ライフサイエンスコーパス: sedoheptulose

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1 cycle enzymes triose-phosphate isomerase and sedoheptulose 1,7-bisphosphate phosphatase.

2 to accumulation of fructose 1-phosphate and sedoheptulose 1-phosphate but not glucose 6-phosphate, f

3 ponding labels into fructose 1-phosphate and sedoheptulose 1-phosphate in FK866-treated cells.

4 oxyacetone phosphate and glyceraldehyde, and sedoheptulose 1-phosphate was derived from dihydroxyacet

5 e dark, and in the dark with the addition of sedoheptulose-1,7-bisphosphatase (normally inactive in t

6 atory members of the cycle, our knowledge of sedoheptulose-1,7-bisphosphatase (SBPase) is particularl

7 d to sedoheptulose-7-phosphate by the enzyme sedoheptulose-1,7-bisphosphatase (SHB17), whose activity

8 chloroplast fructose-1,6-bisphosphatase and sedoheptulose-1,7-bisphosphatase activity showed that th

9 o calculate the flux control coefficients of sedoheptulose-1,7-bisphosphatase over photosynthetic ass

10 The effect of introducing sedoheptulose-1,7-bisphosphatase to the system are relat

11 PCOP enzymes and underinvestment in Rubisco, sedoheptulose-1,7-bisphosphatase, and fructose-1,6-bisph

12 ich the activity of the Calvin cycle enzyme, sedoheptulose-1,7-bisphosphatase, is reduced by an antis

13 ydryl groups of fructose-1,6-bisphosphatase, sedoheptulose-1,7-bisphosphatase, phosphoribulokinase, N

14 e crystal structure of Shb17 in complex with sedoheptulose-1,7-bisphosphate reveals that the substrat

15 of the seven-carbon bisphosphorylated sugar sedoheptulose-1,7-bisphosphate.

16 nerated from an open-chain C(7) precursor, D-sedoheptulose 7-phosphate (5), by a DHQ synthase-like cy

17 ucose 6-phosphate, fructose 6-phosphate, and sedoheptulose 7-phosphate as previously thought.

18 ed by LmbR using D-fructose 6-phosphate or D-sedoheptulose 7-phosphate as the C(3) donor and D-ribose

19 Sedoheptulose 7-phosphate cyclases are enzymes that util

20 These enzymes catalyze the conversion of sedoheptulose 7-phosphate to 2-epi-valiolone, which is p

21 -regulation of cell wall biosynthesis (via D-sedoheptulose 7-phosphate) and nucleotide metabolism (vi

22 ers was characterized by the accumulation of sedoheptulose 7-phosphate, failure to recycle ribose 5-p

23 the pentose phosphate pathway intermediate, sedoheptulose 7-phosphate, to generate cyclic precursors

24 es are ultimately derived from a C(7) sugar, sedoheptulose 7-phosphate, which is cyclized to 2-epi-5-

25 sedoheptulose bisphosphate is hydrolyzed to sedoheptulose-7-phosphate by the enzyme sedoheptulose-1,

26 e is GmhA, which catalyzes the conversion of sedoheptulose-7-phosphate into D-glycero-D-manno-heptopy

27 Sedoheptulose-7-phosphate is ultimately converted by kno

28 ting for their specificity for seven-carbon (sedoheptulose) and six-carbon (fructose) sugar bisphosph

29 l structure of the Chlamydomonas reinhardtii sedoheptulose bisphosphatase (EC 3.1.3.37) there are two

30 Examination of the redox modulation of this sedoheptulose bisphosphatase confirms that it resembles

31 boxylase/oxygenase, phosphoribulokinase, and sedoheptulose bisphosphatase.

32 in modulation in the algal and higher plant sedoheptulose bisphosphatases.

33 In the pathway's committed step, sedoheptulose bisphosphate is hydrolyzed to sedoheptulos

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