| Literature DB >> 15474004 |
Torsten Meissner1, Eberhard Krause, Uwe Vinkemeier.
Abstract
Research on the export of proteins and nucleic acids from the nucleus to the cytoplasm has greatly gained from the discovery that the actinobacterial toxin leptomycin B (LMB) specifically inactivates the export receptor chromosomal region maintenance 1 (CRM1). Recently, it was shown that myxobacterial cytotoxins, named ratjadones (RATs), also bind to CRM1 and inhibit nuclear export. However, the reaction mechanism of RATs was not resolved. Here, we show that LMB and RAT A employ the same molecular mechanism to inactivate CRM1. Alkylation of residue Cys528 of CRM1 determines both LMB and RAT sensitivity and prevents nuclear export of CRM1 cargo proteins. Copyright 2004 Federation of European Biochemical SocietiesEntities:
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Year: 2004 PMID: 15474004 DOI: 10.1016/j.febslet.2004.08.056
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124