Efficient integration and visualization of heterogeneous biomedical information in a
single view is a key challenge. In this study, we present Arena3D
web
, the
first, fully interactive and dependency-free, web application which allows the
visualization of multilayered graphs in 3D space. With Arena3D
web
, users can
integrate multiple networks in a single view along with their intra- and inter-layer
connections. For clearer and more informative views, users can choose between a plethora
of layout algorithms and apply them on a set of selected layers either individually or in
combination. Users can align networks and highlight node topological features, whereas
each layer as well as the whole scene can be translated, rotated and scaled in 3D space.
User-selected edge colors can be used to highlight important paths, while node
positioning, coloring and resizing can be adjusted on-the-fly. In its current version,
Arena3D
web
supports weighted and unweighted undirected graphs and is written
in R, Shiny and JavaScript. We demonstrate the functionality of Arena3D
web
using two different use-case scenarios; one regarding drug repurposing for SARS-CoV-2 and
one related to GPCR signaling pathways implicated in melanoma. Arena3D
web
is
available at
http://bib.fleming.gr:3838/Arena3D
or
http://bib.fleming.gr/Arena3D
.
A significant amount of experimental evidence suggests that G-protein coupled receptors (GPCRs) do not act exclusively as monomers but also form biologically relevant dimers and oligomers. However, the structural determinants, stoichiometry and functional importance of GPCR oligomerization remain topics of intense speculation. In this study we attempted to evaluate the nature and dynamics of GPCR oligomeric interactions. A representative set of GPCR homodimers were studied through Coarse-Grained Molecular Dynamics simulations, combined with interface analysis and concepts from network theory for the construction and analysis of dynamic structural networks. Our results highlight important structural determinants that seem to govern receptor dimer interactions. A conserved dynamic behavior was observed among different GPCRs, including receptors belonging in different GPCR classes. Specific GPCR regions were highlighted as the core of the interfaces. Finally, correlations of motion were observed between parts of the dimer interface and GPCR segments participating in ligand binding and receptor activation, suggesting the existence of mechanisms through which dimer formation may affect GPCR function. The results of this study can be used to drive experiments aimed at exploring GPCR oligomerization, as well as in the study of transmembrane protein-protein interactions in general.
Functional enrichment is a widely used method for interpreting experimental results by identifying classes of proteins/genes associated with certain biological functions, pathways, diseases, or phenotypes. Despite the variety of existing tools, most of them can process a single list per time, thus making a more combinatorial analysis more complicated and prone to errors. In this article, we present FLAME, a web tool for combining multiple lists prior to enrichment analysis. Users can upload several lists and use interactive UpSet plots, as an alternative to Venn diagrams, to handle unions or intersections among the given input files. Functional and literature enrichment, along with gene conversions, are offered by g:Profiler and aGOtool applications for 197 organisms. FLAME can analyze genes/proteins for related articles, Gene Ontologies, pathways, annotations, regulatory motifs, domains, diseases, and phenotypes, and can also generate protein–protein interactions derived from STRING. We have validated FLAME by interrogating gene expression data associated with the sensitivity of the distal part of the large intestine to experimental colitis-propelled colon cancer. FLAME comes with an interactive user-friendly interface for easy list manipulation and exploration, while results can be visualized as interactive and parameterizable heatmaps, barcharts, Manhattan plots, networks, and tables.
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