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
Isolation of a cDNA representing the Fanconi anemia complementation group E gene.
FANCE: the link between Fanconi anaemia complex assembly and activity.
Fanconi anemia protein complex: mapping protein interactions in the yeast 2- and 3-hybrid systems.
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.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Systematic discovery of mutation-directed neo-protein-protein interactions in cancer.
Chk1-mediated phosphorylation of FANCE is required for the Fanconi anemia/BRCA pathway.
The Fanconi anemia protein, FANCE, promotes the nuclear accumulation of FANCC.
FANCC, FANCE, and FANCD2 form a ternary complex essential to the integrity of the Fanconi anemia DNA damage response pathway.
The nuclear accumulation of the Fanconi anemia protein FANCE depends on FANCC.
The carboxyl terminus of FANCE recruits FANCD2 to the Fanconi Anemia (FA) E3 ligase complex to promote the FA DNA repair pathway.
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