Annotation inferences using phylogenetic trees

Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt

Electronic Gene Ontology annotations created by ARBA machine learning models

Combined Automated Annotation using Multiple IEA Methods

Exit from mitosis is triggered by Tem1-dependent release of the protein phosphatase Cdc14 from nucleolar RENT complex.

Characterization of the Net1 cell cycle-dependent regulator of the Cdc14 phosphatase from budding yeast.

Functional organization of the yeast proteome by systematic analysis of protein complexes.

Subcellular localization of the yeast proteome.

Mitotic exit network controls the localization of Cdc14 to the spindle pole body in Saccharomyces cerevisiae.

The Cdc14 phosphatase and the FEAR network control meiotic spindle disassembly and chromosome segregation.

Association of the RENT complex with nontranscribed and coding regions of rDNA and a regional requirement for the replication fork block protein Fob1 in rDNA silencing.

Novel regulation of mitotic exit by the Cdc42 effectors Gic1 and Gic2.

Budding yeast silencing complexes and regulation of Sir2 activity by protein-protein interactions.

Proteome survey reveals modularity of the yeast cell machinery.

Downregulation of PP2A(Cdc55) phosphatase by separase initiates mitotic exit in budding yeast.

Transcription of ribosomal genes can cause nondisjunction.

Inhibition of homologous recombination by a cohesin-associated clamp complex recruited to the rDNA recombination enhancer.

Cdk and APC activities limit the spindle-stabilizing function of Fin1 to anaphase.

Structure-templated predictions of novel protein interactions from sequence information.

A nucleolus-localized activator of Cdc14 phosphatase supports rDNA segregation in yeast mitosis.

Putting the brake on FEAR: Tof2 promotes the biphasic release of Cdc14 phosphatase during mitotic exit.

The Polo-like kinase Cdc5 interacts with FEAR network components and Cdc14.

Cdc14 inhibits transcription by RNA polymerase I during anaphase.

A global protein kinase and phosphatase interaction network in yeast.

Defining the budding yeast chromatin-associated interactome.

A quantitative model for ordered Cdk substrate dephosphorylation during mitotic exit.

Global analysis of cdc14 dephosphorylation sites reveals essential regulatory role in mitosis and cytokinesis.

Molecular mechanisms that restrict yeast centrosome duplication to one event per cell cycle.

Identification of Cdk targets that control cytokinesis.

Pathway connectivity and signaling coordination in the yeast stress-activated signaling network.

Dephosphorylation of Iqg1 by Cdc14 regulates cytokinesis in budding yeast.

Cdc14 Early Anaphase Release, FEAR, Is Limited to the Nucleus and Dispensable for Efficient Mitotic Exit.

Cdc14 Phosphatase Promotes TORC1-Regulated Autophagy in Yeast.

Cdc14 spatiotemporally dephosphorylates Atg13 to activate autophagy during meiotic divisions.

Interphase chromosome condensation in nutrient-starved conditions requires Cdc14 and Hmo1, but not condensin, in yeast.

Phosphosites of the yeast centrosome component Spc110 contribute to cell cycle progression and mitotic exit.

The social and structural architecture of the yeast protein interactome.

Safeguarding genome integrity: Polo-like kinase Cdc5 and phosphatase Cdc14 orchestrate Topoisomerase II-mediated catenane resolution in mitosis.

Determination of the order of gene function in the yeast nuclear division pathway using cs and ts mutants.

The activity of Cdc14p, an oligomeric dual specificity protein phosphatase from Saccharomyces cerevisiae, is required for cell cycle progression.

Deep research report for CDC14 (falcon/Edison)