Two glycosylase families diffusively scan DNA using a wedge residue to probe for and identify oxidatively damaged bases

Proceedings of the National Academy of Sciences of the United States of America

Volumn 111, Issue 20, 2014, Pages

  Nelson, Shane R ^a   Dunn, Andrew R ^b,c   Kathe, Scott D ^b   Warshaw, David M ^a   Wallace, Susan S ^b  

^a UNIVERSITY OF VERMONT   (United States)

^b UNIVERSITY OF VERMONT COLLEGE OF MEDICINE   (United States)

^c N of One   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE; BACTERIAL ENZYME; DNA FORMAMIDOPYRIMIDINE GLYCOSYLASE; DNA GLYCOSYLTRANSFERASE; NEI PROTEIN; NTH PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; DIFFUSION; DIFFUSION COEFFICIENT; DNA DAMAGE; ENZYME BINDING; ESCHERICHIA COLI; EXCISION REPAIR; MUTATION; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL;

DNA REPAIR; SEARCH MECHANISMS;

ALANINE; CATALYTIC DOMAIN; DEOXYRIBONUCLEASE (PYRIMIDINE DIMER); DIFFUSION; DNA DAMAGE; DNA MUTATIONAL ANALYSIS; DNA REPAIR; DNA, BACTERIAL; DNA-FORMAMIDOPYRIMIDINE GLYCOSYLASE; ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; MOLECULAR CONFORMATION; MUTATION; OXYGEN; PROTEIN BINDING; STRESS, MECHANICAL;

EID: 84901022837     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1400386111     Document Type: Article

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