| scholarly article | Q13442814 |
| P2093 | author name string | I Schildkraut | |
| A K Aggarwal | |||
| D A Wah | |||
| J Bitinaite | |||
| P2860 | cites work | Hybrid restriction enzymes: zinc finger fusions to Fok I cleavage domain | Q24567623 |
| FokI dimerization is required for DNA cleavage | Q24657843 | ||
| Improved methods for building protein models in electron density maps and the location of errors in these models | Q26776980 | ||
| Processing of X-ray diffraction data collected in oscillation mode | Q26778468 | ||
| Structure of Bam HI endonuclease bound to DNA: partial folding and unfolding on DNA binding | Q27729783 | ||
| The crystal structure of EcoRV endonuclease and of its complexes with cognate and non-cognate DNA fragments | Q27732162 | ||
| Structure of the multimodular endonuclease FokI bound to DNA | Q27740190 | ||
| The CCP4 suite: programs for protein crystallography | Q27861090 | ||
| Crystal structure of a CAP-DNA complex: the DNA is bent by 90 degrees | Q28301788 | ||
| Atomic structure of a fragment of human CD4 containing two immunoglobulin-like domains | Q30195771 | ||
| The role of the alpha-helix dipole in protein function and structure | Q34051011 | ||
| Structure of restriction endonuclease BamHI and its relationship to EcoRI. | Q34338704 | ||
| Crystal structure of an HIV-binding recombinant fragment of human CD4. | Q34637157 | ||
| Alteration of the cleavage distance of Fok I restriction endonuclease by insertion mutagenesis | Q36198386 | ||
| Single amino acid substitutions uncouple the DNA binding and strand scission activities of Fok I endonuclease. | Q36601344 | ||
| Construction of a Z-DNA-specific restriction endonuclease | Q36710750 | ||
| Functional domains in Fok I restriction endonuclease. | Q37000625 | ||
| Chimeric restriction endonuclease | Q37558156 | ||
| Stsl, a newFokl isoschizomer fromSteptococcus sanguis 54, cleaves 5' GGATG(N)10/143' | Q40411945 | ||
| The significance of distance and orientation of restriction endonuclease recognition sites in viral DNA genomes. | Q40479056 | ||
| Cloning and sequence analysis of the StsI restriction-modification gene: presence of homology to FokI restriction-modification enzymes | Q40533662 | ||
| Cleaving DNA at any predetermined site with adapter-primers and class-IIS restriction enzymes | Q43569455 | ||
| New restriction endonucleases from Flavobacterium okeanokoites (FokI) and Micrococcus luteus (MluI). | Q48407304 | ||
| A novel class of FokI restriction endonuclease mutants that cleave hemi-methylated substrates. | Q54635287 | ||
| Site-specific cleavage of DNA–RNA hybrids by zinc finger/FokI cleavage domain fusions | Q58375256 | ||
| Surface, subunit interfaces and interior of oligomeric proteins | Q68014868 | ||
| The SfiI restriction endonuclease makes a four-strand DNA break at two copies of its recognition sequence | Q72241576 | ||
| Crystallization and preliminary X-ray analysis of restriction endonuclease FokI bound to DNA | Q73094721 | ||
| [33] AMoRe: An automated molecular replacement program package | Q88661432 | ||
| P433 | issue | 18 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 10564-9 | |
| P577 | publication date | 1998-09-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Structure of FokI has implications for DNA cleavage | |
| P478 | volume | 95 |
| Q39798515 | A new Thermus sp. class-IIS enzyme sub-family: isolation of a 'twin' endonuclease TspDTI with a novel specificity 5'-ATGAA(N(11/9))-3', related to TspGWI, TaqII and Tth111II. |
| Q78834328 | A new method for mapping macromolecular topography |
| 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. |
| Q39876124 | A unique family of Mrr-like modification-dependent restriction endonucleases |
| Q38877482 | Activities and specificities of homodimeric TALENs in Saccharomyces cerevisiae. |
| Q56256572 | An Asymmetric Complex of Restriction Endonuclease MspI on Its Palindromic DNA Recognition Site |
| Q37243964 | An EM view of the FokI synaptic complex by single particle analysis |
| Q37260380 | An alternative novel tool for DNA editing without target sequence limitation: the structure-guided nuclease |
| Q28307951 | An improved zinc-finger nuclease architecture for highly specific genome editing |
| Q53523781 | Binding of MmeI restriction-modification enzyme to its specific recognition sequence is stimulated by S-adenosyl-L-methionine. |
| Q34222841 | Binding of two zinc finger nuclease monomers to two specific sites is required for effective double-strand DNA cleavage |
| Q38536582 | Biotechnological strategies and tools for Plum pox virus resistance: trans-, intra-, cis-genesis, and beyond |
| Q24671370 | Catalytic domain of restriction endonuclease BmrI as a cleavage module for engineering endonucleases with novel substrate specificities |
