| scholarly article | Q13442814 |
| P50 | author | H. Jane Dyson | Q30513249 |
| P2860 | cites work | Short Linear Motifs recognized by SH2, SH3 and Ser/Thr Kinase domains are conserved in disordered protein regions | Q21263144 |
| 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 | ||
| Intrinsic disorder explains diverse nuclear roles of chromatin remodeling proteins | Q22061745 | ||
| Cdk-inhibitory activity and stability of p27Kip1 are directly regulated by oncogenic tyrosine kinases | Q24294546 | ||
| Monomeric complex of human orphan estrogen related receptor-2 with DNA: a pseudo-dimer interface mediates extended half-site recognition | Q24298361 | ||
| Structure of the MDM2 oncoprotein bound to the p53 tumor suppressor transactivation domain | Q24314763 | ||
| Structure of factor-inhibiting hypoxia-inducible factor (HIF) reveals mechanism of oxidative modification of HIF-1 alpha | Q24320267 | ||
| Structural basis for recruitment of CBP/p300 by hypoxia-inducible factor-1 alpha | Q24534120 | ||
| Grasping at molecular interactions and genetic networks in Drosophila melanogaster using FlyNets, an Internet database | Q24548382 | ||
| Alternative splicing in concert with protein intrinsic disorder enables increased functional diversity in multicellular organisms | Q24548466 | ||
| Identification, analysis, and prediction of protein ubiquitination sites | Q24624622 | ||
| Structural diversity in p160/CREB-binding protein coactivator complexes | Q82842846 | ||
| Influence of flanking sequences on signaling between the activation function AF1 and DNA-binding domain of the glucocorticoid receptor | Q83061141 | ||
| Phosphorylation-induced transient intrinsic structure in the kinase-inducible domain of CREB facilitates its recognition by the KIX domain of CBP | Q83949081 | ||
| Searching DNA via a "Monkey Bar" mechanism: the significance of disordered tails | Q84976179 | ||
| Smoothing molecular interactions: the "kinetic buffer" effect of intrinsically disordered proteins | Q85200800 | ||
| Mapping the interactions of the p53 transactivation domain with the KIX domain of CBP | Q24650130 | ||
| Structural basis for p300 Taz2-p53 TAD1 binding and modulation by phosphorylation | Q24653926 | ||
| Cooperative regulation of p53 by modulation of ternary complex formation with CBP/p300 and HDM2 | Q24655602 | ||
| MeDor: a metaserver for predicting protein disorder | Q24658193 | ||
| Residual structure, backbone dynamics, and interactions within the synuclein family | Q24671058 | ||
| DisProt: the Database of Disordered Proteins | Q24675789 | ||
| Polyelectrostatic interactions of disordered ligands suggest a physical basis for ultrasensitivity | Q24676374 | ||
| Serine/arginine-rich splicing factors belong to a class of intrinsically disordered proteins | Q25257115 | ||
| Regulating highly dynamic unstructured proteins and their coding mRNAs | Q27488434 | ||
| Inherent flexibility in a potent inhibitor of blood coagulation, recombinant nematode anticoagulant protein c2 | Q27619799 | ||
| Mutual synergistic folding in recruitment of CBP/p300 by p160 nuclear receptor coactivators | Q27637572 | ||
| Structural basis for Hif-1 alpha /CBP recognition in the cellular hypoxic response | Q27638869 | ||
| Structure of human FIH-1 reveals a unique active site pocket and interaction sites for HIF-1 and von Hippel-Lindau | Q27640157 | ||
| Antibody multispecificity mediated by conformational diversity | Q27640592 | ||
| Structural basis for negative regulation of hypoxia-inducible factor-1alpha by CITED2 | Q27641363 | ||
| Interaction of the TAZ1 domain of the CREB-binding protein with the activation domain of CITED2: regulation by competition between intrinsically unstructured ligands for non-identical binding sites | Q27642464 | ||
| Allosteric Activation of E2-RING Finger-Mediated Ubiquitylation by a Structurally Defined Specific E2-Binding Region of gp78 | Q27646351 | ||
| Conformational Dynamics and Structural Plasticity Play Critical Roles in the Ubiquitin Recognition of a UIM Domain | Q27646623 | ||
| Structure of the retinoblastoma protein bound to adenovirus E1A reveals the molecular basis for viral oncoprotein inactivation of a tumor suppressor | Q27648933 | ||
| Structural basis for recruitment of CBP/p300 coactivators by STAT1 and STAT2 transactivation domains | Q27653760 | ||
| Structural basis for subversion of cellular control mechanisms by the adenoviral E1A oncoprotein | Q27656864 | ||
| Structure and dynamics of NBD1 from CFTR characterized using crystallography and hydrogen/deuterium exchange mass spectrometry | Q27658358 | ||
| Allostery and intrinsic disorder mediate transcription regulation by conditional cooperativity | Q27663130 | ||
| Conformational selection in the molten globule state of the nuclear coactivator binding domain of CBP | Q27663290 | ||
| Structure of the p53 Transactivation Domain in Complex with the Nuclear Receptor Coactivator Binding Domain of CREB Binding Protein | Q27665216 | ||
| Arginine Kinase: Joint Crystallographic and NMR RDC Analyses Link Substrate-Associated Motions to Intrinsic Flexibility | Q27665875 | ||
| Three-dimensional solution structure of a single zinc finger DNA-binding domain | Q27694563 | ||
| Structural basis for DNA bending by the architectural transcription factor LEF-1 | Q27729834 | ||
| Solution Structure of the KIX Domain of CBP Bound to the Transactivation Domain of CREB: A Model for Activator:Coactivator Interactions | Q27748755 | ||
| Structure of the retinoblastoma tumour-suppressor pocket domain bound to a peptide from HPV E7 | Q27748910 | ||
| High-resolution solution structure of the retinoid X receptor DNA-binding domain | Q27764990 | ||
| Intrinsically disordered protein | Q28191444 | ||
| Intrinsic disorder in cell-signaling and cancer-associated proteins | Q28207698 | ||
| Extended disordered proteins: targeting function with less scaffold | Q28208096 | ||
| Plasmodium falciparum merozoite surface protein 2 is unstructured and forms amyloid-like fibrils | Q37270041 | ||
