Amyloid beta A4 precursor protein-binding family B member 2 is a
protein that in humans is encoded by the APBB2gene.[5][6][7]
The protein encoded by this gene interacts with the
cytoplasmic domains of
amyloid beta (A4) precursor protein and amyloid beta (A4) precursor-like protein 2. This protein contains two
phosphotyrosine binding (PTB) domains, which are thought to function in
signal transduction.[7]
^Blanco G, Irving NG, Brown SD, Miller CC, McLoughlin DM (Jun 1998). "Mapping of the human and murine X11-like genes (APBA2 and apba2), the murine Fe65 gene (Apbb1), and the human Fe65-like gene (APBB2): genes encoding phosphotyrosine-binding domain proteins that interact with the Alzheimer's disease amyloid precursor protein". Mamm Genome. 9 (6): 473–5.
doi:
10.1007/s003359900800.
PMID9585438.
S2CID31066473.
Lange A, Thon L, Mathieu S, Adam D (2005). "The apoptosis inhibitory domain of FE65-like protein 1 regulates both apoptotic and caspase-independent programmed cell death mediated by tumor necrosis factor". Biochem. Biophys. Res. Commun. 335 (2): 575–83.
doi:
10.1016/j.bbrc.2005.07.125.
PMID16083851.
Amyloid beta A4 precursor protein-binding family B member 2 is a
protein that in humans is encoded by the APBB2gene.[5][6][7]
The protein encoded by this gene interacts with the
cytoplasmic domains of
amyloid beta (A4) precursor protein and amyloid beta (A4) precursor-like protein 2. This protein contains two
phosphotyrosine binding (PTB) domains, which are thought to function in
signal transduction.[7]
^Blanco G, Irving NG, Brown SD, Miller CC, McLoughlin DM (Jun 1998). "Mapping of the human and murine X11-like genes (APBA2 and apba2), the murine Fe65 gene (Apbb1), and the human Fe65-like gene (APBB2): genes encoding phosphotyrosine-binding domain proteins that interact with the Alzheimer's disease amyloid precursor protein". Mamm Genome. 9 (6): 473–5.
doi:
10.1007/s003359900800.
PMID9585438.
S2CID31066473.
Lange A, Thon L, Mathieu S, Adam D (2005). "The apoptosis inhibitory domain of FE65-like protein 1 regulates both apoptotic and caspase-independent programmed cell death mediated by tumor necrosis factor". Biochem. Biophys. Res. Commun. 335 (2): 575–83.
doi:
10.1016/j.bbrc.2005.07.125.
PMID16083851.