Homology modeling and docking studies of δ19-fatty acid desaturase from a Cold-tolerant Pseudomonas sp. AMS8

Membrane-bound fatty acid desaturases perform oxygenated desaturation reactions to insert double bonds within fatty acyl chains in regioselective and stereoselective manners. The Δ9-fatty acid desaturase strictly creates the first double bond between C9 and 10 positions of most saturated substrates....

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Main Authors:	Garba, Lawal, Mohamad Yussoff, Mohamad Ariff, Abd Halim, Khairul Bariyyah, Ishak, Siti Nor Hasmah, Mohamad Ali, Mohd Shukuri, Oslan, Siti Nurbaya, Raja Abd Rahman, Raja Noor Zaliha
Format:	Article
Language:	English English English
Published:	PeerJ 2018
Subjects:	Q Science (General)
Online Access:	http://irep.iium.edu.my/63377/ http://irep.iium.edu.my/63377/ http://irep.iium.edu.my/63377/ http://irep.iium.edu.my/63377/7/63377_Homology%20modeling%20and%20docking%20studies_scopus.pdf http://irep.iium.edu.my/63377/13/63377_Homology%20modeling%20and%20docking%20studies.pdf http://irep.iium.edu.my/63377/14/63377_Homology%20modeling%20and%20docking%20studies_WOS.pdf

