Application of the Subtractive Genomics and Molecular Docking Analysis for the Identification of Novel Putative Drug Targets against<i> Salmonella enterica</i> subsp.<i> enterica serovar</i> Poona

<div>Important residues of the binding site of UDP-3-O-[3-hydroxymyristoyl] N-acetyl glucosamine deacetylase of<i> Salmonella enterica </i>subsp.<i> enterica serovar </i>Poona observed to be interactive with the (2R)-N–hydroxy–3–naphthalen–2-yl-2-[(naphthalen-2ylsulfonyl)amino]propanamideas ligand.</div>

BioMed Research International

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Figure 3

Figure 3: Application of the Subtractive Genomics and Molecular Docking Analysis for the Identification of Novel Putative Drug Targets against<i> Salmonella enterica</i> subsp.<i> enterica serovar</i> Poona 

Figure 3 | Application of the Subtractive Genomics and Molecular Docking Analysis for the Identification of Novel Putative Drug Targets against Salmonella enterica subsp. enterica serovar Poona 