(Q38298992)

1 September 2017

title

N-terminal extension of N-methylpurine DNA glycosylase is required for turnover in hypoxanthine excision reaction (English)

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1 September 2017

Sanjay Adhikari

1

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1 September 2017

Aykut Uren

series ordinal

2

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1 September 2017

Rabindra Roy

series ordinal

3

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1 September 2017

language of work or name

English

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publication date

22 August 2007

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Journal of Biological Chemistry

1 September 2017

published in

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1 September 2017

volume

282

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1 September 2017

issue

41

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1 September 2017

page(s)

30078-30084

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Instability and decay of the primary structure of DNA

1 September 2017

cites work

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https://api.crossref.org/works/10.1074%2FJBC.M704051200

What structural features determine repair enzyme specificity and mechanism in chemically modified DNA?

21 January 2018

1 reference

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Specific interaction of wild-type and truncated mouse N-methylpurine-DNA glycosylase with ethenoadenine-containing DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M704051200

Purification and biochemical characterization of recombinant N-methylpurine-DNA glycosylase of the mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M704051200

Distinct substrate preference of human and mouse N-methylpurine-DNA glycosylases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M704051200

Purification and characterization of human 3-methyladenine-DNA glycosylase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M704051200

Excision of hypoxanthine from DNA containing dIMP residues by the Escherichia coli, yeast, rat, and human alkylpurine DNA glycosylases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M704051200

1,N6-ethenoadenine is preferred over 3-methyladenine as substrate by a cloned human N-methylpurine-DNA glycosylase (3-methyladenine-DNA glycosylase)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M704051200

The domains of mammalian base excision repair enzyme N-methylpurine-DNA glycosylase. Interaction, conformational change, and role in DNA binding and damage recognition.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M704051200

Structural basis for the excision repair of alkylation-damaged DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M704051200

1,N(2)-ethenoguanine, a mutagenic DNA adduct, is a primary substrate of Escherichia coli mismatch-specific uracil-DNA glycosylase and human alkylpurine-DNA-N-glycosylase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M704051200

Dissecting the broad substrate specificity of human 3-methyladenine-DNA glycosylase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M704051200

Magnesium, essential for base excision repair enzymes, inhibits substrate binding of N-methylpurine-DNA glycosylase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M704051200

Interaction of the recombinant human methylpurine-DNA glycosylase (MPG protein) with oligodeoxyribonucleotides containing either hypoxanthine or abasic sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M704051200

Single-turnover and pre-steady-state kinetics of the reaction of the adenine glycosylase MutY with mismatch-containing DNA substrates

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M704051200

Truncation of amino-terminal tail stimulates activity of human endonuclease III (hNTH1)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M704051200

Substrate binding by human apurinic/apyrimidinic endonuclease indicates a Briggs-Haldane mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M704051200

Excision of DNA adducts of nitrogen mustards by bacterial and mammalian 3-methyladenine-DNA glycosylases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M704051200

21 January 2018

Identifiers

DOI

10.1074/JBC.M704051200

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1 September 2017

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