IndraLab

Statements


2 | 1 6

sparser
"FAM188B binds to USP7 and destabilizes the USP7-p53 interaction, thereby promoting p53 ubiquitination and degradation ( xref (iv))."

sparser
"By systematically analyzing, Yu Zhao et al. demonstrated that the OTUD4 could complex with USP7-USP9X. They proved that the OTUD4-USP7-USP9X complex was required for alkylation damage resistance and repair via promoting stability of ALKBH3, a demethylases for alkylation damage repair [ xref ]."

No evidence text available

No evidence text available

sparser
"To achieve this, the 181–550 region of OTUD4, which does not include the OTU catalytic domain, forms a complex with USP7 and USP9X. These two enzymes remove the K48-linked ubiquitin chains of ALKBH2 and ALKBH3 by their DUB activity, thereby preventing their degradation by the proteasome ( xref )."

sparser
"In our study, however, the amount of FAM188B-bound USP7 dramatically increased upon FAM188B overexpression in HCT-116 cells."

sparser
"The specificity of the USP9X and USP7 interaction was examined using unrelated DUBs, including USP4 ( xref ) and USP8 (data not shown), neither of which affected MARCH7 levels."

sparser
"Conversely, USP7 interacts with FAM188B and enhances tumor growth and survival of colon cancer cells[ xref , xref ]."

reach
"Additionally, we conducted Co-IP experiments in NRK-52E cells to verify the binding situation, and the results demonstrated varying degrees of binding between Usp49, Stambp, Usp8, Usp9x, Usp33, Usp20, and Usp7 with TLR4."