Chloramphenicol (Clm) is one of the most widely used broad spectrum antibiotic in veterinary medicine. Recent studies have shown that there is a development of an acquired resistance against Clm by FexB protein which is encoded by its fexB phenicol resistant gene. However, the structural mechanism of its antibiotic resistance towards Clm is unknown due to lack of structural data on FexB protein. Therefore, we have build a 3D structural model of FexB protein using MdfA as template structure by homology modeling and validated it by structure-verification programs. This was followed by binding pocket analysis, molecular docking and molecular dynamic (MD) simulations. Docking results showed the presence of intermolecular hydrogen bonding of Clm with THR151 amino acid residue and changes in the binding orientation of Clm. Analysis from MD simulations revealed significant differences in conformational dynamics of Clm binding in FexB model when compared to MdfA. Our analysis showed that despite of FexB structural similarity with MdfA, it also revealed some distinct features such as mutation of ALA30 and SER93 amino acid residues and large substrate binding pocket that may play important role in contributing its resistance towards Clm. Our detailed data analysis on the FexB protein model and its interactions with Clm on a structural basis is novel and has not been reported earlier. We believe that our work will provide a significant insight in designing more potent inhibitors against antibiotic-resistant FexB protein.
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