## Abstract The text‐based similarity searching method Pharmacophore Alignment Search Tool is grounded on pairwise comparisons of potential pharmacophoric points between a query and screening compounds. The underlying scoring matrix is of critical importance for successful virtual screening and hit
Pharmacophore alignment search tool: Influence of canonical atom labeling on similarity searching
✍ Scribed by Volker Hähnke; Matthias Rupp; Mireille Krier; Friedrich Rippmann; Gisbert Schneider
- Book ID
- 102879118
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 599 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0192-8651
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✦ Synopsis
Abstract
Previously, (Hähnke et al., J Comput Chem 2009, 30, 761) we presented the Pharmacophore Alignment Search Tool (PhAST), a ligand‐based virtual screening technique representing molecules as strings coding pharmacophoric features and comparing them by global pairwise sequence alignment. To guarantee unambiguity during the reduction of two‐dimensional molecular graphs to one‐dimensional strings, PhAST employs a graph canonization step. Here, we present the results of the comparison of 11 different algorithms for graph canonization with respect to their impact on virtual screening. Retrospective screenings of a drug‐like data set were evaluated using the BEDROC metric, which yielded averaged values between 0.4 and 0.14 for the best‐performing and worst‐performing canonization technique. We compared five scoring schemes for the alignments and found preferred combinations of canonization algorithms and scoring functions. Finally, we introduce a performance index that helps prioritize canonization approaches without the need for extensive retrospective evaluation. © 2010 Wiley Periodicals, Inc. J Comput Chem, 2010
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