Human copper transporter ATP7B (Wilson disease protein) forms stable dimers in vitro and in cells
Author:
Funder
National Institute of General Medical Sciences
National Institute of Diabetes and Digestive and Kidney Diseases
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference40 articles.
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4. ATP7B variants as modulators of copper dyshomeostasis in Alzheimer’s disease;Squitti;Neuromolecular Med,2013
5. The role of metal binding and phosphorylation domains in the regulation of cisplatin-induced trafficking of ATP7B;Safaei;Metallomics,2013
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1. Structure and mechanism of the human copper transporting ATPases: Fitting the pieces into a moving puzzle;Biochimica et Biophysica Acta (BBA) - Biomembranes;2024-04
2. Epidemiology of Wilson’s Disease and Pathogenic Variants of the ATP7B Gene Leading to Diversified Protein Disfunctions;International Journal of Molecular Sciences;2024-02-18
3. Copper in Gynecological Diseases;International Journal of Molecular Sciences;2023-12-17
4. Diagnóstico de la enfermedad de Wilson y sus fenotipos usando inteligencia artificial;Magna Scientia UCEVA;2023-08-23
5. Copper binding leads to increased dynamics in the regulatory N-terminal domain of full-length human copper transporter ATP7B;PLOS Computational Biology;2022-09-07
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