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BRCA1-associated protein (BRAP) is an E3 ubiquitin ligase with roles in the regulation of nuclear protein import and cell signaling.1 It is composed of a nucleotide-binding α/β plait, RING-finger, UBP-like zinc-finger (ZfUBP), and coiled-coil domain and localizes to the cytoplasm.1,2 BRAP binds to a variety of transcription factors and kinases in the cytosol to both inhibit nuclear translocation and impede signal propagation. SNPs in BRAP are associated with an increased risk of myocardial infarction and with a predisposition to alcohol use disorder.3,4 Cayman’s BRAP (human, recombinant) protein can be used for enzyme activity and Western blot (WB) applications and has a calculated molecular weight of 67.3 kDa.
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1. Central catalytic domain of BRAP (RNF52) recognizes the types of ubiquitin chains and utilizes oligo-
2. The BRCA-
3. SNPs in BRAP associated with risk of myocardial infarction in Asian populations. Nat. Genet. 41(3), 329-333 (2009).
4. Associations of BRAP polymorphisms with the risk of alcohol dependence and scores on the alcohol use disorders identification test. Neuropsychiatr. Dis. Treat. 15, 83-94 (2018).