Graphics credits: COMPARTMENTS | More Info
Parameter | Value |
---|---|
Gene | MEF2C |
Protein Name | MEF2C_HUMAN |
Organism | Homo sapiens (Human) |
Alternative name(s) | Myocyte-specific enhancer factor 2C (Myocyte enhancer factor 2C) |
Protein Family | MEF2 family |
NCBI Gene ID | 4208 |
UniProt ID | Q06413 |
Enzyme Class | - |
Molecular Weight | 51221 |
Protein Length | 473 |
Protein Domain | InterPro | Pfam |
3D Structure |
PDBe |
PDBj |
RCSB PDB |
DrugPort
ModBase | SwissModel |
Gene Expression | Gene Expression Atlas |
Function and Disease | OMIM |
Protein-protein Interaction Database | STRING | IntAct | MINT |
Kinase Database | Phospho.ELM | PhosphoSite | NetworKIN |
Catalytic Activity (UniProt annotation) | - |
Localization | Nucleus |
Function (UniProt annotation) | Transcription activator which binds specifically to the MEF2 element present in the regulatory regions of many muscle-specific genes. Controls cardiac morphogenesis and myogenesis, and is also involved in vascular development. Plays an essential role in hippocampal-dependent learning and memory by suppressing the number of excitatory synapses and thus regulating basal and evoked synaptic transmission. Crucial for normal neuronal development, distribution, and electrical activity in the neocortex. Necessary for proper development of megakaryocytes and platelets and for bone marrow B-lymphopoiesis. Required for B-cell survival and proliferation in response to BCR stimulation, efficient IgG1 antibody responses to T-cell-dependent antigens and for normal induction of germinal center B-cells. May also be involved in neurogenesis and in the development of cortical architecture (By similarity). Isoform 3 and isoform 4, which lack the repressor domain, are more active than isoform 1 and isoform 2. |
Gene Ontology | GO:0000122; GO:0000165; GO:0000790; GO:0000977; GO:0000978; GO:0000980; GO:0000981; GO:0000983; GO:0001077; GO:0001205; GO:0001568; GO:0001649; GO:0001764; GO:0001782; GO:0001947; GO:0001958; GO:0001974; GO:0002062; GO:0002467; GO:0002634; GO:0002931; GO:0003138; GO:0003139; GO:0003151; GO:0003185; GO:0003211; GO:0003677; GO:0003680; GO:0003682; GO:0003700; GO:0005634; GO:0005654; GO:0005737; GO:0005829; GO:0006355; GO:0006915; GO:0006959; GO:0007399; GO:0007507; GO:0007517; GO:0007519; GO:0007521; GO:0007611; GO:0010628; GO:0010629; GO:0010694; GO:0014033; GO:0014898; GO:0014902; GO:0016528; GO:0016607; GO:0030182; GO:0030220; GO:0030224; GO:0030279; GO:0030318; GO:0030501; GO:0030890; GO:0032991; GO:0033613; GO:0035690; GO:0035914; GO:0035984; GO:0042100; GO:0042826; GO:0043231; GO:0043406; GO:0043523; GO:0043524; GO:0043537; GO:0044212; GO:0045652; GO:0045663; GO:0045666; GO:0045669; GO:0045893; GO:0045944; GO:0046928; GO:0046982; GO:0048167; GO:0048643; GO:0048666; GO:0048667; GO:0048703; GO:0050853; GO:0051145; GO:0051149; GO:0051963; GO:0051966; GO:0055012; GO:0060021; GO:0060025; GO:0060045; GO:0060079; GO:0060297; GO:0060536; GO:0060998; GO:0061333; GO:0071222; GO:0071277; GO:0071374; GO:0071498; GO:0071560; GO:0071837; GO:0071864; GO:0072102; GO:0072160; GO:0090073; GO:0098794; GO:1904706; GO:1904753; GO:1905563; GO:2000111; GO:2000310; GO:2000311; GO:2000727; GO:2000987; GO:2001013; GO:2001016 |
Gene Name | Organism | P-Site | Sequence(+/-7) | Conservation | Disorder | Curator Assessment | Reliability | Evidence Class | Evidence Logic | PubMed | Phospho-ELM | PhosphoSite-Plus |
---|---|---|---|---|---|---|---|---|---|---|---|---|
RPS6KA2 (Q15349) | Homo sapiens | S192 | GVTHRPPSAGNTGGL | 0.696 | 0.8623 | - | - | - | - | 17630987 | Non high throughput (17630987) |
|
MYLK2 (Q9H1R3) | Homo sapiens | T80 | NEPHESRTNSDIVET | 0.797 | 0.6661 | - | - | - | - | - | - |
|
Reactome Pathways
KEGG Pathways
Pathway ID | Pathway Name |
---|---|
hsa04010 | MAPK signaling pathway |
NCI Nature PID Pathways