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Ferroxidase Activity in Eukaryotic Ferritin is Controlled by Accessory-Iron-Binding Sites in the Catalytic CavityThe structure of the human glutaminyl cyclase–SEN177 complex indicates routes for developing new potent inhibitors as possible agents for the treatment of neurological disordersAtomic-Resolution Structure of a Class C β-Lactamase and Its Complex with AvibactamStructural and Functional Characterization of the Human Thymidylate Synthase (hTS) Interface Variant R175C, New Perspectives for the Development of hTS InhibitorsStructural Comparison of Enterococcus faecalis and Human Thymidylate Synthase Complexes with the Substrate dUMP and Its Analogue FdUMP Provides Hints about Enzyme Conformational VariabilitiesTargeting Methyltransferases in Human Pathogenic Bacteria: Insights into Thymidylate Synthase (TS) and Flavin-Dependent TS (FDTS)Evidence of Destabilization of the Human Thymidylate Synthase (hTS) Dimeric Structure Induced by the Interface Mutation Q62R.Iron Biomineral Growth from the Initial Nucleation Seed in L-FerritinIdentification of Phosphate-Containing Compounds as New Inhibitors of 14-3-3/c-Abl Protein-Protein InteractionStructural Insights into the Development of Cycloguanil Derivatives as Trypanosoma brucei Pteridine-Reductase-1 InhibitorsDiscovery of Taniborbactam (VNRX-5133): A Broad-Spectrum Serine- and Metallo-β-lactamase Inhibitor for Carbapenem-Resistant Bacterial InfectionsVNRX-5133 (Taniborbactam), a Broad-Spectrum Inhibitor of Serine- and Metallo-β-Lactamases, Restores Activity of Cefepime in Enterobacterales and Pseudomonas aeruginosaFibrils of α-Synuclein Abolish the Affinity of Cu2+-Binding Site to His50 and Induce Hopping of Cu2+ Ions in the TerminiBreakthroughs in Medicinal Chemistry: New Targets and Mechanisms, New Drugs, New Hopes-6Enhancement of Benzothiazoles as Pteridine Reductase-1 Inhibitors for the Treatment of Trypanosomatidic InfectionsSAR Studies Leading to the Identification of a Novel Series of Metallo-β-lactamase Inhibitors for the Treatment of Carbapenem-Resistant Enterobacteriaceae Infections That Display Efficacy in an Animal Infection ModelHigh-resolution crystal structure of Trypanosoma brucei pteridine reductase 1 in complex with an innovative tricyclic-based inhibitor
P50
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P50
description
researcher ORCID ID = 0000-0003-4824-7478
@en
name
Stefano Mangani
@ast
Stefano Mangani
@en
Stefano Mangani
@es
Stefano Mangani
@nl
type
label
Stefano Mangani
@ast
Stefano Mangani
@en
Stefano Mangani
@es
Stefano Mangani
@nl
prefLabel
Stefano Mangani
@ast
Stefano Mangani
@en
Stefano Mangani
@es
Stefano Mangani
@nl
P21
P31
P496
0000-0003-4824-7478