Mitosis persists in the absence of Cdk1 activity when proteolysis or protein phosphatase activity is suppressed. - Wikidata - awgldk - TriplyDB

Mitosis persists in the absence of Cdk1 activity when proteolysis or protein phosphatase activity is suppressed.

Mitosis persists in the absence of Cdk1 activity when proteolysis or protein phosphatase activity is suppressed.

http://www.wikidata.org/entity/Q36149275

about

Live-cell imaging RNAi screen identifies PP2A-B55alpha and importin-beta1 as key mitotic exit regulators in human cells The decision to enter mitosis: feedback and redundancy in the mitotic entry network Identification and characterization of a novel human PP1 phosphatase complex Cyclin-dependent kinase 1-mediated Bcl-xL/Bcl-2 phosphorylation acts as a functional link coupling mitotic arrest and apoptosis Fcp1-dependent dephosphorylation is required for M-phase-promoting factor inactivation at mitosis exit Resetting a functional G1 nucleus after mitosis A mitotic phosphorylation feedback network connects Cdk1, Plk1, 53BP1, and Chk2 to inactivate the G(2)/M DNA damage checkpoint Fine tuning the cell cycle: activation of the Cdk1 inhibitory phosphorylation pathway during mitotic exit.alpha-Endosulfine is a conserved protein required for oocyte meiotic maturation in Drosophila Microtubule cytoskeleton remodeling by acentriolar microtubule-organizing centers at the entry and exit from mitosis in Drosophila somatic cells Glioblastoma motility occurs in the absence of actin polymer.Inhibitory phosphorylation of cyclin-dependent kinase 1 as a compensatory mechanism for mitosis exit.TD-60 is required for interphase cell cycle progression Protein Phosphatase 2A (PP2A) Regulates EG5 to Control Mitotic Progression Binding partner switching on microtubules and aurora-B in the mitosis to cytokinesis transition.Sustained spindle-assembly checkpoint response requires de novo transcription and translation of cyclin B1.Phosphorylation of AIB1 at mitosis is regulated by CDK1/CYCLIN B.A virtual cycle: theory and experiment converge on the exit from mitosis.The traffic of proteins between nucleolar organizer regions and prenucleolar bodies governs the assembly of the nucleolus at exit of mitosis.PP2A/B55 and Fcp1 regulate Greatwall and Ensa dephosphorylation during mitotic exit.Phosphorylation of targeting protein for Xenopus kinesin-like protein 2 (TPX2) at threonine 72 in spindle assembly.Cdc14 phosphatases preferentially dephosphorylate a subset of cyclin-dependent kinase (Cdk) sites containing phosphoserine Identification of Candidate Cyclin-dependent kinase 1 (Cdk1) Substrates in Mitosis by Quantitative Phosphoproteomics.Human cells enter mitosis with damaged DNA after treatment with pharmacological concentrations of genotoxic agents.Acetylation of Aurora B by TIP60 ensures accurate chromosomal segregation CaM kinase II initiates meiotic spindle depolymerization independently of APC/C activation.Mitotic protein kinase CDK1 phosphorylation of mRNA translation regulator 4E-BP1 Ser83 may contribute to cell transformation Cell fate determination in cisplatin resistance and chemosensitization Cdk-counteracting phosphatases unlock mitotic exit.The multiple layers of ubiquitin-dependent cell cycle control.Regulated protein kinases and phosphatases in cell cycle decisions.Phosphatases: providing safe passage through mitotic exit.Cdk1 orders mitotic events through coordination of a chromosome-associated phosphatase switch.Bistability of mitotic entry and exit switches during open mitosis in mammalian cells.Aurora B potentiates Mps1 activation to ensure rapid checkpoint establishment at the onset of mitosis.Partial inhibition of Cdk1 in G 2 phase overrides the SAC and decouples mitotic events.PP1-mediated dephosphorylation of phosphoproteins at mitotic exit is controlled by inhibitor-1 and PP1 phosphorylation.The BEG (PP2A-B55/ENSA/Greatwall) pathway ensures cytokinesis follows chromosome separation Furry protein promotes aurora A-mediated Polo-like kinase 1 activation.FAM29A, a target of Plk1 regulation, controls the partitioning of NEDD1 between the mitotic spindle and the centrosomes.

P2860

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P2860

Mitosis persists in the absence of Cdk1 activity when proteolysis or protein phosphatase activity is suppressed.

http://www.wikidata.org/entity/Q36149275

description

2007 nî lūn-bûn

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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2007年论文

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2007年论文

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name

Mitosis persists in the absenc ...... hatase activity is suppressed.

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Mitosis persists in the absenc ...... hatase activity is suppressed.

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type

label

Mitosis persists in the absenc ...... hatase activity is suppressed.

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Mitosis persists in the absenc ...... hatase activity is suppressed.

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prefLabel

Mitosis persists in the absenc ...... hatase activity is suppressed.

@ast

Mitosis persists in the absenc ...... hatase activity is suppressed.

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P1433

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P1433

Journal of Cell Biology

P1476

Mitosis persists in the absenc ...... hatase activity is suppressed.

@en

P2093

Andreas Panopoulos

http://www.w3.org/2001/XMLSchema#string

Dimitrios A Skoufias

http://www.w3.org/2001/XMLSchema#string

Françoise Lacroix

http://www.w3.org/2001/XMLSchema#string

Robert L Margolis

http://www.w3.org/2001/XMLSchema#string

Rose-Laure Indorato

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P2860

PRC1: a human mitotic spindle-associated CDK substrate protein required for cytokinesis

Functional analysis of a human homologue of the Drosophila actin binding protein anillin suggests a role in cytokinesis

Mitotic phosphorylation of histone H3 is governed by Ipl1/aurora kinase and Glc7/PP1 phosphatase in budding yeast and nematodes

Prophase destruction of Emi1 by the SCF(betaTrCP/Slimb) ubiquitin ligase activates the anaphase promoting complex to allow progression beyond prometaphase

The mammalian passenger protein TD-60 is an RCC1 family member with an essential role in prometaphase to metaphase progression

Serine/threonine protein phosphatases

Mitotic phosphorylation of histone H3: spatio-temporal regulation by mammalian Aurora kinases

Securin degradation is mediated by fzy and fzr, and is required for complete chromatid separation but not for cytokinesis

The KEN box: an APC recognition signal distinct from the D box targeted by Cdh1

Mitotic checkpoint slippage in humans occurs via cyclin B destruction in the presence of an active checkpoint.

P304

671-685

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10.1083/JCB.200704117

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4

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179

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5822526

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18025303

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P932

2080905

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