| Conformational selection or induced fit: a flux description of reaction mechanism | Q37310586 | ||
| Thermodynamic basis for the optimization of binding-induced biomolecular switches and structure-switching biosensors | Q37310615 | ||
| Colicins exploit native disorder to gain cell entry: a hitchhiker's guide to translocation | Q37330470 | ||
| Flexible structures and ligand interactions of tandem repeats consisting of proline, glycine, asparagine, serine, and/or threonine rich oligopeptides in proteins | Q37347477 | ||
| Protein disorder is positively correlated with gene expression in Escherichia coli | Q37369375 | ||
| Binding of small-molecule ligands to proteins: "what you see" is not always "what you get". | Q37372747 | ||
| Linking folding and binding | Q37373866 | ||
| Biophysical characterization of intrinsically disordered proteins | Q37375367 | ||
| Large-scale analysis of thermostable, mammalian proteins provides insights into the intrinsically disordered proteome | Q37383520 | ||
| Coiled-coils in type III secretion systems: structural flexibility, disorder and biological implications. | Q37392278 | ||
| Reconciling binding mechanisms of intrinsically disordered proteins. | Q37407776 | ||
| Kinetic enhancement of NF-kappaBxDNA dissociation by IkappaBalpha | Q37428998 | ||
| The rules of disorder or why disorder rules | Q37432471 | ||
| Sending signals dynamically | Q37440289 | ||
| Multiple conformations of full-length p53 detected with single-molecule fluorescence resonance energy transfer | Q37469636 | ||
| Intrinsic disorder in proteins associated with neurodegenerative diseases | Q37501827 | ||
| Identical short peptide sequences in unrelated proteins can have different conformations: a testing ground for theories of immune recognition. | Q37527235 | ||
| Acetylation regulates the differentiation-specific functions of the retinoblastoma protein | Q37544561 | ||
| Dynamic interactions of proteins in complex networks: a more structured view. | Q37588014 | ||
| Intrinsically disordered proteins and their environment: effects of strong denaturants, temperature, pH, counter ions, membranes, binding partners, osmolytes, and macromolecular crowding | Q37600691 | ||
| Protein-protein interaction networks: how can a hub protein bind so many different partners? | Q37616866 | ||
| CFTR regulatory region interacts with NBD1 predominantly via multiple transient helices | Q37618800 | ||
| Observing biological dynamics at atomic resolution using NMR. | Q37619100 | ||
| Protein intrinsic disorder and oligomericity in cell signaling | Q37696321 | ||
| Viral disorder or disordered viruses: do viral proteins possess unique features? | Q37745117 | ||
| Reaching biological timescales with all-atom molecular dynamics simulations | Q37799077 | ||
| Angiogenic signaling aberrantly induced by tumor hypoxia | Q37825127 | ||
| Mapping alpha-helical induced folding within the intrinsically disordered C-terminal domain of the measles virus nucleoprotein by site-directed spin-labeling EPR spectroscopy | Q38290276 | ||
| Solution structure of the first three zinc fingers of TFIIIA bound to the cognate DNA sequence: determinants of affinity and sequence specificity | Q38341722 | ||
| Prevalent structural disorder in E. coli and S. cerevisiae proteomes. | Q38517953 | ||
| Amyloid-like aggregates sequester numerous metastable proteins with essential cellular functions | Q39610788 | ||
| Biological regulation via ankyrin repeat folding | Q39895014 | ||
| Mechanism of coupled folding and binding of an intrinsically disordered protein | Q40210194 | ||
| Inferring function using patterns of native disorder in proteins | Q33295214 | ||
| High-speed atomic force microscopy for observing dynamic biomolecular processes | Q33300689 | ||
| Modeling the accessible conformations of the intrinsically unstructured transactivation domain of p53. | Q33304501 | ||
| Flexible nets: disorder and induced fit in the associations of p53 and 14-3-3 with their partners | Q33325589 | ||
| Intrinsically disordered proteins display no preference for chaperone binding in vivo | Q33325882 | ||
| Binding-induced folding of a natively unstructured transcription factor. | Q33327692 | ||
| Dual coding in alternative reading frames correlates with intrinsic protein disorder. | Q33348728 | ||
| Protein intrinsic disorder toolbox for comparative analysis of viral proteins | Q33373579 | ||
| Intrinsic disorder in protein interactions: insights from a comprehensive structural analysis | Q33417626 | ||
| ProtSA: a web application for calculating sequence specific protein solvent accessibilities in the unfolded ensemble. | Q33428317 | ||
| Development of an accurate classification system of proteins into structured and unstructured regions that uncovers novel structural domains: its application to human transcription factors | Q33436460 | ||
| Insights into the regulation of intrinsically disordered proteins in the human proteome by analyzing sequence and gene expression data. | Q33443462 | ||
| Biophysics of Parkinson's disease: structure and aggregation of alpha-synuclein | Q33470625 | ||
| Exploring functional roles of multibinding protein interfaces | Q33480594 | ||
| The mechanism of ubiquitination in the cullin-RING E3 ligase machinery: conformational control of substrate orientation | Q33508245 | ||
| Intrinsic structural disorder confers cellular viability on oncogenic fusion proteins | Q33514873 | ||
| Unfoldomics of human genetic diseases: illustrative examples of ordered and intrinsically disordered members of the human diseasome | Q33517783 | ||
| Extensive and modular intrinsically disordered segments in C. elegans TTN-1 and implications in filament binding, elasticity and oblique striation | Q33546833 | ||
| The importance of being flexible: the case of basic region leucine zipper transcriptional regulators | Q33566030 | ||
| Archaic chaos: intrinsically disordered proteins in Archaea | Q33593571 | ||
