| Q24530739 | A human homologue of Escherichia coli ClpP caseinolytic protease: recombinant expression, intracellular processing and subcellular localization |
| Q35968116 | A molecular chaperone, ClpA, functions like DnaK and DnaJ. |
| Q33726457 | A single ClpS monomer is sufficient to direct the activity of the ClpA hexamer |
| Q34463606 | AAA+ chaperones and acyldepsipeptides activate the ClpP protease via conformational control |
| Q37254059 | ATP-dependent proteases differ substantially in their ability to unfold globular proteins |
| Q89826547 | Acyldepsipeptide Antibiotics and a Bioactive Fragment Thereof Differentially Perturb Mycobacterium tuberculosis ClpXP1P2 Activity in vitro |
| Q27664573 | Acyldepsipeptide antibiotics induce the formation of a structured axial channel in ClpP: A model for the ClpX/ClpA-bound state of ClpP. |
| Q37052768 | Adenosine diphosphate restricts the protein remodeling activity of the Hsp104 chaperone to Hsp70 assisted disaggregation |
| Q34093535 | Alternating translocation of protein substrates from both ends of ClpXP protease |
| Q54494643 | Binding and degradation of heterodimeric substrates by ClpAP and ClpXP. |
| Q33824950 | Binding of the ClpA unfoldase opens the axial gate of ClpP peptidase |
| Q44639277 | Clp protease complexes from photosynthetic and non-photosynthetic plastids and mitochondria of plants, their predicted three-dimensional structures, and functional implications. |
| Q34036663 | ClpAP and ClpXP degrade proteins with tags located in the interior of the primary sequence |
| Q57460374 | ClpAP protease is a universal factor that activates the parDE toxin-antitoxin system from a broad host range RK2 plasmid |
| Q73019220 | ClpB cooperates with DnaK, DnaJ, and GrpE in suppressing protein aggregation. A novel multi-chaperone system from Escherichia coli |
| Q64955662 | ClpP Protease, a Promising Antimicrobial Target. |
| Q36804382 | Complex regulation of the DnaJ homolog CbpA by the global regulators sigmaS and Lrp, by the specific inhibitor CbpM, and by the proteolytic degradation of CbpM. |
| Q77927011 | Concurrent chaperone and protease activities of ClpAP and the requirement for the N-terminal ClpA ATP binding site for chaperone activity |
| Q27639561 | Crystal structure of ClpA, an Hsp100 chaperone and regulator of ClpAP protease |
| Q36092514 | Deletion mutations in N-terminal alpha1 helix render heat labile enterotoxin B subunit susceptible to degradation |
| Q35565304 | Design principles of the proteolytic cascade governing the sigmaE-mediated envelope stress response in Escherichia coli: keys to graded, buffered, and rapid signal transduction. |
| Q33289276 | Discovery of antibacterial cyclic peptides that inhibit the ClpXP protease |
| Q50727347 | Downregulation of ClpR2 leads to reduced accumulation of the ClpPRS protease complex and defects in chloroplast biogenesis in Arabidopsis. |
| Q34456129 | Dysregulation of bacterial proteolytic machinery by a new class of antibiotics |
| Q46395974 | Dystonia-associated forms of torsinA are deficient in ATPase activity |
| Q37570875 | E. coli ClpA catalyzed polypeptide translocation is allosterically controlled by the protease ClpP. |
| Q41535637 | Effects of nucleotides on assembly of the 26S proteasome and degradation of ubiquitin conjugates |
| Q38300971 | Functional domains of the ClpA and ClpX molecular chaperones identified by limited proteolysis and deletion analysis |
| Q24292867 | Functional proteolytic complexes of the human mitochondrial ATP-dependent protease, hClpXP |
| Q64464391 | HSP100/Clp proteins: a common mechanism explains diverse functions |
| Q33580338 | Handcuffing reversal is facilitated by proteases and replication initiator monomers |
| Q34733264 | HslV-HslU: A novel ATP-dependent protease complex in Escherichia coli related to the eukaryotic proteasome |
| Q92501257 | Hsp90 of E. coli modulates assembly of FtsZ, the bacterial tubulin homolog |
| Q24314752 | Human ClpP protease: cDNA sequence, tissue-specific expression and chromosomal assignment of the gene |
| Q30984811 | Identification of a 350-kDa ClpP protease complex with 10 different Clp isoforms in chloroplasts of Arabidopsis thaliana. |
| Q54203694 | In vivo and in vitro effects of a ClpP activating antibiotic against vancomycin resistant enterococci. |
| Q27676956 | Insights into Structural Network Responsible for Oligomerization and Activity of Bacterial Virulence Regulator Caseinolytic Protease P (ClpP) Protein |
| Q38676181 | Insights into the Clp/HSP100 chaperone system from chloroplasts of Arabidopsis thaliana. |
| Q33736607 | Interactions of the chaperone Hsp104 with yeast Sup35 and mammalian PrP. |
| Q34744115 | Isolation and characterization of the phage T4 PinA protein, an inhibitor of the ATP-dependent lon protease of Escherichia coli |
