| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1028650180 |
| P356 | DOI | 10.1038/86188 |
| P3181 | OpenCitations bibliographic resource ID | 682062 |
| P698 | PubMed publication ID | 11276250 |
| P5875 | ResearchGate publication ID | 12057639 |
| P50 | author | Mariusz Jaskólski | Q11770106 |
| Anders Grubb | Q50855618 | ||
| Maciej Kozak | Q58147440 | ||
| P2093 | author name string | E Jankowska | |
| M Abrahamson | |||
| R Janowski | |||
| Z Grzonka | |||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 316-20 | |
| P577 | publication date | 2001-04-01 | |
| P1433 | published in | Nature structural biology | Q26842658 |
| P1476 | title | Human cystatin C, an amyloidogenic protein, dimerizes through three-dimensional domain swapping | |
| P478 | volume | 8 |
| Q89619309 | 3D domain swapping in the TIM barrel of the α subunit of Streptococcus pneumoniae tryptophan synthase |
| Q24644990 | 3D domain swapping: as domains continue to swap |
| Q35804628 | 3DSwap: curated knowledgebase of proteins involved in 3D domain swapping |
| Q53807797 | A Single Amino Acid in the Hinge Loop Region of the FOXP Forkhead Domain is Significant for Dimerisation. |
| Q61443307 | A five-residue motif for the design of domain swapping in proteins |
| Q47432033 | A mechanistic model to predict effects of cathepsin B and cystatin C on β-amyloid aggregation and degradation |
| Q27642242 | A protein contortionist: core mutations of GB1 that induce dimerization and domain swapping |
| Q34640009 | ACHESYM: an algorithm and server for standardized placement of macromolecular models in the unit cell |
| Q53344121 | Aberrant expression of cystatin C in prostate cancer is associated with neuroendocrine differentiation. |
| Q36354413 | Acidic pH promotes oligomerization and membrane insertion of the BclXL apoptotic repressor |
| Q47921291 | Amino-acid composition after loop deletion drives domain swapping |
| Q58179795 | Amyloid fibril formation by human stefin B: influence of pH and TFE on fibril growth and morphology |
| Q35652946 | Amyloid properties of the mouse egg zona pellucida |
| Q34756441 | Amyloid-fibril formation. Proposed mechanisms and relevance to conformational disease |
| Q35309786 | Amyloid-like fibrils from a domain-swapping protein feature a parallel, in-register conformation without native-like interactions. |
| Q30351368 | Amyloid-like fibrils of ribonuclease A with three-dimensional domain-swapped and native-like structure. |
| Q36986109 | An amyloid-forming segment of beta2-microglobulin suggests a molecular model for the fibril |
| Q34357767 | Analysis of domain-swapped oligomers reveals local sequence preferences and structural imprints at the linker regions and swapped interfaces |
| Q47788351 | Appendant structure plays an important role in amyloidogenic cystatin dimerization prior to domain swapping |
| Q37410752 | Application of amide hydrogen/deuterium exchange mass spectrometry for epitope mapping in human cystatin C. |
| Q27666546 | Atomic structure of a nanobody-trapped domain-swapped dimer of an amyloidogenic 2-microglobulin variant |
| Q34377103 | Biochemistry and clinical role of human cystatin C. |
| Q92071855 | Biological Activities of Secretory RNases: Focus on Their Oligomerization to Design Antitumor Drugs |
| Q42396970 | CEREBRAL AMYLOID ANGIOPATHY AND ALZHEIMER'S DISEASE. |
| Q57740813 | Carboxy terminal extended phytocystatins are bifunctional inhibitors of papain and legumain cysteine proteinases |
| Q36136387 | Cerebral amyloidosis: amyloid subunits, mutants and phenotypes. |
| Q39313522 | Characteristics of C-terminal, β-amyloid peptide binding fragment of neuroprotective protease inhibitor, cystatin C. |
| Q40725030 | Characterization of a cysteine proteinase inhibitor induced during neuronal cell differentiation |
| Q46977409 | Characterization of the dimerization process of a domain-swapped dimeric variant of human pancreatic ribonuclease. |
| Q35177052 | Collapse transitions in thermosensitive multi-block copolymers: a Monte Carlo study. |
| Q27659998 | Crystal structure of human cystatin C stabilized against amyloid formation |
| Q34397220 | Crystal structure of human cystatin D, a cysteine peptidase inhibitor with restricted inhibition profile |
| Q27639362 | Crystal structure of the FHA domain of the Chfr mitotic checkpoint protein and its complex with tungstate |
| Q27642485 | Crystal structure of the dimeric unswapped form of bovine seminal ribonuclease |
| Q24291661 | Crystal structure of the extracellular segment of integrin alpha Vbeta3 |
