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1 ctures of the enzyme in complex with ATP and ADP-glucose.
2 g GDP-mannose, ADP-mannose, UDP-glucose, and ADP-glucose.
3 quent rapid conformational change induced by ADP-glucose.
4 pyrophosphorylase catalyzes the synthesis of ADP-glucose (ADP-Glc) from Glc-1-phosphate (G-1-P) and A
7 e activity is activated by a incubation with ADP-glucose and dithiothreitol or by ATP, glucose- 1-pho
8 (1) and K(m) values of 6.9 and 90 microM for ADP-glucose and phosphate, respectively, at pH 8.5 and 2
12 ranslocator with a KTGGL motif common to the ADP-glucose-binding site of starch synthases and bacteri
13 glucose derivatives as glucosyl donors, i.e. ADP-glucose, CDP-glucose, GDP-glucose, TDP-glucose and U
14 P-glucose, TDP-glucose and UDP-glucose, with ADP-glucose, GDP-glucose and UDP-glucose being the prefe
15 he purified enzyme displays no activity with ADP-glucose, GDP-mannose, UDP-glucose, or UDP-galactose.
17 ined to be involved in the regulation of the ADP-glucose (Glc) pyrophosphorylase from spinach leaf an
20 t of SUS in the synthesis of UDP-glucose and ADP-glucose linked to Arabidopsis cellulose and starch b
22 ing late seed development, such as those for ADP glucose pyrophosphorylase and starch synthase, do no
24 bacter sphaeroides adenosine 5'-diphosphate-(ADP)-glucose pyrophosphorylase (ADPGlc PPase) using affi
36 ucture-function analysis of the higher-plant ADP-glucose pyrophosphorylase (AGP), we used a random mu
41 ids were used to investigate the location of ADP-glucose pyrophosphorylase (AGPase) in the developing
46 ed uniquely with the small subunit (APS1) of ADP-glucose pyrophosphorylase (AGPase), the first commit
58 most probably the inhibitor-binding site, of ADP-glucose pyrophosphorylase from the cyanobacterium An
59 chlorophyll a/b-binding protein gene (CAB1), ADP-glucose pyrophosphorylase gene (APL3), and chalcone
60 esis of the large subunit (LS) of the potato ADP-glucose pyrophosphorylase generated an enzyme, P52L,
64 osphorylase, indicating that little, if any, ADP-glucose pyrophosphorylase is granule associated.
65 ue (Lys 419) near the C-terminus of Anabaena ADP-glucose pyrophosphorylase is involved in the binding
66 regulatory sequences of the sugar inducible ADP-glucose pyrophosphorylase subunit ApL3 were fused to
67 subcellular compartment-specific isoforms of ADP-glucose pyrophosphorylase were detected, thus provid
68 Treatment of the Agrobacterium tumefaciens ADP-glucose pyrophosphorylase with the arginyl reagent p
70 pes of gene encoding small subunits (SSU) of ADP-glucose pyrophosphorylase, a starch-biosynthetic enz
71 osynthetic enzymes, namely starch synthases, ADP-glucose pyrophosphorylase, and starch branching and
72 dikinase (PPDK), large and small subunits of ADP-glucose pyrophosphorylase, and the sucrose synthase
73 tion that Asp(142) might play in the E. coli ADP-glucose pyrophosphorylase, aspartate was replaced by
74 ion of VAC-INVcis-QTL were also detected for ADP-glucose pyrophosphorylase, fumarase, and phosphogluc
75 resulted in near-complete solubilization of ADP-glucose pyrophosphorylase, indicating that little, i
76 adg1 mutation disables the small subunit of ADP-glucose pyrophosphorylase, the first step in starch
77 se pathways, fructose-1,6-bisphosphatase and ADP-glucose pyrophosphorylase, was almost completely abo
78 crease in sink capacity, such as increase in ADP-glucose pyrophosphorylase, was also indicated to lea
79 to derepression of the reaction catalyzed by ADP-glucose pyrophosphorylase, we evaluated whether the
87 lgC and glgD) respectively encoding putative ADP-glucose pyrophosphorylases (ADP-Glc PPase), a key en
88 on the allosteric regulation of higher plant ADP-glucose pyrophosphorylases and validates a strategy
89 gulated, suggesting that redox regulation of ADP-glucose pyrophosphorylases appeared later in evoluti
90 erved insensitivity to effector molecules by ADP-glucose pyrophosphorylases from other non-photosynth
91 al prediction of several bacterial and plant ADP-glucose pyrophosphorylases, as well as of other suga
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