| ComSin: database of protein structures in bound (complex) and unbound (single) states in relation to their intrinsic disorder | Q33601021 | ||
| Reduction in structural disorder and functional complexity in the thermal adaptation of prokaryotes | Q33658850 | ||
| Molecular dynamics reveal the essential role of linker motions in the function of cullin-RING E3 ligases | Q33665546 | ||
| Theory, practice, and applications of paramagnetic relaxation enhancement for the characterization of transient low-population states of biological macromolecules and their complexes. | Q33671554 | ||
| Structure of the recombinant full-length hamster prion protein PrP(29-231): the N terminus is highly flexible | Q33705415 | ||
| Library of disordered patterns in 3D protein structures. | Q33728497 | ||
| Cryoprotective mechanism of a small intrinsically disordered dehydrin protein | Q33732719 | ||
| Multitude of binding modes attainable by intrinsically disordered proteins: a portrait gallery of disorder-based complexes | Q33737866 | ||
| Nonnative interactions in coupled folding and binding processes of intrinsically disordered proteins | Q33747704 | ||
| Conformational analysis of the partially disordered measles virus N(TAIL)-XD complex by SDSL EPR spectroscopy | Q33767753 | ||
| Release of long-range tertiary interactions potentiates aggregation of natively unstructured alpha-synuclein | Q33817987 | ||
| Phosphorylation-induced structural changes in smooth muscle myosin regulatory light chain | Q33929417 | ||
| Net charge per residue modulates conformational ensembles of intrinsically disordered proteins | Q33929602 | ||
| Role of secondary structure in discrimination between constitutive and inducible activators | Q33958946 | ||
| Reduced amino acid alphabet is sufficient to accurately recognize intrinsically disordered protein. | Q51595638 | ||
| NMR characterization of long-range order in intrinsically disordered proteins. | Q51695027 | ||
| Low-resolution structures of transient protein-protein complexes using small-angle X-ray scattering. | Q51775382 | ||
| The C-terminal domain of the HIV-1 Vif protein is natively unfolded in its unbound state. | Q51820176 | ||
| Intrinsically disordered p53 extreme C-terminus binds to S100B(betabeta) through "fly-casting". | Q51822571 | ||
| Protein intrinsic disorder and human papillomaviruses: increased amount of disorder in E6 and E7 oncoproteins from high risk HPVs. | Q51936092 | ||
| The protein trinity--linking function and disorder. | Q52055900 | ||
| "Partly folded" state, a new equilibrium state of protein molecules: four-state guanidinium chloride-induced unfolding of beta-lactamase at low temperature. | Q52379831 | ||
| Disorder and sequence repeats in hub proteins and their implications for network evolution. | Q52673882 | ||
| Isoform-specific variation in the intrinsic disorder of the ecdysteroid receptor N-terminal domain. | Q52696012 | ||
| The pairwise energy content estimated from amino acid composition discriminates between folded and intrinsically unstructured proteins. | Q52974739 | ||
| Solution NMR studies of an intrinsically unstructured protein within a dilute, 75 kDa eukaryotic protein assembly; probing the practical limits for efficiently assigning polypeptide backbone resonances. | Q53650419 | ||
| Assessing induced folding of an intrinsically disordered protein by site-directed spin-labeling electron paramagnetic resonance spectroscopy. | Q54453977 | ||
| The 'fuzzy' interactome. | Q55051107 | ||
| Multiple hTAF(II)31-binding motifs in the intrinsically unfolded transcriptional activation domain of VP16. | Q55052108 | ||
| Structural Basis for Cooperative Transcription Factor Binding to the CBP Coactivator | Q57078210 | ||
| DNA-induced α-helix capping in conserved linker sequences is a determinant of binding affinity in Cys2-His2 zinc fingers | Q57078232 | ||
| Conformational distributions of unfolded polypeptides from novel NMR techniques | Q57080193 | ||
| Residual Dipolar Couplings in Short Peptides Reveal Systematic Conformational Preferences of Individual Amino Acids | Q57080210 | ||
| Local Structural Elements in the Mostly Unstructured Transcriptional Activation Domain of Human p53 | Q57650265 | ||
| Protein interactions: is seeing believing? | Q57843262 | ||
| Order, Disorder, and Flexibility | Q57961420 | ||
| G protein-coupled receptors show unusual patterns of intrinsic unfolding | Q57998428 | ||
| Protein interactions: integration leads to belief | Q58062729 | ||
| Effect of sampling on topology predictions of protein-protein interaction networks | Q58067825 | ||
| Thermodynamic characterization of interactions between p27Kip1 and activated and non-activated Cdk2: Intrinsically unstructured proteins as thermodynamic tethers | Q58157265 | ||
| Structural Characterization of the Intrinsically Unfolded Protein β-Synuclein, a Natural Negative Regulator of α-Synuclein Aggregation | Q58484313 | ||
| The reactivity of anti-peptide antibodies is a function of the atomic mobility of sites in a protein | Q59071650 | ||
| The C-terminal half of the anti-sigma factor, FlgM, becomes structured when bound to its target, σ28 | Q59210031 | ||
| Stages in the mechanism of self-organization of protein molecules | Q69556345 | ||
| Zinc-dependent structure of a single-finger domain of yeast ADR1 | Q70212486 | ||
| Further evidence on the equilibrium "pre-molten globule state": four-state guanidinium chloride-induced unfolding of carbonic anhydrase B at low temperature | Q70918140 | ||
| Predicting Disordered Regions from Amino Acid Sequence: Common Themes Despite Differing Structural Characterization | Q73174424 | ||
| Folding minimal sequences: the lower bound for sequence complexity of globular proteins | Q73327910 | ||
| Macromolecular interactions: tracing the roots | Q73493196 | ||
| The protein non-folding problem: amino acid determinants of intrinsic order and disorder | Q73658941 | ||
| Structural basis of thermostability in hyperthermophilic proteins, or "there's more than one way to skin a cat" | Q73995814 | ||
