| scholarly article | Q13442814 |
| P50 | author | Darren M Gowers | Q61865872 |
| P2093 | author name string | Stephen E Halford | |
| Stuart R W Bellamy | |||
| P2860 | cites work | PspGI, a type II restriction endonuclease from the extreme thermophile Pyrococcus sp.: structural and functional studies to investigate an evolutionary relationship with several mesophilic restriction enzymes | Q38353751 |
| The metal-independent type IIs restriction enzyme BfiI is a dimer that binds two DNA sites but has only one catalytic centre | Q38357645 | ||
| Functional analysis of putative restriction-modification system genes in the Helicobacter pylori J99 genome | Q39584191 | ||
| Protein motion from non-specific to specific DNA by three-dimensional routes aided by supercoiling | Q39738169 | ||
| Diversity of type II restriction endonucleases that require two DNA recognition sites | Q40240500 | ||
| One- and three-dimensional pathways for proteins to reach specific DNA sites | Q40388353 | ||
| Structure and function of restriction endonucleases | Q40540883 | ||
| EcoRII can be activated to cleave refractory DNA recognition sites | Q40545771 | ||
| Recombination by resolvase to analyse DNA communications by the SfiI restriction endonuclease | Q41064313 | ||
| Repercussions of DNA tracking by the type IC restriction endonuclease EcoR124I on linear, circular and catenated substrates. | Q41078620 | ||
| Cloning and sequencing the HinfI restriction and modification genes | Q42653249 | ||
| Ability of DNA and spermidine to affect the activity of restriction endonucleases from several bacterial species | Q43886671 | ||
| Generation of the BfiI restriction endonuclease from the fusion of a DNA recognition domain to a non-specific nuclease from the phospholipase D superfamily | Q44740553 | ||
| DNA excision by the Sfi I restriction endonuclease | Q47708855 | ||
| Subunit assembly for DNA cleavage by restriction endonuclease SgrAI. | Q54528761 | ||
| Evolutionary relationship between different subgroups of restriction endonucleases | Q56900882 | ||
| Plasmid DNA Cleavage byMunI Restriction Enzyme: Single-Turnover and Steady-State Kinetic Analysis† | Q57267696 | ||
| The Cfr10I restriction enzyme is functional as a tetramer | Q60500600 | ||
| The kinetic mechanism of EcoRI endonuclease | Q64388761 | ||
| The activity of the EcoRV restriction endonuclease is influenced by flanking DNA sequences both inside and outside the DNA-protein complex | Q67731871 | ||
| 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 | ||
| Reactions of BglI and other type II restriction endonucleases with discontinuous recognition sites | Q73509790 | ||
| Communications between distant sites on supercoiled DNA from non-exponential kinetics for DNA synapsis by resolvase | Q73545861 | ||
| Sau3AI, a monomeric type II restriction endonuclease that dimerizes on the DNA and thereby induces DNA loops | Q73794058 | ||
| 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 | ||
| Alternative arrangements of catalytic residues at the active sites of restriction enzymes | Q78067597 | ||
| Crystal structure of the Bse634I restriction endonuclease: comparison of two enzymes recognizing the same DNA sequence | Q24514776 | ||
| Structure and function of type II restriction endonucleases | Q24555230 | ||
| A nomenclature for restriction enzymes, DNA methyltransferases, homing endonucleases and their genes | Q24684053 | ||
| Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors | Q26778475 | ||
| 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 | ||
| Repair of the Escherichia coli chromosome after in vivo scission by the EcoRI endonuclease | Q33847038 | ||
| DNA nicks inflicted by restriction endonucleases are repaired by a RecA- and RecB-dependent pathway in Escherichia coli | Q33876047 | ||
| Reactions of type II restriction endonucleases with 8-base pair recognition sites | Q33883325 | ||
| Many type IIs restriction endonucleases interact with two recognition sites before cleaving DNA. | Q34103727 | ||
| Organization of restriction-modification systems | Q34111928 | ||
| Complex restriction enzymes: NTP-driven molecular motors | Q34178514 | ||
| Evidence for an evolutionary relationship among type-II restriction endonucleases | Q34301710 | ||
| Fidelity of DNA recognition by the EcoRV restriction/modification system in vivo | Q34631053 | ||
| How the Bfi I restriction enzyme uses one active site to cut two DNA strands | Q35143107 | ||
| REBASE: restriction enzymes and methyltransferases | Q35158752 | ||
