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• W2891915040 abstract "Cryptosporidium parvum is a protozoan parasite which causes waterborne diseases known as Cryptosporidiosis. It is an acute enteric diarrheal disease being severe in the case of immunocompromised individuals and children. C. parvum mainly depends on the glycolysis process for energy production and LDH (Lactate Dehydrogenase) is a key controller of this process. In this study from different in-silico approaches such as structure-based, ligand-based and de novo drug design; a total of 40 compounds were selected for docking studies against LDH. The study reported a compound CHEMBL1784973 from Pathogen Box as the best inhibitor in terms of docking score and pharmacophoric features. Furthermore, the binding mode of the best-reported inhibitor was validated through molecular dynamics simulation for a time interval of 70 ns in water environment. The findings resulted in the stable conformation of the inhibitor in the active site of the protein. This study will be helpful for experimental validation." @default.
• W2891915040 created "2018-09-27" @default.
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• W2891915040 date "2018-12-01" @default.
• W2891915040 modified "2023-09-26" @default.
• W2891915040 title "In-silico screening of small molecule inhibitors against Lactate Dehydrogenase (LDH) of Cryptosporidium parvum" @default.
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• W2891915040 doi "https://doi.org/10.1016/j.compbiolchem.2018.09.002" @default.
• W2891915040 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30240985" @default.
• W2891915040 hasPublicationYear "2018" @default.
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