5aek
From Proteopedia
(Difference between revisions)
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<StructureSection load='5aek' size='340' side='right'caption='[[5aek]], [[Resolution|resolution]] 3.00Å' scene=''> | <StructureSection load='5aek' size='340' side='right'caption='[[5aek]], [[Resolution|resolution]] 3.00Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>[[5aek]] is a 24 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[5aek]] is a 24 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=5AEK OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5AEK FirstGlance]. <br> |
- | </td></tr> | + | </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=5aek FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5aek OCA], [https://pdbe.org/5aek PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5aek RCSB], [https://www.ebi.ac.uk/pdbsum/5aek PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5aek ProSAT]</span></td></tr> |
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- | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | |
</table> | </table> | ||
- | == Disease == | ||
- | [[http://www.uniprot.org/uniprot/SUMO1_HUMAN SUMO1_HUMAN]] Defects in SUMO1 are the cause of non-syndromic orofacial cleft type 10 (OFC10) [MIM:[http://omim.org/entry/613705 613705]]; also called non-syndromic cleft lip with or without cleft palate 10. OFC10 is a birth defect consisting of cleft lips with or without cleft palate. Cleft lips are associated with cleft palate in two-third of cases. A cleft lip can occur on one or both sides and range in severity from a simple notch in the upper lip to a complete opening in the lip extending into the floor of the nostril and involving the upper gum. Note=A chromosomal aberation involving SUMO1 is the cause of OFC10. Translocation t(2;8)(q33.1;q24.3). The breakpoint occurred in the SUMO1 gene and resulted in haploinsufficiency confirmed by protein assays.<ref>PMID:16990542</ref> | ||
== Function == | == Function == | ||
- | [ | + | [https://www.uniprot.org/uniprot/SENP2_HUMAN SENP2_HUMAN] Protease that catalyzes two essential functions in the SUMO pathway: processing of full-length SUMO1, SUMO2 and SUMO3 to their mature forms and deconjugation of SUMO1, SUMO2 and SUMO3 from targeted proteins. May down-regulate CTNNB1 levels and thereby modulate the Wnt pathway (By similarity).<ref>PMID:12192048</ref> <ref>PMID:11896061</ref> |
==See Also== | ==See Also== | ||
- | *[[SUMO|SUMO]] | + | *[[SUMO 3D Structures|SUMO 3D Structures]] |
*[[Sentrin-specific protease|Sentrin-specific protease]] | *[[Sentrin-specific protease|Sentrin-specific protease]] | ||
== References == | == References == | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
- | [[Category: | + | [[Category: Homo sapiens]] |
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
- | + | [[Category: Castillo V]] | |
- | [[Category: Castillo | + | [[Category: Espargaro A]] |
- | [[Category: Espargaro | + | [[Category: Gallego P]] |
- | [[Category: Gallego | + | [[Category: Grana-Montes R]] |
- | [[Category: Grana-Montes | + | [[Category: Lange R]] |
- | [[Category: Lange | + | [[Category: Lindorff-Larsend K]] |
- | [[Category: Lindorff-Larsend | + | [[Category: Papaleo E]] |
- | [[Category: Papaleo | + | [[Category: Reverter D]] |
- | [[Category: Reverter | + | [[Category: Torrent J]] |
- | [[Category: Torrent | + | [[Category: Ventura S]] |
- | [[Category: Ventura | + | |
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Revision as of 04:53, 25 May 2023
Crystal structure of the human SENP2 C548S in complex with the human SUMO1 K48M F66W
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