru5P) to l-3,4-dihydroxy-2-butanon

38 e (PRK) is responsible for the conversion of ribulose 5-phosphate (Ru5P) to ribulose 1,5-bisphosphate

39 4-epimerase catalyzes the epimerization of L-ribulose 5-phosphate to D-xylulose 5-phosphate by an ald

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