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Structures of human cytosolic and mitochondrial nucleotidases: implications for structure-based design of selective inhibitors
P. Pachl, M. Fábry, I. Rosenberg, O. Simák, P. Rezáčová, J. Brynda,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Cytosol chemistry enzymology MeSH
- Deoxyribonucleotides chemistry MeSH
- Escherichia coli genetics metabolism MeSH
- Eukaryotic Cells chemistry enzymology MeSH
- Phosphates chemistry MeSH
- Enzyme Inhibitors chemistry MeSH
- Isoenzymes antagonists & inhibitors chemistry genetics MeSH
- Catalytic Domain MeSH
- Protein Conformation MeSH
- Crystallography, X-Ray MeSH
- Humans MeSH
- Mitochondria chemistry enzymology MeSH
- Models, Molecular MeSH
- Nucleotidases antagonists & inhibitors chemistry genetics MeSH
- Organophosphonates chemistry MeSH
- Organ Specificity MeSH
- Drug Design MeSH
- Recombinant Proteins chemistry genetics MeSH
- Molecular Docking Simulation MeSH
- Structure-Activity Relationship MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
The human 5'(3')-deoxyribonucleotidases catalyze the dephosphorylation of deoxyribonucleoside monophosphates to the corresponding deoxyribonucleosides and thus help to maintain the balance between pools of nucleosides and nucleotides. Here, the structures of human cytosolic deoxyribonucleotidase (cdN) at atomic resolution (1.08 Å) and mitochondrial deoxyribonucleotidase (mdN) at near-atomic resolution (1.4 Å) are reported. The attainment of an atomic resolution structure allowed interatomic distances to be used to assess the probable protonation state of the phosphate anion and the side chains in the enzyme active site. A detailed comparison of the cdN and mdN active sites allowed the design of a cdN-specific inhibitor.
References provided by Crossref.org
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