BAIT
FURIN
FUR, PACE, PCSK3, SPC1
furin (paired basic amino acid cleaving enzyme)
GO Process (29)
GO Function (7)
GO Component (10)
Gene Ontology Biological Process
- Notch signaling pathway [TAS]
- cell proliferation [IMP]
- cellular protein metabolic process [TAS]
- collagen catabolic process [TAS]
- extracellular matrix disassembly [TAS]
- extracellular matrix organization [TAS]
- negative regulation of endopeptidase activity [IDA]
- negative regulation of low-density lipoprotein particle receptor catabolic process [IDA]
- negative regulation of nerve growth factor production [IDA]
- negative regulation of transforming growth factor beta1 production [IMP]
- nerve growth factor processing [TAS]
- nerve growth factor production [IDA]
- neurotrophin TRK receptor signaling pathway [TAS]
- peptide biosynthetic process [IDA]
- peptide hormone processing [IDA]
- peptidyl-glutamic acid carboxylation [TAS]
- positive regulation of membrane protein ectodomain proteolysis [IC]
- post-translational protein modification [TAS]
- protein processing [IDA, IMP]
- proteolysis [TAS]
- regulation of endopeptidase activity [IDA]
- regulation of protein catabolic process [IMP]
- secretion by cell [IDA]
- signal peptide processing [IDA]
- transforming growth factor beta receptor signaling pathway [TAS]
- viral life cycle [IEP]
- viral process [TAS]
- viral protein processing [TAS]
- virion assembly [TAS]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Homo sapiens
PREY
HNRNPM
CEAR, HNRNPM4, HNRPM, HNRPM4, HTGR1, NAGR1, hnRNP M
heterogeneous nuclear ribonucleoprotein M
GO Process (4)
GO Function (4)
GO Component (9)
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Homo sapiens
Proximity Label-MS
An interaction is inferred when a bait-enzyme fusion protein selectively modifies a vicinal protein with a diffusible reactive product, followed by affinity capture of the modified protein and identification by mass spectrometric methods.
Publication
Histone Interaction Landscapes Visualized by Crosslinking Mass Spectrometry in Intact Cell Nuclei.
Cells organize their actions partly through tightly controlled protein-protein interactions-collectively termed the interactome. Here we use crosslinking mass spectrometry (XL-MS) to chart the protein-protein interactions in intact human nuclei. Overall, we identified ∼8,700 crosslinks, of which 2/3 represent links connecting distinct proteins. From these data, we gain insights on interactions involving histone proteins. We observed that core histones on the ... [more]
Mol. Cell Proteomics Dec. 01, 2017; 17(10);2018-2033 [Pubmed: 30021884]
Throughput
- High Throughput
Additional Notes
- interaction identified using XL-MS (cross-linking mass spectrometry): TX100-insoluble fractions from cells were treated with cross-linker and cross-linked proteins were identified by mass-spectrometry; interaction is undirectional; therefore bait and prey/hit have been assigned arbitrarily; interactions with FDRs (false discovery rates) of 1% or less were reported; this interaction was not detected in parallel experiments using unfractionated cells or TX100-soluble fractions
Curated By
- BioGRID