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- W2084004489 abstract "Abstract Structural models for three alkaline conformers of yeast iso ‐1‐ferricytochrome c have been calculated from the atomic coordinates of the native protein through the use of molecular dynamics simulation. In the three models produced by this work, the Met80 axial ligand to the heme iron has been replaced by either Lys72, Lys73, or Lys79, and the related changes in structure of the cyto‐chrome are described. The principal changes in cytochrome structure predicted to result from this pH‐linked change in axial ligation involve location of residues 70–80, a region of the protein sequence that is phylogenetically conserved. The remainder of the protein fold in each model is essentially unchanged from the structure of the native protein, which is consistent with available spectroscopic information. The observation that this highly conserved region is apparently integrally involved in this conformational change may be interpreted as indicating a possible physiological role for the pH‐linkage of ferricytochrome c structure." @default.
- W2084004489 created "2016-06-24" @default.
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- W2084004489 date "2000-06-01" @default.
- W2084004489 modified "2023-09-23" @default.
- W2084004489 title "Structural models for the alkaline conformers of yeast<i>iso</i>-1-ferricytochrome<i>c</i>" @default.
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- W2084004489 doi "https://doi.org/10.1560/pk7u-lepj-etb5-997x" @default.
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