1q02: Difference between revisions
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New page: left|200px<br /> <applet load="1q02" size="450" color="white" frame="true" align="right" spinBox="true" caption="1q02" /> '''NMR structure of the UBA domain of p62 (SQS... |
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[[Image:1q02.gif|left|200px]]<br /> | [[Image:1q02.gif|left|200px]]<br /><applet load="1q02" size="350" color="white" frame="true" align="right" spinBox="true" | ||
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'''NMR structure of the UBA domain of p62 (SQSTM1)'''<br /> | '''NMR structure of the UBA domain of p62 (SQSTM1)'''<br /> | ||
==Overview== | ==Overview== | ||
The p62 protein (also known as SQSTM1) mediates diverse cellular functions | The p62 protein (also known as SQSTM1) mediates diverse cellular functions including control of NFkappaB signaling and transcriptional activation. p62 binds non-covalently to ubiquitin and co-localizes with ubiquitylated inclusions in a number of human protein aggregation diseases. Mutations in the gene encoding p62 cause Paget's disease of bone (PDB), a common disorder of the elderly characterized by excessive bone resorption and formation. All of the p62 PDB mutations identified to date cluster within the C-terminal region of the protein, which shows low sequence identity to previously characterized ubiquitin-associated (UBA) domains. We report the first NMR structure of a recombinant polypeptide that contains the C-terminal UBA domain of the human p62 protein (residues 387-436). This sequence, which confers multiubiquitin chain binding, forms a compact three-helix bundle with a structure analogous to the UBA domains of HHR23A but with differences in the loop regions connecting helices that may be involved in binding accessory proteins. We show that the Pro392 --> Leu PDB substitution mutation modifies the structure of the UBA domain by extending the N terminus of helix 1. In contrast to the p62 PDB deletion mutations that remove the UBA domain and ablate multiubiquitin chain binding, the Pro392 --> Leu substitution does not affect interaction of the UBA domain with multiubiquitin chains. Thus, phenotypically identical substitution and deletion mutations do not appear to predispose to PDB through a mechanism dependent on a common loss of ubiquitin chain binding by p62. | ||
==Disease== | ==Disease== | ||
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==About this Structure== | ==About this Structure== | ||
1Q02 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http:// | 1Q02 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1Q02 OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Cavey, J | [[Category: Cavey, J R.]] | ||
[[Category: Ciani, B.]] | [[Category: Ciani, B.]] | ||
[[Category: Layfield, R.]] | [[Category: Layfield, R.]] | ||
[[Category: Searle, M | [[Category: Searle, M S.]] | ||
[[Category: Sheppard, P | [[Category: Sheppard, P W.]] | ||
[[Category: helical bundle]] | [[Category: helical bundle]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:34:24 2008'' | ||