scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1041073895 |
P356 | DOI | 10.1186/1471-2164-9-S2-S1 |
P932 | PMC publication ID | 2559873 |
P698 | PubMed publication ID | 18831774 |
P50 | author | Vladimir Vacic | Q42850794 |
Vladimir N. Uversky | Q59698496 | ||
P2093 | author name string | Pedro Romero | |
A Keith Dunker | |||
Jingwei Meng | |||
Christopher J Oldfield | |||
Zoran Obradovic | |||
Jack Y Yang | |||
Jessica Walton Chen | |||
P2860 | cites work | Calmodulin signaling: analysis and prediction of a disorder-dependent molecular recognition | Q82627891 |
Disordered domains and high surface charge confer hubs with the ability to interact with multiple proteins in interaction networks | Q82855583 | ||
Intrinsically Disordered Proteins in Human Diseases: Introducing the D 2 Concept | Q22061726 | ||
Intrinsically unstructured proteins and their functions | Q22061731 | ||
Prediction and Functional Analysis of Native Disorder in Proteins from the Three Kingdoms of Life | Q22061741 | ||
A practical overview of protein disorder prediction methods | Q22061753 | ||
Cdk-inhibitory activity and stability of p27Kip1 are directly regulated by oncogenic tyrosine kinases | Q24294546 | ||
A Y chromosome gene family with RNA-binding protein homology: candidates for the azoospermia factor AZF controlling human spermatogenesis | Q24323950 | ||
Crystal structure of the p27Kip1 cyclin-dependent-kinase inhibitor bound to the cyclin A-Cdk2 complex | Q24336704 | ||
Crystal structures of two human pyrophosphorylase isoforms in complexes with UDPGlc(Gal)NAc: role of the alternatively spliced insert in the enzyme oligomeric assembly and active site architecture | Q24535935 | ||
Alternative splicing in concert with protein intrinsic disorder enables increased functional diversity in multicellular organisms | Q24548466 | ||
Nucleation, rapid folding, and globular intrachain regions in proteins | Q24564344 | ||
Altered phosphorylation and intracellular distribution of a (CUG)n triplet repeat RNA-binding protein in patients with myotonic dystrophy and in myotonin protein kinase knockout mice | Q24654728 | ||
ELM server: A new resource for investigating short functional sites in modular eukaryotic proteins | Q24672414 | ||
DisProt: the Database of Disordered Proteins | Q24675789 | ||
A database of protein structure families with common folding motifs | Q24676220 | ||
Systematic discovery of new recognition peptides mediating protein interaction networks | Q24817114 | ||
The crystal structures of glutathione S-transferases isozymes 1-3 and 1-4 from Anopheles dirus species B | Q27635431 | ||
Crystal structure of human cholesterol sulfotransferase (SULT2B1b) in the presence of pregnenolone and 3'-phosphoadenosine 5'-phosphate. Rationale for specificity differences between prototypical SULT2A1 and the SULT2BG1 isoforms | Q27641844 | ||
Alternative splicing of Rac1 generates Rac1b, a self-activating GTPase | Q27642578 | ||
The crystal structures of EDA-A1 and EDA-A2: splice variants with distinct receptor specificity | Q27642694 | ||
Modulation of calmodulin plasticity in molecular recognition on the basis of x-ray structures | Q27731497 | ||
CDK inhibitors: positive and negative regulators of G1-phase progression | Q27860983 | ||
Mechanisms of alternative pre-messenger RNA splicing | Q28131822 | ||
Drug discovery: a historical perspective | Q28138834 | ||
Intrinsically disordered protein | Q28191444 | ||
Domain combinations in archaeal, eubacterial and eukaryotic proteomes | Q28203959 | ||
How did alternative splicing evolve? | Q35930718 | ||
Aberrant and alternative splicing in cancer | Q35936123 | ||
Quantitative characterization of intrinsic disorder in polyglutamine: insights from analysis based on polymer theories | Q35963371 | ||
Showing your ID: intrinsic disorder as an ID for recognition, regulation and cell signaling | Q36226283 | ||
Beyond annotation transfer by homology: novel protein-function prediction methods to assist drug discovery | Q36294114 | ||
Targeting protein-protein interactions for cancer therapy | Q36311496 | ||
Automated protein function prediction--the genomic challenge | Q36505962 | ||
Structural characterization of proteins using residue environments | Q36789994 | ||
Looking into live cells with in-cell NMR spectroscopy | Q36821672 | ||
NACP, a protein implicated in Alzheimer's disease and learning, is natively unfolded | Q36830682 | ||
Conservation of intrinsic disorder in protein domains and families: II. functions of conserved disorder | Q36869604 | ||
Characterization of molecular recognition features, MoRFs, and their binding partners | Q36944291 | ||
Functional anthology of intrinsic disorder. 2. Cellular components, domains, technical terms, developmental processes, and coding sequence diversities correlated with long disordered regions | Q36986347 | ||
TOP-IDP-scale: a new amino acid scale measuring propensity for intrinsic disorder | Q37178764 | ||
Amyloidogenesis of natively unfolded proteins | Q37184755 | ||
