review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Peter Wright | Q7177800 |
H. Jane Dyson | Q30513249 | ||
P2093 | author name string | Wright PE | |
Dyson HJ | |||
P2860 | cites work | Structure of Cdc42 in complex with the GTPase-binding domain of the 'Wiskott-Aldrich syndrome' protein | Q22009957 |
The importance of a mobile loop in regulating chaperonin/ co-chaperonin interaction: humans versus Escherichia coli | Q24290435 | ||
Tcf4 can specifically recognize beta-catenin using alternative conformations | Q24291909 | ||
Structure of a human Tcf4-beta-catenin complex | Q24291910 | ||
Structure of the MDM2 oncoprotein bound to the p53 tumor suppressor transactivation domain | Q24314763 | ||
Solution structure of DFF40 and DFF45 N-terminal domain complex and mutual chaperone activity of DFF40 and DFF45 | Q24629962 | ||
A folding transition and novel zinc finger accessory domain in the transcription factor ADR1 | Q27618287 | ||
Structure of the active domain of the herpes simplex virus protein ICP47 in water/sodium dodecyl sulfate solution determined by nuclear magnetic resonance spectroscopy | Q27619974 | ||
Structure of the S15,S6,S18-rRNA complex: assembly of the 30S ribosome central domain | Q27622112 | ||
Structure of PAK1 in an autoinhibited conformation reveals a multistage activation switch | Q27626911 | ||
Molecular basis of sequence-specific recognition of pre-ribosomal RNA by nucleolin | Q27628932 | ||
Crystal structure of a beta-catenin/Tcf complex | Q27629129 | ||
The structure of the beta-catenin/E-cadherin complex and the molecular basis of diverse ligand recognition by beta-catenin | Q27631714 | ||
Corepressor-induced organization and assembly of the biotin repressor: A model for allosteric activation of a transcriptional regulator | Q27631783 | ||
Recognition of pre-formed and flexible elements of an RNA stem-loop by nucleolin | Q27632444 | ||
Allosteric activation of a spring-loaded natriuretic peptide receptor dimer by hormone | Q27634668 | ||
Solution structure and dynamics of yeast elongin C in complex with a von Hippel-Lindau peptide | Q27634727 | ||
Structural basis for DNA bending by the architectural transcription factor LEF-1 | Q27729834 | ||
Solution conformation of an atrial natriuretic peptide variant selective for the type A receptor | Q27730838 | ||
Structure of a protein photocycle intermediate by millisecond time-resolved crystallography | Q27734830 | ||
Solution Structure of the KIX Domain of CBP Bound to the Transactivation Domain of CREB: A Model for Activator:Coactivator Interactions | Q27748755 | ||
MOLMOL: a program for display and analysis of macromolecular structures | Q27860873 | ||
Binding of elongin A or a von Hippel-Lindau peptide stabilizes the structure of yeast elongin C | Q27933200 | ||
Expression of the Oct-1 transcription factor and characterization of its interactions with the Bob1 coactivator | Q28191274 | ||
Intrinsically disordered protein | Q28191444 | ||
Induced alpha helix in the VP16 activation domain upon binding to a human TAF | Q28247311 | ||
Linked folding and anion binding of the Bacillus subtilis ribonuclease P protein | Q28907143 | ||
The cadherin cytoplasmic domain is unstructured in the absence of beta-catenin. A possible mechanism for regulating cadherin turnover | Q28910197 | ||
An unstructured C-terminal region of the Hsp90 co-chaperone p23 is important for its chaperone function | Q28910360 | ||
Intrinsically unstructured proteins: re-assessing the protein structure-function paradigm | Q29615865 | ||
Coupling of local folding to site-specific binding of proteins to DNA | Q29616464 | ||
Dynamic coupling between the SH2 and SH3 domains of c-Src and Hck underlies their inactivation by C-terminal tyrosine phosphorylation | Q30168286 | ||
Probing the nature of the blue-shifted intermediate of photoactive yellow protein in solution by NMR: hydrogen-deuterium exchange data and pH studies | Q30620073 | ||
A homochiral metal-organic porous material for enantioselective separation and catalysis | Q33901022 | ||
Folding and signaling share the same pathway in a photoreceptor | Q33929677 | ||
Disordered to ordered folding in the regulation of diphtheria toxin repressor activity | Q33944428 | ||
The quorum-sensing transcriptional regulator TraR requires its cognate signaling ligand for protein folding, protease resistance, and dimerization | Q34085916 | ||
Roles of partly unfolded conformations in macromolecular self-assembly | Q34135691 | ||
Current topics in RNA-protein recognition: control of specificity and biological function through induced fit and conformational capture | Q34297707 | ||
Speeding molecular recognition by using the folding funnel: the fly-casting mechanism | Q35189399 | ||
Molecular basis for modulation of biological function by alternate splicing of the Wilms' tumor suppressor protein | Q35351671 | ||
Changes in dynamical behavior of the retinoid X receptor DNA-binding domain upon binding to a 14 base-pair DNA half site | Q38310121 | ||
An accessory DNA binding motif in the zinc finger protein Adr1 assists stable binding to DNA and can be replaced by a third finger | Q38316381 | ||
Identification of a human T-cell leukemia virus type I tax peptide in contact with DNA. | Q38318292 | ||
Molecular and structural basis of target recognition by calmodulin. | Q40476061 | ||
PAS domain receptor photoactive yellow protein is converted to a molten globule state upon activation | Q43586302 | ||
Molecular shapes of transcription factors TFIIB and VP16 in solution: implications for recognition | Q43616285 | ||
Regulation of transcriptional activation domain function by ubiquitin | Q43682027 | ||
Proteins that bind RNA and the labs who love them | Q46563280 | ||
Independent ligand-induced folding of the RNA-binding domain and two functionally distinct antitermination regions in the phage lambda N protein | Q47862787 | ||
The protein trinity--linking function and disorder. | Q52055900 | ||
DNA-induced conformational changes are the basis for cooperative dimerization by the DNA binding domain of the retinoid X receptor. | Q54705142 | ||
DNA-induced α-helix capping in conserved linker sequences is a determinant of binding affinity in Cys2-His2 zinc fingers | Q57078232 | ||
Latent and active p53 are identical in conformation | Q58002479 | ||
Biophysical characterization of elongin C from saccharomyces cerevisiae | Q73030408 | ||
Phosphorylation of T cell receptor zeta is regulated by a lipid dependent folding transition | Q73150636 | ||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | protein folding | Q847556 |
P304 | page(s) | 54-60 | |
P577 | publication date | 2002-02-01 | |
P1433 | published in | Current Opinion in Structural Biology | Q15758416 |
P1476 | title | Coupling of folding and binding for unstructured proteins | |
P478 | volume | 12 |
Q35729373 | "Invisible" conformers of an antifungal disulfide protein revealed by constrained cold and heat unfolding, CEST-NMR experiments, and molecular dynamics calculations. |
Q38325254 | "Natively unfolded" VPg is essential for Sesbania mosaic virus serine protease activity |
Q44372460 | 1H, 15N and 13C resonance assignments for the PTB domain of the signaling protein Shc. |
Q37590711 | A Clostridium difficile-Specific, Gel-Forming Protein Required for Optimal Spore Germination |
Q35902555 | A Method for Systematic Assessment of Intrinsically Disordered Protein Regions by NMR. |
Q27664939 | A Selection Fit Mechanism in BMP Receptor IA as a Possible Source for BMP Ligand-Receptor Promiscuity |
Q60221062 | A comparative proteomic approach to analyse structure, function and evolution of rice chitinases: a step towards increasing plant fungal resistance |
Q28681184 | A decade and a half of protein intrinsic disorder: biology still waits for physics |
Q30544835 | A disorder-to-order structural transition in the COOH-tail of Fz4 determines misfolding of the L501fsX533-Fz4 mutant |
Q99411742 | A disordered encounter complex is central to the yeast Abp1p SH3 domain binding pathway |
Q90490036 | A dynamic charge-charge interaction modulates PP2A:B56 substrate recruitment |
Q40976711 | A fluid salt-bridging cluster and the stabilization of p53. |
Q39731942 | A functionally required unfoldome from the plant kingdom: intrinsically disordered N-terminal domains of GRAS proteins are involved in molecular recognition during plant development. |
Q33656530 | A method to trap transient and weak interacting protein complexes for structural studies |
