Soriano Erika V, Clark Valerie C, Ealick Steven E
Department of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14853-1301, USA.
Acta Crystallogr D Biol Crystallogr. 2007 Dec;63(Pt 12):1201-7. doi: 10.1107/S0907444907048834. Epub 2007 Nov 16.
Human deoxycytidine kinase (dCK) is involved in the nucleotide-biosynthesis salvage pathway and has also been shown to phosphorylate several antitumor and antiviral prodrugs. The structures of dCK alone and the dead-end complex of dCK with substrate nucleoside and product ADP or UDP have previously been reported; however, there is currently no structure available for a substrate or product complex. Here, the structures of dCK complexes with the products dCMP, UDP and Mg2+ ion, and with dAMP, UDP and Mg2+ ion are reported. Structural comparisons show that the product complexes with UDP and a dead-end complex with substrate and UDP have similar active-site conformations.
人类脱氧胞苷激酶(dCK)参与核苷酸生物合成的补救途径,并且已被证明能磷酸化多种抗肿瘤和抗病毒前药。此前已报道了单独的dCK结构以及dCK与底物核苷和产物ADP或UDP形成的终止复合物的结构;然而,目前尚无底物或产物复合物的结构。在此,报道了dCK与产物dCMP、UDP和Mg2+离子以及与dAMP、UDP和Mg2+离子形成的复合物的结构。结构比较表明,与UDP形成的产物复合物以及与底物和UDP形成的终止复合物具有相似的活性位点构象。