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• W2732950593 startingPage "1864" @default.
• W2732950593 abstract "There has been an increased interest in computational methods for amyloid and (or) aggregate prediction, due to the prevalence of these aggregates in numerous diseases and their recently discovered functional importance. To evaluate these methods, several datasets have been compiled. Typically, aggregation-prone regions of proteins, which form aggregates or amyloids in vivo, are more than 15 residues long and intrinsically disordered. However, the number of such experimentally established amyloid forming and non-forming sequences are limited, not exceeding one hundred entries in existing databases. In this work, we parsed all available NMR-resolved protein structures from the PDB and assembled a new, sevenfold larger, dataset of unfolded sequences, soluble at high concentrations. We proposed to use these sequences as a negative set for evaluating methods for predicting aggregation in vivo. We also present the results of benchmarking cutting edge tools for the prediction of aggregation versus solubility propensity." @default.
• W2732950593 created "2017-07-14" @default.
• W2732950593 creator A5019520821 @default.
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• W2732950593 date "2017-07-15" @default.
• W2732950593 modified "2023-10-11" @default.
• W2732950593 title "Usage of a dataset of NMR resolved protein structures to test aggregation versus solubility prediction algorithms" @default.
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• W2732950593 doi "https://doi.org/10.1002/pro.3225" @default.
• W2732950593 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5563137" @default.
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