scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1033621540 |
P356 | DOI | 10.1038/NSB0395-199 |
P698 | PubMed publication ID | 7773788 |
P5875 | ResearchGate publication ID | 15424983 |
P2093 | author name string | Baumeister W | |
Wenzel T | |||
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The conformational properties of somatostatin IV. The conformers contributing to the conformational equilibrium of somatostatin in aqueous solution as found by semi-empirical energy calculations and high-resolution NMR experiments | Q72519289 | ||
Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa | Q27861105 | ||
Inhibitors of the proteasome block the degradation of most cell proteins and the generation of peptides presented on MHC class I molecules | Q28248180 | ||
The ubiquitin-proteasome proteolytic pathway | Q29618638 | ||
A 1.4-nm gold cluster covalently attached to antibodies improves immunolabeling | Q31123677 | ||
Somatostatin conformation: evidence for a stable intramolecular structure from circular dichroism, diffusion, and sedimentation equilibrium | Q34997012 | ||
Proteolysis, proteasomes and antigen presentation | Q35228583 | ||
Constrained peptides: models of bioactive peptides and protein substructures | Q35671045 | ||
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Structural features of 26S and 20S proteasomes. | Q40494212 | ||
Proteasomes: protein degradation machines of the cell | Q40646488 | ||
Sequential degradation of the neuropeptide gonadotropin-releasing hormone by the 20 S granulosa cell proteasomes | Q41461441 | ||
Gamma-interferon and expression of MHC genes regulate peptide hydrolysis by proteasomes | Q41527048 | ||
The three-dimensional structure of proteasomes from Thermoplasma acidophilum as determined by electron microscopy using random conical tilting | Q44032238 | ||
Primary structure of the Thermoplasma proteasome and its implications for the structure, function, and evolution of the multicatalytic proteinase | Q44722342 | ||
Evidence that the nature of amino acid residues in the P3 position directs substrates to distinct catalytic sites of the pituitary multicatalytic proteinase complex (proteasome). | Q48120291 | ||
Conformation of GroEL-bound alpha-lactalbumin probed by mass spectrometry. | Q54622296 | ||
Expression of functional Thermoplasma acidophilum proteasomes in Escherichia coli. | Q54668957 | ||
Electron microscopy and image analysis reveal common principles of organization in two large protein complexes: groEL-type proteins and proteasomes. | Q54714309 | ||
Structure of a molecular chaperone from a thermophilic archaebacterium | Q59070702 | ||
MHC-linked LMP gene products specifically alter peptidase activities of the proteasome | Q59088266 | ||
The multicatalytic proteinase (prosome) is ubiquitous from eukaryotes to archaebacteria | Q69216368 | ||
Thermoplasma acidophilum proteasomes degrade partially unfolded and ubiquitin-associated proteins | Q70464181 | ||
Pathway of disulfide-coupled unfolding and refolding of bovine alpha-lactalbumin | Q70644814 | ||
Structural characterization of the disulfide folding intermediates of bovine alpha-lactalbumin | Q70644817 | ||
Critical elements in proteasome assembly | Q71955022 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 199-204 | |
P577 | publication date | 1995-03-01 | |
P1433 | published in | Nature structural biology | Q26842658 |
P1476 | title | Conformational constraints in protein degradation by the 20S proteasome | |
P478 | volume | 2 |
Q50740999 | 20S proteasomes have the potential to keep substrates in store for continual degradation. |
Q73327194 | A short cut for the immune system |
Q53007185 | A third interferon-gamma-induced subunit exchange in the 20S proteasome. |
Q38575440 | A voyage to the inner space of cells |
Q34398922 | A yeast Ubc9 mutant protein with temperature-sensitive in vivo function is subject to conditional proteolysis by a ubiquitin- and proteasome-dependent pathway |
Q73177832 | AAA-ATPases at the crossroads of protein life and death |
Q44283109 | ATP hydrolysis by the proteasome regulatory complex PAN serves multiple functions in protein degradation |
Q43681662 | ATP-dependent proteases degrade their substrates by processively unraveling them from the degradation signal |
Q73521390 | ATPase and ubiquitin-binding proteins of the yeast proteasome |
Q71996662 | Amyloid β-Protein Inhibits Ubiquitin-dependent Protein Degradation in Vitro |
Q33873082 | An archaebacterial ATPase, homologous to ATPases in the eukaryotic 26 S proteasome, activates protein breakdown by 20 S proteasomes |
Q45018402 | An unstructured initiation site is required for efficient proteasome-mediated degradation |
Q34801818 | Antigen degradation or presentation by MHC class I molecules via classical and non-classical pathways |
Q35209250 | Archaeal proteasomes: potential in metabolic engineering |
Q34418425 | Archaeal proteasomes: proteolytic nanocompartments of the cell |
Q30831374 | Assembly of the Drosophila 26 S proteasome is accompanied by extensive subunit rearrangements |
Q71973342 | Binding of amyloid beta protein to the 20 S proteasome |
Q43943338 | Binding of hydrophobic peptides to several non-catalytic sites promotes peptide hydrolysis by all active sites of 20 S proteasomes. Evidence for peptide-induced channel opening in the alpha-rings |
Q33994076 | Biochemical and physical properties of the Methanococcus jannaschii 20S proteasome and PAN, a homolog of the ATPase (Rpt) subunits of the eucaryal 26S proteasome |
Q34873055 | Can misfolded proteins be beneficial? The HAMLET case |
Q34568997 | Cancer/testis antigens: structural and immunobiological properties |
Q30376143 | Changes in proteasome structure and function caused by HAMLET in tumor cells. |
Q64166868 | Chemical Tools To Study the Proteasome |
Q41052878 | Circular assemblies |
Q44038790 | Concurrent translocation of multiple polypeptide chains through the proteasomal degradation channel |
