BAIT
SHANK3
DEL22q13.3, PROSAP2, PSAP2, SCZD15, SPANK-2
SH3 and multiple ankyrin repeat domains 3
GO Process (27)
GO Function (8)
GO Component (5)
Gene Ontology Biological Process
- MAPK cascade [ISS]
- N-methyl-D-aspartate receptor clustering [ISS]
- adult behavior [IMP]
- alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate selective glutamate receptor clustering [ISS]
- brain morphogenesis [ISS]
- dendritic spine morphogenesis [ISS]
- guanylate kinase-associated protein clustering [ISS]
- learning [IMP, ISS]
- memory [ISS]
- negative regulation of actin filament bundle assembly [ISS]
- negative regulation of cell volume [ISS]
- positive regulation of alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate selective glutamate receptor activity [ISS]
- positive regulation of dendritic spine development [ISS]
- positive regulation of excitatory postsynaptic membrane potential [ISS]
- positive regulation of glutamate receptor signaling pathway [ISS]
- positive regulation of long-term neuronal synaptic plasticity [ISS]
- positive regulation of synapse structural plasticity [ISS]
- positive regulation of synaptic transmission, glutamatergic [ISS]
- postsynaptic density assembly [ISS]
- regulation of dendritic spine morphogenesis [ISS]
- regulation of long term synaptic depression [ISS]
- regulation of long-term synaptic potentiation [ISS]
- social behavior [IMP, ISS]
- striatal medium spiny neuron differentiation [ISS]
- synapse assembly [ISS]
- vocal learning [IMP]
- vocalization behavior [IMP, ISS]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Homo sapiens
PREY
CHCHD3
MINOS3, PPP1R22
coiled-coil-helix-coiled-coil-helix domain containing 3
GO Process (3)
GO Function (4)
GO Component (5)
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-soluble 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-insoluble fractions
Curated By
- BioGRID