Computer Graphics Forum · 2016 · 62 citations · 120 references
EngineeringMicroscopyMolecular BiologyVisualization (Data Visualization)Biomedical EngineeringMolecular GraphicCavity Detection ApproachesComputational VisualizationMolecular SimulationBiological Network VisualizationComputational BiochemistryMacromolecular AssembliesMolecular ImagingBiophysicsVisualization TechnologiesMolecular SciencesMolecular VisualizationVisual AnalysisBiomolecular ScienceUltrastructureNatural SciencesScientific VisualizationBioimage AnalysisBiomedical ImagingMolecular BiophysicsCell ImagingComputational Biophysics
The report introduces key terminology, goals, and the current state of cavity‑analysis methods—including dynamic data—and outlines future challenges. The paper reviews and structures the field of visual analysis of cavities in macromolecular protein structures. The authors present a novel classification of cavity detection methods into grid‑based, Voronoi‑based, surface‑based, and probe‑based categories, link them to visualization techniques such as direct 3D rendering, relational graphs, and contour plots, and survey the most common tools used in structural biology.
Abstract In this report we review and structure the branch of molecular visualization that is concerned with the visual analysis of cavities in macromolecular protein structures. First the necessary background, the domain terminology, and the goals of analytical reasoning are introduced. Based on a comprehensive collection of relevant research works, we present a novel classification for cavity detection approaches and structure them into four distinct classes: grid‐based, Voronoi‐based, surface‐based, and probe‐based methods. The subclasses are then formed by their combinations. We match these approaches with corresponding visualization technologies starting with direct 3D visualization, followed with non‐spatial visualization techniques that for example abstract the interactions between structures into a relational graph, straighten the cavity of interest to see its profile in one view, or aggregate the time sequence into a single contour plot. We also discuss the current state of methods for the visual analysis of cavities in dynamic data such as molecular dynamics simulations. Finally, we give an overview of the most common tools that are actively developed and used in the structural biology and biochemistry research. Our report is concluded by an outlook on future challenges in the field.
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