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Depression: 21st Century Solutions + The Dark Side of Wheat

Abstract Title:

Active site binding modes of curcumin in HIV-1 protease and integrase.

Abstract Source:

Am J Clin Nutr. 1995 Mar;61(3):585-9. PMID: 15950462

Abstract Author(s):

Opa Vajragupta, Preecha Boonchoong, Garrett M Morris, Arthur J Olson

Article Affiliation:

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Mahidol University, 447 Sri-Ayudhya Road, Bangkok 10400, Thailand. pyovj@mahidol.ac.th

Abstract:

Structure models for the interaction of curcumin with HIV-1 integrase (IN) and protease (PR) were investigated using computational docking. Curcumin was found to bind preferentially in similar ways to the active sites of both IN and PR. For IN, the binding site is formed by residues Asp64, His67, Thr66, Glu92, Thr93, Asp116, Ser119, Asn120, and Lys159. Docked curcumin contacts the catalytic residues adjacent to Asp116 and Asp64, and near the divalent metal (Mg2+). In the PR docking, the curcumin structure fitted well to the active site, interacting with residues Asp25, Asp29, Asp30, Gly27', Asp29', and Asp30'. The results suggest that o-hydroxyl and/or keto-enol structures are important for both IN and PR inhibitory actions. The symmetrical structure of curcumin seems to play an important role for binding to the PR protein, whereas the keto-enol and only one side of the terminal o-hydroxyl showed tight binding to the IN active site.

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Sayer Ji
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Depression: 21st Century Solutions + The Dark Side of Wheat

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