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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Dec 2016.

Coactosin-like 1

Top mentioned proteins: ClpP, ATPase, CAN, ACID, ClpX
Papers on Clp
Coarse-Grained Simulations of Topology-Dependent Mechanisms of Protein Unfolding and Translocation Mediated by ClpY ATPase Nanomachines.
Stan et al., Cincinnati, United States. In Plos Comput Biol, Jan 2016
Clp ATPases are powerful ring shaped nanomachines which participate in the degradation pathway of the protein quality control system, coupling the energy from ATP hydrolysis to threading substrate proteins (SP) through their narrow central pore.
Structure of a putative ClpS N-end rule adaptor protein from the malaria pathogen Plasmodium falciparum.
Egea et al., Los Angeles, United States. In Protein Sci, Jan 2016
UNASSIGNED: The N-end rule pathway uses an evolutionarily conserved mechanism in bacteria and eukaryotes that marks proteins for degradation by ATP-dependent chaperones and proteases such as the Clp chaperones and proteases.
The RpfB-dependent Quorum Sensing Signal Turnover System is Required for Adaptation and Virulence in Rice Bacterial Blight Pathogen Xanthomonas oryzae pv. oryzae.
He et al., Shanghai, China. In Mol Plant Microbe Interact, Jan 2016
The RpfC/RpfG-mediated DSF signaling system negatively regulates rpfB expression via the global transcription regulator Clp, whose activity is reversible in the presence of cyclic-di-GMP.
Stability of the GraA antitoxin depends on the growth phase, ATP level and global regulator MexT.
Hõrak et al., Tartu, Estonia. In J Bacteriol, Jan 2016
The degradation of antitoxins is usually rapid and carried out by ATP-dependent proteases Lon or Clp that are activated under stress conditions.
Effect of GTS-21, An Alpha7 Nicotinic Acetylcholine Receptor Agonist, on Clp-Induced Inflammatory, Gastrointestinal Motility and Colonic Permeability Changes in Mice.
De Winter et al., Leuven, Belgium. In Shock, Dec 2015
METHODS: Sepsis was induced in OF-1 mice by caecal ligation and puncture (CLP).
Organization, function and substrates of the essential Clp protease system in plastids.
van Wijk et al., Ithaca, United States. In Biochim Biophys Acta, Sep 2015
We provide a comprehensive review of the Clp protease system present in all plastid types and we draw lessons from structural and functional information of bacterial Clp systems.
Mitochondrial proteases and protein quality control in ageing and longevity.
Friguet et al., Paris, France. In Ageing Res Rev, Sep 2015
In the mitochondrial matrix, protein quality control is mainly achieved by the Lon and Clp proteases which are also key players in damaged mitochondrial proteins degradation.
Regulation of competence for natural transformation in streptococci.
Hols et al., Louvain-la-Neuve, Belgium. In Infect Genet Evol, Jul 2015
Recent findings regarding competence regulation by the ComCDE and ComRS cell-cell signalling pathways and the Clp proteolytic system are specifically highlighted.
Loss of chloroplast ClpP elicits an autophagy-like response in Chlamydomonas.
Rochaix et al., Genève, Switzerland. In Autophagy, 2014
Chloroplast genomes contain a single ClpP1 gene encoding one of the catalytic subunits of the evolutionarily conserved ATP-dependent Clp protease.
Clp chaperones and proteases are central in stress survival, virulence and antibiotic resistance of Staphylococcus aureus.
Ingmer et al., Frederiksberg, Denmark. In Int J Med Microbiol, 2014
The contribution of the Clp proteins to virulence is likely to occur at multiple levels.
D14-SCF(D3)-dependent degradation of D53 regulates strigolactone signalling.
Wan et al., Nanjing, China. In Nature, 2014
The D53 gene product shares predicted features with the class I Clp ATPase proteins and can form a complex with the α/β hydrolase protein DWARF 14 (D14) and the F-box protein DWARF 3 (D3), two previously identified signalling components potentially responsible for SL perception.
Segregation of molecules at cell division reveals native protein localization.
Paulsson et al., Boston, United States. In Nat Methods, 2012
We found that Clp proteases, widely reported to form biologically relevant foci, were uniformly distributed in Escherichia coli cells, and that many commonly used fluorescent proteins caused severe mislocalization when fused to homo-oligomers.
Structure and mechanism of the hexameric MecA-ClpC molecular machine.
Shi et al., Beijing, China. In Nature, 2011
Bacterial ClpC, a member of the Clp/Hsp100 family of AAA+ proteins (ATPases associated with diverse cellular activities) with two nucleotide-binding domains (D1 and D2), requires the adaptor protein MecA for activation and substrate targeting.
Adapting the machine: adaptor proteins for Hsp100/Clp and AAA+ proteases.
Turgay et al., Evanston, United States. In Nat Rev Microbiol, 2009
To manage these many, varied tasks, Hsp100/Clp and AAA+ proteases use specific adaptor proteins to enhance or expand the substrate recognition abilities of their cognate protease.
Dysregulation of bacterial proteolytic machinery by a new class of antibiotics.
Labischinski et al., Wuppertal, Germany. In Nat Med, 2005
ClpP is usually tightly regulated and strictly requires a member of the family of Clp-ATPases and often further accessory proteins for proteolytic activation.
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