Insights into the structure-function relationship of brown plant hopper resistance protein, Bph14 of rice plant: a computational structural biology approach.

ANOLEA: Atomic Non-Local Environment Assessment Bph14 Brown plant hopper CC: Coiled-coil FEL: Free-energy landscape GMXAPBS: GROMACS tool to perform MM/PBSA GROMACS: GROningen MAchine for Chemical Simulations JA: Jasmonic acid LINCS: Linear Constraint Solver LRR: Leucine-rich region MD: Molecular Dynamic MM/PBSA: Molecular Mechanics/Poisson–Boltzmann surface area NBS: Nucleotide: binding site NMR: Nuclear magnetic resonance NPT: constant number of particles, volume and temperature NVT: constant number of particles, pressure and temperature PDB ID: Protein Data Bank identification RMSD: root-mean-square deviations RMSF: root mean square fluctuations SA: Salicylic acid SDF: Structure Data File docking modelling rice

Journal

Journal of biomolecular structure & dynamics
ISSN: 1538-0254
Titre abrégé: J Biomol Struct Dyn
Pays: England
ID NLM: 8404176

Informations de publication

Date de publication:
Apr 2019
Historique:
pubmed: 11 4 2018
medline: 3 6 2020
entrez: 11 4 2018
Statut: ppublish

Résumé

Brown plant hopper (BPH) is one of the major destructive insect pests of rice, causing severe yield loss. Thirty-two BPH resistance genes have been identified in cultivated and wild species of rice Although, molecular mechanism of rice plant resistance against BPH studied through map-based cloning, due to non-existence of NMR/crystal structures of Bph14 protein, recognition of leucine-rich repeat (LRR) domain and its interaction with different ligands are poorly understood. Thus, in the present study, in silico approach was adopted to predict three-dimensional structure of LRR domain of Bph14 using comparative modelling approach followed by interaction study with jasmonic and salicylic acids. LRR domain along with LRR-jasmonic and salicylic acid complexes were subjected to dynamic simulation using GROMACS, individually, for energy minimisation and refinement of the structure. Final binding energy of jasmonic and salicylic acid with LRR domain was calculated using MM/PBSA. Free-energy landscape analysis revealed that overall stability of LRR domain of Bph14 is not much affected after forming complex with jasmonic and salicylic acid. MM/PBSA analysis revealed that binding affinities of LRR domain towards salicylic acid is higher as compared to jasmonic acid. Interaction study of LRR domain with salicylic acid and jasmonic acid reveals that THR987 of LRR form hydrogen bond with both complexes. Thus, THR987 plays active role in the Bph14 and phytochemical interaction for inducing resistance in rice plant against BPH. In future, Bph14 gene and phytochemicals could be used in BPH management and development of novel resistant varieties for increasing rice yield.

Identifiants

pubmed: 29633905
doi: 10.1080/07391102.2018.1462737
doi:

Substances chimiques

Cyclopentanes 0
Ligands 0
Oxylipins 0
Plant Proteins 0
jasmonic acid 6RI5N05OWW
Salicylic Acid O414PZ4LPZ

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1649-1665

Auteurs

Manoj Kumar Gupta (MK)

a Department of Biotechnology & Bioinformatics , Yogi Vemana University , Kadapa , India.

Ramakrishna Vadde (R)

a Department of Biotechnology & Bioinformatics , Yogi Vemana University , Kadapa , India.

Ravindra Donde (R)

b ICAR-National Rice Research Institute (Formerly CRRI) , Cuttack , India.

Gayatri Gouda (G)

b ICAR-National Rice Research Institute (Formerly CRRI) , Cuttack , India.

Jitendra Kumar (J)

b ICAR-National Rice Research Institute (Formerly CRRI) , Cuttack , India.

Subhashree Nayak (S)

b ICAR-National Rice Research Institute (Formerly CRRI) , Cuttack , India.

Mayabini Jena (M)

b ICAR-National Rice Research Institute (Formerly CRRI) , Cuttack , India.

Lambodar Behera (L)

b ICAR-National Rice Research Institute (Formerly CRRI) , Cuttack , India.

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