Abstract

One of the unique characteristics of intrinsically disordered proteins (IPDs) is the existence of functional segments in intrinsically disordered regions (IDRs). A typical function of these segments is binding to partner molecules, such as proteins and DNAs. These segments play important roles in signaling pathways and transcriptional regulation. We conducted bioinformatics analysis to search these functional segments based on IDR predictions and database annotations. We found more than a thousand potential functional IDR segments in disease-related proteins. Large fractions of proteins related to cancers, congenital disorders, digestive system diseases, and reproductive system diseases have these functional IDRs. Some proteins in nervous system diseases have long functional segments in IDRs. The detailed analysis of some of these regions showed that the functional segments are located on experimentally verified IDRs. The proteins with functional IDR segments generally tend to come and go between the cytoplasm and the nucleus. Proteins involved in multiple diseases tend to have more protein-protein interactors, suggesting that hub proteins in the protein-protein interaction networks can have multiple impacts on human diseases.

Highlights

  • Disordered proteins (IDPs) are proteins that do not adopt unique three-dimensional structures under physiological conditions [1,2,3]

  • Out of 18,450 feature annotations found in the disease related proteins, 8.3%, 3.4%, and 24.4% were found in the predicted intrinsically disordered regions (IDRs) for “region of interest”, “mutagenesis site”, and “short sequence motif”, respectively

  • We conducted bioinformatics analyses to survey our knowledge on functional segments in IDRs from the perspective of disease-related proteins

Read more

Summary

Introduction

Disordered proteins (IDPs) are proteins that do not adopt unique three-dimensional structures under physiological conditions [1,2,3]. One of the unique features of IDPs is their ability to bind to binding partners The regions performing such binding are generally short segments ranging from several residues to tens of residues and can adopt local two-dimensional structures in association with this binding. This has been referred to as the coupled folding and binding mechanism. These interactions are transient, specific, and low-affinity. Intrinsically disordered regions (IDRs) play crucial roles in many biological processes, such as signal transduction and transcriptional regulation [1,2,3,7]

Methods
Results
Discussion
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call