| scholarly article | Q13442814 |
| P50 | author | Svetlana Antonyuk | Q51971191 |
| Jennifer Stine Elam | Q75569251 | ||
| Todd O. Yeates | Q32063648 | ||
| P2093 | author name string | Alexander B Taylor | |
| P John Hart | |||
| S Samar Hasnain | |||
| Joan Selverstone Valentine | |||
| Lawrence J Hayward | |||
| Jorge A Rodriguez | |||
| Richard Strange | |||
| Peter A Doucette | |||
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| Decreased metallation and activity in subsets of mutant superoxide dismutases associated with familial amyotrophic lateral sclerosis. | Q38291855 | ||
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| Subunit asymmetry in the three-dimensional structure of a human CuZnSOD mutant found in familial amyotrophic lateral sclerosis | Q42846381 | ||
| Histological evidence of protein aggregation in mutant SOD1 transgenic mice and in amyotrophic lateral sclerosis neural tissues | Q43821139 | ||
| High molecular weight complexes of mutant superoxide dismutase 1: age-dependent and tissue-specific accumulation | Q43918294 | ||
| Fibrillar inclusions and motor neuron degeneration in transgenic mice expressing superoxide dismutase 1 with a disrupted copper-binding site | Q44070818 | ||
| ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions. | Q46135324 | ||
| Arrangement of subunits and ordering of beta-strands in an amyloid sheet | Q46564095 | ||
| Familial amyotrophic lateral sclerosis-associated mutations decrease the thermal stability of distinctly metallated species of human copper/zinc superoxide dismutase | Q46566731 | ||
| Axonal transport of mutant superoxide dismutase 1 and focal axonal abnormalities in the proximal axons of transgenic mice. | Q47692402 | ||
| Neurodegenerative disease: amyloid pores from pathogenic mutations | Q48544171 | ||
| P433 | issue | 6 | |
| P921 | main subject | amyotrophic lateral sclerosis | Q206901 |
| P304 | page(s) | 461-7 | |
| P577 | publication date | 2003-06-01 | |
| P1433 | published in | Nature structural biology | Q26842658 |
| P1476 | title | Amyloid-like filaments and water-filled nanotubes formed by SOD1 mutant proteins linked to familial ALS | |
| P478 | volume | 10 |
| Q37549326 | "Native-like aggregation" of the acylphosphatase from Sulfolobus solfataricus and its biological implications |
| Q40577106 | 3' untranslated region in a light neurofilament (NF-L) mRNA triggers aggregation of NF-L and mutant superoxide dismutase 1 proteins in neuronal cells. |
| Q30668587 | A common 'aggregation-prone' interface possibly participates in the self-assembly of human zona pellucida proteins. |
| Q37431412 | A common property of amyotrophic lateral sclerosis-associated variants: destabilization of the copper/zinc superoxide dismutase electrostatic loop |
| Q38291545 | A limited role for disulfide cross-linking in the aggregation of mutant SOD1 linked to familial amyotrophic lateral sclerosis. |
| Q41659008 | A mechanism for propagated SOD1 misfolding from frustration analysis of a G85R mutant protein assembly. |
| Q51261579 | A misfolded dimer of Cu/Zn-superoxide dismutase leading to pathological oligomerization in amyotrophic lateral sclerosis. |
| Q92863745 | A model for gain of function in superoxide dismutase |
| Q36995776 | A novel variant of human superoxide dismutase 1 harboring amyotrophic lateral sclerosis-associated and experimental mutations in metal-binding residues and free cysteines lacks toxicity in vivo |
| Q33638268 | A prion-like mechanism for the propagated misfolding of SOD1 from in silico modeling of solvated near-native conformers |
| Q37170196 | A quantitative examination of the role of cargo-exerted forces in axonal transport |
| Q40409233 | Aberrantly increased hydrophobicity shared by mutants of Cu,Zn-superoxide dismutase in familial amyotrophic lateral sclerosis. |
| Q34383094 | Aggregation modulating elements in mutant human superoxide dismutase 1. |
