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Crystal structure of human CRM1, covalently modified by 2-mercaptoethanol on Cys528, in complex with RanGTP

CRM1 is a nuclear export receptor that has been intensively targeted over the last decade for the development of antitumor and antiviral drugs. Structural analysis of several inhibitor compounds bound to CRM1 revealed that their mechanism of action relies on the covalent modification of a critical c...

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Detalles Bibliográficos
Autores principales: Shaikhqasem, Alaa, Schmitt, Kerstin, Valerius, Oliver, Ficner, Ralf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7938638/
https://www.ncbi.nlm.nih.gov/pubmed/33682791
http://dx.doi.org/10.1107/S2053230X2100203X