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Palabras clave – provistas por la editorial

IDP; fuzzy interactions; protein complementation assays; split-GFP reassembly; kinetics; membraneless organelles; optical tweezer; liquid–liquid phase separation; protein diffusion; depletion interaction; entropic force; low-complexity sequences; intrinsically disordered proteins; PAGE4; conformational plasticity; order–disorder transition; phosphorylation; intrinsic disordered protein; extremely fuzzy complex; protein interaction; binding mechanism; tumor protein p53; mouse double minute 2; mouse double minute 4; Kinase-inducible domain interacting domain; phosphomimetics; nuclear magnetic resonance; transient secondary structure; COR15A; Late embryogenesis abundant; Trifluoroethanol; Nuclear magnetic resonance; intrinsically disordered regions; functional segments; disease-related proteins; protein-protein interaction; subcellular location; glucocorticoid receptor; intrinsically disordered; transactivation activity; gene regulation; coactivators; microtubule associated protein; tau; intrinsically disordered protein; dynamic configuration; free energy landscape; microtubules; electrostatics; diffusion; protein structure prediction; molecular modelling; molecular dynamics; tau–microtubule association; conformational ensemble; replica exchange molecular dynamics; drug design; n/a