When phosphate levels are low in surface waters, phytoplankton excrete extracellular enzymes called alkaline phosphatases, which have the ability to free phosphate bound to organic molecules. ❋ Unknown (2008)
Receptor protein-tyrosine phosphatases: origin of domains catalytic domain, Ig-related domain, fibronectin type III module based on the sequence of the sponge Geodia cydonium. ❋ Unknown (2006)
I have tried to describe your field of research and elegant discoveries in your studies of reversible protein phosphorylation, going back to the initial detection of the activation mechanism of phosphorylase, and continuing with protein phosphatases. ❋ Unknown (1997)
Their counterparts, the phosphatases, are equally essential in the extended cascade. ❋ Unknown (1992)
In addition, the system includes a large number of phosphatases, which in an opposite manner regulate the removal of the protein phosphate groups from proteins. ❋ Unknown (1992)
Imbalance between kinases and phosphatases can cause disease and nondesirable tissue reactions. ❋ Unknown (1992)
Blood pressure, the inflammatory reaction, and brain signal transduction - just to name a few examples - are being regulated through different hormonal interactions and these interactions in turn are mediated through kinases and phosphatases. ❋ Unknown (1992)
We are looking for a qualified and highly motivated biochemist/protein crystallographer with 0-2 years of postdoctoral experience to work on the structural characterization of protein tyrosine phosphatases involved in T cell signaling regulation. ❋ Unknown (2010)
This study provides a foundation for examining the biological role of this new family of phosphatases and their potential as pharmaceutical targets against infectious diseases. ❋ Unknown (2010)
The mechanism of reversible phosphorylation executed through kinases and phosphatases is a mode of altering biochemical or structural properties of protein and is utilized for all primary biological functions. ❋ Gunjan Arora Et Al. (2010)
Phosphoinositide phosphatases from bacterial pathogens are therefore key players in this modulation and constitute attractive targets for chemotherapy. ❋ Unknown (2010)
Ser/Thr phosphatase, one tyrosine kinase and two tyrosine phosphatases ❋ Gunjan Arora Et Al. (2010)
This new family of enzymes in microorganisms shows distinct sequence and biochemical characteristics to classic eukaryotic lipid phosphatases and they have no homologues in humans. ❋ Unknown (2010)
In this study, we describe phenotypic responses that underscore the importance of the balance between the opposing activities of kinases and phosphatases at the post-synaptic terminals. ❋ Michael Weisenhaus Et Al. (2010)
MptpB, a virulence factor from Mycobacterium tuberculosis, has phosphoinositide phosphatase activity and a distinct active site P-loop signature HCXXGKDR that shares characteristics with eukaryotic lipid phosphatases and protein tyrosine phosphatases. ❋ Unknown (2010)
• Several have obtained crystal structures of ABA bound to its receptor or ABA and the receptor interacting with the PP2C phosphatases that must be shut down to allow ABA to function. ❋ Govindab (2010)
We used this P-loop signature as a "diagnostic motif" to identify related putative phosphatases with phosphoinositide activity in other organisms. ❋ Unknown (2010)
Phylogenetic analysis revealed that these proteins are unrelated to classic eukaryotic lipid phosphatases. ❋ Unknown (2010)
Insulin may also activate protein phosphatases that inactivate HSL ❋ Mnwalkr (2010)
Activated ROCK mediates actin-myosin contraction, stress fiber formation and local adhesion by targeting downstream kinases and phosphatases resulting in increased myosin light chain phosphorylation ❋ Tzu-Ching Chang Et Al. (2010)