| Q35596625 | Crystallization and preliminary X-ray diffraction analysis of Val57 mutants of the amyloidogenic protein human cystatin C. |
| Q43241222 | Cystatin C in macular and neuronal degenerations: implications for mechanism(s) of age-related macular degeneration |
| Q38341202 | Cystatin C is a disease-associated protein subject to multiple regulation |
| Q36274319 | Cystatin F is a biomarker of prion pathogenesis in mice |
| Q37424088 | Cystatin SN neutralizes the inhibitory effect of cystatin C on cathepsin B activity |
| Q44740563 | Cystatin forms a tetramer through structural rearrangement of domain-swapped dimers prior to amyloidogenesis |
| Q37696036 | Cystatin superfamily |
| Q39662527 | Cystatins – Extra- and intracellular cysteine protease inhibitors: High-level secretion and uptake of cystatin C in human neuroblastoma cells |
| Q26860406 | Cysteine cathepsins: from structure, function and regulation to new frontiers |
| Q27318382 | Deciphering the structure, growth and assembly of amyloid-like fibrils using high-speed atomic force microscopy |
| Q33728524 | Detection and Alignment of 3D Domain Swapping Proteins Using Angle-Distance Image-Based Secondary Structural Matching Techniques |
| Q37683390 | Developmental regulation of synthesis and dimerization of the amyloidogenic protease inhibitor cystatin C in the hematopoietic system. |
| Q43897439 | Differences between the prion protein and its homolog Doppel: a partially structured state with implications for scrapie formation |
| Q36526184 | Differences in aggregation properties of three site-specific mutants of recombinant human stefin B. |
| Q52665959 | Distinct structural changes in wild-type and amyloidogenic chicken cystatin caused by disruption of C95-C115 disulfide bond. |
| Q42241154 | Domain swapping and amyloid fibril conformation. |
| Q47743214 | Domain swapping of a llama VHH domain builds a crystal-wide beta-sheet structure |
| Q34447486 | Double domain swapping in bovine seminal RNase: formation of distinct N- and C-swapped tetramers and multimers with increasing biological activities |
| Q52950207 | Effect of environmental conditions on aggregation and fibril formation of barstar. |
| Q50985492 | Effect of methionine80 heme coordination on domain swapping of cytochrome c. |
| Q46098256 | Essential role of Pro 74 in stefin B amyloid-fibril formation: dual action of cyclophilin A on the process |
| Q35877781 | Evaluation of cystatin C activities against HIV |
| Q36639277 | Exploring protein aggregation and self-propagation using lattice models: phase diagram and kinetics |
| Q37519879 | FAMCS: finding all maximal common substructures in proteins |
| Q34138249 | Familial conformational diseases and dementias |
| Q37635821 | Fertility defects in mice expressing the L68Q variant of human cystatin C: a role for amyloid in male infertility. |
| Q48182955 | Fibrillogenic oligomers of human cystatin C are formed by propagated domain swapping |
| Q27312912 | Formation of cystine slipknots in dimeric proteins |
| Q42265622 | Fungal lectin MpL enables entry of protein drugs into cancer cells and their subcellular targeting. |
| Q47605166 | Gelsolin pathogenic Gly167Arg mutation promotes domain-swap dimerization of the protein |
| Q36088829 | Genome-Wide Prediction and Analysis of 3D-Domain Swapped Proteins in the Human Genome from Sequence Information |
| Q31156451 | Glycosylation and specific deamidation of ribonuclease B affect the formation of three-dimensional domain-swapped oligomers. |
| Q44497203 | High pressure induces the formation of aggregation-prone states of proteins under reducing conditions |
| Q34053657 | High throughput testing of drug library substances and monoclonal antibodies for capacity to reduce formation of cystatin C dimers to identify candidates for treatment of hereditary cystatin C amyloid angiopathy. |
| Q38987127 | Human cystatin C monomer, dimer, oligomer, and amyloid structures are related to health and disease. |
| Q34564980 | Human pancreatitis-associated protein forms fibrillar aggregates with a native-like conformation |
| Q43875211 | Human stefin B readily forms amyloid fibrils in vitro |
| Q47563579 | Identification and characterization of antibodies elicited by human cystatin C fragment. |
| Q43057871 | In vitro study of stability and amyloid-fibril formation of two mutants of human stefin B (cystatin B) occurring in patients with EPM1. |
| Q41859753 | Influence of point mutations on the stability, dimerization, and oligomerization of human cystatin C and its L68Q variant |
| Q50882222 | Insights into the mechanism of cystatin C oligomer and amyloid formation and its interaction with β-amyloid. |
