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Journal Article
PLoS ONE, ISSN 1932-6203, 08/2015, Volume 10, Issue 8, p. e0134984
Protein tyrosine phosphatases dephosphorylate tyrosine residues of proteins, whereas, dual specificity phosphatases (DUSPs) are a subgroup of protein tyrosine... 
CELL LUNG-CANCER | CDC25 PHOSPHATASE | ANGSTROM RESOLUTION | ACTIVATION | VIRUS | CRYSTAL-STRUCTURE | KINASE PHOSPHATASE-1 | MULTIDISCIPLINARY SCIENCES | PROTEIN-TYROSINE PHOSPHATASES | INHIBITORS | CATALYTIC MECHANISM | Dual Specificity Phosphatase 1 - genetics | Signal Transduction | Dual-Specificity Phosphatases - metabolism | Humans | Phosphoprotein Phosphatases - metabolism | Substrate Specificity | Dual Specificity Phosphatase 3 - genetics | cdc25 Phosphatases - genetics | Phylogeny | Recombinant Proteins | Mitogen-Activated Protein Kinase Phosphatases - genetics | Amino Acid Motifs | Phosphotyrosine - metabolism | Phosphoprotein Phosphatases - genetics | Dual-Specificity Phosphatases - genetics | Protein Array Analysis | Dual Specificity Phosphatase 1 - metabolism | cdc25 Phosphatases - metabolism | Dual Specificity Phosphatase 3 - metabolism | Mitogen-Activated Protein Kinase Phosphatases - metabolism | Physiological aspects | Phosphorylation | Genetic aspects | Phosphatases | Research | Cluster analysis | Residues | Peptides | Laboratories | Phosphotyrosine | Biochemistry | Catalytic activity | Dephosphorylation | Structure-activity relationships | Kinases | Phosphatase | Crystallography | Subgroups | Proteins | Signal transduction | Cell growth | Pathways | Substrate specificity | Armed forces | Catalysis | Localization | Pharmaceutical sciences | Tyrosine | Smallpox | Medical research | Enzymes | Cell division | Clustering | Substrates | Signaling | Chemistry | Infectious diseases | Alzheimers disease | Recognition | Cancer
Journal Article
Molecular Biology of the Cell, ISSN 1059-1524, 04/2011, Volume 22, Issue 8, pp. 1191 - 1206
Mitosis requires precise coordination of multiple global reorganizations of the nucleus and cytoplasm. Cyclin-dependent kinase 1 (Cdk1) is the primary upstream... 
ANAPHASE-PROMOTING COMPLEX | XENOPUS EGG EXTRACTS | PROTEIN PHOSPHATASES | CYCLE-DEPENDENT PHOSPHORYLATION | UBIQUITIN LIGASE | M-PHASE | CHROMOSOME ALIGNMENT | CELL-CYCLE | TUMOR-CELLS | SPINDLE-ASSEMBLY CHECKPOINT | CELL BIOLOGY | Cyclin-Dependent Kinases - metabolism | Gene Expression - drug effects | Xenopus Proteins - genetics | Mitosis | Protein-Tyrosine Kinases - metabolism | Humans | Phosphoprotein Phosphatases - metabolism | G2 Phase - drug effects | CDC2 Protein Kinase - metabolism | Cell Cycle Proteins - antagonists & inhibitors | Protein-Tyrosine Kinases - genetics | Cyclin B - genetics | cdc25 Phosphatases - antagonists & inhibitors | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Cell Cycle Proteins - genetics | Prometaphase - drug effects | Female | Cyclin-Dependent Kinases - antagonists & inhibitors | Phosphorylation - drug effects | cdc25 Phosphatases - metabolism | Cyclin-Dependent Kinases - genetics | Nuclear Proteins - genetics | Protein-Serine-Threonine Kinases - metabolism | CDC2 Protein Kinase - genetics | Protein Phosphatase 2 - antagonists & inhibitors | CDC2 Protein Kinase - antagonists & inhibitors | Xenopus laevis | Cell Cycle Proteins - metabolism | Protein Phosphatase 2 - genetics | Protein-Serine-Threonine Kinases - genetics | Nuclear Proteins - metabolism | Phosphoprotein Phosphatases - antagonists & inhibitors | cdc25 Phosphatases - genetics | Xenopus Proteins - antagonists & inhibitors | Membrane Proteins | Animals | Phosphoprotein Phosphatases - genetics | Nuclear Proteins - antagonists & inhibitors | Protein Phosphatase 2 - metabolism | Cyclin B - metabolism | Feedback, Physiological - drug effects | Xenopus Proteins - metabolism | Protein Kinase Inhibitors - pharmacology | S Phase - drug effects | HeLa Cells | Protein-Tyrosine Kinases - antagonists & inhibitors
Journal Article
Journal Article
Science Signaling, ISSN 1945-0877, 06/2012, Volume 5, Issue 230, pp. ra46 - ra46
Journal Article