Loading…

Exploring the impact of variations in the mucolipin1 protein that result in mucolipidosis type 4 using the technique of molecular docking and dynamics simulation

Mucolipidosis type IV (MLIV) is classified as an exceptionally autosomal recessive condition due to a change in MCOLN1 that encodes the mucolipin-1 protein. ML-1 is a membrane protein comprising 6 Trans regions, which are situated at the LELs, a serine lipase area, and a nuclear localization sign. T...

Full description

Saved in:
Bibliographic Details
Published in:Journal of biomolecular structure & dynamics 2024-12, p.1-12
Main Authors: K, Priyanka, N, Madhana Priya, Ramasamy, Magesh
Format: Article
Language:English
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites cdi_FETCH-LOGICAL-c187t-221d392c2f3681eb289c0491f3be3c0fd6ba16a46a73c75ebc7cb5d58f76e0cc3
container_end_page 12
container_issue
container_start_page 1
container_title Journal of biomolecular structure & dynamics
container_volume
creator K, Priyanka
N, Madhana Priya
Ramasamy, Magesh
description Mucolipidosis type IV (MLIV) is classified as an exceptionally autosomal recessive condition due to a change in MCOLN1 that encodes the mucolipin-1 protein. ML-1 is a membrane protein comprising 6 Trans regions, which are situated at the LELs, a serine lipase area, and a nuclear localization sign. The characteristic features of the ML4 patients are mental retardation and skeletal deformities due to an increase in lipid molecules in the brain, other tissues, and organs. The fundamental goal of the work is to identify the most significant amino acid variants via a computational pipeline. The twenty-three amino acid variants that are responsible for the condition were retrieved from the public domain: L106P and L447P amino acid variants, with the following categories: extremely conserved, highly pathogenic, most interfering with protein function, more structurally unstable, and having promising Phenotyping characteristics was scrutinized from the series of bioinformatics tools that denote its significant nature. A docking and dynamics study was initiated to identify the interaction profiling and interatomic simulation between the Native, L106P, and L447P and the ligand ML-SA1 (it was known to ease the fatty acid buildup in lysosomes of cellular models of Mucolipidosis type IV) and had a score of -6.19, -5.12, and -5.21 kcal/mol, followed by a duplicate 100-ns run trajectory results, which assisted in detecting the stable nature of all the complex structures. Hence, this work helps to recognize the significant role of the scrutinized amino acid variants and, on the other hand, the stable nature of the ligand using standard computational tools.
doi_str_mv 10.1080/07391102.2024.2439045
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3146710043</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3146710043</sourcerecordid><originalsourceid>FETCH-LOGICAL-c187t-221d392c2f3681eb289c0491f3be3c0fd6ba16a46a73c75ebc7cb5d58f76e0cc3</originalsourceid><addsrcrecordid>eNo9kU1PxCAQhonRuOvHT9Bw9NKVAVraozF-JSZe9NzQKXXRtlSgxv05_lNb3fVEwjzzzsBDyBmwFbCcXTIlCgDGV5xxueJSFEyme2QJqcgTxlO5T5Yzk8zQghyF8MYYB1BwSBaiyBSoQizJ983X0Dpv-1ca14babtAYqWvop_ZWR-v6QG3_W-tGdK0dbA908C6a32sdqTdhbONM7YjaBRto3AyGSjqGXXg0uO7tx2jm_M61BsdWe1o7fJ8R3de03vS6sxhosN1UnOefkINGt8Gcbs9j8nJ783x9nzw-3T1cXz0mCLmKCedQi4Ijb0SWg6l4XiCTBTSiMgJZU2eVhkzLTCuBKjUVKqzSOs0blRmGKI7JxV_u9LhpxxDLzgY0bat748ZQCpDTpzEmxYSmfyh6F4I3TTl422m_KYGVs51yZ6ec7ZRbO1Pf-XbEWHWm_u_a6RA_hfeOng</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3146710043</pqid></control><display><type>article</type><title>Exploring the impact of variations in the mucolipin1 protein that result in mucolipidosis type 4 using the technique of molecular docking and dynamics simulation</title><source>Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Science and Technology Collection (Reading list)</source><creator>K, Priyanka ; N, Madhana Priya ; Ramasamy, Magesh</creator><creatorcontrib>K, Priyanka ; N, Madhana Priya ; Ramasamy, Magesh</creatorcontrib><description>Mucolipidosis type IV (MLIV) is classified as an exceptionally autosomal recessive condition due to a change in MCOLN1 that encodes the mucolipin-1 protein. ML-1 is a membrane protein comprising 6 Trans regions, which are situated at the LELs, a serine lipase area, and a nuclear localization sign. The characteristic features of the ML4 patients are mental retardation and skeletal deformities due to an increase in lipid molecules in the brain, other tissues, and organs. The fundamental goal of the