BAIT
GBA
GBA1, GCB, GLUC
glucosidase, beta, acid
GO Process (12)
GO Function (3)
GO Component (3)
Gene Ontology Biological Process
- cellular response to tumor necrosis factor [IMP]
- ceramide biosynthetic process [IMP]
- glucosylceramide catabolic process [IMP]
- glycosphingolipid metabolic process [TAS]
- negative regulation of MAP kinase activity [IMP]
- negative regulation of inflammatory response [IC]
- negative regulation of interleukin-6 production [IDA]
- positive regulation of protein dephosphorylation [IMP]
- small molecule metabolic process [TAS]
- sphingolipid metabolic process [TAS]
- sphingosine biosynthetic process [IMP]
- termination of signal transduction [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Homo sapiens
PREY
EEA1
MST105, MSTP105, ZFYVE2
early endosome antigen 1
GO Process (4)
GO Function (6)
GO Component (6)
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
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
TRIP12 ubiquitination of glucocerebrosidase contributes to neurodegeneration in Parkinson's disease.
Impairment in glucocerebrosidase (GCase) is strongly associated with the development of Parkinson's disease (PD), yet the regulators responsible for its impairment remain elusive. In this paper, we identify the E3 ligase Thyroid Hormone Receptor Interacting Protein 12 (TRIP12) as a key regulator of GCase. TRIP12 interacts with and ubiquitinates GCase at lysine 293 to control its degradation via ubiquitin proteasomal ... [more]
Neuron Dec. 01, 2020; 109(23);3758-3774.e11 [Pubmed: 34644545]
Throughput
- Low Throughput
Curated By
- BioGRID