Q36519162 | A mobile loop order-disorder transition modulates the speed of chaperonin cycling |
Q47992335 | A natively unfolded toxin domain uses its receptor as a folding template |
Q33331025 | A new protein linear motif benchmark for multiple sequence alignment software |
Q28907138 | A prokaryotic superoxide dismutase paralog lacking two Cu ligands: from largely unstructured in solution to ordered in the crystal |
Q37048844 | A quantitative measure for protein conformational heterogeneity |
Q33784415 | A single intermolecular contact mediates intramolecular stabilization of both RNA and protein |
Q40913581 | A single mutation at residue 25 populates the folding intermediate of E. coli RNase H and reveals a highly dynamic partially folded ensemble |
Q28256953 | A tale of two citrullines--structural and functional aspects of myelin basic protein deimination in health and disease |
Q37528816 | A transient α-helical molecular recognition element in the disordered N-terminus of the Sgs1 helicase is critical for chromosome stability and binding of Top3/Rmi1. |
Q37381486 | ANCHOR: web server for predicting protein binding regions in disordered proteins. |
Q46226823 | Abundance and functional roles of intrinsic disorder in the antimicrobial peptides of the NK-lysin family |
Q57998224 | Accepting its Random Coil Nature Allows a Partial NMR Assignment of the Neuronal Tau Protein |
Q40606661 | Accurate Ab Initio and Template-Based Prediction of Short Intrinsically-Disordered Regions by Bidirectional Recurrent Neural Networks Trained on Large-Scale Datasets |
Q36798972 | Achieving high signal-to-noise in cell regulatory systems: Spatial organization of multiprotein transmembrane assemblies of FGFR and MET receptors. |
Q39148660 | Actinous enigma or enigmatic actin: Folding, structure, and functions of the most abundant eukaryotic protein |
Q50882504 | Adaptation of mRNA structure to control protein folding. |
Q30358999 | Advantages of proteins being disordered. |
Q36681464 | Allosteric modulators of steroid hormone receptors: structural dynamics and gene regulation |
Q35133048 | Allosteric switching by mutually exclusive folding of protein domains |
Q35582539 | Allovalency: A Case of Molecular Entanglement |
Q37511760 | An enzymatic molten globule: efficient coupling of folding and catalysis. |
Q75305854 | An equilibrium thermodynamic model of the sequestration of calcium phosphate by casein phosphopeptides |
Q33651837 | An overview of the importance of conformational flexibility in gene regulation by the transcription factors |
Q42118475 | An unusual intrinsically disordered protein from the model legume Lotus japonicus stabilizes proteins in vitro |
Q30157208 | Analysis of structured and intrinsically disordered regions of transmembrane proteins |
Q57909937 | Are non‐functional, unfolded proteins (‘junk proteins’) common in the genome? |
Q49908026 | Arrestins: structural disorder creates rich functionality. |
Q35128299 | Assembly of a filamin four-domain fragment and the influence of splicing variant-1 on the structure |
Q43638249 | Assessing induced folding within the intrinsically disordered C-terminal domain of the Henipavirus nucleoproteins by site-directed spin labeling EPR spectroscopy |
Q34999872 | At the crossroads of homoeostasis and disease: roles of the PACS proteins in membrane traffic and apoptosis |
Q21131369 | Atomic resolution description of the interaction between the nucleoprotein and phosphoprotein of Hendra virus |
Q30341674 | Automated protein structure homology modeling: a progress report. |
Q47900402 | Backbone conformational preferences of an intrinsically disordered protein in solution. |
Q38630369 | Backbone dynamics of the 18.5 kDa isoform of myelin basic protein reveals transient alpha-helices and a calmodulin-binding site |
Q39361383 | Behaviour of intrinsically disordered proteins in protein-protein complexes with an emphasis on fuzziness |
Q33762505 | Benchmarking B-cell epitope prediction for the design of peptide-based vaccines: problems and prospects |
Q35022626 | Beneficial effect of sugar osmolytes on the refolding of guanidine hydrochloride-denatured trehalose-6-phosphate hydrolase from Bacillus licheniformis |
Q34786728 | Beyond the random coil: stochastic conformational switching in intrinsically disordered proteins |
Q28079899 | Binding Mechanisms of Intrinsically Disordered Proteins: Theory, Simulation, and Experiment |
Q36492875 | Binding of the N-terminal region of coactivator TIF2 to the intrinsically disordered AF1 domain of the glucocorticoid receptor is accompanied by conformational reorganizations |
Q27665108 | Binding-induced folding of prokaryotic ubiquitin-like protein on the Mycobacterium proteasomal ATPase targets substrates for degradation |
Q41891517 | Binding‐induced folding transitions in calpastatin subdomains A and C |
Q28484783 | Biochemical characterization of protein complexes from the Helicobacter pylori protein interaction map: strategies for complex formation and evidence for novel interactions within type IV secretion systems |
Q37653031 | Bioinformatical approaches to characterize intrinsically disordered/unstructured proteins |
Q40200977 | Bioinformatical parsing of folding-on-binding proteins reveals their compositional and evolutionary sequence design |
Q38589803 | Biophysical Methods to Investigate Intrinsically Disordered Proteins: Avoiding an "Elephant and Blind Men" Situation |
Q38042773 | Biophysical and computational fragment-based approaches to targeting protein-protein interactions: applications in structure-guided drug discovery |
Q37375367 | Biophysical characterization of intrinsically disordered proteins |
Q28660230 | Biophysical properties of intrinsically disordered p130Cas substrate domain--implication in mechanosensing |
Q36076140 | Biosensors based on binding-modulated donor-acceptor distances. |
Q27684483 | Broad-Spectrum Allosteric Inhibition of Herpesvirus Proteases |
Q37195737 | CDF it all: consensus prediction of intrinsically disordered proteins based on various cumulative distribution functions |
Q37618800 | CFTR regulatory region interacts with NBD1 predominantly via multiple transient helices |
Q49717521 | CPAP3 proteins in the mineralized cuticle of a decapod crustacean. |
Q24318648 | Calcium-induced tripartite binding of intrinsically disordered calpastatin to its cognate enzyme, calpain |
Q30496929 | Can self-inhibitory peptides be derived from the interfaces of globular protein-protein interactions? |
Q53069240 | Caprice/MISP is a novel F-actin bundling protein critical for actin-based cytoskeletal reorganizations. |
Q50087658 | Carbon dioxide/methanol conversion cycle based on cascade enzymatic reactions supported on superparamagnetic nanoparticles. |
Q34136216 | Catalytic and chaperone-like functions in an intrinsically disordered protein associated with desiccation tolerance |
Q36732525 | Cell-cell communication in the plant pathogen Agrobacterium tumefaciens |
Q44491831 | Cellular and behavioral effects of D2 dopamine receptor hydrophobic eigenmode-targeted peptide ligands |
Q30381690 | Changes in protein structure at the interface accompanying complex formation. |
Q54537736 | Chaperone-independent folding of type 1 pilus domains. |
Q45143473 | Chaperone-like manner of human neuronal tau towards lactate dehydrogenase |
Q30392866 | Chapter 1. Target selection in structural genomics projects to increase knowledge of protein structure and function space |
Q45081629 | Characterisation of a mobile protein-binding epitope in the translocation domain of colicin E9. |
Q39359047 | Characterization and Prediction of Protein Flexibility Based on Structural Alphabets. |
Q48243773 | Characterization of an Hsp90-Independent Interaction between Co-Chaperone p23 and Transcription Factor p53. |
Q36944291 | Characterization of molecular recognition features, MoRFs, and their binding partners |
Q43422418 | Characterization of molten globule PopB in absence and presence of its chaperone PcrH. |
Q42853848 | Characterization of recombinant lysyl oxidase propeptide |
Q41843115 | Characterization of the disordered-to-α-helical transition of IA₃ by SDSL-EPR spectroscopy |
Q34787399 | Characterization of the interactions between the nucleoprotein and the phosphoprotein of Henipavirus |
Q36201794 | Characterization of the structure and intermolecular interactions between the connexin 32 carboxyl-terminal domain and the protein partners synapse-associated protein 97 and calmodulin |