| The C-terminal half of the anti-sigma factor FlgM contains a dynamic equilibrium solution structure favoring helical conformations | Q74137795 | ||
| Intrinsic protein disorder in complete genomes | Q77145749 | ||
| Role of intrinsic disorder in transient interactions of hub proteins | Q79416219 | ||
| Structure of the Tfb1/p53 complex: Insights into the interaction between the p62/Tfb1 subunit of TFIIH and the activation domain of p53 | Q79773486 | ||
| Intrinsic disorder in yeast transcriptional regulatory network | Q80353265 | ||
| Probing single-molecule protein conformational dynamics | Q80392008 | ||
| NMR characterization of the dynamics of biomacromolecules | Q80435130 | ||
| Dynamics of well-folded and natively disordered proteins in solution: a time-of-flight neutron scattering study | Q80567696 | ||
| Mechanism of induced folding: Both folding before binding and binding before folding can be realized in staphylococcal nuclease mutants | Q80660538 | ||
| Helix A stabilization precedes amino-terminal lobe activation upon calcium binding to calmodulin | Q81762087 | ||
| Calmodulin signaling: analysis and prediction of a disorder-dependent molecular recognition | Q82627891 | ||
| Protein allostery, signal transmission and dynamics: a classification scheme of allosteric mechanisms | Q33968222 | ||
| Rbx1 flexible linker facilitates cullin-RING ligase function before neddylation and after deneddylation | Q34032707 | ||
| Narrowing of protein NMR spectral lines broadened by chemical exchange | Q34064443 | ||
| Malleable machines take shape in eukaryotic transcriptional regulation | Q34066027 | ||
| Structure/function implications in a dynamic complex of the intrinsically disordered Sic1 with the Cdc4 subunit of an SCF ubiquitin ligase | Q34074606 | ||
| From the Cover: Charge interactions can dominate the dimensions of intrinsically disordered proteins. | Q34093140 | ||
| Conformational spread as a mechanism for cooperativity in the bacterial flagellar switch | Q34097033 | ||
| Probing structural transitions in the intrinsically disordered C-terminal domain of the measles virus nucleoprotein by vibrational spectroscopy of cyanylated cysteines | Q34098982 | ||
| The structural basis of peptide-protein binding strategies. | Q34099027 | ||
| Modular structure of transcription factors: implications for gene regulation | Q34110705 | ||
| Structural diversity in free and bound states of intrinsically disordered protein phosphatase 1 regulators | Q34116108 | ||
| Osmolyte-induced folding of an intrinsically disordered protein: folding mechanism in the absence of ligand | Q34118594 | ||
| Power law distribution defines structural disorder as a structural element directly linked with function | Q34135998 | ||
| Catalytic and chaperone-like functions in an intrinsically disordered protein associated with desiccation tolerance | Q34136216 | ||
| Structure-independent analysis of the breadth of the positional distribution of disordered groups in macromolecules from order parameters for long, variable-length vectors using NMR paramagnetic relaxation enhancement | Q34152575 | ||
| How viruses hijack cell regulation | Q34154109 | ||
| Flexible Regions within IκBα Create the Ubiquitin-independent Degradation Signal | Q34236735 | ||
| Strategy for complete NMR assignment of disordered proteins with highly repetitive sequences based on resolution-enhanced 5D experiments | Q34252327 | ||
| ‘Molten‐globule state’: a compact form of globular proteins with mobile side‐chains | Q34255230 | ||
| Conformational preferences of synthetic peptides derived from the immunodominant site of the circumsporozoite protein of Plasmodium falciparum by 1H NMR. | Q34276542 | ||
| Graded enhancement of p53 binding to CREB-binding protein (CBP) by multisite phosphorylation | Q34320186 | ||
| CBP/p300 TAZ1 domain forms a structured scaffold for ligand binding | Q34383065 | ||
| FoldIndex: a simple tool to predict whether a given protein sequence is intrinsically unfolded | Q34426417 | ||
| PDZ binding to the BAR domain of PICK1 is elucidated by coarse-grained molecular dynamics | Q34432049 | ||
| Secondary structure and dynamics of an intrinsically unstructured linker domain | Q34439134 | ||
| Induced fit, conformational selection and independent dynamic segments: an extended view of binding events | Q34479883 | ||
| An intrinsically disordered C terminus allows the La protein to assist the biogenesis of diverse noncoding RNA precursors | Q34533704 | ||
| Detection of a ternary complex of NF-kappaB and IkappaBalpha with DNA provides insights into how IkappaBalpha removes NF-kappaB from transcription sites | Q34533797 | ||
| The N-terminus of the intrinsically disordered protein α-synuclein triggers membrane binding and helix folding | Q34590797 | ||
| Intrinsic disorder in scaffold proteins: getting more from less | Q34594105 | ||
| Structure and function of PICK1. | Q34600317 | ||
| Verification of alternative splicing variants based on domain integrity, truncation length and intrinsic protein disorder | Q34609175 | ||
| Natively unstructured regions in proteins identified from contact predictions | Q34665088 | ||
| Asparagine hydroxylation of the HIF transactivation domain a hypoxic switch | Q28217194 | ||
| Roles of phosphorylation and helix propensity in the binding of the KIX domain of CREB-binding protein by constitutive (c-Myb) and inducible (CREB) activators | Q28219104 | ||
| Cooperativity in transcription factor binding to the coactivator CREB-binding protein (CBP). The mixed lineage leukemia protein (MLL) activation domain binds to an allosteric site on the KIX domain | Q28219772 | ||
| A progesterone receptor co-activator (JDP2) mediates activity through interaction with residues in the carboxyl-terminal extension of the DNA binding domain | Q28249810 | ||
| Analysis of molecular recognition features (MoRFs) | Q28260253 | ||