| Enzyme-mediated DNA looping | Q35771536 | ||
| Comparison of the nucleotide and amino acid sequences of the RsrI and EcoRI restriction endonucleases | Q35949088 | ||
| DNA binding and recognition by the IIs restriction endonuclease MboII. | Q38295631 | ||
| Novel subtype of type IIs restriction enzymes. BfiI endonuclease exhibits similarities to the EDTA-resistant nuclease Nuc of Salmonella typhimurium. | Q38310779 | ||
| Use of specific oligonucleotide duplexes to stimulate cleavage of refractory DNA sites by restriction endonucleases | Q38321306 | ||
| Specificity from the synapsis of DNA elements by the Sfi I endonuclease | Q38323728 | ||
| Crystal structure of restriction endonuclease BglI bound to its interrupted DNA recognition sequence | Q38333398 | ||
| Rapid-reaction analysis of plasmid DNA cleavage by the EcoRV restriction endonuclease. | Q38344915 | ||
| P433 | issue | 11 | |
| P304 | page(s) | 3469-3479 | |
| P577 | publication date | 2004-06-29 | |
| P1433 | published in | Nucleic Acids Research | Q135122 |
| P1476 | title | One recognition sequence, seven restriction enzymes, five reaction mechanisms | |
| P478 | volume | 32 |
| Q33871185 | A putative mobile genetic element carrying a novel type IIF restriction-modification system (PluTI) |
| Q40244890 | A switch in the mechanism of communication between the two DNA-binding sites in the SfiI restriction endonuclease |
| Q53286392 | BsaXI/RFLP analysis of initial or selectively reamplified PCR product is unreliable in detecting the V617F mutation in JAK2. |
| Q24816456 | Characterization of the Type III restriction endonuclease PstII from Providencia stuartii. |
| Q38535019 | Concerted action at eight phosphodiester bonds by the BcgI restriction endonuclease. |
| Q42000366 | DNA looping by two-site restriction endonucleases: heterogeneous probability distributions for loop size and unbinding force |
| Q33635112 | DNA recognition by the SwaI restriction endonuclease involves unusual distortion of an 8 base pair A:T-rich target |
| Q41911300 | Differences between Ca2+ and Mg2+ in DNA binding and release by the SfiI restriction endonuclease: implications for DNA looping |
| Q30490896 | Dissecting protein-induced DNA looping dynamics in real time |
| Q41967553 | Dynamics and consequences of DNA looping by the FokI restriction endonuclease |
| Q27664205 | Folding, DNA Recognition, and Function of GIY-YIG Endonucleases: Crystal Structures of R.Eco29kI |
| Q34202850 | Genome stability of Lyme disease spirochetes: comparative genomics of Borrelia burgdorferi plasmids. |
| Q40898041 | Illuminating the reaction pathway of the FokI restriction endonuclease by fluorescence resonance energy transfer |
| Q37713815 | Maintaining a sense of direction during long-range communication on DNA. |
| Q25257159 | Real-time observation of DNA looping dynamics of Type IIE restriction enzymes NaeI and NarI. |
| Q41770197 | Restriction endonucleases that bridge and excise two recognition sites from DNA. |
| Q41814991 | Rpn (YhgA-Like) Proteins of Escherichia coli K-12 and Their Contribution to RecA-Independent Horizontal Transfer. |
| Q34851749 | Tension-dependent DNA cleavage by restriction endonucleases: two-site enzymes are "switched off" at low force |
| Q33911910 | The essential genomic landscape of the commensal Bifidobacterium breve UCC2003. |
| Q36173061 | The restriction endonuclease R.NmeDI from Neisseria meningitidis that recognizes a palindromic sequence and cuts the DNA on both sides of the recognition sequence |
| Q24673408 | The restriction fold turns to the dark side: a bacterial homing endonuclease with a PD-(D/E)-XK motif |
| Q42957729 | The single polypeptide restriction-modification enzyme LlaGI is a self-contained molecular motor that translocates DNA loops |
| Q41132121 | The type II restriction endonuclease MvaI has dual specificity |
| Q34172705 | Translocation, switching and gating: potential roles for ATP in long-range communication on DNA by Type III restriction endonucleases |
| Q33843093 | Type II restriction endonucleases--a historical perspective and more |
| Q37078204 | Type III restriction enzymes communicate in 1D without looping between their target sites |
| Q47766790 | UbaLAI is a monomeric Type IIE restriction enzyme. |
| Q37360403 | Use of next generation sequence to investigate potential novel macrolide resistance mechanisms in a population of Moraxella catarrhalis isolates |
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