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Computational Biology and Chemistry|October 1, 2013
Unintended consequences? Water molecules at biological and crystallographic protein-protein interfacesMostafa H Ahmed, Mesay Habtemariam, Martin K Safo, et al.Journal of Computer-Aided Molecular Design|January 4, 2019
First virtual screening and experimental validation of inhibitors targeting GES-5 carbapenemaseFrancesca Spyrakis, Pierangelo Bellio, Antonio Quotadamo, et al.Biochimie|December 31, 2019
Multiple catalytic activities of human 17β-hydroxysteroid dehydrogenase type 7 respond differently to inhibitorsTerenzio Ferrante, Salvatore Adinolfi, Giulia D'Arrigo, et al.Chemmedchem|April 11, 2018
Tuning the Hydrophobicity of a Mitochondria-Targeted NO PhotodonorFederica Sodano, Barbara Rolando, Francesca Spyrakis, et al.Journal of Medicinal Chemistry|December 15, 2017
From Experiments to a Fast Easy-to-Use Computational Methodology to Predict Human Aldehyde Oxidase Selectivity and Metabolic ReactionsGabriele Cruciani, Nicolò Milani, Paolo Benedetti, et al.The FEBS Journal|November 29, 2020
The allosteric interplay between S-nitrosylation and glycine binding controls the activity of human serine racemaseFrancesco Marchesani, Eleonora Gianquinto, Ida Autiero, et al.RSC Chemical Biology|May 13, 2026
<i>De novo</i> acyl carrier proteins display structure-independent modification and sequence noveltyMichael A Herrera, Grace K King, Zoe Ozols, et al.The Journal of Physical Chemistry Letters|November 13, 2019
Modulating Ligand Dissociation through Methyl Isomerism in Accessory Sites: Binding of Retinol to Cellular CarriersCarolina Estarellas, Salvatore Scaffidi, Giorgio Saladino, et al.Molecules (Basel, Switzerland)|December 11, 2022
<i>N</i>-[1,3-Dialkyl(aryl)-2-oxoimidazolidin-4-ylidene]-aryl(alkyl)sulphonamides as Novel Selective Human Cannabinoid Type 2 Receptor (hCB2R) Ligands; Insights into the Mechanism of Receptor Activation/DeactivationEleonora Gianquinto, Federica Sodano, Barbara Rolando, et al.FEBS Letters|April 14, 2016
Structural insight into the interaction of O-acetylserine sulfhydrylase with competitive, peptidic inhibitors by saturation transfer difference-NMRRoberto Benoni, Thelma A Pertinhez, Francesca Spyrakis, et al.Pageof 13