Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1317554 | Journal of Inorganic Biochemistry | 2013 | 9 Pages |
Abstract
The density functional calculations suggest that the Y1139 residue of methionine synthase (MetH) enzyme forms a stronger Co(I)H interaction than the β-axial H2O ligand. The analysis of the X-ray crystallographic data also indicates that the Y1139 residue in the MetH-bound cobalamin may be the actual β-axial ligand rather than the H2O.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Manoj Kumar, Pawel M. Kozlowski,