Insights into the structure-function relationship of brown plant hopper resistance protein, Bph14 of rice plant: a computational structural biology approach.
Algorithms
Amino Acid Sequence
Animals
Binding Sites
Chemical Phenomena
Cyclopentanes
/ chemistry
Disease Resistance
Hydrogen Bonding
Insecta
Ligands
Models, Molecular
Molecular Docking Simulation
Molecular Dynamics Simulation
Oryza
/ metabolism
Oxylipins
/ chemistry
Plant Proteins
/ chemistry
Protein Binding
Protein Conformation
Protein Interaction Domains and Motifs
Salicylic Acid
/ chemistry
Structure-Activity Relationship
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
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