| + | 
              
              RNF128 | down-regulates quantity by destabilization   
              polyubiquitination
               | 
              CD83 | 
              
              0.352 | 
                    
						
							
								
									| Identifier | 
									Residue | 
									Sequence | 
									Organism | 
									Cell Line | 
								 
							
								
								
									| SIGNOR-271850 | 
									Lys177 | 
									SIFPDFSkAGMERAF | 
									Homo sapiens | 
									HEK-293 Cell | 
								
								 
									| pmid | 
									sentence | 
								 
								 
									| 19542455 | 
								
									In this study, we show that GRAIL can down-modulate the expression of CD83 (previously described as a cell surface marker for mature dendritic cells) on CD4 T cells. GRAIL-mediated down-modulation of CD83 is dependent on an intact GRAIL extracellular protease-associated domain and an enzymatically active cytosolic RING domain, and proceeds via the ubiquitin-dependent 26S proteosome pathway. Ubiquitin modification of lysine residues K168 and K183, but not K192, in the cytoplasmic domain of CD83 was shown to be necessary for GRAIL-mediated degradation of CD83. | 
								 
						 
                     | 
              
               
                    
						
							
								
									| Identifier | 
									Residue | 
									Sequence | 
									Organism | 
									Cell Line | 
								 
							
								
								
									| SIGNOR-271849 | 
									Lys192 | 
									LPVTSPNkHLGLVTP | 
									Homo sapiens | 
									HEK-293 Cell | 
								
								 
									| pmid | 
									sentence | 
								 
								 
									| 19542455 | 
								
									In this study, we show that GRAIL can down-modulate the expression of CD83 (previously described as a cell surface marker for mature dendritic cells) on CD4 T cells. GRAIL-mediated down-modulation of CD83 is dependent on an intact GRAIL extracellular protease-associated domain and an enzymatically active cytosolic RING domain, and proceeds via the ubiquitin-dependent 26S proteosome pathway. Ubiquitin modification of lysine residues K168 and K183, but not K192, in the cytoplasmic domain of CD83 was shown to be necessary for GRAIL-mediated degradation of CD83. | 
								 
						 
                     | 
              
               
			   
					| Publications: | 
					
				
					2 | 
					Organism: | 
							Homo Sapiens | 
				
              | + | 
              
              NfKb-p65/p50 | up-regulates quantity by expression   
              transcriptional regulation
               | 
              CD83 | 
              
              0.26 | 
                    
						
							
								
									| Identifier | 
									Residue | 
									Sequence | 
									Organism | 
									Cell Line | 
								 
							
								
								
									| SIGNOR-254781 | 
									 | 
									 | 
									Homo sapiens | 
									 | 
								
								 
									| pmid | 
									sentence | 
								 
								 
									| 19164127 | 
								
									 We found that upon TLR7 and TLR8 activation, JNK and NF-kappaB positively regulated the expression of CCR7, CD86, CD83, and CD40 and the production of IL-6 and IL-12p40.  | 
								 
						 
                     | 
              
               
			   
					| Publications: | 
					
				
					1 | 
					Organism: | 
							Homo Sapiens |