| P2093 | author name string | Raymond J Williams | |
| P2860 | cites work | Homing endonucleases: keeping the house in order | Q24545192 |
| | BaeI, another unusual BcgI-like restriction endonuclease | Q24548142 |
| | Type I restriction systems: sophisticated molecular machines (a legacy of Bertani and Weigle) | Q24548508 |
| | Structure and function of type II restriction endonucleases | Q24555230 |
| | FokI dimerization is required for DNA cleavage | Q24657843 |
| | A novel endonuclease mechanism directly visualized for I-PpoI | Q27620540 |
| | Understanding the immutability of restriction enzymes: crystal structure of BglII and its DNA substrate at 1.5 A resolution | Q27621185 |
| | Crystallographic snapshots along a protein-induced DNA-bending pathway | Q27622467 |
| | Crystal structure of NaeI--an evolutionary bridge between DNA endonuclease and topoisomerase | Q27624935 |
| | Structure of the tetrameric restriction endonuclease NgoMIV in complex with cleaved DNA | Q27626779 |
| | Structure of the multimodular endonuclease FokI bound to DNA | Q27740190 |
| | Duplex regions in "single-stranded" phiX174 DNA are cleaved by a restriction endonuclease from Haemophilus aegyptius | Q28279042 |
| | Single-site enzymatic cleavage of yeast genomic DNA mediated by triple helix formation | Q33335575 |
| | Type II restriction endonucleases: structural, functional and evolutionary relationships | Q33745019 |
| | Requirements for double-strand cleavage by chimeric restriction enzymes with zinc finger DNA-recognition domains | Q33786657 |
| | Stimulation of homologous recombination through targeted cleavage by chimeric nucleases | Q33927812 |
| | Characterization of the specific DNA nicking activity of restriction endonuclease N.BstNBI. | Q33930994 |
| | The nicking endonuclease N.BstNBI is closely related to type IIs restriction endonucleases MlyI and PleI | Q33939599 |
| | Engineering a nicking endonuclease N.AlwI by domain swapping | Q33949016 |
| | A Suggested nomenclature for bacterial host modification and restriction systems and their enzymes | Q34052438 |
| | High-specificity DNA cleavage agent: design and application to kilobase and megabase DNA substrates | Q34331741 |
| | Recognition and cleavage of DNA by type-II restriction endonucleases | Q34431350 |
| | Comparative genomics of the restriction-modification systems in Helicobacter pylori | Q34489772 |
| | Step-wise DNA relaxation and decatenation by NaeI-43K. | Q34666242 |
| | DNA affinity cleaving analysis of homeodomain-DNA interaction: identification of homeodomain consensus sites in genomic DNA | Q34903207 |
| | Changes in solvation during DNA binding and cleavage are critical to altered specificity of the EcoRI endonuclease | Q35906064 |
| | A family of regulatory genes associated with type II restriction-modification systems | Q36130467 |
| | Structural, functional, and evolutionary relationships between lambda-exonuclease and the type II restriction endonucleases | Q36163748 |
| | Restriction and modification systems | Q37041891 |
| | Chimeric restriction endonuclease | Q37558156 |
| | Introduction of asymmetry in the naturally symmetric restriction endonuclease EcoRV to investigate intersubunit communication in the homodimeric protein | Q37577354 |
| | Finding sequence motifs in groups of functionally related proteins | Q37679318 |
| | Type III restriction endonucleases translocate DNA in a reaction driven by recognition site-specific ATP hydrolysis | Q37698719 |
| | Class-IIS restriction enzymes--a review | Q37765759 |
| | SfiI endonuclease activity is strongly influenced by the non-specific sequence in the middle of its recognition site | Q38302971 |
| | The energetics of the interaction of BamHI endonuclease with its recognition site GGATCC. | Q38303246 |
| | Protein engineering of the restriction endonuclease EcoRV: replacement of an amino acid residue in the DNA binding site leads to an altered selectivity towards unmodified and modified substrates | Q38304399 |
| | Use of specific oligonucleotide duplexes to stimulate cleavage of refractory DNA sites by restriction endonucleases | Q38321306 |
| | Modified DNA fragments activate NaeI cleavage of refractory DNA sites | Q38325335 |
| | Kinetic characterization of linear diffusion of the restriction endonuclease EcoRV on DNA. | Q38339073 |
| | Cloning, expression, and purification of a thermostable nonhomodimeric restriction enzyme, BslI. | Q39498995 |
| | Identification of a base-specific contact between the restriction endonuclease SsoII and its recognition sequence by photocross-linking | Q39542583 |
| | Substrate DNA and cofactor regulate the activities of a multi-functional restriction-modification enzyme, BcgI. | Q39721172 |
| | Cloning and analysis of the four genes coding for Bpu10I restriction-modification enzymes | Q39722909 |
| | A detailed study of the substrate specificity of a chimeric restriction enzyme. | Q39726873 |
