Gene content    
AKT3 ( by HUGO)
V-Akt Murine Thymoma Viral Oncogene Homolog 3
Oncogene
V-Akt Murine Thymoma Viral Oncogene Homolog 3
PKBG
RAC-PK-gamma
STK-2
PKB Gamma
EC 2.7.11.1
MPPH
gamma
Protein Kinase B
PKB-GAMMA
PRKBG
RAC-gamma
RAC-Gamma Serine/Threonine Protein Kinase
RAC-Gamma Serine/Threonine-Protein Kinase
V-Akt Murine Thymoma Viral Oncogene Homolog 3 (Protein Kinase B
Gamma)
Protein Kinase Akt-3
Protein Kinase B Gamma
EC 2.7.11
NCBI: 1q44    Ensembl: 1q44
AKT3_HUMANSize: 479 amino acidsMass: 55775 Da

  • Subunit: Interacts (via PH domain) with TCL1A; this enhances AKT3 phosphorylation and activation. Interacts with TRAF6 Caution: In light of strong homologies in the primary amino acid sequence, the 3 AKT kinases were long surmised to play redundant and overlapping roles. More recent studies has brought into question the redundancy within AKT kinase isoforms and instead pointed to isoform specific functions in different cellular events and diseases. AKT1 is more specifically involved in cellular survival pathways, by inhibiting apoptotic processes; whereas AKT2 is more specific for the insulin receptor signaling pathway. Moreover, while AKT1 and AKT2 are often implicated in many aspects of cellular transformation, the 2 isoforms act in a complementary opposing manner. The role of AKT3 is less clear, though it appears to be predominantly expressed in brain 1 PDB 3D structure from [IMAGE] and Proteopedia [IMAGE] for AKT3: 2X18 (3D) [IMAGE]
  • 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 [IMAGE] Pathway & Disease-focused RT2 Profiler PCR Array
  • 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
                          
    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
  • Catalytic activity:
    ATP + a protein = ADP + a phosphoprotein
  • Similarity:
    Belongs to the protein kinase superfamily. AGC Ser/Thr protein kinase family. RAC subfamily
                          
    Contains 1 AGC-kinase C-terminal domain
                          
    Contains 1 PH domain
                          
    Contains 1 protein kinase domain [IMAGE]
  • Protein Domain/Family    
    Source ID Domain Name Type
    InterProIPR000719Prot_kinase_domProtein kinaseDomain
    IPR000961AGC-kinase_CProtein kinase, C-terminalDomain
    IPR001849Pleckstrin_homologyPleckstrin-likeDomain
    IPR002290Ser/Thr_dual-sp_kinase_domSerine/threonine protein kinaseDomain
    IPR008271Ser/Thr_kinase_ASSerine/threonine protein kinase, active siteActive Sites
    IPR011009Kinase-like_domProtein kinase-likeDomain
    IPR011993PH_like_domPleckstrin homology-typeDomain
    BlocksIPB000961Protein kinase C-terminal domainProtein kinase C-terminal domain
    IPB001849Pleckstrin-likePleckstrin-like

    Gene Ontology    
    Type Term Evidence Source Pub
    Biological Process mitochondrial genome maintenance IMP GOA 18524868
    signal transduction IMP GOA 18524868
    Molecular Function ATP binding IDA GOA 16540465
    protein binding IPI GOA 12176997
    protein kinase activity TAS GOA 10092583
    protein serine/threonine kinase activity IDA GOA 16540465

    Disorder & Mutation    
    Source Disease
    SWISS-PROTNote=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
    SWISS-PROTMegalencephaly-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. Note=The disease is caused by mutations affecting the gene represented in this entry

    AKT3 cross reference    
    PubMed OMIM Entrez Gene NCKU SNP Nucleotide UniProt Genome Data Viewer HomoloGene