scholarly article | Q13442814 |
P2093 | author name string | Robert T Sauer | |
Eyal Gur | |||
P2860 | cites work | A quantitative assessment of the role of the chaperonin proteins in protein folding in vivo. | Q40949130 |
Identification of thermolabile Escherichia coli proteins: prevention and reversion of aggregation by DnaK and ClpB. | Q42247311 | ||
The folding and stability of titin immunoglobulin-like modules, with implications for the mechanism of elasticity | Q42541325 | ||
Use of a real-time, coupled assay to measure the ATPase activity of DNA topoisomerase II. | Q43510390 | ||
Adenosine triphosphate-dependent degradation of a fluorescent lambda N substrate mimic by Lon protease | Q43550142 | ||
Kinetic characterization of the peptidase activity of Escherichia coli Lon reveals the mechanistic similarities in ATP-dependent hydrolysis of peptide and protein substrates | Q44075127 | ||
Proteomic discovery of cellular substrates of the ClpXP protease reveals five classes of ClpX-recognition signals | Q44384522 | ||
Linkage between ATP consumption and mechanical unfolding during the protein processing reactions of an AAA+ degradation machine. | Q44563531 | ||
Overproduction of the Lon protease triggers inhibition of translation in Escherichia coli: involvement of the yefM-yoeB toxin-antitoxin system | Q44792479 | ||
An AAA protease FtsH can initiate proteolysis from internal sites of a model substrate, apo-flavodoxin | Q46948329 | ||
Dynamics of substrate denaturation and translocation by the ClpXP degradation machine | Q47235359 | ||
Mutations in the proteolytic domain of Escherichia coli protease Lon impair the ATPase activity of the enzyme | Q48518551 | ||
Hydrophobicity of amino acid residues in globular proteins. | Q54456958 | ||
ATP-dependent protease La (lon) from Escherichia coli. | Q54645667 | ||
Alternative packing arrangements in the hydrophobic core of λrepresser | Q59096694 | ||
Beta-galactosidase. Rates of synthesis and degradation of incomplete chains | Q69166209 | ||
Coupled assay of Na+,K+-ATPase activity | Q69826419 | ||
Selectivity of intracellular proteolysis: protein substrates activate the ATP-dependent protease (La) | Q69991883 | ||
Regulatory role of C-terminal residues of SulA in its degradation by Lon protease in Escherichia coli | Q73731954 | ||
NMR structure of the bacteriophage lambda N peptide/boxB RNA complex: recognition of a GNRA fold by an arginine-rich motif | Q74502190 | ||
The ClpXP and ClpAP proteases degrade proteins with carboxy-terminal peptide tails added by the SsrA-tagging system | Q24603386 | ||
The crystal structure of a GroEL/peptide complex: plasticity as a basis for substrate diversity | Q27620851 | ||
Regulation of SulA cleavage by Lon protease by the C-terminal amino acid of SulA, histidine | Q28346413 | ||
Its substrate specificity characterizes the DnaJ co-chaperone as a scanning factor for the DnaK chaperone. | Q28354756 | ||
Molecular chaperones and protein quality control | Q29617795 | ||
Sequence requirements for Lon-dependent degradation of the Escherichia coli transcription activator SoxS: identification of the SoxS residues critical to proteolysis and specific inhibition of in vitro degradation by a peptide comprised of the N-ter | Q33233198 | ||
Mechanical and chemical unfolding of a single protein: a comparison | Q33856547 | ||
Binding specificity of Escherichia coli trigger factor | Q33951759 | ||
A conserved domain in Escherichia coli Lon protease is involved in substrate discriminator activity | Q33991680 | ||
ClpAP and ClpXP degrade proteins with tags located in the interior of the primary sequence | Q34036663 | ||
Nucleotide-dependent substrate recognition by the AAA+ HslUV protease. | Q34391837 | ||
The lon Gene and Degradation of β-Galactosidase Nonsense Fragments | Q34699404 | ||
Lon-mediated proteolysis of the Escherichia coli UmuD mutagenesis protein: in vitro degradation and identification of residues required for proteolysis | Q34756168 | ||
The product of the lon (capR) gene in Escherichia coli is the ATP-dependent protease, protease La. | Q35460779 | ||
Proteolysis in Bacterial Regulatory Circuits | Q35564854 | ||
