5en1: Difference between revisions

Line 1:

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

~~The entry~~ 5en1 is ~~ON HOLD until Paper Publication~~

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

~~Authors~~: Wu, B.X., Su, S.C., Ma, J.B.

== Structural highlights ==

<table><tr><td colspan='2'>[[5en1]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5EN1 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5EN1 FirstGlance]. <br>

~~Description~~: ~~Crystal structure~~ of ~~hnRNPA2B1~~ in ~~complex~~ with RNA

</td></tr><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=5en1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5en1 OCA], [http://pdbe.org/5en1 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5en1 RCSB], [http://www.ebi.ac.uk/pdbsum/5en1 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5en1 ProSAT]</span></td></tr>

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

</table>

[[Category: Su, S.C]]

== Disease ==

[[Category: Ma, J.B]]

[[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>

[[Category: ~~Wu, B.X~~]]

== 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 5en1 is ON HOLD  until Paper Publication
+==Crystal structure of hnRNPA2B1 in complex with RNA==
+<StructureSection load='5en1' size='340' side='right' caption='[[5en1]], [[Resolution|resolution]] 2.58&Aring;' scene=''>
-Authors: Wu, B.X., Su, S.C., Ma, J.B.
+== Structural highlights ==
+<table><tr><td colspan='2'>[[5en1]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5EN1 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5EN1 FirstGlance]. <br>
-Description: Crystal structure of hnRNPA2B1 in complex with RNA
+</td></tr><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=5en1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5en1 OCA], [http://pdbe.org/5en1 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5en1 RCSB], [http://www.ebi.ac.uk/pdbsum/5en1 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5en1 ProSAT]</span></td></tr>
-[[Category: Unreleased Structures]]
+</table>
-[[Category: Su, S.C]]
+== Disease ==
-[[Category: Ma, J.B]]
+[[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>
-[[Category: Wu, B.X]]
+== 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]]