scholarly article | Q13442814 |
P356 | DOI | 10.1126/SCIENCE.8310296 |
P698 | PubMed publication ID | 8310296 |
P2093 | author name string | P Christen | |
A Baici | |||
D Schmid | |||
H Gehring | |||
P433 | issue | 5149 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | molecular chaperones | Q422496 |
P304 | page(s) | 971-3 | |
P577 | publication date | 1994-02-18 | |
P1433 | published in | Science | Q192864 |
P1476 | title | Kinetics of molecular chaperone action | |
P478 | volume | 263 |
Q44765749 | 73-kDa molecular chaperone HSP73 is a direct target of antibiotic gentamicin |
Q28190002 | A DnaJ protein, apobec-1-binding protein-2, modulates apolipoprotein B mRNA editing |
Q41063873 | A cycle of binding and release of the DnaK, DnaJ and GrpE chaperones regulates activity of the Escherichia coli heat shock transcription factor sigma32. |
Q41887781 | A dancer caught midstep: the structure of ATP-bound Hsp70 |
Q41834098 | A disulfide-bonded DnaK dimer is maintained in an ATP-bound state |
Q35580778 | A functional DnaK dimer is essential for the efficient interaction with Hsp40 heat shock protein |
Q36769116 | A role for molecular chaperone Hsc70 in reovirus outer capsid disassembly |
Q39538987 | ATPase domain and interdomain linker play a key role in aggregation of mitochondrial Hsp70 chaperone Ssc1. |
Q33996861 | ATPase-defective derivatives of Escherichia coli DnaK that behave differently with respect to ATP-induced conformational change and peptide release |
Q37626722 | Acidic receptor domains on both sides of the outer membrane mediate translocation of precursor proteins into yeast mitochondria |
Q35753003 | All in the family: atypical Hsp70 chaperones are conserved modulators of Hsp70 activity. |
Q27678317 | Allosteric opening of the polypeptide-binding site when an Hsp70 binds ATP |
Q28266387 | Allostery in the Hsp70 chaperone proteins |
Q36580076 | Aptamer-Enabled Manipulation of the Hsp70 Chaperone System Suggests a Novel Strategy for Targeted Ubiquitination |
Q71440821 | Atomic force microscopy visualizes ATP-dependent dissociation of multimeric TATA-binding protein before translocation into the cell nucleus |
Q43664685 | Bag-1M accelerates nucleotide release for human Hsc70 and Hsp70 and can act concentration-dependent as positive and negative cofactor. |
Q36069364 | Beyond transcription--new mechanisms for the regulation of molecular chaperones |
Q28303811 | BiP/Kar2p serves as a molecular chaperone during carboxypeptidase Y folding in yeast |
Q33580742 | Binding of a small molecule at a protein-protein interface regulates the chaperone activity of hsp70-hsp40. |
Q71070590 | Binding of mitochondrial presequences to yeast cytosolic heat shock protein 70 depends on the amphiphilicity of the presequence |
Q92748401 | Biophysical Consequences of EVEN-PLUS Syndrome Mutations for the Function of Mortalin |
Q34629019 | C-terminal amino acids are essential for human heat shock protein 70 dimerization |
Q34051682 | Central domain deletions affect the SAXS solution structure and function of yeast Hsp40 proteins Sis1 and Ydj1. |
Q27936368 | Cer1p functions as a molecular chaperone in the endoplasmic reticulum of Saccharomyces cerevisiae |
Q36069355 | Chaperone-assisted folding of newly synthesized proteins in the cytosol |
Q54571596 | Chaperone-assisted protein folding. |
Q41110607 | Chaperones get Hip. Protein folding |
Q89763905 | Chaperonin-assisted protein folding: a chronologue |
Q30828588 | Characterization of a cDNA clone, encoding a 70 kDa heat shock protein from the dermatophyte pathogen Trichophyton rubrum. |
Q38300849 | Characterization of a lidless form of the molecular chaperone DnaK: deletion of the lid increases peptide on- and off-rate constants |
Q44942951 | Characterization of interactions between the anti-apoptotic protein BAG-1 and Hsc70 molecular chaperones |
Q36235650 | Characterization of the secretion pathway of the collagen adhesin EmaA of Aggregatibacter actinomycetemcomitans. |
Q37788229 | Chemistry and biochemistry of lipid peroxidation products. |
