An interaction is inferred between proteins in vitro. This can include proteins in recombinant form or proteins isolated directly from cells with recombinant or purified bait. For example, GST pull-down assays where a GST-tagged protein is first isolated and then used to fish interactors from cell lysates are considered reconstituted complexes (e.g. PUBMED: 14657240, Fig. 4A or PUBMED: 14761940, Fig. 5). This can also include gel-shifts, surface plasmon resonance, isothermal titration calorimetry (ITC) and bio-layer interferometry (BLI) experiments. The bait-hit directionality may not be clear for 2 interacting proteins. In these cases the directionality is up to the discretion of the curator.

Publication

Molecular Details Underlying Dynamic Structures and Regulation of the Human 26S Proteasome.

Wang X, Cimermancic P, Yu C, Schweitzer A, Chopra N, Engel JL, Greenberg C, Huszagh AS, Beck F, Sakata E, Yang Y, Novitsky EJ, Leitner A, Nanni P, Kahraman A, Guo X, Dixon JE, Rychnovsky SD, Aebersold R, Baumeister W, Sali A, Huang L

The 26S proteasome is the macromolecular machine responsible for ATP/ubiquitin dependent degradation. As aberration in proteasomal degradation has been implicated in many human diseases, structural analysis of the human 26S proteasome complex is essential to advance our understanding of its action and regulation mechanisms. In recent years, cross-linking mass spectrometry (XL-MS) has emerged as a powerful tool for elucidating structural ... [more]

Mol. Cell Proteomics Dec. 01, 2016; 16(5);840-854 [Pubmed: 28292943]

Throughput

High Throughput

Additional Notes

crosslinked peptides

Curated By

BioGRID

Interaction Summary

DNAJA1

Gene Ontology Biological Process

Gene Ontology Molecular Function

G-protein coupled receptor binding [IPI]Hsp70 protein binding [IDA]chaperone binding [IDA, IPI]low-density lipoprotein particle receptor binding [IDA]protein binding [IPI]ubiquitin protein ligase binding [IPI]unfolded protein binding [IBA]

Gene Ontology Cellular Component