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AWESOME: a database of SNPs that affect protein post-translational modifications

Protein post-translational modifications (PTMs), including phosphorylation, ubiquitination, methylation, acetylation, glycosylation et al, are very important biological processes. PTM changes in some critical genes, which may be induced by base-pair substitution, are shown to affect the risk of dise...

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Autores principales: Yang, Yang, Peng, Xiating, Ying, Pingting, Tian, Jianbo, Li, Jiaoyuan, Ke, Juntao, Zhu, Ying, Gong, Yajie, Zou, Danyi, Yang, Nan, Wang, Xiaoyang, Mei, Shufang, Zhong, Rong, Gong, Jing, Chang, Jiang, Miao, Xiaoping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6324025/
https://www.ncbi.nlm.nih.gov/pubmed/30215764
http://dx.doi.org/10.1093/nar/gky821
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author Yang, Yang
Peng, Xiating
Ying, Pingting
Tian, Jianbo
Li, Jiaoyuan
Ke, Juntao
Zhu, Ying
Gong, Yajie
Zou, Danyi
Yang, Nan
Wang, Xiaoyang
Mei, Shufang
Zhong, Rong
Gong, Jing
Chang, Jiang
Miao, Xiaoping
author_facet Yang, Yang
Peng, Xiating
Ying, Pingting
Tian, Jianbo
Li, Jiaoyuan
Ke, Juntao
Zhu, Ying
Gong, Yajie
Zou, Danyi
Yang, Nan
Wang, Xiaoyang
Mei, Shufang
Zhong, Rong
Gong, Jing
Chang, Jiang
Miao, Xiaoping
author_sort Yang, Yang
collection PubMed
description Protein post-translational modifications (PTMs), including phosphorylation, ubiquitination, methylation, acetylation, glycosylation et al, are very important biological processes. PTM changes in some critical genes, which may be induced by base-pair substitution, are shown to affect the risk of diseases. Recently, large-scale exome-wide association studies found that missense single nucleotide polymorphisms (SNPs) play an important role in the susceptibility for complex diseases or traits. One of the functional mechanisms of missense SNPs is that they may affect PTMs and leads to a protein dysfunction and its downstream signaling pathway disorder. Here, we constructed a database named AWESOME (A Website Exhibits SNP On Modification Event, http://www.awesome-hust.com), which is an interactive web-based analysis tool that systematically evaluates the role of SNPs on nearly all kinds of PTMs based on 20 available tools. We also provided a well-designed scoring system to compare the performance of different PTM prediction tools and help users to get a better interpretation of results. Users can search SNPs, genes or position of interest, filter with specific modifications or prediction methods, to get a comprehensive PTM change induced by SNPs. In summary, our database provides a convenient way to detect PTM-related SNPs, which may potentially be pathogenic factors or therapeutic targets.
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spelling pubmed-63240252019-01-10 AWESOME: a database of SNPs that affect protein post-translational modifications Yang, Yang Peng, Xiating Ying, Pingting Tian, Jianbo Li, Jiaoyuan Ke, Juntao Zhu, Ying Gong, Yajie Zou, Danyi Yang, Nan Wang, Xiaoyang Mei, Shufang Zhong, Rong Gong, Jing Chang, Jiang Miao, Xiaoping Nucleic Acids Res Database Issue Protein post-translational modifications (PTMs), including phosphorylation, ubiquitination, methylation, acetylation, glycosylation et al, are very important biological processes. PTM changes in some critical genes, which may be induced by base-pair substitution, are shown to affect the risk of diseases. Recently, large-scale exome-wide association studies found that missense single nucleotide polymorphisms (SNPs) play an important role in the susceptibility for complex diseases or traits. One of the functional mechanisms of missense SNPs is that they may affect PTMs and leads to a protein dysfunction and its downstream signaling pathway disorder. Here, we constructed a database named AWESOME (A Website Exhibits SNP On Modification Event, http://www.awesome-hust.com), which is an interactive web-based analysis tool that systematically evaluates the role of SNPs on nearly all kinds of PTMs based on 20 available tools. We also provided a well-designed scoring system to compare the performance of different PTM prediction tools and help users to get a better interpretation of results. Users can search SNPs, genes or position of interest, filter with specific modifications or prediction methods, to get a comprehensive PTM change induced by SNPs. In summary, our database provides a convenient way to detect PTM-related SNPs, which may potentially be pathogenic factors or therapeutic targets. Oxford University Press 2019-01-08 2018-09-12 /pmc/articles/PMC6324025/ /pubmed/30215764 http://dx.doi.org/10.1093/nar/gky821 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Database Issue
Yang, Yang
Peng, Xiating
Ying, Pingting
Tian, Jianbo
Li, Jiaoyuan
Ke, Juntao
Zhu, Ying
Gong, Yajie
Zou, Danyi
Yang, Nan
Wang, Xiaoyang
Mei, Shufang
Zhong, Rong
Gong, Jing
Chang, Jiang
Miao, Xiaoping
AWESOME: a database of SNPs that affect protein post-translational modifications
title AWESOME: a database of SNPs that affect protein post-translational modifications
title_full AWESOME: a database of SNPs that affect protein post-translational modifications
title_fullStr AWESOME: a database of SNPs that affect protein post-translational modifications
title_full_unstemmed AWESOME: a database of SNPs that affect protein post-translational modifications
title_short AWESOME: a database of SNPs that affect protein post-translational modifications
title_sort awesome: a database of snps that affect protein post-translational modifications
topic Database Issue
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6324025/
https://www.ncbi.nlm.nih.gov/pubmed/30215764
http://dx.doi.org/10.1093/nar/gky821
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