Physical and functional interactions between 3-methyladenine DNA glycosylase and topoisomerase I in mycobacteria

[1]  Li-hua Hu,et al.  Characterization of amino acid residues essential for tetramer formation and DNA-binding activity of ssDNA-binding protein of Mycobacterium tuberculosis , 2011, Biochemistry (Moscow).

[2]  Yi Wang,et al.  Global protein-protein interaction network in the human pathogen Mycobacterium tuberculosis H37Rv. , 2010, Journal of proteome research.

[3]  F. Huang,et al.  Characterization of an interplay between a Mycobacterium tuberculosis MazF homolog, Rv1495 and its sole DNA topoisomerase I , 2010, Nucleic acids research.

[4]  Yi Wang,et al.  Characterization of the Interaction and Cross-Regulation of Three Mycobacterium tuberculosis RelBE Modules , 2010, PloS one.

[5]  J. Zeng,et al.  Over-producing soluble protein complex and validating protein-protein interaction through a new bacterial co-expression system. , 2010, Protein expression and purification.

[6]  Yi Liu,et al.  Archaeal eukaryote-like Orc1/Cdc6 initiators physically interact with DNA polymerase B1 and regulate its functions , 2009, Proceedings of the National Academy of Sciences.

[7]  T. Parish,et al.  Mycobacterium : genomics and molecular biology , 2009 .

[8]  L. Samson,et al.  Substrate specificity and sequence-dependent activity of the Saccharomyces cerevisiae 3-methyladenine DNA glycosylase (Mag). , 2008, DNA repair.

[9]  R. Fleischmann,et al.  Transcriptional Regulation of Multi-Drug Tolerance and Antibiotic-Induced Responses by the Histone-Like Protein Lsr2 in M. tuberculosis , 2007, PLoS pathogens.

[10]  J. Tainer,et al.  The intricate structural chemistry of base excision repair machinery: implications for DNA damage recognition, removal, and repair. , 2007, DNA repair.

[11]  V. Mizrahi,et al.  Tuberculosis Chemotherapy: the Influence of Bacillary Stress and Damage Response Pathways on Drug Efficacy , 2006, Clinical Microbiology Reviews.

[12]  D. Eisenberg,et al.  Unique Transcriptome Signature of Mycobacterium tuberculosis in Pulmonary Tuberculosis , 2006, Infection and Immunity.

[13]  T. Ellenberger,et al.  The Escherichia coli 3-Methyladenine DNA Glycosylase AlkA Has a Remarkably Versatile Active Site* , 2004, Journal of Biological Chemistry.

[14]  T. Ellenberger,et al.  Dissecting the Broad Substrate Specificity of Human 3-Methyladenine-DNA Glycosylase* , 2004, Journal of Biological Chemistry.

[15]  J. Griffith,et al.  The Carboxyl-terminal Domain of Bacteriophage T7 Single-stranded DNA-binding Protein Modulates DNA Binding and Interaction with T7 DNA Polymerase* , 2003, Journal of Biological Chemistry.

[16]  Clifton E. Barry,et al.  DnaE2 Polymerase Contributes to In Vivo Survival and the Emergence of Drug Resistance in Mycobacterium tuberculosis , 2003, Cell.

[17]  J. Jiricny,et al.  Recent progress in the biology, chemistry and structural biology of DNA glycosylases , 2001, BioEssays : news and reviews in molecular, cellular and developmental biology.

[18]  C. Nathan,et al.  Reactive oxygen and nitrogen intermediates in the relationship between mammalian hosts and microbial pathogens. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[19]  T. Lindahl,et al.  Quality control by DNA repair. , 1999, Science.

[20]  L. Samson,et al.  Crystal Structure of a Human Alkylbase-DNA Repair Enzyme Complexed to DNA Mechanisms for Nucleotide Flipping and Base Excision , 1998, Cell.

[21]  L. Samson,et al.  Mammalian 3-methyladenine DNA glycosylase protects against the toxicity and clastogenicity of certain chemotherapeutic DNA cross-linking agents. , 1998, Cancer research.

[22]  B. Barrell,et al.  Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence , 1998, Nature.

[23]  L. Samson,et al.  A Chemical and Genetic Approach Together Define the Biological Consequences of 3-Methyladenine Lesions in the Mammalian Genome* , 1998, The Journal of Biological Chemistry.

[24]  D. Lilley,et al.  DNA Repair , 1998, Nucleic Acids and Molecular Biology.

[25]  J. Alonso,et al.  The recombinant product of the Chryptomonas phi plastid gene hlpA is an architectural HU-like protein that promotes the assembly of complex nucleoprotein structures. , 1997, European journal of biochemistry.

[26]  K. Kleibl,et al.  Escherichia coli, Saccharomyces cerevisiae, rat and human 3-methyladenine DNA glycosylases repair 1,N6-ethenoadenine when present in DNA. , 1995, Nucleic acids research.

[27]  L. Hartwell,et al.  A checkpoint regulates the rate of progression through S phase in S. cerevisiae in Response to DNA damage , 1995, Cell.

[28]  M. Saparbaev,et al.  Excision of hypoxanthine from DNA containing dIMP residues by the Escherichia coli, yeast, rat, and human alkylpurine DNA glycosylases. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[29]  T. Lindahl.  Instability and decay of the primary structure of DNA , 1993, Nature.

[30]  H. Fraenkel-conrat,et al.  Both purified human 1,N6-ethenoadenine-binding protein and purified human 3-methyladenine-DNA glycosylase act on 1,N6-ethenoadenine and 3-methyladenine. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[31]  P. V. von Hippel,et al.  Calculation of protein extinction coefficients from amino acid sequence data. , 1989, Analytical biochemistry.

[32]  T. Lindahl.  DNA glycosylases in DNA repair. , 1986, Basic life sciences.