Degenerate DNA recognition by I-PpoI endonuclease. (Q38340018)

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9 November 2019

title

Degenerate DNA recognition by I-PpoI endonuclease (English)

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9 November 2019

3

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9 November 2019

author name string

P K Wittmayer

series ordinal

1

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9 November 2019

J L McKenzie

series ordinal

2

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9 November 2019

publication date

1 January 1998

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9 November 2019

language of work or name

0 references

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9 November 2019

volume

206

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9 November 2019

issue

1

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9 November 2019

page(s)

11-21

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Site-Directed Mutagenesis by Double Polymerase Chain Reaction: Megaprimer Method

9 November 2019

cites work

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Characterization of the cleavage site and the recognition sequence of the I-CreI DNA endonuclease encoded by the chloroplast ribosomal intron of Chlamydomonas reinhardtii

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Interaction of the intron-encoded mobility endonuclease I-PpoI with its target site

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Searching sequence space by definably random mutagenesis: improving the catalytic potency of an enzyme

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DNA binding sites for the transcriptional activator/repressor YY1.

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The I-CeuI endonuclease recognizes a sequence of 19 base pairs and preferentially cleaves the coding strand of the Chlamydomonas moewusii chloroplast large subunit rRNA gene

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Thermodynamic origins of specificity in the lac repressor-operator interaction. Adaptability in the recognition of mutant operator sites

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Characterization of I-Ppo, an intron-encoded endonuclease that mediates homing of a group I intron in the ribosomal DNA of Physarum polycephalum

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A mobile group I intron from Physarum polycephalum can insert itself and induce point mutations in the nuclear ribosomal DNA of saccharomyces cerevisiae

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In vivo analysis of the Saccharomyces cerevisiae HO nuclease recognition site by site-directed mutagenesis

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Specificity of substrate recognition by the EcoRI restriction endonuclease

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Polymer support oligonucleotide synthesis XVIII: use of beta-cyanoethyl-N,N-dialkylamino-/N-morpholino phosphoramidite of deoxynucleosides for the synthesis of DNA fragments simplifying deprotection and isolation of the final product

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Discrimination between DNA sequences by the EcoRV restriction endonuclease

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Influence of enzyme-substrate contacts located outside the EcoRI recognition site on cleavage of duplex oligodeoxyribonucleotide substrates by EcoRI endonuclease

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Complex recognition site for the group I intron-encoded endonuclease I-SceII

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7 January 2021

Substrate binding and turnover by the highly specific I-PpoI endonuclease.

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7 January 2021

10.1016/S0378-1119(97)00563-5

Identifiers

DOI

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9 November 2019

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