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In this study, we characterised the interactomes of PAXX and its paralogs, XLF and XRCC4, to show that these factors share the ability to interact with DNA polymerase lambda (Poll), stimulate its activityand are required for the recruitment of Poll to laser-induced DNA damage sites.
ORGANISM(S): Homo sapiens (Human) 
2018-09-24 | PXD010891 | Pride
To investigate the RNA binding proteins that change following mTOR inhibition, HeLa cells were treated with and without 200nM Torin1 for an hour. Cells were the UV254 cross-linked, lysed and large scale whole cell oligo(dT) based pulldowns were performed with identification and quantification of pu...
ORGANISM(S): Homo sapiens (Human) 
2020-11-24 | PXD016705 | Pride
Heme-affinity pull-down assays and proteomics of lysates from primary cortical neurons identified and EAG channel, hERG3 (Kv11.3) binds to heme.
ORGANISM(S): Mus musculus (Mouse) 
2020-09-17 | PXD019887 | Pride
Uncovering the molecular architecture of the core FADD:Caspase-8 complex and how this is altered by regulatory partners, such as the cell death inhibitor c-FLIP, is essential to understand co-ordination of cell fate. Here, using electron microscopy, we visualize for the first time fulllength proca...
ORGANISM(S): Homo sapiens (Human) 
2021-02-08 | PXD022408 | Pride
Analysis of the phosphorylation state of a mis-sense variant in MIDEAS (Tyr654Ser). The substitution from YTP to STP generates a CDK kinase site that is phosphorylated in a human cell line.
ORGANISM(S): Homo sapiens (Human) 
2026-08-18 | PXD064578 | Pride
Here we show eIF4A2 is a major effector of the represive miRNA pathway functioning via the Ccr4_Not complex; through its interaction with the Ccr4-Not complex eIF4A2 represses mRNAs at translation initiation. We show evidence that native eIF4A2 has similar properties to chemically inhibited eIF4A1...
ORGANISM(S): Homo sapiens (Human) 
2019-10-10 | PXD015772 | Pride
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