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Cornell, W., Cieplak, B., Bayly, C., Gould, I., Merz, K., Ferguson, D., Spellmeyer, D, Fox, T., Caldwell, J. and Kollman, P. (1995) A Second Generation Force-Field for the Simulation of Proteins, Nucleic-Acids, and Organic Molecules. Journal of the American Chemical Society, 117, 5179-5197.
https://doi.org/10.1021/ja00124a002
has been cited by the following article:
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TITLE:
Comparative Study of the Chemical Reactivity of Helical Peptide Models for Protein Glycation
AUTHORS:
Juan Frau, Daniel Glossman-Mitnik
KEYWORDS:
Helical Model peptides, Protein Glycation, Computational Chemistry, Molecular Modeling, Conceptual DFT, Chemical Reactivity Theory
JOURNAL NAME:
Computational Chemistry,
Vol.5 No.2,
April
28,
2017
ABSTRACT: Non-enzymatic glycation of proteins has been implicated as an important cause of the complications associated with diabetes and Alzheimer disease. It is well known that glycation involves the reactivity of, primarily, the ε-amino group of the lysines present in the protein. The immediate chemical environment of an amino group modulates the glycation reaction. In this work, several model helical peptides for protein glycation has been studied by resorting to QM:MM calculations through the ONIOM methodology. Some Conceptual DFT descriptors have been calculated that allowed the comparison of the chemical reactivity between the different model peptides in terms of the position of the Lys group and other spatially proximate amino acid residues.
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