Elongation factor-2 kinase: effective inhibition by the novel protein kinase inhibitor rottlerin and relative insensitivity towards staurosporine

The elongation factor-2 (eEF-2) is selectively phosphorylated by the eEF-2 kinase (calmodulin-dependent kinase III). This phosphorylation can be inhibited by calmodulin antagonists, such as CGS 9343B (IC 5o = 4 μM). The novel protein kinase inhibitor rottlerin is shown to suppress eEF-2 phosphorylat...

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Veröffentlicht in:FEBS letters 1994-01, Vol.338 (1), p.85-88
Hauptverfasser: Gschwendt, Michael, Kittstein, Walter, Marks, Friedrich
Format: Artikel
Sprache:eng
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Zusammenfassung:The elongation factor-2 (eEF-2) is selectively phosphorylated by the eEF-2 kinase (calmodulin-dependent kinase III). This phosphorylation can be inhibited by calmodulin antagonists, such as CGS 9343B (IC 5o = 4 μM). The novel protein kinase inhibitor rottlerin is shown to suppress eEF-2 phosphorylation with an IC 50 of 5.3 μM. By contrast, the eEF-2 kinase is rather resistant towards the potent but non-selective protein kinase inhibitor staurosporine (IC 50> 50 μM) and thus can be differentiated from most other protein kinases that are suppressed by staurosporine in the nM range.
ISSN:0014-5793
1873-3468
DOI:10.1016/0014-5793(94)80121-5