Computational Modeling and Simulation of Toxin-antitoxin System in Acinetobacter baumannii: HicB as a Dynamic Factor for Therapeutic Target
Acinetobacter baumannii is a ubiquitous Gram-negative bacillus bacterium that is frequently found in the nosocomial infections. Regard to the
rapid development of resistance against various antimicrobial agents due to the high ability of natural genetic transformation, A. baumannii is
resistance to many of the antibiotics. Toxin-antitoxin system is one of the virulence agents in A. baumannii that can be involved in the emergenceof drug resistance. HicB as a toxin system is an ideal target for the design of new classes of antimicrobial agents against A. baumannii. The
goals of this work was to model the complete tridimensional structure of the HicB protein using computational methods and to assess structural
and functional of it. The consistency of modeled structure was confirmed by different servers to high accuracy for modeling and dynamics
simulation. The molecular dynamic simulation and virtual screening results indicate that HicB is a stable protein from A. baumannii. These
results provide new insights for the molecular understanding and development of new antibacterial drugs against toxin system involved in A.
baumannii pathogenesis.
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