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• W2912116791 abstract "Glycosaminoglycans (GAGs), a major constituent of the extracellular matrix, participate in cell‐signaling by binding specific proteins. Structural data on protein–GAG interactions are crucial to understand and modulate these signaling processes, with potential applications in regenerative medicine. However, experimental and theoretical approaches used to study GAG–protein systems are challenged by GAGs high flexibility limiting the conformational sampling above a certain size, and by the scarcity of GAG‐specific docking tools compared to protein–protein or protein–drug docking approaches. We present for the first time an automated fragment‐based method for docking GAGs on a protein binding site. In this approach, trimeric GAG fragments are flexibly docked to the protein, assembled based on their spacial overlap, and refined by molecular dynamics. The method appeared more successful than the classical full‐ligand approach for most of 13 tested complexes with known structure. The approach is particularly promising for docking of long GAG chains, which represents a bottleneck for classical docking approaches applied to these systems. © 2019 Wiley Periodicals, Inc." @default.
• W2912116791 created "2019-02-21" @default.
• W2912116791 creator A5067298493 @default.
• W2912116791 creator A5086671958 @default.
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• W2912116791 date "2019-02-15" @default.
• W2912116791 modified "2023-10-17" @default.
• W2912116791 title "Modeling large protein–glycosaminoglycan complexes using a fragment‐based approach" @default.
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• W2912116791 doi "https://doi.org/10.1002/jcc.25797" @default.
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• W2912116791 hasPublicationYear "2019" @default.
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