Name
Multivesicular Bodies
Namespace Keyword
CellStructure
Namespace
MeSH
Namespace Version
20170511
Namespace URL
https://arty.scai.fraunhofer.de/artifactory/bel/annotation/cell-structure/cell-structure-20170511.belanno

Sample Annotated Edges 5

p(MGI:Mapt, var("p.Pro301Leu")) increases bp(GO:macroautophagy) View Subject | View Object

We found that abundance of autophagic vacuoles (autophagosomes + autolysosomes) significantly increased in cells expressing either of the two tau mutants (Fig. 4d,e). This increase was mainly due to higher content of autolysosomes (red puncta) (Fig. 4d,e), in support of increased macroautophagic flux PubMed:29024336

p(HBP:HBP00053, pmod(Ph, Ser, 214), pmod(Ph, Thr, 212)) decreases deg(p(HBP:HBP00053, pmod(Ph, Ser, 214), pmod(Ph, Thr, 212))) View Subject | View Object

Analysis of e-MI of the pseudophosphorylated forms of tau using LE showed reduced uptake/degradation of hTau40 AT8/AT100/PHF-1 when compared to WT tau (Fig. 7d,e) PubMed:29024336

p(HBP:HBP00053, pmod(Ph, Ser, 202), pmod(Ph, Thr, 205)) decreases deg(p(HBP:HBP00053, pmod(Ph, Ser, 202), pmod(Ph, Thr, 205))) View Subject | View Object

Analysis of e-MI of the pseudophosphorylated forms of tau using LE showed reduced uptake/degradation of hTau40 AT8/AT100/PHF-1 when compared to WT tau (Fig. 7d,e) PubMed:29024336

a(HBP:HBP00055) decreases deg(p(MGI:Mapt)) View Subject | View Object

Absence of the second N-terminal insert also significantly reduced e-MI of tau (Fig. 5e,f) PubMed:29024336

p(MGI:Mapt, var("p.Pro301Leu")) increases a(GO:autolysosome) View Subject | View Object

We found that abundance of autophagic vacuoles (autophagosomes + autolysosomes) significantly increased in cells expressing either of the two tau mutants (Fig. 4d,e). This increase was mainly due to higher content of autolysosomes (red puncta) (Fig. 4d,e), in support of increased macroautophagic flux PubMed:29024336

About

BEL Commons is developed and maintained in an academic capacity by Charles Tapley Hoyt and Daniel Domingo-Fernández at the Fraunhofer SCAI Department of Bioinformatics with support from the IMI project, AETIONOMY. It is built on top of PyBEL, an open source project. Please feel free to contact us here to give us feedback or report any issues. Also, see our Publishing Notes and Data Protection information.

If you find BEL Commons useful in your work, please consider citing: Hoyt, C. T., Domingo-Fernández, D., & Hofmann-Apitius, M. (2018). BEL Commons: an environment for exploration and analysis of networks encoded in Biological Expression Language. Database, 2018(3), 1–11.