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1  below those required to denature Rubisco or phosphoribulokinase.
2 dehyde 3-phosphate dehydrogenase (GAPDH) and phosphoribulokinase.
3 ulose bisphosphate carboxylase (RuBisCO) and phosphoribulokinase.
4 ment of the mobile lid domain as part of the phosphoribulokinase active site, even though this region
5 tional mutations were made in genes encoding phosphoribulokinase and transketolase and in the gene en
6 fructose 1,6-bisphosphatase), cbbP (encoding phosphoribulokinase), and part of cbbT (encoding transke
7 ribulose bisphosphate carboxylase/oxygenase, phosphoribulokinase, and sedoheptulose bisphosphatase.
8 e dehydrogenase) and carbon-fixing (RuBisCO, phosphoribulokinase, carbonic anhydrase) modules.
9                      Rhodobacter sphaeroides phosphoribulokinase contains four invariant arginines (R
10 e 1,5-bisphosphate carboxylase/oxygenase and phosphoribulokinase deletion strains.
11                                              Phosphoribulokinase, glyceraldehyde-3-phosphate dehydrog
12 inine-186, which is conserved in prokaryotic phosphoribulokinases, have not been previously functiona
13 at Rs. rubrum and Rp. palustris Calvin cycle phosphoribulokinase mutants that cannot produce RuBP can
14 osphatase, sedoheptulose-1,7-bisphosphatase, phosphoribulokinase, NADP-glyceraldehyde phosphate dehyd
15  Escherichia coli metabolism by expressing a phosphoribulokinase-neomycin phosphotransferase fusion p
16                                              Phosphoribulokinase (PRK) and glyceraldehyde 3-phosphate
17 , CP12 joins the Calvin-Benson cycle enzymes phosphoribulokinase (PRK) and glyceraldehyde-3-phosphate
18 complex with the Calvin-Benson cycle enzymes phosphoribulokinase (PRK) and glyceraldehyde-3-phosphate
19  enzymes regulated by thioredoxin f, spinach phosphoribulokinase (PRK) and the fructose-1,6-bisphosph
20                      Rhodobacter sphaeroides phosphoribulokinase (PRK) binds ATP substrate, as well a
21                     The N-terminal region of phosphoribulokinase (PRK) has been proposed to contain a
22 e 11 enzymes of the CB cycle, the TRX target phosphoribulokinase (PRK) has yet to be characterized at
23                      Rhodobacter sphaeroides phosphoribulokinase (PRK) is inactivated upon exposure t
24                                              Phosphoribulokinase (PRK) is one of several plant enzyme
25          The essential photosynthetic enzyme phosphoribulokinase (PRK) is responsible for the convers
26 ostulate has not been rigorously tested with phosphoribulokinase (PRK), a fulcrum for redox regulatio
27 athway, there is a need for an enzyme, i.e., phosphoribulokinase (PRK), to catalyze the formation of
28                                              Phosphoribulokinase (PRK), unique to photosynthetic orga
29 e phosphorylation of ribulose 5-phosphate by phosphoribulokinase (PRK).
30               In this study we characterized phosphoribulokinase (PRK, EC 2.7.1.19) from the eukaryot
31                                    Bacterial phosphoribulokinases (PRKs) are octameric members of the
32 dehyde-3-phosphate dehydrogenase (GAPDH) and phosphoribulokinase, two enzymes of the carbon assimilat
33 strains revealed that a product generated by phosphoribulokinase was involved in control of CbbR-medi
34                    Activities of Rubisco and phosphoribulokinase were sufficient to account for signi