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10.1093/bib/bbaa144

http://scihub22266oqcxt.onion/10.1093/bib/bbaa144
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32685972!7454262!32685972
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suck abstract from ncbi


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pmid32685972      Brief+Bioinform 2021 ; 22 (3): ä
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  • FoldRec-C2C: protein fold recognition by combining cluster-to-cluster model and protein similarity network #MMPMID32685972
  • Shao J; Yan K; Liu B
  • Brief Bioinform 2021[May]; 22 (3): ä PMID32685972show ga
  • As a key for studying the protein structures, protein fold recognition is playing an important role in predicting the protein structures associated with COVID-19 and other important structures. However, the existing computational predictors only focus on the protein pairwise similarity or the similarity between two groups of proteins from 2-folds. However, the homology relationship among proteins is in a hierarchical structure. The global protein similarity network will contribute to the performance improvement. In this study, we proposed a predictor called FoldRec-C2C to globally incorporate the interactions among proteins into the prediction. For the FoldRec-C2C predictor, protein fold recognition problem is treated as an information retrieval task in nature language processing. The initial ranking results were generated by a surprised ranking algorithm Learning to Rank, and then three re-ranking algorithms were performed on the ranking lists to adjust the results globally based on the protein similarity network, including seq-to-seq model, seq-to-cluster model and cluster-to-cluster model (C2C). When tested on a widely used and rigorous benchmark dataset LINDAHL dataset, FoldRec-C2C outperforms other 34 state-of-the-art methods in this field. The source code and data of FoldRec-C2C can be downloaded from http://bliulab.net/FoldRec-C2C/download.
  • |*Models, Molecular[MESH]
  • |*Protein Folding[MESH]
  • |Cluster Analysis[MESH]
  • |Computational Biology/methods[MESH]
  • |Datasets as Topic[MESH]


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