The loss of stability of a naturally occurring ATP7A mutant is the cause of
Menkes disease

Copper-transporting ATPase 1(E.C.3.6.3.4)

Information obtained from PDB's Chemical Component Dictionary
at http://wwpdb-remediation.rutgers.edu/downloads.html
Downloaded on Thu Jun 16 11:21:40 2011

An atomic-level investigation of the disease-causing A629P mutant of the Menkes protein, ATP7A.

Solution Structure Of The Cu(I) Form Of The Sixth Soluble Domain Of Menkes Protein

Solution Structure Of The Apo Form Of The Sixth Soluble Domain Of Menkes Protein

Solution Structure Of The Cu(I) Form Of The Sixth Soluble Domain A69p Mutant Of Menkes Protein

Solution Structure Of The Apo Form Of The Sixth Soluble Domain A69p Mutant Of Menkes Protein

torsion angle dynamics coupled with simulated annealing followed by restrained energy minimization