+ |
PLK1 | up-regulates activity
phosphorylation
|
KIF2B |
0.647 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252050 |
Ser204 |
HLDSSKIsVLEPPQE |
Homo sapiens |
|
pmid |
sentence |
22535524 |
We show that Plk1 directly phosphorylates Kif2b at threonine 125 (T125) and serine 204 (S204), and that these two sites differentially regulate Kif2b function. Phosphorylation of S204 is required for the kinetochore localization and activity of Kif2b in prometaphase, and phosphorylation of T125 is required for Kif2b activity in the correction of k-MT attachment errors. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252049 |
Thr125 |
MIPQKNQtASGDSLD |
Homo sapiens |
U2-OS Cell |
pmid |
sentence |
22535524 |
We show that Plk1 directly phosphorylates Kif2b at threonine 125 (T125) and serine 204 (S204), and that these two sites differentially regulate Kif2b function. Phosphorylation of S204 is required for the kinetochore localization and activity of Kif2b in prometaphase, and phosphorylation of T125 is required for Kif2b activity in the correction of k-MT attachment errors. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
KNSTRN | down-regulates activity
relocalization
|
KIF2B |
0.418 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252053 |
|
|
Homo sapiens |
U2-OS Cell |
pmid |
sentence |
22535524 |
The protein astrin has been shown to remove Kif2b from kinetochores in metaphase through competitive binding of CLASP1 (Manning et al., 2010 blue right-pointing triangle). During prometaphase, Aurora B kinase activity prevents astrin from localizing to kinetochores (Manning et al., 2010 blue right-pointing triangle; Schmidt et al., 2010 blue right-pointing triangle). This permits Kif2b to localize to kinetochores to destabilize k-MT attachments to execute error correction through Plk1-dependent recruitment and activation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
KIF2B | up-regulates
|
Minus-end directed microtubule movement |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-272534 |
|
|
Homo sapiens |
|
pmid |
sentence |
19773780 |
In general, N-kinesins and C-kinesins drive microtubule plus end- and minus end-directed motilities, respectively, and M-kinesins depolymerize microtubules1,9 (Box 1).|Forty-five genes that encode kinesin superfamily proteins (also known as KIFs) have been discovered in the mouse and human genomes.|KIFs are molecular motors that directionally transport various cargos, including membranous organelles, protein complexes and mRNAs, along the microtubule system. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
KIF2B | down-regulates
|
Mitotic_checkpoint |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252051 |
|
|
Homo sapiens |
|
pmid |
sentence |
22535524 |
The protein astrin has been shown to remove Kif2b from kinetochores in metaphase through competitive binding of CLASP1 (Manning et al., 2010 blue right-pointing triangle). During prometaphase, Aurora B kinase activity prevents astrin from localizing to kinetochores (Manning et al., 2010 blue right-pointing triangle; Schmidt et al., 2010 blue right-pointing triangle). This permits Kif2b to localize to kinetochores to destabilize k-MT attachments to execute error correction through Plk1-dependent recruitment and activation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |