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1 spread of the branch points directly with T4 endonuclease VII.
2  in the phosphodiester cleavage mechanism of endonuclease VII.
3 xyl radicals, KMnO4, the junction resolvases endonuclease VII and RuvC, and RuvC activation of KMNO4
4 he rate of resolution of the Hol75 DNA by T4 endonuclease VII and T7 endonuclease I, two enzymes know
5 ced the cleavage of Holliday junctions by T4 endonuclease VII and T7 endonuclease I.
6 rly and middle genes, but two late proteins, endonuclease VII and terminase, are uniquely important i
7     This motif is shared by subdomains of T4 endonuclease VII and transcription factor rho, despite n
8 tic lysyl-tRNA synthetases, bacteriophage T4 endonuclease VII, and several uncharacterized proteins.
9                        Furthermore, purified endonuclease VII cleaved the blocked forks in vitro clos
10 uctural folds, namely RNase H, endonuclease, endonuclease VII-colicin E and RusA.
11                                       Active endonuclease VII converts the supercoiled circular DNA d
12 e accumulation of blocked forks increased in endonuclease VII-deficient infections, suggesting that e
13                    Together with colicin E7, endonuclease VII defines a distinct metal-dependent nucl
14 aracter is observed between Hjc and T4-phage endonuclease VII despite a complete lack of structural h
15 uding nondenaturing PAGE, Ferguson analysis, endonuclease VII digestion, and hydroxyl radical autofoo
16                               (3) On binding endonuclease VII E86A to junctions, the configuration of
17                                        Using endonuclease VII E86A we have shown: (1) The protein bin
18                                     Phage T4 endonuclease VII (endo VII) was the first enzyme shown t
19 ication reaction is only partly dependent on endonuclease VII (gp49), suggesting that either another
20                                           T4 endonuclease VII is a junction-selective enzyme that bot
21                             Bacteriophage T4 endonuclease VII is a nuclease that is selective for fou
22 f the cruciform by the junction resolvase T4 endonuclease VII is independent of PARP-1, which indicat
23 imer of active enzyme and an inactive mutant endonuclease VII leads to the formation of nicked circul
24 ber of other DNA junction-resolving enzymes, endonuclease VII of bacteriophage T4 binds to a four-way
25            The DNA junction-resolving enzyme endonuclease VII of bacteriophage T4 contains a zinc-bin
26 n low-GC Gram-positive bacteria and AQUIFEX: Endonuclease VII of phage T4 is shown to serve as a stru
27 rrelation spectroscopy that purified T4 gp49 endonuclease VII resolvase can release DNA compression i
28 hat these blocked forks can be cleaved by T4 endonuclease VII to create overt DNA breaks.
29   Fourth, mutations that inactivate UvsW and endonuclease VII (which cleaves DNA branches) synergisti

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