MAPK8
Gene Ontology Biological Process
- JNK cascade [IDA, ISO]
- JUN phosphorylation [IDA, IMP, ISO]
- cellular response to hydrogen peroxide [IDA]
- cellular response to lipopolysaccharide [ISO]
- cellular response to nitric oxide [IMP]
- determination of dorsal identity [ISO]
- inflammatory response [ISO]
- negative regulation of apoptotic process [ISO]
- negative regulation of protein binding [ISO]
- neuron projection development [ISO]
- ossification [IMP]
- peptidyl-serine phosphorylation [ISO]
- peptidyl-threonine phosphorylation [IMP, ISO]
- positive regulation of DNA replication [ISO]
- positive regulation of apoptotic signaling pathway [IGI]
- positive regulation of cell migration [ISO]
- positive regulation of deacetylase activity [ISO]
- positive regulation of determination of dorsal identity [IDA]
- positive regulation of gene expression [ISO]
- positive regulation of microtubule polymerization [ISO]
- programmed necrotic cell death [IMP]
- protein phosphorylation [IDA]
- regulation of gene expression [IMP]
- regulation of histone deacetylation [ISO]
- regulation of protein localization [ISO]
- regulation of transcription, DNA-templated [ISO]
- response to UV [ISO]
- response to cadmium ion [IGI]
- response to heat [ISO]
- response to hydrogen peroxide [ISO]
- response to osmotic stress [ISO]
- signal transduction [ISO]
Gene Ontology Molecular Function
MAPK8IP3
Gene Ontology Biological Process
- JNK cascade [IDA]
- activation of JUN kinase activity [IDA]
- axon guidance [IMP]
- forebrain development [IMP]
- in utero embryonic development [IMP]
- lung alveolus development [IMP]
- lung morphogenesis [IMP]
- positive regulation of JUN kinase activity [IDA]
- positive regulation of neuron differentiation [ISO]
- positive regulation of signal transduction [IPI]
- post-embryonic development [IMP]
- protein localization [IMP]
- regulation of JNK cascade [IDA]
- regulation of gene expression [IDA]
- respiratory gaseous exchange [IMP]
- vesicle-mediated transport [IDA]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
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.
Publication
Role of the JIP4 scaffold protein in the regulation of mitogen-activated protein kinase signaling pathways.
The c-Jun NH2-terminal kinase (JNK)-interacting protein (JIP) group of scaffold proteins (JIP1, JIP2, and JIP3) can interact with components of the JNK signaling pathway and potently activate JNK. Here we describe the identification of a fourth member of the JIP family. The primary sequence of JIP4 is most closely related to that of JIP3. Like other members of the JIP ... [more]
Throughput
- Low Throughput
Related interactions
Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
---|---|---|---|---|---|---|
MAPK8IP3 MAPK8 | 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 | - | |
MAPK8IP3 MAPK8 | 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 | - | |
MAPK8 MAPK8IP3 | Biochemical Activity Biochemical Activity An interaction is inferred from the biochemical effect of one protein upon another, for example, GTP-GDP exchange activity or phosphorylation of a substrate by a kinase. The bait protein executes the activity on the substrate hit protein. A Modification value is recorded for interactions of this type with the possible values Phosphorylation, Ubiquitination, Sumoylation, Dephosphorylation, Methylation, Prenylation, Acetylation, Deubiquitination, Proteolytic Processing, Glucosylation, Nedd(Rub1)ylation, Deacetylation, No Modification, Demethylation. | Low | - | BioGRID | 838592 |
Curated By
- BioGRID