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PMID: 15933203 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

A fluoroquinolone resistance protein from Mycobacterium tuberculosis that mimics DNA.

Science (New York, N.Y.) ·Vol. 308 ·No. 5727 ·2005-06-03 ·Pages 1480-3

Hegde SS, Vetting MW, Roderick SL, Mitchenall LA, Maxwell A, Takiff HE, Blanchard JS

Abstract

Fluoroquinolones are gaining increasing importance in the treatment of tuberculosis. The expression of MfpA, a member of the pentapeptide repeat family of proteins from Mycobacterium tuberculosis, causes resistance to ciprofloxacin and sparfloxacin. This protein binds to DNA gyrase and inhibits its activity. Its three-dimensional structure reveals a fold, which we have named the right-handed quadrilateral beta helix, that exhibits size, shape, and electrostatic similarity to B-form DNA. This represents a form of DNA mimicry and explains both its inhibitory effect on DNA gyrase and fluoroquinolone resistance resulting from the protein's expression in vivo.

MeSH Terms
Amino Acid Sequence Antitubercular Agents/chemistry,pharmacology Bacterial Proteins/chemistry,physiology Ciprofloxacin/pharmacology Crystallography, X-Ray DNA Gyrase/metabolism DNA, Bacterial/chemistry DNA, Superhelical/chemistry Drug Resistance, Bacterial Drug Resistance, Microbial/physiology Enzyme Inhibitors/chemistry Escherichia coli/enzymology Fluoroquinolones/antagonists & inhibitors,chemistry,pharmacology Models, Molecular Molecular Mimicry Molecular Sequence Data Monomeric GTP-Binding Proteins Mycobacterium tuberculosis/drug effects,physiology Protein Conformation Protein Folding Structure-Activity Relationship Topoisomerase II Inhibitors
Chemicals
Antitubercular Agents Bacterial Proteins DNA, Bacterial DNA, Superhelical Enzyme Inhibitors Fluoroquinolones Topoisomerase II Inhibitors Ciprofloxacin MfpA protein, Mycobacterium smegmatis Monomeric GTP-Binding Proteins DNA Gyrase sparfloxacin
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Hegde Subray S
Department of Biochemistry, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.
Vetting Matthew W
Roderick Steven L
Mitchenall Lesley A
Maxwell Anthony
Takiff Howard E
Blanchard John S
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
1095-9203
Published
2005-06-03
Pages
1480-3
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIAID NIH HHS · AI33696 · United States
NIAID NIH HHS · AI60899 · United States
NIAID NIH HHS · T32 AI07501 · United States
Databases
PDB
Corrections
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