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Proteins|December 14, 2007
Functional and structural features of the oxyanion hole in a thermophilic esterase from Alicyclobacillus acidocaldariusLuigi Mandrich, Valeria Menchise, Vincenzo Alterio, et al.Journal of Molecular Biology|September 24, 2004
The crystal structure of an EST2 mutant unveils structural insights on the H group of the carboxylesterase/lipase familyGiuseppina De Simone, Valeria Menchise, Vincenzo Alterio, et al.Organic & Biomolecular Chemistry|May 28, 2010
The first example of a significant active site conformational rearrangement in a carbonic anhydrase-inhibitor adduct: the carbonic anhydrase I-topiramate complexVincenzo Alterio, Simona Maria Monti, Emanuela Truppo, et al.Biology|February 25, 2023
A Combined in Silico and Structural Study Opens New Perspectives on Aliphatic Sulfonamides, a Still Poorly Investigated Class of CA InhibitorsEmma Langella, Davide Esposito, Simona Maria Monti, et al.Biopolymers|March 9, 2010
Crystal structure of an S-formylglutathione hydrolase from Pseudoalteromonas haloplanktis TAC125Vincenzo Alterio, Vincenzo Aurilia, Alessandra Romanelli, et al.International Journal of Molecular Sciences|October 14, 2022
α-CAs from Photosynthetic OrganismsEmma Langella, Anna Di Fiore, Vincenzo Alterio, et al.International Journal of Biological Macromolecules|October 25, 2024
Exploring the binding mode of phenyl and vinyl boronic acids to human carbonic anhydrasesDavide Esposito, Simona Maria Monti, Claudiu T Supuran, et al.Biopolymers|December 31, 2013
The structural comparison between membrane-associated human carbonic anhydrases provides insights into drug design of selective inhibitorsVincenzo Alterio, Peiwen Pan, Seppo Parkkila, et al.Journal of Medicinal Chemistry|September 2, 2005
Carbonic anhydrase inhibitors: stacking with Phe131 determines active site binding region of inhibitors as exemplified by the X-ray crystal structure of a membrane-impermeant antitumor sulfonamide complexed with isozyme IIValeria Menchise, Giuseppina De Simone, Vincenzo Alterio, et al.Bioorganic & Medicinal Chemistry|June 19, 2016
Kinetic and X-ray crystallographic investigations of substituted 2-thio-6-oxo-1,6-dihydropyrimidine-benzenesulfonamides acting as carbonic anhydrase inhibitorsDaniela Vullo, Claudiu T Supuran, Andrea Scozzafava, et al.Pageof 15