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|Title:||Molecular dynamics simulation of chitinase I from Thermomyces lanuginosus SSBP to ensure optimal activity||Authors:||Khan, Faez Iqbal
Hassan, Md. Imtaiyaz
|Keywords:||Chitinase;TIM-barrel;Protein stability;Molecular docking;GROMAC S;Molecular dynamics simulation||Issue Date:||22-Sep-2016||Publisher:||Taylor and Fancis Online||Source:||Khan, F.I. et al. 2016. Molecular dynamics simulation of chitinase I from Thermomyces lanuginosus SSBP to ensure optimal activity. Molecular Simulation. 43(7): 480-490. DOI: 10.1080/08927022.2016.1237024||Abstract:||The fungal chitinase I obtained from Thermomyces lanuginosus SSBP, a thermophilic deuteromycete, has an optimum growth temperature and pH of 323.15 K and 6.5, respectively. This enzyme plays an important task in the defence mechanism of organisms against chitin-containing parasites by hydrolysing β-1, 4-linkages in chitin. It acts as both anti-fungal and biofouling agents, with some being thermostable and suitable for the industrial applications. Three-dimensional model of chitinase I enzyme was predicted and analysed using various bioinformatics tools. The structure of chitinase I exhibited a well-defined TIM barrel topology with an eight-stranded α/β domain. Structural analysis and folding studies at temperatures ranging from 300 to 375 K using 10 ns molecular dynamics simulations clearly showed the stability of the protein was evenly distributed even at higher temperatures, in accordance with the experimental results. We also carried out a number of 20 ns constant pH molecular dynamics simulations of chitinase I at a pH range 2–6 in a solvent. This work was aimed at establishing the optimum activity and stability profiles of chitinase I. We observed a strong conformational pH dependence of chitinase I and the enzyme retained their characteristic TIM barrel topology at low pH.||URI:||http://hdl.handle.net/10321/2943||ISSN:||0892-7022
|Appears in Collections:||Research Publications (Applied Sciences)|
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