Please use this identifier to cite or link to this item:
|Title:||Structural bioinformatics and molecular dynamics simulations studies of cathepsins as a potential target for drug discovery||Authors:||Pinitglang, Surapong
|Keywords:||Cathepsin;Cysteine proteinase;Homology modeling;Virtual screening||Issue Date:||2012||Publisher:||University of the Thai Chamber of Commerce||Source:||Surapong Pinitglang, Ratchanee Saiprajong, T. Dussadee, Khanok Ratanakhanokchai (2012) Structural bioinformatics and molecular dynamics simulations studies of cathepsins as a potential target for drug discovery., 63-74.||Conference:||(2012) Procedia Computer Science||Abstract:||Prediction of threedimensional structure of cathepsins, and molecular dynamics simulations of cathepsin S were studied by interaction with the drug molecule with virtual screening 681,158 compounds from ZINC database. The result of study showed top 1 ranked was obtained with drug molecule ZINC 23215439 reaction with cathepsin S. This demonstrates that the active site of cathepsin S Cys25, His164 and binding site Gln19 and Gly 20 are essential for interactions of cathepsin SZINC 23215439inhibitor complex. CoulombSR and LennardJonesSRinteractions energy of amino acids and drug molecule ZINC code 23215439 which consisted in active site of cathepsin S have been evaluated.||URI:||https://scholar.utcc.ac.th/handle/6626976254/3532||Rights:||This work is protected by copyright. Reproduction or distribution of the work in any format is prohibited without written permission of the copyright owner.|
|Appears in Collections:||RSO: Conference Papers|
Show full item record Recommend this item
checked on Jul 11, 2019
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.