| Q35010566 | Characterization of the restriction enzyme-like endonuclease encoded by the Entamoeba histolytica non-long terminal repeat retrotransposon EhLINE1. |
| Q48114494 | Chemical Approach to Biological Safety: Molecular-Level Control of an Integrated Zinc Finger Nuclease. |
| Q33737255 | Chimeric restriction enzymes: what is next? |
| Q34178514 | Complex restriction enzymes: NTP-driven molecular motors |
| Q28346667 | Converting MlyI endonuclease into a nicking enzyme by changing its oligomerization state |
| Q28298846 | Creating Designed Zinc-Finger Nucleases with Minimal Cytotoxicity |
| Q43124003 | Creation of a type IIS restriction endonuclease with a long recognition sequence |
| Q28265251 | Crystal structure of human eIF3k, the first structure of eIF3 subunits |
| Q27682253 | Crystal structure of the 5hmC specific endonuclease PvuRts1I |
| Q34067230 | Custom-designed zinc finger nucleases: what is next? |
| Q38295631 | DNA binding and recognition by the IIs restriction endonuclease MboII. |
| 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 |
| Q38810667 | Defining and improving the genome-wide specificities of CRISPR-Cas9 nucleases |
| Q36832214 | Design and Development of Artificial Zinc Finger Transcription Factors and Zinc Finger Nucleases to the hTERT Locus |
| Q33922101 | Design of a colicin E7 based chimeric zinc-finger nuclease |
| Q26787105 | Designed nucleases for targeted genome editing |
| Q42413601 | Discovery of natural nicking endonucleases Nb.BsrDI and Nb.BtsI and engineering of top-strand nicking variants from BsrDI and BtsI. |
| Q43257111 | Distance determination by GIY-YIG intron endonucleases: discrimination between repression and cleavage functions |
| Q34009602 | Divalent metal ion differentially regulates the sequential nicking reactions of the GIY-YIG homing endonuclease I-BmoI. |
| 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 |
| Q38362416 | EcoRII: a restriction enzyme evolving recombination functions? |
| Q40118342 | Endonuclease domain of the Drosophila melanogaster R2 non-LTR retrotransposon and related retroelements: a new model for transposition |
| Q39373513 | Engineering Nt.BtsCI and Nb.BtsCI nicking enzymes and applications in generating long overhangs. |
| Q33949016 | Engineering a nicking endonuclease N.AlwI by domain swapping |
| Q28299915 | Enhancing zinc-finger-nuclease activity with improved obligate heterodimeric architectures |
| Q38217860 | Enzyme-assisted target recycling (EATR) for nucleic acid detection |
| Q36832219 | Expanding the Repertoire of Target Sites for Zinc Finger Nuclease-mediated Genome Modification |
| Q24649467 | Expression and purification of BmrI restriction endonuclease and its N-terminal cleavage domain variants |
| Q24657843 | FokI dimerization is required for DNA cleavage |
| Q42965698 | Functional analysis of MmeI from methanol utilizer Methylophilus methylotrophus, a subtype IIC restriction-modification enzyme related to type I enzymes |
| Q50696210 | Generation of targeted mouse mutants by embryo microinjection of TALENs. |
| Q47168605 | Genome Editing Tools in Plants. |
| Q26741955 | Genome- and Cell-Based Strategies in Therapy of Muscular Dystrophies |
| Q39324308 | Genome-editing technologies and patent landscape overview. |
| Q92124016 | High throughput, efficacious gene editing & genome surveillance in Chinese hamster ovary cells |
| Q54940015 | Homodimerisation-independent cleavage of dsRNA by a pestiviral nicking endoribonuclease. |
| Q35143107 | How the Bfi I restriction enzyme uses one active site to cut two DNA strands |
| Q33794201 | Hybrid lentivirus-phiC31-int-NLS vector allows site-specific recombination in murine and human cells but induces DNA damage. |
| Q36407664 | Identification of the endonuclease domain encoded by R2 and other site-specific, non-long terminal repeat retrotransposable elements |
| Q40898041 | Illuminating the reaction pathway of the FokI restriction endonuclease by fluorescence resonance energy transfer |
| Q31091659 | In vitro selection of restriction endonucleases by in vitro compartmentalization |
| Q42184401 | Light-activated gene editing with a photocaged zinc-finger nuclease |
| Q34103727 | Many type IIs restriction endonucleases interact with two recognition sites before cleaving DNA. |
| Q34510053 | Modification-dependent restriction endonuclease, MspJI, flips 5-methylcytosine out of the DNA helix |
| Q38760604 | Modular construction for function of a ribonucleoprotein enzyme: the catalytic domain of Bacillus subtilis RNase P complexed with B. subtilis RNase P protein |
| 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 |
| Q38840666 | Off-target effects of engineered nucleases |
| Q41429735 | Organization of the BcgI restriction-modification protein for the cleavage of eight phosphodiester bonds in DNA. |