| Q34905853 | Amyloid formation by globular proteins under native conditions |
| Q52856652 | Amyloid formation under physiological conditions proceeds via a native-like folding intermediate. |
| Q33495551 | Amyloidogenic regions and interaction surfaces overlap in globular proteins related to conformational diseases |
| Q36986109 | An amyloid-forming segment of beta2-microglobulin suggests a molecular model for the fibril |
| Q38174873 | An emerging role for misfolded wild-type SOD1 in sporadic ALS pathogenesis |
| Q51591442 | An in silico study of the effect of SOD1 electrostatic loop dynamics on amyloid‑like filament formation. |
| Q35224579 | Analysis of mutant SOD1 electrophoretic mobility by Blue Native gel electrophoresis; evidence for soluble multimeric assemblies |
| Q49907306 | Atomic structures of corkscrew-forming segments of SOD1 reveal varied oligomer conformations |
| Q33891008 | Beta arcades: recurring motifs in naturally occurring and disease-related amyloid fibrils |
| Q44931860 | Bicarbonate and active site zinc modulate the self-peroxidation of bovine copper-zinc superoxide dismutase |
| Q28393352 | Binding mode of Thioflavin T and other molecular probes in the context of amyloid fibrils-current status |
| Q38069389 | Breaking the amyloidogenicity code: methods to predict amyloids from amino acid sequence |
| Q36407372 | Cargo distributions differentiate pathological axonal transport impairments |
| Q38766626 | Cellular Redox Systems Impact the Aggregation of Cu,Zn Superoxide Dismutase Linked to Familial Amyotrophic Lateral Sclerosis |
| Q28277615 | Cellular copper distribution: a mechanistic systems biology approach |
| Q57261217 | Chapter 14 Familial amyotrophic lateral sclerosis |
| Q27658869 | Characterization of a Covalent Polysulfane Bridge in Copper−Zinc Superoxide Dismutase, |
| Q35709805 | Characterization of heparin-induced glyceraldehyde-3-phosphate dehydrogenase early amyloid-like oligomers and their implication in α-synuclein aggregation. |
| Q51017813 | Characterizing Structural Stability of Amyloid Motif Fibrils Mediated by Water Molecules |
| Q41807230 | Characterizing intermolecular interactions that initiate native-like protein aggregation |
| Q26996075 | Chemical approaches to detect and analyze protein sulfenic acids |
| Q24299487 | Chromogranin-mediated secretion of mutant superoxide dismutase proteins linked to amyotrophic lateral sclerosis |
| Q34480306 | Common dynamical signatures of familial amyotrophic lateral sclerosis-associated structurally diverse Cu, Zn superoxide dismutase mutants |
| Q35928006 | Common molecular signature in SOD1 for both sporadic and familial amyotrophic lateral sclerosis. |
| Q39972533 | Complete loss of post-translational modifications triggers fibrillar aggregation of SOD1 in the familial form of amyotrophic lateral sclerosis |
| Q42694170 | Computational methods for identifying a layered allosteric regulatory mechanism for ALS‐causing mutations of Cu‐Zn superoxide dismutase 1 |
| Q38551857 | Conformational Disorder of the Most Immature Cu, Zn-Superoxide Dismutase Leading to Amyotrophic Lateral Sclerosis. |
| Q34310311 | Copper-based pulsed dipolar ESR spectroscopy as a probe of protein conformation linked to disease states |
| Q38769938 | Copper-zinc superoxide dismutase is activated through a sulfenic acid intermediate at a copper ion entry site |
| Q35234117 | Crystallizing ideas about Parkinson's disease |
| Q33680425 | DNA-Triggered Aggregation of Copper, Zinc Superoxide Dismutase in the Presence of Ascorbate |
| Q44971569 | Decrease of Hsp25 protein expression precedes degeneration of motoneurons in ALS-SOD1 mice |
| Q34572921 | Decreased stability and increased formation of soluble aggregates by immature superoxide dismutase do not account for disease severity in ALS. |
| Q57944931 | Dehydration stability of amyloid fibrils studied by AFM |
| Q33897544 | Destabilization of apoprotein is insufficient to explain Cu,Zn-superoxide dismutase-linked ALS pathogenesis. |
| Q36512177 | Detergent-insoluble aggregates associated with amyotrophic lateral sclerosis in transgenic mice contain primarily full-length, unmodified superoxide dismutase-1. |
| Q40496567 | Different immunoreactivity against monoclonal antibodies between wild-type and mutant copper/zinc superoxide dismutase linked to amyotrophic lateral sclerosis |
| Q37646220 | Dimer destabilization in superoxide dismutase may result in disease-causing properties: structures of motor neuron disease mutants. |
| Q50204472 | Direct Conversion of an Enzyme from Native-like to Amyloid-like Aggregates within Inclusion Bodies |
| Q37375549 | Disease-associated mutations at copper ligand histidine residues of superoxide dismutase 1 diminish the binding of copper and compromise dimer stability |
| Q27662078 | Disrupted Zinc-Binding Sites in Structures of Pathogenic SOD1 Variants D124V and H80R |
| Q45107835 | Dissociation of human copper-zinc superoxide dismutase dimers using chaotrope and reductant. Insights into the molecular basis for dimer stability |
| Q24544265 | Disulfide cross-linked protein represents a significant fraction of ALS-associated Cu, Zn-superoxide dismutase aggregates in spinal cords of model mice |
| Q34788369 | Disulfide-reduced ALS variants of Cu, Zn superoxide dismutase exhibit increased populations of unfolded species |
| Q40885460 | Dynamic properties of SOD1 mutants can predict survival time of patients carrying familial amyotrophic lateral sclerosis. |
| Q27690644 | Edge strand engineering prevents native-like aggregation in Sulfolobus solfataricus acylphosphatase |
| Q36507250 | Evaluation of a symmetry-based strategy for assembling protein complexes |
| Q91809748 | Evolutionary Analyses of Sequence and Structure Space Unravel the Structural Facets of SOD1 |
| Q64241123 | Experimental Mutations in Superoxide Dismutase 1 Provide Insight into Potential Mechanisms Involved in Aberrant Aggregation in Familial Amyotrophic Lateral Sclerosis |
| Q34082710 | Exposure of hydrophobic surfaces initiates aggregation of diverse ALS-causing superoxide dismutase-1 mutants |
| Q35012498 | Familial ALS-superoxide dismutases associate with mitochondria and shift their redox potentials. |
| Q36398045 | Fibrillation precursor of superoxide dismutase 1 revealed by gradual tuning of the protein-folding equilibrium |
| Q37619322 | Folding of human superoxide dismutase: disulfide reduction prevents dimerization and produces marginally stable monomers |
| Q57944846 | From Molecular to Supramolecular Amyloid Structures: Contributions from Fiber Diffraction and Electron Microscopy |
| Q46654946 | Fully metallated S134N Cu,Zn-superoxide dismutase displays abnormal mobility and intermolecular contacts in solution |
| Q27655747 | Functional features cause misfolding of the ALS-provoking enzyme SOD1 |
| Q37079411 | Hacking the code of amyloid formation: the amyloid stretch hypothesis |
| Q40389314 | HoxB2 binds mutant SOD1 and is altered in transgenic model of ALS. |
| Q46807674 | Human SOD1 before harboring the catalytic metal: solution structure of copper-depleted, disulfide-reduced form |
| Q34564980 | Human pancreatitis-associated protein forms fibrillar aggregates with a native-like conformation |
| Q64982638 | Hydrogen-Deuterium Exchange Profiles of Polyubiquitin Fibrils. |
| Q34317439 | Identification of a misfolded region in superoxide dismutase 1 that is exposed in amyotrophic lateral sclerosis. |
| Q33772493 | Immature copper-zinc superoxide dismutase and familial amyotrophic lateral sclerosis. |
| Q33541145 | Improving binding specificity of pharmacological chaperones that target mutant superoxide dismutase-1 linked to familial amyotrophic lateral sclerosis using computational methods |
| Q64231004 | Infinite Assembly of Folded Proteins in Evolution, Disease, and Engineering |
| Q38518708 | Informatics-assisted protein profiling in a transgenic mouse model of amyotrophic lateral sclerosis. |
