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complex(a(MESH:"Protein Kinases"), p(HGNC:HSP90AB1))

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Components

Appears in Networks 1

A Quantitative Chaperone Interaction Network Reveals the Architecture of Cellular Protein Homeostasis Pathways v1.0.0

In-Edges 1

p(HGNC:HSP90AB1) directlyIncreases complex(a(MESH:"Protein Kinases"), p(HGNC:HSP90AB1)) View Subject | View Object

Hsp90beta interacted particularly strongly with kinases (Figure 5B, filled blue circles), whereas the transcription factors p53 and HSF1 were among the most Hsp70-biased interactors (Figure 5B,green circles) PubMed:25036637

Appears in Networks:

Out-Edges 2

complex(a(MESH:"Protein Kinases"), p(HGNC:HSP90AB1)) hasComponent a(MESH:"Protein Kinases") View Subject | View Object

Appears in Networks:

complex(a(MESH:"Protein Kinases"), p(HGNC:HSP90AB1)) hasComponent p(HGNC:HSP90AB1) View Subject | View Object

Appears in Networks:

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.