DDBDRAFT_0167145 antikoerper, DDBDRAFT_0185177 antikoerper, DDB_0167145 antikoerper, DDB_0185177 antikoerper, AIP1 antikoerper, ALIX antikoerper, DRIP4 antikoerper, HP95 antikoerper, AI480591 antikoerper, AW544830 antikoerper, Aip1 antikoerper, Alix antikoerper, C76364 antikoerper, Eig2 antikoerper, mKIAA1375 antikoerper, CG12876 antikoerper, DAIP1 antikoerper, Dmel\\CG12876 antikoerper, GB11744 antikoerper, RGD1561176 antikoerper, zgc:63638 antikoerper, wu:fb70d03 antikoerper, wu:fy65h02 antikoerper, PDCD6IP antikoerper, aip1 antikoerper, alix antikoerper, hp95 antikoerper, drip4 antikoerper, ALG-2 interacting protein X antikoerper, programmed cell death 6 interacting protein antikoerper, programmed cell death 6-interacting protein antikoerper, Programmed cell death 6 interacting protein antikoerper, programmed cell death 6 interacting protein L homeolog antikoerper, alxA antikoerper, PDCD6IP antikoerper, Pdcd6ip antikoerper, ALiX antikoerper, LOC412662 antikoerper, pdcd6ip antikoerper, Bm1_48390 antikoerper, pdcd6ip.L antikoerper
Hintergrund
Alix (ALG-2-interacting protein X) is an adaptor protein that was first described for its capacity to bind to the calcium-binding protein ALG-2, the expression of which seemed necessary for cell death. Predicted molecular weight approximately 96 kD. Alix contains an N-terminal Bro1 domain and a C-terminal proline-rich domain (PRD). The PRD contains multiple polyproline motifs, which are potential docking sites for proteins containing SH3 domains, interactwith multiple cellular Alix-binding partners that are involvedin apoptotic induction, endosomal sorting,and endocytosis. Bro1 domain interacts with CHMP4b which is also involved in endosomal sorting.