| Regulation of hypoxia-inducible factor 1 by prolyl and asparaginyl hydroxylases | Q28271592 | ||
| Ubiquitin-independent degradation of proteins by the proteasome | Q28284043 | ||
| Critical scaffolding regions of the tumor suppressor Axin1 are natively unfolded | Q28298690 | ||
| The WW domain: a signalling site in dystrophin? | Q28306741 | ||
| A novel viral oncogene with structural similarity to phospholipase C | Q28307371 | ||
| Structural polymorphism of 441-residue tau at single residue resolution | Q28474834 | ||
| Defining the molecular basis of Arf and Hdm2 interactions | Q28507075 | ||
| The importance of intrinsic disorder for protein phosphorylation | Q28776125 | ||
| Conformational preferences in the Ser133-phosphorylated and non-phosphorylated forms of the kinase inducible transactivation domain of CREB | Q28910220 | ||
| Structural studies of p21Waf1/Cip1/Sdi1 in the free and Cdk2-bound state: conformational disorder mediates binding diversity | Q28910326 | ||
| Peptides derived from two dynamically disordered proteins self-assemble into amyloid-like fibrils | Q28910441 | ||
| A large intrinsically disordered region in SKIP and its disorder-order transition induced by PPIL1 binding revealed by NMR | Q28910448 | ||
| Error and attack tolerance of complex networks | Q29547268 | ||
| Protein disorder prediction: implications for structural proteomics | Q29615736 | ||
| GlobPlot: Exploring protein sequences for globularity and disorder | Q29615737 | ||
| Why are "natively unfolded" proteins unstructured under physiologic conditions? | Q29615739 | ||
| Intrinsically unstructured proteins: re-assessing the protein structure-function paradigm | Q29615865 | ||
| 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 | ||
| Sequence complexity of disordered protein | Q29616420 | ||
| Structural characterization of flexible proteins using small-angle X-ray scattering | Q29617289 | ||
| Funnels, pathways, and the energy landscape of protein folding: a synthesis | Q29617521 | ||
| Steroid receptor interactions with heat shock protein and immunophilin chaperones | Q29619628 | ||
| Analysis of structured and intrinsically disordered regions of transmembrane proteins | Q30157208 | ||
| Paramagnetic relaxation enhancements in unfolded proteins: theory and application to drkN SH3 domain | Q30157222 | ||
| Increased backbone mobility in beta-barrel enhances entropy gain driving binding of N-TIMP-1 to MMP-3. | Q30164834 | ||
| Conformational switch upon phosphorylation: human CDK inhibitor p19INK4d between the native and partially folded state | Q30319246 | ||
| Flexible nets. The roles of intrinsic disorder in protein interaction networks. | Q30351593 | ||
| Length-dependent prediction of protein intrinsic disorder. | Q30353929 | ||
| Computational studies of protein regulation by post-translational phosphorylation. | Q30375915 | ||
| Protein dynamism and evolvability. | Q30376087 | ||
| Modularity of intrinsic disorder in the human proteome. | Q30379187 | ||
| Toward a quantitative theory of intrinsically disordered proteins and their function | Q30382415 | ||
| Structure and Dynamics of Ribosomal Protein L12: An Ensemble Model Based on SAXS and NMR Relaxation | Q40625926 | ||
| Sequence determinants of compaction in intrinsically disordered proteins | Q40626286 | ||
| High-resolution crystal structure of the human Notch 1 ankyrin domain | Q40726164 | ||
| The intermembrane space domain of Tim23 is intrinsically disordered with a distinct binding region for presequences | Q41294423 | ||
| The IkappaBalpha/NF-kappaB complex has two hot spots, one at either end of the interface | Q41492776 | ||
| Spectroscopic studies of GSK3{beta} phosphorylation of the neuronal tau protein and its interaction with the N-terminal domain of apolipoprotein E. | Q41771621 | ||
| Conservation of intrinsic disorder in protein domains and families: I. A database of conserved predicted disordered regions | Q41851853 | ||
| Order within disorder: aggrecan chondroitin sulphate-attachment region provides new structural insights into protein sequences classified as disordered | Q41870328 | ||
| NMR evidence for differential phosphorylation-dependent interactions in WT and DeltaF508 CFTR. | Q41882930 | ||
| Structural characterization of unphosphorylated STAT5a oligomerization equilibrium in solution by small-angle X-ray scattering. | Q41904480 | ||
| An unfolded CH1 domain controls the assembly and secretion of IgG antibodies. | Q41975011 | ||
| Structural characterization of the active and inactive states of Src kinase in solution by small-angle X-ray scattering. | Q42030942 | ||
| Stabilizing IkappaBalpha by "consensus" design | Q42085776 | ||
| The RelA nuclear localization signal folds upon binding to IκBα. | Q42129907 | ||
| Crystal structure of IRF-3 in complex with CBP. | Q42152366 | ||
| Modeling intrinsically disordered proteins with bayesian statistics | Q42408893 | ||
| A robust approach for analyzing a heterogeneous structural ensemble | Q42437093 | ||
| A homeostatic model of IkappaB metabolism to control constitutive NF-kappaB activity | Q42512304 | ||
| Facilitated DNA search by multidomain transcription factors: cross talk via a flexible linker | Q42535577 | ||
| Overlapping genes produce proteins with unusual sequence properties and offer insight into de novo protein creation | Q42570606 | ||
| E46K Parkinson's-linked mutation enhances C-terminal-to-N-terminal contacts in alpha-synuclein | Q42672293 | ||
| Susceptibility of p53 unstructured N terminus to 20 S proteasomal degradation programs the stress response. | Q42680947 | ||
| Detection of transient interchain interactions in the intrinsically disordered protein alpha-synuclein by NMR paramagnetic relaxation enhancement | Q42703911 | ||
| Proteomic studies of the intrinsically unstructured mammalian proteome. | Q42834771 | ||
| The role of disorder in interaction networks: a structural analysis | Q42924615 | ||
| Loss of post-translational modification sites in disease | Q42927113 | ||
