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注意：仅列出部分参考文献，下载原文获取全部文献信息。AAA+ Proteases: ATP-Fueled Machines of Protein Destruction
Robert T. Sauer et al.
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 80 (2011)
Single-Molecule Protein Unfolding and Translocation by an ATP-Fueled Proteolytic Machine
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Stepwise Unfolding of a β Barrel Protein by the AAA plus ClpXP Protease
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Rad23 escapes degradation because it lacks a proteasome initiation region
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ATP-dependent Proteases Differ Substantially in Their Ability to Unfold Globular Proteins
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Protein Unfolding with a Steric Trap
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Targeting proteins for degradation
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Degrons in protein substrates program the speed and operating efficiency of the AAA plus Lon proteolytic machine
Eyal Gur et al.
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Recognition of misfolded proteins by Lon, a AAA+ protease
Eyal Gur et al.
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The Molecular Basis of N-End Rule Recognition
Kevin H. Wang et al.
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Protein unfolding by a AAA plus protease is dependent on ATP-hydrolysis rates and substrate energy landscapes
Andreas Martin et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2008)
Evolution of the ssrA degradation tag in Mycoplasma: Specificity switch to a different protease
Eyal Gur et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Lon protease degrades transfer-messenger RNA-tagged proteins
Jennifer S. Choy et al.
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ClpS modulates but is not essential for bacterial N-end rule degradation
Kevin H. Wang et al.
GENES & DEVELOPMENT (2007)
ATP-dependent proteases of bacteria: recognition logic and operating principles
Tania A. Baker et al.
TRENDS IN BIOCHEMICAL SCIENCES (2006)
A conserved processing mechanism regulates the activity of transcription factors Cubitus interruptus and NF-κB
L Tian et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2005)
Partitioning between unfolding and release of native domains during ClpXP degradation determines substrate selectivity and partial processing
JA Kenniston et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
Kinetics of protein substrate degradation by HslUV
AR Kwon et al.
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Effects of local protein stability and the geometric position of the substrate degradation tag on the efficiency of ClpXP denaturation and degradation
JA Kenniston et al.
JOURNAL OF STRUCTURAL BIOLOGY (2004)
An unstructured initiation site is required for efficient proteasome-mediated degradation
S Prakash et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2004)
Exploring the energy landscape of GFP by single-molecule mechanical experiments
H Dietz et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Nucleotide-dependent substrate handoff from the SspB adaptor to the AAA plus ClpXP protease
DN Bolon et al.
MOLECULAR CELL (2004)
Linkage between ATP consumption and mechanical unfolding during the protein processing reactions of an AAA+ degradation machine
JA Kenniston et al.
CELL (2003)
Lack of a robust unfoldase activity confers a unique level of substrate specificity to the universal AAA protease FtsH
C Herman et al.
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Proteolysis in bacterial regulatory circuits
S Gottesman
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY (2003)
Concurrent translocation of multiple polypeptide chains through the proteasomal degradation channel
C Lee et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
ClpAP and ClpXP degrade proteins with tags located in the interior of the primary sequence
JR Hoskins et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
Overlapping recognition determinants within the ssrA degradation tag allow modulation of proteolysis
JM Flynn et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)
ATP-dependent proteases degrade their substrates by processively unraveling them from the degradation signal
C Lee et al.
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Folding of green fluorescent protein and the cycle3 mutant
H Fukuda et al.
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Unfolding and internalization of proteins by the ATP-dependent proteases ClpXP and ClpAP
SK Singh et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)
Dynamics of substrate denaturation and translocation by the ClpXP degradation machine
YI Kim et al.
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