| scholarly article | Q13442814 |
| P356 | DOI | 10.1074/JBC.M108441200 |
| P698 | PubMed publication ID | 11729187 |
| P2093 | author name string | Stephen E Halford | |
| Niall A Gormley | |||
| Susan E Milsom | |||
| Abigail J Bath | |||
| P2860 | cites work | FokI dimerization is required for DNA cleavage | Q24657843 |
| Structure of FokI has implications for DNA cleavage | Q24657897 | ||
| 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 Bam HI endonuclease bound to DNA: partial folding and unfolding on DNA binding | Q27729783 | ||
| The structure of I-Crel, a group I intron-encoded homing endonuclease | Q27739151 | ||
| Structure of the multimodular endonuclease FokI bound to DNA | Q27740190 | ||
| Construction and characterization of new cloning vehicle. II. A multipurpose cloning system | Q28298407 | ||
| ATP-dependent restriction enzymes | Q33851803 | ||
| Reactions of type II restriction endonucleases with 8-base pair recognition sites | Q33883325 | ||
| The nicking endonuclease N.BstNBI is closely related to type IIs restriction endonucleases MlyI and PleI | Q33939599 | ||
| Restriction endonuclease reactions requiring two recognition sites | Q33985658 | ||
| Organization of restriction-modification systems | Q34111928 | ||
| REBASE--restriction enzymes and methylases. | Q34323893 | ||
| Dynamics of site juxtaposition in supercoiled DNA. | Q34635507 | ||
| Functional domains in Fok I restriction endonuclease. | Q37000625 | ||
| Class-IIS restriction enzymes--a review | Q37765759 | ||
| Sequence-Specific Binding of DNA by the EcoRV Restriction and Modification Enzymes with Nucleic Acid and Cofactor Analogs | Q38292360 | ||
| 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 | ||
| The monomeric homing endonuclease PI-SceI has two catalytic centres for cleavage of the two strands of its DNA substrate | Q38317452 | ||
| 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 | ||
| DNA cleavage by the EcoRV restriction endonuclease: roles of divalent metal ions in specificity and catalysis | Q38324788 | ||
| Crystal structure of restriction endonuclease BglI bound to its interrupted DNA recognition sequence | Q38333398 | ||
| One- and three-dimensional pathways for proteins to reach specific DNA sites | Q40388353 | ||
| Purification and properties of the MboII, a class-IIS restriction endonuclease | Q40411721 | ||
| Purification and properties of the Eco57I restriction endonuclease and methylase--prototypes of a new class (type IV) | Q40535626 | ||
| Cloning and sequence analysis of the genes coding for Eco57I type IV restriction-modification enzymes | Q40535631 | ||
| 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 | ||
| Ability of DNA and spermidine to affect the activity of restriction endonucleases from several bacterial species | Q43886671 | ||
| Cooperative binding properties of restriction endonuclease EcoRII with DNA recognition sites. | Q52995430 | ||
| Trans-complementable copy-number mutants of plasmid ColE1. | Q54559090 | ||
| The Cfr10I restriction enzyme is functional as a tetramer | Q60500600 | ||
| Purification and characterization of the FokI restriction endonuclease | Q69385045 | ||
| MmeI, a class-IIS restriction endonuclease: Purification and characterization | Q71866648 | ||
| 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 | ||
| 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 | ||
| The type IIs restriction endonuclease BspMI is a tetramer that acts concertedly at two copies of an asymmetric DNA sequence | Q77309135 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 10 | |
| P304 | page(s) | 4024-4033 | |
| P577 | publication date | 2001-11-29 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Many type IIs restriction endonucleases interact with two recognition sites before cleaving DNA. | |
| P478 | volume | 277 |
| Q24800162 | A homology model of restriction endonuclease SfiI in complex with DNA |
