B. Cheng

发表

Identification of Anziaic Acid, a Lichen Depside from Hypotrachyna sp., as a New Topoisomerase Poison Inhibitor

J. Clardy, G. Tamayo-Castillo, Y. Tse‐Dinh, 2013, PloS one.

RNase H overproduction allows the expression of stress-induced genes in the absence of topoisomerase I.

T. V. Van Dyk, Y. Tse‐Dinh, B. Cheng, 2003, FEMS microbiology letters.

Insights from the Structure of Mycobacterium tuberculosis Topoisomerase I with a Novel Protein Fold.

A. Joachimiak, K. Tan, Y. Tse‐Dinh, 2016, Journal of molecular biology.

Antimicrobial Susceptibility and SOS-Dependent Increase in Mutation Frequency Are Impacted by Escherichia coli Topoisomerase I C-Terminal Point Mutation

Jenny J. Yang, Y. Tse‐Dinh, B. Cheng, 2015, Antimicrobial Agents and Chemotherapy.

Inhibition of Zn(II) Binding Type IA Topoisomerases by Organomercury Compounds and Hg(II)

Y. Tse‐Dinh, B. Cheng, T. Annamalai, 2015, PloS one.

The DNA relaxation activity and covalent complex accumulation of Mycobacterium tuberculosis topoisomerase I can be assayed in Escherichia coli: application for identification of potential FRET-dye labeling sites

Y. Tse‐Dinh, G. Narula, B. Cheng, 2010, BMC Biochemistry.

Asp-to-Asn substitution at the first position of the DxD TOPRIM motif of recombinant bacterial topoisomerase I is extremely lethal to E. coli.

Sandra J. Aedo, Y. Tse‐Dinh, B. Cheng, 2009, Journal of molecular biology.

Mutation adjacent to the active site tyrosine can enhance DNA cleavage and cell killing by the TOPRIM Gly to Ser mutant of bacterial topoisomerase I

Y. Tse‐Dinh, B. Cheng, Elena P. Sorokin, 2007, Nucleic acids research.

Identification of proximal sites for unwound DNA substrate in Escherichia coli topoisomerase I with oxidative crosslinking

J. Leszyk, Y. Tse‐Dinh, M. Greenberg, 2017, FEBS letters.

Identification of proximal sites for unwound DNA substrate in E . coli topoisomerase I with oxidative crosslinking

J. Leszyk, Y. Tse‐Dinh, M. Greenberg, 2017 .

Structural basis for suppression of hypernegative DNA supercoiling by E. coli topoisomerase I

A. Joachimiak, K. Tan, Zhongtao Zhang, 2015, Nucleic acids research.

Crystal structure of a covalent intermediate in DNA cleavage and rejoining by Escherichia coli DNA topoisomerase I

Zhongtao Zhang, Y. Tse‐Dinh, B. Cheng, 2011, Proceedings of the National Academy of Sciences.

Analysis of DNA relaxation and cleavage activities of recombinant Mycobacterium tuberculosis DNA topoisomerase I from a new expression and purification protocol

Y. Tse‐Dinh, B. Cheng, T. Annamalai, 2009 .

Site-directed Mutagenesis of Residues Involved in G Strand DNA Binding by Escherichia coli DNA Topoisomerase I*

Y. Tse‐Dinh, B. Cheng, Vishwaroop B. Mulay, 2004, Journal of Biological Chemistry.

Compounds with antibacterial activity that enhance DNA cleavage by bacterial DNA topoisomerase I.

Y. Tse‐Dinh, I-Fen Liu, B. Cheng, 2007, The Journal of antimicrobial chemotherapy.

Bacterial Cell Killing Mediated by Topoisomerase I DNA Cleavage Activity*

S. Mukhopadhyay, S. Vasunilashorn, Y. Tse‐Dinh, 2005, Journal of Biological Chemistry.

The Strictly Conserved Arg-321 Residue in the Active Site of Escherichia coli Topoisomerase I Plays a Critical Role in DNA Rejoining*

Sandra J. Aedo, Y. Tse‐Dinh, A. Wong, 2011, The Journal of Biological Chemistry.

Inhibition of Mg2+ binding and DNA religation by bacterial topoisomerase I via introduction of an additional positive charge into the active site region

Sandra J. Aedo, Y. Tse‐Dinh, B. Cheng, 2008, Nucleic acids research.

Experimental and computational investigations of Ser10 and Lys13 in the binding and cleavage of DNA substrates by Escherichia coli DNA topoisomerase I

Y. Tse‐Dinh, Chang-Xi Zhu, D. Strahs, 2006, Nucleic acids research.

3,4-dimethoxyphenyl bis-benzimidazole, a novel DNA topoisomerase inhibitor that preferentially targets Escherichia coli topoisomerase I.

V. Tandon, Sandhya Bansal, Y. Tse‐Dinh, 2012, The Journal of antimicrobial chemotherapy.

Topoisomerase I function during Escherichia coli response to antibiotics and stress enhances cell killing from stabilization of its cleavage complex.

Y. Tse‐Dinh, J. Sutherland, I-Fen Liu, 2011, The Journal of antimicrobial chemotherapy.

Direct Interaction between Escherichia coli RNA Polymerase and the Zinc Ribbon Domains of DNA Topoisomerase I*

Y. Tse‐Dinh, Chang-Xi Zhu, A. Ahumada, 2003, Journal of Biological Chemistry.

SOS Induction by Stabilized Topoisomerase IA Cleavage Complex Occurs via the RecBCD Pathway

Y. Tse‐Dinh, J. Sutherland, I-Fen Liu, 2008, Journal of bacteriology.

A surface plasmon resonance study of the intermolecular interaction between Escherichia coli topoisomerase I and pBAD/Thio supercoiled plasmid DNA.

P. Tiwari, Y. Tse‐Dinh, Jin He, 2014, Biochemical and biophysical research communications.

A Fluorescence-Based Assay for Identification of Bacterial Topoisomerase I Poisons.

Y. Tse‐Dinh, B. Cheng, T. Annamalai, 2018, Methods in molecular biology.

Flexibility at Gly-194 Is Required for DNA Cleavage and Relaxation Activity of Escherichia coli DNA Topoisomerase I*

Y. Tse‐Dinh, B. Cheng, Jingyang Feng, 2004, Journal of Biological Chemistry.

Metal ion and inter-domain interactions as functional networks in E. coli topoisomerase I.

M. Palumbo, Y. Tse‐Dinh, C. Sissi, 2013, Gene.

Growth of Plasmodium falciparum in human erythrocytes containing abnormal membrane proteins.

R. Nagel, R. Schwartz, I. Sussman, 1990, Proceedings of the National Academy of Sciences of the United States of America.

Insights from the Structure of Mycobacterium tuberculosis Topoisomerase I with a Novel Protein Fold.

A. Joachimiak, K. Tan, Y. Tse‐Dinh, 2016, Journal of molecular biology.