scholarly article | Q13442814 |
P50 | author | Detlev H. Krüger | Q1201438 |
Merlind Mucke | Q101542192 | ||
P2093 | author name string | Monika Reuter | |
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Crystal structure of NaeI--an evolutionary bridge between DNA endonuclease and topoisomerase | Q27624935 | ||
Unexpected structural diversity in DNA recombination: the restriction endonuclease connection | Q27625490 | ||
Structure of the tetrameric restriction endonuclease NgoMIV in complex with cleaved DNA | Q27626779 | ||
Structure of NaeI-DNA complex reveals dual-mode DNA recognition and complete dimer rearrangement | Q27633648 | ||
Crystal structure of Citrobacter freundii restriction endonuclease Cfr10I at 2.15 A resolution | Q27732535 | ||
Structure of the multimodular endonuclease FokI bound to DNA | Q27740190 | ||
Subunit assembly and mode of DNA cleavage of the type III restriction endonucleases EcoP1I and EcoP15I. | Q31937862 | ||
Chimeric restriction enzymes: what is next? | Q33737255 | ||
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Structural basis for MutH activation in E.coli mismatch repair and relationship of MutH to restriction endonucleases | Q33888460 | ||
Imaging DNA loops induced by restriction endonuclease EcoRII. A single amino acid substitution uncouples target recognition from cooperative DNA interaction and cleavage | Q33910413 | ||
Self-generated DNA termini relax the specificity of SgrAI restriction endonuclease | Q34008473 | ||
Many type IIs restriction endonucleases interact with two recognition sites before cleaving DNA. | Q34103727 | ||
DNA and spermidine provide a switch mechanism to regulate the activity of restriction enzyme Nae I. | Q34324777 | ||
Similarities and differences among 105 members of the Int family of site-specific recombinases | Q34652687 | ||
Changing endonuclease EcoRII Tyr308 to Phe abolishes cleavage but not recognition: possible homology with the Int-family of recombinases | Q34985243 | ||
The domain organization of NaeI endonuclease: separation of binding and catalysis | Q36003818 | ||
Functional domains in Fok I restriction endonuclease. | Q37000625 | ||
Class-IIS restriction enzymes--a review | Q37765759 | ||
Two subunits of EcoRII restriction endonuclease interact with two DNA recognition sites | Q38311075 | ||
Modified DNA fragments activate NaeI cleavage of refractory DNA sites | Q38325335 | ||
Regions of endonuclease EcoRII involved in DNA target recognition identified by membrane-bound peptide repertoires. | Q38328208 | ||
NaeI endonuclease binding to pBR322 DNA induces looping | Q38336509 | ||
Oligonucleotide duplexes containing CC(A/T)GG stimulate cleavage of refractory DNA by restriction endonuclease EcoRII. | Q38345031 | ||
EcoRII: a restriction enzyme evolving recombination functions? | Q38362416 | ||
Activation of restriction endonuclease EcoRII does not depend on the cleavage of stimulator DNA. | Q40507377 | ||
EcoRII can be activated to cleave refractory DNA recognition sites | Q40545771 | ||
Analysis of DNA looping interactions by type II restriction enzymes that require two copies of their recognition sites | Q43699908 | ||
DNA cleavage by type III restriction-modification enzyme EcoP15I is independent of spacer distance between two head to head oriented recognition sites | Q43749963 | ||
Amino acid substitutions at position 43 of NaeI endonuclease. Evidence for changes in NaeI structure | Q44273168 | ||
Nonidentical DNA-binding sites of endonuclease NaeI recognize different families of sequences flanking the recognition site | Q44501284 | ||
DNA looping by the Sfi I restriction endonuclease | Q47708812 | ||
Cooperative binding properties of restriction endonuclease EcoRII with DNA recognition sites. | Q52995430 | ||
Hyperexpressed EcoRII renatured from inclusion bodies and native enzyme both exhibit essential cooperativity with two DNA sites. | Q53013124 | ||
Interaction of EcoRII endonuclease with DNA substrates containing single recognition sites | Q54261959 | ||
Evolutionary relationship between different subgroups of restriction endonucleases | Q56900882 | ||
