272 related articles for article (PubMed ID: 18779302)
21. Clusterin and COMMD1 independently regulate degradation of the mammalian copper ATPases ATP7A and ATP7B.
Materia S; Cater MA; Klomp LW; Mercer JF; La Fontaine S
J Biol Chem; 2012 Jan; 287(4):2485-99. PubMed ID: 22130675
[TBL] [Abstract][Full Text] [Related]
22. 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.
Ralle M; Lutsenko S; Blackburn NJ
J Inorg Biochem; 2004 May; 98(5):765-74. PubMed ID: 15134922
[TBL] [Abstract][Full Text] [Related]
23. Advances in the understanding of mammalian copper transporters.
Wang Y; Hodgkinson V; Zhu S; Weisman GA; Petris MJ
Adv Nutr; 2011 Mar; 2(2):129-37. PubMed ID: 22332042
[TBL] [Abstract][Full Text] [Related]
24. Molecular features of copper binding proteins involved in copper homeostasis.
Inesi G
IUBMB Life; 2017 Apr; 69(4):211-217. PubMed ID: 27896900
[TBL] [Abstract][Full Text] [Related]
25. Wilson disease.
Harada M
Med Electron Microsc; 2002 Jun; 35(2):61-6. PubMed ID: 12181646
[TBL] [Abstract][Full Text] [Related]
26. The metal chaperone Atox1 regulates the activity of the human copper transporter ATP7B by modulating domain dynamics.
Yu CH; Yang N; Bothe J; Tonelli M; Nokhrin S; Dolgova NV; Braiterman L; Lutsenko S; Dmitriev OY
J Biol Chem; 2017 Nov; 292(44):18169-18177. PubMed ID: 28900031
[TBL] [Abstract][Full Text] [Related]
27. Metal binding domains 3 and 4 of the Wilson disease protein: solution structure and interaction with the copper(I) chaperone HAH1.
Banci L; Bertini I; Cantini F; Rosenzweig AC; Yatsunyk LA
Biochemistry; 2008 Jul; 47(28):7423-9. PubMed ID: 18558714
[TBL] [Abstract][Full Text] [Related]
28. The puzzle posed by COMMD1, a newly discovered protein binding Cu(II).
Sarkar B; Roberts EA
Metallomics; 2011 Jan; 3(1):20-7. PubMed ID: 21275100
[TBL] [Abstract][Full Text] [Related]
29. Trafficking of the copper-ATPases, ATP7A and ATP7B: role in copper homeostasis.
La Fontaine S; Mercer JF
Arch Biochem Biophys; 2007 Jul; 463(2):149-67. PubMed ID: 17531189
[TBL] [Abstract][Full Text] [Related]
30. Conserved residues modulate copper release in human copper chaperone Atox1.
Hussain F; Olson JS; Wittung-Stafshede P
Proc Natl Acad Sci U S A; 2008 Aug; 105(32):11158-63. PubMed ID: 18685091
[TBL] [Abstract][Full Text] [Related]
31. Functional understanding of the versatile protein copper metabolism MURR1 domain 1 (COMMD1) in copper homeostasis.
Fedoseienko A; Bartuzi P; van de Sluis B
Ann N Y Acad Sci; 2014 May; 1314():6-14. PubMed ID: 24697840
[TBL] [Abstract][Full Text] [Related]
32. Expression in mouse kidney of membrane copper transporters Atp7a and Atp7b.
Moore SD; Cox DW
Nephron; 2002; 92(3):629-34. PubMed ID: 12372948
[TBL] [Abstract][Full Text] [Related]
33. Binding of copper(I) by the Wilson disease protein and its copper chaperone.
Wernimont AK; Yatsunyk LA; Rosenzweig AC
J Biol Chem; 2004 Mar; 279(13):12269-76. PubMed ID: 14709553
[TBL] [Abstract][Full Text] [Related]
34. Menkes Copper ATPase (Atp7a) is a novel metal-responsive gene in rat duodenum, and immunoreactive protein is present on brush-border and basolateral membrane domains.
Ravia JJ; Stephen RM; Ghishan FK; Collins JF
J Biol Chem; 2005 Oct; 280(43):36221-7. PubMed ID: 16081413
[TBL] [Abstract][Full Text] [Related]
35. Copper chaperone Atox1 interacts with the metal-binding domain of Wilson's disease protein in cisplatin detoxification.
Dolgova NV; Nokhrin S; Yu CH; George GN; Dmitriev OY
Biochem J; 2013 Aug; 454(1):147-56. PubMed ID: 23751120
[TBL] [Abstract][Full Text] [Related]
36. Congenital cataract, muscular hypotonia, developmental delay and sensorineural hearing loss associated with a defect in copper metabolism.
Horváth R; Freisinger P; Rubio R; Merl T; Bax R; Mayr JA; Shawan ; Müller-Höcker J; Pongratz D; Moller LB; Horn N; Jaksch M
J Inherit Metab Dis; 2005; 28(4):479-92. PubMed ID: 15902551
[TBL] [Abstract][Full Text] [Related]
37. Conformational dynamics of metal-binding domains in Wilson disease protein: molecular insights into selective copper transfer.
Rodriguez-Granillo A; Crespo A; Wittung-Stafshede P
Biochemistry; 2009 Jun; 48(25):5849-63. PubMed ID: 19449859
[TBL] [Abstract][Full Text] [Related]
38. [From gene to disease: copper-transporting P ATPases alteration].
Garcia Hejl C; Vrignaud C; Garcia C; Ceppa F
Pathol Biol (Paris); 2009 May; 57(3):272-9. PubMed ID: 19046832
[TBL] [Abstract][Full Text] [Related]
39. How copper traverses cellular membranes through the mammalian copper transporter 1, Ctr1.
Ohrvik H; Thiele DJ
Ann N Y Acad Sci; 2014 May; 1314():32-41. PubMed ID: 24697869
[TBL] [Abstract][Full Text] [Related]
40. NMR characterization of copper-binding domains 4-6 of ATP7B .
Fatemi N; Korzhnev DM; Velyvis A; Sarkar B; Forman-Kay JD
Biochemistry; 2010 Oct; 49(39):8468-77. PubMed ID: 20799727
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
