Homo sapiens Protein: AKT3
Summary
InnateDB Protein IDBP-107753.7
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol AKT3
Protein Name v-akt murine thymoma viral oncogene homolog 3 (protein kinase B, gamma)
Synonyms MPPH; MPPH2; PKB-GAMMA; PKBG; PRKBG; RAC-gamma; RAC-PK-gamma; STK-2;
Species Homo sapiens
Ensembl Protein ENSP00000336943
InnateDB Gene IDBG-107751 (AKT3)
Protein Structure
UniProt Annotation
Function AKT3 is one of 3 closely related serine/threonine- protein kinases (AKT1, AKT2 and AKT3) called the AKT kinase, and which regulate many processes including metabolism, proliferation, cell survival, growth and angiogenesis. This is mediated through serine and/or threonine phosphorylation of a range of downstream substrates. Over 100 substrate candidates have been reported so far, but for most of them, no isoform specificity has been reported. AKT3 is the least studied AKT isoform. It plays an important role in brain development and is crucial for the viability of malignant glioma cells. AKT3 isoform may also be the key molecule in up-regulation and down-regulation of MMP13 via IL13. Required for the coordination of mitochondrial biogenesis with growth factor-induced increases in cellular energy demands. Down-regulation by RNA interference reduces the expression of the phosphorylated form of BAD, resulting in the induction of caspase- dependent apoptosis. {ECO:0000269PubMed:18524868, ECO:0000269PubMed:21191416}.
Subcellular Localization Nucleus {ECO:0000269PubMed:20018949}. Cytoplasm {ECO:0000269PubMed:20018949}. Membrane {ECO:0000269PubMed:20018949}; Peripheral membrane protein {ECO:0000269PubMed:20018949}. Note=Membrane-associated after cell stimulation leading to its translocation.
Disease Associations Note=AKT3 is a key modulator of several tumors like melanoma, glioma and ovarian cancer. Active AKT3 increases progressively during melanoma tumor progression with highest levels present in advanced-stage metastatic melanomas. Promotes melanoma tumorigenesis by decreasing apoptosis. Plays a key role in the genesis of ovarian cancers through modulation of G2/M phase transition. With AKT2, plays a pivotal role in the biology of glioblastoma.Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome (MPPH) [MIM:603387]: A syndrome characterized by megalencephaly, hydrocephalus, and polymicrogyria; polydactyly may also be seen. There is considerable phenotypic similarity between this disorder and the megalencephaly-capillary malformation syndrome. {ECO:0000269PubMed:22500628, ECO:0000269PubMed:22729223, ECO:0000269PubMed:22729224}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity In adult tissues, it is highly expressed in brain, lung and kidney, but weakly in heart, testis and liver. In fetal tissues, it is highly expressed in heart, liver and brain and not at all in kidney.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 24 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 24 [view]
Protein-Protein 24 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004672 protein kinase activity
GO:0004674 protein serine/threonine kinase activity
GO:0004713 protein tyrosine kinase activity
GO:0005515 protein binding
GO:0005524 ATP binding
GO:0016772 transferase activity, transferring phosphorus-containing groups
Biological Process
GO:0000002 mitochondrial genome maintenance
GO:0006468 protein phosphorylation
GO:0007165 signal transduction
Cellular Component
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005794 Golgi apparatus
GO:0005886 plasma membrane
Protein Structure and Domains
PDB ID
InterPro IPR000719 Protein kinase domain
IPR000961 AGC-kinase, C-terminal
IPR001245 Serine-threonine/tyrosine-protein kinase catalytic domain
IPR001849 Pleckstrin homology domain
IPR002290 Serine/threonine/dual specificity protein kinase, catalytic domain
IPR011009 Protein kinase-like domain
IPR017892 Protein kinase, C-terminal
IPR020635 Tyrosine-protein kinase, catalytic domain
PFAM PF00069
PF07714
PF00169
PF00433
PRINTS PR00109
PIRSF
SMART SM00133
SM00233
SM00220
SM00219
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9Y243
PhosphoSite PhosphoSite-Q9Y243
TrEMBL F8VS91
UniProt Splice Variant
Entrez Gene 10000
UniGene Hs.734019
RefSeq NP_859029
HUGO HGNC:393
OMIM 611223
CCDS CCDS31076
HPRD 06441
IMGT
EMBL AC096539 AF085234 AF124141 AF135794 AJ245709 AL117525 AL591721 AL592151 AL662889 AY005799 BC121154 CH471148
GenPept AAD24196 AAD29089 AAF91073 AAI21155 AAL40392 CAB53537 CAB55977 CAH71866 CAH71867 CAH72891 CAH72892 CAH73072 CAH73073 EAW77093 EAW77094