| | The regulatory C proteins from different restriction-modification systems can cross-complement | Q39839024 |
| | The significance of distance and orientation of restriction endonuclease recognition sites in viral DNA genomes. | Q40479056 |
| | Activation of restriction endonuclease EcoRII does not depend on the cleavage of stimulator DNA. | Q40507377 |
| | RecA-AC: single-site cleavage of plasmids and chromosomes at any predetermined restriction site | Q40535370 |
| | Purification and properties of the Eco57I restriction endonuclease and methylase--prototypes of a new class (type IV) | Q40535626 |
| | Ability of DNA and spermidine to affect the activity of restriction endonucleases from several bacterial species | Q43886671 |
| | EcoRV restriction endonuclease: communication between catalytic metal ions and DNA recognition | Q45108243 |
| | Purification of restriction endonuclease from Acetobacter aceti IFO 3281 (AatII) and its properties | Q45804234 |
| | Reagents for the site-specific cleavage of megabase DNA. | Q45949187 |
| | Analyzing the functional organization of a novel restriction modification system, the BcgI system | Q47923479 |
| | Chimeric restriction enzyme: Gal4 fusion to FokI cleavage domain | Q47970000 |
| | Restriction and modification systems of Neisseria gonorrhoeae. | Q48073660 |
| | Linkage of EcoRI dissociation from its specific DNA recognition site to water activity, salt concentration, and pH: separating their roles in specific and non-specific binding | Q49203449 |
| | Purification of a new restriction endonuclease, StyI, from Escherichia coli carrying the hsd+ miniplasmid | Q50206784 |
| | The energetic basis of specificity in the Eco RI endonuclease--DNA interaction. | Q52484098 |
| | Diversity of restriction-modification gene homologues in Helicobacter pylori. | Q52927779 |
| | Cooperative binding properties of restriction endonuclease EcoRII with DNA recognition sites. | Q52995430 |
| | XcmI as a universal restriction enzyme for single-stranded DNA. | Q53834773 |
| | EcoRV-T94V: a mutant restriction endonuclease with an altered substrate specificity towards modified oligodeoxynucleotides. | Q54053124 |
| | Oligonucleotide activation of the type IIe restriction enzyme NaeI for digestion of refractory sites. | Q54155861 |
| | Towards the design of rare cutting restriction endonucleases: using directed evolution to generate variants of EcoRV differing in their substrate specificity by two orders of magnitude | Q56902829 |
| | Protein engineering of the restriction endonuclease EcoRV . Structure-guided design of enzyme variants that recognize the base pairs flanking the recognition site | Q57267701 |
| | The Mechanism of DNA Cleavage by the Type II. Restriction Enzyme EcoRV: Asp36 Is Not Directly Involved in DNA Cleavage but Serves to Couple Indirect. Readout to Catalysis | Q57267708 |
| | Site-specific cleavage of DNA–RNA hybrids by zinc finger/FokI cleavage domain fusions | Q58375256 |
| | The Cfr10I restriction enzyme is functional as a tetramer | Q60500600 |
| | Cloning the modification methylase gene of Bacillus sphaericus R in Escherichia coli | Q60505834 |
| | [N.BstSE--a site-specific nickase from Bacillus stearothermophilus SE-589] | Q64382667 |
| | Incorporation of an EDTA-metal complex at a rationally selected site within a protein: application to EDTA-iron DNA affinity cleaving with catabolite gene activator protein (CAP) and Cro | Q67505524 |
| | DNA cleavage at two recognition sites by the SfiI restriction endonuclease: salt dependence of cis and trans interactions between distant DNA sites | Q71751602 |
| | Minimum duplex requirements for restriction enzyme cleavage near the termini of linear DNA fragments | Q72045587 |
| | The SfiI restriction endonuclease makes a four-strand DNA break at two copies of its recognition sequence | Q72241576 |
| | Cleavage of single strand oligonucleotides and bacteriophage phi X174 DNA by Msp I endonuclease | Q72620657 |
| | DNA topoisomerase and recombinase activities in Nae I restriction endonuclease | Q72635901 |
| | Evidence for mutations that break communication between the Endo and Topo domains in NaeI endonuclease/topoisomerase | Q73185528 |
| | Evolutionary role of restriction/modification systems as revealed by comparative genome analysis | Q73943265 |
| | 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 |
| | Digestion of terminal restriction endonuclease recognition sites on PCR products | Q74492699 |
| | Phosphorothioate substrates for the SfiI restriction endonuclease | Q74653655 |
| | Does BcgI, a unique restriction endonuclease, require two recognition sites for cleavage? | Q74653661 |
| P433 | issue | 3 | |
| P304 | page(s) | 225-243 | |
| P577 | publication date | 2003-03-01 | |
| P1433 | published in | Molecular Biotechnology | Q15761195 |
| P1476 | title | Restriction endonucleases: classification, properties, and applications | |
| P478 | volume | 23 | |