8YF3

DNA cytosine C5-carboxymethyltransferase in complex with Cx-SAM

Summary for 8YF3

• Entry DOI: 10.2210/pdb8yf3/pdb
• Descriptor: Cytosine-specific methyltransferase, (2S)-4-[{[(2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl}(carboxylatomethyl)sulfonio] -2-ammoniobutanoate (3 entities in total)
• Functional Keywords: dna cytosine-5-carboxymethyltransferase, carboxy-sam, transferase
• Biological source: Synechococcus phage S-B43
• Total number of polymer chains: 1
• Total formula weight: 41404.36

Authors

Yang, Q.,Zhang, Y. (deposition date: 2024-02-23, release date: 2025-09-03, Last modification date: 2026-03-18)

Primary citation

Yang, Q.,Zhang, L.,Liang, Y.,Ma, H.,Song, L.,Luo, L.,Tan, J.,Hu, Y.,Ma, K.,Chen, Y.,Tong, Y.,Zhang, C.,Zhao, S.,Wang, M.,Zhang, L.,Wei, Y.,Zhang, Y.
Carboxymethylcytosine is a natural base modification and a handle for bacteriophage DNA hypermodification.
Nat Commun, 17:281-281, 2025

PubMed Abstract: Bacteriophages possess a wide array of DNA modifications, with many acting as molecular camouflage to evade host immune defenses. Sequence databases contain numerous bacteriophage enzymes of unknown function, with some potentially involved in yet to be identified DNA modifications. Here we report the discovery of a DNA cytosine C5-carboxymethyltransferase (CmoX) in Synechococcus phage S-B43, which catalyzes the formation of a 5-carboxymethylcytosine (5cxmC), previously reported as an unnatural DNA modification formed by an engineered cytosine methyltransferase. The carboxy-S-adenosyl-L-methionine (Cx-SAM) cofactor required by CmoX is provided by a phage-encoded Cx-SAM synthase (CmoA), a homolog of the bacterial CmoA involved in tRNA modification. A crystal structure of CmoX in complex with Cx-SAM revealed the basis for its substrate selectivity, involving a key Arg residue interacting with the substrate carboxy group. In addition, we characterize a phage-encoded ATP-dependent amide ligase, CmoY that catalyzes the formation of 5cxmC-glycine amide. CmoA is present in many bacteriophage genomes, typically alongside CmoX and homologs of CmoY, suggesting that 5cxmC modification is a widespread naturally occurring DNA modification serving as a handle for further hypermodifications in bacteriophages. Our study underscores the ability of bacteriophages to repurpose RNA modification enzymes to expand their repertoire of DNA modifications.

PubMed: 41354841
DOI: 10.1038/s41467-025-66999-9

Experimental method

X-RAY DIFFRACTION (1.9 Å)