The Journal of Antibiotics · 1994 · 17 citations · 14 references
Life SciencesBiochemistryMolecular BiologyCell SignalingEnzymologySignal TransductionEnzyme InhibitionProtein Kinase CascadesSignal Transduction PathwaysKinase Inhibitor Library DesignKinase InhibitorsKinase Signaling InhibitorsMyosin BiochemistryMyosin Inhibitors
MS-282a and MS-282b were isolated from the culture broth of Streptomyces tauricus ATCC 27470 as inhibitors of smooth muscle myosin light chain kinase (MLCK). MS-282a and MS-282b inhibited the activity of chicken gizzard MLCK with IC50 values of 3.8 microM and 5.2 microM, respectively. Cyclic AMP-dependent protein kinase, cyclic GMP-dependent protein kinase and protein kinase C were not inhibited by 150 microM MS-282a at all. It is likely that MS-282a blocks MLCK activity by antagonizing calmodulin since 1) the compound inhibited calmodulin-dependent but not calmodulin-independent activity of MLCK; 2) the inhibition of MLCK was antagonized by increasing concentrations of calmodulin, and 3) the compound inhibited calmodulin-dependent cyclic nucleotide phosphodiesterase.
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Wortmannin, a microbial product inhibitor of myosin light chain kinase.
S. Nakanishi, Shingo Kakita, ISAMI TAKAHASHI et al. · Journal of Biological Chemistry · 1992 · 430 citations · Full text
KT5926, a potent and selective inhibitor of myosin light chain kinase.
S. Nakanishi, Keisuke Yamada, K Iwahashi et al. · Molecular Pharmacology · 1990 · 128 citations