» Articles » PMID: 24850495

Analyses of Cobalt-ligand and Potassium-ligand Bond Lengths in Metalloproteins: Trends and Patterns

Overview
Journal J Mol Model
Publisher Springer
Specialty Molecular Biology
Date 2014 May 23
PMID 24850495
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Cobalt and potassium are biologically important metal elements that are present in a large array of proteins. Cobalt is mostly found in vivo associated with a corrin ring, which represents the core of the vitamin B12 molecule. Potassium is the most abundant metal in the cytosol, and it plays a crucial role in maintaining membrane potential as well as correct protein function. Here, we report a thorough analysis of the geometric properties of cobalt and potassium coordination spheres that was performed with high resolution on a representative set of structures from the Protein Data Bank and complemented by quantum mechanical calculations realized at the DFT level of theory (B3LYP/ SDD) on mononuclear model systems. The results allowed us to draw interesting conclusions on the structural characteristics of both Co and K centers, and to evaluate the importance of effects such as their association energies and intrinsic thermodynamic stabilities. Overall, the results obtained provide useful data for enhancing the atomic models normally applied in theoretical and computational studies of Co or K proteins performed at the quantum mechanical level, and for developing molecular mechanical parameters for treating Co or K coordination spheres in molecular mechanics or molecular dynamics studies.

Citing Articles

A database overview of metal-coordination distances in metalloproteins.

Bazayeva M, Andreini C, Rosato A Acta Crystallogr D Struct Biol. 2024; 80(Pt 5):362-376.

PMID: 38682667 PMC: 11066882. DOI: 10.1107/S2059798324003152.


Mechanisms for the synthesis of conjugated enynes from diphenylacetylene and trimethylsilylacetylene catalyzed by a nickel(0) complex: DFT study of ligand-controlled selectivity.

Huang C, He R, Shen W, Li M J Mol Model. 2015; 21(5):135.

PMID: 25935335 DOI: 10.1007/s00894-015-2672-7.

References
1.
Morgunova E, Meining W, Illarionov B, Haase I, Jin G, Bacher A . Crystal structure of lumazine synthase from Mycobacterium tuberculosis as a target for rational drug design: binding mode of a new class of purinetrione inhibitors. Biochemistry. 2005; 44(8):2746-58. DOI: 10.1021/bi047848a. View

2.
Liao R, Yu J, Himo F . Quantum Chemical Modeling of Enzymatic Reactions: The Case of Decarboxylation. J Chem Theory Comput. 2015; 7(5):1494-501. DOI: 10.1021/ct200031t. View

3.
Masuda J, Shibata N, Morimoto Y, Toraya T, Yasuoka N . How a protein generates a catalytic radical from coenzyme B(12): X-ray structure of a diol-dehydratase-adeninylpentylcobalamin complex. Structure. 2000; 8(7):775-88. DOI: 10.1016/s0969-2126(00)00164-7. View

4.
Berman H, Henrick K, Nakamura H, Markley J . The worldwide Protein Data Bank (wwPDB): ensuring a single, uniform archive of PDB data. Nucleic Acids Res. 2006; 35(Database issue):D301-3. PMC: 1669775. DOI: 10.1093/nar/gkl971. View

5.
Ramos M, Fernandes P . Computational enzymatic catalysis. Acc Chem Res. 2008; 41(6):689-98. DOI: 10.1021/ar7001045. View