Structural basis for effector protein recognition by the Dot/Icm Type IVB coupling protein complex

Hyunmin Kim, Tomoko Kubori, Kohei Yamazaki, Mi Jeong Kwak, Suk Youl Park, Hiroki Nagai, Joseph P. Vogel, Byung Ha Oh

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

The Legionella pneumophila Dot/Icm type IVB secretion system (T4BSS) is extremely versatile, translocating ~300 effector proteins into host cells. This specialized secretion system employs the Dot/Icm type IVB coupling protein (T4CP) complex, which includes IcmS, IcmW and LvgA, that are known to selectively assist the export of a subclass of effectors. Herein, the crystal structure of a four-subunit T4CP subcomplex bound to the effector protein VpdB reveals an interaction between LvgA and a linear motif in the C-terminus of VpdB. The same binding interface of LvgA also interacts with the C-terminal region of three additional effectors, SidH, SetA and PieA. Mutational analyses identified a FxxxLxxxK binding motif that is shared by VpdB and SidH, but not by SetA and PieA, showing that LvgA recognizes more than one type of binding motif. Together, this work provides a structural basis for how the Dot/Icm T4CP complex recognizes effectors, and highlights the multiple substrate-binding specificities of its adaptor subunit.

Original languageEnglish
Article number2623
JournalNature communications
Volume11
Issue number1
DOIs
StatePublished - Dec 1 2020

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