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. 2018 Jul 31;20(5):1878–1912. doi: 10.1093/bib/bby061

Figure 3.

Figure 3.

(A) In conventional virtual screening, multiple compounds are screened against a pre-specified target, and candidate interacting compounds (i.e. ligands) are identified, whereas (B) in target prediction (i.e. reverse virtual screening), a compound is searched against multiple proteins and candidate targets are identified.