Structural Aspects of the Fibrinogen to Fibrin Conversion | Q39935581 | ||
Mechanism of coupled folding and binding of an intrinsically disordered protein | Q40210194 | ||
Small-molecule antagonists of p53-MDM2 binding: research tools and potential therapeutics. | Q40581450 | ||
Close encounters: why unstructured, polymeric domains can increase rates of specific macromolecular association | Q40823855 | ||
Design of a synthetic Mdm2-binding mini protein that activates the p53 response in vivo. | Q41063629 | ||
Translational control of p27Kip1 accumulation during the cell cycle | Q41213467 | ||
Alzheimer's disease-like phosphorylation of the microtubule-associated protein tau by glycogen synthase kinase-3 in transfected mammalian cells. | Q41423732 | ||
Inhibitors of the Cip/Kip family. | Q41710956 | ||
Conservation of intrinsic disorder in protein domains and families: I. A database of conserved predicted disordered regions | Q41851853 | ||
SLiMDisc: short, linear motif discovery, correcting for common evolutionary descent | Q42415695 | ||
Intrinsic disorder in cell-signaling and cancer-associated proteins | Q28207698 | ||
Genome-wide survey of human alternative pre-mRNA splicing with exon junction microarrays | Q28235146 | ||
Analysis of molecular recognition features (MoRFs) | Q28260253 | ||
Redesigning enzyme topology by directed evolution | Q28265020 | ||
One thousand families for the molecular biologist | Q28266140 | ||
The anatomy and taxonomy of protein structure | Q28277011 | ||
Distinct and opposite activities of human terminal deoxynucleotidyltransferase splice variants | Q28281082 | ||
Shuffled domains in extracellular proteins | Q28288029 | ||
Solvent-induced collapse of alpha-synuclein and acid-denatured cytochrome c | Q28361893 | ||
Structural studies of p21Waf1/Cip1/Sdi1 in the free and Cdk2-bound state: conformational disorder mediates binding diversity | Q28910326 | ||
p27 binds cyclin-CDK complexes through a sequential mechanism involving binding-induced protein folding | Q28910366 | ||
Structural studies of tau protein and Alzheimer paired helical filaments show no evidence for beta-structure | Q28910456 | ||
The molecular surface package | Q29039306 | ||
A Bayesian Networks Approach for Predicting Protein-Protein Interactions from Genomic Data | Q29395063 | ||
Reaching for high-hanging fruit in drug discovery at protein-protein interfaces | Q29547258 | ||
Lethality and centrality in protein networks | Q29547267 | ||
Principles of CDK regulation | Q29547820 | ||
Evidence for dynamically organized modularity in the yeast protein-protein interaction network | Q29614449 | ||
Why are "natively unfolded" proteins unstructured under physiologic conditions? | Q29615739 | ||
Intrinsically unstructured proteins: re-assessing the protein structure-function paradigm | Q29615865 | ||
An evolutionary trace method defines binding surfaces common to protein families | Q29615880 | ||
SCOP database in 2004: refinements integrate structure and sequence family data | Q29615988 | ||
Intrinsic disorder and protein function | Q29616415 | ||
Natively unfolded proteins: a point where biology waits for physics | Q29616416 | ||
Coupling of folding and binding for unstructured proteins | Q29616417 | ||
Coupling of local folding to site-specific binding of proteins to DNA | Q29616464 | ||
Role of the ubiquitin-proteasome pathway in regulating abundance of the cyclin-dependent kinase inhibitor p27 | Q29617346 | ||
Small-molecule inhibitors of protein-protein interactions: progressing towards the dream | Q29617758 | ||
Why genes in pieces? | Q29618207 | ||
Alternative splicing: increasing diversity in the proteomic world | Q29618730 | ||
Local structural disorder imparts plasticity on linear motifs. | Q30158016 | ||
Protein structure and enzyme action. | Q30334053 | ||
Comparing and combining predictors of mostly disordered proteins. | Q30350136 | ||
Flexible nets. The roles of intrinsic disorder in protein interaction networks. | Q30351593 | ||
Length-dependent prediction of protein intrinsic disorder. | Q30353929 | ||
Functional anthology of intrinsic disorder. 1. Biological processes and functions of proteins with long disordered regions. | Q30360720 | ||
Functional anthology of intrinsic disorder. 3. Ligands, post-translational modifications, and diseases associated with intrinsically disordered proteins. | Q30360723 | ||
Assessment of disorder predictions in CASP7. | Q30363273 | ||
Characterizing the microenvironment surrounding protein sites | Q30417434 | ||
Structural basis for the attachment of a paramyxoviral polymerase to its template | Q30448746 | ||
What properties characterize the hub proteins of the protein-protein interaction network of Saccharomyces cerevisiae? | Q42625650 | ||
Evaluation of features for catalytic residue prediction in novel folds | Q42958224 | ||
Protein dynamics in living cells | Q43153025 | ||
Splice variants: a homology modeling approach | Q44745632 | ||