Differential protease-mediated turnover of H-NS and StpA revealed by a mutation altering protein stability and stationary-phase survival of Escherichia coli | Q35631720 | ||
Sculpting the proteome with AAA(+) proteases and disassembly machines. | Q35904074 | ||
Lon protease degrades transfer-messenger RNA-tagged proteins | Q36098313 | ||
lon gene product of Escherichia coli is a heat-shock protein | Q36301710 | ||
Deg phenotype of Escherichia coli lon mutants | Q36418299 | ||
Biological roles of the Lon ATP-dependent protease | Q36541141 | ||
Degradation of Escherichia coli beta-galactosidase fragments in protease-deficient mutants of Salmonella typhimurium | Q36600309 | ||
ATP-dependent proteases of bacteria: recognition logic and operating principles | Q36639201 | ||
Substrate specificity of the DnaK chaperone determined by screening cellulose-bound peptide libraries | Q36857677 | ||
ATP hydrolysis is not stoichiometrically linked with proteolysis in the ATP-dependent protease La from Escherichia coli | Q38315068 | ||
Classification of ATP-dependent proteases Lon and comparison of the active sites of their proteolytic domains | Q38332946 | ||
Core-packing constraints, hydrophobicity and protein design | Q40535073 | ||
Intermediate steps in the degradation of a specific abnormal protein in Escherichia coli | Q40829271 | ||
P433 | issue | 16 | |
P304 | page(s) | 2267-2277 | |
P577 | publication date | 2008-08-01 | |
P1433 | published in | Genes & Development | Q1524533 |
P1476 | title | Recognition of misfolded proteins by Lon, a AAA(+) protease | |
P478 | volume | 22 |
Q34336038 | A Lon-like protease with no ATP-powered unfolding activity |
Q64267505 | A facile forward-genetic screen for Arabidopsis autophagy mutants reveals twenty-one loss-of-function mutations disrupting six ATG genes |
Q37469756 | A mutation in the N domain of Escherichia coli lon stabilizes dodecamers and selectively alters degradation of model substrates. |
Q49309498 | A set of synthetic versatile genetic control elements for the efficient expression of genes in Actinobacteria |
Q60932175 | Active degradation of MarA controls coordination of its downstream targets |
Q37553901 | Adapting the machine: adaptor proteins for Hsp100/Clp and AAA+ proteases |
Q34926673 | Adaptor-mediated Lon proteolysis restricts Bacillus subtilis hyperflagellation |
Q97676621 | Altered expression of a quality control protease in E. coli reshapes the in vivo mutational landscape of a model enzyme |
Q41583908 | An extracelluar protease, SepM, generates functional competence-stimulating peptide in Streptococcus mutans UA159. |
Q91967377 | Asymmetric division yields progeny cells with distinct modes of regulating cell cycle-dependent chromosome methylation |
Q38047828 | Bacterial proteolytic complexes as therapeutic targets |
Q91651412 | Chaperone activity of serine protease HtrA of Helicobacter pylori as a crucial survival factor under stress conditions |
Q36033652 | Characterization of the ATP-Dependent Lon-Like Protease in Methanobrevibacter smithii |
Q34251772 | Chloroplastic Hsp100 chaperones ClpC2 and ClpD interact in vitro with a transit peptide only when it is located at the N-terminus of a protein. |
Q44983747 | ClpAP is an auxiliary protease for DnaA degradation in Caulobacter crescentus. |
Q33591989 | Co-evolution of multipartite interactions between an extended tmRNA tag and a robust Lon protease in Mycoplasma |
Q35806272 | Complete Genome Sequence of Thermus aquaticus Y51MC23. |
Q37875825 | Context-dependent resistance to proteolysis of intrinsically disordered proteins |
Q41430702 | Control of lipopolysaccharide biosynthesis by FtsH-mediated proteolysis of LpxC is conserved in enterobacteria but not in all gram-negative bacteria. |
Q27664441 | Crystal structure of Lon protease: molecular architecture of gated entry to a sequestered degradation chamber |
Q50959628 | Defining the crucial domain and amino acid residues in bacterial Lon protease for DNA binding and processing of DNA-interacting substrates. |
Q37413548 | Degrons in protein substrates program the speed and operating efficiency of the AAA+ Lon proteolytic machine. |
