2f42: Difference between revisions
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[[Image:2f42.gif|left|200px]] | [[Image:2f42.gif|left|200px]] | ||
'''dimerization and U-box domains of Zebrafish C-terminal of HSP70 interacting protein''' | {{Structure | ||
|PDB= 2f42 |SIZE=350|CAPTION= <scene name='initialview01'>2f42</scene>, resolution 2.50Å | |||
|SITE= | |||
|LIGAND= <scene name='pdbligand=CL:CHLORIDE ION'>CL</scene> | |||
|ACTIVITY= | |||
|GENE= stub1 (amino acids 112-284) ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=7955 Danio rerio]) | |||
}} | |||
'''dimerization and U-box domains of Zebrafish C-terminal of HSP70 interacting protein''' | |||
==Overview== | ==Overview== | ||
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==About this Structure== | ==About this Structure== | ||
2F42 is a [ | 2F42 is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Danio_rerio Danio rerio]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2F42 OCA]. | ||
==Reference== | ==Reference== | ||
Structure and interactions of the helical and U-box domains of CHIP, the C terminus of HSP70 interacting protein., Xu Z, Devlin KI, Ford MG, Nix JC, Qin J, Misra S, Biochemistry. 2006 Apr 18;45(15):4749-59. PMID:[http:// | Structure and interactions of the helical and U-box domains of CHIP, the C terminus of HSP70 interacting protein., Xu Z, Devlin KI, Ford MG, Nix JC, Qin J, Misra S, Biochemistry. 2006 Apr 18;45(15):4749-59. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/16605243 16605243] | ||
[[Category: Danio rerio]] | [[Category: Danio rerio]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
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[[Category: u-box]] | [[Category: u-box]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 16:47:50 2008'' | ||
Revision as of 17:47, 20 March 2008
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| , resolution 2.50Å | |||||||
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| Ligands: | |||||||
| Gene: | stub1 (amino acids 112-284) (Danio rerio) | ||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||
dimerization and U-box domains of Zebrafish C-terminal of HSP70 interacting protein
OverviewOverview
The heat-shock proteins Hsp70 and Hsp90 play a crucial role in regulating protein quality control both by refolding and by preventing the aggregation of misfolded proteins. It has recently been shown that Hsp70 and Hsp90 act not only in protein refolding but also cooperate with the C terminus of Hsp70 interacting protein (CHIP), a multidomain ubiquitin ligase, to mediate the degradation of unfolded proteins. We present the crystal structure of the helical linker domain and U-box domain of zebrafish CHIP (DrCHIP-HU). The structure of DrCHIP-HU shows a symmetric homodimer. The conformation of the helical linker domains and the relative positions of the helical and U-box domains differ substantially in DrCHIP-HU from those in a recently published structure of an asymmetric dimer of mammalian (mouse) CHIP. We used an in vitro ubiquitination assay to identify residues, located on two long loops and a central alpha helix of the CHIP U-box domain, that are important for interacting with the ubiquitin-conjugating enzyme UbcH5b. In addition, we used NMR spectroscopy to define a complementary interaction surface located on the N-terminal alpha helix and the L4 and L7 loops of UbcH5b. Our results provide insights into conformational variability in the domain arrangement of CHIP and into U-box-mediated recruitment of UbcH5b for the ubiquitination of Hsp70 and Hsp90 substrates.
About this StructureAbout this Structure
2F42 is a Single protein structure of sequence from Danio rerio. Full crystallographic information is available from OCA.
ReferenceReference
Structure and interactions of the helical and U-box domains of CHIP, the C terminus of HSP70 interacting protein., Xu Z, Devlin KI, Ford MG, Nix JC, Qin J, Misra S, Biochemistry. 2006 Apr 18;45(15):4749-59. PMID:16605243
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