| Q39502110 | A sequence-specific nicking endonuclease from streptomyces: purification, physical and catalytic properties. |
| Q40244890 | A switch in the mechanism of communication between the two DNA-binding sites in the SfiI restriction endonuclease |
| Q39876124 | A unique family of Mrr-like modification-dependent restriction endonucleases |
| Q43048971 | A view of consecutive binding events from structures of tetrameric endonuclease SfiI bound to DNA. |
| Q38361433 | AarI, a restriction endonuclease from Arthrobacter aurescens SS2-322, which recognizes the novel non-palindromic sequence 5'-CACCTGC(N)4/8-3'. |
| Q37243964 | An EM view of the FokI synaptic complex by single particle analysis |
| Q59358913 | Argonaute-based programmable RNase as a tool for cleavage of highly-structured RNA |
| Q42587210 | Bacteriophage T4 endonuclease II, a promiscuous GIY-YIG nuclease, binds as a tetramer to two DNA substrates |
| Q34222841 | Binding of two zinc finger nuclease monomers to two specific sites is required for effective double-strand DNA cleavage |
| Q34530273 | BioVector, a flexible system for gene specific-expression in plants |
| Q58771597 | BtsCI and BseGI display sequence preference in the nucleotides flanking the recognition sequence |
| Q35883923 | Challenging the Roles of NSP3 and Untranslated Regions in Rotavirus mRNA Translation. |
| Q27670651 | Characterization and crystal structure of the type IIG restriction endonuclease RM.BpuSI |
| Q33456218 | Cloning and analysis of a bifunctional methyltransferase/restriction endonuclease TspGWI, the prototype of a Thermus sp. enzyme family |
| Q38288505 | Communications between catalytic sites in the protein-DNA synapse by the SfiI endonuclease |
| Q38535019 | Concerted action at eight phosphodiester bonds by the BcgI restriction endonuclease. |
| Q43124003 | Creation of a type IIS restriction endonuclease with a long recognition sequence |
| Q38295631 | DNA binding and recognition by the IIs restriction endonuclease MboII. |
| Q39946292 | DNA communications by Type III restriction endonucleases--confirmation of 1D translocation over 3D looping |
| 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 |
| Q39922663 | DNA supercoiling enables the type IIS restriction enzyme BspMI to recognise the relative orientation of two DNA sequences |
| Q90239384 | Detection of Marker-Free Precision Genome Editing and Genetic Variation through the Capture of Genomic Signatures |
| Q58581575 | Direct AFM Visualization of the Nanoscale Dynamics of Biomolecular Complexes |
| Q42413601 | Discovery of natural nicking endonucleases Nb.BsrDI and Nb.BtsI and engineering of top-strand nicking variants from BsrDI and BtsI. |
| Q30490896 | Dissecting protein-induced DNA looping dynamics in real time |
| Q40240500 | Diversity of type II restriction endonucleases that require two DNA recognition sites |
| Q41967553 | Dynamics and consequences of DNA looping by the FokI restriction endonuclease |
| Q35751446 | Dynamics of synaptic SfiI-DNA complex: single-molecule fluorescence analysis |
| Q39750969 | Glycosylases and AP-cleaving enzymes as a general tool for probe-directed cleavage of ssDNA targets |
| Q35143107 | How the Bfi I restriction enzyme uses one active site to cut two DNA strands |
| Q42009522 | Identification of a single HNH active site in type IIS restriction endonuclease Eco31I. |
| Q40898041 | Illuminating the reaction pathway of the FokI restriction endonuclease by fluorescence resonance energy transfer |
| Q36991424 | Imaging of DNA and Protein-DNA Complexes with Atomic Force Microscopy |
| Q73636278 | Kinetic analysis of the coordinated interaction of SgrAI restriction endonuclease with different DNA targets |
| Q37713815 | Maintaining a sense of direction during long-range communication on DNA. |
| Q34091428 | Measurement of the contributions of 1D and 3D pathways to the translocation of a protein along DNA. |
| Q34598959 | MmeI: a minimal Type II restriction-modification system that only modifies one DNA strand for host protection |