Q33834096 | CoESPRIT: a library-based construct screening method for identification and expression of soluble protein complexes |
Q34598294 | Common attributes of native-state structures of proteins, disordered proteins, and amyloid. |
Q24813518 | Comparative genomics and disorder prediction identify biologically relevant SH3 protein interactions |
Q36216371 | Competitive binding between dynamic p53 transactivation subdomains to human MDM2 protein: implications for regulating the p53·MDM2/MDMX interaction. |
Q39966854 | Composition, Assembly, and Trafficking of a Wheat Xylan Synthase Complex |
Q63740433 | Computational Prediction of MoRFs, Short Disorder-to-order Transitioning Protein Binding Regions |
Q30783773 | Concerted folding and binding of a flexible colicin domain to its periplasmic receptor TolA. |
Q91822502 | Concomitant disorder and high-affinity zinc binding in the human zinc- and iron-regulated transport protein 4 intracellular loop |
Q33875537 | Conditionally and transiently disordered proteins: awakening cryptic disorder to regulate protein function |
Q37856774 | Conformation and thermodynamic stability of pre-molten and molten globule states of mammalian cytochromes-c |
Q39869280 | Conformational Ensembles of an Intrinsically Disordered Protein pKID with and without a KIX Domain in Explicit Solvent Investigated by All-Atom Multicanonical Molecular Dynamics |
Q33767753 | Conformational analysis of the partially disordered measles virus N(TAIL)-XD complex by SDSL EPR spectroscopy |
Q27334093 | Conformational frustration in calmodulin-target recognition |
Q38116495 | Conformational propensities of intrinsically disordered proteins from NMR chemical shifts |
Q54545986 | Conformational selection versus induced fit in kinases: the case of PI3K-γ. |
Q41851853 | Conservation of intrinsic disorder in protein domains and families: I. A database of conserved predicted disordered regions |
Q36869604 | Conservation of intrinsic disorder in protein domains and families: II. functions of conserved disorder |
Q33786355 | Conserved Helix-Flanking Prolines Modulate Intrinsically Disordered Protein:Target Affinity by Altering the Lifetime of the Bound Complex |
Q48503561 | Conserved, unstructured regions in Pseudomonas aeruginosa PilO are important for type IVa pilus function. |
Q35105348 | Continuous wave W- and D-band EPR spectroscopy offer "sweet-spots" for characterizing conformational changes and dynamics in intrinsically disordered proteins |
Q44669072 | Contribution of the Per/Arnt/Sim (PAS) domains to DNA binding by the basic helix-loop-helix PAS transcriptional regulators |
Q57358066 | Cooperativity Principles in Self-Assembled Nanomedicine |
Q30419579 | Counteracting chemical chaperone effects on the single-molecule α-synuclein structural landscape |
Q35036023 | Coupled folding and specific binding: fishing for amphiphilicity |
Q40929494 | Coupled folding-binding in a hydrophobic/polar protein model: impact of synergistic folding and disordered flanks. |
Q51642594 | Coupled folding-binding versus docking: a lattice model study. |
Q27641793 | Coupling of folding and binding in the PTB domain of the signaling protein Shc |
Q47897313 | Coupling of folding and binding of thymosin beta4 upon interaction with monomeric actin monitored by nuclear magnetic resonance |
Q47867146 | Cyclization of pyrrhocoricin retains structural elements crucial for the antimicrobial activity of the native peptide. |
Q30407509 | Cysteine and histidine shuffling: mixing and matching cysteine and histidine residues in zinc finger proteins to afford different folds and function |
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 |
Q47821476 | Deciphering the promiscuous interactions between intrinsically disordered transactivation domains and the KIX domain. |
Q53315698 | Defining structural domains of an intrinsically disordered protein: Sic1, the cyclin-dependent kinase inhibitor of Saccharomyces cerevisiae. |
Q33818465 | Describing sequence-ensemble relationships for intrinsically disordered proteins |
Q51926130 | Desiccation and zinc binding induce transition of tomato abscisic acid stress ripening 1, a water stress- and salt stress-regulated plant-specific protein, from unfolded to folded state. |
Q34184921 | Designing human m1 muscarinic receptor-targeted hydrophobic eigenmode matched peptides as functional modulators |
Q40297593 | Destabilizing missense mutations in the tumour suppressor protein p53 enhance its ubiquitination in vitro and in vivo |
Q37105049 | Detailed structural characterization of unbound protein phosphatase 1 inhibitors |
Q21030644 | Determining biophysical protein stability in lysates by a fast proteolysis assay, FASTpp |
Q89745010 | Development of imaging scaffolds for cryo-electron microscopy |
Q36939730 | Differences in β-strand populations of monomeric Aβ40 and Aβ42. |
Q37586962 | Differential regulation of the transcriptional activity of the glucocorticoid receptor through site-specific phosphorylation |
Q30402101 | Digested disorder: Quarterly intrinsic disorder digest (April-May-June, 2013). |
Q22061724 | Digested disorder: Quarterly intrinsic disorder digest (January/February/March, 2013). |
Q44391914 | Direct prediction of NMR residual dipolar couplings from the primary sequence of unfolded proteins |
Q33972273 | DisMeta: a meta server for construct design and optimization |
Q28550591 | DisPredict: A Predictor of Disordered Protein Using Optimized RBF Kernel |
Q34341031 | DisProt: a database of protein disorder |
Q58789775 | Discerning evolutionary trends in post-translational modification and the effect of intrinsic disorder: Analysis of methylation, acetylation and ubiquitination sites in human proteins |
Q30422189 | Disease-associated mutations disrupt functionally important regions of intrinsic protein disorder |
Q26796658 | Disorder Prediction Methods, Their Applicability to Different Protein Targets and Their Usefulness for Guiding Experimental Studies |
Q34563791 | Disorder in cholesterol-binding functionality of CRAC peptides: a molecular dynamics study |
Q38779717 | Disorder in the lifetime of a protein |
Q24554044 | Disorder in the nuclear pore complex: the FG repeat regions of nucleoporins are natively unfolded |
Q34442227 | Disordered binding regions and linear motifs--bridging the gap between two models of molecular recognition. |
Q41880608 | Disordered plant LEA proteins as molecular chaperones |
Q28652765 | Disordered proteinaceous machines |
Q90024659 | Disruption of the MBD2-NuRD complex but not MBD3-NuRD induces high level HbF expression in human adult erythroid cells |
Q38288151 | Dissecting physical structure of calreticulin, an intrinsically disordered Ca2+-buffering chaperone from endoplasmic reticulum |
Q28754659 | Distribution patterns of small-molecule ligands in the protein universe and implications for origin of life and drug discovery |
Q83375657 | Dominant kinetic paths on biomolecular binding-folding energy landscape |
Q57128184 | Drawing on disorder: How viruses use histone mimicry to their advantage |
Q35938545 | Dynamic Protein Interaction Networks and New Structural Paradigms in Signaling |
Q43715232 | Dynamic behavior of an intrinsically unstructured linker domain is conserved in the face of negligible amino acid sequence conservation |
Q37588014 | Dynamic interactions of proteins in complex networks: a more structured view. |
Q42563954 | Dynamic surface activity by folding and unfolding an amphiphilic alpha-helix |
Q34452418 | Dynamics of the C-terminal region of TnI in the troponin complex in solution. |
Q74764013 | Dynamics-modulated biological activity of transforming growth factor beta3 |
Q24672414 | ELM server: A new resource for investigating short functional sites in modular eukaryotic proteins |
Q24811801 | Early-stage folding in proteins (in silico) sequence-to-structure relation |
Q37178747 | Effect of methionine oxidation on the structural properties, conformational stability, and aggregation of immunoglobulin light chain LEN. |
Q30392544 | Effect of natural polymorphism on structure and function of the Yersinia pestis outer membrane porin F (OmpF protein): a computational study |
Q51537335 | Effectiveness of Φ-value analysis in the binding process of Arc repressor dimer. |
Q42715067 | Effects of different osmolytes on the induced folding of the N-terminal activation domain (AF1) of the glucocorticoid receptor |
Q34493912 | Effects of molecular crowding on the dynamics of intrinsically disordered proteins |
