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4rcw
From Proteopedia
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==Crystal structure of human Slitrk1== | ==Crystal structure of human Slitrk1== | ||
| - | <StructureSection load='4rcw' size='340' side='right' caption='[[4rcw]], [[Resolution|resolution]] 3.19Å' scene=''> | + | <StructureSection load='4rcw' size='340' side='right'caption='[[4rcw]], [[Resolution|resolution]] 3.19Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[4rcw]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4RCW OCA]. For a <b>guided tour on the structure components</b> use [ | + | <table><tr><td colspan='2'>[[4rcw]] is a 2 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=4RCW OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4RCW 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]] 3.1925Å</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=4rcw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4rcw OCA], [https://pdbe.org/4rcw PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4rcw RCSB], [https://www.ebi.ac.uk/pdbsum/4rcw PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4rcw ProSAT]</span></td></tr> |
</table> | </table> | ||
== Disease == | == Disease == | ||
| - | [ | + | [https://www.uniprot.org/uniprot/SLIK1_HUMAN SLIK1_HUMAN] Tourette syndrome. The disease may be caused by mutations affecting the gene represented in this entry. The disease may be caused by mutations affecting the gene represented in this entry. |
== Function == | == Function == | ||
| - | [ | + | [https://www.uniprot.org/uniprot/SLIK1_HUMAN SLIK1_HUMAN] Enhances neuronal dendrite outgrowth.<ref>PMID:16224024</ref> |
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
</div> | </div> | ||
| + | <div class="pdbe-citations 4rcw" style="background-color:#fffaf0;"></div> | ||
== References == | == References == | ||
<references/> | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| - | [[Category: | + | [[Category: Homo sapiens]] |
| - | [[Category: | + | [[Category: Large Structures]] |
| - | [[Category: | + | [[Category: Kim D]] |
| - | [[Category: | + | [[Category: Kim HM]] |
| - | [[Category: | + | [[Category: Lee SG]] |
| - | [[Category: | + | [[Category: Park BS]] |
| - | + | ||
Current revision
Crystal structure of human Slitrk1
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Categories: Homo sapiens | Large Structures | Kim D | Kim HM | Lee SG | Park BS
