BAIT
NMRAL1
HSCARG, SDR48A1
NmrA-like family domain containing 1
GO Process (0)
GO Function (0)
GO Component (2)
Homo sapiens
PREY
ACOT8
HNAACTE, PTE-1, PTE-2, PTE1, PTE2, hACTE-III, hTE, RP3-337O18.2
acyl-CoA thioesterase 8
GO Process (10)
GO Function (5)
GO Component (1)
Gene Ontology Biological Process
- acyl-CoA metabolic process [IDA]
- alpha-linolenic acid metabolic process [TAS]
- bile acid biosynthetic process [TAS]
- bile acid metabolic process [TAS]
- cellular lipid metabolic process [TAS]
- dicarboxylic acid catabolic process [IDA]
- fatty acid beta-oxidation using acyl-CoA oxidase [TAS]
- peroxisome fission [IDA]
- small molecule metabolic process [TAS]
- unsaturated fatty acid metabolic process [TAS]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
- peroxisomal matrix [IDA, IMP, TAS]
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
Cellular redox sensor HSCARG negatively regulates the translesion synthesis pathway and exacerbates mammary tumorigenesis.
The translesion synthesis (TLS) pathway is a double-edged sword in terms of genome integrity. Deficiency in TLS leads to generation of DNA double strand break (DSB) during replication stress, while excessive activation of the TLS pathway increases the risk of point mutation. Here we demonstrate that HSCARG, a cellular redox sensor, directly interacts with the key protein PCNA in the ... [more]
Proc Natl Acad Sci U S A Dec. 17, 2018; 116(51);25624-25633 [Pubmed: 31796584]
Throughput
- High Throughput
Curated By
- BioGRID