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本文引用的文献
1
Nucleotide-dependent substrate handoff from the SspB adaptor to the AAA+ ClpXP protease.
Mol Cell. 2004 Nov 5;16(3):343-50. doi: 10.1016/j.molcel.2004.10.001.
2
An unstructured initiation site is required for efficient proteasome-mediated degradation.
Nat Struct Mol Biol. 2004 Sep;11(9):830-7. doi: 10.1038/nsmb814. Epub 2004 Aug 15.
3
SspB delivery of substrates for ClpXP proteolysis probed by the design of improved degradation tags.
Proc Natl Acad Sci U S A. 2004 Aug 17;101(33):12136-41. doi: 10.1073/pnas.0404733101. Epub 2004 Aug 5.
4
Substrate recognition by the AAA+ chaperone ClpB.
Nat Struct Mol Biol. 2004 Jul;11(7):607-15. doi: 10.1038/nsmb787. Epub 2004 Jun 20.
5
Communication between ClpX and ClpP during substrate processing and degradation.
Nat Struct Mol Biol. 2004 May;11(5):404-11. doi: 10.1038/nsmb752. Epub 2004 Apr 4.
6
Effects of local protein stability and the geometric position of the substrate degradation tag on the efficiency of ClpXP denaturation and degradation.
J Struct Biol. 2004 Apr-May;146(1-2):130-40. doi: 10.1016/j.jsb.2003.10.023.
7
Role of the processing pore of the ClpX AAA+ ATPase in the recognition and engagement of specific protein substrates.
Genes Dev. 2004 Feb 15;18(4):369-74. doi: 10.1101/gad.1170304.
8
Bivalent tethering of SspB to ClpXP is required for efficient substrate delivery: a protein-design study.
Mol Cell. 2004 Feb 13;13(3):443-9. doi: 10.1016/s1097-2765(04)00027-9.
9
Distinct peptide signals in the UmuD and UmuD' subunits of UmuD/D' mediate tethering and substrate processing by the ClpXP protease.
Proc Natl Acad Sci U S A. 2003 Nov 11;100(23):13219-24. doi: 10.1073/pnas.2235804100. Epub 2003 Oct 31.
10
Determination of the cleavage sites in SulA, a cell division inhibitor, by the ATP-dependent HslVU protease from Escherichia coli.
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