| Q57204416 | Inhibition of Chaperone Activity Is a Shared Property of Several Cu,Zn-Superoxide Dismutase Mutants That Cause Amyotrophic Lateral Sclerosis |
| Q33942778 | Insights into SOD1-linked amyotrophic lateral sclerosis from NMR studies of Ni(2+)- and other metal-ion-substituted wild-type copper-zinc superoxide dismutases |
| Q30155471 | Intermolecular transmission of superoxide dismutase 1 misfolding in living cells |
| Q30159818 | Local unfolding in a destabilized, pathogenic variant of superoxide dismutase 1 observed with H/D exchange and mass spectrometry |
| Q35873804 | Local unfolding of Cu, Zn superoxide dismutase monomer determines the morphology of fibrillar aggregates |
| Q58608539 | Loss of charge mutations in solvent exposed Lys residues of superoxide dismutase 1 do not induce inclusion formation in cultured cell models |
| Q46851121 | Many roads lead to Rome? Multiple modes of Cu,Zn superoxide dismutase destabilization, misfolding and aggregation in amyotrophic lateral sclerosis |
| Q37707829 | Mapping superoxide dismutase 1 domains of non-native interaction: roles of intra- and intermolecular disulfide bonding in aggregation |
| Q37448164 | Metal deficiency increases aberrant hydrophobicity of mutant superoxide dismutases that cause amyotrophic lateral sclerosis |
| Q33559671 | Metal-free ALS variants of dimeric human Cu,Zn-superoxide dismutase have enhanced populations of monomeric species |
| Q64084482 | Microsecond sub-domain motions and the folding and misfolding of the mouse prion protein |
| Q47382895 | Molecular dynamics of a far positioned SOD1 mutant V14M reveals pathogenic misfolding behavior |
| Q27645269 | Molecular dynamics using atomic-resolution structure reveal structural fluctuations that may lead to polymerization of human Cu Zn superoxide dismutase |
| Q50069615 | Molecular mechanisms underlying the impact of mutations in SOD1 on its conformational properties associated with amyotrophic lateral sclerosis as revealed with molecular modelling |
| Q36062875 | Mutant SOD1 forms ion channel: implications for ALS pathophysiology |
| Q30159679 | Mutant SOD1 instability: implications for toxicity in amyotrophic lateral sclerosis |
| Q34438898 | Nonamyloid aggregates arising from mature copper/zinc superoxide dismutases resemble those observed in amyotrophic lateral sclerosis |
| Q89706496 | Nucleation and kinetics of SOD1 aggregation in human cells for ALS1 |
| Q30101060 | Parsing Disease-relevant Protein Modifications from Epiphenomena: Perspective on the Structural Basis of SOD1-Mediated ALS. |
| Q46171494 | Pathogenic Mutations Induce Partial Structural Changes in the Native β-Sheet Structure of Transthyretin and Accelerate Aggregation. |
| Q46375493 | Photoinduced fibrils formation of chicken egg white lysozyme under native conditions |
| Q35125315 | Posttranslational modifications in Cu,Zn-superoxide dismutase and mutations associated with amyotrophic lateral sclerosis. |
| Q38176187 | Prion-like activity of Cu/Zn superoxide dismutase: implications for amyotrophic lateral sclerosis. |
| Q37417809 | Probing the free energy landscapes of ALS disease mutants of SOD1 by NMR spectroscopy |
| Q46728737 | Proteasomal degradation of mutant superoxide dismutases linked to amyotrophic lateral sclerosis |
| Q33356197 | Protein aggregation and protein instability govern familial amyotrophic lateral sclerosis patient survival |
| Q35592405 | Protein aggregation in motor neurone disorders. |
| Q47126292 | Real-Time Observation of the Interaction between Thioflavin T and an Amyloid Protein by Using High-Sensitivity Rheo-NMR. |
| Q36497696 | Redox properties of the disulfide bond of human Cu,Zn superoxide dismutase and the effects of human glutaredoxin 1 |
| Q36673087 | SOD1 exhibits allosteric frustration to facilitate metal binding affinity |
| Q37479003 | SOD1-associated ALS: a promising system for elucidating the origin of protein-misfolding disease |
