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Appears in Networks 1

In-Edges 8

Out-Edges 6

p(HGNC:PSMD2) directlyIncreases complex(p(HGNC:BAG1), p(HGNC:PSMD2)) View Subject | View Object

RPN1 interacted strongly with four BAG proteins and with the ubiquitin ligase CHIP. This was in contrast to the three other subunits (RPN10, RPN13, and RPT2) that primarily interacted with other proteasome subunits (Figures 5I, 5J, and S4E) PubMed:25036637

p(HGNC:PSMD2) directlyIncreases complex(p(HGNC:BAG2), p(HGNC:PSMD2)) View Subject | View Object

RPN1 interacted strongly with four BAG proteins and with the ubiquitin ligase CHIP. This was in contrast to the three other subunits (RPN10, RPN13, and RPT2) that primarily interacted with other proteasome subunits (Figures 5I, 5J, and S4E) PubMed:25036637

p(HGNC:PSMD2) directlyIncreases complex(p(HGNC:BAG3), p(HGNC:PSMD2)) View Subject | View Object

RPN1 interacted strongly with four BAG proteins and with the ubiquitin ligase CHIP. This was in contrast to the three other subunits (RPN10, RPN13, and RPT2) that primarily interacted with other proteasome subunits (Figures 5I, 5J, and S4E) PubMed:25036637

p(HGNC:PSMD2) directlyIncreases complex(p(HGNC:BAG5), p(HGNC:PSMD2)) View Subject | View Object

RPN1 interacted strongly with four BAG proteins and with the ubiquitin ligase CHIP. This was in contrast to the three other subunits (RPN10, RPN13, and RPT2) that primarily interacted with other proteasome subunits (Figures 5I, 5J, and S4E) PubMed:25036637

p(HGNC:PSMD2) directlyIncreases complex(p(HGNC:PSMD2), p(HGNC:STUB1)) View Subject | View Object

RPN1 interacted strongly with four BAG proteins and with the ubiquitin ligase CHIP. This was in contrast to the three other subunits (RPN10, RPN13, and RPT2) that primarily interacted with other proteasome subunits (Figures 5I, 5J, and S4E) PubMed:25036637

p(HGNC:PSMD2) directlyIncreases complex(p(HGNC:PSMD2), p(INTERPRO:"Heat shock protein 70 family")) View Subject | View Object

Although all four subunits are part of the base of the proteasome regulatory particle (Lander et al., 2012), RPN1 clustered together with Hsp70 rather than with the other proteasome subunits (Figure 5A) PubMed:25036637

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.