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"  
<applet load="1q02" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1q02" />
caption="1q02" />
'''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, 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 --&gt; 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 --&gt; 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.
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 --&gt; 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 --&gt; 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://ispc.weizmann.ac.il/oca-bin/ocashort?id=1Q02 OCA].  
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.R.]]
[[Category: Cavey, J R.]]
[[Category: Ciani, B.]]
[[Category: Ciani, B.]]
[[Category: Layfield, R.]]
[[Category: Layfield, R.]]
[[Category: Searle, M.S.]]
[[Category: Searle, M S.]]
[[Category: Sheppard, P.W.]]
[[Category: Sheppard, P W.]]
[[Category: helical bundle]]
[[Category: helical bundle]]


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