BAIT
FAM46C
family with sequence similarity 46, member C
GO Process (0)
GO Function (0)
GO Component (0)
Homo sapiens
PREY
GSTO1
GSTO 1-1, GSTTLp28, HEL-S-21, P28, SPG-R, RP11-99N20.1
glutathione S-transferase omega 1
GO Process (11)
GO Function (4)
GO Component (3)
Gene Ontology Biological Process
- L-ascorbic acid metabolic process [IDA]
- cellular response to arsenic-containing substance [IDA]
- glutathione derivative biosynthetic process [TAS]
- negative regulation of ryanodine-sensitive calcium-release channel activity [IDA]
- positive regulation of ryanodine-sensitive calcium-release channel activity [IDA]
- positive regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion [IC]
- regulation of cardiac muscle contraction by regulation of the release of sequestered calcium ion [IC]
- regulation of release of sequestered calcium ion into cytosol by sarcoplasmic reticulum [IDA]
- small molecule metabolic process [TAS]
- xenobiotic catabolic process [IDA]
- xenobiotic metabolic process [TAS]
Gene Ontology Molecular Function
Homo sapiens
Affinity Capture-MS
An interaction is inferred when a bait protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and the associated interaction partner is identified by mass spectrometric methods.
Publication
FAM46C and FNDC3A Are Multiple Myeloma Tumor Suppressors That Act in Concert to Impair Clearing of Protein Aggregates and Autophagy.
Multiple myeloma is a plasma cell neoplasm characterized by the production of unfolded immunoglobulins, which cause endoplasmic reticulum (ER) stress and sensitivity to proteasome inhibition. The genomic landscape of multiple myeloma is characterized by the loss of several genes rarely mutated in other cancers that may underline specific weaknesses of multiple myeloma cells. One of these is FAM46C that is ... [more]
Cancer Res Nov. 01, 2020; 80(21);4693-4706 [Pubmed: 32963011]
Throughput
- High Throughput
Additional Notes
- False discovery rate (FDR) of all peptide identifications was set to a maximum of 1%.
- LP-1 multiple myeloma cell line
- Statistically significant enriched proteins were filtered using a threshold setting for differential analysis where S0=1 and FDR=0.05 comparing IP-FAM46C versus mock experiments.
Curated By
- BioGRID