4FYK
Crystal structure of rcl with 5'-phiosphorothioate-adenosine
Summary for 4FYK
| Entry DOI | 10.2210/pdb4fyk/pdb |
| Related | 4FYH 4FYI |
| Descriptor | Deoxyribonucleoside 5'-monophosphate N-glycosidase, ADENOSINE -5'-THIO-MONOPHOSPHATE, SULFATE ION, ... (4 entities in total) |
| Functional Keywords | deoxyribonucleoside 5'-monophosphate n-glycosidase, hydrolase |
| Biological source | Rattus norvegicus (brown rat,rat,rats) |
| Cellular location | Cytoplasm : O35820 |
| Total number of polymer chains | 4 |
| Total formula weight | 70434.67 |
| Authors | Labesse, G.,Padilla, A.,Kaminski, P.A. (deposition date: 2012-07-04, release date: 2013-01-02, Last modification date: 2024-02-28) |
| Primary citation | Padilla, A.,Amiable, C.,Pochet, S.,Kaminski, P.A.,Labesse, G. Structure of the oncoprotein Rcl bound to three nucleotide analogues. Acta Crystallogr.,Sect.D, 69:247-255, 2013 Cited by PubMed Abstract: Rcl is a novel N-glycoside hydrolase found in mammals that shows specificity for the hydrolysis of 5'-monophosphate nucleotides. Its role in nucleotide catabolism and the resulting production of 2-deoxyribose 5-phosphate has suggested that it might fuel cancer growth. Its expression is regulated by c-Myc, but its role as an oncoprotein remains to be clarified. In parallel, various nucleosides have been shown to acquire pro-apoptotic properties upon 5'-monophosphorylation in cells. These include triciribine, a tricyclic nucleoside analogue that is currently in clinical trials in combination with a farnesyltransferase inhibitor. Similarly, an N(6)-alkyl-AMP has been shown to be cytotoxic. Interestingly, Rcl has been shown to be inhibited by such compounds in vitro. In order to gain better insight into the precise ligand-recognition determinants, the crystallization of Rcl with these nucleotide analogues was attempted. The first crystal structure of Rcl was solved by molecular replacement using its NMR structure in combination with distantly related crystal structures. The structures of Rcl bound to two other nucleotides were then solved by molecular replacement using the previous crystal structure as a template. The resulting structures, solved at high resolution, led to a clear characterization of the protein-ligand interactions that will guide further rational drug design. PubMed: 23385460DOI: 10.1107/S0907444912045039 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.79 Å) |
Structure validation
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