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==Crystal structure of human WDR41== | ==Crystal structure of human WDR41== | ||
<StructureSection load='6whh' size='340' side='right'caption='[[6whh]]' scene=''> | <StructureSection load='6whh' size='340' side='right'caption='[[6whh]], [[Resolution|resolution]] 2.71Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6WHH OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=6WHH FirstGlance]. <br> | <table><tr><td colspan='2'>[[6whh]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6WHH OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=6WHH FirstGlance]. <br> | ||
</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://proteopedia.org/fgij/fg.htm?mol=6whh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6whh OCA], [http://pdbe.org/6whh PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6whh RCSB], [http://www.ebi.ac.uk/pdbsum/6whh PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6whh ProSAT]</span></td></tr> | </td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://proteopedia.org/fgij/fg.htm?mol=6whh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6whh OCA], [http://pdbe.org/6whh PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6whh RCSB], [http://www.ebi.ac.uk/pdbsum/6whh PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6whh ProSAT]</span></td></tr> | ||
</table> | </table> | ||
== Function == | |||
[[http://www.uniprot.org/uniprot/WDR41_HUMAN WDR41_HUMAN]] Non-catalytic component of the C9orf72-SMCR8 complex, a complex that has guanine nucleotide exchange factor (GEF) activity and regulates autophagy (PubMed:27193190, PubMed:27103069, PubMed:27617292, PubMed:28195531). The C9orf72-SMCR8 complex promotes the exchange of GDP to GTP, converting inactive GDP-bound RAB8A and RAB39B into their active GTP-bound form, thereby promoting autophagosome maturation (PubMed:27103069). The C9orf72-SMCR8 complex also acts as a negative regulator of autophagy initiation by interacting with the ATG1/ULK1 kinase complex and inhibiting its protein kinase activity (PubMed:27103069, PubMed:27617292).<ref>PMID:27103069</ref> <ref>PMID:27193190</ref> <ref>PMID:27617292</ref> <ref>PMID:28195531</ref> | |||
== References == | |||
<references/> | |||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Arrowsmith | [[Category: Arrowsmith, C H]] | ||
[[Category: Bountra C]] | [[Category: Bountra, C]] | ||
[[Category: Edwards | [[Category: Edwards, A M]] | ||
[[Category: Halabelian L]] | [[Category: Halabelian, L]] | ||
[[Category: Hutchinson A]] | [[Category: Hutchinson, A]] | ||
[[Category: Li Y]] | [[Category: Li, Y]] | ||
[[Category: Seitova A]] | [[Category: Structural genomic]] | ||
[[Category: Tempel W]] | [[Category: Seitova, A]] | ||
[[Category: Tempel, W]] | |||
[[Category: Protein binding]] | |||
[[Category: Sgc]] | |||
[[Category: Wd-repeat]] | |||
[[Category: Wdr41]] |
Revision as of 09:14, 20 May 2020
Crystal structure of human WDR41Crystal structure of human WDR41
Structural highlights
Function[WDR41_HUMAN] Non-catalytic component of the C9orf72-SMCR8 complex, a complex that has guanine nucleotide exchange factor (GEF) activity and regulates autophagy (PubMed:27193190, PubMed:27103069, PubMed:27617292, PubMed:28195531). The C9orf72-SMCR8 complex promotes the exchange of GDP to GTP, converting inactive GDP-bound RAB8A and RAB39B into their active GTP-bound form, thereby promoting autophagosome maturation (PubMed:27103069). The C9orf72-SMCR8 complex also acts as a negative regulator of autophagy initiation by interacting with the ATG1/ULK1 kinase complex and inhibiting its protein kinase activity (PubMed:27103069, PubMed:27617292).[1] [2] [3] [4] References
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