In the nucleus of the many sorts of traditional cells, the BRCA1 super molecule interacts with RAD51 throughout repair of deoxyribonucleic acid double-strand breaks. These breaks are often caused by natural radiation or different exposures, however conjointly occur once chromosomes exchange genetic material (homologous recombination, e.g., "crossing over" throughout meiosis). The BRCA2 super molecule that contains a performance just like that of BRCA1  conjointly interacts with the RAD51 super molecule. By influencing deoxyribonucleic acid injury repair, these 3 proteins play a task in maintaining the soundness of the human ordering.

BRCA1 is additionally concerned in another kind of deoxyribonucleic acid repair, termed miss-match repair. BRCA1 interacts with the deoxyribonucleic acid couple repair super molecule MSH2. MSH2, MSH6, PARP and a few different proteins concerns in single strand repair square measure reportable to be elevated in BRCA1-deficient duct gland tumors.

A super molecule known as violin-containing super molecule (VCP, conjointly called p97) plays a task to recruit BRCA1 to the broken deoxyribonucleic acid sites. Once radiation, VCP is recruited to deoxyribonucleic acid lesions and cooperates with the ubiquity legate RNF8 to orchestrate assembly of sign complexes for economical DSB repair.

 BRCA1 interacts with VCP. BRCA1 conjointly interacts with c-Myc, other proteins that square measure vital to take care of ordering stability.