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Fraternal twins at work: Structures of PLD3/4 reveal mechanism for lysosomal nucleic acid breakdown
1Structural Biology, Max Delbrück Center for Molecular Medicine (MDC), 13125 Berlin, Germany; Institute for Chemistry and Biochemistry, Freie Universität Berlin, 14195 Berlin, Germany.
Abstract:
Phospholipase D (PLD) family proteins degrade phospholipids and nucleic acids. In the current issue of Structure, Yuan et al.1 report crystal structures of lysosomal PLD3 and PLD4 with and without a single-stranded DNA substrate. Their manuscript reveals a catalytic ping-pong mechanism and explains how disease-associated mutations compromise PLD3/4 function.
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