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1 RTPR also catalyzes the exchange of the C5'-hydrogens of
2 RTPR, in the presence of allosteric effector dGTP and in
3 interpreted to support the proposal that an RTPR-based thiyl radical can give rise to a nucleotide-b
6 e constants for epimerization by RTPR, C408A-RTPR, and C408S-RTPRs in the presence of dGTP are 5.1, 0
7 ed with RTPR or the Cys 408 viariants, C408A-RTPR and C408S-RTPR in the presence of dGTP, the deuteri
9 the Cys 408 viariants, C408A-RTPR and C408S-RTPR in the presence of dGTP, the deuterium at the 5'-ca
10 epimerization by RTPR, C408A-RTPR, and C408S-RTPRs in the presence of dGTP are 5.1, 0.28, and 0.42 s(
13 ne 5'-triphosphate, and isotopically labeled RTPR and AdoCbl in conjunction with EPR spectroscopy has
14 Observation of epimerization with mutated RTPR proves that transient cleavage of the Co-C5' bond o
19 The ribonucleoside triphosphate reductase (RTPR) from Lactobacillus leichmannii catalyzes adenosylc
20 tion, ribonucleoside triphosphate reductase (RTPR) from Lactobacillus leichmannii catalyzes the homol
21 ndent ribonucleoside triphosphate reductase (RTPR) from Lactobacillus leichmannii catalyzes the reduc
22 The ribonucleoside triphosphate reductase (RTPR) from Lactobacillus leichmannii catalyzes the reduc
24 oncentration remained unchanged at 1.4 spins/RTPR, twice that predicted by the amount of cob(II)alami
30 lcobalamin (5'R/S = 3:1), was incubated with RTPR or the Cys 408 viariants, C408A-RTPR and C408S-RTPR
31 Mechanistic implications with respect to wt-RTPR-mediated carbon cobalt bond homolysis and the inter
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