| Q42664185 | Small molecules present in the cerebrospinal fluid metabolome influence superoxide dismutase 1 aggregation |
| Q27648424 | Structural Characterization of Zinc-deficient Human Superoxide Dismutase and Implications for ALS |
| Q27679379 | Structural Consequences of Cysteinylation of Cu/Zn-Superoxide Dismutase |
| Q27653849 | Structural and Biophysical Properties of the Pathogenic SOD1 Variant H46R/H48Q † |
| Q27657645 | Structural and biophysical properties of metal-free pathogenic SOD1 mutants A4V and G93A |
| Q27654799 | Structural and dynamic aspects related to oligomerization of apo SOD1 and its mutants |
| Q36944974 | Structural basis of infectious and non-infectious amyloids |
| Q42252269 | Structural consequences of the familial amyotrophic lateral sclerosis SOD1 mutant His46Arg. |
| Q34947293 | Structural insights into functional and pathological amyloid |
| Q36693082 | Structural models of amyloid-like fibrils |
| Q27670773 | Structural switching of Cu,Zn-superoxide dismutases at loop VI: insights from the crystal structure of 2-mercaptoethanol-modified enzyme |
| Q36297476 | Structural, Functional, and Immunogenic Insights on Cu,Zn Superoxide Dismutase Pathogenic Virulence Factors from Neisseria meningitidis and Brucella abortus |
| Q27664114 | Structures of mouse SOD1 and human/mouse SOD1 chimeras |
| Q21136374 | Superoxide dismutase 1 and tgSOD1 mouse spinal cord seed fibrils, suggesting a propagative cell death mechanism in amyotrophic lateral sclerosis |
| Q35049047 | Superoxide dismutases and superoxide reductases |
| Q37771718 | Taking charge of proteins from neurodegeneration to industrial biotechnology |
| Q91419222 | The biophysics of superoxide dismutase-1 and amyotrophic lateral sclerosis |
| Q35928026 | The effect of amyotrophic lateral sclerosis-linked exogenous SOD1-G93A on electrophysiological properties and intracellular calcium in cultured rat astrocytes |
| Q33891158 | The effect of red pigment on the amyloidization of yeast proteins |
| Q37375579 | The effects of glutaredoxin and copper activation pathways on the disulfide and stability of Cu,Zn superoxide dismutase |
| Q28287224 | The rate and equilibrium constants for a multistep reaction sequence for the aggregation of superoxide dismutase in amyotrophic lateral sclerosis |
| Q44697040 | The role of solvent exclusion in the interaction between D124 and the metal site in SOD1: implications for ALS. |
| Q34993111 | The structural biochemistry of the superoxide dismutases. |
| Q33356208 | The threat of instability: neurodegeneration predicted by protein destabilization and aggregation propensity |
| Q35623240 | Therapeutic effects of immunization with mutant superoxide dismutase in mice models of amyotrophic lateral sclerosis |
| Q92032360 | Therapeutic vaccines for amyotrophic lateral sclerosis directed against disease specific epitopes of superoxide dismutase 1 |
| Q35763674 | Thermal fluctuations of immature SOD1 lead to separate folding and misfolding pathways |
| Q27687002 | Three-dimensional domain swapping and supramolecular protein assembly: insights from the X-ray structure of a dimeric swapped variant of human pancreatic RNase |
| Q27002139 | Top-down proteomics in health and disease: challenges and opportunities |
| Q37416520 | Transient structural distortion of metal-free Cu/Zn superoxide dismutase triggers aberrant oligomerization |
| Q93061331 | Tryptophan residue 32 in human Cu-Zn superoxide dismutase modulates prion-like propagation and strain selection |
| Q37877295 | Understanding the complex mechanisms of β2-microglobulin amyloid assembly |
| Q40440970 | Unsaturated fatty acids induce cytotoxic aggregate formation of amyotrophic lateral sclerosis-linked superoxide dismutase 1 mutants. |
| Q92021353 | β-Methylamino-L-alanine substitution of serine in SOD1 suggests a direct role in ALS etiology |
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