The C-terminal domain of measles virus nucleoprotein belongs to the class of intrinsically disordered proteins that fold upon binding to their physiological partner | Q44746385 | ||
Alternative splicing in the N-terminus of Alzheimer's presenilin 1. | Q45104033 | ||
Rational drug design via intrinsically disordered protein | Q47193604 | ||
Analysis of ordered and disordered protein complexes reveals structural features discriminating between stable and unstable monomers | Q47609385 | ||
Preformed structural elements feature in partner recognition by intrinsically unstructured proteins | Q47692263 | ||
Flavors of protein disorder | Q47700031 | ||
Protein disorder and the evolution of molecular recognition: theory, predictions and observations | Q47715145 | ||
Coupled folding and binding with alpha-helix-forming molecular recognition elements | Q48122045 | ||
Combining prediction, computation and experiment for the characterization of protein disorder. | Q51635477 | ||
Protein intrinsic disorder and human papillomaviruses: increased amount of disorder in E6 and E7 oncoproteins from high risk HPVs. | Q51936092 | ||
Assessment of disorder predictions in CASP6. | Q51963679 | ||
The protein trinity--linking function and disorder. | Q52055900 | ||
Intrinsic disorder is a key characteristic in partners that bind 14-3-3 proteins. | Q52664522 | ||
Disorder and sequence repeats in hub proteins and their implications for network evolution. | Q52673882 | ||
EST comparison indicates 38% of human mRNAs contain possible alternative splice forms. | Q52971558 | ||
Signal transduction via unstructured protein conduits. | Q53491312 | ||
Macromolecular crowding in the Escherichia coli periplasm maintains alpha-synuclein disorder. | Q54473816 | ||
Evaluation of disorder predictions in CASP5 | Q57972076 | ||
Probabilistic model of the human protein-protein interaction network | Q58482561 | ||
Unspinning the web | Q59087483 | ||
Adenovirus amazes at Cold Spring Harbor | Q64382281 | ||
Specific sequence homology and three-dimensional structure of an aminoacyl transfer RNA synthetase | Q70398900 | ||
Predicting Disordered Regions from Amino Acid Sequence: Common Themes Despite Differing Structural Characterization | Q73174424 | ||
Predicting Binding Regions within Disordered Proteins | Q73174434 | ||
Light-scattering study of effect of electrolytes on alpha- and beta-casein solutions | Q73556264 | ||
The protein non-folding problem: amino acid determinants of intrinsic order and disorder | Q73658941 | ||
Intrinsic protein disorder in complete genomes | Q77145749 | ||
Effects of macromolecular crowding on the intrinsically disordered proteins c-Fos and p27(Kip1) | Q77366460 | ||
Abundance of intrinsic disorder in protein associated with cardiovascular disease | Q80181937 | ||
Intrinsic disorder in yeast transcriptional regulatory network | Q80353265 | ||
Virtual identification of essential proteins within the protein interaction network of yeast | Q81466184 | ||
Optimizing long intrinsic disorder predictors with protein evolutionary information | Q81484824 | ||
Antagonists of protein-protein interactions. | Q30861865 | ||
The N-terminal domain of p53 is natively unfolded. | Q30879982 | ||
Fluorescence correlation spectroscopy shows that monomeric polyglutamine molecules form collapsed structures in aqueous solutions | Q31072074 | ||
Intrinsic disorder in the Protein Data Bank | Q31090109 | ||
Method for prediction of protein function from sequence using the sequence-to-structure-to-function paradigm with application to glutaredoxins/thioredoxins and T1 ribonucleases | Q32032853 | ||
Studies of the RNA degradosome-organizing domain of the Escherichia coli ribonuclease RNase E. | Q33204492 | ||
Intrinsic disorder is a common feature of hub proteins from four eukaryotic interactomes | Q33252616 | ||
Composition Profiler: a tool for discovery and visualization of amino acid composition differences | Q33288198 | ||
Inferring function using patterns of native disorder in proteins | Q33295214 | ||
Flexible nets: disorder and induced fit in the associations of p53 and 14-3-3 with their partners | Q33325589 | ||
InterPro: an integrated documentation resource for protein families, domains and functional sites | Q33961349 | ||
Normalization of nomenclature for peptide motifs as ligands of modular protein domains | Q34120337 | ||
FlgM gains structure in living cells | Q34189211 | ||
Structural genomics analysis of alternative splicing and application to isoform structure modeling | Q34244987 | ||
DisProt: a database of protein disorder | Q34341031 | ||
Protein-protein interactions and cancer: small molecules going in for the kill | Q34424260 | ||
Gene family evolution and homology: genomics meets phylogenetics | Q34433357 | ||
Analysis of protein-protein interaction sites using surface patches | Q34439363 | ||
What does it mean to be natively unfolded? | Q34488954 | ||
Function of alternative splicing | Q34554255 | ||
The CATH domain structure database: new protocols and classification levels give a more comprehensive resource for exploring evolution | Q34585750 | ||
