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. 2021 Aug 5;7:203. doi: 10.1038/s41420-021-00594-x

Table 2.

Topology and function of ERdj proteins.

Topology Function
ERdj1 Integral membrane protein with a luminal J-domain and cytosolic C-terminus

Binding to the ribosome (60 S subunit) near the tunnel exit

In the absence of BiP: translational block

In the presence of BiP: translational release

ERdj2 Integral membrane protein with the luminal J-domain and a cytosolic C-domain

At the cytosolic site: association with the translocon proteins Sec61 α, β, γ, and Sec62

Transport of proteins across the ER membrane to control the protein load in the ER

ERdj3

Within the ER lumen:

Major pool: part of large protein complexes

Minor pool: as free protein pool

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Integral membrane protein: minor pool

In the absence of accessory proteins: head-on insertion (cytosolic orientation)

In the presence of accessory proteins: loop insertion (luminal orientation)

Interaction with the Sec61 translocon

Promoting protein degradation via ERAD

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Putative transcription factor in the nucleus

ERdj4

70–75% of the protein: soluble in the ER lumen

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25–30% of the protein: integral membrane protein facing the cytosol

Targeting of proteins to the ERAD pathway

Protein folding

Induction of apoptosis

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ERdj5 Luminal localization

Acceleration of the ERAD pathway

Protein folding

Apoptosis

ERdj6

Major pool: luminal localization

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Minor pool: integral membrane protein facing the cytosol

Protein maturation and post-ER transport of target proteins

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Inhibition of protein synthesis by

- Direct binding to the kinase domains of PKR, PERK, and GCN2 kinases

- Very efficient control of eIF2a phosphorylation

ERdj7 ER-localization