Q33842677 | Differential protein acetylation assists import of excess SOD2 into mitochondria and mediates SOD2 aggregation associated with cardiac hypertrophy in the murine SOD2-tg heart |
Q39366122 | Diphenylarsinic acid promotes degradation of glutaminase C by mitochondrial Lon protease |
Q89186855 | Dissecting Substrate Specificities of the Mitochondrial AFG3L2 Protease |
Q34651849 | Distinct quaternary structures of the AAA+ Lon protease control substrate degradation. |
Q32884587 | Engineered AAA+ proteases reveal principles of proteolysis at the mitochondrial inner membrane. |
Q37027096 | Engineering fluorescent protein substrates for the AAA+ Lon protease. |
Q27003925 | Evolution and significance of the Lon gene family in Arabidopsis organelle biogenesis and energy metabolism |
Q24649663 | Evolution of the ssrA degradation tag in Mycoplasma: specificity switch to a different protease |
Q90407013 | Feedback Control of a Two-Component Signaling System by an Fe-S-Binding Receiver Domain |
Q90230248 | Global Proteome of LonP1+/- Mouse Embryonal Fibroblasts Reveals Impact on Respiratory Chain, but No Interdependence between Eral1 and Mitoribosomes |
Q47970826 | Identification of a Degradation Signal Sequence within Substrates of the Mitochondrial i-AAA Protease |
Q40101707 | Identification of novel oxidized protein substrates and physiological partners of the mitochondrial ATP-dependent Lon-like protease Pim1. |
Q48274506 | Importance of the E. coli DinJ antitoxin carboxy terminus for toxin suppression and regulated proteolysis |
Q27320857 | Individual and collective contributions of chaperoning and degradation to protein homeostasis in E. coli |
Q30506460 | Insights into the gene expression profile of uncultivable hemotrophic Mycoplasma suis during acute infection, obtained using proteome analysis |
Q37858328 | Integrating protein homeostasis strategies in prokaryotes |
Q33452525 | Intrinsic thermal sensing controls proteolysis of Yersinia virulence regulator RovA. |
Q94545150 | Iron Limitation in Klebsiella pneumoniae Defines New Roles for Lon Protease in Homeostasis and Degradation by Quantitative Proteomics |
Q46163099 | Knots can impair protein degradation by ATP-dependent proteases |
Q41811406 | LON is the master protease that protects against protein aggregation in human mitochondria through direct degradation of misfolded proteins |
Q50998985 | Lon protease modulates virulence traits in Erwinia amylovora by direct monitoring of major regulators and indirectly through the Rcs and Gac-Csr regulatory systems. |
Q34004070 | Lon protease quality control of presecretory proteins in Escherichia coli and its dependence on the SecB and DnaJ (Hsp40) chaperones |
Q57029703 | Lon recognition of the replication initiator DnaA requires a bipartite degron |
Q40368471 | Loss-of-Function Mutations in HspR Rescue the Growth Defect of a Mycobacterium tuberculosis Proteasome Accessory Factor E (pafE) Mutant |
Q41954811 | MazF-induced growth inhibition and persister generation in Escherichia coli. |
Q34308388 | Mechanochemical basis of protein degradation by a double-ring AAA+ machine |
Q38772212 | Mini review: ATP-dependent proteases in bacteria |
Q38758114 | Mitochondrial cereblon functions as a Lon-type protease |
Q28083423 | Mitochondrial protein quality control: the mechanisms guarding mitochondrial health |
Q28394612 | Molecular mechanisms of ethanol-induced pathogenesis revealed by RNA-sequencing |
Q33710845 | Multifunctional Mitochondrial AAA Proteases |
Q58770991 | Multiple domains of bacterial and human Lon proteases define substrate selectivity |
Q41898305 | Multiple sequence signals direct recognition and degradation of protein substrates by the AAA+ protease HslUV. |
Q27003208 | Multitasking in the mitochondrion by the ATP-dependent Lon protease |
Q36459359 | Oxidization without substrate unfolding triggers proteolysis of the peroxide-sensor, PerR. |
Q37068583 | Oxygen-sensitive mitochondrial accumulation of cystathionine β-synthase mediated by Lon protease |
Q40324445 | Placing a disrupted degradation motif at the C terminus of proteasome substrates attenuates degradation without impairing ubiquitylation |
Q42732678 | Polyphosphate, cyclic AMP, guanosine tetraphosphate, and c-di-GMP reduce in vitro Lon activity |
