2mxw
From Proteopedia
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==Solution NMR Structure of the OCRE Domain of RBM10== | ==Solution NMR Structure of the OCRE Domain of RBM10== | ||
| - | <StructureSection load='2mxw' size='340' side='right'caption='[[2mxw | + | <StructureSection load='2mxw' size='340' side='right'caption='[[2mxw]]' scene=''> |
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[2mxw]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/ | + | <table><tr><td colspan='2'>[[2mxw]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. 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 [https://proteopedia.org/fgij/fg.htm?mol=2MXW FirstGlance]. <br> |
| - | </td></tr> | + | </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=2mxw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2mxw OCA], [https://pdbe.org/2mxw PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2mxw RCSB], [https://www.ebi.ac.uk/pdbsum/2mxw PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2mxw ProSAT]</span></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=2mxw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2mxw OCA], [https://pdbe.org/2mxw PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2mxw RCSB], [https://www.ebi.ac.uk/pdbsum/2mxw PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2mxw ProSAT]</span></td></tr> | + | |
</table> | </table> | ||
== Disease == | == Disease == | ||
| - | + | [https://www.uniprot.org/uniprot/RBM10_HUMAN RBM10_HUMAN] TARP syndrome. TARP syndrome (TARPS) [MIM:[https://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 == | == Function == | ||
| - | + | [https://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 == | ||
<references/> | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| - | [[Category: | + | [[Category: Homo sapiens]] |
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
| - | [[Category: Geralt | + | [[Category: Geralt M]] |
| - | + | [[Category: Martin BT]] | |
| - | [[Category: Martin | + | [[Category: Serrano P]] |
| - | [[Category: Serrano | + | [[Category: Wuthrich K]] |
| - | [[Category: Wuthrich | + | |
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Revision as of 08:10, 8 March 2023
Solution NMR Structure of the OCRE Domain of RBM10
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