protein
| CARD11 |
|
death domain of MALT1 and the CARD of BCL10 also contribute to BCL10-MALT1 interactions |
|
IL2-independent STAT5B target gene |
|
interacting with CALM1 (CALM1 regulates T cell responses to antigens by binding to BCL10, thereby modulating its interaction with CARD11 and subsequent activation of NF-kappaB) |
|
interacting with CAMK2G (phosphorylates the CARD domain of BCL10, which regulates the interactions within the important CARD11, BCL10, MALT1 signalling complex) |
|
CARD11 serves as a scaffold for BCL10, MALT1 and other effector proteins and regulates various signaling pathways related to the immune response |
|
interaction mode between CARD11 CARD and BCL10 CARD based on a structure-based modeling study |
|
ATM-dependent phosphorylation of BCL10 promotes its interaction with and presentation of UBE2N to RNF8, and RNF8-mediated ubiquitination of BCL10 enhances binding of BCL10 and UBE2N to RNF168 |
|
novel function for CRADD in endothelial cells as an inducible suppressor of BCL10, a key mediator of responses to proinflammatory agonists |
|
AIP augments CARMA1-BCL10-MALT1 complex formation to facilitate NFKB1 signaling upon T cell activation |
|
CARD14 recruits BCL10 and MALT1 to form the CARD-BCL10-MALT1 complex, which modulates NFKB1 and MAPK signalling pathway |
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
tumoral
|  
| translocation
|  
|  
|
t (1;14)(p22;q32) as uncommon but recurrent events in MALT lymphoma | tumoral
|  
| deletion
|  
|  
|
involving 1, 10, 17 chromosome in Sezary syndrome and chromosome instability | tumoral
| fusion
|  
|  
|  
|
an IGH-BCL2-fusion with t(1;14)(p22;q32), in MALT lymphoma | |