IndraLab

Statements


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reach
"One, we hypothesized that USP11 binds and deubiquitylates SMAD7, thereby inhibiting the TGFbeta pathway."

sparser
"To confirm the specificity of the USP11SMAD7 interaction, SMADs carrying an N-terminal FLAG tag were transiently transfected into HEK293 cells with or without the N-terminal HA-tagged USP11."

sparser
"USP11 but not USP15 binds specifically to SMAD7."

sparser
"USP11SMAD7 interaction and potential complex formation raised two distinct possibilities for USP11 targets within the TGFβ pathway."

sparser
"One, we hypothesized that USP11 binds and deubiquitylates SMAD7, thereby inhibiting the TGFβ pathway."

sparser
"USP11 binds to Smad7, which then recruits USP11 to TGFβ receptor I where it interacts, deubiquitinates and stabilizes TGFβ receptor I to sustain Smad-mediated TGFβ signaling [ xref ]."

No evidence text available

reach
"USP11 binds to Smad7, which then recruits USP11 to TGFbeta receptor I where it interacts, deubiquitinates and stabilizes TGFbeta receptor I to sustain Smad mediated TGFbeta signaling [XREF_BIBR]."

reach
"Conversely, a SMAD7 and USP11 complex would deubiquitylate the receptor, preventing its degradation and allow continued signalling (XREF_FIG)."

sparser
"TGFβ stimulation did not alter the SMAD7USP11 interactions (see the electronic supplementary material, figure S1)."

reach
"We found that USP11 interacted more robustly with SMAD7 compared with any of the other SMAD proteins (XREF_FIG b)."

reach
"Size-exclusion chromatography also alluded to the possibility of potential complex formation between USP11 and SMAD7."

sparser
"In the case of USP11, SMAD7 does not appear to act exclusively as a scaffold for as SMAD7 does not appear to mediate the interaction between USP11 and TβRI, despite the fact that SMAD7 and USP11 being[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

No evidence text available

sparser
"This confirms our previous observation that USP11 interacts with SMAD7 [ xref ]."

reach
"We performed size-exclusion chromatography on HaCaT cell extracts in order to detect potential endogenous USP11 and SMAD7 complex formation."

No evidence text available