work is to identify the most significant amino acid variants via a computational pipeline. The twenty-three amino acid variants that are responsible for the condition were retrieved from the public domain: L106P and L447P amino acid variants, with the following categories: extremely conserved, highly pathogenic, most interfering with protein function, more structurally unstable, and having promising Phenotyping characteristics was scrutinized from the series of bioinformatics tools that denote its significant nature. A docking and dynamics study was initiated to identify the interaction profiling and interatomic simulation between the Native, L106P, and L447P and the ligand ML-SA1 (it was known to ease the fatty acid buildup in lysosomes of cellular models of Mucolipidosis type IV) and had a score of -6.19, -5.12, and -5.21 kcal/mol, followed by a duplicate 100-ns run trajectory results, which assisted in detecting the stable nature of all the complex structures. Hence, this work helps to recognize the significant role of the scrutinized amino acid variants and, on the other hand, the stable nature of the ligand using standard computational tools.</description><identifier>ISSN: 0739-1102</identifier><identifier>ISSN: 1538-0254</identifier><identifier>EISSN: 1538-0254</identifier><identifier>DOI: 10.1080/07391102.2024.2439045</identifier><identifier>PMID: 39671793</identifier><language>eng</language><publisher>England</publisher><ispartof>Journal of biomolecular structure &amp; dynamics, 2024-12, p.1-12</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c187t-221d392c2f3681eb289c0491f3be3c0fd6ba16a46a73c75ebc7cb5d58f76e0cc3</cites><orcidid>0000-0002-9508-8097</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39671793$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>K, Priyanka</creatorcontrib><creatorcontrib>N, Madhana Priya</creatorcontrib><creatorcontrib>Ramasamy, Magesh</creatorcontrib><title>Exploring the impact of variations in the mucolipin1 protein that result in mucolipidosis type 4 using the technique of molecular docking and dynamics simulation</title><title>Journal of biomolecular structure &amp; dynamics</title><addtitle>J Biomol Struct Dyn</addtitle><description>Mucolipidosis type IV (MLIV) is classified as an exceptionally autosomal recessive condition due to a change in MCOLN1 that encodes the mucolipin-1 protein. ML-1 is a membrane protein comprising 6 Trans regions, which are situated at the LELs, a serine lipase area, and a nuclear localization sign. The characteristic features of the ML4 patients are mental retardation and skeletal deformities due to an increase in lipid molecules in the brain, other tissues, and organs. The fundamental goal of the work is to identify the most significant amino acid variants via a computational pipeline. The twenty-three amino acid variants that are responsible for the condition were retrieved from the public domain: L106P and L447P amino acid variants, with the following categories: extremely conserved, highly pathogenic, most interfering with protein function, more structurally unstable, and having promising Phenotyping characteristics was scrutinized from the series of bioinformatics tools that denote its significant nature. A docking and dynamics study was initiated to identify the interaction profiling and interatomic simulation between the Native, L106P, and L447P and the ligand ML-SA1 (it was known to ease the fatty acid buildup in lysosomes of cellular models of Mucolipidosis type IV) and had a score of -6.19, -5.12, and -5.21 kcal/mol, followed by a duplicate 100-ns run trajectory results, which assisted in detecting the stable nature of all the complex structures. Hence, this work helps to recognize the significant role of the scrutinized amino acid variants and, on the other hand, the stable nature of the ligand using standard computational tools.