ADPriboDB 2.0: an updated database of ADP-ribosylated proteins

被引:34
作者
Ayyappan, Vinay [1 ]
Wat, Ricky [2 ]
Barber, Calvin [3 ]
Vivelo, Christina A. [2 ]
Gauch, Kathryn [4 ]
Visanpattanasin, Pat [4 ]
Cook, Garth [4 ]
Sazeides, Christos [2 ]
Leung, Anthony K. L. [2 ,5 ,6 ]
机构
[1] Johns Hopkins Univ, GWC Whiting Sch Engn, Dept Biomed Engn, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Biochem & Mol Biol, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Krieger Sch Arts & Sci, Dept Biophys, Baltimore, MD 21218 USA
[4] Johns Hopkins Univ, Krieger Sch Arts & Sci, Dept Biol, Baltimore, MD 21218 USA
[5] Johns Hopkins Univ, Sch Med, Dept Mol Biol & Genet, Baltimore, MD 21205 USA
[6] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21205 USA
关键词
REVEALS; PARPS;
D O I
10.1093/nar/gkaa941
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
ADP-ribosylation is a protein modification responsible for biological processes such as DNA repair, RNA regulation, cell cycle and biomolecular condensate formation. Dysregulation of ADP-ribosylation is implicated in cancer, neurodegeneration and viral infection. We developed ADPriboDB (adpribodb.leunglab.org) to facilitate studies in uncovering insights into the mechanisms and biological significance of ADP-ribosylation. ADPriboDB 2.0 serves as a one-stop repository comprising 48 346 entries and 9097 ADP-ribosylated proteins, of which 6708 were newly identified since the original database release. In this updated version, we provide information regarding the sites of ADP-ribosylation in 32 946 entries. The wealth of information allows us to interrogate existing databases or newly available data. For example, we found that ADP-ribosylated substrates are significantly associated with the recently identified human protein interaction networks associated with SARS-CoV-2, which encodes a conserved protein domain called macrodomain that binds and removes ADP-ribosylation. In addition, we create a new interactive tool to visualize the local context of ADP-ribosylation, such as structural and functional features as well as other post-translational modifications (e.g. phosphorylation, methylation and ubiquitination). This information provides opportunities to explore the biology of ADP-ribosylation and generate new hypotheses for experimental testing.
引用
收藏
页码:D261 / D265
页数:5
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