| Polyglutamine disruption of the huntingtin exon 1 N terminus triggers a complex aggregation mechanism | Q43100835 | ||
| Thermodynamics reveal that helix four in the NLS of NF-kappaB p65 anchors IkappaBalpha, forming a very stable complex. | Q43130560 | ||
| Characterization of the regions involved in the calcium-induced folding of the intrinsically disordered RTX motifs from the bordetella pertussis adenylate cyclase toxin. | Q43185587 | ||
| The specificity of cross‐reactivity: Promiscuous antibody binding involves specific hydrogen bonds rather than nonspecific hydrophobic stickiness | Q43205446 | ||
| Increase in backbone mobility of the VTS1p-SAM domain on binding to SRE-RNA. | Q43224776 | ||
| Transfer of flexibility between ankyrin repeats in IkappaB* upon formation of the NF-kappaB complex | Q43227326 | ||
| Thermodynamic aspects of coupled binding and folding of an intrinsically disordered protein: a computational alanine scanning study | Q43247103 | ||
| Characterization of intrinsically disordered proteins with electrospray ionization mass spectrometry: conformational heterogeneity of alpha-synuclein | Q43256880 | ||
| The nanny model for IDPs. | Q43258539 | ||
| Conformational changes specific for pseudophosphorylation at serine 262 selectively impair binding of tau to microtubules | Q43273610 | ||
| Kinetics and thermodynamics of the interaction of 1-anilino-naphthalene-8-sulfonate with proteins | Q43291463 | ||
| Structural rationale for the coupled binding and unfolding of the c-Myc oncoprotein by small molecules | Q43945988 | ||
| Direct observation of structural heterogeneity in a beta-sheet | Q44126837 | ||
| Activation of the redox-regulated chaperone Hsp33 by domain unfolding. | Q44801421 | ||
| The LEF-1 high-mobility group domain undergoes a disorder-to-order transition upon formation of a complex with cognate DNA. | Q44965707 | ||
| The zinc-dependent redox switch domain of the chaperone Hsp33 has a novel fold | Q45029981 | ||
| Energetics of structural transitions of the addiction antitoxin MazE: is a programmed bacterial cell death dependent on the intrinsically flexible nature of the antitoxins? | Q45285817 | ||
| Alpha-synuclein structures probed by 5-fluorotryptophan fluorescence and 19F NMR spectroscopy. | Q45950766 | ||
| Energetics of MazG unfolding in correlation with its structural features. | Q45970578 | ||
| Structural characterization of the natively unfolded N-terminal domain of human c-Src kinase: insights into the role of phosphorylation of the unique domain. | Q45972692 | ||
| Local structural plasticity of the prion protein. Analysis of NMR relaxation dynamics | Q46074568 | ||
| The cell as a collection of protein machines: preparing the next generation of molecular biologists | Q46148013 | ||
| Small-molecule perturbation of competing interactions between c-Myc and Max. | Q46180274 | ||
| RTX calcium binding motifs are intrinsically disordered in the absence of calcium: implication for protein secretion. | Q46241353 | ||
| Role of backbone-solvent interactions in determining conformational equilibria of intrinsically disordered proteins | Q46594558 | ||
| Reconciling observations of sequence-specific conformational propensities with the generic polymeric behavior of denatured proteins | Q46662533 | ||
| Uncovering the unfoldome: enriching cell extracts for unstructured proteins by acid treatment | Q46741729 | ||
| All-atom Monte Carlo approach to protein-peptide binding | Q46751333 | ||
| A novel two-dimensional electrophoresis technique for the identification of intrinsically unstructured proteins | Q46751790 | ||
| Rational drug design via intrinsically disordered protein | Q47193604 | ||
| Alternate states of proteins revealed by detailed energy landscape mapping | Q30396213 | ||
| Single-stranded DNA mimicry in the p53 transactivation domain interaction with replication protein A | Q30446685 | ||
| Structure and kinetics of a transient antibody binding intermediate reveal a kinetic discrimination mechanism in antigen recognition | Q30476133 | ||
| A high-speed atomic force microscope for studying biological macromolecules. | Q30732098 | ||
| NMR relaxation studies on the hydrate layer of intrinsically unstructured proteins | Q30979050 | ||
| EspB from enterohaemorrhagic Escherichia coli is a natively partially folded protein | Q30981321 | ||
| Residual structure in disordered peptides and unfolded proteins from multivariate analysis and ab initio simulation of Raman optical activity data | Q31122954 | ||
| Biophysical characterization of the free IkappaBalpha ankyrin repeat domain in solution. | Q33204174 | ||
| Intrinsic disorder is a common feature of hub proteins from four eukaryotic interactomes | Q33252616 | ||
| Prediction of amyloidogenic and disordered regions in protein chains | Q33267899 | ||
| Energetic determinants of protein binding specificity: insights into protein interaction networks | Q47590562 | ||
| Intrinsic disorder in pathogenic and non-pathogenic microbes: discovering and analyzing the unfoldomes of early-branching eukaryotes | Q47702038 | ||
| Protein disorder and the evolution of molecular recognition: theory, predictions and observations | Q47715145 | ||
| Thousands of proteins likely to have long disordered regions. | Q47715178 | ||
| Use of protonless NMR spectroscopy to alleviate the loss of information resulting from exchange-broadening. | Q47830265 | ||
| Multiple independent binding sites for small-molecule inhibitors on the oncoprotein c-Myc. | Q47830329 | ||
| Sequence similarity of phospholipase C with the non-catalytic region of src. | Q48099424 | ||
| Coupled folding and binding with alpha-helix-forming molecular recognition elements | Q48122045 | ||
| Evolutionary rate heterogeneity in proteins with long disordered regions. | Q48626135 | ||
| Biochemistry. An ensemble view of allostery. | Q50334078 | ||
| Fuzzy complexes: polymorphism and structural disorder in protein-protein interactions | Q34720702 | ||