</description><issn>0739-1102</issn><issn>1538-0254</issn><issn>1538-0254</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNo9kU1PxCAQhonRuOvHT9Bw9NKVAVraozF-JSZe9NzQKXXRtlSgxv05_lNb3fVEwjzzzsBDyBmwFbCcXTIlCgDGV5xxueJSFEyme2QJqcgTxlO5T5Yzk8zQghyF8MYYB1BwSBaiyBSoQizJ983X0Dpv-1ca14babtAYqWvop_ZWR-v6QG3_W-tGdK0dbA908C6a32sdqTdhbONM7YjaBRto3AyGSjqGXXg0uO7tx2jm_M61BsdWe1o7fJ8R3de03vS6sxhosN1UnOefkINGt8Gcbs9j8nJ783x9nzw-3T1cXz0mCLmKCedQi4Ijb0SWg6l4XiCTBTSiMgJZU2eVhkzLTCuBKjUVKqzSOs0blRmGKI7JxV_u9LhpxxDLzgY0bat748ZQCpDTpzEmxYSmfyh6F4I3TTl422m_KYGVs51yZ6ec7ZRbO1Pf-XbEWHWm_u_a6RA_hfeOng</recordid><startdate>20241213</startdate><enddate>20241213</enddate><creator>K, Priyanka</creator><creator>N, Madhana Priya</creator><creator>Ramasamy, Magesh</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9508-8097</orcidid></search><sort><creationdate>20241213</creationdate><title>Exploring the impact of variations in the mucolipin1 protein that result in mucolipidosis type 4 using the technique of molecular docking and dynamics simulation</title><author>K, Priyanka ; N, Madhana Priya ; Ramasamy, Magesh</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c187t-221d392c2f3681eb289c0491f3be3c0fd6ba16a46a73c75ebc7cb5d58f76e0cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>K, Priyanka</creatorcontrib><creatorcontrib>N, Madhana Priya</creatorcontrib><creatorcontrib>Ramasamy, Magesh</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of biomolecular structure &amp; dynamics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>K, Priyanka</au><au>N, Madhana Priya</au><au>Ramasamy, Magesh</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Exploring the impact of variations in the mucolipin1 protein that result in mucolipidosis type 4 using the technique of molecular docking and dynamics simulation</atitle><jtitle>Journal of biomolecular structure &amp; dynamics</jtitle><addtitle>J Biomol Struct Dyn</addtitle><date>2024-12-13</date><risdate>2024</risdate><spage>1</spage><epage>12</epage><pages>1-12</pages><issn>0739-1102</issn><issn>1538-0254</issn><eissn>1538-0254</eissn><abstract>Mucolipidosis type IV (MLIV) is classified as an exceptionally autosomal recessive condition due to a change in MCOLN1 that encodes the mucolipin-1 protein. ML-1 is a membrane protein comprising 6 Trans regions, which are situated at the LELs, a serine lipase area, and a nuclear localization sign. The characteristic features of the ML4 patients are mental retardation and skeletal deformities due to an increase in lipid molecules in the brain, other tissues, and organs. The fundamental goal of the work is to identify the most significant amino acid variants via a computational pipeline. The twenty-three amino acid variants that are responsible for the condition were retrieved from the public domain: L106P and L447P amino acid variants, with the following categories: extremely conserved, highly pathogenic, most interfering with protein function, more structurally unstable, and having promising Phenotyping characteristics was scrutinized from the series of bioinformatics tools that denote its significant nature. A docking and dynamics study was initiated to identify the interaction profiling and interatomic simulation between the Native, L106P, and L447P and the ligand ML-SA1 (it was known to ease the fatty acid buildup in lysosomes of cellular models of Mucolipidosis type IV) and had a score of -6.19, -5.12, and -5.21 kcal/mol, followed by a duplicate 100-ns run trajectory results, which assisted in detecting the stable nature of all the complex structures. Hence, this work helps to recognize the significant role of the scrutinized amino acid variants and, on the other hand, the stable nature of the ligand using standard computational tools.</abstract><cop>England</cop><pmid>39671793</pmid><doi>10.1080/07391102.2024.2439045</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-9508-8097</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0739-1102
ispartof Journal of biomolecular structure & dynamics, 2024-12, p.1-12
issn 0739-1102
1538-0254
1538-0254
language eng
recordid cdi_proquest_miscellaneous_3146710043
source Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Science and Technology Collection (Reading list)
title Exploring the impact of variations in the mucolipin1 protein that result in mucolipidosis type 4 using the technique of molecular docking and dynamics simulation
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T06%3A35%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Exploring%20the%20impact%20of%20variations%20in%20the%20mucolipin1%20protein%20that%20result%20in%20mucolipidosis%20type%204%20using%20the%20technique%20of%20molecular%20docking%20and%20dynamics%20simulation&rft.jtitle=Journal%20of%20biomolecular%20structure%20&%20dynamics&rft.au=K,%20Priyanka&rft.date=2024-12-13&rft.spage=1&rft.epage=12&rft.pages=1-12&rft.issn=0739-1102&rft.eissn=1538-0254&rft_id=info:doi/10.1080/07391102.2024.2439045&rft_dat=%3Cproquest_cross%3E3146710043%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c187t-221d392c2f3681eb289c0491f3be3c0fd6ba16a46a73c75ebc7cb5d58f76e0cc3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3146710043&rft_id=info:pmid/39671793&rfr_iscdi=true