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Journal ArticleDOI

Structural and Functional Aspects of Metal Sites in Biology

TLDR
A protein-bound metal site consists of one or more metal ions and all protein side chain and exogenous bridging and terminal ligands that define the first coordination sphere of each metal ion as discussed by the authors.
Abstract
For present purposes, a protein-bound metal site consists of one or more metal ions and all protein side chain and exogenous bridging and terminal ligands that define the first coordination sphere of each metal ion. Such sites can be classified into five basic types with the indicated functions: (1) structural -- configuration (in part) of protein tertiary and/or quaternary structure; (2) storage -- uptake, binding, and release of metals in soluble form: (3) electron transfer -- uptake, release, and storage of electrons; (4) dioxygen binding -- metal-O{sub 2} coordination and decoordination; and (5) catalytic -- substrate binding, activation, and turnover. The authors present here a classification and structure/function analysis of native metal sites based on these functions, where 5 is an extensive class subdivided by the type of reaction catalyzed. Within this purview, coverage of the various site types is extensive, but not exhaustive. The purpose of this exposition is to present examples of all types of sites and to relate, insofar as is currently feasible, the structure and function of selected types. The authors largely confine their considerations to the sites themselves, with due recognition that these site features are coupled to protein structure at all levels. In themore » next section, the coordination chemistry of metalloprotein sites and the unique properties of a protein as a ligand are briefly summarized. Structure/function relationships are systematically explored and tabulations of structurally defined sites presented. Finally, future directions in bioinorganic research in the context of metal site chemistry are considered. 620 refs.« less

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Versatility of biological non-heme Fe(II) centers in oxygen activation reactions

TL;DR: Data from several studies are presented showing that reductive O2 activation within this family is initiated by substrate (and in some cases cosubstrate or cofactor) binding, which then allows coordination of O2 to the metal.
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The structural biochemistry of the superoxide dismutases

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Nickel superoxide dismutase structure and mechanism.

TL;DR: The 1.30 A resolution crystal structure of nickel superoxide dismutase (NiSOD) identifies a novel SOD fold, assembly, and Ni active site that provides almost all interactions critical for metal binding and catalysis, and thus will likely be diagnostic of NiSODs.
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Biosensors Based on Two-Dimensional MoS2

TL;DR: In this article, the current progress on 2D MoS2 based biosensors is presented and the prospects for future possibilities of expanding its applications for a variety of biosensing applications are discussed.
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Hydrolytic catalysis and structural stabilization in a designed metalloprotein

TL;DR: The kinetic and structural analysis of this first de novo designed hydrolytic metalloenzyme uncovers necessary design features for future meetalloenzymes containing one or more metals.
References
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Journal ArticleDOI

Structural and Functional Aspects of Metal Sites in Biology

TL;DR: The authors present here a classification and structure/function analysis of native metal sites based on these functions, and the coordination chemistry of metalloprotein sites and the unique properties of a protein as a ligand are briefly summarized.
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