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Literature summary for 7.2.2.8 extracted from
- The Structure of metal binding domain 1 of the copper transporter ATP7B reveals mechanism of a singular Wilson disease mutation (2018), Sci. Rep., 8, 581 .
Crystallization (Commentary)
| Crystallization (Comment) | Organism |
|---|---|
| NMR structure of metal-binding domain MBD1, shows the characteristic beta,alpha,beta,beta,alpha,beta ferredoxin fold. The copper binding motif CxxC appears to experience complex dynamics | Homo sapiens |
Protein Variants
| Protein Variants | Comment | Organism |
|---|---|---|
| G85V | mutation involved in Wilson disease. Mutation causes disruption of the structure of metal-binding domain MBD1 | Homo sapiens |
Organism
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Homo sapiens | P35670 | - |
- |
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Release 2023.1 (January 2023)
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