Intrinsically disordered regions (IDRs) account for one-third of the human proteome and play essential biological roles. However, predicting the functions of IDRs remains a major challenge due to their lack of stable structures, rapid sequence evolution, and context-dependent behavior. Many predictors of protein function neglect or underperform on IDRs. Recent advances in computational biology and machine learning, including protein language models, alignment-free approaches, and IDR-specific methods, have revealed conserved bulk features and local motifs within IDRs that are linked to function. This review highlights emerging computational methods that map the sequence-function relationship in IDRs, outlines critical challenges in IDR function annotation, and proposes a community-driven framework to accelerate interpretable functional predictions for IDRs.
@article{arxiv.2506.06004,
title = {Into the Unknown: From Structure to Disorder in Protein Function Prediction},
author = {Đesika Kolarić and Chi Fung Willis Chow and Rita Zi Zhu and Agnes Toth-Petroczy and T. Reid Alderson and Iva Pritišanac},
journal= {arXiv preprint arXiv:2506.06004},
year = {2025}
}