The Cfr10I restriction enzyme is functional as a tetramer | Q60500600 | ||
DNA looping | Q68008374 | ||
The SfiI restriction endonuclease makes a four-strand DNA break at two copies of its recognition sequence | Q72241576 | ||
DNA topoisomerase and recombinase activities in Nae I restriction endonuclease | Q72635901 | ||
[Kinetic modeling of the mechanism of allosteric interactions of restriction endonuclease EcoRII with two DNA segments] | Q73078700 | ||
Sau3AI, a monomeric type II restriction endonuclease that dimerizes on the DNA and thereby induces DNA loops | Q73794058 | ||
FokI requires two specific DNA sites for cleavage | Q74326486 | ||
DNA cleavage reactions by type II restriction enzymes that require two copies of their recognition sites | Q74328897 | ||
EcoRII endonuclease has two identical DNA-binding sites and cleaves one of two co-ordinated recognition sites in one catalytic event | Q74440419 | ||
DNA restriction dependent on two recognition sites: activities of the SfiI restriction-modification system in Escherichia coli | Q74649181 | ||
Alternative arrangements of catalytic residues at the active sites of restriction enzymes | Q78067597 | ||
P433 | issue | 21 | |
P304 | page(s) | 6079-6084 | |
P577 | publication date | 2003-11-01 | |
P1433 | published in | Nucleic Acids Research | Q135122 |
P1476 | title | Diversity of type II restriction endonucleases that require two DNA recognition sites | |
P478 | volume | 31 |
Q33871185 | A putative mobile genetic element carrying a novel type IIF restriction-modification system (PluTI) |
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Q40244890 | A switch in the mechanism of communication between the two DNA-binding sites in the SfiI restriction endonuclease |
Q38535019 | Concerted action at eight phosphodiester bonds by the BcgI restriction endonuclease. |
Q42002446 | DNA looping and translocation provide an optimal cleavage mechanism for the type III restriction enzymes |
Q42183834 | DNA looping by FokI: the impact of synapse geometry on loop topology at varied site orientations. |
Q41911300 | Differences between Ca2+ and Mg2+ in DNA binding and release by the SfiI restriction endonuclease: implications for DNA looping |
Q40421023 | Direct monitoring of allosteric recognition of type IIE restriction endonuclease EcoRII. |
Q39094209 | Dynamics of single DNA looping and cleavage by Sau3AI and effect of tension applied to the DNA. |
Q40898041 | Illuminating the reaction pathway of the FokI restriction endonuclease by fluorescence resonance energy transfer |
Q98176844 | Modular prophage interactions driven by capsule serotype select for capsule loss under phage predation |
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Q41023221 | One recognition sequence, seven restriction enzymes, five reaction mechanisms. |
Q41429735 | Organization of the BcgI restriction-modification protein for the cleavage of eight phosphodiester bonds in DNA. |
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Q41770197 | Restriction endonucleases that bridge and excise two recognition sites from DNA. |
Q30491964 | Single-molecule dynamics of the DNA-EcoRII protein complexes revealed with high-speed atomic force microscopy. |
Q33209323 | Specificity changes in the evolution of type II restriction endonucleases: a biochemical and bioinformatic analysis of restriction enzymes that recognize unrelated sequences |
Q34851749 | Tension-dependent DNA cleavage by restriction endonucleases: two-site enzymes are "switched off" at low force |
Q37856408 | The reaction mechanism of FokI excludes the possibility of targeting zinc finger nucleases to unique DNA sites. |
Q39770852 | TstI, a Type II restriction-modification protein with DNA recognition, cleavage and methylation functions in a single polypeptide |
Q33843093 | Type II restriction endonucleases--a historical perspective and more |
Q37880722 | Unraveling DNA dynamics using atomic force microscopy |
Q35627759 | Visual analysis of concerted cleavage by type IIF restriction enzyme SfiI in subsecond time region |
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