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4AF9

Crystal Structure of Epithelial Adhesin 1 A domain (Epa1A) from Candida glabrata in complex with Galb1-3Glc

Summary for 4AF9
Entry DOI10.2210/pdb4af9/pdb
Related4A3X 4AFA 4AFB 4AFC 4ASL
DescriptorEPA1P, beta-D-galactopyranose-(1-3)-beta-D-glucopyranose, CALCIUM ION, ... (6 entities in total)
Functional Keywordscell adhesion, lectin, tissue invasion, pathogenicity
Biological sourceCANDIDA GLABRATA
Total number of polymer chains1
Total formula weight30201.40
Authors
Maestre-Reyna, M.,Diderrich, R.,Veelders, M.S.,Eulenburg, G.,Kalugin, V.,Brueckner, S.,Keller, P.,Rupp, S.,Moesch, H.-U.,Essen, L.-O. (deposition date: 2012-01-18, release date: 2012-10-17, Last modification date: 2024-10-09)
Primary citationMaestre-Reyna, M.,Diderrich, R.,Veelders, M.S.,Eulenburg, G.,Kalugin, V.,Bruckner, S.,Keller, P.,Rupp, S.,Mosch, H.,Essen, L.
Structural Basis for Promiscuity and Specificity During Candida Glabrata Invasion of Host Epithelia.
Proc.Natl.Acad.Sci.USA, 109:16864-, 2012
Cited by
PubMed Abstract: The human pathogenic yeast Candida glabrata harbors more than 20 surface-exposed, epithelial adhesins (Epas) for host cell adhesion. The Epa family recognizes host glycans and discriminates between target tissues by their adhesin (A) domains, but a detailed structural basis for ligand-binding specificity of Epa proteins has been lacking so far. In this study, we provide high-resolution crystal structures of the Epa1A domain in complex with different carbohydrate ligands that reveal how host cell mucin-type O-glycans are recognized and allow a structure-guided classification of the Epa family into specific subtypes. Further detailed structural and functional characterization of subtype-switched Epa1 variants shows that specificity is governed by two inner loops, CBL1 and CBL2, involved in calcium binding as well as by three outer loops, L1, L2, and L3. In summary, our study provides the structural basis for promiscuity and specificity of Epa adhesins, which might further contribute to developing anti-adhesive antimycotics and combating Candida colonization.
PubMed: 23035251
DOI: 10.1073/PNAS.1207653109
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.5 Å)
Structure validation

237992

數據於2025-06-25公開中

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