Related references
Note: Only part of the references are listed.Conformational Dynamics of Metal-Binding Domains in Wilson Disease Protein: Molecular Insights into Selective Copper Transfer
Agustina Rodriguez-Granillo et al.
BIOCHEMISTRY (2009)
The Loop Connecting Metal-Binding Domains 3 and 4 of ATP7B Is a Target of a Kinase-Mediated Phosphorylation
Mee Y. Bartee et al.
BIOCHEMISTRY (2009)
High Yield Heterologous Expression of Wild-type and Mutant Cu+-ATPase (ATP7B, Wilson Disease Protein) for Functional Characterization of Catalytic Activity and Serine Residues Undergoing Copper-dependent Phosphorylation
Rajendra Pilankatta et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
A selenocysteine variant of the human copper chaperone for superoxide dismutase. A Se-XAS probe of cluster composition at the domain 3 domain 3 dimer interface
Amanda N. Barry et al.
BIOCHEMISTRY (2008)
Metal binding domains 3 and 4 of the Wilson disease protein: solution Structure and interaction with the copper(I) chaperone HAH1
Lucia Banci et al.
BIOCHEMISTRY (2008)
Structure and dynamics of Cu(I) binding in copper chaperones Atox1 and CopZ: A computer simulation study
Agustina Rodriguez-Granillo et al.
JOURNAL OF PHYSICAL CHEMISTRY B (2008)
Menkes disease
I. Bertini et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2008)
Oxidative modification to cysteine sulfonic acid of Cys111 in human copper-zinc superoxide dismutase
Noriko Fujiwara et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
Biochemical basis of regulation of human copper-transporting ATPases
Svetlana Lutsenko et al.
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS (2007)
Cu(I) binding and transfer by the N terminus of the Wilson disease protein
Liliya A. Yatsunyk et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
Solution structure and intermolecular interactions of the third metal-binding domain of ATP7A, the Menkes disease protein
Lucia Banci et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Copper-dependent interaction of glutaredoxin with the N termini of the copper-ATPases (ATP7A and ATP7B) defective in Menkes and Wilson diseases
Chris M. Lim et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2006)
Copper-dependent interaction of dynactin subunit p62 with the N terminus of ATP7B but not ATP7A
Chris M. Lim et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Structure of human Wilson protein domains 5 and 6 and their interplay with domain 4 and the copper chaperone HAM in copper uptake
D Achila et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Solution structures of the reduced and Cu(I) bound forms of the first metal binding sequence of ATP7A associated with Menkes disease
TM DeSilva et al.
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS (2005)
NH2-terminal signals in ATP7B Cu-ATPase mediate its Cu-dependent anterograde traffic in polarized hepatic cells
Y Guo et al.
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY (2005)
Dynamic mechanism for the serpin loop insertion as revealed by quantitative kinetics
N Takahashi et al.
JOURNAL OF MOLECULAR BIOLOGY (2005)
An NMR study of the interaction between the human copper(I) chaperone and the second and fifth metal-binding domains of the Menkes protein
L Banci et al.
FEBS JOURNAL (2005)
The N-terminal metal-binding site 2 of the Wilson's disease protein plays a key role in the transfer of copper from Atox1
JM Walker et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Solution structure and backbone dynamics of the Cu(I) and apo forms of the second metal-binding domain of the Menkes protein ATP7A
L Banci et al.
BIOCHEMISTRY (2004)
Positive selection dictates the choice between kinetic and thermodynamic protein folding and stability in subtilases
E Subbian et al.
BIOCHEMISTRY (2004)
Copper transfer to the N-terminal domain of the Wilson disease protein (ATP7B): X-ray absorption spectroscopy of reconstituted and chaperone-loaded metal binding domains and their interaction with exogenous ligands
M Ralle et al.
JOURNAL OF INORGANIC BIOCHEMISTRY (2004)
Metallochaperone Atox1 transfers copper to the NH2-terminal domain of the Wilson's disease protein and regulates its catalytic activity
JM Walker et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
The Lys1010-Lys1325 fragment of the Wilson's disease protein binds nucleotides and interacts with the N-terminal domain of this protein in a copper-dependent manner
R Tsivkovskii et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Copper-induced conformational changes in the N-terminal domain of the Wilson disease copper-transporting ATPase
M DiDonato et al.
BIOCHEMISTRY (2000)
Share Paper
