Author/Authors :
Mortazavi, M Department of Biotechnology - Institute of Science and High Technology and Environmental Science - Graduate University of Advanced Technology, Kerman , Torkzadeh-Mahani, M Department of Biotechnology - Institute of Science and High Technology and Environmental Science - Graduate University of Advanced Technology, Kerman , Nezafat, N Department of Pharmaceutical Biotechnology - School of Pharmacy - Shiraz University of Medical Sciences, Shiraz , Malekpour, A Legal Medicine Research Center - Legal Medicine Organization of Iran, Tehran , Zarenezhad, M Legal Medicine Research Center - Legal Medicine Organization of Iran, Tehran , Hemmati, R Department of Biology - Faculty of Basic Sciences - Shahrekord University - Charmahal va Bakhtiari , Maleki, M Department of Biotechnology - Institute of Science and High Technology and Environmental Science - Graduate University of Advanced Technology, Kerman , Hosseini, Y Gastroentero Hepatology Research Center - Shiraz University of Medical Sciences , Pazhoomand, R Legal Medicine Research Center - Legal Medicine Organization of Iran, Tehran
Abstract :
Luciferase enzymes are involved in the bioluminescence reaction (light emission by living organisms). The bioluminescence process
is a widespread phenomenon in the Nature. These enzymes are identified in some domains of life, but the luciferases from lampyrid genus
are considered of for biological applications. The molecular cloning of a new type of firefly luciferase from Luciola lateralis was
reported, previously. Here, we study its substrate binding site and rare codon with molecular docking and bioinformatics studies. By
molecular modelling, some rare codons were identified that may have a critical role in structure and function of this luciferase. AutoDock
Vina was used in the molecular docking that recognizes some residues that yield closely related with luciferin and AMP binding site.
These types of studies help in the discovery of the light production reaction. Evaluation of these hidden information’s can improve the
knowledge of luciferases folding and protein expression challenges and help in design of new drugs.
Keywords :
Luciola lateralis , Luciferase , Rare codon , Docking , Substrate binding site