Abstract
Motivation: A large fraction of eukaryotic proteins contain unstructured tails or linkers. The presence of flexible regions allows these systems to experience a high level of mobility facilitating their biological function. The complex nature of protein rotation in such flexible modular systems precludes a straightforward application of hydrodynamic methods to calculate their rotational motional properties. We describe the workflow of HYdrodynamic CoUpling of Domains (HYCUD), a program for prediction of effective rotational correlation times in multidomain proteins. The usage of HYCUD is demonstrated by its application to the ribosomal protein L7/L12. Rotational correlation times predicted by HYCUD might be used to detect molecular switch events mediated by disorder-order transitions in interdomain linkers. Availability and implementation: The source code and documentation are available at www.mpibpc.mpg.de/106144/software.
Cite
CITATION STYLE
Rezaei-Ghaleh, N., Klama, F., Munari, F., & Zweckstetter, M. (2015). HYCUD: A computational tool for prediction of effective rotational correlation time in flexible proteins. Bioinformatics, 31(8), 1319–1321. https://doi.org/10.1093/bioinformatics/btu824
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.