9WLV
The Crystal Structure of Alpha-Beta-fold_hydrolase from Microlunatus sagamiharensis.
This is a non-PDB format compatible entry.
Summary for 9WLV
| Entry DOI | 10.2210/pdb9wlv/pdb |
| Descriptor | Pimeloyl-ACP methyl ester carboxylesterase, SULFATE ION, CHLORIDE ION, ... (7 entities in total) |
| Functional Keywords | hydrolase |
| Biological source | Microlunatus sagamiharensis |
| Total number of polymer chains | 2 |
| Total formula weight | 61794.74 |
| Authors | |
| Primary citation | Wang, Q.,Ye, Y.,Wang, L.,Guan, Y.,Wang, S.,Wang, Z.,Sun, H.,Smith, S.M.,Huang, J. Independent horizontal transfer of genes encoding alpha / beta-hydrolases with strigolactone binding and hydrolytic activities from bacteria to fungi and plants. Mol Plant, 18:1949-1961, 2025 Cited by PubMed Abstract: Strigolactones (SLs) are not only phytohormones that influence multiple aspects of plant growth and development but also signaling molecules for interactions between plants and certain fungi or bacteria. In plants, the SL receptor is an α/β-hydrolase (ABH) encoded by the DWARF14 (D14)/KARRIKIN INSENSITIVE2 (KAI2) gene family, which is known to be derived from proteobacterial RsbQ through horizontal gene transfer (HGT). In the phytopathogenic fungus Cryphonectria parasitica, another ABH named CpD14 was found to possess SL binding and hydrolytic activities and mediate SL responses, exhibiting potential SL perception functions. Here, we demonstrate that CpD14 and its homologs in Leotiomyceta fungi were derived from Actinobacteria through an independent HGT event, forming a distinct CpD14-like (CDL) family across fungi and bacteria. X-ray crystallography and structural analyses reveal that actinobacterial and fungal CDL proteins share a conserved core "α/β fold" domain with D14/KAI2/RsbQ but possess a unique lid domain. Biochemical assays show that both actinobacterial CDL and proteobacterial RsbQ can recognize and hydrolyze SLs, suggesting that they are pre-adapted for SL responses and potential perception. Both plant D14/KAI2 and fungal CDL proteins retained these functional activities, whereas they evolved distinct ligand specificities for SL structural variants. Collectively, this work reveals that independent HGT events from two bacterial groups provided plants and their interacting fungi with pre-adapted ABH proteins, which were deployed for SL perception or responses. PubMed: 41039777DOI: 10.1016/j.molp.2025.09.021 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.9 Å) |
Structure validation
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