Secondly, to our knowledge none of the present top interactions have previously been reported to interact in risk for MDD.
Since several binding partners have been reported to interact with the C-terminus of FLNa molecule, these mutations may perturb their interaction as well [1], [26].
Interestingly, many of them have been reported to interact with other viruses.
E3 SUMO-protein ligase PIAS has been reported to interact with and reduce the levels of claudin-2.
Several proteins related to the coagulation cascade, such as fibrinogen and fibrinogen degradation products, have been reported to interact with histones [31].
A murine monoclonal antibody, 14B7, has been reported to interact with domain 4 of PA (PAD4) and block its binding to CMG2.
Some foods have also been reported to interact with warfarin.
The LIM domains of several proteins have been reported to interact with F-actin.
Consistent with this hypothesis, A-type lamins have been reported to interact with actin [10].
VP24 has been reported to interact with VP28 and to be involved in virus infection [22].
Grp78 has previously been reported to interact with APP under pharmacologically induced ER stress conditions [9].
