These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
214 related articles for article (PubMed ID: 12679332)
1. Kinetic analysis of the interaction of the copper chaperone Atox1 with the metal binding sites of the Menkes protein. Strausak D; Howie MK; Firth SD; Schlicksupp A; Pipkorn R; Multhaup G; Mercer JF J Biol Chem; 2003 Jun; 278(23):20821-7. PubMed ID: 12679332 [TBL] [Abstract][Full Text] [Related]
2. Copper-induced trafficking of the cU-ATPases: a key mechanism for copper homeostasis. Mercer JF; Barnes N; Stevenson J; Strausak D; Llanos RM Biometals; 2003 Mar; 16(1):175-84. PubMed ID: 12572677 [TBL] [Abstract][Full Text] [Related]
3. Cu(I) binding and transfer by the N terminus of the Wilson disease protein. Yatsunyk LA; Rosenzweig AC J Biol Chem; 2007 Mar; 282(12):8622-31. PubMed ID: 17229731 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. Metallochaperone Atox1 transfers copper to the NH2-terminal domain of the Wilson's disease protein and regulates its catalytic activity. Walker JM; Tsivkovskii R; Lutsenko S J Biol Chem; 2002 Aug; 277(31):27953-9. PubMed ID: 12029094 [TBL] [Abstract][Full Text] [Related]
6. The role of GMXCXXC metal binding sites in the copper-induced redistribution of the Menkes protein. Strausak D; La Fontaine S; Hill J; Firth SD; Lockhart PJ; Mercer JF J Biol Chem; 1999 Apr; 274(16):11170-7. PubMed ID: 10196202 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Characterization of the interaction between the Wilson and Menkes disease proteins and the cytoplasmic copper chaperone, HAH1p. Larin D; Mekios C; Das K; Ross B; Yang AS; Gilliam TC J Biol Chem; 1999 Oct; 274(40):28497-504. PubMed ID: 10497213 [TBL] [Abstract][Full Text] [Related]
10. The N-terminal metal-binding site 2 of the Wilson's Disease Protein plays a key role in the transfer of copper from Atox1. Walker JM; Huster D; Ralle M; Morgan CT; Blackburn NJ; Lutsenko S J Biol Chem; 2004 Apr; 279(15):15376-84. PubMed ID: 14754885 [TBL] [Abstract][Full Text] [Related]
11. Functional analysis of the N-terminal CXXC metal-binding motifs in the human Menkes copper-transporting P-type ATPase expressed in cultured mammalian cells. Voskoboinik I; Strausak D; Greenough M; Brooks H; Petris M; Smith S; Mercer JF; Camakaris J J Biol Chem; 1999 Jul; 274(31):22008-12. PubMed ID: 10419525 [TBL] [Abstract][Full Text] [Related]
12. Copper transporting P-type ATPases and human disease. Cox DW; Moore SD J Bioenerg Biomembr; 2002 Oct; 34(5):333-8. PubMed ID: 12539960 [TBL] [Abstract][Full Text] [Related]
13. An NMR study of the interaction between the human copper(I) chaperone and the second and fifth metal-binding domains of the Menkes protein. Banci L; Bertini I; Ciofi-Baffoni S; Chasapis CT; Hadjiliadis N; Rosato A FEBS J; 2005 Feb; 272(3):865-71. PubMed ID: 15670166 [TBL] [Abstract][Full Text] [Related]
14. N-terminal domains of human copper-transporting adenosine triphosphatases (the Wilson's and Menkes disease proteins) bind copper selectively in vivo and in vitro with stoichiometry of one copper per metal-binding repeat. Lutsenko S; Petrukhin K; Cooper MJ; Gilliam CT; Kaplan JH J Biol Chem; 1997 Jul; 272(30):18939-44. PubMed ID: 9228074 [TBL] [Abstract][Full Text] [Related]
15. In vitro thermodynamic dissection of human copper transfer from chaperone to target protein. Niemiec MS; Weise CF; Wittung-Stafshede P PLoS One; 2012; 7(5):e36102. PubMed ID: 22574136 [TBL] [Abstract][Full Text] [Related]
16. Functional properties of the human copper-transporting ATPase ATP7B (the Wilson's disease protein) and regulation by metallochaperone Atox1. Lutsenko S; Tsivkovskii R; Walker JM Ann N Y Acad Sci; 2003 Apr; 986():204-11. PubMed ID: 12763797 [TBL] [Abstract][Full Text] [Related]
17. An expanding range of functions for the copper chaperone/antioxidant protein Atox1. Hatori Y; Lutsenko S Antioxid Redox Signal; 2013 Sep; 19(9):945-57. PubMed ID: 23249252 [TBL] [Abstract][Full Text] [Related]
18. Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B. de Bie P; van de Sluis B; Burstein E; van de Berghe PV; Muller P; Berger R; Gitlin JD; Wijmenga C; Klomp LW Gastroenterology; 2007 Oct; 133(4):1316-26. PubMed ID: 17919502 [TBL] [Abstract][Full Text] [Related]
19. Chaperone-mediated Cu+ delivery to Cu+ transport ATPases: requirement of nucleotide binding. González-Guerrero M; Hong D; Argüello JM J Biol Chem; 2009 Jul; 284(31):20804-11. PubMed ID: 19525226 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]