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Molecular characterization of farnesyl pyrophosphate synthase from Bacopa monniera by comparative modeling and docking studies

Farnesyl pyrophosphate synthase (FPS; EC 2.5.1.10) is a key enzyme in isoprenoid biosynthetic pathway and provides precursors for the biosynthesis of various pharmaceutically important metabolites. It catalyzes head to tail condensation of two isopentenyl pyrophosphate molecules with dimethylallyl p...

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Autores principales: Vishwakarma, Rishi Kishore, Patel, Krunal Arvind, Sonawane, Prashant, Singh, Somesh, Ruby, Kumari, Uma, Agrawal, Dinesh Chandra, Khan, Bashir Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Biomedical Informatics 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3523221/
https://www.ncbi.nlm.nih.gov/pubmed/23251041
http://dx.doi.org/10.6026/97320630081075
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author Vishwakarma, Rishi Kishore
Patel, Krunal Arvind
Sonawane, Prashant
Singh, Somesh
Ruby,
Kumari, Uma
Agrawal, Dinesh Chandra
Khan, Bashir Mohammad
author_facet Vishwakarma, Rishi Kishore
Patel, Krunal Arvind
Sonawane, Prashant
Singh, Somesh
Ruby,
Kumari, Uma
Agrawal, Dinesh Chandra
Khan, Bashir Mohammad
author_sort Vishwakarma, Rishi Kishore
collection PubMed
description Farnesyl pyrophosphate synthase (FPS; EC 2.5.1.10) is a key enzyme in isoprenoid biosynthetic pathway and provides precursors for the biosynthesis of various pharmaceutically important metabolites. It catalyzes head to tail condensation of two isopentenyl pyrophosphate molecules with dimethylallyl pyrophosphate to form C15 compound farnesyl pyrophosphate. Recent studies have confirmed FPS as a molecular target of bisphosphonates for drug development against bone diseases as well as pathogens. Although large numbers of FPSs from different sources are known, very few protein structures have been reported till date. In the present study, FPS gene from medicinal plant Bacopa monniera (BmFPS) was characterized by comparative modeling and docking. Multiple sequence alignment showed two highly conserved aspartate rich motifs FARM and SARM (DDXXD). The 3-D model of BmFPS was generated based on structurally resolved FPS crystal information of Gallus gallus. The generated models were validated by various bioinformatics tools and the final model contained only α-helices and coils. Further, docking studies of modeled BmFPS with substrates and inhibitors were performed to understand the protein ligand interactions. The two Asp residues from FARM (Asp100 and Asp104) as well as Asp171, Lys197 and Lys262 were found to be important for catalytic activity. Interaction of nitrogen containing bisphosphonates (risedronate, alendronate, zoledronate and pamidronate) with modeled BmFPS showed competitive inhibition; where, apart from Asp (100, 104 and 171), Thr175 played an important role. The results presented here could be useful for designing of mutants for isoprenoid biosynthetic pathway engineering well as more effective drugs against osteoporosis and human pathogens. ABBREVIATIONS: IPP - Isopentenyl Pyrophosphate, DMAPP - Dimethylallyl Pyrophosphate, GPP - Geranyl Pyrophosphate, FPP - FPPFarnesyl Pyrophosphate, DOPE - Discrete Optimized Protein Energy, BmFPS - Bacopa monniera Farnesyl Pyrophosphate Synthase, RMSD - Root Mean square Deviation, OPLS-AA - Optimized Potentials for Liquid Simulations- All Atom, FARM - First Aspartate Rich Motif, SARM - Second Aspartate Rich Motif.
