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http://krishi.icar.gov.in/jspui/handle/123456789/73839
Title: | Structural insights into the RNA interaction with Yam bean Mosaic virus (coat protein) from Pachyrhizus erosus using bioinformatics approach |
Other Titles: | Not Available |
Authors: | Varsha Acharya R. Arutselvan Kalidas Pati Ajaya Kumar Rout Budheswar Dehury V. B. S. Chauhan M. Nedunchezhiyan |
ICAR Data Use Licennce: | http://krishi.icar.gov.in/PDF/ICAR_Data_Use_Licence.pdf |
Author's Affiliated institute: | Regional Centre, ICAR-Central Tuber Crops Research Institute Bhubaneswar, Odisha, India ICAR-Central Inland Fisheries Research Institute, Barrackpore, Kolkata, West Bengal, India |
Published/ Complete Date: | 2022-07-22 |
Project Code: | Not Available |
Keywords: | Potyvirus Coat protein Yam bean mosaic virus RNA binding MD Simulation |
Publisher: | PLOS ONE |
Citation: | Acharya V, Arutselvan R, Pati K, Rout AK, Dehury B, Chauhan VBS, et al. (2022) Structural insights into the RNA interaction with Yam bean Mosaic virus (coat protein) from Pachyrhizus erosus using bioinformatics approach. PLoS ONE 17(7): e0270534 |
Series/Report no.: | Not Available; |
Abstract/Description: | Plants are constantly threatened by a virus infection, i.e., Potyviruses, the second largest genus of plant viruses which results in several million-dollar losses in various essential crops globally. Yam bean (Pachyrhizus erosus) is considered to be one of the essential tuberous legume crops holding a great potential source of starch. Yam Bean Mosaic Virus (YBMV) of Potyvirus group belonging to the family potyviridae affects Yam bean and several angiosperms both in the tropical and sub-tropical regions causing large economical losses in crops. In this study, we attempted to understand the sequence-structure relationship and mode of RNA binding mechanism in YBMV CP using in silico integrative modeling and allatoms molecular dynamics (MD) simulations. The assembly of coat protein (CP) subunits from YBMV and the plausible mode of RNA binding were compared with the experimental structure of CP from Watermelon mosaic virus potyvirus (5ODV). The transmembrane helix region is present in the YBMV CP sequence ranging from 76 to 91 amino acids. Like the close structural-homolog, 24 CPs monomeric sub-units formed YBMV a conserved fold. Our computational study showed that ARG124, ARG155 , and TYR151 orient towards the inner side of the virion, while, THR122, GLN125, SER92, ASP94 reside towards the outer side of the virion. Despite sharing very low sequence similarity with CPs from other plant viruses, the strongly conserved residues Ser, Arg, and Asp within the RNA binding pocket of YBMV CP indicate the presence of a highly conserved RNA binding site in CPs from different families. Using several bioinformatics tools and comprehensive analysis from MD simulation, our study has provided novel insights into the RNA binding mechanism in YBMV CP. Thus, we anticipate that our findings from this study will be useful for the development of new therapeutic agents against the pathogen, paving the way for researchers to better control this destructive plant virus. |
Description: | Not Available |
ISSN: | 1932-6203 |
Type(s) of content: | Article |
Sponsors: | Not Available |
Language: | English |
Name of Journal: | PLOS ONE |
Journal Type: | International |
NAAS Rating: | 9.24 |
Impact Factor: | 3.752 |
Volume No.: | 17(7) |
Page Number: | 1-25 |
Name of the Division/Regional Station: | Regional Centre, ICAR-Central Tuber Crops Research Institute Bhubaneswar, Odisha, India |
Source, DOI or any other URL: | https://doi.org/10.1371/journal. pone.0270534 |
URI: | http://krishi.icar.gov.in/jspui/handle/123456789/73839 |
Appears in Collections: | HS-CTCRI-Publication |
Files in This Item:
File | Description | Size | Format | |
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journal.pone.0270534.pdf | 5.47 MB | Adobe PDF | View/Open |
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