6wpq

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==GNYNVF from hnRNPA2-low complexity domain segment, residues 286-291, D290V variant==
==GNYNVF from hnRNPA2-low complexity domain segment, residues 286-291, D290V variant==
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<StructureSection load='6wpq' size='340' side='right'caption='[[6wpq]]' scene=''>
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<StructureSection load='6wpq' size='340' side='right'caption='[[6wpq]], [[Resolution|resolution]] 1.10&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6WPQ OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=6WPQ FirstGlance]. <br>
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<table><tr><td colspan='2'>[[6wpq]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6WPQ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6WPQ FirstGlance]. <br>
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</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://proteopedia.org/fgij/fg.htm?mol=6wpq FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6wpq OCA], [http://pdbe.org/6wpq PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6wpq RCSB], [http://www.ebi.ac.uk/pdbsum/6wpq PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6wpq ProSAT]</span></td></tr>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.1&#8491;</td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6wpq FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6wpq OCA], [https://pdbe.org/6wpq PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6wpq RCSB], [https://www.ebi.ac.uk/pdbsum/6wpq PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6wpq ProSAT]</span></td></tr>
</table>
</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/ROA2_HUMAN ROA2_HUMAN] Inclusion body myopathy with Paget disease of bone and frontotemporal dementia. The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:23455423</ref>
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== Function ==
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[https://www.uniprot.org/uniprot/ROA2_HUMAN ROA2_HUMAN] Involved with pre-mRNA processing. Forms complexes (ribonucleosomes) with at least 20 other different hnRNP and heterogeneous nuclear RNA in the nucleus.
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== References ==
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<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
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[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Large Structures]]
[[Category: Boyer DR]]
[[Category: Boyer DR]]

Current revision

GNYNVF from hnRNPA2-low complexity domain segment, residues 286-291, D290V variant

PDB ID 6wpq

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