Q42666155 | Cloning, sequencing, and expression of dnaK-operon proteins from the thermophilic bacterium Thermus thermophilus |
Q28270851 | Close and Allosteric Opening of the Polypeptide-Binding Site in a Human Hsp70 Chaperone BiP |
Q42055821 | Co-expression of human chaperone Hsp70 and Hsdj or Hsp40 co-factor increases solubility of overexpressed target proteins in insect cells |
Q37396817 | Compartmentalized cancer drug discovery targeting mitochondrial Hsp90 chaperones |
Q24653464 | Complexes between nascent polypeptides and their molecular chaperones in the cytosol of mammalian cells |
Q44710284 | Conformation transitions of the polypeptide-binding pocket support an active substrate release from Hsp70s |
Q49819851 | Conserved conformational selection mechanism of Hsp70 chaperone-substrate interactions. |
Q39494827 | Construction and analysis of hybrid Escherichia coli-Bacillus subtilis dnaK genes |
Q74325958 | Control of the DnaK chaperone cycle by substoichiometric concentrations of the co-chaperones DnaJ and GrpE |
Q27678812 | Crystal Structure of DnaK Protein Complexed with Nucleotide Exchange Factor GrpE in DnaK Chaperone System: INSIGHT INTO INTERMOLECULAR COMMUNICATION |
Q27650298 | Crystal Structures of the 70-kDa Heat Shock Proteins in Domain Disjoining Conformation |
Q77355829 | Current views in intracellular transport: insights from studies in immunology |
Q40016232 | Cyclophilin 20 is involved in mitochondrial protein folding in cooperation with molecular chaperones Hsp70 and Hsp60 |
Q57751808 | Cytosolic Hsp70 and Hsp40 chaperones enable the biogenesis of mitochondrial β-barrel proteins |
Q35868832 | Cytosolic and ER J-domains of mammalian and parasitic origin can functionally interact with DnaK. |
Q44362204 | D-Peptides as inhibitors of the DnaK/DnaJ/GrpE chaperone system |
Q74516752 | D-peptide ligands for the co-chaperone DnaJ |
Q44371542 | Detection of a concerted conformational change in the ATPase domain of DnaK triggered by peptide binding |
Q44014747 | Detection of a very rapid first phase in complex formation of DnaK and peptide substrate |
Q47961119 | Detection of low affinity interactions between peptides and heat shock proteins by chemiluminescence of enhanced avidity reactions (CLEAR). |
Q42941290 | Development of fluorescence polarization assays for the molecular chaperone Hsp70 family members: Hsp72 and DnaK. |
Q38296271 | Different combinations of the heat-shock cognate protein 70 (hsc70) C-terminal functional groups are utilized to interact with distinct tetratricopeptide repeat-containing proteins |
Q54598078 | Differential effects of molecular chaperones on refolding of homologous proteins. |
Q31962372 | Divergent Hsc70 binding properties of mitochondrial and cytosolic aspartate aminotransferase. Implications for their segregation to different cellular compartments |
Q54606140 | Divergent effects of ATP on the binding of the DnaK and DnaJ chaperones to each other, or to their various native and denatured protein substrates. |
Q38850197 | DnaJ-promoted binding of DnaK to multiple sites on σ32 in the presence of ATP. |
Q28203002 | Domain structure of the HSC70 cochaperone, HIP |
Q37291056 | E. coli chaperones DnaK, Hsp33 and Spy inhibit bacterial functional amyloid assembly. |
Q35039971 | Effect of hsp70 chaperone on the folding and misfolding of polypeptides modeling an elongating protein chain |
Q71245482 | Effect of nucleotides, peptides, and unfolded proteins on the self-association of the molecular chaperone HSC70 |
Q92039391 | Efficient conversion of chemical energy into mechanical work by Hsp70 chaperones |
Q73864357 | Empirical calculation of the relative free energies of peptide binding to the molecular chaperone DnaK |
Q37982692 | Environmentally sensitive fluorescent sensors based on synthetic peptides |
Q50136458 | Enzymatic characterization of FliI. An ATPase involved in flagellar assembly in Salmonella typhimurium. |
