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1 ontains the recognition sequence of the NarI Type II restriction endonuclease.
2 ific mitochondrial DNA binding protein and a type II restriction endonuclease.
3 Surprisingly, the TnsA fold is that of a type II restriction endonuclease.
4 group II intron reverse transcriptase and a type II restriction endonuclease.
5 NaeI is a remarkable type II restriction endonuclease.
6 targets has not been observed hitherto among type II restriction endonucleases.
7 onstrates that H. pylori is a rich source of type II restriction endonucleases.
8 e subunits similar to that seen with certain type II restriction endonucleases.
9 cific DNA-protein interactions using several type II restriction endonucleases.
10 kely to contain target sites for all natural type IIS restriction endonucleases.
11 without binding specificity, but like other type II restriction endonucleases achieves sequence spec
12 repeated cycles of enzymatic cleavage with a type IIs restriction endonuclease, adaptor ligation, and
15 uding the PD(D/E)XK superfamily (typified by type II restriction endonucleases and many recombination
17 N-terminal domain core folds like the other type II restriction endonucleases as well as lambda-exon
18 milarity of the FokI catalytic domain to the type II restriction endonuclease BamHI monomer suggested
19 metal ions bound in the active sites of the type II restriction endonucleases BamHI and BglI, sugges
24 This work provides strong evidence that some type IIS restriction endonucleases carry two separate ac
28 ignificant amino acid sequence similarity to Type II restriction endonuclease CviJI that recognizes a
29 pylori natural transformation, a markerless type II restriction endonuclease-deficient (REd) mutant
30 ribed as site I in the related blunt cutting type II restriction endonuclease EcoRV, as well as that
31 tion (PCR) combined with the capacity of the type-IIS restriction endonuclease (ENase) Eam1104I to cu
32 divergent evolution, and this suggests that type II restriction endonucleases evolved from a common
35 lower selectivity for the dcm sequence than type II restriction endonucleases have for their target
36 l artificial chromosome (BAC) clones using a Type IIS restriction endonuclease, HgaI, paired with a T
38 The 2.1A crystal structure of the unliganded type II restriction endonuclease, HincII, is described.
39 e deleted the genes encoding all four active type II restriction endonucleases in H. pylori strain 26
42 etic screening method was devised to convert type IIS restriction endonucleases into strand-specific
45 one of the active sites is inactivated, the type IIS restriction endonuclease may nick only one stra
51 nded genetic information systems (AEGIS), 24 type-II restriction endonucleases (REases) were challeng
53 e flipping mechanism as found for some other type II restriction endonuclease recognizing similarly d
56 -ray crystal structure of the 'rare cutting' type II restriction endonuclease SgrAI bound to cognate
62 hods presented are readily applicable to all type II restriction endonucleases that cleave both stran
63 long pieces of DNA, we have engineered a new type IIS restriction endonuclease that combines the spec
66 at after an initial round of indexing uses a Type IIS restriction endonuclease to expose additional s
69 Fragments produced from human genomic DNA by Type II restriction endonucleases were sorted using six
70 ational change to that observed in the other type II restriction endonucleases where DNA bound and un
72 re the structure of BstYI, an "intermediate" type II restriction endonuclease with overlapping sequen
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