Solution structue of the N-domain of Wilson disease protein: Distinct nucleotide-binding environment and effects of disease mutations

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[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-hydroxy-phosphoryl] phosphono hydrogen phosphate

adenosine 5'-(tetrahydrogen triphosphate)

Proceedings of the National Academy of Sciences of the United States of America
Solution structure of the N-domain of Wilson disease protein: distinct nucleotide-binding environment and effects of disease mutations.

Solution Structure Of The Wilson Atpase N-Domain In The Presence Of Atp

ATPase, Cu++ transporting, beta polypeptide isoform a variant [Homo sapiens]

copper transporting ATPase [Homo sapiens]

copper-transporting ATPase (EC 3.6.1.-) beta chain - human

copper-transporting ATPase 2 isoform a [Homo sapiens]

copper-transporting ATPase 2 isoform b [Homo sapiens]

copper-transporting ATPase 2 isoform c [Homo sapiens]

PREDICTED: copper-transporting ATPase 2 [Macaca mulatta]

PREDICTED: LOW QUALITY PROTEIN: copper-transporting ATPase 2 [Nomascus leucogenys]

RecName: Full=Copper-transporting ATPase 2; AltName: Full=Copper pump 2; AltName: Full=Wilson disease-associated protein; Conta

torsion angle dynamics, simulated annealing

room temperature specified for incubation

Zimmerman, Moseley, Kulikowski and Montelione

Brunger, Adams, Clore, Gros, Nilges and Read