The planar cell polarity protein Vangl2 interacts with the PDZ-domains of Scribble but not with a unique PDZ-like domain in Inturned

  • FEBS Lett. 2026 Mar 8. doi: 10.1002/1873-3468.70319.
Stephan Wilmes  1 Jan Brysch  1 Carmen Gelze  1 Lilli Meier  1 Daniel Kümmel  1
Affiliations
  • 1. Department of Chemistry and Pharmacy, Institute of Biochemistry, University of Münster, Germany.
Abstract

The proteins Inturned and Fuzzy are members of the tri-longin domain (TLD) RabGEF family and activate the GTPase Rab23 downstream of the core planar cell polarity (PCP) proteins Vangl2 and Prickle. To gain insight into the function of a predicted PDZ domain unique to Inturned among TLD proteins, we performed structural and biochemical characterisations. We show that this domain does not interact with membranes or Vangl2. Instead, we find a phosphorylation-dependent interaction between Vangl2 and a PDZ domain of the apical-basal polarity protein Scribble. A crystal structure of Intu-PDZ reveals a unique PDZ-like fold lacking an interaction site for PDZ-binding motifs. Our data provide new insight into the role of PDZ domains in coordinating cell polarity downstream of Vangl2.

Keywords
Intu; PDZ domain; Scrib; Vang; X‐ray crystallography; protein–protein interaction.
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