3egn: Difference between revisions
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<StructureSection load='3egn' size='340' side='right'caption='[[3egn]], [[Resolution|resolution]] 2.50Å' scene=''> | <StructureSection load='3egn' size='340' side='right'caption='[[3egn]], [[Resolution|resolution]] 2.50Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[3egn]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/ | <table><tr><td colspan='2'>[[3egn]] is a 1 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=3EGN OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3EGN 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]] 2.5Å</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=3egn FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3egn OCA], [https://pdbe.org/3egn PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3egn RCSB], [https://www.ebi.ac.uk/pdbsum/3egn PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3egn 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=3egn FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3egn OCA], [https://pdbe.org/3egn PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3egn RCSB], [https://www.ebi.ac.uk/pdbsum/3egn PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3egn ProSAT]</span></td></tr> | ||
</table> | </table> | ||
== Disease == | |||
[https://www.uniprot.org/uniprot/RNPC3_HUMAN RNPC3_HUMAN] Isolated growth hormone deficiency type IA. The disease is caused by variants affecting the gene represented in this entry. | |||
== Function == | == Function == | ||
[https://www.uniprot.org/uniprot/RNPC3_HUMAN RNPC3_HUMAN] Participates in pre-mRNA U12-dependent splicing, performed by the minor spliceosome which removes U12-type introns. U12-type introns comprises less than 1% of all non-coding sequences. Binds to the 3'-stem-loop of m(7)G-capped U12 snRNA.<ref>PMID:16096647</ref> <ref>PMID:19447915</ref> <ref>PMID:24480542</ref> <ref>PMID:29255062</ref> | |||
== Evolutionary Conservation == | == Evolutionary Conservation == | ||
[[Image:Consurf_key_small.gif|200px|right]] | [[Image:Consurf_key_small.gif|200px|right]] | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Netter | [[Category: Netter C]] | ||
[[Category: Wahl | [[Category: Wahl MC]] | ||