Title :
Interaction simulation of Lipoxygenase with arachidonate acid using NAMD
Author :
Li, Zhongwei ; Khosravi, Ebrahim ; Bai, Shuju
Author_Institution :
Dept. of Comput. Sci., Southern Univ., Baton Rouge, LA, USA
Abstract :
Lipoxygenase (LOX) family is believed as the major cause of pathological symptoms in asthma by biosynthesis of leukotrienes. The physiological function is known as firstly producing 8R-HPETE (derived from arachidonate acid, referred as AA), which is transformed in further enzymatic step into leukotrienes. However, much less detail is known about the role of 5-Lox in the inflammatory reaction. We have used the 1.85Å resolution structure of a wild coral Lipoxygenase (8R-LOX) (with 41% sequence identical to the human arachidonate 5-LOX) as a foundation to model the interactions between 8R-Lox and its substrate AA, and its binding site was identified using ICM. In this research, the 8R-Lox:AA complex obtained was refined and analyzed by molecular dynamic method (NAMD). Parameterization scheme for unknown structure of non-heme iron ligated by a series of residues was developed using VMD paratool plugin. All quantum mechanical calculation were performed by Gaussian03 with the Becke3LYP functional at 6-31G(d) basis set.
Keywords :
density functional theory; diseases; enzymes; molecular biophysics; molecular dynamics method; 6-31G(d) basis set; 8R-HPETE; Becke3LYP functional; Gaussian03; LOX family; Lipoxygenase; VMD paratool plugin; arachidonate acid; asthma; biosynthesis; inflammatory reaction; interaction simulation; leukotrienes; molecular dynamic method; pathological symptom; Biological system modeling; Conferences; Force; Iron; Physiology; Substrates; Trajectory; NAMD; arachidonic acid; force field parameter; lipoxygenases; mocular dynamics;
Conference_Titel :
Bioinformatics and Biomedicine Workshops (BIBMW), 2011 IEEE International Conference on
Conference_Location :
Atlanta, GA
Print_ISBN :
978-1-4577-1612-6
DOI :
10.1109/BIBMW.2011.6112525