All Stories

  1. A novel class of spectral conjugate gradient methods for unconstrained multiobjective optimization with practical application in image processing
  2. Affinity isolation and biochemical characterization of N-degron ligands using the N-recognin, ClpS
  3. Novel modification by L/F-tRNA-protein transferase (LFTR) generates a Leu/N-degron ligand in Escherichia coli
  4. ClpXP-mediated Degradation of the TAC Antitoxin is Neutralized by the SecB-like Chaperone in Mycobacterium tuberculosis
  5. Polymerase delta-interacting protein 38 (PDIP38) modulates the stability and activity of the mitochondrial AAA+ protease CLPXP
  6. Exploring a potential Achilles heel of Mycobacterium tuberculosis : defining the ClpC1 interactome
  7. PDIP38 is a novel adaptor-like modulator of the mitochondrial AAA+ protease CLPXP
  8. Insight into the RssB-Mediated Recognition and Delivery of σs to the AAA+ Protease, ClpXP
  9. Molecular and structural insights into an asymmetric proteolytic complex (ClpP1P2) from Mycobacterium smegmatis
  10. The Direct Molecular Target for Imipridone ONC201 Is Finally Established
  11. N‐degron specificity of chloroplast ClpS1 in plants
  12. Perrault syndrome type 3 caused by diverse molecular defects in CLPP
  13. The structural biology of mitochondrial respiratory complex assembly
  14. Dysregulating ClpP: From Antibiotics to Anticancer?
  15. Understanding the Pro/N-end rule pathway
  16. Crystal structure of bacterial succinate:quinone oxidoreductase flavoprotein SdhA in complex with its assembly factor SdhE
  17. Pupylation of PafA or Pup inhibits components of the Pup-Proteasome System
  18. AAA+ Machines of Protein Destruction in Mycobacteria
  19. Pro(moting) the Turnover of Gluconeogenic Enzymes by a New Branch of the N-end Rule Pathway
  20. The N-end rule adaptor protein ClpS from Plasmodium falciparum exhibits broad substrate specificity
  21. LON is the master protease that protects against protein aggregation in human mitochondria through direct degradation of misfolded proteins
  22. Anti-adaptors use distinct modes of binding to inhibit the RssB-dependent turnover of RpoS (σS) by ClpXP
  23. Mitochondrial matrix proteostasis is linked to hereditary paraganglioma: LON-mediated turnover of the human flavinylation factor SDH5 is regulated by its interaction with SDHA
  24. Control of Protein Function through Regulated Protein Degradation: Biotechnological and Biomedical Applications
  25. Machines of Destruction – AAA+ Proteases and the Adaptors That Control Them
  26. Proteolytic Regulation of Stress Response Pathways in Escherichia coli
  27. Regulated Proteolysis in Microorganisms
  28. Substrate recognition and processing by a Walker B mutant of the human mitochondrial AAA+ protein CLPX
  29. The N-end rule pathway: From recognition by N-recognins, to destruction by AAA+proteases
  30. Unfolded protein responses in bacteria and mitochondria: A central role for the ClpXP machine
  31. Chemical Activators of ClpP: Turning Jekyll into Hyde
  32. The bacterial N-end rule pathway: expect the unexpected
  33. Diverse functions of mitochondrial AAA+ proteins: protein activation, disaggregation, and degradationThis paper is one of a selection of papers published in this special issue entitled 8th International Conference on AAA Proteins and has undergone the ...
  34. Adapting the machine: adaptor proteins for Hsp100/Clp and AAA+ proteases
  35. Modification of PATase by L/F-transferase generates a ClpS-dependent N-end rule substrate in Escherichia coli
  36. Structural basis of N-end rule substrate recognition in Escherichia coli by the ClpAP adaptor protein ClpS
  37. Structural basis of N‐end rule substrate recognition in Escherichia coli by the ClpAP adaptor protein ClpS
  38. Conserved residues in the N‐domain of the AAA+ chaperone ClpA regulate substrate recognition and unfolding
  39. The tyrosine kinase McsB is a regulated adaptor protein for ClpCP
  40. Adaptor protein controlled oligomerization activates the AAA+ protein ClpC
  41. ClpS is an essential component of the N-end rule pathway in Escherichia coli
  42. Thermotolerance Requires Refolding of Aggregated Proteins by Substrate Translocation through the Central Pore of ClpB
  43. Broad yet high substrate specificity: the challenge of AAA+ proteins
  44. Targeted Delivery of an ssrA-Tagged Substrate by the Adaptor Protein SspB to Its Cognate AAA+ Protein ClpX
  45. MecA, an adaptor protein necessary for ClpC chaperone activity
  46. A folding machine for many but a master of none
  47. Structural analysis of the adaptor protein ClpS in complex with the N-terminal domain of ClpA
  48. Protein folding and degradation in bacteria:¶To degrade or not to degrade? That is the question
  49. Insertion and Assembly of Human Tom7 into the Preprotein Translocase Complex of the Outer Mitochondrial Membrane
  50. AAA+ proteins and substrate recognition, it all depends on their partner in crime
  51. Crystallization and preliminary X-ray analysis of theEscherichia coliadaptor protein ClpS, free and in complex with the N-terminal domain of ClpA
  52. ClpS, a Substrate Modulator of the ClpAP Machine
  53. Effects of substitutions in the binding surface of an antibody on antigen affinity
  54. Heat shock proteins of barley mitochondria and chloroplasts Identification of organellar hsp 10 and 12: putative chaperonin 10 homologues