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1 ous N-glycan core oligosaccharide by reverse phosphorolysis.
2 ed to attack the glycosidic bond and promote phosphorolysis.
3 ffects of (p)ppGpp on the polymerization and phosphorolysis activities of PNPase from Streptomyces co
4 ioadenosine nucleosidase (MTAN) catalyze the phosphorolysis and hydrolysis of 5'-methylthioadenosine
5 proved to be susceptible to PNPHyor-mediated phosphorolysis, and a markedly decreased or increased cy
8 nosine (F-dAdo) is a "subversive substrate." Phosphorolysis by TvPNP of F-dAdo, which is not a substr
9 y of the indicated substrates including: for phosphorolysis, higher chitin oliogsaccharides, (GlcNAc)
10 osphorylase (PNP) catalyzes N-ribosidic bond phosphorolysis in 6-oxypurine nucleosides and deoxynucle
11 se) catalyzes RNA polymerization and 3'-->5' phosphorolysis in vitro, but its roles in plant organell
17 ith the high efficiency of PNPHyor-catalyzed phosphorolysis of cladribine to its less toxic base 2-ch
18 r reaction catalyzed by these enzymes is the phosphorolysis of GDP-D-glucose to GDP and D-glucose 1-p
21 phosphorylase (PNP) catalyzes the reversible phosphorolysis of purine (2'-deoxy)ribonucleosides to gi
22 ucleoside phosphorylase catalyzes reversible phosphorolysis of purine nucleosides and 2'-deoxypurine
23 ms a ribocation-like transition state in the phosphorolysis of purine nucleosides and fast protein mo
24 dopsis VTC2 and VTC5 enzymes catalyze simple phosphorolysis of the guanylylated enzyme, forming GDP a
25 icroM ADP, CDP, GDP, and UDP, the Km for the phosphorolysis of the substrate with the 3' stem-loop wa
26 Hyor cells and observed a rapid and complete phosphorolysis of this drug when it was exposed to the s
29 idine phosphorylase catalyzes the reversible phosphorolysis of uridine and 2'-deoxyuridine to generat
34 nthesis direction and as the reactant in the phosphorolysis reaction; their interconversion can occur
35 omyces antibioticus, and Escherichia coli in phosphorolysis using substrates derived from the rpsO-pn
36 CB) and alpha-glucose 1-phosphate by reverse phosphorolysis, using enzymes cellodextrin phosphorylase
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