2mxw
From Proteopedia
(Difference between revisions)
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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]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''> | + | <StructureSection load='2mxw' size='340' side='right'caption='[[2mxw]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''> |
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[2mxw]] is a 1 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[2mxw]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Human Human]. 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><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">DXS8237E, GPATC9, GPATCH9, KIAA0122, RBM10 ([ | + | </td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">DXS8237E, GPATC9, GPATCH9, KIAA0122, RBM10 ([https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr> |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | <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/> | ||
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</StructureSection> | </StructureSection> | ||
[[Category: Human]] | [[Category: Human]] | ||
| + | [[Category: Large Structures]] | ||
[[Category: Geralt, M]] | [[Category: Geralt, M]] | ||
[[Category: Structural genomic]] | [[Category: Structural genomic]] | ||
Revision as of 15:23, 2 June 2021
Solution NMR Structure of the OCRE Domain of RBM10
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Categories: Human | Large Structures | Geralt, M | Structural genomic | Martin, B T | Serrano, P | Wuthrich, K | Jcsg | Ocre domain | Psi-biology | Rbm10 | Unknown function