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spelling	iium-633772019-03-13T07:11:29Z http://irep.iium.edu.my/63377/ Homology modeling and docking studies of δ19-fatty acid desaturase from a Cold-tolerant Pseudomonas sp. AMS8 Garba, Lawal Mohamad Yussoff, Mohamad Ariff Abd Halim, Khairul Bariyyah Ishak, Siti Nor Hasmah Mohamad Ali, Mohd Shukuri Oslan, Siti Nurbaya Raja Abd Rahman, Raja Noor Zaliha Q Science (General) Membrane-bound fatty acid desaturases perform oxygenated desaturation reactions to insert double bonds within fatty acyl chains in regioselective and stereoselective manners. The Δ9-fatty acid desaturase strictly creates the first double bond between C9 and 10 positions of most saturated substrates. As the three-dimensional structures of the bacterial membrane fatty acid desaturases are not available, relevant information about the enzymes are derived from their amino acid sequences, site-directed mutagenesis and domain swapping in similar membrane-bound desaturases. The cold-tolerant Pseudomonas sp. AMS8 was found to produce high amount of monounsaturated fatty acids at low temperature. Subsequently, an active Δ9-fatty acid desaturase was isolated and functionally expressed in Escherichia coli. In this paper we report homology modeling and docking studies of a Δ9-fatty acid desaturase from a Cold-tolerant Pseudomonas sp. AMS8 for the first time to the best of our knowledge. Three dimensional structure of the enzyme was built using MODELLER version 9.18 using a suitable template. The protein model contained the three conserved-histidine residues typical for all membrane-bound desaturase catalytic activity. The structure was subjected to energy minimization and checked for correctness using Ramachandran plots and ERRAT, which showed a good quality model of 91.6 and 65.0%, respectively. The protein model was used to preform MD simulation and docking of palmitic acid using CHARMM36 force field in GROMACS Version 5 and Autodock tool Version 4.2, respectively. The docking simulation with the lowest binding energy, −6.8 kcal/mol had a number of residues in close contact with the docked palmitic acid namely, Ile26, Tyr95, Val179, Gly180, Pro64, Glu203, His34, His206, His71, Arg182, Thr85, Lys98 and His177. Interestingly, among the binding residues are His34, His71 and His206 from the first, second, and third conserved histidine motif, respectively, which constitute the active site of the enzyme. The results obtained are in compliance with the in vivo activity of the Δ9-fatty acid desaturase on the membrane phospholipids. PeerJ 2018-03-19 Article PeerReviewed application/pdf en http://irep.iium.edu.my/63377/7/63377_Homology%20modeling%20and%20docking%20studies_scopus.pdf application/pdf en http://irep.iium.edu.my/63377/13/63377_Homology%20modeling%20and%20docking%20studies.pdf application/pdf en http://irep.iium.edu.my/63377/14/63377_Homology%20modeling%20and%20docking%20studies_WOS.pdf Garba, Lawal and Mohamad Yussoff, Mohamad Ariff and Abd Halim, Khairul Bariyyah and Ishak, Siti Nor Hasmah and Mohamad Ali, Mohd Shukuri and Oslan, Siti Nurbaya and Raja Abd Rahman, Raja Noor Zaliha (2018) Homology modeling and docking studies of δ19-fatty acid desaturase from a Cold-tolerant Pseudomonas sp. AMS8. PeerJ, 2018 (3). pp. 1-21. ISSN 2167-8359 https://peerj.com/articles/4347.pdf 10.7717/peerj.4347
repository_type	Digital Repository
institution_category	Local University
institution	International Islamic University Malaysia
building	IIUM Repository
collection	Online Access
language	English English English
topic	Q Science (General)
spellingShingle	Q Science (General) Garba, Lawal Mohamad Yussoff, Mohamad Ariff Abd Halim, Khairul Bariyyah Ishak, Siti Nor Hasmah Mohamad Ali, Mohd Shukuri Oslan, Siti Nurbaya Raja Abd Rahman, Raja Noor Zaliha Homology modeling and docking studies of δ19-fatty acid desaturase from a Cold-tolerant Pseudomonas sp. AMS8
description	Membrane-bound fatty acid desaturases perform oxygenated desaturation reactions to insert double bonds within fatty acyl chains in regioselective and stereoselective manners. The Δ9-fatty acid desaturase strictly creates the first double bond between C9 and 10 positions of most saturated substrates. As the three-dimensional structures of the bacterial membrane fatty acid desaturases are not available, relevant information about the enzymes are derived from their amino acid sequences, site-directed mutagenesis and domain swapping in similar membrane-bound desaturases. The cold-tolerant Pseudomonas sp. AMS8 was found to produce high amount of monounsaturated fatty acids at low temperature. Subsequently, an active Δ9-fatty acid desaturase was isolated and functionally expressed in Escherichia coli. In this paper we report homology modeling and docking studies of a Δ9-fatty acid desaturase from a Cold-tolerant Pseudomonas sp. AMS8 for the first time to the best of our knowledge. Three dimensional structure of the enzyme was built using MODELLER version 9.18 using a suitable template. The protein model contained the three conserved-histidine residues typical for all membrane-bound desaturase catalytic activity. The structure was subjected to energy minimization and checked for correctness using Ramachandran plots and ERRAT, which showed a good quality model of 91.6 and 65.0%, respectively. The protein model was used to preform MD simulation and docking of palmitic acid using CHARMM36 force field in GROMACS Version 5 and Autodock tool Version 4.2, respectively. The docking simulation with the lowest binding energy, −6.8 kcal/mol had a number of residues in close contact with the docked palmitic acid namely, Ile26, Tyr95, Val179, Gly180, Pro64, Glu203, His34, His206, His71, Arg182, Thr85, Lys98 and His177. Interestingly, among the binding residues are His34, His71 and His206 from the first, second, and third conserved histidine motif, respectively, which constitute the active site of the enzyme. The results obtained are in compliance with the in vivo activity of the Δ9-fatty acid desaturase on the membrane phospholipids.
format	Article
author	Garba, Lawal Mohamad Yussoff, Mohamad Ariff Abd Halim, Khairul Bariyyah Ishak, Siti Nor Hasmah Mohamad Ali, Mohd Shukuri Oslan, Siti Nurbaya Raja Abd Rahman, Raja Noor Zaliha
author_facet	Garba, Lawal Mohamad Yussoff, Mohamad Ariff Abd Halim, Khairul Bariyyah Ishak, Siti Nor Hasmah Mohamad Ali, Mohd Shukuri Oslan, Siti Nurbaya Raja Abd Rahman, Raja Noor Zaliha
author_sort	Garba, Lawal
title	Homology modeling and docking studies of δ19-fatty acid desaturase from a Cold-tolerant Pseudomonas sp. AMS8
title_short	Homology modeling and docking studies of δ19-fatty acid desaturase from a Cold-tolerant Pseudomonas sp. AMS8
title_full	Homology modeling and docking studies of δ19-fatty acid desaturase from a Cold-tolerant Pseudomonas sp. AMS8
title_fullStr	Homology modeling and docking studies of δ19-fatty acid desaturase from a Cold-tolerant Pseudomonas sp. AMS8
title_full_unstemmed	Homology modeling and docking studies of δ19-fatty acid desaturase from a Cold-tolerant Pseudomonas sp. AMS8
title_sort	homology modeling and docking studies of δ19-fatty acid desaturase from a cold-tolerant pseudomonas sp. ams8
publisher	PeerJ
publishDate	2018
url	http://irep.iium.edu.my/63377/ http://irep.iium.edu.my/63377/ http://irep.iium.edu.my/63377/ http://irep.iium.edu.my/63377/7/63377_Homology%20modeling%20and%20docking%20studies_scopus.pdf http://irep.iium.edu.my/63377/13/63377_Homology%20modeling%20and%20docking%20studies.pdf http://irep.iium.edu.my/63377/14/63377_Homology%20modeling%20and%20docking%20studies_WOS.pdf
first_indexed	2023-09-18T21:29:54Z
last_indexed	2023-09-18T21:29:54Z
_version_	1777412440642813952

Homology modeling and docking studies of δ19-fatty acid desaturase from a Cold-tolerant Pseudomonas sp. AMS8

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