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Protein Kinases: A family of enzymes that catalyze the conversion of Atp and a protein to Adp and a phosphoprotein.

Phosphorylation

JoVE 10733

The addition or removal of phosphate groups from proteins is the most common chemical modification that regulates cellular processes. These modifications can affect the structure, activity, stability, and localization of proteins within cells as well as their interactions with other proteins.

During phosphorylation, protein kinases transfer the terminal phosphate group of ATP to specific amino acid side chains of substrate proteins. Serine, threonine, and tyrosine are the most commonly phosphorylated amino acids. Accordingly, protein kinases are classified as serine/threonine kinases, tyrosine kinases, or dual action kinases if they can phosphorylate all three amino acids. Conversely, protein phosphatases catalyze the removal of the phosphate group (dephosphorylation), restoring the original properties of the protein. Under physiological conditions, phosphorylation and dephosphorylation are tightly regulated to prevent prolonged changes in protein structure and function. Disruption of this balance can cause diseases, including cancer and various neurodegenerative disorders. For instance, a protein called tau is hyperphosphorylated in Alzheimer’s disease (AD). Physiologically, tau regulates the shape, structure, and development of neurons. The tau protein contains over 80 serine, threonine, and tyrosine residues, of which only a fraction is usually pho

 Core: Metabolism

Light-mediated Reversible Modulation of the Mitogen-activated Protein Kinase Pathway during Cell Differentiation and Xenopus Embryonic Development

1Department of Biochemistry, University of Illinois at Urbana-Champaign, 2Department of Comparative Biosciences, University of Illinois at Urbana-Champaign, 3Neuroscience Program, University of Illinois at Urbana-Champaign, 4Center for Biophysics and Quantitative Biology, University of Illinois at Urbana-Champaign

JoVE 55823

 Developmental Biology

Identification of Mediators of T-cell Receptor Signaling via the Screening of Chemical Inhibitor Libraries

1Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of Singapore, 2Singapore Immunology Network, A*STAR, 3Curiox Biosystems, 4Department of Immunobiology, Rega Institute for Medical Research, Katholieke Universiteit (KU) Leuven

JoVE 58946

 Immunology and Infection

Inactivation of mTor: A Tool to Investigate Meiotic Progression and Translational Control During Bovine Oocyte Maturation

1BVN Neustadt/Aisch, 2Faculty of Veterinary Medicine, Clinic for Obstetrics, Gynecology and Andrology of Large and Small Animals, Justus-Liebig-University Giessen, 3Reproductive Cell Biology Unit, Leibniz Institute for Farm Animal Biology, 4Reproductive Biochemistry Unit, Leibniz Institute for Farm Animal Biology

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JoVE 53689

 JoVE In-Press
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