Enables MAP kinase kinase kinase activity; mitogen-activated protein kinase kinase binding activity; and small GTPase binding activity. Involved in several processes, including cellular response to nerve growth factor stimulus; positive regulation of ERK1 and ERK2 cascade; and response to cAMP. Predicted to be located in several cellular components, including cell body; intracellular membrane-bounded organelle; and neuron projection. Predicted to be active in cytosol; mitochondrion; and plasma membrane. Used to study bile duct adenoma; cholangiocarcinoma; intrahepatic cholangiocarcinoma; and thyroid gland papillary carcinoma. Human ortholog(s) of this gene implicated in several diseases, including Noonan syndrome 7; carcinoma (multiple); cardiofaciocutaneous syndrome (multiple); central nervous system benign neoplasm (multiple); and melanoma (multiple). Orthologous to human BRAF (B-Raf proto-oncogene, serine/threonine kinase); PARTICIPATES IN the extracellular signal-regulated Raf/Mek/Erk signaling pathway; adenosine signaling pathway; altered extracellular signal-regulated Raf/Mek/Erk signaling pathway; INTERACTS WITH 17alpha-ethynylestradiol; 2,3,7,8-tetrachlorodibenzodioxine; 2,3,7,8-Tetrachlorodibenzofuran.
[Pentoxifylline results in increased abundance of Cyclic AMP] which results in increased activity of BRAF protein and [Theophylline results in increased abundance of Cyclic AMP] which results in increased activity of BRAF protein
ABT-737 inhibits the reaction [[MET protein affects the susceptibility to HGF protein] affects the reaction [BRAF protein mutant form results in increased susceptibility to Vemurafenib]]
[Cannabidiol co-treated with moringin] results in decreased expression of BRAF mRNA and [Oxygen co-treated with Ozone co-treated with Cannabidiol] results in decreased expression of BRAF mRNA
[Cisplatin co-treated with jinfukang] results in decreased expression of BRAF mRNA and [Cisplatin co-treated with Quercetin] results in increased expression of BRAF mRNA
2-(1H-indazol-4-yl)-6-(4-methanesulfonylpiperazin-1-ylmethyl)-4-morpholin-4-ylthieno(3 and 2-d)pyrimidine promotes the reaction [BRAF protein mutant form results in increased susceptibility to cobimetinib]
MIR22 mRNA inhibits the reaction [pirarubicin results in increased phosphorylation of BRAF protein] and Rutin inhibits the reaction [pirarubicin results in increased phosphorylation of BRAF protein]
Sorafenib inhibits the reaction [BRAF protein mutant form results in increased phosphorylation of MAPK1 protein] and Sorafenib inhibits the reaction [BRAF protein mutant form results in increased phosphorylation of MAPK3 protein]
BRAF gene mutant form results in increased susceptibility to vemurafenib and BRAF protein mutant form results in increased susceptibility to vemurafenib
BRAF protein mutant form affects the reaction [vorinostat affects the reaction [[TSHB protein co-treated with vemurafenib] affects the expression of SLC5A5 mRNA]] more ...
Hepatic epidermal growth factor-regulated mitogen-activated protein kinase kinase kinase activity in the rat: lack of identity with known forms of raf and MEKK.
In papillary thyroid carcinoma BRAFV600E is associated with increased expression of the urokinase plasminogen activator and its cognate receptor, but not with disease-free interval.