Enzymes
| UniProtKB help_outline | 1 proteins |
Reaction participants Show >> << Hide
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Namehelp_outline
5-phosphomethyl-dUMP in DNA
Identifier
RHEA-COMP:18039
Reactive part
help_outline
- Name help_outline 5-phosphomethyl-dUMP residue Identifier CHEBI:190918 Charge -3 Formula C10H11N2O11P2 SMILEShelp_outline C1=C(COP(=O)([O-])[O-])C(NC(N1[C@@H]2O[C@H](COP(=O)([O-])*)[C@H](C2)O*)=O)=O 2D coordinates Mol file for the small molecule Search links Involved in 4 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline L-serine Identifier CHEBI:33384 Charge 0 Formula C3H7NO3 InChIKeyhelp_outline MTCFGRXMJLQNBG-REOHCLBHSA-N SMILEShelp_outline [NH3+][C@@H](CO)C([O-])=O 2D coordinates Mol file for the small molecule Search links Involved in 85 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
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Namehelp_outline
5-O-(L-seryl)-dTMP in DNA
Identifier
RHEA-COMP:18046
Reactive part
help_outline
- Name help_outline 5-O-(L-seryl)-dTMP residue Identifier CHEBI:190922 Charge -1 Formula C13H17N3O10P SMILEShelp_outline C1=C(COC[C@@H](C([O-])=O)[NH3+])C(NC(N1[C@@H]2O[C@H](COP(=O)([O-])*)[C@H](C2)O*)=O)=O 2D coordinates Mol file for the small molecule Search links Involved in 2 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline phosphate Identifier CHEBI:43474 Charge -2 Formula HO4P InChIKeyhelp_outline NBIIXXVUZAFLBC-UHFFFAOYSA-L SMILEShelp_outline OP([O-])([O-])=O 2D coordinates Mol file for the small molecule Search links Involved in 1,041 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
Cross-references
| RHEA:71567 | RHEA:71568 | RHEA:71569 | RHEA:71570 | |
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| Reaction direction help_outline | undefined | left-to-right | right-to-left | bidirectional |
| UniProtKB help_outline |
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Publications
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Pathways of thymidine hypermodification.
Lee Y.J., Dai N., Mueller S.I., Guan C., Parker M.J., Fraser M.E., Walsh S.E., Sridar J., Mulholland A., Nayak K., Sun Z., Lin Y.C., Comb D.G., Marks K., Gonzalez R., Dowling D.P., Bandarian V., Saleh L., Correa I.R., Weigele P.R.
The DNAs of bacterial viruses are known to contain diverse, chemically complex modifications to thymidine that protect them from the endonuclease-based defenses of their cellular hosts, but whose biosynthetic origins are enigmatic. Up to half of thymidines in the Pseudomonas phage M6, the Salmonel ... >> More
The DNAs of bacterial viruses are known to contain diverse, chemically complex modifications to thymidine that protect them from the endonuclease-based defenses of their cellular hosts, but whose biosynthetic origins are enigmatic. Up to half of thymidines in the Pseudomonas phage M6, the Salmonella phage ViI, and others, contain exotic chemical moieties synthesized through the post-replicative modification of 5-hydroxymethyluridine (5-hmdU). We have determined that these thymidine hypermodifications are derived from free amino acids enzymatically installed on 5-hmdU. These appended amino acids are further sculpted by various enzyme classes such as radical SAM isomerases, PLP-dependent decarboxylases, flavin-dependent lyases and acetyltransferases. The combinatorial permutations of thymidine hypermodification genes found in viral metagenomes from geographically widespread sources suggests an untapped reservoir of chemical diversity in DNA hypermodifications. << Less
Nucleic Acids Res. 0:0-0(2021) [PubMed] [EuropePMC]
This publication is cited by 8 other entries.