The loss of stability of a naturally occurring ATP7A mutant is the cause of Menkes disease
| ID | Type | Value order | Atom ID 1 | Atom ID 2 |
|---|---|---|---|---|
| 1 | na | sing | 1:CYS15:SG | 2:CU11:CU |
| 2 | na | sing | 1:CYS18:SG | 2:CU11:CU |
Polymer type: polypeptide(L)
| Total | 1H | 15N | |
|---|---|---|---|
| All | 87.6 % (446 of 509) | 86.4 % (376 of 435) | 94.6 % (70 of 74) |
| Backbone | 94.7 % (215 of 227) | 94.8 % (146 of 154) | 94.5 % (69 of 73) |
| Sidechain | 81.9 % (231 of 282) | 81.9 % (230 of 281) | 100.0 % (1 of 1) |
| Aromatic | 52.4 % (11 of 21) | 52.4 % (11 of 21) | |
| Methyl | 92.5 % (49 of 53) | 92.5 % (49 of 53) |
1. Copper-transporting ATPase 1(E.C.3.6.3.4)
MGDGVLELVV RGMTCASCVH KIESSLTKHR GILYCSVALA TNKAHIKYDP EIIGPRDIIH TIESLGFEAS LVKIEPressure 1 atm, Temperature 298 K, pH 7
| # | Name | Isotope labeling | Type | Concentration |
|---|---|---|---|---|
| 1 | Copper-transporting ATPase 1(E.C.3.6.3.4) | [U-15N] | 0.8 mM | |
| 2 | DTT | 5 mM | ||
| 3 | phosphate buffer | 100 mM | ||
| 4 | H2O | 90 % | ||
| 5 | D2O | 10 % |