Q34007449 | Expression pattern of heat-shock cognate 70 gene of humphead snapper, Lutjanus sanguineus (Cuvier), infected by Vibrio harveyi |
Q36287776 | Flo11p-independent control of "mat" formation by hsp70 molecular chaperones and nucleotide exchange factors in yeast |
Q36347784 | Francisella DnaK inhibits tissue-nonspecific alkaline phosphatase |
Q33493419 | Function of SSA subfamily of Hsp70 within and across species varies widely in complementing Saccharomyces cerevisiae cell growth and prion propagation |
Q27680671 | Functional analysis of Hsp70 inhibitors |
Q54067842 | Functional defects of the DnaK756 mutant chaperone of Escherichia coli indicate distinct roles for amino- and carboxyl-terminal residues in substrate and co-chaperone interaction and interdomain communication. |
Q27935347 | Functional interaction of cytosolic hsp70 and a DnaJ-related protein, Ydj1p, in protein translocation in vivo |
Q35221600 | Functional significance of point mutations in stress chaperone mortalin and their relevance to Parkinson disease. |
Q41447461 | Fusion protein analysis reveals the precise regulation between Hsp70 and Hsp100 during protein disaggregation |
Q43517706 | Gentamicin inhibits HSP70-assisted protein folding by interfering with substrate recognition |
Q30402933 | Geranylgeranylacetone selectively binds to the HSP70 of Helicobacter pylori and alters its coccoid morphology |
Q24536019 | GrpE-like regulation of the hsc70 chaperone by the anti-apoptotic protein BAG-1 |
Q90424090 | Guiding tail-anchored membrane proteins to the endoplasmic reticulum in a chaperone cascade |
Q28216531 | HSP40 binding is the first step in the HSP90 chaperoning pathway for the progesterone receptor |
Q89978558 | HSP70 Multi-Functionality in Cancer |
Q39175124 | HSPA5 Gene encoding Hsp70 chaperone BiP in the endoplasmic reticulum |
Q34195771 | Heat shock protein 70 binds caspase-activated DNase and enhances its activity in TCR-stimulated T cells |
Q35431324 | Heat shock proteins in association with heat tolerance in grasses |
Q28569622 | Hip, a novel cochaperone involved in the eukaryotic hsc70/hsp40 reaction cycle |
Q35852998 | Hsp60-independent protein folding in the matrix of yeast mitochondria |
Q92509338 | Hsp70 and Hsp40 inhibit an inter-domain interaction necessary for transcriptional activity in the androgen receptor |
Q34545594 | Hsp70 chaperone machines. |
Q33648403 | Hsp70 chaperones are non-equilibrium machines that achieve ultra-affinity by energy consumption |
Q24644472 | Hsp70 chaperones: cellular functions and molecular mechanism |
Q48216572 | Hsp70 displaces small heat shock proteins from aggregates to initiate protein refolding. |
Q50906468 | Hsp70's RNA-binding and mRNA-stabilizing activities are independent of its protein chaperone functions. |
Q34271504 | Hsp72 functions as a natural inhibitory protein of c-Jun N-terminal kinase |
Q28213524 | HspBP1, a homologue of the yeast Fes1 and Sls1 proteins, is an Hsc70 nucleotide exchange factor |
Q46858675 | Human and yeast Hsp110 chaperones exhibit functional differences |
Q34660530 | Human heat shock protein 70 enhances tumor antigen presentation through complex formation and intracellular antigen delivery without innate immune signaling. |
Q24291143 | Identification and characterization of a human mitochondrial homologue of the bacterial co-chaperone GrpE |
Q43508426 | Identification of an inhibitor of hsc70-mediated protein translocation and ATP hydrolysis |
Q47884028 | Immediate response of the DnaK molecular chaperone system to heat shock |
Q44205703 | Induction of antibodies against murine full-length prion protein in wild-type mice |
Q52537294 | Inferences concerning the ATPase properties of DnaK and other HSP70s are affected by the ADP kinase activity of copurifying nucleoside-diphosphate kinase. |
Q36801199 | Influence of specific HSP70 domains on fibril formation of the yeast prion protein Ure2 |
Q34207265 | Inhibition of Hsp72-mediated protein refolding by 4-hydroxy-2-nonenal |
Q26779247 | Insights into the molecular mechanism of allostery in Hsp70s |
