Abstract
Background: Fungal tyrosinase maturation involves multiple processes of the dinuclear copper assembly and proteolytic activation. Results: Structural examinations and mutational studies of the pro-tyrosinases revealed that three endogenous cysteines contribute to the copper incorporation. Conclusion: The three highly flexible cysteines are essential for assembly of the active site across the protein shell. Significance: Elucidation of such a copper incorporation process provides useful insights into metal homeostasis.
| Original language | English |
|---|---|
| Pages (from-to) | 22128-22140 |
| Number of pages | 13 |
| Journal | Journal of Biological Chemistry |
| Volume | 288 |
| Issue number | 30 |
| DOIs | |
| Publication status | Published - 2013 Jul 26 |
| Externally published | Yes |
ASJC Scopus subject areas
- Biochemistry
- Molecular Biology
- Cell Biology
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