scholarly article | Q13442814 |
P2093 | author name string | Stephen E Halford | |
Lucy E Catto | |||
Susan E Milsom | |||
Abigail J Welsh | |||
Sumita Ganguly | |||
P2860 | cites work | Nucleoside triphosphate-dependent restriction enzymes | Q24555228 |
FokI dimerization is required for DNA cleavage | Q24657843 | ||
Structure of FokI has implications for DNA cleavage | Q24657897 | ||
A nomenclature for restriction enzymes, DNA methyltransferases, homing endonucleases and their genes | Q24684053 | ||
REBASE--restriction enzymes and DNA methyltransferases | Q24793693 | ||
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 | ||
Structure of the multimodular endonuclease FokI bound to DNA | Q27740190 | ||
Measurement of the contributions of 1D and 3D pathways to the translocation of a protein along DNA. | Q34091428 | ||
Many type IIs restriction endonucleases interact with two recognition sites before cleaving DNA. | Q34103727 | ||
Site-specific DNA-nicking mutants of the heterodimeric restriction endonuclease R.BbvCI. | Q34410970 | ||
Type II restriction endonucleases: structure and mechanism | Q34555997 | ||
How the Bfi I restriction enzyme uses one active site to cut two DNA strands | Q35143107 | ||
Enzyme-mediated DNA looping | Q35771536 | ||
Functional domains in Fok I restriction endonuclease. | Q37000625 | ||
DNA binding and recognition by the IIs restriction endonuclease MboII. | Q38295631 | ||
The energetics of the interaction of BamHI endonuclease with its recognition site GGATCC. | Q38303246 | ||
The monomeric homing endonuclease PI-SceI has two catalytic centres for cleavage of the two strands of its DNA substrate | Q38317452 | ||
Specificity from the synapsis of DNA elements by the Sfi I endonuclease | Q38323728 | ||
Rapid-reaction analysis of plasmid DNA cleavage by the EcoRV restriction endonuclease. | Q38344915 | ||
The metal-independent type IIs restriction enzyme BfiI is a dimer that binds two DNA sites but has only one catalytic centre | Q38357645 | ||
DNA supercoiling enables the type IIS restriction enzyme BspMI to recognise the relative orientation of two DNA sequences | Q39922663 | ||
Diversity of type II restriction endonucleases that require two DNA recognition sites | Q40240500 | ||
Structure and function of restriction endonucleases | Q40540883 | ||
EcoRII can be activated to cleave refractory DNA recognition sites | Q40545771 | ||
Transposition and site-specific recombination: adapting DNA cut-and-paste mechanisms to a variety of genetic rearrangements | Q41625243 | ||
A view of consecutive binding events from structures of tetrameric endonuclease SfiI bound to DNA. | Q43048971 | ||
DNA looping by the Sfi I restriction endonuclease | Q47708812 | ||
Subunit assembly for DNA cleavage by restriction endonuclease SgrAI. | Q54528761 | ||
Plasmid DNA Cleavage byMunI Restriction Enzyme: Single-Turnover and Steady-State Kinetic Analysis†| Q57267696 | ||
Sequence-dependent helical periodicity of DNA | Q59073903 | ||
The Cfr10I restriction enzyme is functional as a tetramer | Q60500600 | ||
Cleavage of Individual DNA Strands by the Different Subunits of the Heterodimeric Restriction Endonuclease BbvCI | Q63362548 | ||
The kinetic mechanism of EcoRI endonuclease | Q64388761 | ||
DNA looping | Q68008374 | ||
Purification and characterization of the FokI restriction endonuclease | Q69385045 | ||
DNA cleavage at two recognition sites by the SfiI restriction endonuclease: salt dependence of cis and trans interactions between distant DNA sites | Q71751602 | ||
The SfiI restriction endonuclease makes a four-strand DNA break at two copies of its recognition sequence | Q72241576 | ||
Atypical DNA-binding properties of class-IIS restriction endonucleases: evidence for recognition of the cognate sequence by a FokI monomer | Q72383650 | ||
Crystallization and preliminary X-ray analysis of restriction endonuclease FokI bound to DNA | Q73094721 | ||
Alternative geometries of DNA looping: an analysis using the SfiI endonuclease | Q73692909 | ||
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 | ||
Hopping, jumping and looping by restriction enzymes | Q74347698 | ||
Does BcgI, a unique restriction endonuclease, require two recognition sites for cleavage? | Q74653661 | ||
The type IIs restriction endonuclease BspMI is a tetramer that acts concertedly at two copies of an asymmetric DNA sequence | Q77309135 | ||
[Type IIE and IIF restriction endonucleases interacting with two recognition sites in DNA] | Q81034176 | ||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 1711-1720 | |
P577 | publication date | 2006-03-23 | |
P1433 | published in | Nucleic Acids Research | Q135122 |
P1476 | title | Protein assembly and DNA looping by the FokI restriction endonuclease | |
P478 | volume | 34 |
Q39986656 | A novel mechanism for the scission of double-stranded DNA: BfiI cuts both 3'-5' and 5'-3' strands by rotating a single active site |
Q41959958 | A novel zinc-finger nuclease platform with a sequence-specific cleavage module. |
Q47114521 | A single active site in the mariner transposase cleaves DNA strands of opposite polarity. |
Q41901647 | Adding fingers to an engineered zinc finger nuclease can reduce activity |
Q37243964 | An EM view of the FokI synaptic complex by single particle analysis |
Q46506838 | Analysis of P element transposase protein-DNA interactions during the early stages of transposition |
Q38535019 | Concerted action at eight phosphodiester bonds by the BcgI restriction endonuclease. |
Q28298846 | Creating Designed Zinc-Finger Nucleases with Minimal Cytotoxicity |
Q43124003 | Creation of a type IIS restriction endonuclease with a long recognition sequence |
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. |
Q42052270 | DNA looping by FokI: the impact of twisting and bending rigidity on protein-induced looping dynamics. |
Q42000366 | DNA looping by two-site restriction endonucleases: heterogeneous probability distributions for loop size and unbinding force |
Q41967553 | Dynamics and consequences of DNA looping by the FokI restriction endonuclease |
Q40898041 | Illuminating the reaction pathway of the FokI restriction endonuclease by fluorescence resonance energy transfer |
Q35991442 | Monomeric site-specific nucleases for genome editing |
Q41429735 | Organization of the BcgI restriction-modification protein for the cleavage of eight phosphodiester bonds in DNA. |
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Q39048699 | Restriction endonuclease AgeI is a monomer which dimerizes to cleave DNA |
Q24682734 | Restriction endonuclease BpuJI specific for the 5'-CCCGT sequence is related to the archaeal Holliday junction resolvase family |
Q41770197 | Restriction endonucleases that bridge and excise two recognition sites from DNA. |
Q28307957 | Structure-based redesign of the dimerization interface reduces the toxicity of zinc-finger nucleases |
Q35070354 | TALE-PvuII fusion proteins--novel tools for gene targeting. |
Q38855439 | Target site cleavage by the monomeric restriction enzyme BcnI requires translocation to a random DNA sequence and a switch in enzyme orientation |
Q43141069 | Targeting individual subunits of the FokI restriction endonuclease to specific DNA strands |
Q37856408 | The reaction mechanism of FokI excludes the possibility of targeting zinc finger nucleases to unique DNA sites. |
Q37948867 | Towards artificial metallonucleases for gene therapy: recent advances and new perspectives |
Q33843093 | Type II restriction endonucleases--a historical perspective and more |
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