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 |
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Hauptverfasser: | , , |
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. |
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ISSN: | 0014-5793 1873-3468 |
DOI: | 10.1016/0014-5793(94)80121-5 |