Neuropathology, biochemistry, and biophysics of alpha-synuclein aggregation | Q34648491 | ||
Mining alpha-helix-forming molecular recognition features with cross species sequence alignments | Q34708119 | ||
Fuzzy complexes: polymorphism and structural disorder in protein-protein interactions | Q34720702 | ||
Role of intrinsic flexibility in signal transduction mediated by the cell cycle regulator, p27 Kip1. | Q34733508 | ||
Identification and functions of usefully disordered proteins | Q34989882 | ||
Speeding molecular recognition by using the folding funnel: the fly-casting mechanism | Q35189399 | ||
A protein-chameleon: conformational plasticity of alpha-synuclein, a disordered protein involved in neurodegenerative disorders | Q35212177 | ||
Protein folding revisited. A polypeptide chain at the folding ? misfolding ? nonfolding cross-roads: which way to go? | Q35549177 | ||
Intrinsic disorder and functional proteomics | Q35632957 | ||
Inhibition of the p53-MDM2 interaction: targeting a protein-protein interface. | Q35646494 | ||
Splice variants of G protein-coupled receptors | Q35679333 | ||
firestar--prediction of functionally important residues using structural templates and alignment reliability | Q35914235 | ||
P407 | language of work or name | English | Q1860 |
P304 | page(s) | S1 | |
P577 | publication date | 2008-09-16 | |
P1433 | published in | BMC Genomics | Q15765854 |
P1476 | title | The unfoldomics decade: an update on intrinsically disordered proteins. | |
P478 | volume | 9 Suppl 2 |
Q35672250 | (13)C-detected NMR experiments for automatic resonance assignment of IDPs and multiple-fixing SMFT processing. |
Q51745948 | 3D J-resolved NMR spectroscopy for unstructured polypeptides: fast measurement of 3J HNH alpha coupling constants with outstanding spectral resolution. |
Q33378970 | A comparative analysis of viral matrix proteins using disorder predictors |
Q33869871 | A comprehensive benchmark study of multiple sequence alignment methods: current challenges and future perspectives |
Q47133883 | A conserved ankyrin repeat-containing protein regulates conoid stability, motility and cell invasion in Toxoplasma gondii. |
Q28681184 | A decade and a half of protein intrinsic disorder: biology still waits for physics |
Q41984210 | A frustrated binding interface for intrinsically disordered proteins |
Q34523989 | A genomic scale map of genetic diversity in Trypanosoma cruzi |
Q33924598 | Accurate in silico identification of species-specific acetylation sites by integrating protein sequence-derived and functional features. |
Q39148660 | Actinous enigma or enigmatic actin: Folding, structure, and functions of the most abundant eukaryotic protein |
Q50979566 | Advantages of synchrotron radiation circular dichroism spectroscopy to study intrinsically disordered proteins. |
Q39967413 | Amino acid recognition for automatic resonance assignment of intrinsically disordered proteins |
Q58621641 | Amyloid assembly and disassembly |
Q26783068 | An Overview of Predictors for Intrinsically Disordered Proteins over 2010-2014 |
Q37958616 | An omics perspective of protein disorder |
Q34787939 | Analysis and consensus of currently available intrinsic protein disorder annotation sources in the MobiDB database. |
Q30157208 | Analysis of structured and intrinsically disordered regions of transmembrane proteins |
Q42647821 | Annotation of novel transcripts putatively relevant for bovine fat metabolism. |
Q64980510 | Anti-Correlation between the Dynamics of the Active Site Loop and C-Terminal Tail in Relation to the Homodimer Asymmetry of the Mouse Erythroid 5-Aminolevulinate Synthase. |
Q42316830 | Architecture and coevolution of allosteric materials. |
Q51576437 | Are protein hubs faster folders? Exploration based on Escherichia coli proteome. |
Q43638249 | Assessing induced folding within the intrinsically disordered C-terminal domain of the Henipavirus nucleoproteins by site-directed spin labeling EPR spectroscopy |
Q33901421 | Assessing the contribution of alternative splicing to proteome diversity in Arabidopsis thaliana using proteomics data |
Q36672683 | Assessment of 3D models for allergen research |
Q34594687 | Assisted peptide folding by surface pattern recognition. |
Q30481562 | At low concentrations, 3,4-dihydroxyphenylacetic acid (DOPAC) binds non-covalently to alpha-synuclein and prevents its fibrillation |
Q33762505 | Benchmarking B-cell epitope prediction for the design of peptide-based vaccines: problems and prospects |
Q38019703 | Beyond 'furballs' and 'dumpling soups' - towards a molecular architecture of signaling complexes and networks |
Q42821660 | Bidirectional modulation of thermal and chemical sensitivity of TRPM8 channels by the initial region of the N-terminal domain. |
Q35001468 | Biochemical and structural studies of the oligomerization domain of the Nipah virus phosphoprotein: evidence for an elongated coiled-coil homotrimer |
