Structural Basis for Error-Free Bypass of the 5-N-Methylformamidopyrimidine-dG Lesion by Human DNA Polymerase η and Sulfolobus solfataricus P2 Polymerase IV-Reference-Cited by-同舟云学术

Structural Basis for Error-Free Bypass of the 5-N-Methylformamidopyrimidine-dG Lesion by Human DNA Polymerase η and Sulfolobus solfataricus P2 Polymerase IV

Published:2015-05-27 Issue:22 Volume:137 Page:7011-7014
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Patra Amritraj¹,Banerjee Surajit²³,Johnson Salyard Tracy L.²,Malik Chanchal K.²,Christov Plamen P.²,Rizzo Carmelo J.²,Stone Michael P.²,Egli Martin¹

Affiliation:

1. Department of Biochemistry, Center in Molecular Toxicology, Vanderbilt-Ingram Cancer Center, Vanderbilt Institute of Chemical Biology, Center for Structural Biology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, United States

2. Department of Chemistry, Center in Molecular Toxicology, Vanderbilt-Ingram Cancer Center, Vanderbilt Institute of Chemical Biology, Center for Structural Biology, Vanderbilt University, Nashville, Tennessee 37235, United States

3. Northeastern Collaborative Access Team and Department of Chemistry and Chemical Biology, Cornell University, Argonne National Laboratory, Building 436E, Argonne, Illinois 60439, United States

Funder

National Institute of Environmental Health Sciences

National Cancer Institute

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.5b02701

Reference26 articles.

1. Distribution of methyl and ethyl adducts following alkylation with monofunctional alkylating agents

2. STUDIES ON THE CHEMICALLY REACTIVE GROUPS OF DEOXYRIBONUCLEIC ACIDS