Q44173685 | Effects of the osmolyte trimethylamine-N-oxide on conformation, self-association, and two-dimensional crystallization of myelin basic protein |
Q52325095 | Ehrlichia chaffeensis TRP120 nucleomodulin binds DNA with disordered tandem repeat domain. |
Q30502244 | Electrochemical interrogation of conformational changes as a reagentless method for the sequence-specific detection of DNA |
Q90713865 | Electrostatic control of calcineurin's intrinsically-disordered regulatory domain binding to calmodulin |
Q46286448 | Elucidation of the protein folding landscape by NMR. |
Q34546674 | Emergence of new regulatory mechanisms in the Benson-Calvin pathway via protein-protein interactions: a glyceraldehyde-3-phosphate dehydrogenase/CP12/phosphoribulokinase complex. |
Q45285817 | Energetics of structural transitions of the addiction antitoxin MazE: is a programmed bacterial cell death dependent on the intrinsically flexible nature of the antitoxins? |
Q38589795 | Ensemble Calculation for Intrinsically Disordered Proteins Using NMR Parameters |
Q30392517 | Estimation of Position Specific Energy as a Feature of Protein Residues from Sequence Alone for Structural Classification |
Q38826569 | Evidence for a Strong Correlation Between Transcription Factor Protein Disorder and Organismic Complexity. |
Q54376376 | Evidences of a natively unfolded state for the human topoisomerase IB N-terminal domain. |
Q35037936 | Evolution and disorder |
Q36145469 | Evolution of Protein Domain Repeats in Metazoa |
Q58735294 | Evolution of Protein Ductility in Duplicated Genes of Plants |
Q34203400 | Evolution of a derived protein-protein interaction between HoxA11 and Foxo1a in mammals caused by changes in intramolecular regulation |
Q34310281 | Evolution of specificity in protein-protein interactions |
Q90593521 | Evolutionary Analysis of the Lysine-Rich N-terminal Cytoplasmic Domains of the Gastric H+,K+-ATPase and the Na+,K+-ATPase |
Q61807386 | Evolutionary Features in the Structure and Function of Bacterial Toxins |
Q34671764 | Evolutionary capacitance and control of protein stability in protein-protein interaction networks |
Q42211815 | Exceptionally abundant exceptions: comprehensive characterization of intrinsic disorder in all domains of life |
Q34197530 | Expanding the proteome: disordered and alternatively folded proteins |
Q27692089 | Exploring intrinsically disordered proteins using site-directed spin labeling electron paramagnetic resonance spectroscopy. |
Q28208096 | Extended disordered proteins: targeting function with less scaffold |
Q38779757 | Extracting structural information from charge-state distributions of intrinsically disordered proteins by non-denaturing electrospray-ionization mass spectrometry |
Q37239949 | Extrinsic interactions dominate helical propensity in coupled binding and folding of the lactose repressor protein hinge helix |
Q37534629 | Fast folding of a helical protein initiated by the collision of unstructured chains |
Q30351593 | Flexible nets. The roles of intrinsic disorder in protein interaction networks. |
Q39370444 | Fly Fishing for Histones: Catch and Release by Histone Chaperone Intrinsically Disordered Regions and Acidic Stretches |
Q80275118 | Folding and assembly of hemoglobin monitored by electrospray mass spectrometry using an on-line dialysis system |
Q55287194 | Folding and binding pathways of BH3-only proteins are encoded within their intrinsically disordered sequence, not templated by partner proteins. |
Q79086585 | Folding for binding or binding for folding? |
Q40319333 | Folding thermodynamics of peptides |
Q34856957 | Forced folding of a disordered protein accesses an alternative folding landscape |
Q28730747 | Free cysteine modulates the conformation of human C/EBP homologous protein |
Q43459132 | Frustration-induced protein intrinsic disorder. |
Q36101573 | Functional advantages of dynamic protein disorder |
Q30360720 | Functional anthology of intrinsic disorder. 1. Biological processes and functions of proteins with long disordered regions. |
Q36986347 | Functional anthology of intrinsic disorder. 2. Cellular components, domains, technical terms, developmental processes, and coding sequence diversities correlated with long disordered regions |
Q30375717 | Functional aspects of protein flexibility. |
Q42061600 | Functional dissection of an intrinsically disordered protein: understanding the roles of different domains of Knr4 protein in protein-protein interactions |
Q35167516 | Functional genomics and proteomics: charting a multidimensional map of the yeast cell |
Q28085662 | Functional roles of transiently and intrinsically disordered regions within proteins |
Q38659937 | Functionality of Intrinsic Disorder in Tumor Necrosis Factor-α and its Receptors |
Q22061730 | Fuzziness: linking regulation to protein dynamics |
Q50922689 | Fuzzy regions in an intrinsically disordered protein impair protein-protein interactions. |
Q40954956 | GADIS: Algorithm for designing sequences to achieve target secondary structure profiles of intrinsically disordered proteins. |
Q33352897 | GRAS proteins: the versatile roles of intrinsically disordered proteins in plant signalling. |
Q45693599 | Genetically tunable frustration controls allostery in an intrinsically disordered transcription factor |
Q34531340 | Guanidine-HCl dependent structural unfolding of M-crystallin: fluctuating native state like topologies and intermolecular association. |
Q35191557 | HMGA proteins: flexibility finds a nuclear niche? |
Q34044981 | Hamiltonian Switch Metropolis Monte Carlo Simulations for Improved Conformational Sampling of Intrinsically Disordered Regions Tethered to Ordered Domains of Proteins |
Q58045256 | Helical Propensity in an Intrinsically Disordered Protein Accelerates Ligand Binding |
Q38321196 | Heparan sulfate mimicry: a synthetic glycoconjugate that recognizes the heparin binding domain of interferon-gamma inhibits the cytokine activity |
Q38734798 | Heterotrimeric G protein signaling via GIV/Girdin: Breaking the rules of engagement, space, and time. |
Q47163099 | Hidden α-helical propensity segments within disordered regions of the transcriptional activator CHOP. |
Q24337888 | High levels of structural disorder in scaffold proteins as exemplified by a novel neuronal protein, CASK-interactive protein1 |
Q41098679 | High-resolution structural characterization of Noxa, an intrinsically disordered protein, by microsecond molecular dynamics simulations |
Q36756201 | How adenylate cyclase choreographs the pas de deux of the receptors heteromerization dance |
Q50559161 | How to Predict Disorder in a Protein of Interest. |
Q34204011 | Hydration layer coupling and cooperativity in phase behavior of stimulus responsive peptide polymers. |
Q33847013 | Hydrogen exchange mass spectrometry: what is it and what can it tell us? |
Q38779738 | Hypothesis: The unfolding power of protein dielectricity |
Q90010481 | IDPpi: Protein-Protein Interaction Analyses of Human Intrinsically Disordered Proteins |
Q31136649 | Identification and characterization of peptide probes directed against PKCalpha conformations. |
Q41974143 | Identification of DNA-binding proteins using structural, electrostatic and evolutionary features |
Q38275632 | Identification of intrinsically disordered regions in PTEN and delineation of its function via a network approach |
Q21143869 | Improved disorder prediction by combination of orthogonal approaches |
Q35538193 | Improving protein order-disorder classification using charge-hydropathy plots |
Q35172387 | In situ visualization of protein interactions in sensory neurons: glutamic acid-rich proteins (GARPs) play differential roles for photoreceptor outer segment scaffolding |
Q50864208 | In various protein complexes, disordered protomers have large per-residue surface areas and area of protein-, DNA- and RNA-binding interfaces. |
Q47246041 | InSiDDe: A Server for Designing Artificial Disordered Proteins |
Q34190132 | Induced fit and the entropy of structural adaptation in the complexation of CAP and lambda-repressor with cognate DNA sequences |
Q35372743 | Influence of domain interactions on conformational mobility of the progesterone receptor detected by hydrogen/deuterium exchange mass spectrometry |
Q30380392 | Influence of sequence changes and environment on intrinsically disordered proteins. |
Q42606718 | Insight into a novel p53 single point mutation (G389E) by Molecular Dynamics Simulations. |
Q34465001 | Insights into the evolutionary features of human neurodegenerative diseases |