Q38326190 | Interaction between the nucleotide exchange factor Mge1 and the mitochondrial Hsp70 Ssc1. |
Q38322966 | Interaction of BiP with the J-domain of the Sec63p component of the endoplasmic reticulum protein translocation complex. |
Q41465900 | Interaction of Hsp70 chaperones with substrates |
Q24681842 | Interaction of murine BiP/GRP78 with the DnaJ homologue MTJ1 |
Q44141092 | Interaction of the DnaK and DnaJ chaperone system with a native substrate, P1 RepA. |
Q33574540 | Interaction of the Hsp70 molecular chaperone, DnaK, with its cochaperone DnaJ. |
Q44021081 | Interaction of the chaperone BiP with an antibody domain: implications for the chaperone cycle |
Q52073360 | Interaction of the targeting sequence of chloroplast precursors with Hsp70 molecular chaperones. |
Q42685750 | Interdomain communication in the molecular chaperone DnaK. |
Q88596142 | Intra-molecular pathways of allosteric control in Hsp70s |
Q35601345 | Intragenic suppressors of Hsp70 mutants: interplay between the ATPase- and peptide-binding domains |
Q48493458 | Intrinsic ADP-ATP exchange activity is a novel function of the molecular chaperone, Hsp70. |
Q74531665 | Involvement of molecular chaperonins in nucleotide excision repair. Dnak leads to increased thermal stability of UvrA, catalytic UvrB loading, enhanced repair, and increased UV resistance |
Q77652505 | J proteins catalytically activate Hsp70 molecules to trap a wide range of peptide sequences |
Q35653384 | Keep the traffic moving: mechanism of the Hsp70 motor |
Q33919575 | Kinetic and structural characterization of human mortalin |
Q41724423 | Kinetic characterization of the ATPase cycle of the molecular chaperone Hsc66 from Escherichia coli |
Q33852559 | Maturation-induced conformational changes of HIV-1 capsid protein and identification of two high affinity sites for cyclophilins in the C-terminal domain |
Q54369498 | Mechanics of Hsp70 chaperones enables differential interaction with client proteins. |
Q36351463 | Mechanism of regulation of hsp70 chaperones by DnaJ cochaperones |
Q44374505 | Mechanism of the targeting action of DnaJ in the DnaK molecular chaperone system |
Q36556555 | Mitochondrial GrpE modulates the function of matrix Hsp70 in translocation and maturation of preproteins |
Q27936101 | Mitochondrial Hsp70 Ssc1: role in protein folding. |
Q77377946 | Mitochondrial Hsp70 cannot replace BiP in driving protein translocation into the yeast endoplasmic reticulum |
Q72534381 | Mitochondrial presequences can induce aggregation of unfolded proteins |
Q58419056 | Mitotic phosphorylation regulates Hsp72 spindle localization by uncoupling ATP binding from substrate release |
Q41666510 | Modeling Hsp70-mediated protein folding |
Q44485303 | Modulation of the ATPase cycle of BiP by peptides and proteins |
Q33251546 | Module-based analysis of robustness tradeoffs in the heat shock response system |
Q34081455 | Molecular basis for interactions of the DnaK chaperone with substrates. |
Q45045971 | Molecular biology: Mature proteins braced by a chaperone |
Q29547795 | Molecular chaperones in cellular protein folding |
Q41026044 | Molecular chaperones in protein folding and translocation |
Q34165962 | Molecular chaperones--cellular machines for protein folding |
Q33895353 | Molecular characterization of heat shock protein 70 gene transcripts during Vibrio harveyi infection of humphead snapper, Lutjanus sanguineus |
Q28578347 | Molecular composition of staufen2-containing ribonucleoproteins in embryonic rat brain |
Q37200825 | Multiple hsp70 isoforms in the eukaryotic cytosol: mere redundancy or functional specificity? |
Q34011971 | Mutagenesis of a functional chimeric gene in yeast identifies mutations in the simian virus 40 large T antigen J domain |
Q33967227 | Mutagenesis reveals the complex relationships between ATPase rate and the chaperone activities of Escherichia coli heat shock protein 70 (Hsp70/DnaK) |