| Q33853445 | Local and global mobility in the ClpA AAA+ chaperone detected by cryo-electron microscopy: functional connotations |
| Q35145217 | Location of dual sites in E. coli FtsZ important for degradation by ClpXP; one at the C-terminus and one in the disordered linker |
| Q78038063 | Marked instability of the sigma(32) heat shock transcription factor at high temperature. Implications for heat shock regulation |
| Q36762714 | Mechanism of protein remodeling by ClpA chaperone |
| Q64931192 | Medicinal chemistry optimization of acyldepsipeptides of the enopeptin class antibiotics. |
| Q64086968 | Mitochondrial Protease ClpP is a Target for the Anticancer Compounds ONC201 and Related Analogues |
| Q34649165 | Modulating RssB activity: IraP, a novel regulator of sigma(S) stability in Escherichia coli |
| Q40016654 | Modulating substrate choice: the SspB adaptor delivers a regulator of the extracytoplasmic-stress response to the AAA+ protease ClpXP for degradation |
| Q44456263 | Mu transpososome architecture ensures that unfolding by ClpX or proteolysis by ClpXP remodels but does not destroy the complex |
| Q91966164 | New Insights into Multistep-Phosphorelay (MSP)/ Two-Component System (TCS) Regulation: Are Plants and Bacteria that Different? |
| Q36281630 | Nucleotide-dependent oligomerization of ClpB from Escherichia coli |
| Q40898115 | Opposing effects of DNA on proteolysis of a replication initiator |
| Q33943642 | Overlapping recognition determinants within the ssrA degradation tag allow modulation of proteolysis. |
| Q54515038 | Plasmid P1 RepA is homologous to the F plasmid RepE class of initiators. |
| Q35190125 | Protein binding and unfolding by the chaperone ClpA and degradation by the protease ClpAP. |
| Q30397832 | Proteolysis-Dependent Remodeling of the Tubulin Homolog FtsZ at the Division Septum in Escherichia coli |
| Q39044453 | Restriction of the conformational dynamics of the cyclic acyldepsipeptide antibiotics improves their antibacterial activity |
| Q30598763 | Role of a conserved pore residue in the formation of a prehydrolytic high substrate affinity state in the AAA+ chaperone ClpA |
| Q36827402 | Sclerotiamide: The First Non-Peptide-Based Natural Product Activator of Bacterial Caseinolytic Protease P. |
| Q34737150 | Six-fold rotational symmetry of ClpQ, the E. coli homolog of the 20S proteasome, and its ATP-dependent activator, ClpY. |
| Q93039158 | Structural basis for inhibition of a response regulator of σS stability by a ClpXP antiadaptor |
| Q42251896 | Structural determinants stabilizing the axial channel of ClpP for substrate translocation |
| Q34490504 | Subunit-specific degradation of the UmuD/D' heterodimer by the ClpXP protease: the role of trans recognition in UmuD' stability |
| Q34089946 | Synchrotron protein footprinting supports substrate translocation by ClpA via ATP-induced movements of the D2 loop |
| Q54571568 | The ATP-dependent HslVU protease from Escherichia coli is a four-ring structure resembling the proteasome. |
| Q47982221 | The ATPase activity of Hsp104, effects of environmental conditions and mutations. |
| Q34061068 | The ClpP N-terminus coordinates substrate access with protease active site reactivity |
| Q33633994 | The Protein Chaperone ClpX Targets Native and Non-native Aggregated Substrates for Remodeling, Disassembly, and Degradation with ClpP |
| Q28359852 | The RssB response regulator directly targets sigma(S) for degradation by ClpXP |
| Q42554554 | The active ClpP protease from M. tuberculosis is a complex composed of a heptameric ClpP1 and a ClpP2 ring. |
| Q50748896 | The chloroplast ClpP complex in Chlamydomonas reinhardtii contains an unusual high molecular mass subunit with a large apical domain. |
| Q34742836 | The heat-shock protein HslVU from Escherichia coli is a protein-activated ATPase as well as an ATP-dependent proteinase |
| Q77163867 | The isolated proteolytic domain of Escherichia coli ATP-dependent protease Lon exhibits the peptidase activity |
| Q45228992 | The molecular chaperone, ClpA, has a single high affinity peptide binding site per hexamer |
| Q36406990 | The purification of the Chlamydomonas reinhardtii chloroplast ClpP complex: additional subunits and structural features |
| Q36518957 | The role of the ClpA chaperone in proteolysis by ClpAP |
| Q35243928 | Translocation pathway of protein substrates in ClpAP protease. |
| Q34304801 | Two peptide sequences can function cooperatively to facilitate binding and unfolding by ClpA and degradation by ClpAP |
| Q35190292 | Unfolding and internalization of proteins by the ATP-dependent proteases ClpXP and ClpAP. |
| Q54486455 | Versatile modes of peptide recognition by the AAA+ adaptor protein SspB. |
| Q43542803 | Visualization of substrate binding and translocation by the ATP-dependent protease, ClpXP. |
| Q64464378 | [34] Purification and properties of Hsp104 from yeast |