7ZOB
Metagenomic cytidine deaminase Cdd
Summary for 7ZOB
Entry DOI | 10.2210/pdb7zob/pdb |
Descriptor | Metagenomic cytidine deaminase Cdd, ZINC ION, (4S)-2-METHYL-2,4-PENTANEDIOL, ... (5 entities in total) |
Functional Keywords | hydrolase |
Biological source | uncultured bacterium |
Total number of polymer chains | 8 |
Total formula weight | 125671.73 |
Authors | Tamulaitiene, G.,Urbeliene, N.,Meskys, R. (deposition date: 2022-04-25, release date: 2023-02-01, Last modification date: 2024-02-07) |
Primary citation | Urbeliene, N.,Tiskus, M.,Tamulaitiene, G.,Gasparaviciute, R.,Lapinskaite, R.,Jauniskis, V.,Sudzius, J.,Meskiene, R.,Tauraite, D.,Skrodenyte, E.,Urbelis, G.,Vaitekunas, J.,Meskys, R. Cytidine deaminases catalyze the conversion of N ( S , O ) 4 -substituted pyrimidine nucleosides. Sci Adv, 9:eade4361-eade4361, 2023 Cited by PubMed Abstract: Cytidine deaminases (CDAs) catalyze the hydrolytic deamination of cytidine and 2'-deoxycytidine to uridine and 2'-deoxyuridine. Here, we report that prokaryotic homo-tetrameric CDAs catalyze the nucleophilic substitution at the fourth position of -acyl-cytidines, -alkyl-cytidines, and -alkyloxycarbonyl-cytidines, and -alkylthio-uridines and -alkyl-uridines, converting them to uridine and corresponding amide, amine, carbamate, thiol, or alcohol as leaving groups. The x-ray structure of a metagenomic CDA_F14 and the molecular modeling of the CDAs used in this study show a relationship between the bulkiness of a leaving group and the volume of the binding pocket, which is partly determined by the flexible β3α3 loop of CDAs. We propose that CDAs that are active toward a wide range of substrates participate in salvage and/or catabolism of variously modified pyrimidine nucleosides. This identified promiscuity of CDAs expands the knowledge about the cellular turnover of cytidine derivatives, including the pharmacokinetics of pyrimidine-based prodrugs. PubMed: 36735785DOI: 10.1126/sciadv.ade4361 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.2 Å) |
Structure validation
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