| Q34250442 | Model-guided ligation strategy for optimal assembly of DNA libraries |
| Q34510053 | Modification-dependent restriction endonuclease, MspJI, flips 5-methylcytosine out of the DNA helix |
| Q38319941 | Mva1269I: a monomeric type IIS restriction endonuclease from Micrococcus varians with two EcoRI- and FokI-like catalytic domains |
| Q34474076 | Natural and engineered nicking endonucleases--from cleavage mechanism to engineering of strand-specificity |
| Q33206170 | Near-field-magnetic-tweezer manipulation of single DNA molecules |
| Q64084068 | Novel parameter describing restriction endonucleases: Secondary-Cognate-Specificity and chemical stimulation of TsoI leading to substrate specificity change |
| 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. |
| Q25257871 | Protein assembly and DNA looping by the FokI restriction endonuclease |
| Q24680513 | Pseudocomplementary PNAs as selective modifiers of protein activity on duplex DNA: the case of type IIs restriction enzymes |
| Q33925242 | R2 target-primed reverse transcription: ordered cleavage and polymerization steps by protein subunits asymmetrically bound to the target DNA. |
| Q33283369 | REPSA: general combinatorial approach for identifying preferred ligand-DNA binding sequences |
| Q25257159 | Real-time observation of DNA looping dynamics of Type IIE restriction enzymes NaeI and NarI. |
| 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. |
| Q41473721 | Restriction site free cloning (RSFC) plasmid family for seamless, sequence independent cloning in Pichia pastoris |
| Q44608364 | S-Adenosyl Methionine Prevents Promiscuous DNA Cleavage by the EcoP1I type III Restriction Enzyme |
| Q38329393 | Secondary binding sites for heavily modified triplex forming oligonucleotides |
| Q41132592 | Sequence-specific cleavage of RNA by Type II restriction enzymes |
| Q33977674 | Single molecular investigation of DNA looping and aggregation by restriction endonuclease BspMI. |
| Q51542428 | Single-tube linear DNA amplification for genome-wide studies using a few thousand cells. |
| Q24535057 | Structure of the metal-independent restriction enzyme BfiI reveals fusion of a specific DNA-binding domain with a nonspecific nuclease |
| Q58611623 | Structure, subunit organization and behavior of the asymmetric Type IIT restriction endonuclease BbvCI |
| Q54528761 | Subunit assembly for DNA cleavage by restriction endonuclease SgrAI. |
| Q40399754 | Tailoring the activity of restriction endonuclease PleI by PNA-induced DNA looping |
| Q43141069 | Targeting individual subunits of the FokI restriction endonuclease to specific DNA strands |
| Q34851749 | Tension-dependent DNA cleavage by restriction endonucleases: two-site enzymes are "switched off" at low force |
| Q41820271 | Tetrameric restriction enzymes: expansion to the GIY-YIG nuclease family |
| Q34990708 | The MmeI family: type II restriction-modification enzymes that employ single-strand modification for host protection |
| Q31091708 | The isolation of strand-specific nicking endonucleases from a randomized SapI expression library |
| Q38357645 | The metal-independent type IIs restriction enzyme BfiI is a dimer that binds two DNA sites but has only one catalytic centre |
| Q37856408 | The reaction mechanism of FokI excludes the possibility of targeting zinc finger nucleases to unique DNA sites. |
| 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 |
| Q77309135 | The type IIs restriction endonuclease BspMI is a tetramer that acts concertedly at two copies of an asymmetric DNA sequence |
| Q42656840 | Thermostable proteins bioprocesses: The activity of restriction endonuclease-methyltransferase from Thermus thermophilus (RM.TthHB27I) cloned in Escherichia coli is critically affected by the codon composition of the synthetic gene |
| Q39770852 | TstI, a Type II restriction-modification protein with DNA recognition, cleavage and methylation functions in a single polypeptide |
Search more.