Q34610710 | Mutation of the ATP-binding pocket of SSA1 indicates that a functional interaction between Ssa1p and Ydj1p is required for post-translational translocation into the yeast endoplasmic reticulum. |
Q37288233 | Mutations in the C-terminal fragment of DnaK affecting peptide binding |
Q33575042 | Mutations in the DnaK chaperone affecting interaction with the DnaJ cochaperone. |
Q43619818 | Mutations in the interdomain linker region of DnaK abolish the chaperone action of the DnaK/DnaJ/GrpE system |
Q77717254 | Mydj2 as a potent partner of hsc70 in mammalian cells |
Q28205098 | NEMO trimerizes through its coiled-coil C-terminal domain |
Q42628534 | NMR study of nucleotide-induced changes in the nucleotide binding domain of Thermus thermophilus Hsp70 chaperone DnaK: implications for the allosteric mechanism |
Q28143100 | Negative regulation of the Apaf-1 apoptosome by Hsp70 |
Q27932135 | Nucleotide binding by Lhs1p is essential for its nucleotide exchange activity and for function in vivo. |
Q27931293 | Nucleotide exchange factor for the yeast Hsp70 molecular chaperone Ssa1p |
Q71921283 | Nucleotide-induced conformational changes in the ATPase and substrate binding domains of the DnaK chaperone provide evidence for interdomain communication |
Q39777855 | Overexpression of the cochaperone CHIP enhances Hsp70-dependent folding activity in mammalian cells. |
Q30667048 | Pathways of allosteric regulation in Hsp70 chaperones. |
Q24798059 | Peptide substrate identification for yeast Hsp40 Ydj1 by screening the phage display library |
Q33923929 | Polypeptide release by Hsp90 involves ATP hydrolysis and is enhanced by the co-chaperone p23. |
Q41298313 | Polypeptide translocation machinery of the yeast endoplasmic reticulum |
Q47336036 | Post-termination-induced and hormonally dependent expression of low-molecular-weight heat shock protein genes in Douglas fir. |
Q44853354 | Preferential substrate binding orientation by the molecular chaperone HscA. |
Q34587831 | Primate chaperones Hsc70 (constitutive) and Hsp70 (induced) differ functionally in supporting growth and prion propagation in Saccharomyces cerevisiae |
Q30530315 | Protein folding rates and thermodynamic stability are key determinants for interaction with the Hsp70 chaperone system |
Q54580451 | Purification and biochemical properties of Saccharomyces cerevisiae's Mge1p, the mitochondrial cochaperone of Ssc1p. |
Q35596639 | Quantifying the role of chaperones in protein translocation by computational modeling |
Q47334829 | Real time kinetics of the DnaK/DnaJ/GrpE molecular chaperone machine action |
Q93222384 | Recent advances in the structural and mechanistic aspects of Hsp70 molecular chaperones |
Q54528186 | Recombinant expression and purification of Ssa1p (Hsp70) from Saccharomyces cerevisiae using Pichia pastoris. |
Q24324029 | Regulated association of misfolded endoplasmic reticulum lumenal proteins with P58/DNAJc3 |
Q38354169 | Regulation of the heat-shock protein 70 reaction cycle by the mammalian DnaJ homolog, Hsp40. |
Q88867226 | Response to Persistent ER Stress in Plants: A Multiphasic Process That Transitions Cells from Prosurvival Activities to Cell Death |
Q31578047 | Reversible thermal transition in GrpE, the nucleotide exchange factor of the DnaK heat-shock system |
Q35160700 | Role of Hsc70 binding cycle in CFTR folding and endoplasmic reticulum-associated degradation |
Q38335127 | Role of the C-terminal region of mouse inducible Hsp72 in the recognition of peptide substrate for chaperone activity |
Q37380910 | Role of the J-domain in the cooperation of Hsp40 with Hsp70. |
Q34775640 | Roles of DEAD-box proteins in RNA and RNP Folding |
Q44257199 | Roles of cytosolic Hsp70 and Hsp40 molecular chaperones in post-translational translocation of presecretory proteins into the endoplasmic reticulum |
Q34208996 | Salicylic acid signaling controls the maturation and localization of the arabidopsis defense protein ACCELERATED CELL DEATH6 |
Q41951622 | Salivary histatin 3 inhibits heat shock cognate protein 70-mediated inflammatory cytokine production through toll-like receptors in human gingival fibroblasts |
