Homo sapiens Protein: AKT3 | |||||||||||||||||||||||
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Summary | |||||||||||||||||||||||
InnateDB Protein | IDBP-107755.7 | ||||||||||||||||||||||
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 | ENSP00000355498 | ||||||||||||||||||||||
InnateDB Gene | IDBG-107751 (AKT3) | ||||||||||||||||||||||
Protein Structure |
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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.
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Gene Ontology | |||||||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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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 |
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PFAM |
PF00069
PF07714 PF00169 PF00433 |
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PRINTS |
PR00109
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PIRSF | |||||||||||||||||||||||
SMART |
SM00133
SM00233 SM00220 SM00219 |
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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_001193658 | ||||||||||||||||||||||
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 | ||||||||||||||||||||||