7X4T
LpCdnE UMPNPP Mg complex
Summary for 7X4T
Entry DOI | 10.2210/pdb7x4t/pdb |
Related | 7X4A 7X4C 7X4F 7X4G 7X4P 7X4Q |
Descriptor | Cyclic dipyrimidine nucleotide synthase, 5'-O-[(S)-hydroxy{[(S)-hydroxy(phosphonooxy)phosphoryl]amino}phosphoryl]uridine, MAGNESIUM ION, ... (6 entities in total) |
Functional Keywords | cd-ntase, cgas, cyclic dinucleotide, complex, substrate analogue, transferase |
Biological source | Legionella pneumophila |
Total number of polymer chains | 2 |
Total formula weight | 72260.69 |
Authors | Chen, Y.,Ko, T.P.,Yang, C.S.,Wang, Y.C.,Hou, M.H. (deposition date: 2022-03-03, release date: 2023-03-08, Last modification date: 2023-11-29) |
Primary citation | Yang, C.S.,Ko, T.P.,Chen, C.J.,Hou, M.H.,Wang, Y.C.,Chen, Y. Crystal structure and functional implications of cyclic di-pyrimidine-synthesizing cGAS/DncV-like nucleotidyltransferases. Nat Commun, 14:5078-5078, 2023 Cited by PubMed Abstract: Purine-containing nucleotide second messengers regulate diverse cellular activities. Cyclic di-pyrimidines mediate anti-phage functions in bacteria; however, the synthesis mechanism remains elusive. Here, we determine the high-resolution structures of cyclic di-pyrimidine-synthesizing cGAS/DncV-like nucleotidyltransferases (CD-NTases) in clade E (CdnE) in its apo, substrate-, and intermediate-bound states. A conserved (R/Q)xW motif controlling the pyrimidine specificity of donor nucleotide is identified. Mutation of Trp or Arg from the (R/Q)xW motif to Ala rewires its specificity to purine nucleotides, producing mixed purine-pyrimidine cyclic dinucleotides (CDNs). Preferential binding of uracil over cytosine bases explains the product specificity of cyclic di-pyrimidine-synthesizing CdnE to cyclic di-UMP (cUU). Based on the intermediate-bound structures, a synthetic pathway for cUU containing a unique 2'3'-phosphodiester linkage through intermediate pppU[3'-5']pU is deduced. Our results provide a framework for pyrimidine selection and establish the importance of conserved residues at the C-terminal loop for the specificity determination of CD-NTases. PubMed: 37604815DOI: 10.1038/s41467-023-40787-9 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.2 Å) |
Structure validation
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