SMAD4 | Mothers against decapentaplegic homolog 4
 
image/svg+xmlExtracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion None Substrate Localization legend

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Sequence Viewer
Gene
Synonyms
DPC4 MADH4
Protein Name
Mothers against decapentaplegic homolog 4
UniProt ID
Q13485 [go to UniProt ] [go to PDBe-KB ]
Ensembl Gene ID
NCBI Gene ID
Molecular Weight
60439
Protein Length
552
Protein Domain
3D Structure
(PDB ID : 1dd1)
Target by Small Molecules
Protein-protein Interaction Database
Gene Expression
Drugs and Diseases
Enzyme Class
-
Catalytic Site
Catalytic Activity
-
Localization
Cytoplasm,Nucleus;
Function
In muscle physiology, plays a central role in the balance between atrophy and hypertrophy. When recruited by MSTN, promotes atrophy response via phosphorylated SMAD2/4. MSTN decrease causes SMAD4 release and subsequent recruitment by the BMP pathway to promote hypertrophy via phosphorylated SMAD1/5/8. Acts synergistically with SMAD1 and YY1 in bone morphogenetic protein (BMP)-mediated cardiac-specific gene expression. Binds to SMAD binding elements (SBEs) (5'-GTCT/AGAC-3') within BMP response element (BMPRE) of cardiac activating regions (By similarity). Common SMAD (co-SMAD) is the coactivator and mediator of signal transduction by TGF-beta (transforming growth factor). Component of the heterotrimeric SMAD2/SMAD3-SMAD4 complex that forms in the nucleus and is required for the TGF-mediated signaling (PubMed:25514493). Promotes binding of the SMAD2/SMAD4/FAST-1 complex to DNA and provides an activation function required for SMAD1 or SMAD2 to stimulate transcription. Component of the multimeric SMAD3/SMAD4/JUN/FOS complex which forms at the AP1 promoter site; required for synergistic transcriptional activity in response to TGF-beta. May act as a tumor suppressor. Positively regulates PDPK1 kinase activity by stimulating its dissociation from the 14-3-3 protein YWHAQ which acts as a negative regulator.
Gene Ontology
GO:0032444; GO:0005813; GO:0005737; GO:0005829; GO:0000790; GO:0005654; GO:0005634; GO:0071141; GO:0005667; GO:0003682; GO:0005518; GO:0001228; GO:0000981; GO:0070411; GO:0042802; GO:0046872; GO:0046982; GO:0042803; GO:0000987; GO:0070412; GO:0000978; GO:0001085; GO:0043199; GO:0003712; GO:0044212; GO:0030616; GO:0036302; GO:0003190; GO:0007411; GO:0030509; GO:0003360; GO:0001658; GO:0008283; GO:0006879; GO:0071773; GO:0048589; GO:0042733; GO:0060956; GO:0007492; GO:0042118; GO:0003198; GO:0061040; GO:0048859; GO:0001702; GO:0001701; GO:0070102; GO:0035556; GO:0003220; GO:0007498; GO:0072133; GO:0010614; GO:1905305; GO:0060548; GO:0030308; GO:0008285; GO:0070373; GO:0000122; GO:0045892; GO:0072134; GO:0014033; GO:0048663; GO:0003148; GO:0001541; GO:0030513; GO:0003251; GO:0010718; GO:0046881; GO:0051571; GO:2000617; GO:0033686; GO:0010862; GO:0060391; GO:0045944; GO:1901522; GO:0045893; GO:0030511; GO:0061614; GO:0016579; GO:0070207; GO:0051098; GO:0051797; GO:0017015; GO:0032909; GO:0001666; GO:0071559; GO:0048733; GO:0062009; GO:0072520; GO:0007338; GO:0007183; GO:0060395; GO:0035019; GO:0032525; GO:0007283; GO:0007179; GO:0060065; GO:0060412
 
Gene Ontology