| Q34862258 | Integrin structure: new twists and turns in dynamic cell adhesion |
| Q33661328 | Interaction between oligomers of stefin B and amyloid-beta in vitro and in cells. |
| Q43999627 | Interaction of serum amyloid A with human cystatin C--assessment of amino acid residues crucial for hCC-SAA formation (part II). |
| Q44530124 | Interaction of serum amyloid A with human cystatin C--identification of binding sites. |
| Q49885401 | Involvement of Cystatin C in Immunity and Apoptosis. |
| Q48287384 | Isolation and characterization of autoantibodies against human cystatin C. |
| Q38557771 | Journey of cystatins from being mere thiol protease inhibitors to at heart of many pathological conditions |
| Q35712841 | Ligand binding and membrane insertion compete with oligomerization of the BclXL apoptotic repressor |
| Q26749121 | Lysosomal cathepsins and their regulation in aging and neurodegeneration |
| Q42428466 | Mapping local structural perturbations in the native state of stefin B (cystatin B) under amyloid forming conditions. |
| Q37871074 | Mechanisms of amyloid fibril formation--focus on domain-swapping |
| Q36609753 | Mechanistic biomarkers for cytotoxic acute kidney injury |
| Q51334586 | Modelling family 2 cystatins and their interaction with papain. |
| Q30497091 | Molecular determinants of improved cathepsin B inhibition by new cystatins obtained by DNA shuffling |
| Q30165046 | Molecular dynamics simulation of the SH3 domain aggregation suggests a generic amyloidogenesis mechanism |
| Q45796784 | Molecular dynamics simulation to investigate the impact of disulfide bond formation on conformational stability of chicken cystatin I66Q mutant |
| Q42629832 | Molecular dynamics simulations of human cystatin C and its L68Q varient to investigate the domain swapping mechanism |
| Q51024224 | Molecular dynamics simulations to investigate the domain swapping mechanism of human cystatin C. |
| Q50467116 | Monomers of the NhaA Na+/H+ antiporter of Escherichia coli are fully functional yet dimers are beneficial under extreme stress conditions at alkaline pH in the presence of Na+ or Li+. |
| Q34452395 | Oligomerization and aggregation of bovine pancreatic ribonuclease A: characteristic events observed by FTIR spectroscopy |
| Q46220803 | Oligomerization and transglutaminase cross-linking of the cystatin CRES in the mouse epididymal lumen: potential mechanism of extracellular quality control |
| Q34315788 | Oligomerization of bovine ribonuclease A: structural and functional features of its multimers |
| Q44952066 | Oligomerization of ribonuclease A: two novel three-dimensional domain-swapped tetramers |
| Q21256421 | On the origin of the histone fold |
| Q40320734 | Open interface and large quaternary structure movements in 3D domain swapped proteins: insights from molecular dynamics simulations of the C-terminal swapped dimer of ribonuclease A. |
| Q38617150 | Partial rotational lattice order-disorder in stefin B crystals. |
| Q30417671 | Pressure as a denaturing agent in studies of single-point mutants of an amyloidogenic protein human cystatin c. |
| Q41275437 | Pretreatment Serum Cystatin C Levels Predict Renal Function, but Not Tumor Characteristics, in Patients with Prostate Neoplasia. |
| Q33232435 | Prevention of amyloid fibril formation of amyloidogenic chicken cystatin by site-specific glycosylation in yeast |
| Q33199753 | Prevention of domain swapping inhibits dimerization and amyloid fibril formation of cystatin C: use of engineered disulfide bridges, antibodies, and carboxymethylpapain to stabilize the monomeric form of cystatin C. |
| Q42378672 | Production of Cystatin C Wild Type and Stabilized Mutants |
| Q42105214 | Proline Residues as Switches in Conformational Changes Leading to Amyloid Fibril Formation |
| Q43093815 | Protein aggregation determinants from a simplified model: cooperative folders resist aggregation |
| Q34525881 | Protein folding and three-dimensional domain swapping: a strained relationship? |
| Q30365413 | Protein reconstitution and three-dimensional domain swapping: benefits and constraints of covalency. |
| Q33920260 | Protein-folding landscapes in multichain systems. |
| Q48098677 | Proteomics identification of proteins in human cortex using multidimensional separations and MALDI tandem mass spectrometer |
| Q27336041 | Rapid sampling of molecular motions with prior information constraints |
| Q50931817 | Rational design of a low-affinity peptide for the detection of cystatin C in a fast homogeneous immunoassay. |
| Q27696139 | Rational design of heterodimeric protein using domain swapping for myoglobin |