Q37875825 | Context-dependent resistance to proteolysis of intrinsically disordered proteins |
Q27640057 | Crystal structure of the protease domain of a heat-shock protein HtrA from Thermotoga maritima |
Q36342153 | Dynamic association of proteasomal machinery with the centrosome |
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Q41603733 | Electron Microscopy and Image Processing: Essential Tools for Structural Analysis of Macromolecules |
Q38237803 | Emerging mechanistic insights into AAA complexes regulating proteasomal degradation |
Q36450745 | Endoproteolytic activity of the proteasome |
Q34463371 | Enzymes catalyzing ubiquitination and proteolytic processing of the p105 precursor of nuclear factor kappaB1. |
Q41535709 | Eubacterial proteasomes |
Q33930855 | Evidence that proteolysis of Gal4 cannot explain the transcriptional effects of proteasome ATPase mutations |
Q30576410 | HAMLET: functional properties and therapeutic potential |
Q33993001 | Halophilic 20S proteasomes of the archaeon Haloferax volcanii: purification, characterization, and gene sequence analysis |
Q58322274 | Identification of the gal4 suppressor Sug1 as a subunit of the yeast 26S proteasome |
Q42583535 | Involvement of a eukaryotic-like ubiquitin-related modifier in the proteasome pathway of the archaeon Sulfolobus acidocaldarius. |
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Q37086732 | Knotting and unknotting of a protein in single molecule experiments. |
Q30474083 | Missense mutations in the NF2 gene result in the quantitative loss of merlin protein and minimally affect protein intrinsic function |
Q64087496 | Modulation of Disordered Proteins with a Focus on Neurodegenerative Diseases and Other Pathologies |
Q47072449 | Molecular characterization of the Rpt1/p48B ATPase subunit of the Drosophila melanogaster 26S proteasome. |
Q34116003 | Multiple modes of interaction of the deglycosylation enzyme, mouse peptide N-glycanase, with the proteasome |
Q33869201 | New frontiers in gold labeling |
Q33796113 | Oligomers of mutant glial fibrillary acidic protein (GFAP) Inhibit the proteasome system in alexander disease astrocytes, and the small heat shock protein alphaB-crystallin reverses the inhibition |
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Q41053715 | Processing and delivery of peptides presented by MHC class I molecules |
Q37826501 | Proteasome activators |
Q34976438 | Proteasome degradation of brain cytosolic tau in Alzheimer's disease |
Q34341985 | Proteasome inhibitors: from research tools to drug candidates |
Q40476345 | Proteasome: a complex protease with a new fold and a distinct mechanism |
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Q41656243 | Protein translocation channels in the proteasome and other proteases |
Q40427886 | Proteolysis: The proteasome: a protein-degrading organelle? |
Q41189449 | Proteostasis, oxidative stress and aging |
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Q38303135 | Rad23 provides a link between the Png1 deglycosylating enzyme and the 26 S proteasome in yeast. |
Q34188164 | Rearrangement of the 16S precursor subunits is essential for the formation of the active 20S proteasome |
Q24291760 | Selective chemical inactivation of AAA proteins reveals distinct functions of proteasomal ATPases |
Q41633142 | Self-compartmentalizing proteases. |
Q72033286 | Sighting the cellular shredder |
Q36254901 | Single-particle selection and alignment with heavy atom cluster-antibody conjugates |
Q83225722 | Specific lid-base contacts in the 26s proteasome control the conformational switching required for substrate degradation |
Q31096459 | Specific orientation and two-dimensional crystallization of the proteasome at metal-chelating lipid interfaces |
Q27628418 | Structural basis for the activation of 20S proteasomes by 11S regulators |
Q38081952 | Structural biology of the proteasome |
Q41535692 | Structure and structure formation of the 20S proteasome |
Q27748362 | Structure of the proteasome activator REGalpha (PA28alpha) |
Q22010425 | Subcellular localization, stoichiometry, and protein levels of 26 S proteasome subunits in yeast |
Q44121715 | Substrate size selectivity of 20S proteasomes: analysis with variable-sized synthetic substrates |
Q39702656 | Subunit topology of two 20S proteasomes from Haloferax volcanii |
Q63383896 | The 19S Regulatory Complex of the Proteasome Functions Independently of Proteolysis in Nucleotide Excision Repair |
Q39843088 | The DegP and DegQ periplasmic endoproteases of Escherichia coli: specificity for cleavage sites and substrate conformation |
Q41862238 | The Ubiquitin-Proteasome System in Huntington's Disease: Are Proteasomes Impaired, Initiators of Disease, or Coming to the Rescue? |
Q26785503 | The different roles of selective autophagic protein degradation in mammalian cells |
Q48072601 | The first characterization of a eubacterial proteasome: the 20S complex of Rhodococcus |
Q54567772 | The human alpha-type proteasomal subunit HsC8 forms a double ringlike structure, but does not assemble into proteasome-like particles with the beta-type subunits HsDelta or HsBPROS26. |
Q36065854 | The pore of activated 20S proteasomes has an ordered 7-fold symmetric conformation |
Q73204803 | The proteasome |
Q24673577 | The proteasome 11S regulator subunit REG alpha (PA28 alpha) is a heptamer |
Q33785021 | The proteasome: a macromolecular assembly designed for controlled proteolysis |
Q36862775 | The proteasome: a macromolecular assembly designed to confine proteolysis to a nanocompartment |
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Q39498144 | Zn2+-induced reversible dissociation of subunit Rpn10/p54 of the Drosophila 26 S proteasome |
Q36402945 | alpha v beta3-dependent cross-presentation of matrix metalloproteinase-2 by melanoma cells gives rise to a new tumor antigen. |
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