(Q22061740)

Synucleinopathies: clinical and pathological implications

PubMed

volume

18

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page(s)

756-764

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issue

6

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cites work

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Dynamic behavior of an intrinsically unstructured linker domain is conserved in the face of negligible amino acid sequence conservation

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The interplay between structure and function in intrinsically unstructured proteins.

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Disordered domains and high surface charge confer hubs with the ability to interact with multiple proteins in interaction networks

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Prediction and Functional Analysis of Native Disorder in Proteins from the Three Kingdoms of Life

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Are amyloid diseases caused by protein aggregates that mimic bacterial pore-forming toxins?

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Intrinsic disorder and protein function

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Urea promotes polyproline II helix formation: implications for protein denatured states

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Helical alpha-synuclein forms highly conductive ion channels

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Functional anthology of intrinsic disorder. 2. Cellular components, domains, technical terms, developmental processes, and coding sequence diversities correlated with long disordered regions

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The protein trinity--linking function and disorder.

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Intrinsically unstructured proteins and their functions

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Amyloid ion channels: a common structural link for protein-misfolding disease

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Alternative splicing in concert with protein intrinsic disorder enables increased functional diversity in multicellular organisms

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Fluorescence correlation spectroscopy shows that monomeric polyglutamine molecules form collapsed structures in aqueous solutions

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Lipid binding inhibits alpha-synuclein fibril formation

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Structure and dynamics of micelle-bound human alpha-synuclein

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Local structural disorder imparts plasticity on linear motifs.

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p53 isoforms can regulate p53 transcriptional activity.

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Molecular determinants of the aggregation behavior of alpha- and beta-synuclein

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Flexible nets. The roles of intrinsic disorder in protein interaction networks.

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Dynamics of alpha-synuclein aggregation and inhibition of pore-like oligomer development by beta-synuclein

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Structural biology of the tumor suppressor p53.

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Intrinsically Disordered Proteins in Human Diseases: Introducing the D 2 Concept

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Flexible nets: disorder and induced fit in the associations of p53 and 14-3-3 with their partners

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7 January 2021

Short Linear Motifs recognized by SH2, SH3 and Ser/Thr Kinase domains are conserved in disordered protein regions

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7 January 2021

What properties characterize the hub proteins of the protein-protein interaction network of Saccharomyces cerevisiae?

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7 January 2021

Intrinsic disorder is a common feature of hub proteins from four eukaryotic interactomes

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7 January 2021

SLiMFinder: a probabilistic method for identifying over-represented, convergently evolved, short linear motifs in proteins.

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Hierarchical extensibility in the PEVK domain of skeletal-muscle titin

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7 January 2021

Intrinsic disorder and functional proteomics

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7 January 2021

Biophysical characterization of the unstructured cytoplasmic domain of the human neuronal adhesion protein neuroligin 3.

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7 January 2021

Amyloidogenesis of natively unfolded proteins

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