MLXIPL
Gene Ontology Biological Process
- anatomical structure morphogenesis [TAS]
- cellular response to carbohydrate stimulus [IBA]
- energy reserve metabolic process [TAS]
- fatty acid homeostasis [ISS]
- glucose homeostasis [ISS]
- glucose mediated signaling pathway [ISS]
- intracellular signal transduction [TAS]
- negative regulation of cell cycle arrest [IMP]
- negative regulation of oxidative phosphorylation [IMP]
- negative regulation of peptidyl-serine phosphorylation [IMP]
- negative regulation of transcription, DNA-templated [ISS]
- positive regulation of cell proliferation [IMP]
- positive regulation of cellular metabolic process [TAS]
- positive regulation of fatty acid biosynthetic process [ISS]
- positive regulation of glycolytic process [IMP]
- positive regulation of lipid biosynthetic process [IMP]
- positive regulation of transcription from RNA polymerase II promoter [ISS]
- positive regulation of transcription, DNA-templated [ISS]
- regulation of energy homeostasis [ISS]
- regulation of fatty acid biosynthetic process [TAS]
- regulation of transcription from RNA polymerase II promoter [IBA]
- regulation of transcription, DNA-templated [NAS]
- small molecule metabolic process [TAS]
- triglyceride homeostasis [NAS]
Gene Ontology Molecular Function
DDB1
Gene Ontology Biological Process
- DNA repair [TAS]
- UV-damage excision repair [IDA]
- histone H2A monoubiquitination [IDA]
- nucleotide-excision repair [TAS]
- nucleotide-excision repair, DNA damage removal [TAS]
- proteasome-mediated ubiquitin-dependent protein catabolic process [IMP]
- protein ubiquitination involved in ubiquitin-dependent protein catabolic process [IDA]
- regulation of mitotic cell cycle phase transition [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
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
DDB1 E3 ligase controls dietary fructose-induced ChREBP? stabilization and liver steatosis via CRY1.
Fructose over-consumption contributes to the development of liver steatosis in part by stimulating ChREBP?-driven de novo lipogenesis. However, the mechanisms by which fructose activates ChREBP pathway remain largely undefined. Here we performed affinity purification of ChREBP? followed by mass spectrometry and identified DDB1 as a novel interaction protein of ChREBP? in the presence of fructose. Depletion and overexpression of Ddb1 ... [more]
Throughput
- High Throughput
Additional Notes
- Source of ChREBP/MLXIPL not clear
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| MLXIPL DDB1 | Affinity Capture-Western Affinity Capture-Western 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 identified by Western blot with a specific polyclonal antibody or second epitope tag. This category is also used if an interacting protein is visualized directly by dye stain or radioactivity. Note that this differs from any co-purification experiment involving affinity capture in that the co-purification experiment involves at least one extra purification step to get rid of potential contaminating proteins. | Low | - | BioGRID | 2936972 | |
| DDB1 MLXIPL | Affinity Capture-Western Affinity Capture-Western 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 identified by Western blot with a specific polyclonal antibody or second epitope tag. This category is also used if an interacting protein is visualized directly by dye stain or radioactivity. Note that this differs from any co-purification experiment involving affinity capture in that the co-purification experiment involves at least one extra purification step to get rid of potential contaminating proteins. | Low | - | BioGRID | 2936973 |
Curated By
- BioGRID