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Updated: Jan 22, 2026

Crystallization and Structural Determination of an Enzyme:Substrate Complex by Serial Crystallography in a Versatile Microfluidic Chip
Published on: March 20, 2021
Crystal structure of the tubulin tyrosine carboxypeptidase complex VASH1-SVBP
Athanassios Adamopoulos1,2, Lisa Landskron1,2, Tatjana Heidebrecht1,2
1Division of Biochemistry, the Netherlands Cancer Institute, Amsterdam, the Netherlands.
Abstract:
The cyclic enzymatic removal and ligation of the C-terminal tyrosine of α-tubulin generates heterogeneous microtubules and affects their functions. Here we describe the crystal and solution structure of the tubulin carboxypeptidase complex between vasohibin (VASH1) and small vasohibin-binding protein (SVBP), which folds in a long helix, which stabilizes the VASH1 catalytic domain. This structure, combined with molecular docking and mutagenesis experiments, reveals which residues are responsible for recognition and cleavage of the tubulin C-terminal tyrosine.
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