5wwe: Difference between revisions

Line 1:

~~'''Unreleased structure'''~~

The entry ~~5wwe is ON HOLD~~ ~~until Paper Publication~~

==Crystal structure of hnRNPA2B1 in complex with RNA==

~~Authors~~:

== Structural highlights ==

<table><tr><td colspan='2'>[[5wwe]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5WWE OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5WWE FirstGlance]. <br>

~~Description~~:

</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5wwf|5wwf]], [[5wwg|5wwg]], [[5wwh|5wwh]]</td></tr>

[[Category: ~~Unreleased Structures~~]]

<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5wwe FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5wwe OCA], [http://pdbe.org/5wwe PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5wwe RCSB], [http://www.ebi.ac.uk/pdbsum/5wwe PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5wwe ProSAT]</span></td></tr>

</table>

== Disease ==

[[http://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 ==

[[http://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.

== References ==

__TOC__

</StructureSection>

[[Category: Ma, J B]]

[[Category: Su, S C]]

[[Category: Wu, B X]]

[[Category: Hnrnp]]

[[Category: Rna binding protein-rna complex]]

[[Category: Rrm]]

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
-The entry 5wwe is ON HOLD  until Paper Publication
+==Crystal structure of hnRNPA2B1 in complex with RNA==
+<StructureSection load='5wwe' size='340' side='right' caption='[[5wwe]], [[Resolution|resolution]] 2.40&Aring;' scene=''>
-Authors:
+== Structural highlights ==
+<table><tr><td colspan='2'>[[5wwe]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5WWE OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5WWE FirstGlance]. <br>
-Description:
+</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5wwf|5wwf]], [[5wwg|5wwg]], [[5wwh|5wwh]]</td></tr>
-[[Category: Unreleased Structures]]
+<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5wwe FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5wwe OCA], [http://pdbe.org/5wwe PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5wwe RCSB], [http://www.ebi.ac.uk/pdbsum/5wwe PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5wwe ProSAT]</span></td></tr>
+</table>
+== Disease ==
+[[http://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 ==
+[[http://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.
+== References ==
+<references/>
+__TOC__
+</StructureSection>
+[[Category: Ma, J B]]
+[[Category: Su, S C]]
+[[Category: Wu, B X]]
+[[Category: Hnrnp]]
+[[Category: Rna binding protein-rna complex]]
+[[Category: Rrm]]