脱氧胞苷激酶
前药
基质(水族馆)
化学
核苷酸
核苷
脱氧胞苷
核苷酸回收
激酶
核苷类似物
立体化学
生物化学
生物
吉西他滨
生态学
化疗
基因
遗传学
作者
Erika Soriano,Valerie C. Clark,S.E. Ealick
标识
DOI:10.1107/s0907444907048834
摘要
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.
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