{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["8(1)"],"submitter":["Yadav DK"],"pubmed_abstract":["SIRT6 and COX-2 are oncogenes target that promote the expression of proinflammatory and pro-survival proteins through a signaling pathway, which leads to increased survival and proliferation of tumor cells. However, COX-2 also suppresses skin tumorigenesis and their relationship with SIRT6, making it an interesting target for the discovery of drugs with anti-inflammatory and anti-cancer properties. Herein, we studied the interaction of thieno[3,2-c]pyran analogs and RONS species with SIRT6 and COX-2 through the use of molecular docking and molecular dynamic simulations. Molecular docking studies revealed the importance of hydrophobic and hydrophilic amino acid residues for the stability. The molecular dynamics study examined conformational changes in the enzymes caused by the binding of th"],"journal":["Scientific reports"],"pagination":["4777"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC5859274"],"repository":["biostudies-literature"],"pubmed_title":["Molecular Insights into the Interaction of RONS and Thieno[3,2-c]pyran Analogs with SIRT6/COX-2: A Molecular Dynamics Study."],"pmcid":["PMC5859274"],"pubmed_authors":["Yadav DK","Choi EH","Yadav L","Teli M","Sharma P","Chaudhary S","Saloni","Kim HS","Kim MH","Kumar N","Kumar S","Misra S"],"additional_accession":[]},"is_claimable":false,"name":"Molecular Insights into the Interaction of RONS and Thieno[3,2-c]pyran Analogs with SIRT6/COX-2: A Molecular Dynamics Study.","description":"SIRT6 and COX-2 are oncogenes target that promote the expression of proinflammatory and pro-survival proteins through a signaling pathway, which leads to increased survival and proliferation of tumor cells. However, COX-2 also suppresses skin tumorigenesis and their relationship with SIRT6, making it an interesting target for the discovery of drugs with anti-inflammatory and anti-cancer properties. Herein, we studied the interaction of thieno[3,2-c]pyran analogs and RONS species with SIRT6 and COX-2 through the use of molecular docking and molecular dynamic simulations. Molecular docking studies revealed the importance of hydrophobic and hydrophilic amino acid residues for the stability. The molecular dynamics study examined conformational changes in the enzymes caused by the binding of th","dates":{"release":"2018-01-01T00:00:00Z","publication":"2018 Mar","modification":"2026-05-03T06:36:31.241Z","creation":"2019-03-26T23:20:20Z"},"accession":"S-EPMC5859274","cross_references":{"pubmed":["29556059"],"doi":["10.1038/s41598-018-22972-9"]}}