Q34989920 | Insights into the structure and dynamics of unfolded proteins from nuclear magnetic resonance |
Q42030822 | Insights into the structure-function relationships of pneumococcal cell wall lysozymes, LytC and Cpl-1. |
Q50105520 | Interaction of the disordered terminal regions of flagellin upon flagellar filament formation. |
Q34541386 | Interaction of the transactivation domain of B-Myb with the TAZ2 domain of the coactivator p300: molecular features and properties of the complex |
Q42137229 | Interactions between DNA, transcriptional regulator Dreb2a and the Med25 mediator subunit from Arabidopsis thaliana involve conformational changes |
Q64943644 | Interactions of Casein and Polypeptides in Multilayer Films Studied by FTIR and Molecular Dynamics. |
Q42565088 | Interactions of TolB with the translocation domain of colicin E9 require an extended TolB box. |
Q38614473 | Interpreting functional effects of coding variants: challenges in proteome-scale prediction, annotation and assessment |
Q55066708 | Intrinsic Disorder and Posttranslational Modifications: The Darker Side of the Biological Dark Matter. |
Q47351608 | Intrinsic Disorder in Proteins with Pathogenic Repeat Expansions. |
Q35632957 | Intrinsic disorder and functional proteomics |
Q43121399 | Intrinsic disorder in PTEN and its interactome confers structural plasticity and functional versatility |
Q51574262 | Intrinsic disorder in S100 proteins. |
Q37114136 | Intrinsic disorder in Viral Proteins Genome-Linked: experimental and predictive analyses |
Q28207698 | Intrinsic disorder in cell-signaling and cancer-associated proteins |
Q33417626 | Intrinsic disorder in protein interactions: insights from a comprehensive structural analysis |
Q34594105 | Intrinsic disorder in scaffold proteins: getting more from less |
Q35928939 | Intrinsic disorder in the C-terminal domain of the Shaker voltage-activated K+ channel modulates its interaction with scaffold proteins |
Q36882145 | Intrinsic disorder in transcription factors |
Q33252616 | Intrinsic disorder is a common feature of hub proteins from four eukaryotic interactomes |
Q35044139 | Intrinsic disorder mediates hepatitis C virus core-host cell protein interactions. |
Q34167396 | Intrinsic disorder mediates the diverse regulatory functions of the Cdk inhibitor p21 |
Q98775878 | Intrinsic disorder perspective of an interplay between the renin-angiotensin-aldosterone system and SARS-CoV-2 |
Q34051941 | Intrinsic protein disorder in human pathways |
Q47171932 | Intrinsic protein disorder reduces small-scale gene duplicability |
Q47811118 | Intrinsically Disordered Proteins and Desiccation Tolerance: Elucidating Functional and Mechanistic Underpinnings of Anhydrobiosis |
Q90107802 | Intrinsically Disordered Transactivation Domains Bind to TAZ1 Domain of CBP via Diverse Mechanisms |
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 |
Q33755622 | Intrinsically disordered domains deviate significantly from random sequences in mammalian proteins |
Q28910465 | Intrinsically disordered human C/EBP homologous protein regulates biological activity of colon cancer cells during calcium stress |
Q35228279 | Intrinsically disordered proteins (IDPs) in trypanosomatids. |
Q37600691 | Intrinsically disordered proteins and their environment: effects of strong denaturants, temperature, pH, counter ions, membranes, binding partners, osmolytes, and macromolecular crowding |
Q30389323 | Intrinsically disordered proteins in bcl-2 regulated apoptosis. |
Q35510300 | Intrinsically disordered proteins in cellular signalling and regulation. |
Q57354509 | Intrinsically disordered proteins in crowded milieu: when chaos prevails within the cellular gumbo |
Q36508892 | Intrinsically disordered proteins in the neurodegenerative processes: formation of tau protein paired helical filaments and their analysis |
Q38002804 | Intrinsically disordered proteins: from sequence and conformational properties toward drug discovery |
Q37932415 | Intrinsically disordered regions as affinity tuners in protein-DNA interactions |
Q39335014 | Intrinsically disordered regions in autophagy proteins |
Q33640094 | Intrinsically disordered regions may lower the hydration free energy in proteins: a case study of nudix hydrolase in the bacterium Deinococcus radiodurans |
Q37528149 | Intrinsically disordered regions of p53 family are highly diversified in evolution |
Q38259350 | Intrinsically disordered tubulin tails: complex tuners of microtubule functions? |
Q27649732 | Intrinsically disordered -subunit of cGMP phosphodiesterase encodes functionally relevant transient secondary and tertiary structure |
Q29614784 | Intrinsically unstructured proteins |
Q22061731 | Intrinsically unstructured proteins and their functions |
Q100738796 | Investigating the trade-off between folding and function in a multidomain Y-family DNA polymerase |
Q89982899 | Investigations of the underlying mechanisms of HIF-1α and CITED2 binding to TAZ1 |
Q44792787 | Ion mobility spectrometry focusing on speciation analysis of metals/metalloids bound to carbonic anhydrase. |
Q57080287 | Is there a biological cost of protein disorder? Analysis of cancer-associated mutations |
Q40308402 | Kinetics of protein-DNA interaction: facilitated target location in sequence-dependent potential |
Q30393021 | Large-scale analysis of intrinsic disorder flavors and associated functions in the protein sequence universe |
Q46151834 | Leucine-rich hydrophobic clusters promote folding of the N-terminus of the intrinsically disordered transactivation domain of p53. |
Q33728497 | Library of disordered patterns in 3D protein structures. |
Q91817045 | Life in Phases: Intra- and Inter- Molecular Phase Transitions in Protein Solutions |
Q27681049 | Ligand concentration regulates the pathways of coupled protein folding and binding. |
Q44222236 | Limits of cooperativity in a structurally modular protein: response of the Notch ankyrin domain to analogous alanine substitutions in each repeat |
Q37373866 | Linking folding and binding |
Q30158016 | Local structural disorder imparts plasticity on linear motifs. |
Q36748344 | Long range recognition and selection in IDPs: the interactions of the C-terminus of p53 |
Q30369339 | Low complexity and disordered regions of proteins have different structural and amino acid preferences. |
Q24672581 | MAP2 and tau bind longitudinally along the outer ridges of microtubule protofilaments |
Q33394559 | Malleable machines in transcription regulation: the mediator complex |
Q34066027 | Malleable machines take shape in eukaryotic transcriptional regulation |
Q30430063 | Malleable ribonucleoprotein machine: protein intrinsic disorder in the Saccharomyces cerevisiae spliceosome |
Q40210194 | Mechanism of coupled folding and binding of an intrinsically disordered protein |
Q28477146 | Mechanism of the interaction between the intrinsically disordered C-terminus of the pro-apoptotic ARTS protein and the Bir3 domain of XIAP |
Q46435011 | Mechanism of transcription factor recruitment by acidic activators. |
Q34417638 | Mechanisms of small-molecule binding to intrinsically disordered proteins |
Q44026039 | Methionine oxidation inhibits fibrillation of human alpha-synuclein in vitro |
Q38669148 | Methods of probing the interactions between small molecules and disordered proteins |
Q22061750 | Micelle-induced folding of spinach thylakoid soluble phosphoprotein of 9 kDa and its functional implications |
Q27313374 | Microsecond molecular dynamics simulations of intrinsically disordered proteins involved in the oxidative stress response |
Q34708119 | Mining alpha-helix-forming molecular recognition features with cross species sequence alignments |
Q52593918 | Modeling the Early Stages of Phase Separation in Disordered Elastin-like Proteins. |
Q47709393 | Modular organization of SARS coronavirus nucleocapsid protein |
Q42154324 | Modulation of the structural integrity of helix F in apomyoglobin by single amino acid replacements |
Q28202717 | Molecular and Functional Characterization of Clathrin- and AP-2-binding Determinants within a Disordered Domain of Auxilin |
Q38453820 | Molecular recognition features (MoRFs) in three domains of life |
Q34782212 | Multiple intrinsically disordered sequences alter DNA binding by the homeodomain of the Drosophila hox protein ultrabithorax |
Q33737866 | Multitude of binding modes attainable by intrinsically disordered proteins: a portrait gallery of disorder-based complexes |