Q35961848 | Similarity of nucleotide interactions of BiP and GTP-binding proteins |
Q34218169 | Single-molecule spectroscopy reveals chaperone-mediated expansion of substrate protein |
Q27938635 | Sls1p stimulates Sec63p-mediated activation of Kar2p in a conformation-dependent manner in the yeast endoplasmic reticulum. |
Q40479992 | Small molecule modulators of endogenous and co-chaperone-stimulated Hsp70 ATPase activity. |
Q42096150 | Spatial localisation of chaperone distribution in the endoplasmic reticulum of yeast |
Q71841804 | Spinach leaf 70-kilodalton heat-shock cognate stabilizes bovine adrenal glucose-6-phosphate dehydrogenase in vitro without apparent stable binding |
Q34167528 | Strong precursor-pore interactions constrain models for mitochondrial protein import |
Q27732810 | Structural analysis of substrate binding by the molecular chaperone DnaK |
Q90058716 | Structural and functional analysis of the Hsp70/Hsp40 chaperone system |
Q41072966 | Structural basis of interdomain communication in the Hsc70 chaperone. |
Q41696207 | Structural features required for the interaction of the Hsp70 molecular chaperone DnaK with its cochaperone DnaJ. |
Q27650814 | Structure of the Hsp110:Hsc70 nucleotide exchange machine |
Q42030110 | Structure-based mutagenesis studies of the peptide substrate binding fragment of type I heat-shock protein 40 |
Q42524938 | Structure-function analysis of HscC, the Escherichia coli member of a novel subfamily of specialized Hsp70 chaperones |
Q41077127 | Structure-function analysis of the Escherichia coli GrpE heat shock protein |
Q36289632 | Subcellular distribution of non-muscle myosin IIb is controlled by FILIP through Hsc70 |
Q38332859 | Substrate binding induces depolymerization of the C-terminal peptide binding domain of murine GRP78/BiP. |
Q27932701 | Substrate binding to the molecular chaperone Hsp104 and its regulation by nucleotides |
Q37402365 | Subtilase cytotoxin cleaves newly synthesized BiP and blocks antibody secretion in B lymphocytes |
Q45012676 | Successive and synergistic action of the Hsp70 and Hsp100 chaperones in protein disaggregation |
Q34662543 | T antigens of simian virus 40: molecular chaperones for viral replication and tumorigenesis |
Q35327865 | Tangled web of interactions among proteins involved in iron-sulfur cluster assembly as unraveled by NMR, SAXS, chemical crosslinking, and functional studies. |
Q33899676 | Temperature differentially affects adenosine triphosphatase activity in Hsc70 orthologs from Antarctic and New Zealand notothenioid fishes |
Q28239456 | The ATP hydrolysis-dependent reaction cycle of the Escherichia coli Hsp70 system DnaK, DnaJ, and GrpE |
Q42645780 | The ATPase cycle of the mitochondrial Hsp90 analog Trap1. |
Q54512126 | The ATPase domain of HscC (DnaK homolog) is essential for interfering sigma70 activity in E. coli. |
Q28118960 | The C-terminal helices of heat shock protein 70 are essential for J-domain binding and ATPase activation |
Q28301089 | The ClpX heat-shock protein of Escherichia coli, the ATP-dependent substrate specificity component of the ClpP-ClpX protease, is a novel molecular chaperone |
Q42549105 | The DNLZ/HEP zinc-binding subdomain is critical for regulation of the mitochondrial chaperone HSPA9. |
Q34107961 | The DnaJ chaperone catalytically activates the DnaK chaperone to preferentially bind the sigma 32 heat shock transcriptional regulator |
Q54540763 | The DnaK chaperone system facilitates 30S ribosomal subunit assembly. |
Q44037002 | The Fe/S assembly protein IscU behaves as a substrate for the molecular chaperone Hsc66 from Escherichia coli |
Q29547601 | The Hsp70 and Hsp60 chaperone machines |
Q36962268 | The Hsp70 chaperone machines of Escherichia coli: a paradigm for the repartition of chaperone functions. |
Q42434719 | The Hsp70 chaperone system maintains high concentrations of active proteins and suppresses ATP consumption during heat shock |
Q40992366 | The assembly of progesterone receptor-hsp90 complexes using purified proteins |