| Q41429898 | Organization of the BcgI restriction-modification protein for the transfer of one methyl group to DNA. |
| Q26778501 | Origins of Programmable Nucleases for Genome Engineering |
| Q60912966 | Programmable Molecular Scissors: Applications of a New Tool for Genome Editing in Biotech |
| Q25257871 | Protein assembly and DNA looping by the FokI restriction endonuclease |
| Q30331241 | Protein stability indicates divergent evolution of PD-(D/E)XK type II restriction endonucleases. |
| Q36497080 | Rational design of a chimeric endonuclease targeted to NotI recognition site |
| Q37197777 | Rationally designed coiled-coil DNA looping peptides control DNA topology |
| Q33786657 | Requirements for double-strand cleavage by chimeric restriction enzymes with zinc finger DNA-recognition domains |
| Q39048699 | Restriction endonuclease AgeI is a monomer which dimerizes to cleave DNA |
| Q73794058 | Sau3AI, a monomeric type II restriction endonuclease that dimerizes on the DNA and thereby induces DNA loops |
| Q92203109 | Sequence motifs recognized by the casposon integrase of Aciduliprofundum boonei |
| Q36180207 | Sequence, structure and functional diversity of PD-(D/E)XK phosphodiesterase superfamily |
| Q38308094 | Specificity of DNA binding and methylation by the M.FokI DNA methyltransferase |
| Q33927812 | Stimulation of homologous recombination through targeted cleavage by chimeric nucleases |
| Q39634823 | Structural and evolutionary classification of Type II restriction enzymes based on theoretical and experimental analyses |
| Q42707053 | Structural flexibility allows the functional diversity of potyvirus genome-linked protein VPg |
| Q27671003 | Structure and cleavage activity of the tetrameric MspJI DNA modification-dependent restriction endonuclease |
| Q24555230 | Structure and function of type II restriction endonucleases |
| Q27682042 | Structure and mutagenesis of the DNA modification-dependent restriction endonuclease AspBHI |
| Q24806247 | Structure of HinP1I endonuclease reveals a striking similarity to the monomeric restriction enzyme MspI. |
| 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 |
| Q28307957 | Structure-based redesign of the dimerization interface reduces the toxicity of zinc-finger nucleases |
| Q24603277 | TAL nucleases (TALNs): hybrid proteins composed of TAL effectors and FokI DNA-cleavage domain |
| Q43141069 | Targeting individual subunits of the FokI restriction endonuclease to specific DNA strands |
| Q35857263 | The DNA binding domain of a papillomavirus E2 protein programs a chimeric nuclease to cleave integrated human papillomavirus DNA in HeLa cervical carcinoma cells. |
| Q39160939 | The Role of Gene Editing in Neurodegenerative Diseases |
| Q55709239 | The Role of Gene Editing in Neurodegenerative Diseases. |
| Q34974737 | The dynamics of DNA damage repair and transcription |
| Q38357645 | The metal-independent type IIs restriction enzyme BfiI is a dimer that binds two DNA sites but has only one catalytic centre |
| Q33939599 | The nicking endonuclease N.BstNBI is closely related to type IIs restriction endonucleases MlyI and PleI |
| Q38139120 | The potential for genetically altered microglia to influence glioma treatment. |
| Q37856408 | The reaction mechanism of FokI excludes the possibility of targeting zinc finger nucleases to unique DNA sites. |
| Q27765729 | The role of metals in catalysis by the restriction endonuclease BamHI |
| Q77309135 | The type IIs restriction endonuclease BspMI is a tetramer that acts concertedly at two copies of an asymmetric DNA sequence |
| Q52050322 | Three-dimensional modeling of the I-TevI homing endonuclease catalytic domain, a GIY-YIG superfamily member, using NMR restraints and Monte Carlo dynamics. |
| Q37948867 | Towards artificial metallonucleases for gene therapy: recent advances and new perspectives |
| Q36476697 | Two crystal forms of the restriction enzyme MspI-DNA complex show the same novel structure |
| Q38143721 | Type I restriction enzymes and their relatives. |
| Q33843093 | Type II restriction endonucleases--a historical perspective and more |
| Q27625490 | Unexpected structural diversity in DNA recombination: the restriction endonuclease connection |
| Q38850483 | Use of genome-editing tools to treat sickle cell disease |
| Q88592264 | Zinc finger nuclease-mediated precision genome editing of an endogenous gene in hexaploid bread wheat (Triticum aestivum) using a DNA repair template |
| Q33622931 | Zinc finger nucleases as tools to understand and treat human diseases |
| Q24535831 | Zinc finger nucleases: custom-designed molecular scissors for genome engineering of plant and mammalian cells |
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