| Literature DB >> 34184738 |
Hao Lv1, Fu-Ying Dao1, Hasan Zulfiqar1, Hao Lin1.
Abstract
The rapid spread of SARS-CoV-2 infection around the globe has caused a massive health and socioeconomic crisis. Identification of phosphorylation sites is an important step for understanding the molecular mechanisms of SARS-CoV-2 infection and the changes within the host cells pathways. In this study, we present DeepIPs, a first specific deep-learning architecture to identify phosphorylation sites in host cells infected with SARS-CoV-2. DeepIPs consists of the most popular word embedding method and convolutional neural network-long short-term memory network architecture to make the final prediction. The independent test demonstrates that DeepIPs improves the prediction performance compared with other existing tools for general phosphorylation sites prediction. Based on the proposed model, a web-server called DeepIPs was established and is freely accessible at http://lin-group.cn/server/DeepIPs. The source code of DeepIPs is freely available at the repository https://github.com/linDing-group/DeepIPs.Entities:
Keywords: CNN; LSTM; SARS-CoV-2; phosphorylation; word embedding
Year: 2021 PMID: 34184738 DOI: 10.1093/bib/bbab244
Source DB: PubMed Journal: Brief Bioinform ISSN: 1467-5463 Impact factor: 11.622