Q27939861 | The biochemical properties of the ATPase activity of a 70-kDa heat shock protein (Hsp70) are governed by the C-terminal domains |
Q34177320 | The brownian ratchet and power stroke models for posttranslational protein translocation into the endoplasmic reticulum |
Q28575687 | The carboxy-terminal domain of Hsc70 provides binding sites for a distinct set of chaperone cofactors |
Q39200186 | The chaperone toolbox at the single-molecule level: From clamping to confining |
Q38298937 | The conserved G/F motif of the DnaJ chaperone is necessary for the activation of the substrate binding properties of the DnaK chaperone |
Q27627141 | The crystal structure of the peptide-binding fragment from the yeast Hsp40 protein Sis1 |
Q41065567 | The delta psi- and Hsp70/MIM44-dependent reaction cycle driving early steps of protein import into mitochondria |
Q27935038 | The dissociation of ATP from hsp70 of Saccharomyces cerevisiae is stimulated by both Ydj1p and peptide substrates |
Q33593911 | The endoplasmic reticulum chaperone Cosmc directly promotes in vitro folding of T-synthase |
Q44967706 | The four hydrophobic residues on the Hsp70 inter-domain linker have two distinct roles |
Q33960355 | The glycine-phenylalanine-rich region determines the specificity of the yeast Hsp40 Sis1. |
Q40419483 | The human escort protein Hep binds to the ATPase domain of mitochondrial hsp70 and regulates ATP hydrolysis |
Q45261031 | The importance of having thermosensor control in the DnaK chaperone system |
Q36279709 | The mitochondrial protein import motor: dissociation of mitochondrial hsp70 from its membrane anchor requires ATP binding rather than ATP hydrolysis |
Q48610642 | The molecular chaperone Hsc70 assists the in vitro folding of the N-terminal nucleotide-binding domain of the cystic fibrosis transmembrane conductance regulator. |
Q27935359 | The molecular chaperone Ssb from Saccharomyces cerevisiae is a component of the ribosome-nascent chain complex |
Q41479027 | The role of molecular chaperones in mitochondrial protein import and folding |
Q44564172 | The roles of the two zinc binding sites in DnaJ. |
Q41958304 | The second metal-binding site of 70 kDa heat-shock protein is essential for ADP binding, ATP hydrolysis and ATP synthesis |
Q34808336 | The unfolding story of the Escherichia coli Hsp70 DnaK: is DnaK a holdase or an unfoldase? |
Q39496540 | The unique chaperone operon of Thermotoga maritima: cloning and initial characterization of a functional Hsp70 and small heat shock protein. |
Q48024832 | Thermodynamic Bounds on the Ultra- and Infra-affinity of Hsp70 for Its Substrates |
Q44363996 | Thermosensor action of GrpE. The DnaK chaperone system at heat shock temperatures |
Q35939823 | Tight complex formation between Cosmc chaperone and its specific client non-native T-synthase leads to enzyme activity and client-driven dissociation |
Q36889334 | Tissue-specific expression of dominant negative mutant Drosophila HSC70 causes developmental defects and lethality |
Q40267302 | Toc12, a novel subunit of the intermembrane space preprotein translocon of chloroplasts |
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Q41885020 | Translocation of a long amino-terminal domain through ER membrane by following signal-anchor sequence |
Q54456793 | Tuning of DnaK chaperone action by nonnative protein sensor DnaJ and thermosensor GrpE. |
Q43695967 | Unassembled Ig heavy chains do not cycle from BiP in vivo but require light chains to trigger their release |
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Q73066915 | What is the driving force for protein import into mitochondria? |
Q28585314 | XBP-1 Regulates a Subset of Endoplasmic Reticulum Resident Chaperone Genes in the Unfolded Protein Response |
Q27933106 | Zuotin, a ribosome-associated DnaJ molecular chaperone |
Q34311002 | cis-Effect of DnaJ on DnaK in ternary complexes with chimeric DnaK/DnaJ-binding peptides |
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