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Journal Abstract Search
188 related items for PubMed ID: 21323310
1. Copper trafficking mechanism of CXXC-containing domains: insight from the pH-dependence of their Cu(I) affinities. Badarau A, Dennison C. J Am Chem Soc; 2011 Mar 09; 133(9):2983-8. PubMed ID: 21323310 [Abstract] [Full Text] [Related]
2. Dynamics and stability of the metal binding domains of the Menkes ATPase and their interaction with metallochaperone HAH1. Arumugam K, Crouzy S. Biochemistry; 2012 Nov 06; 51(44):8885-906. PubMed ID: 23075277 [Abstract] [Full Text] [Related]
3. Structure of human Wilson protein domains 5 and 6 and their interplay with domain 4 and the copper chaperone HAH1 in copper uptake. Achila D, Banci L, Bertini I, Bunce J, Ciofi-Baffoni S, Huffman DL. Proc Natl Acad Sci U S A; 2006 Apr 11; 103(15):5729-34. PubMed ID: 16571664 [Abstract] [Full Text] [Related]
4. Dynamic multibody protein interactions suggest versatile pathways for copper trafficking. Keller AM, Benítez JJ, Klarin D, Zhong L, Goldfogel M, Yang F, Chen TY, Chen P. J Am Chem Soc; 2012 May 30; 134(21):8934-43. PubMed ID: 22578168 [Abstract] [Full Text] [Related]
5. 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 15; 48(49):11640-54. PubMed ID: 19883117 [Abstract] [Full Text] [Related]
7. Cu(I) binding and transfer by the N terminus of the Wilson disease protein. Yatsunyk LA, Rosenzweig AC. J Biol Chem; 2007 Mar 23; 282(12):8622-31. PubMed ID: 17229731 [Abstract] [Full Text] [Related]
8. 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 15; 47(28):7423-9. PubMed ID: 18558714 [Abstract] [Full Text] [Related]
11. NMR structural analysis of the soluble domain of ZiaA-ATPase and the basis of selective interactions with copper metallochaperone Atx1. Banci L, Bertini I, Ciofi-Baffoni S, Poggi L, Vanarotti M, Tottey S, Waldron KJ, Robinson NJ. J Biol Inorg Chem; 2010 Jan 15; 15(1):87-98. PubMed ID: 19609573 [Abstract] [Full Text] [Related]
12. X-ray absorption spectroscopy of the copper chaperone HAH1 reveals a linear two-coordinate Cu(I) center capable of adduct formation with exogenous thiols and phosphines. Ralle M, Lutsenko S, Blackburn NJ. J Biol Chem; 2003 Jun 20; 278(25):23163-70. PubMed ID: 12686548 [Abstract] [Full Text] [Related]
13. Copper-mediated homo-dimerisation for the HAH1 metallochaperone. Tanchou V, Gas F, Urvoas A, Cougouluègne F, Ruat S, Averseng O, Quéméneur E. Biochem Biophys Res Commun; 2004 Dec 10; 325(2):388-94. PubMed ID: 15530404 [Abstract] [Full Text] [Related]
15. Solution structures of the reduced and Cu(I) bound forms of the first metal binding sequence of ATP7A associated with Menkes disease. DeSilva TM, Veglia G, Opella SJ. Proteins; 2005 Dec 01; 61(4):1038-49. PubMed ID: 16211579 [Abstract] [Full Text] [Related]
19. A NMR study of the interaction of a three-domain construct of ATP7A with copper(I) and copper(I)-HAH1: the interplay of domains. Banci L, Bertini I, Cantini F, Chasapis CT, Hadjiliadis N, Rosato A. J Biol Chem; 2005 Nov 18; 280(46):38259-63. PubMed ID: 16172131 [Abstract] [Full Text] [Related]