Pages that link to "Q30322959"
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The following pages link to Global unfolding of a substrate protein by the Hsp100 chaperone ClpA. (Q30322959):
Displaying 50 items.
- The ubiquitin-proteasome proteolytic pathway: destruction for the sake of construction (Q24292709) (← links)
- Recognition of C-terminal amino acids in tubulin by pore loops in Spastin is important for microtubule severing (Q24300949) (← links)
- Human mitochondrial ClpP is a stable heptamer that assembles into a tetradecamer in the presence of ClpX (Q24317060) (← links)
- Regulation of Torsin ATPases by LAP1 and LULL1 (Q24338125) (← links)
- Evolution of the ssrA degradation tag in Mycoplasma: specificity switch to a different protease (Q24649663) (← links)
- Chaperone machines for protein folding, unfolding and disaggregation (Q27026110) (← links)
- The structures of HsIU and the ATP-dependent protease HsIU-HsIV (Q27621563) (← links)
- Crystal and solution structures of an HslUV protease-chaperone complex (Q27628834) (← links)
- Crystal structures of the HslVU peptidase-ATPase complex reveal an ATP-dependent proteolysis mechanism (Q27630654) (← links)
- Crystal structure of E. coli Hsp100 ClpB nucleotide-binding domain 1 (NBD1) and mechanistic studies on ClpB ATPase activity (Q27639122) (← links)
- Crystal structure of the heterodimeric complex of the adaptor, ClpS, with the N-domain of the AAA+ chaperone, ClpA (Q27639658) (← links)
- Structure of a Delivery Protein for an AAA+ Protease in Complex with a Peptide Degradation Tag (Q27642327) (← links)
- The structure of ClpB: a molecular chaperone that rescues proteins from an aggregated state (Q27642377) (← links)
- The Molecular Basis of N-End Rule Recognition (Q27652824) (← links)
- Crystal structure of Lon protease: molecular architecture of gated entry to a sequestered degradation chamber (Q27664441) (← links)
- Structure and mechanism of the hexameric MecA-ClpC molecular machine (Q27666868) (← links)
- The ClpS Adaptor Mediates Staged Delivery of N-End Rule Substrates to the AAA+ ClpAP Protease (Q27670922) (← links)
- Head-to-tail interactions of the coiled-coil domains regulate ClpB activity and cooperation with Hsp70 in protein disaggregation (Q27683847) (← links)
- Selective degradation of ubiquitinated Sic1 by purified 26S proteasome yields active S phase cyclin-Cdk (Q27931597) (← links)
- Substrate binding to the molecular chaperone Hsp104 and its regulation by nucleotides (Q27932701) (← links)
- The axial channel of the proteasome core particle is gated by the Rpt2 ATPase and controls both substrate entry and product release (Q27933726) (← links)
- Structural properties of substrate proteins determine their proteolysis by the mitochondrial AAA+ protease Pim1. (Q27936117) (← links)
- The 19S regulatory particle of the proteasome is required for efficient transcription elongation by RNA polymerase II. (Q27939755) (← links)
- Complementary roles for Rpn11 and Ubp6 in deubiquitination and proteolysis by the proteasome (Q27939996) (← links)
- Torsins: not your typical AAA+ ATPases (Q28087663) (← links)
- An asymmetric interface between the regulatory and core particles of the proteasome (Q28251784) (← links)
- Cooperative kinetics of both Hsp104 ATPase domains and interdomain communication revealed by AAA sensor-1 mutants (Q28344719) (← links)
- Clp-mediated proteolysis in Gram-positive bacteria is autoregulated by the stability of a repressor (Q28348879) (← links)
- Characterization of the N-terminal repeat domain of Escherichia coli ClpA-A class I Clp/HSP100 ATPase (Q28364580) (← links)
- Effects of protein stability and structure on substrate processing by the ClpXP unfolding and degradation machine (Q28366801) (← links)
- A distinct structural region of the prokaryotic ubiquitin-like protein (Pup) is recognized by the N-terminal domain of the proteasomal ATPase Mpa (Q28486354) (← links)
- Mycobacterium tuberculosis ClpC1: characterization and role of the N-terminal domain in its function (Q28486809) (← links)
- The mycobacterial Mpa-proteasome unfolds and degrades pupylated substrates by engaging Pup's N-terminus (Q28486892) (← links)
- Suramin inhibits Hsp104 ATPase and disaggregase activity (Q28543672) (← links)
- Recognition and processing of ubiquitin-protein conjugates by the proteasome (Q29547616) (← links)
- Proteasomes and their kin: proteases in the machine age (Q29614359) (← links)
- AAA+ proteins: have engine, will work (Q29617410) (← links)
- Architecture and molecular mechanism of PAN, the archaeal proteasome regulatory ATPase (Q30490705) (← links)
- Unfolding and translocation pathway of substrate protein controlled by structure in repetitive allosteric cycles of the ClpY ATPase (Q30498176) (← links)
- Marine microbial symbiosis heats up: the phylogenetic and functional response of a sponge holobiont to thermal stress (Q30584195) (← links)
- Role of a conserved pore residue in the formation of a prehydrolytic high substrate affinity state in the AAA+ chaperone ClpA (Q30598763) (← links)
- Unfolding the mechanism of the AAA+ unfoldase VAT by a combined cryo-EM, solution NMR study (Q30789737) (← links)
- Stress genes and proteins in the archaea (Q33334155) (← links)
- Molecular determinants of MecA as a degradation tag for the ClpCP protease (Q33553568) (← links)
- Coupling ATP utilization to protein remodeling by ClpB, a hexameric AAA+ protein (Q33564124) (← links)
- GroEL dependency affects codon usage--support for a critical role of misfolding in gene evolution (Q33668518) (← links)
- Substrate Discrimination by ClpB and Hsp104. (Q33734726) (← links)
- Binding of the ClpA unfoldase opens the axial gate of ClpP peptidase (Q33824950) (← links)
- Local and global mobility in the ClpA AAA+ chaperone detected by cryo-electron microscopy: functional connotations (Q33853445) (← links)
- Conditionally and transiently disordered proteins: awakening cryptic disorder to regulate protein function (Q33875537) (← links)