| Literature DB >> 11756419 |
Toshiyuki Shimizu1, Azusa Seto, Nobuo Maita, Keisuke Hamada, Shoichiro Tsukita, Sachiko Tsukita, Toshio Hakoshima.
Abstract
Neurofibromatosis type 2 (NF2) is a dominantly inherited disease associated with the central nervous system. The NF2 gene product merlin is a tumor suppressor, and its mutation or inactivation causes this disease. We report here the crystal structure of the merlin FERM domain containing a 22-residue alpha-helical segment. The structure reveals that the merlin FERM domain consists of three subdomains displaying notable features of the electrostatic surface potentials, although the overall surface potentials similar to those of ezrin/radixin/moesin (ERM) proteins indicate electrostatic membrane association. The structure also is consistent with inactivation mechanisms caused by the pathogenic mutations associated with NF2.Entities:
Mesh:
Substances:
Year: 2001 PMID: 11756419 DOI: 10.1074/jbc.M109979200
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157