PDBsum entry 4b3g

Hydrolase/RNA

PDB id: 4b3g

Contents

Protein chain

614 a.a.

DNA/RNA

Waters ×145

References listed in PDB file

Key reference

• Title: The ighmbp2 helicase structure reveals the molecular basis for disease-Causing mutations in dmsa1.
• Authors: S.C.Lim, M.W.Bowler, T.F.Lai, H.Song.
• Ref.: Nucleic Acids Res, 2012, 40, 11009-11022.
• PubMed id: 22965130

Abstract

Mutations in immunoglobulin µ-binding protein 2 (Ighmbp2) cause distal spinal muscular atrophy type 1 (DSMA1), an autosomal recessive disease that is clinically characterized by distal limb weakness and respiratory distress. However, despite extensive studies, the mechanism of disease-causing mutations remains elusive. Here we report the crystal structures of the Ighmbp2 helicase core with and without bound RNA. The structures show that the overall fold of Ighmbp2 is very similar to that of Upf1, a key helicase involved in nonsense-mediated mRNA decay. Similar to Upf1, domains 1B and 1C of Ighmbp2 undergo large conformational changes in response to RNA binding, rotating 30° and 10°, respectively. The RNA binding and ATPase activities of Ighmbp2 are further enhanced by the R3H domain, located just downstream of the helicase core. Mapping of the pathogenic mutations of DSMA1 onto the helicase core structure provides a molecular basis for understanding the disease-causing consequences of Ighmbp2 mutations.