Q36103418 | Multivalent IDP assemblies: Unique properties of LC8-associated, IDP duplex scaffolds |
Q24337446 | Multivalent Microtubule Recognition by Tubulin Tyrosine Ligase-like Family Glutamylases |
Q47597641 | Mutations designed to destabilize the receptor-bound conformation increase MICA-NKG2D association rate and affinity |
Q93039579 | Mutual population-shift driven antibody-peptide binding elucidated by molecular dynamics simulations |
Q37246459 | Mutual synergistic protein folding in split intein |
Q34257524 | Myelin basic protein induces neuron-specific toxicity by directly damaging the neuronal plasma membrane |
Q33799817 | N-terminal domains of DELLA proteins are intrinsically unstructured in the absence of interaction with GID1/gibberellic acid receptors. |
Q26852394 | NAC Transcription Factors in Senescence: From Molecular Structure to Function in Crops |
Q24792064 | NMR chemical shift and relaxation measurements provide evidence for the coupled folding and binding of the p53 transactivation domain |
Q30979050 | NMR relaxation studies on the hydrate layer of intrinsically unstructured proteins |
Q56993044 | NOT THAT RIGID MIDGETS AND NOT SO FLEXIBLE GIANTS: ON THE ABUNDANCE AND ROLES OF INTRINSIC DISORDER IN SHORT AND LONG PROTEINS |
Q33292014 | Natively unstructured loops differ from other loops |
Q34665088 | Natively unstructured regions in proteins identified from contact predictions |
Q35318712 | New Insights into Protein (Un)Folding Dynamics |
Q42706787 | New insights into the Lpt machinery for lipopolysaccharide transport to the cell surface: LptA-LptC interaction and LptA stability as sensors of a properly assembled transenvelope complex |
Q89849097 | New technologies to analyse protein function: an intrinsic disorder perspective |
Q80194726 | Nm23-H1/NDP kinase folding intermediates and cancer: a hypothesis |
Q33747704 | Nonnative interactions in coupled folding and binding processes of intrinsically disordered proteins |
Q46977931 | Novel DNA binding by a basic helix-loop-helix protein. The role of the dioxin receptor PAS domain |
Q57786842 | Nuclear magnetic resonance as a quantitative tool to study interactions in biomacromolecules |
Q42945520 | Off-Pathway Status for the Alkali Molten Globule of Horse Ferricytochromec |
Q41906667 | On the intrinsic disorder status of the major players in programmed cell death pathways |
Q30393176 | On the mechanism of protein fold‐switching by a molecular sensor |
Q35812281 | Optimal specificity and function for flexible biomolecular recognition |
Q36739680 | Order-disorder-order transitions mediate the activation of cholera toxin. |
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 |
Q33308396 | Overexpression of post-translationally modified peptides in Escherichia coli by co-expression with modifying enzymes |
Q42169778 | Overview of the purification of recombinant proteins produced in Escherichia coli. |
Q35541296 | Overview of the purification of recombinant proteins. |
Q78067723 | Partially structured state of the functional VH domain of the mouse anti-ferritin antibody F11 |
Q35578839 | Peptide Binding to a PDZ Domain by Electrostatic Steering via Nonnative Salt Bridges |
Q35154360 | Performance of protein disorder prediction programs on amino acid substitutions |
Q38326965 | Pex5p, the peroxisomal cycling receptor, is a monomeric non-globular protein. |
Q47661120 | Phase transition and winding properties of a flexible polymer adsorbed to a rigid perioidic copolymer |
Q35397840 | Phosphorylation in intrinsically disordered regions regulates the activity of Neurogenin2. |
Q38910392 | Phosphorylation-induced conformational dynamics in an intrinsically disordered protein and potential role in phenotypic heterogeneity |
Q37981477 | Physical chemistry of polyglutamine: intriguing tales of a monotonous sequence |
Q26823798 | Physicochemical properties of cells and their effects on intrinsically disordered proteins (IDPs) |
Q27973484 | Plasmodium falciparum inhibitor-3 homolog increases protein phosphatase type 1 activity and is essential for parasitic survival |
Q37270041 | Plasmodium falciparum merozoite surface protein 2 is unstructured and forms amyloid-like fibrils |
Q41849419 | Polycation-induced oligomerization and accelerated fibrillation of human alpha-synuclein in vitro |
Q35826191 | Polymorphism Analysis Reveals Reduced Negative Selection and Elevated Rate of Insertions and Deletions in Intrinsically Disordered Protein Regions |
Q91820539 | Position-, disorder-, and salt-dependent diffusion in binding-coupled-folding of intrinsically disordered proteins |
Q57789346 | PreSMo Target-Binding Signatures in Intrinsically Disordered Proteins |
Q22061741 | Prediction and Functional Analysis of Native Disorder in Proteins from the Three Kingdoms of Life |
Q48104723 | Prediction of Disordered Regions and Their Roles in the Anti-Pathogenic and Immunomodulatory Functions of Butyrophilins. |
Q48347994 | Prediction of disordered regions in proteins based on the meta approach |
Q21145360 | Prediction of protein binding regions in disordered proteins |
Q34082751 | Prepaying the entropic cost for allosteric regulation in KIX |
Q37377772 | Pro-interleukin (IL)-1beta shares a core region of stability as compared with mature IL-1beta while maintaining a distinctly different configurational landscape: a comparative hydrogen/deuterium exchange mass spectrometry study |
Q34098982 | Probing structural transitions in the intrinsically disordered C-terminal domain of the measles virus nucleoprotein by vibrational spectroscopy of cyanylated cysteines |
Q47371568 | Prosystemin, a prohormone that modulates plant defense barriers, is an intrinsically disordered protein. |
Q92818075 | Protein Abundance Biases the Amino Acid Composition of Disordered Regions to Minimize Non-functional Interactions |
Q40065481 | Protein crystallography and drug discovery: recollections of knowledge exchange between academia and industry |
Q33481211 | Protein disorder in the human diseasome: unfoldomics of human genetic diseases |
Q37369375 | Protein disorder is positively correlated with gene expression in Escherichia coli |
Q35053327 | Protein expression systems for structural genomics and proteomics |
Q43104940 | Protein flexibility and intrinsic disorder |
Q30368801 | Protein folding and misfolding: mechanism and principles. |
Q30399457 | Protein folding at single-molecule resolution |
Q35165260 | Protein informatics towards function identification |
Q37696321 | Protein intrinsic disorder and oligomericity in cell signaling |
Q36675634 | Protein intrinsic disorder in the acetylome of intracellular and extracellular Toxoplasma gondii |
Q46324799 | Protein intrinsic disorder negatively associates with gene age in different eukaryotic lineages |
Q30365413 | Protein reconstitution and three-dimensional domain swapping: benefits and constraints of covalency. |
Q33351985 | Protein solubility and folding enhancement by interaction with RNA |
Q35734060 | Protein topology determines binding mechanism |
Q36947477 | Protein translocation into peroxisomes by ring-shaped import receptors |
Q93229444 | Proteins of generalist and specialist pathogens differ in their amino acid composition |
Q28479221 | Proteins with complex architecture as potential targets for drug design: a case study of Mycobacterium tuberculosis |
Q36936200 | Proteins with weakly funneled energy landscapes challenge the classical structure-function paradigm |
Q38257180 | Proteins without unique 3D structures: biotechnological applications of intrinsically unstable/disordered proteins |
Q42673758 | Proteome-wide analysis of human disease mutations in short linear motifs: neglected players in cancer? |
Q24681633 | Quaternary structures of tumor suppressor p53 and a specific p53 DNA complex |
Q38007407 | Recent progress in NMR spectroscopy: toward the study of intrinsically disordered proteins of increasing size and complexity |
Q33989616 | Recognition of the HIV capsid by the TRIM5α restriction factor is mediated by a subset of pre-existing conformations of the TRIM5α SPRY domain |
Q51595638 | Reduced amino acid alphabet is sufficient to accurately recognize intrinsically disordered protein. |
Q36446093 | Regulation of Escherichia coli SOS mutagenesis by dimeric intrinsically disordered umuD gene products. |
Q42089987 | Regulation of the E3 ubiquitin ligase activity of MDM2 by an N-terminal pseudo-substrate motif |
Q28245681 | Regulation of the neuron-specific Ras GTPase-activating protein, synGAP, by Ca2+/calmodulin-dependent protein kinase II |
Q24534363 | Regulatory interaction of phosducin-like protein with the cytosolic chaperonin complex |
Q42935134 | Remarkably fast coupled folding and binding of the intrinsically disordered transactivation domain of cMyb to CBP KIX. |
Q64106354 | Role of Phosphorylation in the Modulation of the Glucocorticoid Receptor's Intrinsically Disordered Domain |
Q36331739 | Role of non-native electrostatic interactions in the coupled folding and binding of PUMA with Mcl-1 |
Q28910369 | Role of structural plasticity in signal transduction by the cryptochrome blue-light photoreceptor |
Q33978783 | SPA: Short peptide analyzer of intrinsic disorder status of short peptides |
Q34439134 | Secondary structure and dynamics of an intrinsically unstructured linker domain |
Q90225140 | Self-assembly in elastin-like recombinamers: a mechanism to mimic natural complexity |
Q35110852 | Sequence complexity of amyloidogenic regions in intrinsically disordered human proteins |
Q40626286 | Sequence determinants of compaction in intrinsically disordered proteins |
Q30424441 | Sequence repeats and protein structure. |
Q25257115 | Serine/arginine-rich splicing factors belong to a class of intrinsically disordered proteins |
Q34774628 | Side-chain conformational changes upon Protein-Protein Association |
Q37577009 | Signaling from the secretory granule to the nucleus |
Q36397878 | Simple few-state models reveal hidden complexity in protein folding |
Q34982184 | Simulating disorder-order transitions in molecular recognition of unstructured proteins: where folding meets binding |
Q29299846 | Simulations of proteins with inhomogeneous degrees of freedom: The effect of thermostats |
Q33250076 | Single-molecule dynamics reveals cooperative binding-folding in protein recognition |
Q34314714 | Slow, reversible, coupled folding and binding of the spectrin tetramerization domain |
Q28479168 | Small cofactors may assist protein emergence from RNA world: clues from RNA-protein complexes |
Q37142494 | Solution Behavior of the Intrinsically Disordered N-Terminal Domain of Retinoid X Receptor α in the Context of the Full-Length Protein |
Q53650419 | 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. |
Q57902578 | Solution structures of the putative anti-σ-factor antagonist TM1442 fromThermotoga maritima in the free and phosphorylated states |
Q48526269 | Spatial and temporal organization of multi-protein assemblies: achieving sensitive control in information-rich cell-regulatory systems. |
Q89843916 | Specific Conformational Dynamics and Expansion Underpin a Multi-Step Mechanism for Specific Binding of p27 with Cdk2/Cyclin A |
Q42151102 | Specificity and affinity quantification of flexible recognition from underlying energy landscape topography |
Q24304144 | Spinophilin directs protein phosphatase 1 specificity by blocking substrate binding sites |
Q46942411 | Spontaneous assembly of photosynthetic supramolecular complexes as mediated by the intrinsically unstructured protein CP12. |
Q30355526 | Spritz: a server for the prediction of intrinsically disordered regions in protein sequences using kernel machines. |
Q36835434 | Stepwise protein folding at near amino acid resolution by hydrogen exchange and mass spectrometry |
Q27640497 | Structural analysis of Bacillus subtilis SPP1 phage helicase loader protein G39P |
Q42041151 | Structural and Biochemical Characterization of Poly-ADP-ribose Polymerase from Trypanosoma brucei |
Q27671736 | Structural and Functional Analysis of the Tandem -Zipper Interaction of a Streptococcal Protein with Human Fibronectin |
Q37576700 | Structural and functional relationships of the steroid hormone receptors' N-terminal transactivation domain |
Q35672949 | Structural basis for activation of calcineurin by calmodulin |
Q34504260 | Structural basis for activation of trimeric Gi proteins by multiple growth factor receptors via GIV/Girdin |
Q27640917 | Structural basis for antibiotic recognition by the TipA class of multidrug-resistance transcriptional regulators |
Q27641363 | Structural basis for negative regulation of hypoxia-inducible factor-1alpha by CITED2 |
Q27641812 | Structural basis for recognition and catalysis by the bifunctional dCTP deaminase and dUTPase from Methanococcus jannaschii |
Q24534120 | Structural basis for recruitment of CBP/p300 by hypoxia-inducible factor-1 alpha |
Q30448746 | Structural basis for the attachment of a paramyxoviral polymerase to its template |
Q24676096 | Structural basis for the recognition of ldb1 by the N-terminal LIM domains of LMO2 and LMO4 |
Q35029571 | Structural basis of the fibrinogen-fibrin transformation: contributions from X-ray crystallography |
Q34964228 | Structural basis of α-catenin recognition by EspB from enterohaemorrhagic E. coli based on hybrid strategy using low-resolution structural and protein dissection |
Q28910332 | Structural characterization of partially disordered human Chibby: insights into its function in the Wnt-signaling pathway |
Q33301958 | Structural disorder promotes assembly of protein complexes |
Q36346815 | Structural disorder within the replicative complex of measles virus: functional implications |
Q34680376 | Structural divergence is more extensive than sequence divergence for a family of intrinsically disordered proteins |
Q34116108 | Structural diversity in free and bound states of intrinsically disordered protein phosphatase 1 regulators |
Q35562822 | Structural dynamics, intrinsic disorder, and allostery in nuclear receptors as transcription factors |
Q24817012 | Structural genomics of human proteins--target selection and generation of a public catalogue of expression clones |
Q24313019 | Structural insight into the TFIIE-TFIIH interaction: TFIIE and p53 share the binding region on TFIIH |
Q33967718 | Structural insights into the SNARE mechanism |
Q35040942 | Structural insights into the dynamics and function of the C-terminus of the E. coli RNA chaperone Hfq. |
Q36736139 | Structural landscape of the proline-rich domain of Sos1 nucleotide exchange factor |
Q34366754 | Structural study of the H/ACA snoRNP components Nop10p and the 3' hairpin of U65 snoRNA. |
Q57850970 | Structure and Interactions of PAS Kinase N-Terminal PAS Domain |
Q27642408 | Structure and stability of the ankyrin domain of the Drosophila Notch receptor |
Q24296040 | Structure of Cdc42 in a complex with the GTPase-binding domain of the cell polarity protein, Par6 |
Q90207565 | Structure of E3 ligase E6AP with a proteasome-binding site provided by substrate receptor hRpn10 |
Q27675055 | Structure of a Blinkin-BUBR1 Complex Reveals an Interaction Crucial for Kinetochore-Mitotic Checkpoint Regulation via an Unanticipated Binding Site |
Q33558203 | Structured and disordered regions cooperatively mediate DNA-binding autoinhibition of ETS factors ETV1, ETV4 and ETV5. |
Q35128412 | Studies on titin PEVK peptides and their interaction |
Q33961599 | TBP binding-induced folding of the glucocorticoid receptor AF1 domain facilitates its interaction with steroid receptor coactivator-1 |
Q28600879 | Tandem amino acid repeats in the green anole (Anolis carolinensis) and other squamates may have a role in increasing genetic variability |
Q36020398 | Targeting intrinsically disordered proteins in neurodegenerative and protein dysfunction diseases: another illustration of the D(2) concept |
Q40182215 | Targeting of the Sendai virus C protein to the plasma membrane via a peptide-only membrane anchor |
Q36919983 | Targeting the human cancer pathway protein interaction network by structural genomics |
Q41975597 | Temperature-dependent structural changes in intrinsically disordered proteins: formation of alpha-helices or loss of polyproline II? |
Q40594143 | Terminal deletion mutants of myelin basic protein: new insights into self-association and phospholipid interactions |
Q27679793 | The Arginine-Rich RNA-Binding Motif of HIV-1 Rev Is Intrinsically Disordered and Folds upon RRE Binding |
Q44746385 | The C-terminal domain of measles virus nucleoprotein belongs to the class of intrinsically disordered proteins that fold upon binding to their physiological partner |
Q45728875 | The C-terminal domain of the measles virus nucleoprotein is intrinsically disordered and folds upon binding to the C-terminal moiety of the phosphoprotein |
Q41120778 | The C-terminus of ICln is natively disordered but displays local structural preformation |
Q55351373 | The Disordered C-Terminus of Yeast Hsf1 Contains a Cryptic Low-Complexity Amyloidogenic Region. |
