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6j60

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(New page: '''Unreleased structure''' The entry 6j60 is ON HOLD Authors: Luo, F., Zhou, H., Gui, X., Li, D., Li, X., Liu, C. Description: hnRNP A1 reversible amyloid core GFGGNDNFG (residues 209-...)
Current revision (10:36, 27 March 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 6j60 is ON HOLD
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==hnRNP A1 reversible amyloid core GFGGNDNFG (residues 209-217)==
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<StructureSection load='6j60' size='340' side='right'caption='[[6j60]], [[Resolution|resolution]] 0.96&Aring;' scene=''>
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Authors: Luo, F., Zhou, H., Gui, X., Li, D., Li, X., Liu, C.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6j60]] 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=6J60 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6J60 FirstGlance]. <br>
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Description: hnRNP A1 reversible amyloid core GFGGNDNFG (residues 209-217)
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron crystallography, [[Resolution|Resolution]] 0.96&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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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=6j60 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6j60 OCA], [https://pdbe.org/6j60 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6j60 RCSB], [https://www.ebi.ac.uk/pdbsum/6j60 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6j60 ProSAT]</span></td></tr>
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[[Category: Li, D]]
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</table>
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[[Category: Zhou, H]]
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== Disease ==
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[[Category: Gui, X]]
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[https://www.uniprot.org/uniprot/ROA1_HUMAN ROA1_HUMAN] Amyotrophic lateral sclerosis;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> The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:23455423</ref>
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[[Category: Li, X]]
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== Function ==
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[[Category: Liu, C]]
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[https://www.uniprot.org/uniprot/ROA1_HUMAN ROA1_HUMAN] Involved in the packaging of pre-mRNA into hnRNP particles, transport of poly(A) mRNA from the nucleus to the cytoplasm and may modulate splice site selection. May play a role in HCV RNA replication.<ref>PMID:17229681</ref>
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[[Category: Luo, F]]
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Gui X]]
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[[Category: Li D]]
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[[Category: Li X]]
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[[Category: Liu C]]
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[[Category: Luo F]]
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[[Category: Zhou H]]

Current revision

hnRNP A1 reversible amyloid core GFGGNDNFG (residues 209-217)

PDB ID 6j60

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