183 related articles for article (PubMed ID: 11527979)
21. The role of the invariant His-1069 in folding and function of the Wilson's disease protein, the human copper-transporting ATPase ATP7B.
Tsivkovskii R; Efremov RG; Lutsenko S
J Biol Chem; 2003 Apr; 278(15):13302-8. PubMed ID: 12551905
[TBL] [Abstract][Full Text] [Related]
22. Copper transport and its defect in Wilson disease: characterization of the copper-binding domain of Wilson disease ATPase.
Sarkar B
J Inorg Biochem; 2000 Apr; 79(1-4):187-91. PubMed ID: 10830865
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. The ATP hydrolytic activity of purified ZntA, a Pb(II)/Cd(II)/Zn(II)-translocating ATPase from Escherichia coli.
Sharma R; Rensing C; Rosen BP; Mitra B
J Biol Chem; 2000 Feb; 275(6):3873-8. PubMed ID: 10660539
[TBL] [Abstract][Full Text] [Related]
25. Expression of ZntA, a zinc-transporting P1-type ATPase, is specifically regulated by zinc and cadmium.
Noll M; Lutsenko S
IUBMB Life; 2000 Apr; 49(4):297-302. PubMed ID: 10995032
[TBL] [Abstract][Full Text] [Related]
26. Purification and functional reconstitution of the human Wilson copper ATPase, ATP7B.
Portmann R; Solioz M
FEBS Lett; 2005 Jul; 579(17):3589-95. PubMed ID: 15963506
[TBL] [Abstract][Full Text] [Related]
27. A new zinc-protein coordination site in intracellular metal trafficking: solution structure of the Apo and Zn(II) forms of ZntA(46-118).
Banci L; Bertini I; Ciofi-Baffoni S; Finney LA; Outten CE; O'Halloran TV
J Mol Biol; 2002 Nov; 323(5):883-97. PubMed ID: 12417201
[TBL] [Abstract][Full Text] [Related]
28. Metal binding affinities of Arabidopsis zinc and copper transporters: selectivities match the relative, but not the absolute, affinities of their amino-terminal domains.
Zimmermann M; Clarke O; Gulbis JM; Keizer DW; Jarvis RS; Cobbett CS; Hinds MG; Xiao Z; Wedd AG
Biochemistry; 2009 Dec; 48(49):11640-54. PubMed ID: 19883117
[TBL] [Abstract][Full Text] [Related]
29. Analysis of functional domains of Wilson disease protein (ATP7B) in Saccharomyces cerevisiae.
Iida M; Terada K; Sambongi Y; Wakabayashi T; Miura N; Koyama K; Futai M; Sugiyama T
FEBS Lett; 1998 May; 428(3):281-5. PubMed ID: 9654149
[TBL] [Abstract][Full Text] [Related]
30. Identification of the "missing domain" of the rat copper-transporting ATPase, atp7b: insight into the structural and metal binding characteristics of its N-terminal copper-binding domain.
Tsay MJ; Fatemi N; Narindrasorasak S; Forbes JR; Sarkar B
Biochim Biophys Acta; 2004 Jan; 1688(1):78-85. PubMed ID: 14732483
[TBL] [Abstract][Full Text] [Related]
31. Apical targeting and Golgi retention signals reside within a 9-amino acid sequence in the copper-ATPase, ATP7B.
Braiterman L; Nyasae L; Guo Y; Bustos R; Lutsenko S; Hubbard A
Am J Physiol Gastrointest Liver Physiol; 2009 Feb; 296(2):G433-44. PubMed ID: 19033537
[TBL] [Abstract][Full Text] [Related]
32. CopA: An Escherichia coli Cu(I)-translocating P-type ATPase.
Rensing C; Fan B; Sharma R; Mitra B; Rosen BP
Proc Natl Acad Sci U S A; 2000 Jan; 97(2):652-6. PubMed ID: 10639134
[TBL] [Abstract][Full Text] [Related]
33. Molecular events initiating exit of a copper-transporting ATPase ATP7B from the trans-Golgi network.
Hasan NM; Gupta A; Polishchuk E; Yu CH; Polishchuk R; Dmitriev OY; Lutsenko S
J Biol Chem; 2012 Oct; 287(43):36041-50. PubMed ID: 22898812
[TBL] [Abstract][Full Text] [Related]
34. Critical roles for the COOH terminus of the Cu-ATPase ATP7B in protein stability, trans-Golgi network retention, copper sensing, and retrograde trafficking.
Braiterman L; Nyasae L; Leves F; Hubbard AL
Am J Physiol Gastrointest Liver Physiol; 2011 Jul; 301(1):G69-81. PubMed ID: 21454443
[TBL] [Abstract][Full Text] [Related]
35. Zinc binding to the NH2-terminal domain of the Wilson disease copper-transporting ATPase: implications for in vivo metal ion-mediated regulation of ATPase activity.
DiDonato M; Zhang J; Que L; Sarkar B
J Biol Chem; 2002 Apr; 277(16):13409-14. PubMed ID: 11823463
[TBL] [Abstract][Full Text] [Related]
36. Functional analysis and drug response to zinc and D-penicillamine in stable ATP7B mutant hepatic cell lines.
Chandhok G; Horvath J; Aggarwal A; Bhatt M; Zibert A; Schmidt HH
World J Gastroenterol; 2016 Apr; 22(16):4109-19. PubMed ID: 27122662
[TBL] [Abstract][Full Text] [Related]
37. Functional characterization of new mutations in Wilson disease gene (ATP7B) using the yeast model.
Papur OS; Terzioglu O; Koc A
J Trace Elem Med Biol; 2015; 31():33-6. PubMed ID: 26004889
[TBL] [Abstract][Full Text] [Related]
38. Conserved aspartic acid 714 in transmembrane segment 8 of the ZntA subgroup of P1B-type ATPases is a metal-binding residue.
Dutta SJ; Liu J; Hou Z; Mitra B
Biochemistry; 2006 May; 45(18):5923-31. PubMed ID: 16669635
[TBL] [Abstract][Full Text] [Related]
39. Functional expression of AtHMA4, a P1B-type ATPase of the Zn/Co/Cd/Pb subclass.
Mills RF; Krijger GC; Baccarini PJ; Hall JL; Williams LE
Plant J; 2003 Jul; 35(2):164-76. PubMed ID: 12848823
[TBL] [Abstract][Full Text] [Related]
40. Conservative and nonconservative mutations of the transmembrane CPC motif in ZntA: effect on metal selectivity and activity.
Dutta SJ; Liu J; Stemmler AJ; Mitra B
Biochemistry; 2007 Mar; 46(12):3692-703. PubMed ID: 17326661
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]