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2lxi

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{{STRUCTURE_2lxi| PDB=2lxi | SCENE= }}
 
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===NMR structure of the N-terminal RNA Binding domain 1 (RRM1) of the protein RBM10 from Homo sapiens===
 
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==Disease==
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==NMR structure of the N-terminal RNA Binding domain 1 (RRM1) of the protein RBM10 from Homo sapiens==
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[[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>
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<StructureSection load='2lxi' size='340' side='right'caption='[[2lxi]]' scene=''>
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== Structural highlights ==
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==Function==
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<table><tr><td colspan='2'>[[2lxi]] 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=2LXI OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2LXI FirstGlance]. <br>
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[[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>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2lxi FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lxi OCA], [https://pdbe.org/2lxi PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2lxi RCSB], [https://www.ebi.ac.uk/pdbsum/2lxi PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2lxi ProSAT]</span></td></tr>
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==About this Structure==
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</table>
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[[2lxi]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LXI OCA].
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== Disease ==
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[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>
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==Reference==
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== Function ==
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<references group="xtra"/><references/>
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[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>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Dutta, S K.]]
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[[Category: Large Structures]]
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[[Category: Geralt, M.]]
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[[Category: Dutta SK]]
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[[Category: JCSG, Joint Center for Structural Genomics.]]
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[[Category: Geralt M]]
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[[Category: Serrano, P.]]
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[[Category: Serrano P]]
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[[Category: TCELL, Partnership for T-Cell Biology.]]
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[[Category: Wuthrich K]]
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[[Category: Wuthrich, K.]]
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[[Category: Rna binding]]
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[[Category: Rna binding protein]]
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Current revision

NMR structure of the N-terminal RNA Binding domain 1 (RRM1) of the protein RBM10 from Homo sapiens

PDB ID 2lxi

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