3siv
From Proteopedia
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<StructureSection load='3siv' size='340' side='right'caption='[[3siv]], [[Resolution|resolution]] 3.30Å' scene=''> | <StructureSection load='3siv' size='340' side='right'caption='[[3siv]], [[Resolution|resolution]] 3.30Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>[[3siv]] is a 12 chain structure with sequence from [https://en.wikipedia.org/wiki/ | + | <table><tr><td colspan='2'>[[3siv]] is a 12 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3SIV OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3SIV FirstGlance]. <br> |
- | </td></tr><tr id=' | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.304Å</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=3siv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3siv OCA], [https://pdbe.org/3siv PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3siv RCSB], [https://www.ebi.ac.uk/pdbsum/3siv PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3siv 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=3siv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3siv OCA], [https://pdbe.org/3siv PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3siv RCSB], [https://www.ebi.ac.uk/pdbsum/3siv PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3siv ProSAT]</span></td></tr> | ||
</table> | </table> | ||
- | == Disease == | ||
- | [[https://www.uniprot.org/uniprot/PRP31_HUMAN PRP31_HUMAN]] Defects in PRPF31 are the cause of retinitis pigmentosa type 11 (RP11) [MIM:[https://omim.org/entry/600138 600138]]. RP leads to degeneration of retinal photoreceptor cells. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. RP11 inheritance is autosomal dominant.<ref>PMID:17412961</ref> <ref>PMID:12444105</ref> <ref>PMID:11545739</ref> <ref>PMID:8808602</ref> <ref>PMID:12923864</ref> | ||
== Function == | == Function == | ||
- | + | [https://www.uniprot.org/uniprot/NH2L1_HUMAN NH2L1_HUMAN] Binds to the 5'-stem-loop of U4 snRNA and may play a role in the late stage of spliceosome assembly. The protein undergoes a conformational change upon RNA-binding.<ref>PMID:10545122</ref> <ref>PMID:17412961</ref> | |
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==See Also== | ==See Also== | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
- | [[Category: | + | [[Category: Homo sapiens]] |
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
- | [[Category: Ghalei | + | [[Category: Ghalei H]] |
- | [[Category: Liu | + | [[Category: Liu S]] |
- | [[Category: Luhrmann | + | [[Category: Luhrmann R]] |
- | [[Category: Wahl | + | [[Category: Wahl MC]] |
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Current revision
Structure of a hPrp31-15.5K-U4atac 5' stem loop complex, dimeric form
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Categories: Homo sapiens | Large Structures | Ghalei H | Liu S | Luhrmann R | Wahl MC