Molecular modeling studies of peptide drug candidates against SARS.

Kuo-Chen Chou, Dong-Qing Wei, Qi-Shi Du, Rui Zhang

Journal: Medicinal chemistry (Shariqah (United Arab Emirates)) 2006;2(3):309-14

PMID: 16948478

Abstract

Flexible alignment and docking studies were conducted for the three octapeptides, ATLQANEV, AVLQSGFR, and ATLQAIAS, that were cleavable by SARS-CoV Mpro. It has been observed that all pharmacophores of the three peptides overlap very well, and that ATLQANEV binds best with the receptor, followed by AVLQSGFR, and then ATLQAIAS. During the process of docking the octapeptides to the SARS enzyme, the residues of the catalytic dyad, i.e., His-41 and Cys-145 are actively involved in forming the hydrogen bonds, so is the center residue (Gln) of all the three octapeptides. The findings are fully consistent with experimental observations. The present studies suggest that the octapeptides ATLQANEV and ATLQAIAS, like AVLQSGFR, might also be the good starting points for designing potential drugs against SARS.

Address: Tianjin Institute of Bioinformatics and Drug Discoveries and Tianjin Normal University, China.

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