284 related articles for article (PubMed ID: 28107647)
1. Programmed Ribosomal Frameshifting Generates a Copper Transporter and a Copper Chaperone from the Same Gene.
Meydan S; Klepacki D; Karthikeyan S; Margus T; Thomas P; Jones JE; Khan Y; Briggs J; Dinman JD; Vázquez-Laslop N; Mankin AS
Mol Cell; 2017 Jan; 65(2):207-219. PubMed ID: 28107647
[TBL] [Abstract][Full Text] [Related]
2. One gene, two proteins: coordinated production of a copper chaperone by differential transcript formation and translational frameshifting in Escherichia coli.
Drees SL; Klinkert B; Helling S; Beyer DF; Marcus K; Narberhaus F; Lübben M
Mol Microbiol; 2017 Nov; 106(4):635-645. PubMed ID: 28925527
[TBL] [Abstract][Full Text] [Related]
3. Mechanism of ATPase-mediated Cu+ export and delivery to periplasmic chaperones: the interaction of Escherichia coli CopA and CusF.
Padilla-Benavides T; George Thompson AM; McEvoy MM; Argüello JM
J Biol Chem; 2014 Jul; 289(30):20492-501. PubMed ID: 24917681
[TBL] [Abstract][Full Text] [Related]
4. Conditional Switch between Frameshifting Regimes upon Translation of dnaX mRNA.
Caliskan N; Wohlgemuth I; Korniy N; Pearson M; Peske F; Rodnina MV
Mol Cell; 2017 May; 66(4):558-567.e4. PubMed ID: 28525745
[TBL] [Abstract][Full Text] [Related]
5. Mechanism of Cu+-transporting ATPases: soluble Cu+ chaperones directly transfer Cu+ to transmembrane transport sites.
González-Guerrero M; Argüello JM
Proc Natl Acad Sci U S A; 2008 Apr; 105(16):5992-7. PubMed ID: 18417453
[TBL] [Abstract][Full Text] [Related]
6. The transport mechanism of bacterial Cu+-ATPases: distinct efflux rates adapted to different function.
Raimunda D; González-Guerrero M; Leeber BW; Argüello JM
Biometals; 2011 Jun; 24(3):467-75. PubMed ID: 21210186
[TBL] [Abstract][Full Text] [Related]
7. Biochemical characterization of CopA, the Escherichia coli Cu(I)-translocating P-type ATPase.
Fan B; Rosen BP
J Biol Chem; 2002 Dec; 277(49):46987-92. PubMed ID: 12351646
[TBL] [Abstract][Full Text] [Related]
8. Measurement of cytoplasmic copper, silver, and gold with a lux biosensor shows copper and silver, but not gold, efflux by the CopA ATPase of Escherichia coli.
Stoyanov JV; Magnani D; Solioz M
FEBS Lett; 2003 Jul; 546(2-3):391-4. PubMed ID: 12832075
[TBL] [Abstract][Full Text] [Related]
9. An NMR study of the interaction of the N-terminal cytoplasmic tail of the Wilson disease protein with copper(I)-HAH1.
Banci L; Bertini I; Cantini F; Massagni C; Migliardi M; Rosato A
J Biol Chem; 2009 Apr; 284(14):9354-60. PubMed ID: 19181666
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Characterization and comparison of metal accumulation in two Escherichia coli strains expressing either CopA or MntA, heavy metal-transporting bacterial P-type adenosine triphosphatases.
Zagorski N; Wilson DB
Appl Biochem Biotechnol; 2004 Apr; 117(1):33-48. PubMed ID: 15126702
[TBL] [Abstract][Full Text] [Related]
12. A mechanical explanation of RNA pseudoknot function in programmed ribosomal frameshifting.
Namy O; Moran SJ; Stuart DI; Gilbert RJ; Brierley I
Nature; 2006 May; 441(7090):244-7. PubMed ID: 16688178
[TBL] [Abstract][Full Text] [Related]
13. Correlation between mechanical strength of messenger RNA pseudoknots and ribosomal frameshifting.
Hansen TM; Reihani SN; Oddershede LB; Sørensen MA
Proc Natl Acad Sci U S A; 2007 Apr; 104(14):5830-5. PubMed ID: 17389398
[TBL] [Abstract][Full Text] [Related]
14. Control of copper homeostasis in Escherichia coli by a P-type ATPase, CopA, and a MerR-like transcriptional activator, CopR.
Petersen C; Møller LB
Gene; 2000 Dec; 261(2):289-98. PubMed ID: 11167016
[TBL] [Abstract][Full Text] [Related]
15. The ATPases CopA and CopB both contribute to copper resistance of the thermoacidophilic archaeon Sulfolobus solfataricus.
Völlmecke C; Drees SL; Reimann J; Albers SV; Lübben M
Microbiology (Reading); 2012 Jun; 158(Pt 6):1622-1633. PubMed ID: 22361944
[TBL] [Abstract][Full Text] [Related]
16. Lack of evidence for ribosomal frameshifting in ATP7B mRNA decoding.
Loughran G; Fedorova AD; Khan YA; Atkins JF; Baranov PV
Mol Cell; 2022 Oct; 82(19):3745-3749.e2. PubMed ID: 36115342
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Characterization and structure of a Zn2+ and [2Fe-2S]-containing copper chaperone from Archaeoglobus fulgidus.
Sazinsky MH; LeMoine B; Orofino M; Davydov R; Bencze KZ; Stemmler TL; Hoffman BM; Argüello JM; Rosenzweig AC
J Biol Chem; 2007 Aug; 282(35):25950-9. PubMed ID: 17609202
[TBL] [Abstract][Full Text] [Related]
19. Purification and functional analysis of the copper ATPase CopA of Enterococcus hirae.
Wunderli-Ye H; Solioz M
Biochem Biophys Res Commun; 2001 Jan; 280(3):713-9. PubMed ID: 11162579
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
