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大肠杆菌Nudix水解酶二氢新蝶呤三磷酸焦磷酸酶中的金属离子配位:催化机制的新线索

Metal ion coordination in the E. coli Nudix hydrolase dihydroneopterin triphosphate pyrophosphatase: New clues into catalytic mechanism.

作者信息

Hill Shannon E, Nguyen Elaine, Ukachukwu Chiamaka U, Freeman Dana M, Quirk Stephen, Lieberman Raquel L

机构信息

School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Georgia, United States of America.

Kimberly-Clark Corporation, Roswell, Georgia, United States of America.

出版信息

PLoS One. 2017 Jul 25;12(7):e0180241. doi: 10.1371/journal.pone.0180241. eCollection 2017.

Abstract

Dihydroneopterin triphosphate pyrophosphatase (DHNTPase), a member of the Mg2+ dependent Nudix hydrolase superfamily, is the recently-discovered enzyme that functions in the second step of the pterin branch of the folate biosynthetic pathway in E. coli. DHNTPase is of interest because inhibition of enzymes in bacterial folate biosynthetic pathways is a strategy for antibiotic development. We determined crystal structures of DHNTPase with and without activating, Mg2+-mimicking metals Co2+ and Ni2+. Four metal ions, identified by anomalous scattering, and stoichiometrically confirmed in solution by isothermal titration calorimetry, are held in place by Glu56 and Glu60 within the Nudix sequence motif, Glu117, waters, and a sulfate ion, of which the latter is further stabilized by a salt bridge with Lys7. In silico docking of the DHNTP substrate reveals a binding mode in which the pterin ring moiety is nestled in a largely hydrophobic pocket, the β-phosphate activated for nucleophilic attack overlays with the crystallographic sulfate and is in line with an activated water molecule, and remaining phosphate groups are stabilized by all four identified metal ions. The structures and binding data provide new details regarding DHNTPase metal requirements, mechanism, and suggest a strategy for efficient inhibition.

摘要

二氢新蝶呤三磷酸焦磷酸酶(DHNTPase)是Mg2+依赖性Nudix水解酶超家族的成员,是最近发现的一种在大肠杆菌叶酸生物合成途径的蝶呤分支第二步中发挥作用的酶。DHNTPase之所以受到关注,是因为抑制细菌叶酸生物合成途径中的酶是一种抗生素开发策略。我们确定了含有和不含有激活的、模拟Mg2+的金属Co2+和Ni2+的DHNTPase的晶体结构。通过反常散射鉴定并通过等温滴定量热法在溶液中进行化学计量学确认的四个金属离子,由Nudix序列基序中的Glu56和Glu60、Glu117、水分子和一个硫酸根离子固定在适当位置,其中后者通过与Lys7的盐桥进一步稳定。DHNTP底物的计算机对接揭示了一种结合模式,其中蝶呤环部分嵌套在一个主要为疏水的口袋中,被激活用于亲核攻击的β-磷酸与晶体学硫酸根重叠并与一个激活的水分子对齐,其余磷酸基团由所有四个鉴定出的金属离子稳定。这些结构和结合数据提供了关于DHNTPase金属需求、机制的新细节,并提出了一种有效抑制的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5aa/5526541/e2e70617cd9d/pone.0180241.g001.jpg

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