Homo sapiens Protein: MAPK8IP1
Summary
InnateDB Protein IDBP-41202.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol MAPK8IP1
Protein Name mitogen-activated protein kinase 8 interacting protein 1
Synonyms IB1; JIP-1; JIP1; PRKM8IP;
Species Homo sapiens
Ensembl Protein ENSP00000241014
InnateDB Gene IDBG-41200 (MAPK8IP1)
Protein Structure
UniProt Annotation
Function The JNK-interacting protein (JIP) group of scaffold proteins selectively mediates JNK signaling by aggregating specific components of the MAPK cascade to form a functional JNK signaling module. Required for JNK activation in response to excitotoxic stress. Cytoplasmic MAPK8IP1 causes inhibition of JNK- regulated activity by retaining JNK in the cytoplasm and inhibiting JNK phosphorylation of c-Jun. May also participate in ApoER2-specific reelin signaling. Directly, or indirectly, regulates GLUT2 gene expression and beta-cell function. Appears to have a role in cell signaling in mature and developing nerve terminals. May function as a regulator of vesicle transport, through interactions with the JNK-signaling components and motor proteins (By similarity). Functions as an anti-apoptotic protein and whose level seems to influence the beta-cell death or survival response. {ECO:0000250}.
Subcellular Localization Cytoplasm {ECO:0000250}. Cytoplasm, perinuclear region {ECO:0000250}. Nucleus {ECO:0000250}. Endoplasmic reticulum membrane. Mitochondrion membrane. Note=Accumulates in cell surface projections. Under certain stress conditions, translocates to the perinuclear region of neurons. In insulin-secreting cells, detected in both the cytoplasm and nucleus (By similarity). {ECO:0000250}.
Disease Associations Diabetes mellitus, non-insulin-dependent (NIDDM) [MIM:125853]: A multifactorial disorder of glucose homeostasis caused by a lack of sensitivity to the body's own insulin. Affected individuals usually have an obese body habitus and manifestations of a metabolic syndrome characterized by diabetes, insulin resistance, hypertension and hypertriglyceridemia. The disease results in long-term complications that affect the eyes, kidneys, nerves, and blood vessels. {ECO:0000269PubMed:10700186}. Note=The disease may be caused by mutations affecting the gene represented in this entry.
Tissue Specificity Highly expressed in brain. Expressed in neurons, localizing to neurite tips in differentiating cells. Also expressed in the pancreas, testis and prostate. Low levels in heart, ovary and small intestine. Decreased levels in pancreatic beta cells sensitize cells to IL-1-beta-induced apoptosis.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 51 experimentally validated interaction(s) in this database.
They are also associated with 12 interaction(s) predicted by orthology.
Experimentally validated
Total 51 [view]
Protein-Protein 51 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 12 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004860 protein kinase inhibitor activity
GO:0005078 MAP-kinase scaffold activity
GO:0005515 protein binding
GO:0008432 JUN kinase binding
GO:0019894 kinesin binding
GO:0019901 protein kinase binding
GO:0031434 mitogen-activated protein kinase kinase binding
GO:0031435 mitogen-activated protein kinase kinase kinase binding
GO:0042802 identical protein binding
Biological Process
GO:0006355 regulation of transcription, DNA-templated
GO:0007165 signal transduction
GO:0007258 JUN phosphorylation
GO:0009967 positive regulation of signal transduction
GO:0016192 vesicle-mediated transport
GO:0043066 negative regulation of apoptotic process
GO:0043508 negative regulation of JUN kinase activity
GO:0046328 regulation of JNK cascade
GO:0046329 negative regulation of JNK cascade
GO:2001243 negative regulation of intrinsic apoptotic signaling pathway
Cellular Component
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005789 endoplasmic reticulum membrane
GO:0005829 cytosol
GO:0016020 membrane
GO:0030424 axon
GO:0030425 dendrite
GO:0031966 mitochondrial membrane
GO:0043005 neuron projection
GO:0044294 dendritic growth cone
GO:0044295 axonal growth cone
GO:0044297 cell body
GO:0044302 dentate gyrus mossy fiber
GO:0045202 synapse
GO:0048471 perinuclear region of cytoplasm
Protein Structure and Domains
PDB ID
InterPro IPR001452 SH3 domain
IPR006020 PTB/PI domain
PFAM PF00018
PF14604
PF00640
PF14719
PRINTS PR00452
PIRSF
SMART SM00326
SM00462
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9UQF2
PhosphoSite PhosphoSite-Q9UQF2
TrEMBL Q59EU1
UniProt Splice Variant
Entrez Gene 9479
UniGene Hs.234249
RefSeq NP_005447
HUGO HGNC:6882
OMIM 604641
CCDS CCDS7916
HPRD 05223
IMGT
EMBL AB209720 AF007134 AF074091 AK295942 CH471064
GenPept AAC19150 AAD20443 BAD92957 BAG58726 EAW68027 EAW68028