Comparison stability Rusticyanin ۲۳۲۷۰ wild-type and mutant His۱۴۳Leu using molecular dynamics simulation

Publish Year: 1401
نوع سند: مقاله ژورنالی
زبان: English
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JR_JORNA-2-1_001

تاریخ نمایه سازی: 14 اسفند 1401

Abstract:

The Acidithiobacillus ferroxidans bacterium plays an important role in the bioleaching process of uranium. The rusticyanin protein is the second most crucial component in the electron transport chain in the membrane of the Acidithiobacillus ferroxidnas bacterium. This protein belongs to the large family of copper blue proteins. The protein sequence rusticyanin ۲۳۲۷۰ was derived from UniProtKB database. A suitable template for modeling was prepared from the Swiss model server, and the best protein model was made with Modeller software. The His۱۴۳Leu mutation was developed using the Pymol software in the protein. The effect of the mutation on the stability of the protein structure was investigated by analysing the results of molecular dynamics simulation on the wild-type and mutant protein. The values RMSD and RMSF are the same for both wild-type and mutant. The amount of Rg in mutant protein is reduced. His۱۴۳Leu mutation in the rusticyanin ۲۳۲۷۰ protein does not affect the secondary structure protein and slightly increases the folding and stability of the tertiary structure.

Authors

R. Jafarpour

Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran

F. Fatemi

Materials and Nuclear Fuel Research School, Nuclear Science and Technology Research Institute, Tehran, Iran

M. Dehghan Shasaltane

Department of Biology, Faculty of Sciences, University of Zanjan, Zanjan, Iran

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