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6wqk
From Proteopedia
(Difference between revisions)
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==hnRNPA2 Low complexity domain (LCD) determined by cryoEM== | ==hnRNPA2 Low complexity domain (LCD) determined by cryoEM== | ||
| - | <StructureSection load='6wqk' size='340' side='right'caption='[[6wqk]]' scene=''> | + | <StructureSection load='6wqk' size='340' side='right'caption='[[6wqk]], [[Resolution|resolution]] 3.10Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6WQK OCA]. For a <b>guided tour on the structure components</b> use [ | + | <table><tr><td colspan='2'>[[6wqk]] is a 5 chain structure with sequence from [https://en.wikipedia.org/wiki/Anaplasma_marginale Anaplasma marginale] and [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6WQK OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6WQK FirstGlance]. <br> |
| - | </td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.1Å</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=6wqk FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6wqk OCA], [https://pdbe.org/6wqk PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6wqk RCSB], [https://www.ebi.ac.uk/pdbsum/6wqk PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6wqk ProSAT]</span></td></tr> | ||
</table> | </table> | ||
| + | == Disease == | ||
| + | [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> | ||
| + | == Function == | ||
| + | [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.[https://www.uniprot.org/uniprot/X5DSL3_ANAMA X5DSL3_ANAMA] | ||
| + | |||
| + | ==See Also== | ||
| + | *[[Green Fluorescent Protein 3D structures|Green Fluorescent Protein 3D structures]] | ||
| + | == References == | ||
| + | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| + | [[Category: Anaplasma marginale]] | ||
| + | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Boyer DR]] | [[Category: Boyer DR]] | ||
Current revision
hnRNPA2 Low complexity domain (LCD) determined by cryoEM
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Categories: Anaplasma marginale | Homo sapiens | Large Structures | Boyer DR | Cao Q | Cascio D | Eisenberg DS | Hughes MP | Lu J | Sawaya MR