| Sticking together? Falling apart? Exploring the dynamics of the interactome | Q34771682 | ||
| Tight regulation of unstructured proteins: from transcript synthesis to protein degradation | Q34890013 | ||
| The client protein p53 adopts a molten globule-like state in the presence of Hsp90. | Q34928219 | ||
| Phosphorylated intrinsically disordered region of FACT masks its nucleosomal DNA binding elements | Q34992426 | ||
| Cell regulation: determined to signal discrete cooperation | Q35002154 | ||
| Synergistic interplay between promoter recognition and CBP/p300 coactivator recruitment by FOXO3a | Q35007540 | ||
| Speeding molecular recognition by using the folding funnel: the fly-casting mechanism | Q35189399 | ||
| Molecular mechanisms of amyloidosis | Q35194628 | ||
| Regions of IkappaBalpha that are critical for its inhibition of NF-kappaB.DNA interaction fold upon binding to NF-kappaB | Q35539707 | ||
| The intrinsically disordered cytoplasmic domain of the T cell receptor zeta chain binds to the nef protein of simian immunodeficiency virus without a disorder-to-order transition | Q35580612 | ||
| Sequence-specific solvent accessibilities of protein residues in unfolded protein ensembles. | Q35606668 | ||
| The role of structural disorder in the function of RNA and protein chaperones | Q35850848 | ||
| Unfolded proteins and protein folding studied by NMR. | Q35860163 | ||
| Macromolecular crowding in biological systems: hydrodynamics and NMR methods. | Q35884786 | ||
| Natively disordered proteins: functions and predictions | Q36031548 | ||
| Dynamical binding of proline-rich peptides to their recognition domains | Q36276155 | ||
| What drives proteins into the major or minor grooves of DNA? | Q36630637 | ||
| Towards proteomic approaches for the identification of structural disorder | Q36789770 | ||
| 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 | ||
| Tailoring relaxation dispersion experiments for fast-associating protein complexes | Q36871716 | ||
| Characterization of molecular recognition features, MoRFs, and their binding partners | Q36944291 | ||
| Principles of flexible protein-protein docking | Q36952164 | ||
| Intrinsically unstructured domains of Arf and Hdm2 form bimolecular oligomeric structures in vitro and in vivo | Q37032577 | ||
| The effects of conformational heterogeneity on the binding of the Notch intracellular domain to effector proteins: a case of biologically tuned disorder | Q37117911 | ||
| Interplay of alpha-synuclein binding and conformational switching probed by single-molecule fluorescence. | Q37153744 | ||
| TOP-IDP-scale: a new amino acid scale measuring propensity for intrinsic disorder | Q37178764 | ||
| CDF it all: consensus prediction of intrinsically disordered proteins based on various cumulative distribution functions | Q37195737 | ||
| Chemical and biological folding contribute to temperature-sensitive DeltaF508 CFTR trafficking | Q37196094 | ||
| Prediction of the rotational tumbling time for proteins with disordered segments | Q37223434 | ||
| Protein intrinsic disorder and influenza virulence: the 1918 H1N1 and H5N1 viruses | Q37241586 | ||
| Amino acid repeats and the structure and evolution of proteins | Q37254903 | ||
| P433 | issue | 4 | |
| P921 | main subject | protein folding | Q847556 |
| P304 | page(s) | 467-518 | |
| P577 | publication date | 2011-07-01 | |
| P1433 | published in | Quarterly Reviews of Biophysics | Q2361372 |
| P1476 | title | Expanding the proteome: disordered and alternatively folded proteins | |
| P478 | volume | 44 |
| Q34575566 | A novel inhibitor of α9α10 nicotinic acetylcholine receptors from Conus vexillum delineates a new conotoxin superfamily. |
| Q38124811 | A serendipitous survey of prediction algorithms for amyloidogenicity |
| Q30358999 | Advantages of proteins being disordered. |
| Q38019703 | Beyond 'furballs' and 'dumpling soups' - towards a molecular architecture of signaling complexes and networks |
| Q37145661 | CD44 receptor unfolding enhances binding by freeing basic amino acids to contact carbohydrate ligand |
| Q34295598 | Computational analysis of position-dependent disorder content in DisProt database |
| Q37214509 | Computational characterization of moonlighting proteins |
| Q34302314 | Conditional disorder in chaperone action |
| Q30402882 | Conditionally disordered proteins: bringing the environment back into the fold |
| Q38116495 | Conformational propensities of intrinsically disordered proteins from NMR chemical shifts |
| Q37428842 | Construction and application of a protein interaction map for white spot syndrome virus (WSSV). |
| Q35036034 | Deciphering the binding between Nupr1 and MSL1 and their DNA-repairing activity |
| Q30402101 | Digested disorder: Quarterly intrinsic disorder digest (April-May-June, 2013). |
| Q38779717 | Disorder in the lifetime of a protein |
| Q46125144 | Do intrinsically disordered proteins possess high specificity in protein-protein interactions? |
| Q36071932 | Dynamical coupling of intrinsically disordered proteins and their hydration water: comparison with folded soluble and membrane proteins |
| Q37354855 | Effects of Macromolecular Crowding on the Conformational Ensembles of Disordered Proteins |
| Q39005050 | Erythropoietin and co.: intrinsic structure and functional disorder |
| Q34107289 | Expanding the proteome of an RNA virus by phosphorylation of an intrinsically disordered viral protein |
| Q34390377 | Fast association and slow transitions in the interaction between two intrinsically disordered protein domains |
| Q44486815 | From protein sequence to dynamics and disorder with DynaMine |
| Q26830798 | From systems to structure: bridging networks and mechanism |
| Q27316805 | Functional diversity and structural disorder in the human ubiquitination pathway |
| Q44205166 | Genetic separation of Sae2 nuclease activity from Mre11 nuclease functions in budding yeast |
| Q36747788 | How bacteria survive an acid trip |
| Q39398150 | Human cytomegalovirus phosphoproteins are hypophosphorylated and intrinsically disordered. |
