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complex(a(CHEBI:ATP), p(HGNC:HSPA1B))

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Components

Appears in Networks 1

Model systems of protein-misfolding diseases reveal chaperone modifiers of proteotoxicity v1.0.0

In-Edges 1

a(PUBCHEM:40009526) decreases complex(a(CHEBI:ATP), p(HGNC:HSPA1B)) View Subject | View Object

Compounds such as the allosteric inhibitor of ATP-binding for the inducible HSP70 isoform HSPA1A/HSPA1B, called HS-72, will likely lead to beneficial consequences (Howe et al., 2014). PubMed:27491084

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Out-Edges 2

complex(a(CHEBI:ATP), p(HGNC:HSPA1B)) hasComponent a(CHEBI:ATP) View Subject | View Object

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complex(a(CHEBI:ATP), p(HGNC:HSPA1B)) hasComponent p(HGNC:HSPA1B) View Subject | View Object

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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.