نتایج جستجو برای: rsk method

تعداد نتایج: 1630648  

2013
Mykhaylo Artamonov Ko Momotani Darkhan Utepbergenov Aaron Franke Alexander Khromov Zygmunt S. Derewenda Avril V. Somlyo

In the canonical model of smooth muscle (SM) contraction, the contractile force is generated by phosphorylation of the myosin regulatory light chain (RLC20) by the myosin light chain kinase (MLCK). Moreover, phosphorylation of the myosin targeting subunit (MYPT1) of the RLC20 phosphatase (MLCP) by the RhoA-dependent ROCK kinase, inhibits the phosphatase activity and consequently inhibits dephos...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2016
Kirsty Sawicka Alexander Pyronneau Miranda Chao Michael V L Bennett R Suzanne Zukin

Fragile X syndrome (FXS) is the most common heritable cause of intellectual disability and a leading genetic form of autism. The Fmr1 KO mouse, a model of FXS, exhibits elevated translation in the hippocampus and the cortex. ERK (extracellular signal-regulated kinase) and mTOR (mechanistic target of rapamycin) signaling regulate protein synthesis by activating downstream targets critical to tra...

2013
Malihe Keramati Farzin Roohvand Mohammad Mehdi Aslani Shohreh Khatami MohammadReza Aghasadeghi Mehdi Sadat Arash Memarnejadian Fatemeh Motevalli

INTRODUCTION Streptokinase (SK) is a fibrinolytic protein secreted by β-hemolytic streptococci (βHS) groups A, C and G. Due to its importance as a thrombolytic drug, national screening programs in different countries for isolation of βHS and especially SK-producing group C (GCS) strains have been conducted. Herein, we provide data of the first screening study on βHS isolates in Iran for the aim...

Journal: :The Journal of biological chemistry 2000
M Delehedde M Seve N Sergeant I Wartelle M Lyon P S Rudland D G Fernig

Fibroblast growth factor-2 (FGF-2) interacts with a dual receptor system consisting of tyrosine kinase receptors and heparan sulfate proteoglycans (HSPGs). In rat mammary fibroblasts, FGF-2 stimulated DNA synthesis and induced a sustained phosphorylation of p42/44(MAPK) and of its downstream target, p90(RSK). Moreover, FGF-2 also stimulated the transient degradation of IkappaBalpha and IkappaBb...

2014
Roman M. Mrozowski Zachary M. Sandusky Rajender Vemula Bulan Wu Qi Zhang Deborah A. Lannigan George A. O’Doherty

In an effort to improve upon the in vivo half-life of the known ribosomal s6 kinase (RSK) inhibitor SL0101, C4″-amide/C6″-alkyl substituted analogues of SL0101 were synthesized and evaluated in cell-based assays. The analogues were prepared using a de novo asymmetric synthetic approach, which featured Pd-π-allylic catalyzed glycosylation for the introduction of a C4″-azido group. Surprisingly r...

2011
Ersheng Kuang Bishi Fu Qiming Liang Jinjong Myoung Fanxiu Zhu

PHOSPHORYLATION OF EIF4B BY THE ORF45/RSK SIGNALING AXIS FACILITATES PROTEIN TRANSLATION DURING KSHV LYTIC REPLICATION Ersheng Kuang, Bishi Fu, Qiming Liang, Jinjong Myoung, and Fanxiu Zhu From Department of Biological Science, Florida State University, Tallahassee, FL 32306-4370, and Novartis Institutes for Biomedical Research, Emeryville, CA 94608-2916 Running head: ORF45/RSK axis facilitates...

2014
Shyamashree Upadhyay

A Richardson variety X α in the Orthogonal Grassmannian is defined to be the intersection of a Schubert variety X in the Orthogonal Grassmannian and an opposite Schubert variety X α therein. We give an explicit description of the initial ideal (with respect to certain conveniently chosen term order) for the ideal of the tangent cone at any T-fixed point of X α , thus generalizing a result of Ra...

Journal: :Science 2005
Michael S Cohen Chao Zhang Kevan M Shokat Jack Taunton

The active sites of 491 human protein kinase domains are highly conserved, which makes the design of selective inhibitors a formidable challenge. We used a structural bioinformatics approach to identify two selectivity filters, a threonine and a cysteine, at defined positions in the active site of p90 ribosomal protein S6 kinase (RSK). A fluoromethylketone inhibitor, designed to exploit both se...

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