Literature DB >> 12009927

3-methyladenine-DNA glycosylase II: the crystal structure of an AlkA-hypoxanthine complex suggests the possibility of product inhibition.

Michael Teale1, Jindrich Symersky, Larry DeLucas.   

Abstract

Escherichia coli (E. coli) protein 3-methyladenine-DNA glycosylase II (AlkA) functions primarily by removing alkylation damage from duplex and single stranded DNA. A crystal structure of AlkA was refined to 2.0 A resolution. This structure in turn was used to refine an AlkA-hypoxanthine (substrate) complex structure to 2.4 A resolution. The complex structure shows hypoxanthine located in AlkA's active site stacked between residues W218 and Y239. The structural analysis of the AlkA and AlkA-hypoxanthine structures indicate that free hypoxanthine binding in the active site may inhibit glycosylase activity.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12009927     DOI: 10.1021/bc015527v

Source DB:  PubMed          Journal:  Bioconjug Chem        ISSN: 1043-1802            Impact factor:   4.774


  3 in total

1.  Substrate specificity and sequence-dependent activity of the Saccharomyces cerevisiae 3-methyladenine DNA glycosylase (Mag).

Authors:  Gondichatnahalli M Lingaraju; Maria Kartalou; Lisiane B Meira; Leona D Samson
Journal:  DNA Repair (Amst)       Date:  2008-05-12

2.  Breaking the Rules: Protein Sculpting in NEIL2 Regulation.

Authors:  Susan E Tsutakawa; Altaf H Sarker
Journal:  Structure       Date:  2021-01-07       Impact factor: 5.006

Review 3.  Ada response - a strategy for repair of alkylated DNA in bacteria.

Authors:  Damian Mielecki; Elżbieta Grzesiuk
Journal:  FEMS Microbiol Lett       Date:  2014-06-06       Impact factor: 2.742

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.