This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.


Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.


1jei

From Proteopedia

Revision as of 14:06, 15 February 2008 by OCA (Talk | contribs)
Jump to: navigation, search

1jei

Drag the structure with the mouse to rotate

LEM DOMAIN OF HUMAN INNER NUCLEAR MEMBRANE PROTEIN EMERIN

Contents

Overview

Like Duchenne and Becker muscular dystrophies, Emery-Dreifuss muscular, dystrophy (EDMD) is characterized by myopathic and cardiomyopathic, abnormalities. EDMD has the particularity of being linked to mutations in, nuclear proteins. The X-linked form of EDMD is caused by mutations in the, emerin gene, whereas autosomal dominant EDMD is caused by mutations in the, lamin A/C gene. Emerin colocalizes with lamin A/C in interphase cells, and, binds in vitro to lamin A/C. Recent work suggests that lamin A/C might, serve as a receptor for emerin. We have undertaken a structural analysis, of emerin, and in particular of its N-terminal domain, which is comprised, in the emerin segment critical for binding to lamin A/C. We show that, region 2-54 of emerin adopts the LEM fold. This fold was originally, described in the two N-terminal domains of another inner nuclear membrane, protein called lamina-associated protein 2 (LAP2). The existence of a, conserved solvent-exposed surface on the LEM domains of LAP2 and emerin is, discussed, as well as the nature of a possible common target.

Disease

Known diseases associated with this structure: Emery-Dreifuss muscular dystrophy OMIM:[300384]

About this Structure

1JEI is a Single protein structure of sequence from [1]. Full crystallographic information is available from OCA.

Reference

Structural analysis of emerin, an inner nuclear membrane protein mutated in X-linked Emery-Dreifuss muscular dystrophy., Wolff N, Gilquin B, Courchay K, Callebaut I, Worman HJ, Zinn-Justin S, FEBS Lett. 2001 Jul 20;501(2-3):171-6. PMID:11470279

Page seeded by OCA on Fri Feb 15 16:06:57 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools