about
Classification of intrinsically disordered regions and proteinsMotif co-regulation and co-operativity are common mechanisms in transcriptional, post-transcriptional and post-translational regulationWrecked regulation of intrinsically disordered proteins in diseases: pathogenicity of deregulated regulatorsExon-phase symmetry and intrinsic structural disorder promote modular evolution in the human genome.Genome-wide analysis of protein disorder in Arabidopsis thaliana: implications for plant environmental adaptation.Proteins that switch foldsAssemblages: functional units formed by cellular phase separationCatalytic and chaperone-like functions in an intrinsically disordered protein associated with desiccation toleranceDetecting remote sequence homology in disordered proteins: discovery of conserved motifs in the N-termini of Mononegavirales phosphoproteinsExpanding the proteome: disordered and alternatively folded proteins.Genome-scale prediction of proteins with long intrinsically disordered regions.The intrinsically disordered amino-terminal region of human RecQL4: multiple DNA-binding domains confer annealing, strand exchange and G4 DNA binding.Distinct types of disorder in the human proteome: functional implications for alternative splicing.KMAD: knowledge-based multiple sequence alignment for intrinsically disordered proteins.Analyses of the general rule on residue pair frequencies in local amino acid sequences of soluble, ordered proteins.An omics perspective of protein disorder.Comprehensive review of methods for prediction of intrinsic disorder and its molecular functions.Autophagy-related intrinsically disordered proteins in intra-nuclear compartments.Structural and functional analyses of Barth syndrome-causing mutations and alternative splicing in the tafazzin acyltransferase domain.Compartmentalization and Functionality of Nuclear Disorder: Intrinsic Disorder and Protein-Protein Interactions in Intra-Nuclear Compartments.Identifying Similar Patterns of Structural Flexibility in Proteins by Disorder Prediction and Dynamic Programming.Tissue-specific splicing of disordered segments that embed binding motifs rewires protein interaction networks.Exceptionally abundant exceptions: comprehensive characterization of intrinsic disorder in all domains of life.Probing Medin Monomer Structure and its Amyloid Nucleation Using 13C-Direct Detection NMR in Combination with Structural BioinformaticsCharacterization of the impact of alternative splicing on protein dynamics: the cases of glutathione S-transferase and ectodysplasin-A isoforms.From protein sequence to dynamics and disorder with DynaMine.Disordered nucleiome: Abundance of intrinsic disorder in the DNA- and RNA-binding proteins in 1121 species from Eukaryota, Bacteria and Archaea.Deciphering the cause of evolutionary variance within intrinsically disordered regions in human proteins.Functional Analysis of Human Hub Proteins and Their Interactors Involved in the Intrinsic Disorder-Enriched Interactions.Not an exception to the rule: the functional significance of intrinsically disordered protein regions in enzymes.
P2860
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P2860
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Modularity of intrinsic disorder in the human proteome.
@ast
Modularity of intrinsic disorder in the human proteome.
@en
type
label
Modularity of intrinsic disorder in the human proteome.
@ast
Modularity of intrinsic disorder in the human proteome.
@en
prefLabel
Modularity of intrinsic disorder in the human proteome.
@ast
Modularity of intrinsic disorder in the human proteome.
@en
P2860
P356
P1433
P1476
Modularity of intrinsic disorder in the human proteome.
@en
P2093
David T Jones
Melissa M Pentony
P2860
P304
P356
10.1002/PROT.22504
P407
P577
2010-01-01T00:00:00Z