Fig. 5From: Genomic landscape of the emerging XDR Salmonella Typhi for mining druggable targets clpP, hisH, folP and gpmI and screening of novel TCM inhibitors, molecular docking and simulation analysesDiagram showing In Silico interactions of 2 best ZINC compounds (ZINC19340748 and ZINC08738207) with the identified putative target STY0490_ATP-dependent CLP protease proteolytic subunit. The 2D interactions (left panel) were determined via MOE software (v2016–17) while their respective 3D interactions (right panel - target protein in surface representation) were developed using PyMOL visualizing toolBack to article page