Nucleotide flipping by restriction enzymes analyzed by 2-aminopurine steady-state fluorescence.
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Base flipping in tn10 transposition: an active flip and capture mechanismStructural mechanisms for the 5'-CCWGG sequence recognition by the N- and C-terminal domains of EcoRIIThe recognition domain of the methyl-specific endonuclease McrBC flips out 5-methylcytosineCas9-crRNA ribonucleoprotein complex mediates specific DNA cleavage for adaptive immunity in bacteriaCas3 is a single-stranded DNA nuclease and ATP-dependent helicase in the CRISPR/Cas immune systemDNA synapsis through transient tetramerization triggers cleavage by Ecl18kI restriction enzyme.Chemical mapping of cytosines enzymatically flipped out of the DNA helix.Time-resolved fluorescence studies of nucleotide flipping by restriction enzymes.Base flipping in open complex formation at bacterial promotersDNA base flipping by both members of the PspGI restriction-modification systemCentral base pair flipping and discrimination by PspGI.Characterization of Mycobacterium leprae RecA intein, a LAGLIDADG homing endonuclease, reveals a unique mode of DNA binding, helical distortion, and cleavage compared with a canonical LAGLIDADG homing endonucleaseAn O6-methylguanine-DNA methyltransferase-like protein from Thermus thermophilus interacts with a nucleotide excision repair protein.Quadruplex formation as a molecular switch to turn on intrinsically fluorescent nucleotide analogs.Restriction endonuclease TseI cleaves A:A and T:T mismatches in CAG and CTG repeats.Evidence for a tyrosine-adenine stacking interaction and for a short-lived open intermediate subsequent to initial binding of Escherichia coli RNA polymerase to promoter DNAMutational analysis of active-site residues in the Mycobacterium leprae RecA intein, a LAGLIDADG homing endonuclease: Asp(122) and Asp(193) are crucial to the double-stranded DNA cleavage activity whereas Asp(218) is not.Functional significance of protein assemblies predicted by the crystal structure of the restriction endonuclease BsaWI.How PspGI, catalytic domain of EcoRII and Ecl18kI acquire specificities for different DNA targets.UbaLAI is a monomeric Type IIE restriction enzyme.Highly emissive deoxyguanosine analogue capable of direct visualization of B-Z transition.
P2860
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P2860
Nucleotide flipping by restriction enzymes analyzed by 2-aminopurine steady-state fluorescence.
description
2007 nî lūn-bûn
@nan
2007年の論文
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2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
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2007年论文
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name
Nucleotide flipping by restric ...... ine steady-state fluorescence.
@en
type
label
Nucleotide flipping by restric ...... ine steady-state fluorescence.
@en
prefLabel
Nucleotide flipping by restric ...... ine steady-state fluorescence.
@en
P2093
P2860
P356
P1476
Nucleotide flipping by restric ...... ine steady-state fluorescence.
@en
P2093
Gintautas Tamulaitis
Mindaugas Zaremba
Roman H Szczepanowski
Virginijus Siksnys
P2860
P304
P356
10.1093/NAR/GKM513
P407
P577
2007-07-07T00:00:00Z