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In this work, we explored the aromatic cage flexibility of the histone methyllysine reader protein Spindlin1 and its impact on binding mode prediction by means of in silico approaches. We first investigated the Spindlin1 aromatic cage plasticity by analyzing the available crystal structures and through molecular dynamic simulations. Then we assessed the ability of rigid docking and flexible docking to rightly reproduce the binding mode of a known ligand into Spindlin1, as an example of a reader protein displaying flexibility in the binding pocket. The ability of induced fit docking was further probed to test if the right ligand binding mode could be obtained through flexible docking regardless of the initial protein conformation. Finally, the stability of generated docking poses was verified by molecular dynamic simulations. Accurate binding mode prediction was obtained showing that the herein reported approach is a highly promising combination of in silico methods able to rightly predict the binding mode of small molecule ligands in flexible binding pockets, such as those observed in some reader proteins.<\/jats:p>","DOI":"10.1007\/s10822-021-00391-9","type":"journal-article","created":{"date-parts":[[2021,6,3]],"date-time":"2021-06-03T05:09:02Z","timestamp":1622696942000},"page":"695-706","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":4,"title":["Exploring aromatic cage flexibility of the histone methyllysine reader protein Spindlin1 and its impact on binding mode prediction: an in silico study"],"prefix":"10.1007","volume":"35","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-6916-8213","authenticated-orcid":false,"given":"Chiara","family":"Luise","sequence":"first","affiliation":[]},{"ORCID":"https:\/\/orcid.org\/0000-0003-4297-8130","authenticated-orcid":false,"given":"Dina","family":"Robaa","sequence":"additional","affiliation":[]},{"ORCID":"https:\/\/orcid.org\/0000-0002-5985-9261","authenticated-orcid":false,"given":"Wolfgang","family":"Sippl","sequence":"additional","affiliation":[]}],"member":"297","published-online":{"date-parts":[[2021,6,3]]},"reference":[{"issue":"11","key":"391_CR1","doi-asserted-by":"publisher","first-page":"546","DOI":"10.1016\/j.tibs.2013.08.002","volume":"38","author":"R Lu","year":"2013","unstructured":"Lu R, Wang GG (2013) Tudor: a versatile family of histone methylation \u201creaders.\u201d Trends Biochem Sci 38(11):546\u2013555. https:\/\/doi.org\/10.1016\/j.tibs.2013.08.002","journal-title":"Trends Biochem Sci"},{"issue":"48","key":"391_CR2","doi-asserted-by":"publisher","first-page":"37725","DOI":"10.1074\/jbc.M110.139527","volume":"285","author":"LE West","year":"2010","unstructured":"West LE, Roy S, Lachmi-Weiner K, Hayashi R, Shi X, Appella E, Kutateladze TG, Gozani O (2010) The MBT repeats of L3MBTL1 link SET8-mediated p53 methylation at lysine 382 to target gene repression. 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