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25QC

Crystal structure of Pseudomonas phage YuA Pplase2 in complex with 5hmdU-DNA and glycine

Summary for 25QC
Entry DOI10.2210/pdb25qc/pdb
DescriptorAmino acid:DNA transferase domain-containing protein, DNA (5'-D(P*CP*GP*AP*TP*(5HU)P*GP*CP*CP*CP*AP*TP*CP*G)-3'), octyl beta-D-glucopyranoside, ... (8 entities in total)
Functional Keywordscomplex. dna modification, thymine hypermodification, transferase
Biological sourcePseudomonas virus Yua
More
Total number of polymer chains2
Total formula weight38191.16
Authors
Li, W.,Zhao, S. (deposition date: 2026-04-14, release date: 2026-08-05, Last modification date: 2026-08-26)
Primary citationLi, W.,Chen, H.,Ma, H.,Pan, H.,Jia, Y.,He, P.,Zhao, S.
Discovery and biosynthesis of a novel diaminopropane-modified thymine in phage DNA.
Nucleic Acids Res., 54:-, 2026
Cited by
PubMed Abstract: Bacteriophage genomes exhibit exceptional diversity in nucleotide modifications, which primarily function to counteract host defense systems. However, the diversity of phage DNA hypermodifications remains largely unexplored in post genome era. Here, we discovered a novel thymine hypermodification, α-1,3-diaminopropanylthymine (α-dapT), in the Acinetobacter baumannii phage SH-Ab 15599, and elucidated its biosynthetic pathway, featuring the phage-encoded key diamine DNA transferase (DADT, formerly αGPT-Pplase2). DADT utilizes the metabolite 1,3-diaminopropane, which is the major polyamine in the host to modify phage DNA. DADT exhibits broad in vitro substrate specificity but a strong in vivo preference for 1,3-diaminopropane. Structural and mutagenesis analyses revealed the molecular basis for substrate recognition and catalysis. The α-dapT modification occurs preferentially at TG dinucleotides and confers resistance to multiple host restriction enzymes. Furthermore, RNA-seq analysis showed that phage infection upregulates genes for 1,3-diaminopropane synthesis, and downregulates genes for 1,3-diaminoproprane consumption to supply the modification precursor. Given that 1,3-diaminopropane functions as a key regulator in mobility of A. baumannii, its metabolic reprograming may impair host biofilm formation.
PubMed: 42578370
DOI: 10.1093/nar/gkag763
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.2 Å)
Structure validation

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