Q27675763 | The Escherichia coli Lpt Transenvelope Protein Complex for Lipopolysaccharide Export Is Assembled via Conserved Structurally Homologous Domains |
Q36227793 | The Identification and Characterization of Two Novel Epitopes on the Nucleocapsid Protein of the Porcine Epidemic Diarrhea Virus |
Q27652627 | The Interplay of Ligand Binding and Quaternary Structure in the Diverse Interactions of Dynein Light Chain LC8 |
Q42121729 | The N(0)-binding region of the vesicular stomatitis virus phosphoprotein is globally disordered but contains transient α-helices |
Q34590106 | The N-terminal intrinsically disordered domain of Mgm101p is localized to the mitochondrial nucleoid |
Q90043286 | The Nopp140 gene in Drosophila melanogaster displays length polymorphisms in its large repetitive second exon |
Q79149287 | The N‐terminus is unstructured, but not dynamically disordered, in the complex between HK022 Nun protein and λ‐phage BoxB RNA hairpin |
Q28909797 | The PIR domain of Grb14 is an intrinsically unstructured protein: implication in insulin signaling |
Q42129907 | The RelA nuclear localization signal folds upon binding to IκBα. |
Q41768887 | The SCHOOL of nature: II. Protein order, disorder and oligomericity in transmembrane signaling |
Q30385977 | The Unstructured N-terminal Region of Arabidopsis Group 4 Late Embryogenesis Abundant (LEA) Proteins Is Required for Folding and for Chaperone-like Activity under Water Deficit. |
Q41915186 | The calponin regulatory region is intrinsically unstructured: novel insight into actin-calponin and calmodulin-calponin interfaces using NMR spectroscopy |
Q55043836 | The continuing conundrum of the LEA proteins. |
Q28080017 | The contribution of intrinsically disordered regions to protein function, cellular complexity, and human disease |
Q37572324 | The cytoplasmic domain of the T-cell receptor zeta subunit does not form disordered dimers |
Q37187941 | The disordered C-terminal domain of human DNA glycosylase NEIL1 contributes to its stability via intramolecular interactions |
Q30165009 | The dynamic behavior of CheW from Thermotoga maritima in solution, as determined by nuclear magnetic resonance: implications for potential protein-protein interaction sites |
Q40720904 | The dynamic structure of the estrogen receptor |
Q34264016 | The dynamics of signal amplification by macromolecular assemblies for the control of chromosome segregation |
Q33775584 | The effects of alpha-helical structure and cyanylated cysteine on each other |
Q34251310 | The hepatitis E virus polyproline region is involved in viral adaptation |
Q33566030 | The importance of being flexible: the case of basic region leucine zipper transcriptional regulators |
Q28776125 | The importance of intrinsic disorder for protein phosphorylation |
Q43152748 | The inactivating factor of glutamine synthetase, IF7, is a "natively unfolded" protein |
Q104064637 | The intracellular lipid-binding domain of human Na+/H+ exchanger 1 forms a lipid-protein co-structure essential for activity |
Q50914408 | The intrinsically disordered C-terminal region of Arabidopsis thaliana TCP8 transcription factor acts both as a transactivation and self-assembly domain. |
Q41940615 | The intrinsically disordered TC-1 interacts with Chibby via regions with high helical propensity |
Q30364875 | The intrinsically disordered structural platform of the plant defence hub protein RPM1-interacting protein 4 provides insights into its mode of action in the host-pathogen interface and evolution of the nitrate-induced domain protein family. |
Q38334792 | The key role of protein flexibility in modulating IgE interactions |
Q38105815 | The most important thing is the tail: multitudinous functionalities of intrinsically disordered protein termini |
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. |
Q30379937 | The protein meta-structure: a novel concept for chemical and molecular biology. |
Q41774157 | The relationship between relative solvent accessible surface area (rASA) and irregular structures in protean segments (ProSs) |
Q34632794 | The role of conformational entropy in molecular recognition by calmodulin |
Q37462213 | The role of disordered ribosomal protein extensions in the early steps of eubacterial 50 S ribosomal subunit assembly |
Q42972255 | The structure of human CD23 and its interactions with IgE and CD21. |
Q51281223 | The tumor suppressor inhibitor of growth 4 binds double-stranded DNA through its disordered central region. |
Q40895923 | The twilight zone between protein order and disorder |
Q30372413 | The unfoldomics decade: an update on intrinsically disordered proteins. |
Q54484534 | The unstructured N-terminal tail of ParG modulates assembly of a quaternary nucleoprotein complex in transcription repression. |
Q38710732 | The untapped potential of tyrosine-based G protein signaling |
Q36137400 | Thermodynamic dissection of the intrinsically disordered N-terminal domain of human glucocorticoid receptor |
Q47701859 | Thermotoga maritima IscU. Structural characterization and dynamics of a new class of metallochaperone |
Q38453379 | Time window expansion for HDX analysis of an intrinsically disordered protein |
Q37923322 | Towards a robust description of intrinsic protein disorder using nuclear magnetic resonance spectroscopy. |
Q38779721 | Transient disorder: Calcineurin as an example |
Q34963539 | Transient-state kinetic analysis of transcriptional activator·DNA complexes interacting with a key coactivator |
Q87381218 | Trehalose-Induced Structural Transition Accelerates Aggregation of α-Synuclein |
Q36218535 | Two Isoforms of Yersinia pestis Plasminogen Activator Pla: Intraspecies Distribution, Intrinsic Disorder Propensity, and Contribution to Virulence |
Q24533476 | Two sequence motifs from HIF-1alpha bind to the DNA-binding site of p53. |
Q89063745 | Uncoupling the Folding and Binding of an Intrinsically Disordered Protein |
Q50919522 | Under-folded proteins: Conformational ensembles and their roles in protein folding, function, and pathogenesis. |
Q30385084 | Understanding protein non-folding. |
Q33481254 | Unfoldomics of human diseases: linking protein intrinsic disorder with diseases |
Q53629521 | Unified perspective on proteins: a physics approach. |
Q73104353 | Unmasking ligand binding motifs: identification of a chemokine receptor motif by NMR studies of antagonist peptides |
Q42542563 | Unravelling the structure of the pneumococcal autolytic lysozyme |
Q41864976 | Unusual biophysics of immune signaling-related intrinsically disordered proteins |
Q24339439 | Unusual bipartite mode of interaction between the nonsense-mediated decay factors, UPF1 and UPF2 |
Q38044420 | Using NMR chemical shifts to calculate the propensity for structural order and disorder in proteins. |
Q27644406 | Using hydrogen deuterium exchange mass spectrometry to engineer optimized constructs for crystallization of protein complexes: Case study of PI4KIIIβ with Rab11 |
Q37451071 | Vaccine potentials of an intrinsically unstructured fragment derived from the blood stage-associated Plasmodium falciparum protein PFF0165c |
Q46735392 | VirtualSpectrum, a tool for simulating peak list for multi-dimensional NMR spectra |
Q34469965 | Visualization of coupled protein folding and binding in bacteria and purification of the heterodimeric complex |
Q47402805 | WITHDRAWN: Role of osmolytes in protein folding and aggregation in cells and its applications in biotechnology |
Q90346190 | What Drives 15N Spin Relaxation in Disordered Proteins? Combined NMR/MD Study of the H4 Histone Tail |
Q27012942 | What macromolecular crowding can do to a protein |
Q60302049 | Where differences resemble: sequence-feature analysis in curated databases of intrinsically disordered proteins |
Q28909275 | Yeast cox17 solution structure and Copper(I) binding |
Q36126137 | Yersinia pestis Caf1 Protein: Effect of Sequence Polymorphism on Intrinsic Disorder Propensity, Serological Cross-Reactivity and Cross-Protectivity of Isoforms |
Q41910014 | p25alpha is flexible but natively folded and binds tubulin with oligomeric stoichiometry |
Q28079390 | p53 Proteoforms and Intrinsic Disorder: An Illustration of the Protein Structure-Function Continuum Concept |
Q44788631 | pH and cation-induced thermodynamic stability of human hyaluronan binding protein 1 regulates its hyaluronan affinity |
Q34351764 | pH dependence of amide chemical shifts in natively disordered polypeptides detects medium-range interactions with ionizable residues |
Search more.