Q38932643 | Protease regulation and capacity during Caulobacter growth |
Q35814404 | Protein Homeostasis Imposes a Barrier on Functional Integration of Horizontally Transferred Genes in Bacteria |
Q36532990 | Protein quality control acts on folding intermediates to shape the effects of mutations on organismal fitness |
Q35884522 | Protein unfolding and degradation by the AAA+ Lon protease |
Q37320446 | Proteins altered by elevated levels of palmitate or glucose implicated in impaired glucose-stimulated insulin secretion |
Q37847387 | Proteolysis in the Escherichia coli heat shock response: a player at many levels. |
Q90124570 | Proteolysis mediated by the membrane-integrated ATP-dependent protease FtsH has a unique nonlinear dependence on ATP hydrolysis rates |
Q37110188 | Proteotoxic stress induces a cell-cycle arrest by stimulating Lon to degrade the replication initiator DnaA |
Q44372505 | Quality control of a molybdoenzyme by the Lon protease. |
Q52323704 | Regulated Proteolysis in Bacteria. |
Q39022244 | Regulated Proteolysis in Bacteria: Caulobacter |
Q37948597 | Regulated proteolysis in Gram-negative bacteria--how and when? |
Q41171940 | Regulated proteolysis of a transcription factor complex is critical to cell cycle progression in Caulobacter crescentus |
Q39217558 | Roles of the N domain of the AAA+ Lon protease in substrate recognition, allosteric regulation and chaperone activity. |
Q39273861 | Selective adaptor dependent protein degradation in bacteria |
Q42117075 | SepM, a Streptococcal Protease Involved in Quorum Sensing, Displays Strict Substrate Specificity |
Q30155499 | Stepwise unfolding of a β barrel protein by the AAA+ ClpXP protease. |
Q38213227 | Stress-induced remodeling of the bacterial proteome |
Q96110646 | Structural basis for distinct operational modes and protease activation in AAA+ protease Lon |
Q27663923 | Structure of the N-terminal fragment ofEscherichia coliLon protease |
Q27685291 | Structures of an ATP-independent Lon-like protease and its complexes with covalent inhibitors |
Q42539267 | Sulfur-34S stable isotope labeling of amino acids for quantification (SULAQ34) of proteomic changes in Pseudomonas fluorescens during naphthalene degradation |
Q47222966 | The C-terminal region of Bacillus subtilis SwrA is required for activity and adaptor-dependent LonA-proteolysis |
Q41840280 | The Copper Efflux Regulator CueR Is Subject to ATP-Dependent Proteolysis in Escherichia coli. |
Q53259155 | The Escherichia coli replication inhibitor CspD is subject to growth-regulated degradation by the Lon protease. |
Q34616752 | The IbpA and IbpB small heat-shock proteins are substrates of the AAA+ Lon protease |
Q27685452 | The N-terminal substrate-recognition domain of a LonC protease exhibits structural and functional similarity to cytosolic chaperones |
Q33633994 | The Protein Chaperone ClpX Targets Native and Non-native Aggregated Substrates for Remodeling, Disassembly, and Degradation with ClpP |
Q64273419 | The Role of Proteases in the Virulence of Plant Pathogenic Bacteria |
Q37949008 | The multifaceted role of Lon proteolysis in seedling establishment and maintenance of plant organelle function: living from protein destruction. |
Q37507163 | The peroxisomal Lon protease LonP2 in aging and disease: functions and comparisons with mitochondrial Lon protease LonP1 |
Q41366279 | Translation readthrough mitigation. |
Q24630346 | Tuning the dials of Synthetic Biology |
Q38794976 | Two isoforms of Clp peptidase in Pseudomonas aeruginosa control distinct aspects of cellular physiology |
Q24293436 | Two proteases, trypsin domain-containing 1 (Tysnd1) and peroxisomal lon protease (PsLon), cooperatively regulate fatty acid β-oxidation in peroxisomal matrix |
Q41891328 | Utilization of synthetic peptides to evaluate the importance of substrate interaction at the proteolytic site of Escherichia coli Lon protease |
Q40403943 | Versatile modes of peptide recognition by the ClpX N domain mediate alternative adaptor-binding specificities in different bacterial species |
Q36010478 | YoeB toxin is activated during thermal stress |
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