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Best Matching Protein Conformations and Docking Programs for a Virtual Screening Campaign Against SMO Receptor
Author(s) -
Amendola Giorgio,
Di Maio Danilo,
La Pietra Valeria,
Cosconati Sandro
Publication year - 2016
Publication title -
molecular informatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.481
H-Index - 68
eISSN - 1868-1751
pISSN - 1868-1743
DOI - 10.1002/minf.201501021
Subject(s) - virtual screening , docking (animal) , computer science , smoothened , dock , computational biology , bioinformatics , chemistry , hedgehog , pharmacophore , biology , medicine , biochemistry , signal transduction , nursing
SMO receptor is one of the main components of the Hedgehog biochemical pathway. In the last decades compelling body of evidence demonstrated that this receptor is a pertinent target for the treatment of various types of solid tumors. Recently, the X‐ray determination of the three‐dimensional structure of SMO in complex with different antagonists opened up the way for the structure‐based design of new antagonists for this receptor that could possibly overcome the limitations connected with the induction of acquired tumor resistance. Herein, taking advantage of three different docking software (namely Glide, PLANTS, and Vina) and of the available SMO structures we set up a retrospective virtual screening (VS) protocol. A database, made up by known SMO antagonists and compounds with no alleged activity against the receptor was created and screened against the different SMO structures. To evaluate the performance of the ranking in VS calculations different statistical metrics (EF, AUAC and BEDROC) were employed allowing to identify the best performing VS docking protocol. Results of these studies will serve as a platform for the application of structure‐based VS against the pharmaceutically relevant SMO receptor.