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New page: left|200px<br /> <applet load="1iyf" size="450" color="white" frame="true" align="right" spinBox="true" caption="1iyf" /> '''Solution structure of ubiquitin-like domain...
 
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[[Image:1iyf.gif|left|200px]]<br />
[[Image:1iyf.gif|left|200px]]<br /><applet load="1iyf" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1iyf" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1iyf" />
caption="1iyf" />
'''Solution structure of ubiquitin-like domain of human parkin'''<br />
'''Solution structure of ubiquitin-like domain of human parkin'''<br />


==Overview==
==Overview==
Parkin, a product of the causative gene of autosomal-recessive juvenile, parkinsonism (AR-JP), is a RING-type E3 ubiquitin ligase and has an, amino-terminal ubiquitin-like (Ubl) domain. Although a single mutation, that causes an Arg to Pro substitution at position 42 of the Ubl domain, (the Arg 42 mutation) has been identified in AR-JP patients, the function, of this domain is not clear. In this study, we determined the, three-dimensional structure of the Ubl domain of parkin by NMR, in, particular by extensive use of backbone (15)N-(1)H residual, dipolar-coupling data. Inspection of chemical-shift-perturbation data, showed that the parkin Ubl domain binds the Rpn10 subunit of 26S, proteasomes via the region of parkin that includes position 42. Our, findings suggest that the Arg 42 mutation induces a conformational change, in the Rpn10-binding site of Ubl, resulting in impaired proteasomal, binding of parkin, which could be the cause of AR-JP.
Parkin, a product of the causative gene of autosomal-recessive juvenile parkinsonism (AR-JP), is a RING-type E3 ubiquitin ligase and has an amino-terminal ubiquitin-like (Ubl) domain. Although a single mutation that causes an Arg to Pro substitution at position 42 of the Ubl domain (the Arg 42 mutation) has been identified in AR-JP patients, the function of this domain is not clear. In this study, we determined the three-dimensional structure of the Ubl domain of parkin by NMR, in particular by extensive use of backbone (15)N-(1)H residual dipolar-coupling data. Inspection of chemical-shift-perturbation data showed that the parkin Ubl domain binds the Rpn10 subunit of 26S proteasomes via the region of parkin that includes position 42. Our findings suggest that the Arg 42 mutation induces a conformational change in the Rpn10-binding site of Ubl, resulting in impaired proteasomal binding of parkin, which could be the cause of AR-JP.


==Disease==
==Disease==
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==About this Structure==
==About this Structure==
1IYF is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Active as [http://en.wikipedia.org/wiki/Ubiquitin--protein_ligase Ubiquitin--protein ligase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=6.3.2.19 6.3.2.19] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1IYF OCA].  
1IYF is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Active as [http://en.wikipedia.org/wiki/Ubiquitin--protein_ligase Ubiquitin--protein ligase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=6.3.2.19 6.3.2.19] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1IYF OCA].  


==Reference==
==Reference==
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[[Category: Kurimoto, E.]]
[[Category: Kurimoto, E.]]
[[Category: Mizuno, Y.]]
[[Category: Mizuno, Y.]]
[[Category: RSGI, RIKEN.Structural.Genomics/Proteomics.Initiative.]]
[[Category: RSGI, RIKEN Structural Genomics/Proteomics Initiative.]]
[[Category: Sakata, E.]]
[[Category: Sakata, E.]]
[[Category: Tanaka, K.]]
[[Category: Tanaka, K.]]
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[[Category: ubiquitin fold]]
[[Category: ubiquitin fold]]


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