首页> 外文期刊>Journal of Inorganic Biochemistry: An Interdisciplinary Journal >A chemical approach to systematically designate the pyranopterin centersof molybdenum and tungsten enzymes and synthetic models
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A chemical approach to systematically designate the pyranopterin centersof molybdenum and tungsten enzymes and synthetic models

机译:一种化学方法,系统地指定钼和钨酶的吡opter呤中心和合成模型

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The recent growth in the chemistry of the oxo-molybdenum enzymes has demonstrated the need for developing systematic methods for naming and abbreviating the novel pterin cofactors that bind to the metal ion via the sulfur atoms of an ene-1,2-dithiolate moiety. Historically, the term "molybdopterin" was coined to designate a special pterin that binds molybdenum and the molybdenum-bound form was termed the "molybdenum cofactor". However, recent studies have demonstrated that this novel pterin also binds tungsten. Furthermore, considerable variation has been found in the pterin entity itself. Taken together, these facts show that molybdenum- and tungsten-containing enzymes possess a family of cofactors rather than a single "molybdenum cofactor". This article proposes a unified methodology for describing these cofactors and their metal-free pterin units in light of recent results from protein crystallography. The various numbering schemes that have been used for this heterocycle are considered, as well as the IUPAC rules which are currently being used for related tricyclic compounds. A unified methodology for uniquely designating and abbreviating each cofactor is proposed. The available chemical and spectroscopic information on the pyranopterin entities that are present in the molybdenum and tungsten enzymes, the precursors to these centers, and synthetic pyranopterins are in part the basis of the systematic names and simplifying abbreviations.
机译:氧-钼酶化学的最新发展表明,需要开发系统的方法来命名和缩写新颖的蝶呤辅因子,该新的蝶呤辅因子通过ene-1,2-二硫代硫酸盐部分的硫原子与金属离子结合。历史上,术语“钼蝶呤”被创造来表示结合钼的特殊蝶呤,并且与钼结合的形式被称为“钼辅因子”。然而,最近的研究表明,这种新型的蝶呤也结合钨。此外,在蝶呤实体本身中发现了相当大的变化。综上所述,这些事实表明,含钼和钨的酶具有一族辅因子,而不是单一的“钼辅因子”。本文提出了一种统一的方法,用于根据蛋白质晶体学的最新结果来描述这些辅因子及其不含金属的蝶呤单元。考虑了已用于该杂环的各种编号方案,以及目前用于相关三环化合物的IUPAC规则。提出了用于唯一指定和缩写每个辅因子的统一方法。有关存在于钼和钨酶中的吡喃蝶呤实体,这些中心的前体以及合成吡喃蝶呤的可用化学和光谱信息,部分是系统名称和简化缩写的基础。

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