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spelling pubmed-35232212012-12-18 Molecular characterization of farnesyl pyrophosphate synthase from Bacopa monniera by comparative modeling and docking studies Vishwakarma, Rishi Kishore Patel, Krunal Arvind Sonawane, Prashant Singh, Somesh Ruby, Kumari, Uma Agrawal, Dinesh Chandra Khan, Bashir Mohammad Bioinformation Hypothesis Farnesyl pyrophosphate synthase (FPS; EC 2.5.1.10) is a key enzyme in isoprenoid biosynthetic pathway and provides precursors for the biosynthesis of various pharmaceutically important metabolites. It catalyzes head to tail condensation of two isopentenyl pyrophosphate molecules with dimethylallyl pyrophosphate to form C15 compound farnesyl pyrophosphate. Recent studies have confirmed FPS as a molecular target of bisphosphonates for drug development against bone diseases as well as pathogens. Although large numbers of FPSs from different sources are known, very few protein structures have been reported till date. In the present study, FPS gene from medicinal plant Bacopa monniera (BmFPS) was characterized by comparative modeling and docking. Multiple sequence alignment showed two highly conserved aspartate rich motifs FARM and SARM (DDXXD). The 3-D model of BmFPS was generated based on structurally resolved FPS crystal information of Gallus gallus. The generated models were validated by various bioinformatics tools and the final model contained only α-helices and coils. Further, docking studies of modeled BmFPS with substrates and inhibitors were performed to understand the protein ligand interactions. The two Asp residues from FARM (Asp100 and Asp104) as well as Asp171, Lys197 and Lys262 were found to be important for catalytic activity. Interaction of nitrogen containing bisphosphonates (risedronate, alendronate, zoledronate and pamidronate) with modeled BmFPS showed competitive inhibition; where, apart from Asp (100, 104 and 171), Thr175 played an important role. The results presented here could be useful for designing of mutants for isoprenoid biosynthetic pathway engineering well as more effective drugs against osteoporosis and human pathogens. ABBREVIATIONS: IPP - Isopentenyl Pyrophosphate, DMAPP - Dimethylallyl Pyrophosphate, GPP - Geranyl Pyrophosphate, FPP - FPPFarnesyl Pyrophosphate, DOPE - Discrete Optimized Protein Energy, BmFPS - Bacopa monniera Farnesyl Pyrophosphate Synthase, RMSD - Root Mean square Deviation, OPLS-AA - Optimized Potentials for Liquid Simulations- All Atom, FARM - First Aspartate Rich Motif, SARM - Second Aspartate Rich Motif. Biomedical Informatics 2012-11-13 /pmc/articles/PMC3523221/ /pubmed/23251041 http://dx.doi.org/10.6026/97320630081075 Text en © 2012 Biomedical Informatics This is an open-access article, which permits unrestricted use, distribution, and reproduction in any medium, for non-commercial purposes, provided the original author and source are credited.
spellingShingle Hypothesis
Vishwakarma, Rishi Kishore
Patel, Krunal Arvind
Sonawane, Prashant
Singh, Somesh
Ruby,
Kumari, Uma
Agrawal, Dinesh Chandra
Khan, Bashir Mohammad
Molecular characterization of farnesyl pyrophosphate synthase from Bacopa monniera by comparative modeling and docking studies
title Molecular characterization of farnesyl pyrophosphate synthase from Bacopa monniera by comparative modeling and docking studies
title_full Molecular characterization of farnesyl pyrophosphate synthase from Bacopa monniera by comparative modeling and docking studies
title_fullStr Molecular characterization of farnesyl pyrophosphate synthase from Bacopa monniera by comparative modeling and docking studies
title_full_unstemmed Molecular characterization of farnesyl pyrophosphate synthase from Bacopa monniera by comparative modeling and docking studies
title_short Molecular characterization of farnesyl pyrophosphate synthase from Bacopa monniera by comparative modeling and docking studies
title_sort molecular characterization of farnesyl pyrophosphate synthase from bacopa monniera by comparative modeling and docking studies
topic Hypothesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3523221/
https://www.ncbi.nlm.nih.gov/pubmed/23251041
http://dx.doi.org/10.6026/97320630081075
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