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肌醇多磷酸1-磷酸酶2.3埃分辨率的晶体结构。

Crystal structure of inositol polyphosphate 1-phosphatase at 2.3-A resolution.

作者信息

York J D, Ponder J W, Chen Z W, Mathews F S, Majerus P W

机构信息

Division of Hematology/Oncology, Washington University School of Medicine, St. Louis, Missouri 63110.

出版信息

Biochemistry. 1994 Nov 15;33(45):13164-71. doi: 10.1021/bi00249a002.

Abstract

Bovine inositol polyphosphate 1-phosphatase (1-ptase), M(r) = 44,000, is a Mg(2+)-dependent/Li(+)-sensitive enzyme that catalyzes the hydrolysis of the 1-position phosphate from inositol 1,4-bisphosphate and inositol 1,3,4-trisphosphate. We have determined the crystal structure of recombinant bovine 1-ptase in the presence of Mg2+ by multiple isomorphous replacement. The structure is currently refined to an R value of 0.198 for 15,563 reflections within a resolution range of 8.0-2.3 A. 1-Ptase is monomeric in the crystal, consistent with biochemical data, and folds into an alternatively layered alpha/beta/alpha/beta sandwich. The central core of 1-ptase consists of a six-stranded antiparallel beta sheet perpendicular to two parallel three-turn alpha-helices. The beta sheet is flanked by two antiparallel six-turn alpha-helices aligned parallel to the beta sheet, and the central helices are flanked by a five-stranded largely parallel beta sheet. Two neighboring metal binding sites are located in adjacent acidic pockets formed by the intersection of several secondary structure elements including an unusual kink structure formed by the "DPIDST" sequence motif. The fold of 1-ptase is similar to that of two other metal-dependent/Li(+)-sensitive phosphatases, inositol monophosphate phosphatase and fructose 1,6-bisphosphatase despite minimal amino acid identity. Comparison of the active-site pockets of these proteins will likely provide insight into substrate binding and the mechanisms of metal-dependent catalysis and Li+ inhibition.

摘要

牛肌醇多磷酸1-磷酸酶(1-磷酸酶),分子量为44,000,是一种依赖Mg(2+)且对Li(+)敏感的酶,可催化肌醇1,4-二磷酸和肌醇1,3,4-三磷酸1位磷酸的水解。我们通过多同晶置换法确定了重组牛1-磷酸酶在Mg2+存在下的晶体结构。目前该结构在8.0 - 2.3 Å分辨率范围内对15,563个反射的R值精修至0.198。1-磷酸酶在晶体中为单体,这与生化数据一致,其折叠成交替分层的α/β/α/β三明治结构。1-磷酸酶的中心核心由一个垂直于两个平行三圈α螺旋的六股反平行β折叠组成。β折叠两侧是两个与β折叠平行排列的反平行六圈α螺旋,中心螺旋两侧是一个五股大致平行的β折叠。两个相邻的金属结合位点位于由几个二级结构元件相交形成的相邻酸性口袋中,这些元件包括由“DPIDST”序列基序形成的不寻常扭结结构。尽管氨基酸一致性极低,但1-磷酸酶的折叠与另外两种依赖金属且对Li(+)敏感的磷酸酶——肌醇单磷酸磷酸酶和果糖1,6-二磷酸酶相似。比较这些蛋白质的活性位点口袋可能会为底物结合以及金属依赖催化和Li+抑制机制提供深入了解。

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