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HawkDock: a web server to predict and analyze the protein–protein complex based on computational docking and MM/GBSA

Open access
Weng, Gaoqi, Wang, Ercheng, Wang, Zhe, Liu, Hui, Zhu, Feng, Li, Dan, Hou, Tingjun·2019·Nucleic Acids Research

Abstract

Protein–protein interactions (PPIs) play an important role in the different functions of cells, but accurate prediction of the three-dimensional structures for PPIs is still a notoriously difficult task. In this study, HawkDock, a free and open accessed web server, was developed to predict and analyze the structures of PPIs. In the HawkDock server, the ATTRACT docking algorithm, the HawkRank scoring function developed in our group and the MM/GBSA free energy decomposition analysis were seamlessly integrated into a multi-functional platform. The structures of PPIs were predicted by combining the ATTRACT docking and the HawkRank re-scoring, and the key residues for PPIs were highlighted by the MM/GBSA free energy decomposition. The molecular visualization was supported by 3Dmol.js. For the structural modeling of PPIs, HawkDock could achieve a better performance than ZDOCK 3.0.2 in the benchmark testing. For the prediction of key residues, the important residues that play an essential role in PPIs could be identified in the top 10 residues for ∼81.4% predicted models and ∼95.4% crystal structures in the benchmark dataset. To sum up, the HawkDock server is a powerful tool to predict the binding structures and identify the key residues of PPIs. The HawkDock server is accessible free of charge at http://cadd.zju.edu.cn/hawkdock/.

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Metadata

Authors
Weng, G., Wang, E., Wang, Z., Liu, H., Zhu, F., Li, D., & Hou, T.
Venue
Nucleic Acids Research
Published
2019-05-20
Volume
47
Issue
W1
Pages
W322-W330
ISSN
  • 0305-1048 (ISSN-L)
  • 1362-4962
OpenAlex
W2945172910
Cited by
637
References
4
FWCI
16.76
Type
journal article
Language
en
Open access
gold

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