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New page: left|200px<br /><applet load="1jru" size="450" color="white" frame="true" align="right" spinBox="true" caption="1jru" /> '''NMR STRUCTURE OF THE UBX DOMAIN FROM P47 (EN...
 
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[[Image:1jru.jpg|left|200px]]<br /><applet load="1jru" size="450" color="white" frame="true" align="right" spinBox="true"
caption="1jru" />
'''NMR STRUCTURE OF THE UBX DOMAIN FROM P47 (ENERGY MINIMISED AVERAGE)'''<br />


==Overview==
==NMR STRUCTURE OF THE UBX DOMAIN FROM P47 (ENERGY MINIMISED AVERAGE)==
p47 is the major protein identified in complex with the cytosolic AAA, ATPase p97. It functions as an essential cofactor of p97-regulated, membrane fusion, which has been suggested to disassemble t-t-SNARE, complexes and prepare them for further rounds of membrane fusion. Here, we, report the high-resolution NMR structure of the C-terminal domain from, p47. It comprises a UBX domain and a 13 residue long structured N-terminal, extension. The UBX domain adopts a characteristic ubiquitin fold with a, betabetaalphabetabetaalphabeta secondary structure arrangement. Three, hydrophobic residues from the N-terminal extension pack closely against a, cleft in the UBX domain. We also identify, for the first time, the p97, interaction surface using NMR chemical shift perturbation studies.
<StructureSection load='1jru' size='340' side='right'caption='[[1jru]]' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[1jru]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Rattus_norvegicus Rattus norvegicus]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1JRU OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1JRU FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1jru FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1jru OCA], [https://pdbe.org/1jru PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1jru RCSB], [https://www.ebi.ac.uk/pdbsum/1jru PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1jru ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/NSF1C_RAT NSF1C_RAT] Reduces the ATPase activity of VCP. Necessary for the fragmentation of Golgi stacks during mitosis and for VCP-mediated reassembly of Golgi stacks after mitosis. May play a role in VCP-mediated formation of transitional endoplasmic reticulum (tER).<ref>PMID:9214505</ref> <ref>PMID:9824302</ref> <ref>PMID:10930451</ref> <ref>PMID:12411482</ref>
== Evolutionary Conservation ==
[[Image:Consurf_key_small.gif|200px|right]]
Check<jmol>
  <jmolCheckbox>
    <scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/jr/1jru_consurf.spt"</scriptWhenChecked>
    <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
    <text>to colour the structure by Evolutionary Conservation</text>
  </jmolCheckbox>
</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=1jru ConSurf].
<div style="clear:both"></div>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
p47 is the major protein identified in complex with the cytosolic AAA ATPase p97. It functions as an essential cofactor of p97-regulated membrane fusion, which has been suggested to disassemble t-t-SNARE complexes and prepare them for further rounds of membrane fusion. Here, we report the high-resolution NMR structure of the C-terminal domain from p47. It comprises a UBX domain and a 13 residue long structured N-terminal extension. The UBX domain adopts a characteristic ubiquitin fold with a betabetaalphabetabetaalphabeta secondary structure arrangement. Three hydrophobic residues from the N-terminal extension pack closely against a cleft in the UBX domain. We also identify, for the first time, the p97 interaction surface using NMR chemical shift perturbation studies.


==About this Structure==
Solution structure and interaction surface of the C-terminal domain from p47: a major p97-cofactor involved in SNARE disassembly.,Yuan X, Shaw A, Zhang X, Kondo H, Lally J, Freemont PS, Matthews S J Mol Biol. 2001 Aug 10;311(2):255-63. PMID:11478859<ref>PMID:11478859</ref>
1JRU is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Rattus_norvegicus Rattus norvegicus]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1JRU OCA].


==Reference==
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
Solution structure and interaction surface of the C-terminal domain from p47: a major p97-cofactor involved in SNARE disassembly., Yuan X, Shaw A, Zhang X, Kondo H, Lally J, Freemont PS, Matthews S, J Mol Biol. 2001 Aug 10;311(2):255-63. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=11478859 11478859]
</div>
<div class="pdbe-citations 1jru" style="background-color:#fffaf0;"></div>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Large Structures]]
[[Category: Rattus norvegicus]]
[[Category: Rattus norvegicus]]
[[Category: Single protein]]
[[Category: Freemont PS]]
[[Category: Freemont, P.S.]]
[[Category: Kondo H]]
[[Category: Kondo, H.]]
[[Category: Lally J]]
[[Category: Lally, J.]]
[[Category: Matthews SJ]]
[[Category: Matthews, S.J.]]
[[Category: Shaw A]]
[[Category: Shaw, A.]]
[[Category: Yuan XM]]
[[Category: Yuan, X.M.]]
[[Category: Zhang XD]]
[[Category: Zhang, X.D.]]
[[Category: ubiquitin superfold]]
[[Category: ubx]]
[[Category: unusual n-terminal feature]]
 
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