Himo Fahmi, Guo Jing-Dong, Rinaldo-Matthis Agnes, Nordlund Pär
Theoretical Chemistry, Department of Biotechnology, Royal Institute of Technology, ALBANOVA, SE-106 91 Stockholm, Sweden.
J Phys Chem B. 2005 Oct 27;109(42):20004-8. doi: 10.1021/jp0546150.
The reaction mechanism of human deoxyribonucleotidase (dN) is studied using high-level quantum-chemical methods. dN catalyzes the dephosphorylation of deoxyribonucleoside monophosphates (dNMPs) to their nucleoside form in human cells. Large quantum models are employed (99 atoms) based on a recent X-ray crystal structure. The calculations support the proposed mechanism in which Asp41 performs a nucleophilic attack on the phosphate to form a phospho-enzyme intermediate. Asp43 acts in the first step as an acid, protonating the leaving nucleoside, and in the second step as a base, deprotonating the lytic water. No pentacoordinated intermediates could be located.
采用高级量子化学方法研究了人类脱氧核糖核苷酸酶(dN)的反应机制。dN在人体细胞中催化脱氧核糖核苷单磷酸(dNMPs)脱磷酸化为核苷形式。基于最近的X射线晶体结构构建了大型量子模型(99个原子)。计算结果支持了所提出的机制,即Asp41对磷酸进行亲核攻击以形成磷酶中间体。Asp43在第一步中作为酸,使离去的核苷质子化,在第二步中作为碱,使裂解水去质子化。未找到五配位中间体。