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The orientation of the mitotic spindle (MS) is tightly regulated, but the molecular mechanisms are incompletely understood. Here we report a novel role for the multifunctional adaptor protein ALG-2-interacting protein X (ALIX) in regulating MS orientation in addition to its well-established role in ...
ORGANISM(S): Homo sapiens (Human) 
2018-06-04 | PXD009747 | Pride
CARM1 is an arginine methyltransferase with a well-established role in regulating gene expression, but its cytoplasmic functions remain largely uncharacterized. We identified ALIX, a protein acting with the ESCRT-III machinery in numerous membrane remodeling events, as a main cytoplasmic partner and...
ORGANISM(S): Homo sapiens (Human) 
2026-09-24 | PXD064697 | Pride
Hela Cells were treated with a CARM1 inhibitor or with DMSO for 48h. Endogenous ALIX was then immunoprecipitated and sujected to lysarginase digestion. The level of arginine methylation of Arg745 and Arg 757 of ALIX were then analyzed, and compared between the two conditions (CARM1 inhibition versus...
ORGANISM(S): Homo sapiens (Human) 
2026-09-24 | PXD064974 | Pride
Alix is a ubiquitously expressed scaffold protein that participates in numerous cellular processes, relating to the remodeling/repair of membranes and the actin cytoskeleton. Alix exists in monomeric and dimeric/multimeric configurations, but how dimer formation occurs and what role the dimer has ...
ORGANISM(S): Mus musculus (Mouse) 
2022-10-14 | PXD031450 | Pride
To characterize ALIX interactome in BT549 cells and in HeLa cells, endogenous ALIX was immunoprecipitated followed by mass spectrometry based analysis
ORGANISM(S): Homo sapiens (Human) 
2026-09-24 | PXD064975 | Pride
Human ALIX (Uniprot accession no. Q8WUM4) Bro1 and proline-rich domains were recombinantly expressed, purified, and phosphorylated in vitro by tyrosine kinase Src. Phosphorylation products were analyzed by mass spectrometry.
ORGANISM(S): Homo Sapiens (ncbitaxon:9606) 
Background: Huntington’s disease (HD) is an inherited autosomal dominant disorder characterized by progressive degeneration of the striatum and cerebral cortex, caused by a mutation in the huntingtin gene, which includes an aberrant expansion of a CAG repeat. The mutant huntingtin protein accumulate...
ORGANISM(S): Homo sapiens (Human) 
2025-12-10 | PXD060574 | Pride
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