CARDIO-PRED:一个预测心血管疾病相关蛋白的计算机工具。

Systems and Synthetic Biology Pub Date : 2015-06-01 Epub Date: 2015-03-14 DOI:10.1007/s11693-015-9164-z
Prerna Jain, Nitin Thukral, Lokesh Kumar Gahlot, Yasha Hasija
{"title":"CARDIO-PRED:一个预测心血管疾病相关蛋白的计算机工具。","authors":"Prerna Jain,&nbsp;Nitin Thukral,&nbsp;Lokesh Kumar Gahlot,&nbsp;Yasha Hasija","doi":"10.1007/s11693-015-9164-z","DOIUrl":null,"url":null,"abstract":"<p><p>Interactions between proteins largely govern cellular processes and this has led to numerous efforts culminating in enormous information related to the proteins, their interactions and the function which is determined by their interactions. The main concern of the present study is to present interface analysis of cardiovascular-disorder (CVD) related proteins to shed lights on details of interactions and to emphasize the importance of using structures in network studies. This study combines the network-centred approach with three dimensional studies to comprehend the fundamentals of biology. Interface properties were used as descriptors to classify the CVD associated proteins and non-CVD associated proteins. Machine learning algorithm was used to generate a classifier based on the training set which was then used to predict potential CVD related proteins from a set of polymorphic proteins which are not known to be involved in any disease. Among several classifying algorithms applied to generate models, best performance was achieved using Random Forest with an accuracy of 69.5 %. The tool named CARDIO-PRED, based on the prediction model is present at http://www.genomeinformatics.dce.edu/CARDIO-PRED/. The predicted CVD related proteins may not be the causing factor of particular disease but can be involved in pathways and reactions yet unknown to us thus permitting a more rational analysis of disease mechanism. Study of their interactions with other proteins can significantly improve our understanding of the molecular mechanism of diseases. </p>","PeriodicalId":22161,"journal":{"name":"Systems and Synthetic Biology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2015-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s11693-015-9164-z","citationCount":"3","resultStr":"{\"title\":\"CARDIO-PRED: an in silico tool for predicting cardiovascular-disorder associated proteins.\",\"authors\":\"Prerna Jain,&nbsp;Nitin Thukral,&nbsp;Lokesh Kumar Gahlot,&nbsp;Yasha Hasija\",\"doi\":\"10.1007/s11693-015-9164-z\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Interactions between proteins largely govern cellular processes and this has led to numerous efforts culminating in enormous information related to the proteins, their interactions and the function which is determined by their interactions. The main concern of the present study is to present interface analysis of cardiovascular-disorder (CVD) related proteins to shed lights on details of interactions and to emphasize the importance of using structures in network studies. This study combines the network-centred approach with three dimensional studies to comprehend the fundamentals of biology. Interface properties were used as descriptors to classify the CVD associated proteins and non-CVD associated proteins. Machine learning algorithm was used to generate a classifier based on the training set which was then used to predict potential CVD related proteins from a set of polymorphic proteins which are not known to be involved in any disease. Among several classifying algorithms applied to generate models, best performance was achieved using Random Forest with an accuracy of 69.5 %. The tool named CARDIO-PRED, based on the prediction model is present at http://www.genomeinformatics.dce.edu/CARDIO-PRED/. The predicted CVD related proteins may not be the causing factor of particular disease but can be involved in pathways and reactions yet unknown to us thus permitting a more rational analysis of disease mechanism. Study of their interactions with other proteins can significantly improve our understanding of the molecular mechanism of diseases. </p>\",\"PeriodicalId\":22161,\"journal\":{\"name\":\"Systems and Synthetic Biology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2015-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1007/s11693-015-9164-z\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Systems and Synthetic Biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1007/s11693-015-9164-z\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2015/3/14 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Systems and Synthetic Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s11693-015-9164-z","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2015/3/14 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3

摘要

蛋白质之间的相互作用在很大程度上控制着细胞过程,这导致了许多努力,最终获得了与蛋白质、它们的相互作用和由它们的相互作用决定的功能相关的大量信息。本研究主要关注的是对心血管疾病(CVD)相关蛋白进行界面分析,以揭示相互作用的细节,并强调在网络研究中使用结构的重要性。本研究结合以网络为中心的方法与三维研究来理解生物学的基本原理。用界面性质作为描述符对CVD相关蛋白和非CVD相关蛋白进行分类。使用机器学习算法生成基于训练集的分类器,然后使用该分类器从一组未知与任何疾病相关的多态性蛋白中预测潜在的CVD相关蛋白。在几种用于生成模型的分类算法中,随机森林算法的准确率为69.5%,达到了最佳效果。基于预测模型的CARDIO-PRED工具出现在http://www.genomeinformatics.dce.edu/CARDIO-PRED/。预测的CVD相关蛋白可能不是特定疾病的致病因素,但可能涉及我们未知的途径和反应,从而允许对疾病机制进行更合理的分析。研究它们与其他蛋白质的相互作用可以显著提高我们对疾病分子机制的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

CARDIO-PRED: an in silico tool for predicting cardiovascular-disorder associated proteins.

CARDIO-PRED: an in silico tool for predicting cardiovascular-disorder associated proteins.

CARDIO-PRED: an in silico tool for predicting cardiovascular-disorder associated proteins.

CARDIO-PRED: an in silico tool for predicting cardiovascular-disorder associated proteins.

Interactions between proteins largely govern cellular processes and this has led to numerous efforts culminating in enormous information related to the proteins, their interactions and the function which is determined by their interactions. The main concern of the present study is to present interface analysis of cardiovascular-disorder (CVD) related proteins to shed lights on details of interactions and to emphasize the importance of using structures in network studies. This study combines the network-centred approach with three dimensional studies to comprehend the fundamentals of biology. Interface properties were used as descriptors to classify the CVD associated proteins and non-CVD associated proteins. Machine learning algorithm was used to generate a classifier based on the training set which was then used to predict potential CVD related proteins from a set of polymorphic proteins which are not known to be involved in any disease. Among several classifying algorithms applied to generate models, best performance was achieved using Random Forest with an accuracy of 69.5 %. The tool named CARDIO-PRED, based on the prediction model is present at http://www.genomeinformatics.dce.edu/CARDIO-PRED/. The predicted CVD related proteins may not be the causing factor of particular disease but can be involved in pathways and reactions yet unknown to us thus permitting a more rational analysis of disease mechanism. Study of their interactions with other proteins can significantly improve our understanding of the molecular mechanism of diseases.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信