| Q41987667 | Regions which are Responsible for Swapping are also Responsible for Folding and Misfolding |
| Q34650054 | Runaway domain swapping in amyloid-like fibrils of T7 endonuclease I. |
| Q30365734 | Self-assembly of human latexin into amyloid-like oligomers. |
| Q52012637 | Sequence-structure signals of 3D domain swapping in proteins. |
| Q34932013 | Serpinopathies and the conformational dementias |
| Q55382081 | Serum Cystatin C Level Is Not a Promising Biomarker for Predicting Clinicopathological Characteristics of Bladder Urothelial Tumors. |
| Q57186606 | Similar toxicity of the oligomeric molten globule state and the prefibrillar oligomers |
| Q43477001 | Size and morphology of toxic oligomers of amyloidogenic proteins: a case study of human stefin B. |
| Q36910057 | Stabilization, characterization, and selective removal of cystatin C amyloid oligomers. |
| Q46161037 | Steered molecular dynamics simulation of the binding of the β2 and β3 regions in domain-swapped human cystatin C dimer |
| Q47579578 | Steered molecular dynamics simulations on the binding of the appendant structure and helix-β2 in domain-swapped human cystatin C dimer |
| Q43189990 | Structural and dynamic properties of a new amyloidogenic chicken cystatin mutant I108T. |
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| Q34511593 | Structural basis of reduction-dependent activation of human cystatin F. |
| Q27676957 | Structural characterization of V57D and V57P mutants of human cystatin C, an amyloidogenic protein |
| Q34947293 | Structural insights into functional and pathological amyloid |
| Q36693082 | Structural models of amyloid-like fibrils |
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| Q28084296 | The Landscape of Intertwined Associations in Homooligomeric Proteins |
| Q27680786 | The Multidrug Resistance IncA/C Transferable Plasmid Encodes a Novel Domain-swapped Dimeric Protein-disulfide Isomerase |
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| Q27662251 | The crystal structures of two salivary cystatins from the tick Ixodes scapularis and the effect of these inhibitors on the establishment of Borrelia burgdorferi infection in a murine model |
| Q64994075 | The domain swapping of human cystatin C induced by synchrotron radiation. |
| Q27639001 | The domain-swapped dimer of cyanovirin-N is in a metastable folded state: reconciliation of X-ray and NMR structures |
| Q30165352 | The dual role of a loop with low loop contact distance in folding and domain swapping |
| Q45872079 | The mammalian DUF59 protein Fam96a forms two distinct types of domain-swapped dimer |
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| Q28307028 | The role of cystatin C in cerebral amyloid angiopathy and stroke: cell biology and animal models |
| Q36650672 | The role of cystatins in cells of the immune system |
| Q34177517 | The role of dimerization in prion replication |
| Q36596587 | The structural biology of protein aggregation diseases: Fundamental questions and some answers |
| Q35080182 | The unfolding story of three-dimensional domain swapping. |
| Q44281858 | Thermal aggregation of ribonuclease A. A contribution to the understanding of the role of 3D domain swapping in protein aggregation |
| Q44743859 | Thermal and guanidine hydrochloride-induced denaturation of human cystatin C. |
| Q27687002 | Three-dimensional domain swapping and supramolecular protein assembly: insights from the X-ray structure of a dimeric swapped variant of human pancreatic RNase |
| Q27634658 | Three-dimensional domain swapping in the folded and molten-globule states of cystatins, an amyloid-forming structural superfamily |
| Q43205499 | Trinucleotide expansions leading to an extended poly-L-alanine segment in the poly (A) binding protein PABPN1 cause fibril formation |
| Q42943805 | Two new types of assays to determine protein concentrations in biological fluids using mass spectrometry of intact proteins with cystatin C in spinal fluid as an example |
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| Q33368470 | Viral cystatin evolution and three-dimensional structure modelling: a case of directional selection acting on a viral protein involved in a host-parasitoid interaction |
| Q30382591 | Wetting of nonconserved residue-backbones: A feature indicative of aggregation associated regions of proteins. |
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| Q27666185 | β2-microglobulin forms three-dimensional domain-swapped amyloid fibrils with disulfide linkages |
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