8YSS
Crystal structure of the apo form of Deinococcus wulumuqiensis CD-NTase DwCdnB
Summary for 8YSS
Entry DOI | 10.2210/pdb8yss/pdb |
Descriptor | Nucleotidyltransferase (2 entities in total) |
Functional Keywords | cd-ntase, transferase |
Biological source | Deinococcus wulumuqiensis |
Total number of polymer chains | 1 |
Total formula weight | 39499.29 |
Authors | |
Primary citation | Yang, C.S.,Shie, M.Y.,Huang, S.W.,Wang, Y.C.,Hou, M.H.,Chen, C.J.,Chen, Y. Structural insights into signaling promiscuity of the CBASS anti-phage defense system from a radiation-resistant bacterium. Int.J.Biol.Macromol., 295:139534-139534, 2025 Cited by PubMed Abstract: Radiation-resistant bacteria are of great application potential in various fields, including bioindustry and bioremediation of radioactive waste. However, how radiation-resistant bacteria combat against invading phages is seldom addressed. Here, we present a series of crystal structures of a sensor and an effector of the cyclic oligonucleotide-based anti-phage signaling system (CBASS) from a radioresistant bacterium Deinococcus wulumuqiensis. We found that the sensor CD-NTase enzyme, DwCdnB, can bind all four ribonucleotides and synthesize a variety of cyclic di-nucleotides, including the novel second messenger 3'3'-cyclic di-CMP. Crystal structures of DwCdnB in complex with ATP and dATP provide structural explanations for specific recognition of ribonucleotides via metal coordination with ribose 2'-OH. Crystal structures of DwCdnB in complex with purine and/or pyrimidine nucleotides in the presence of Mg revealed similar binding modes; however, in the presence of Mn, the UTP/CTP rotates and flips into the donor pocket and make extensive contacts with additional five residues, suggesting essential role of Mn for catalytic production of cyclic di-pyrimidines. Finally, structural analysis of the downstream effector DwCap5 further provides a structural explanation for its non-specific recognition of a broad range of cyclic di-nucleotides. In sum, this work provides key structural insights into the immune mechanisms of radioresistant bacteria. PubMed: 39761885DOI: 10.1016/j.ijbiomac.2025.139534 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.83 Å) |
Structure validation
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