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Computational Modeling of Cellulose Synthase Heterotrimer Assembly and Identification of Antimicrobial Compounds Targeting Interface Sites in Phytophthora infestans
by
Amritha, V. S.
, Chellappan, Biju Vadakkemukadiyil
, El-Ganainy, Sherif Mohamed
, Almalki, Mohammed A.
, Shidhi, P. R.
in
AlphaFold-multimer
/ Analysis
/ Artificial intelligence
/ Biosynthesis
/ Cell walls
/ Cellulose
/ Cellulose synthase
/ cellulose synthases
/ Computer simulation
/ Computer-generated environments
/ Disease control
/ Geometry
/ Glycosyltransferase
/ glycosyltransferase family 2
/ Homology
/ Hydrogen bonds
/ Interfaces
/ Late blight
/ Ligands
/ Maximum likelihood method
/ Metabolites
/ oomycete pathogenesis
/ Pathogens
/ Phylogenetics
/ Physiological aspects
/ Physiology
/ Phytophthora infestans
/ Pleckstrin
/ pleckstrin homology domain
/ Protection and preservation
/ Proteins
/ Simulation
/ Virulence
2026
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Computational Modeling of Cellulose Synthase Heterotrimer Assembly and Identification of Antimicrobial Compounds Targeting Interface Sites in Phytophthora infestans
by
Amritha, V. S.
, Chellappan, Biju Vadakkemukadiyil
, El-Ganainy, Sherif Mohamed
, Almalki, Mohammed A.
, Shidhi, P. R.
in
AlphaFold-multimer
/ Analysis
/ Artificial intelligence
/ Biosynthesis
/ Cell walls
/ Cellulose
/ Cellulose synthase
/ cellulose synthases
/ Computer simulation
/ Computer-generated environments
/ Disease control
/ Geometry
/ Glycosyltransferase
/ glycosyltransferase family 2
/ Homology
/ Hydrogen bonds
/ Interfaces
/ Late blight
/ Ligands
/ Maximum likelihood method
/ Metabolites
/ oomycete pathogenesis
/ Pathogens
/ Phylogenetics
/ Physiological aspects
/ Physiology
/ Phytophthora infestans
/ Pleckstrin
/ pleckstrin homology domain
/ Protection and preservation
/ Proteins
/ Simulation
/ Virulence
2026
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Computational Modeling of Cellulose Synthase Heterotrimer Assembly and Identification of Antimicrobial Compounds Targeting Interface Sites in Phytophthora infestans
by
Amritha, V. S.
, Chellappan, Biju Vadakkemukadiyil
, El-Ganainy, Sherif Mohamed
, Almalki, Mohammed A.
, Shidhi, P. R.
in
AlphaFold-multimer
/ Analysis
/ Artificial intelligence
/ Biosynthesis
/ Cell walls
/ Cellulose
/ Cellulose synthase
/ cellulose synthases
/ Computer simulation
/ Computer-generated environments
/ Disease control
/ Geometry
/ Glycosyltransferase
/ glycosyltransferase family 2
/ Homology
/ Hydrogen bonds
/ Interfaces
/ Late blight
/ Ligands
/ Maximum likelihood method
/ Metabolites
/ oomycete pathogenesis
/ Pathogens
/ Phylogenetics
/ Physiological aspects
/ Physiology
/ Phytophthora infestans
/ Pleckstrin
/ pleckstrin homology domain
/ Protection and preservation
/ Proteins
/ Simulation
/ Virulence
2026
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Computational Modeling of Cellulose Synthase Heterotrimer Assembly and Identification of Antimicrobial Compounds Targeting Interface Sites in Phytophthora infestans
Journal Article
Computational Modeling of Cellulose Synthase Heterotrimer Assembly and Identification of Antimicrobial Compounds Targeting Interface Sites in Phytophthora infestans
2026
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Overview
Phytophthora infestans, a devastating oomycete pathogen responsible for late blight in solanaceous crops, relies on cellulose synthase (CesA) complexes for cell wall biosynthesis and virulence. Unlike plant CesAs that form homomeric trimers, oomycete CesA complexes are hypothesized to assemble as heteromeric units, yet their structural organization remains poorly defined. Here, we employed AlphaFold-Multimer and molecular docking to resolve the structural assembly of the PiCesA1–PiCesA2–PiCesA4 heterotrimer in P. infestans and identify potential ligand-binding sites for targeted inhibition. Structural modeling revealed a conserved transmembrane architecture combined with a distinctive cytosolic organization, in which N-terminal pleckstrin homology domains play a central role in heteromeric assembly. AlphaFold-Multimer consistently predicted a stable heterotrimer stabilized by cyclic interactions between pleckstrin homology domains and glycosyltransferase-A domains, forming an extensive interface network that is spatially segregated from the conserved UDP-glucose–binding catalytic core. Structure-guided docking identified potential ligands targeting pleckstrin homology–glycosyltransferase interface regions. Notably, these sites are absent or structurally divergent in plant cellulose synthases, underscoring their potential for pathogen-selective targeting. This work advances mechanistic understanding of cellulose biosynthesis in filamentous pathogens and proposes new avenues for selective disease control in agriculture.
Publisher
MDPI AG,Multidisciplinary Digital Publishing Institute (MDPI)
Subject
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