| Literature DB >> 34290238 |
Gang Hu1, Akila Katuwawala2, Kui Wang3, Zhonghua Wu3, Sina Ghadermarzi2, Jianzhao Gao3, Lukasz Kurgan4.
Abstract
Identification of intrinsic disorder in proteins relies in large part on computational predictors, which demands that their accuracy should be high. Since intrinsic disorder carries out a broad range of cellular functions, it is desirable to couple the disorder and disorder function predictions. We report a computational tool, flDPnn, that provides accurate, fast and comprehensive disorder and disorder function predictions from protein sequences. The recent Critical Assessment of protein Intrinsic Disorder prediction (CAID) experiment and results on other test datasets demonstrate that flDPnn offers accurate predictions of disorder, fully disordered proteins and four common disorder functions. These predictions are substantially better than the results of the existing disorder predictors and methods that predict functions of disorder. Ablation tests reveal that the high predictive performance stems from innovative ways used in flDPnn to derive sequence profiles and encode inputs. flDPnn's webserver is available at http://biomine.cs.vcu.edu/servers/flDPnn/.Entities:
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Year: 2021 PMID: 34290238 DOI: 10.1038/s41467-021-24773-7
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919