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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.
10 inine-186, which is conserved in prokaryotic phosphoribulokinases, have not been previously functiona
11 at Rs. rubrum and Rp. palustris Calvin cycle phosphoribulokinase mutants that cannot produce RuBP can
12 osphatase, sedoheptulose-1,7-bisphosphatase, phosphoribulokinase, NADP-glyceraldehyde phosphate dehyd
13 Escherichia coli metabolism by expressing a phosphoribulokinase-neomycin phosphotransferase fusion p
14 complex with the Calvin-Benson cycle enzymes phosphoribulokinase (PRK) and glyceraldehyde-3-phosphate
15 enzymes regulated by thioredoxin f, spinach phosphoribulokinase (PRK) and the fructose-1,6-bisphosph
21 ostulate has not been rigorously tested with phosphoribulokinase (PRK), a fulcrum for redox regulatio
22 athway, there is a need for an enzyme, i.e., phosphoribulokinase (PRK), to catalyze the formation of
26 dehyde-3-phosphate dehydrogenase (GAPDH) and phosphoribulokinase, two enzymes of the carbon assimilat
27 strains revealed that a product generated by phosphoribulokinase was involved in control of CbbR-medi
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