2mxw: Difference between revisions

Line 1:

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

==Solution NMR Structure of the OCRE Domain of RBM10==

~~The entry~~ 2mxw is ~~ON HOLD until Paper Publication~~

== Structural highlights ==

<table><tr><td colspan='2'>[[2mxw]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2MXW OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2MXW FirstGlance]. <br>

~~Authors~~: ~~Martin~~, B.T., ~~Geralt~~, M., ~~Serrano~~, P., ~~Wuthrich, K~~., ~~Joint Center~~ for ~~Structural Genomics~~ (~~JCSG~~)

</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=2mxw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2mxw OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2mxw RCSB], [http://www.ebi.ac.uk/pdbsum/2mxw PDBsum]</span></td></tr>

</table>

~~Description~~: ~~Solution NMR Structure of the OCRE Domain of RBM10~~

== Disease ==

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

[[http://www.uniprot.org/uniprot/RBM10_HUMAN RBM10_HUMAN]] TARP syndrome. TARP syndrome (TARPS) [MIM:[http://omim.org/entry/311900 311900]]: A disorder characterized by the Robin sequence (micrognathia, glossoptosis and cleft palate), talipes equinovarus and cardiac defects. Note=The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:20451169</ref>

== Function ==

[[http://www.uniprot.org/uniprot/RBM10_HUMAN RBM10_HUMAN]] May be involved in post-transcriptional processing, most probably in mRNA splicing. Binds to RNA homopolymers, with a preference for poly(G) and poly(U) and little for poly(A) (By similarity).<ref>PMID:18315527</ref>

== References ==

__TOC__

</StructureSection>

[[Category: Geralt, M]]

[[Category: Structural genomic]]

[[Category: Martin, B T]]

[[Category: Serrano, P]]

[[Category: Wuthrich, K]]

[[Category: ~~Martin, B.T~~]]

[[Category: Jcsg]]

[[Category: ~~Serrano, P~~]]

[[Category: Ocre domain]]

[[Category: ~~Joint Center For Structural Genomics (Jcsg)~~]]

[[Category: Psi-biology]]

[[Category: ~~Geralt, M~~]]

[[Category: Rbm10]]

[[Category: Unknown function]]

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
+==Solution NMR Structure of the OCRE Domain of RBM10==
+<StructureSection load='2mxw' size='340' side='right' caption='[[2mxw]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''>
-The entry 2mxw is ON HOLD  until Paper Publication
+== Structural highlights ==
+<table><tr><td colspan='2'>[[2mxw]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2MXW OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2MXW FirstGlance]. <br>
-Authors: Martin, B.T., Geralt, M., Serrano, P., Wuthrich, K., Joint Center for Structural Genomics (JCSG)
+</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=2mxw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2mxw OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2mxw RCSB], [http://www.ebi.ac.uk/pdbsum/2mxw PDBsum]</span></td></tr>
+</table>
-Description: Solution NMR Structure of the OCRE Domain of RBM10
+== Disease ==
-[[Category: Unreleased Structures]]
+[[http://www.uniprot.org/uniprot/RBM10_HUMAN RBM10_HUMAN]] TARP syndrome. TARP syndrome (TARPS) [MIM:[http://omim.org/entry/311900 311900]]: A disorder characterized by the Robin sequence (micrognathia, glossoptosis and cleft palate), talipes equinovarus and cardiac defects. Note=The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:20451169</ref>
+== Function ==
+[[http://www.uniprot.org/uniprot/RBM10_HUMAN RBM10_HUMAN]] May be involved in post-transcriptional processing, most probably in mRNA splicing. Binds to RNA homopolymers, with a preference for poly(G) and poly(U) and little for poly(A) (By similarity).<ref>PMID:18315527</ref>
+== References ==
+<references/>
+__TOC__
+</StructureSection>
+[[Category: Geralt, M]]
+[[Category: Structural genomic]]
+[[Category: Martin, B T]]
+[[Category: Serrano, P]]
 [[Category: Wuthrich, K]]
-[[Category: Martin, B.T]]
+[[Category: Jcsg]]
-[[Category: Serrano, P]]
+[[Category: Ocre domain]]
-[[Category: Joint Center For Structural Genomics (Jcsg)]]
+[[Category: Psi-biology]]
-[[Category: Geralt, M]]
+[[Category: Rbm10]]
+[[Category: Unknown function]]