The Blobulator: A Toolkit for Identification and Visual Exploration of Hydrophobic Modularity in Protein Sequences
While contiguous subsequences of hydrophobic residues are essential to protein structure and function, as in the hydrophobic core and transmembrane regions, there are no current bioinformatics tools for module identification focused on hydrophobicity. To fill this gap, we created the <i>blobulator</i> toolkit for detecting, visualizing, and characterizing hydrophobic modules in protein sequences. This toolkit uses our previously developed algorithm, blobulation, which was critical in both interpreting intraprotein contacts in a series of intrinsically disordered protein simulations (Lohia et al., 2019) and defining the "local context" around disease-associated mutations across the human proteome (Lohia et al., 2022). The <i>blobulator</i> toolkit provides accessible, interactive, and scalable implementations of blobulation. These are available via a webtool, a visual molecular dynamics (VMD) plugin, and a command line interface. We highlight use cases for visualization, interaction analysis, and modular annotation through three example applications: a globular protein, two orthologous membrane proteins, and an intrinsically disordered protein. The <i>blobulator</i> webtool can be found at www.blobulator.branniganlab.org, and the source code with pip installable command line tool, as well as the VMD plugin with installation instructions, can be found on GitHub at www.GitHub.com/BranniganLab/blobulator.
Authors
- Kaitlin Bassi
- Ruchi Lohia
- Ezry Santiago-McRae
- Connor Pitman
- Lindsey M. Riggs
- Ryan Lamb
- Grace Brannigan
- Thomas T. Joseph
- Matthew E. B. Hansen
Institutions
- Rutgers, The State University of New Jersey (US)
- University of Pennsylvania (US)
Publication Details
- Journal
- Journal of Chemical Information and Modeling
- Published
- 2026-01-13
- DOI
- https://doi.org/10.1021/acs.jcim.5c01585
- Primary Topic
- Protein Structure and Dynamics
- Type
- article
- Field-Weighted Citation Impact
- 0.00