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 | 87.1 % (446 of 512) | 85.4 % (375 of 439) | 97.3 % (71 of 73) |
Backbone | 96.4 % (217 of 225) | 96.1 % (147 of 153) | 97.2 % (70 of 72) |
Sidechain | 79.8 % (229 of 287) | 79.7 % (228 of 286) | 100.0 % (1 of 1) |
Aromatic | 57.1 % (12 of 21) | 57.1 % (12 of 21) | |
Methyl | 100.0 % (52 of 52) | 100.0 % (52 of 52) |
1. Copper-transporting ATPase 1
MGDGVLELVV RGMTCASCVH KIESSLTKHR GILYCSVALA TNKAHIKYDP EIIGPRDIIH TIESLGFEPS LVKIEPressure 1 atm, Temperature 298 K, pH 7
# | Name | Isotope labeling | Type | Concentration |
---|---|---|---|---|
1 | Copper-transporting ATPase 1 | [U-15N] | 0.8 mM | |
2 | DTT | 5 mM | ||
3 | phosphate buffer | 100 mM | ||
4 | H2O | 90 % | ||
5 | D2O | 10 % |