Background: Studying the patterns of protein-protein interactions (PPIs) is fundamental for understanding the structure and function of protein complexes. The exploration of the vast space of possible mutual configurations of interacting proteins and their contact zones is very time consuming and requires the proteomic expert knowledge.
Results: In this paper, we propose a novel tool containing a set of visual abstraction techniques for the guided exploration of PPI configuration space. It helps proteomic experts to select the most relevant configurations and explore their contact zones at different levels of detail. The system integrates a set of methods that follow and support the workflow of proteomics experts. The first visual abstraction method, the Matrix view, is based on customized interactive heat maps and provides the users with an overview of all possible residue-residue contacts in all PPI configurations and their interactive filtering. In this step, the user can traverse all input PPI configurations and obtain an overview of their interacting amino acids. Then, the models containing a particular pair of interacting amino acids can be selectively picked and traversed. Detailed information on the individual amino acids in the contact zones and their properties is presented in the Contact-Zone list-view. The list-view provides a comparative tool to rank the best models based on the similarity of their contacts to the template-structure contacts. All these techniques are interactively linked with other proposed methods, the Exploded view and the Open-Book view, which represent individual configurations in three-dimensional space. These representations solve the high overlap problem associated with many configurations. Using these views, the structural alignment of the best models can also be visually confirmed.
Conclusions: We developed a system for the exploration of large sets of protein-protein complexes in a fast and intuitive way. The usefulness of our system has been tested and verified on several docking structures covering the three major types of PPIs, including coiled-coil, pocket-string, and surface-surface interactions. Our case studies prove that our tool helps to analyse and filter protein-protein complexes in a fraction of the time compared to using previously available techniques.
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http://dx.doi.org/10.1186/s12859-018-2113-6 | DOI Listing |
Materials (Basel)
January 2025
Department of Machine Design and Manufacturing Engineering, Kielce University of Technology, al. Tysiaclecia Panstwa Polskiego 7, 25-314 Kielce, Poland.
The minimum cutting thickness is a key value in machining processes, as below this value the material will only undergo elastic and plastic deformation without chip removal. Existing measurement methods require time-consuming preparation and complicated procedures. This work focuses on the development of a new, simplified method for determining the minimum cutting thickness (h) using a contact profilometer that can be used in industry.
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January 2025
Museum of Natural History, University of Wroclaw, Wroclaw, Poland.
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Plants (Basel)
December 2024
Institute of Botany and Botanical Garden, Faculty of Biology, University of Belgrade, Takovska 43, 11000 Belgrade, Serbia.
Materials (Basel)
December 2024
Department of Geomechanics, Civil Engineering and Geotechnics, Faculty of Civil Engineering and Resource Management, AGH University of Krakow, al. Adama Mickiewicza 30, 30-059 Cracow, Poland.
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December 2024
Department of Mechanics of Materials and Constructions, Faculty of Engineering, Vrije Universiteit Brussel, B-1050 Brussels, Belgium.
Cementitious materials are susceptible to damage not only from mechanical loading, but also from environmental (physical, chemical, and biological) factors. For Textile-Reinforced Cementitious (TRC) composites, durability poses a significant challenge, and a reliable method to assess long-term performance is still lacking. Among various durability attacks, freeze-thaw can induce internal cracking within the cementitious matrix, and weaken the textile-matrix bond.
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