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1 hardtii starchless mutant, sta6, which lacks ADP-glucose pyrophosphorylase.
2 is was not linked to reductive activation of ADP-glucose pyrophosphorylase.
3 he rate-limiting starch biosynthetic enzyme, ADP-glucose pyrophosphorylase.
4 ort the first atomic resolution structure of ADP-glucose pyrophosphorylase.
5 synthase, UDP-glucose pyrophosphorylase, and ADP-glucose pyrophosphorylase.
6 losteric regulatory properties of the potato ADP-glucose pyrophosphorylase.
7 edback regulation of phosphofructokinase and ADP-glucose pyrophosphorylase.
8 relatively conserved in similarly regulated ADP-glucose pyrophosphorylases.
9 ing TaNAC019, a repressor of cytosolic small ADP-glucose pyrophosphorylase 1a (TacAGPS1a), sucrose sy
10 pes of gene encoding small subunits (SSU) of ADP-glucose pyrophosphorylase, a starch-biosynthetic enz
17 lgC and glgD) respectively encoding putative ADP-glucose pyrophosphorylases (ADP-Glc PPase), a key en
19 bacter sphaeroides adenosine 5'-diphosphate-(ADP)-glucose pyrophosphorylase (ADPGlc PPase) using affi
22 ity of enzymes involved in starch synthesis (ADP-glucose pyrophosphorylase, ADPGlc PPase; granule bou
28 ucture-function analysis of the higher-plant ADP-glucose pyrophosphorylase (AGP), we used a random mu
33 ids were used to investigate the location of ADP-glucose pyrophosphorylase (AGPase) in the developing
38 o1;2 mutant, which inhibited the activity of ADP-glucose pyrophosphorylase (AGPase), important for st
39 ed uniquely with the small subunit (APS1) of ADP-glucose pyrophosphorylase (AGPase), the first commit
42 ing late seed development, such as those for ADP glucose pyrophosphorylase and starch synthase, do no
43 en metabolic pathway comprises the action of ADP-glucose pyrophosphorylase and glycogen synthase, whe
44 on the allosteric regulation of higher plant ADP-glucose pyrophosphorylases and validates a strategy
45 osynthetic enzymes, namely starch synthases, ADP-glucose pyrophosphorylase, and starch branching and
46 dikinase (PPDK), large and small subunits of ADP-glucose pyrophosphorylase, and the sucrose synthase
47 gulated, suggesting that redox regulation of ADP-glucose pyrophosphorylases appeared later in evoluti
48 al prediction of several bacterial and plant ADP-glucose pyrophosphorylases, as well as of other suga
49 tion that Asp(142) might play in the E. coli ADP-glucose pyrophosphorylase, aspartate was replaced by
59 report pyruvate-bound crystal structures of ADP-glucose pyrophosphorylase from the bacterium Agrobac
60 most probably the inhibitor-binding site, of ADP-glucose pyrophosphorylase from the cyanobacterium An
61 erved insensitivity to effector molecules by ADP-glucose pyrophosphorylases from other non-photosynth
62 ion of VAC-INVcis-QTL were also detected for ADP-glucose pyrophosphorylase, fumarase, and phosphogluc
63 chlorophyll a/b-binding protein gene (CAB1), ADP-glucose pyrophosphorylase gene (APL3), and chalcone
64 esis of the large subunit (LS) of the potato ADP-glucose pyrophosphorylase generated an enzyme, P52L,
66 resulted in near-complete solubilization of ADP-glucose pyrophosphorylase, indicating that little, i
69 osphorylase, indicating that little, if any, ADP-glucose pyrophosphorylase is granule associated.
70 ue (Lys 419) near the C-terminus of Anabaena ADP-glucose pyrophosphorylase is involved in the binding
71 acterized five isoforms of Manihot esculenta ADP-glucose pyrophosphorylase large subunit (MeAPL1-MeAP
72 Starch structure is impacted by enzymes like ADP-glucose pyrophosphorylase, starch synthases, and deb
73 regulatory sequences of the sugar inducible ADP-glucose pyrophosphorylase subunit ApL3 were fused to
74 adg1 mutation disables the small subunit of ADP-glucose pyrophosphorylase, the first step in starch
75 etic, regulatory and evolutionary aspects of ADP-glucose pyrophosphorylase, the regulatory enzyme for
76 se pathways, fructose-1,6-bisphosphatase and ADP-glucose pyrophosphorylase, was almost completely abo
77 crease in sink capacity, such as increase in ADP-glucose pyrophosphorylase, was also indicated to lea
78 to derepression of the reaction catalyzed by ADP-glucose pyrophosphorylase, we evaluated whether the
79 subcellular compartment-specific isoforms of ADP-glucose pyrophosphorylase were detected, thus provid
81 Treatment of the Agrobacterium tumefaciens ADP-glucose pyrophosphorylase with the arginyl reagent p