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Mini Rev Med Chem ; 23(3): 246-264, 2023.
Article in English | MEDLINE | ID: mdl-35549880

ABSTRACT

The selection of a protein structure is an important step for the success of the drug discovery process using structure-based design. Selection of the right crystal structure is critical as multiple crystal structures are available for the same protein in the Protein Data Bank (PDB). In this communication, we have discussed a systematic approach for selecting the right type of protein structure. Selecting crystal structures of TACE, 11ß-HSD1, DprE1, and SARS-CoV-2 Mpro enzymes for some case studies have been discussed for illustration.


Subject(s)
COVID-19 , Enzyme Inhibitors , Humans , Enzyme Inhibitors/chemistry , SARS-CoV-2 , Drug Design , Drug Discovery
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