Q57035312 | Biomolecular Assemblies: Moving from Observation to Predictive Design |
Q49329183 | Biophysical Evidence for Intrinsic Disorder in the C-terminal Tails of the Epidermal Growth Factor Receptor (EGFR) and HER3 Receptor Tyrosine Kinases. |
Q28660230 | Biophysical properties of intrinsically disordered p130Cas substrate domain--implication in mechanosensing |
Q35547360 | Brain expressed and X-linked (Bex) proteins are intrinsically disordered proteins (IDPs) and form new signaling hubs |
Q30399739 | Bringing order to protein disorder through comparative genomics and genetic interactions |
Q37195737 | CDF it all: consensus prediction of intrinsically disordered proteins based on various cumulative distribution functions |
Q33810210 | CFP: a web-server for constructing sequence-based protein conformational flexibility profiles |
Q55514345 | Calcium-Binding Proteins with Disordered Structure and Their Role in Secretion, Storage, and Cellular Signaling. |
Q37398192 | Caulobacter PopZ forms an intrinsically disordered hub in organizing bacterial cell poles |
Q35036093 | Chaperoning roles of macromolecules interacting with proteins in vivo |
Q43256880 | Characterization of intrinsically disordered proteins with electrospray ionization mass spectrometry: conformational heterogeneity of alpha-synuclein |
Q34787399 | Characterization of the interactions between the nucleoprotein and the phosphoprotein of Henipavirus |
Q37848764 | Chlamydia co-opts the rod shape-determining proteins MreB and Pbp2 for cell division |
Q36355194 | Cholesterol: its regulation and role in central nervous system disorders |
Q22061736 | Classification of intrinsically disordered regions and proteins |
Q92059386 | Clustering of atomic displacement parameters in bovine trypsin reveals a distributed lattice of atoms with shared chemical properties |
Q54348285 | Compaction and binding properties of the intrinsically disordered C-terminal domain of Henipavirus nucleoprotein as unveiled by deletion studies. |
Q34657052 | Comparative studies of disordered proteins with similar sequences: application to Aβ40 and Aβ42 |
Q28483769 | Computational and statistical analyses of amino acid usage and physico-chemical properties of the twelve late embryogenesis abundant protein classes |
Q33875537 | Conditionally and transiently disordered proteins: awakening cryptic disorder to regulate protein function |
Q38116495 | Conformational propensities of intrinsically disordered proteins from NMR chemical shifts |
Q36997794 | Connecting autophagy: AMBRA1 and its network of regulation |
Q24616986 | Constructing ensembles for intrinsically disordered proteins |
Q42777346 | Controllability of protein-protein interaction phosphorylation-based networks: Participation of the hub 14-3-3 protein family |
Q33654343 | Correcting for differential transcript coverage reveals a strong relationship between alternative splicing and organism complexity. |
Q27653453 | Crystal Structures of Human MdmX (HdmX) in Complex with p53 Peptide Analogues Reveal Surprising Conformational Changes |
Q30392650 | DNA-binding protects p53 from interactions with cofactors involved in transcription-independent functions |
Q38724766 | Dancing Protein Clouds: The Strange Biology and Chaotic Physics of Intrinsically Disordered Proteins |
Q30009894 | Dancing retro: solution structure and micelle interactions of the retro-SH3-domain, retro-SHH-'Bergerac'. |
Q46607962 | Deciphering the cause of evolutionary variance within intrinsically disordered regions in human proteins |
Q43241621 | DeepCNF-D: Predicting Protein Order/Disorder Regions by Weighted Deep Convolutional Neural Fields |
Q36010061 | Did the prion protein become vulnerable to misfolding after an evolutionary divide and conquer event? |
Q22061724 | Digested disorder: Quarterly intrinsic disorder digest (January/February/March, 2013). |
Q27666038 | Directed epitope delivery across the Escherichia coli outer membrane through the porin OmpF |
Q30375859 | DisoMCS: Accurately Predicting Protein Intrinsically Disordered Regions Using a Multi-Class Conservative Score Approach. |
Q38779717 | Disorder in the lifetime of a protein |
Q42564287 | Disorder targets misorder in nuclear quality control degradation: a disordered ubiquitin ligase directly recognizes its misfolded substrates. |
Q28652765 | Disordered proteinaceous machines |
Q35938545 | Dynamic Protein Interaction Networks and New Structural Paradigms in Signaling |
Q38965660 | Dynamic footprint of sequestration in the molecular fluctuations of osteopontin |
Q42177256 | Dynamics of the intrinsically disordered C-terminal domain of the nipah virus nucleoprotein and interaction with the x domain of the phosphoprotein as unveiled by NMR spectroscopy |
Q34100061 | Economical evolution: microbes reduce the synthetic cost of extracellular proteins |
Q47955285 | Efficient protocol for backbone and side-chain assignments of large, intrinsically disordered proteins: transient secondary structure analysis of 49.2 kDa microtubule associated protein 2c. |
