+ |
AURKB | up-regulates
phosphorylation
|
CHMP4C |
0.483 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-197967 |
Ser210 |
MSSTARRsRAASSQR |
Homo sapiens |
|
pmid |
sentence |
22724069 |
Moreover, we find that the cpc's catalytic subunit, aurora b kinase, phosphorylates one of the three human snf7 paralogues-chmp4c-in its c-terminal tail, a region known to regulate its ability to form polymers and associate with membranes. Phosphorylation at these sites appears essential for chmp4c function because their mutation leads to cytokinesis defects. The introduction of the s214a and s215a mutations together with s210a almost completely abolished aurora b phosphorylation |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-197971 |
Ser214 |
ARRSRAAsSQRAEEE |
Homo sapiens |
|
pmid |
sentence |
22724069 |
Moreover, we find that the cpc's catalytic subunit, aurora b kinase, phosphorylates one of the three human snf7 paralogues-chmp4c-in its c-terminal tail, a region known to regulate its ability to form polymers and associate with membranes. Phosphorylation at these sites appears essential for chmp4c function because their mutation leads to cytokinesis defects. The introduction of the s214a and s215a mutations together with s210a almost completely abolished aurora b phosphorylation |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-196728 |
Ser215 |
RRSRAASsQRAEEED |
Homo sapiens |
|
pmid |
sentence |
22422861 |
Chmp4c functioned in the aurora b-dependent abscission checkpoint to prevent both premature resolution of intercellular chromosome bridges and accumulation of dna damage. Chmp4c engaged the chromosomal passenger complex (cpc) via interaction with borealin, which suggested a model whereby chmp4c inhibits abscission upon phosphorylation by aurora b |
|
Publications: |
3 |
Organism: |
Homo Sapiens |
+ |
CHMP4C | form complex
binding
|
ESCRT-III |
0.631 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265528 |
|
|
in vitro |
|
pmid |
sentence |
26775243 |
The ESCRT machinery drives a diverse collection of membrane remodeling events, including multivesicular body biogenesis, release of enveloped retroviruses and both reformation of the nuclear envelope and cytokinetic abscission during mitotic exit. ESCRT-III subunits (CHMPs, for Charged Multivesicular Body Proteins [32], or Chromatin Modifying Proteins [33]) transition between soluble and polymerising states, and assemble in a defined order to form a membrane-remodeling filament that brings about membrane fission. |
|
Publications: |
1 |
Organism: |
In Vitro |