| Q91806556 | Identification of Moonlighting Proteins in Genomes Using Text Mining Techniques |
| Q35899015 | Insights into Unfolded Proteins from the Intrinsic ϕ/ψ Propensities of the AAXAA Host-Guest Series |
| Q38163534 | Intrinsic Disorder in the Kinesin Superfamily. |
| Q37649609 | Intrinsic disorder in biomarkers of insulin resistance, hypoadiponectinemia, and endothelial dysfunction among the type 2 diabetic patients |
| Q28542604 | Intrinsically disordered and pliable Starmaker-like protein from medaka (Oryzias latipes) controls the formation of calcium carbonate crystals |
| Q40488052 | Intrinsically disordered caldesmon binds calmodulin via the "buttons on a string" mechanism |
| Q42318119 | Intrinsically disordered proteins drive enamel formation via an evolutionarily conserved self-assembly motif |
| Q38044411 | Intrinsically disordered proteins: administration not executive. |
| Q36218605 | Kinesin tail domains are intrinsically disordered. |
| Q44458262 | Kinetic modulation of a disordered protein domain by phosphorylation |
| Q91817045 | Life in Phases: Intra- and Inter- Molecular Phase Transitions in Protein Solutions |
| Q36678743 | Making Sense of Intrinsically Disordered Proteins |
| Q42536043 | Mechanism of cell cycle entry mediated by the intrinsically disordered protein p27(Kip1). |
| Q38724763 | Modulation of Intrinsically Disordered Protein Function by Post-translational Modifications |
| Q36615930 | Molecular Recognition by Templated Folding of an Intrinsically Disordered Protein |
| Q37218609 | Multiscaled exploration of coupled folding and binding of an intrinsically disordered molecular recognition element in measles virus nucleoprotein. |
| Q89849097 | New technologies to analyse protein function: an intrinsic disorder perspective |
| Q40912194 | Phosphorylation-coupled intramolecular dynamics of unstructured regions in chromatin remodeler FACT. |
| Q37981477 | Physical chemistry of polyglutamine: intriguing tales of a monotonous sequence |
| Q35051967 | Prediction of Intrinsic Disorder in MERS-CoV/HCoV-EMC Supports a High Oral-Fecal Transmission |
| Q39775009 | Promising in Vitro anti-Alzheimer Properties for a Ruthenium(III) Complex |
| Q41842857 | Protein flexibility, not disorder, is intrinsic to molecular recognition |
| Q60238099 | Q&A: repeat-containing proteins |
| Q33558920 | RAG2's acidic hinge restricts repair-pathway choice and promotes genomic stability |
| Q36397739 | Regulation of the H4 tail binding and folding landscapes via Lys-16 acetylation. |
| Q35746730 | Revealing the Mechanisms of Protein Disorder and N-Glycosylation in CD44-Hyaluronan Binding Using Molecular Simulation |
| Q37923321 | Roles of intrinsic disorder in protein-nucleic acid interactions |
| Q36374431 | SS-map: Visualizing cooperative secondary structure elements in protein ensembles |
| Q41520412 | Serine phosphorylation suppresses huntingtin amyloid accumulation by altering protein aggregation properties. |
| Q56890280 | Single-molecule force spectroscopy of rapidly fluctuating, marginally stable structures in the intrinsically disordered protein α-synuclein |
| Q42151102 | Specificity and affinity quantification of flexible recognition from underlying energy landscape topography |
| Q34270022 | Stereospecific binding of a disordered peptide segment mediates BK channel inactivation. |
| Q92565853 | Structural Basis of the Subcellular Topology Landscape of Escherichia coli |
| Q27690266 | Structural analysis of poly-SUMO chain recognition by the RNF4-SIMs domain |
| Q34845322 | Structural disorder provides increased adaptability for vesicle trafficking pathways |
| Q35608572 | Structural snapshots of actively translating human ribosomes |
| Q27683700 | Structure of the Neisserial outer membrane protein Opa₆₀: loop flexibility essential to receptor recognition and bacterial engulfment |
| Q37173275 | Structure of the transition state for the binding of c-Myb and KIX highlights an unexpected order for a disordered system |
| Q41774543 | T4 lysozyme as a Pac-Man: how fast can it chew? |
| Q35050915 | The DNMT1 intrinsically disordered domain regulates genomic methylation during development |
| Q42279450 | The DynaMine webserver: predicting protein dynamics from sequence |
| Q52593699 | The Recombinant Inhibitor of DNA Binding Id2 Forms Multimeric Structures via the Helix-Loop-Helix Domain and the Nuclear Export Signal. |
| Q30357836 | The SARS coronavirus nucleocapsid protein--forms and functions. |
| Q35062460 | The binding mechanisms of intrinsically disordered proteins. |
| Q35448836 | The carboxy-terminal domain of Erb1 is a seven-bladed ß-propeller that binds RNA. |
| Q24298721 | The chaperone-like protein 14-3-3η interacts with human α-synuclein aggregation intermediates rerouting the amyloidogenic pathway and reducing α-synuclein cellular toxicity |
| Q28481319 | The impact of small molecule binding on the energy landscape of the intrinsically disordered protein C-myc |
| Q38105815 | The most important thing is the tail: multitudinous functionalities of intrinsically disordered protein termini |
| Q55402086 | The transition state structure for binding between TAZ1 of CBP and the disordered Hif-1α CAD. |
| Q31121568 | The transition state structure for coupled binding and folding of disordered protein domains |
| Q41917487 | Translational diffusion of hydration water correlates with functional motions in folded and intrinsically disordered proteins |
| Q47602277 | Triple resonance ¹⁵Ν NMR relaxation experiments for studies of intrinsically disordered proteins |
| Q27688964 | Two potential therapeutic antibodies bind to a peptide segment of membrane-bound IgE in different conformations |
| Q50919522 | Under-folded proteins: Conformational ensembles and their roles in protein folding, function, and pathogenesis. |
| Q27000495 | Wrecked regulation of intrinsically disordered proteins in diseases: pathogenicity of deregulated regulators |
Search more.