Q30010028 | Engineering of an elastic scaffolding polyprotein based on an SH3-binding intrinsically disordered titin PEVK module |
Q39005050 | Erythropoietin and co.: intrinsic structure and functional disorder |
Q29048164 | Evaluation of disorder predictions in CASP9 |
Q35129656 | Evidence of trem2 variant associated with triple risk of Alzheimer's disease |
Q35037936 | Evolution and disorder |
Q36246401 | Evolution of the hepatitis E virus polyproline region: order from disorder |
Q61798267 | Evolutionary Approach of Intrinsically Disordered CIP/KIP Proteins |
Q36120928 | FLEXc: protein flexibility prediction using context-based statistics, predicted structural features, and sequence information |
Q35622155 | Fairy "tails": flexibility and function of intrinsically disordered extensions in the photosynthetic world |
Q36868063 | Fast, cheap and out of control--Insights into thermodynamic and informatic constraints on natural protein sequences from de novo protein design. |
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Q30377510 | Folding by numbers: primary sequence statistics and their use in studying protein folding |
Q35670426 | Force field-dependent solution properties of glycine oligomers |
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Q35800480 | Functional Advantages of Conserved Intrinsic Disorder in RNA-Binding Proteins |
Q30375717 | Functional aspects of protein flexibility. |
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Q33352897 | GRAS proteins: the versatile roles of intrinsically disordered proteins in plant signalling. |
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Q33373534 | Genomics, molecular imaging, bioinformatics, and bio-nano-info integration are synergistic components of translational medicine and personalized healthcare research |
Q54257512 | Hepatitis E Virus Genome Structure and Replication Strategy. |
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Q38370771 | How do disordered regions achieve comparable functions to structured domains? |
Q34154833 | How sequence determines elasticity of disordered proteins |
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Q33385232 | Importance of backbone and solvent properties for conformational dynamics in polypeptides |
Q24615841 | Improved sequence-based prediction of disordered regions with multilayer fusion of multiple information sources |
Q50864208 | In various protein complexes, disordered protomers have large per-residue surface areas and area of protein-, DNA- and RNA-binding interfaces. |
Q36846728 | In vivo protein complex topologies: sights through a cross-linking lens |
Q48245958 | In-cell NMR: from metabolites to macromolecules |
Q33935454 | In-silico prediction of disorder content using hybrid sequence representation |
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Q41814829 | Interaction between the C-terminal domains of measles virus nucleoprotein and phosphoprotein: a tight complex implying one binding site |
Q37453424 | Interaction of human laminin receptor with Sup35, the [PSI⁺] prion-forming protein from S. cerevisiae: a yeast model for studies of LamR interactions with amyloidogenic proteins |
Q48198768 | Interactome INSIDER: a structural interactome browser for genomic studies. |
Q34442046 | Interplay between partner and ligand facilitates the folding and binding of an intrinsically disordered protein |
Q55066708 | Intrinsic Disorder and Posttranslational Modifications: The Darker Side of the Biological Dark Matter. |
Q38163534 | Intrinsic Disorder in the Kinesin Superfamily. |
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Q57354509 | Intrinsically disordered proteins in crowded milieu: when chaos prevails within the cellular gumbo |
Q39335014 | Intrinsically disordered regions in autophagy proteins |
Q36218605 | Kinesin tail domains are intrinsically disordered. |
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Q33671056 | Lipoprotein Complex of Equine Lysozyme with Oleic Acid (ELOA) Interactions with the Plasma Membrane of Live Cells |
Q43238987 | MEPE evolution in mammals reveals regions and residues of prime functional importance |
Q38779764 | MFDp2: Accurate predictor of disorder in proteins by fusion of disorder probabilities, content and profiles |
Q30430063 | Malleable ribonucleoprotein machine: protein intrinsic disorder in the Saccharomyces cerevisiae spliceosome |
Q39410121 | Mapping of Chikungunya virus interactions with host proteins identified nsP2 as a highly connected viral component |
Q35117017 | Mapping the amino acid properties of constituent nucleoporins onto the yeast nuclear pore complex |
Q58337134 | Mapping the domain of interaction of PVBV VPg with NIa-Pro: Role of N-terminal disordered region of VPg in the modulation of structure and function |
Q34688655 | Marked variability in the extent of protein disorder within and between viral families |
Q28478338 | Markov models of amino acid substitution to study proteins with intrinsically disordered regions |
