4ASL
Structure of Epa1A in complex with the T-antigen (Gal-b1-3- GalNAc)
Summary for 4ASL
| Entry DOI | 10.2210/pdb4asl/pdb |
| Related | 4A3X 4AF9 4AFA 4AFB 4AFC |
| Descriptor | EPA1P, beta-D-galactopyranose-(1-3)-2-acetamido-2-deoxy-beta-D-galactopyranose, CALCIUM ION, ... (6 entities in total) |
| Functional Keywords | cell adhesion, lectin, tissue invasion, pathogenicity |
| Biological source | CANDIDA GLABRATA |
| Total number of polymer chains | 1 |
| Total formula weight | 29883.86 |
| 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: 2012-05-02, release date: 2012-10-17, Last modification date: 2024-11-06) |
| Primary citation | Maestre-Reyna, M.,Diderrich, R.,Veelders, M.S.,Eulenburg, G.,Kalugin, V.,Bruckner, S.,Keller, P.,Rupp, S.,Mosch, H.,Essen, L.-O. 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: 23035251DOI: 10.1073/PNAS.1207653109 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.24 Å) |
Structure validation
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