2yrl: Difference between revisions
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==Solution structure of the PKD domain from KIAA 1837 protein== | ==Solution structure of the PKD domain from KIAA 1837 protein== | ||
<StructureSection load='2yrl' size='340' side='right' caption='[[2yrl]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''> | <StructureSection load='2yrl' size='340' side='right'caption='[[2yrl]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[2yrl]] is a 1 chain structure with sequence from [ | <table><tr><td colspan='2'>[[2yrl]] 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=2YRL OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2YRL FirstGlance]. <br> | ||
</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">KIAA1837 ([ | </td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">KIAA1837 ([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=2yrl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2yrl OCA], [https://pdbe.org/2yrl PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2yrl RCSB], [https://www.ebi.ac.uk/pdbsum/2yrl PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2yrl ProSAT], [https://www.topsan.org/Proteins/RSGI/2yrl TOPSAN]</span></td></tr> | ||
</table> | </table> | ||
== Disease == | == Disease == | ||
[[ | [[https://www.uniprot.org/uniprot/K319L_HUMAN K319L_HUMAN]] Systemic lupus erythematosus;Limited cutaneous systemic sclerosis. | ||
== Function == | == Function == | ||
[[ | [[https://www.uniprot.org/uniprot/K319L_HUMAN K319L_HUMAN]] Possible role in axon guidance through interaction with RTN4R.<ref>PMID:20697954</ref> | ||
== Evolutionary Conservation == | == Evolutionary Conservation == | ||
[[Image:Consurf_key_small.gif|200px|right]] | [[Image:Consurf_key_small.gif|200px|right]] | ||
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</StructureSection> | </StructureSection> | ||
[[Category: Human]] | [[Category: Human]] | ||
[[Category: Large Structures]] | |||
[[Category: Hayashi, F]] | [[Category: Hayashi, F]] | ||
[[Category: Qin, X R]] | [[Category: Qin, X R]] | ||
Revision as of 13:36, 24 November 2021
Solution structure of the PKD domain from KIAA 1837 protein
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