Q21245770 | Messing up disorder: how do missense mutations in the tumor suppressor protein APC lead to cancer? |
Q21284325 | MetaDisorder: a meta-server for the prediction of intrinsic disorder in proteins |
Q41035075 | Microenvironmentally controlled secondary structure motifs of apolipoprotein A-I derived peptides |
Q47259639 | Modulating protein amyloid aggregation with nanomaterials. |
Q37311893 | Modulating the intrinsic disorder in the cytoplasmic domain alters the biological activity of the N-methyl-D-aspartate-sensitive glutamate receptor |
Q64087496 | Modulation of Disordered Proteins with a Focus on Neurodegenerative Diseases and Other Pathologies |
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Q34318423 | Molecular phylogeny of OVOL genes illustrates a conserved C2H2 zinc finger domain coupled by hypervariable unstructured regions. |
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Q37746989 | Molecular simulations of protein disorder |
Q37770057 | Multicolor single-molecule FRET to explore protein folding and binding |
Q38077753 | Multifarious roles of intrinsic disorder in proteins illustrate its broad impact on plant biology |
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Q35006989 | Musite, a tool for global prediction of general and kinase-specific phosphorylation sites. |
Q37919366 | Mutual effects of disorder and order in fusion proteins between intrinsically disordered domains and fluorescent proteins. |
Q33999903 | N-termini of fungal CSL transcription factors are disordered, enriched in regulatory motifs and inhibit DNA binding in fission yeast |
Q30666950 | NMR based solvent exchange experiments to understand the conformational preference of intrinsically disordered proteins using FG-nucleoporin peptide as a model |
Q28478425 | NMR studies of the C-terminus of alpha4 reveal possible mechanism of its interaction with MID1 and protein phosphatase 2A |
Q56993044 | NOT THAT RIGID MIDGETS AND NOT SO FLEXIBLE GIANTS: ON THE ABUNDANCE AND ROLES OF INTRINSIC DISORDER IN SHORT AND LONG PROTEINS |
Q89849097 | New technologies to analyse protein function: an intrinsic disorder perspective |
Q37891686 | Novel strategies for drug discovery based on Intrinsically Disordered Proteins (IDPs) |
Q41870328 | Order within disorder: aggrecan chondroitin sulphate-attachment region provides new structural insights into protein sequences classified as disordered |
Q34981100 | Ordered disorder of the astrocytic dystrophin-associated protein complex in the norm and pathology |
Q34118594 | Osmolyte-induced folding of an intrinsically disordered protein: folding mechanism in the absence of ligand |
Q33531518 | Parameterization of disorder predictors for large-scale applications requiring high specificity by using an extended benchmark dataset |
Q38650728 | PhosphoPredict: A bioinformatics tool for prediction of human kinase-specific phosphorylation substrates and sites by integrating heterogeneous feature selection |
Q34097567 | Phosphoproteomics by mass spectrometry: insights, implications, applications and limitations |
Q35874419 | Plasticity in structural and functional interactions between the phosphoprotein and nucleoprotein of measles virus. |
Q47710367 | Potential functions of LEA proteins from the brine shrimp Artemia franciscana - anhydrobiosis meets bioinformatics |
Q43484080 | Potential of mean force and transient states in polyelectrolyte pair complexation. |
Q37549950 | Predicting intrinsic disorder in proteins: an overview |
Q30399245 | Predicting protein flexibility through the prediction of local structures |
Q28476679 | Prediction and analysis of protein hydroxyproline and hydroxylysine |
Q35051967 | Prediction of Intrinsic Disorder in MERS-CoV/HCoV-EMC Supports a High Oral-Fecal Transmission |
Q38132466 | Promiscuity as a functional trait: intrinsically disordered regions as central players of interactomes |
Q47371568 | Prosystemin, a prohormone that modulates plant defense barriers, is an intrinsically disordered protein. |
Q50856198 | Protein Complexes in the Nucleus: The Control of Chromosome Segregation. |
Q83667091 | Protein dynamics: bridging the gap |
Q37241586 | Protein intrinsic disorder and influenza virulence: the 1918 H1N1 and H5N1 viruses |
Q37541123 | Protein intrinsic disorder and network connectivity. The case of 14-3-3 proteins |
Q36675634 | Protein intrinsic disorder in the acetylome of intracellular and extracellular Toxoplasma gondii |
Q30403541 | Protein structure along the order-disorder continuum |
Q38257180 | Proteins without unique 3D structures: biotechnological applications of intrinsically unstable/disordered proteins |
Q39183554 | Proteome-wide evidence for enhanced positive Darwinian selection within intrinsically disordered regions in proteins |
Q41809289 | Proteomic phenotyping of Novosphingobium nitrogenifigens reveals a robust capacity for simultaneous nitrogen fixation, polyhydroxyalkanoate production, and resistance to reactive oxygen species |
