Gene Ontology annotation through association of InterPro records with GO terms
Annotation inferences using phylogenetic trees
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
Gene Ontology annotation based on curation of immunofluorescence data
Electronic Gene Ontology annotations created by ARBA machine learning models
Strong FANCA/FANCG but weak FANCA/FANCC interaction in the yeast 2-hybrid system.
Investigation of Fanconi anemia protein interactions by yeast two-hybrid analysis.
The Fanconi anemia protein FANCF forms a nuclear complex with FANCA, FANCC and FANCG.
Fanconi anemia protein complex: mapping protein interactions in the yeast 2- and 3-hybrid systems.
Fanconi anemia FANCG protein in mitigating radiation- and enzyme-induced DNA double-strand breaks by homologous recombination in vertebrate cells.
Towards a proteome-scale map of the human protein-protein interaction network.
Defective mitochondrial peroxiredoxin-3 results in sensitivity to oxidative stress in Fanconi anemia.
Identification of FAAP24, a Fanconi anemia core complex protein that interacts with FANCM.
FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway.
FANCG promotes formation of a newly identified protein complex containing BRCA2, FANCD2 and XRCC3.
The SH3 domain of alphaII spectrin is a target for the Fanconi anemia protein, FANCG.
The Fanconi anemia pathway promotes replication-dependent DNA interstrand cross-link repair.
A histone-fold complex and FANCM form a conserved DNA-remodeling complex to maintain genome stability.
Regulation of Rev1 by the Fanconi anemia core complex.
FAAP20: a novel ubiquitin-binding FA nuclear core-complex protein required for functional integrity of the FA-BRCA DNA repair pathway.
Host-pathogen interactome mapping for HTLV-1 and -2 retroviruses.
A ubiquitin-binding protein, FAAP20, links RNF8-mediated ubiquitination to the Fanconi anemia DNA repair network.
Architecture of the human interactome defines protein communities and disease networks.
Maximizing binary interactome mapping with a minimal number of assays.
A reference map of the human binary protein interactome.
Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
AI-guided pipeline for protein-protein interaction drug discovery identifies a SARS-CoV-2 inhibitor.
Multimodal cell maps as a foundation for structural and functional genomics.
The human XRCC9 gene corrects chromosomal instability and mutagen sensitivities in CHO UV40 cells.
The Fanconi anaemia group G gene FANCG is identical with XRCC9.
FA core complex assembles at DNA interstrand crosslinks (ICLs)
FANCD2:FANCI complex and UBE2T bind ICL-DNA associated with the FA core complex
Monoubiquitination of FANCD2:FANCI
DNA nucleases bind monoubiquitinated ID2 complex
DNA nucleases unhook the interstrand crosslink (ICL)
Translesion synthesis across unhooked ICL by POLN
FANCD2 deubiquitination by USP1:WDR48
The complex of ATR and ATRIP is recruited to ICL-DNA
ATR phosphorylates RPA2, FANCI, FANCD2 and FANCM at ICL-DNA
FA core complex:HSP70s binds PKR