This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.
Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.
8e22
From Proteopedia
(Difference between revisions)
| Line 1: | Line 1: | ||
| - | '''Unreleased structure''' | ||
| - | + | ==VPS37A_21-148== | |
| - | + | <StructureSection load='8e22' size='340' side='right'caption='[[8e22]]' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[8e22]] 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=8E22 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8E22 FirstGlance]. <br> | |
| - | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr> | |
| - | [[Category: | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8e22 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8e22 OCA], [https://pdbe.org/8e22 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8e22 RCSB], [https://www.ebi.ac.uk/pdbsum/8e22 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8e22 ProSAT]</span></td></tr> |
| - | [[Category: | + | </table> |
| - | [[Category: Tian | + | == Disease == |
| + | [https://www.uniprot.org/uniprot/VP37A_HUMAN VP37A_HUMAN] Autosomal recessive spastic paraplegia type 53. The disease is caused by variants affecting the gene represented in this entry. | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/VP37A_HUMAN VP37A_HUMAN] Component of the ESCRT-I complex, a regulator of vesicular trafficking process. Required for the sorting of endocytic ubiquitinated cargos into multivesicular bodies. May be involved in cell growth and differentiation.<ref>PMID:15240819</ref> | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Tian F]] | ||
| + | [[Category: Ye YS]] | ||
Revision as of 05:26, 9 August 2023
VPS37A_21-148
| |||||||||||