Q51112497 | Quantitative mapping of microtubule-associated protein 2c (MAP2c) phosphorylation and regulatory protein 14-3-3ζ-binding sites reveals key differences between MAP2c and its homolog Tau. |
Q38589800 | Recombinant Intrinsically Disordered Proteins for NMR: Tips and Tricks |
Q33766662 | Refining orthologue groups at the transcript level |
Q37255426 | Residual structure within the disordered C-terminal segment of p21(Waf1/Cip1/Sdi1) and its implications for molecular recognition. |
Q30379606 | SDSL-ESR-based protein structure characterization. |
Q33978783 | SPA: Short peptide analyzer of intrinsic disorder status of short peptides |
Q37440289 | Sending signals dynamically |
Q33997189 | Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population. |
Q42124997 | Small acid-soluble proteins with intrinsic disorder are required for UV resistance in Myxococcus xanthus spores |
Q42151102 | Specificity and affinity quantification of flexible recognition from underlying energy landscape topography |
Q51362509 | Stochastic simulation of structural properties of natively unfolded and denatured proteins. |
Q33640276 | Structural disorder within Henipavirus nucleoprotein and phosphoprotein: from predictions to experimental assessment |
Q34680376 | Structural divergence is more extensive than sequence divergence for a family of intrinsically disordered proteins |
Q42707053 | Structural flexibility allows the functional diversity of potyvirus genome-linked protein VPg |
Q27658157 | Structure of the Flexible Amino-Terminal Domain of Prion Protein Bound to a Sulfated Glycan |
Q36638977 | Structure-based Inhibitor Design for the Intrinsically Disordered Protein c-Myc |
Q36020398 | Targeting intrinsically disordered proteins in neurodegenerative and protein dysfunction diseases: another illustration of the D(2) concept |
Q57043848 | The 124202 candidate effector ofMelampsora larici-populinainteracts with membranes inNicotianaandArabidopsis |
Q40326289 | The BECN1 N-terminal domain is intrinsically disordered |
Q30009088 | The Disordered Region of the HCV Protein NS5A: Conformational Dynamics, SH3 Binding, and Phosphorylation |
Q39957451 | The challenge of increasing Pfam coverage of the human proteome |
Q28080017 | The contribution of intrinsically disordered regions to protein function, cellular complexity, and human disease |
Q34264016 | The dynamics of signal amplification by macromolecular assemblies for the control of chromosome segregation |
Q30361131 | The evolution of protein structures and structural ensembles under functional constraint. |
Q51066033 | The functional roles of the unstructured N- and C-terminal regions in αB-crystallin and other mammalian small heat-shock proteins. |
Q27685219 | The hepatitis B virus preS1 domain hijacks host trafficking proteins by motif mimicry |
Q34251310 | The hepatitis E virus polyproline region is involved in viral adaptation |
Q33977801 | The high-molecular-weight kininogen domain 5 is an intrinsically unstructured protein and its interaction with ferritin is metal mediated. |
Q42252683 | The human selenoprotein VCP-interacting membrane protein (VIMP) is non-globular and harbors a reductase function in an intrinsically disordered region |
Q39850928 | The interaction between the measles virus nucleoprotein and the Interferon Regulator Factor 3 relies on a specific cellular environment |
Q28749496 | The intrinsically disordered N-terminal domain of thymidylate synthase targets the enzyme to the ubiquitin-independent proteasomal degradation pathway |
Q39032659 | The multifaceted benefits of protein co-expression in Escherichia coli |
Q38527462 | The multifaceted roles of intrinsic disorder in protein complexes |
Q37462521 | The mysterious unfoldome: structureless, underappreciated, yet vital part of any given proteome |
Q34046537 | The protein kingdom extended: ordered and intrinsically disordered proteins, their folding, supramolecular complex formation, and aggregation. |
Q35907671 | The relationship between proteome size, structural disorder and organism complexity |
Q37938718 | The role of protein disorder in the 14-3-3 interaction network |
Q38806231 | Therapeutic Interventions of Cancers Using Intrinsically Disordered Proteins as Drug Targets: c-Myc as Model System. |
Q41650438 | Towards the Analysis of High Molecular Weight Proteins and Protein complexes using TIMS-MS. |
Q53143914 | Troponins, intrinsic disorder, and cardiomyopathy. |
Q51060526 | Tuning the precision of predictors to reduce overestimation of protein disorder over large datasets. |
Q30385084 | Understanding protein non-folding. |
Q36821293 | Understanding the structural ensembles of a highly extended disordered protein |
Q27660091 | Urea denatured state ensembles contain extensive secondary structure that is increased in hydrophobic proteins |
Q27012942 | What macromolecular crowding can do to a protein |
Q46237020 | Zoonotic Hepatitis E Virus: An Ignored Risk for Public Health |
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