NITFID, School of Statistics and Data Science, LPMC and KLMDASR, Nankai University, Tianjin, China.
School of Mathematical Sciences and LPMC, Nankai University, Tianjin, China.
Methods Mol Biol. 2025;2867:201-218. doi: 10.1007/978-1-0716-4196-5_12.
Intrinsically disordered proteins (IDPs) that include one or more intrinsically disordered regions (IDRs) are abundant across all domains of life and viruses and play numerous functional roles in various cellular processes. Due to a relatively low throughput and high cost of experimental techniques for identifying IDRs, there is a growing need for fast and accurate computational algorithms that accurately predict IDRs/IDPs from protein sequences. We describe one of the leading disorder predictors, flDPnn. Results from a recent community-organized Critical Assessment of Intrinsic Disorder (CAID) experiment show that flDPnn provides fast and state-of-the-art predictions of disorder, which are supplemented with the predictions of several major disorder functions. This chapter provides a practical guide to flDPnn, which includes a brief explanation of its predictive model, descriptions of its web server and standalone versions, and a case study that showcases how to read and understand flDPnn's predictions.
无规则蛋白质(IDPs)在所有生命领域和病毒中都很丰富,包含一个或多个无规则区域(IDR),并在各种细胞过程中发挥着多种功能作用。由于用于识别 IDR 的实验技术的通量相对较低且成本较高,因此需要快速且准确的计算算法,以便从蛋白质序列中准确预测 IDR/IDPs。我们描述了领先的无序预测器之一,flDPnn。最近由社区组织的内在无序性(CAID)实验的结果表明,flDPnn 可以快速且最先进地预测无序性,并且还补充了几个主要无序功能的预测。本章提供了 flDPnn 的实用指南,其中包括对其预测模型的简要说明,对其网络服务器和独立版本的描述,以及一个案例研究,展示了如何阅读和理解 flDPnn 的预测。