93 related articles for article (PubMed ID: 23354150)
1. Periplasmic response upon disruption of transmembrane Cu transport in Pseudomonas aeruginosa.
Raimunda D; Padilla-Benavides T; Vogt S; Boutigny S; Tomkinson KN; Finney LA; Argüello JM
Metallomics; 2013 Feb; 5(2):144-51. PubMed ID: 23354150
[TBL] [Abstract][Full Text] [Related]
2. Distinct functional roles of homologous Cu+ efflux ATPases in Pseudomonas aeruginosa.
González-Guerrero M; Raimunda D; Cheng X; Argüello JM
Mol Microbiol; 2010 Dec; 78(5):1246-58. PubMed ID: 21091508
[TBL] [Abstract][Full Text] [Related]
3. The Two-Component System CopRS Maintains Subfemtomolar Levels of Free Copper in the Periplasm of Pseudomonas aeruginosa Using a Phosphatase-Based Mechanism.
Novoa-Aponte L; Xu C; Soncini FC; Argüello JM
mSphere; 2020 Dec; 5(6):. PubMed ID: 33361129
[TBL] [Abstract][Full Text] [Related]
4. Copper homeostasis networks in the bacterium
Quintana J; Novoa-Aponte L; Argüello JM
J Biol Chem; 2017 Sep; 292(38):15691-15704. PubMed ID: 28760827
[TBL] [Abstract][Full Text] [Related]
5. Effect of pH and ligand binding on the structure of the Cu site of the Met121Glu mutant of azurin from Pseudomonas aeruginosa.
Strange RW; Murphy LM; Karlsson BG; Reinhammar B; Hasnain SS
Biochemistry; 1996 Dec; 35(50):16391-8. PubMed ID: 8973215
[TBL] [Abstract][Full Text] [Related]
6. The interplay of the metallosensor CueR with two distinct CopZ chaperones defines copper homeostasis in
Novoa-Aponte L; Ramírez D; Argüello JM
J Biol Chem; 2019 Mar; 294(13):4934-4945. PubMed ID: 30718281
[TBL] [Abstract][Full Text] [Related]
7. Mimicking protein-protein electron transfer: voltammetry of Pseudomonas aeruginosa azurin and the Thermus thermophilus Cu(A) domain at omega-derivatized self-assembled-monolayer gold electrodes.
Fujita K; Nakamura N; Ohno H; Leigh BS; Niki K; Gray HB; Richards JH
J Am Chem Soc; 2004 Nov; 126(43):13954-61. PubMed ID: 15506756
[TBL] [Abstract][Full Text] [Related]
8. An important role for periplasmic storage in Pseudomonas aeruginosa copper homeostasis revealed by a combined experimental and computational modeling study.
Parmar JH; Quintana J; Ramírez D; Laubenbacher R; Argüello JM; Mendes P
Mol Microbiol; 2018 Nov; 110(3):357-369. PubMed ID: 30047562
[TBL] [Abstract][Full Text] [Related]
9. Analysis of the periplasmic proteome of Pseudomonas aeruginosa, a metabolically versatile opportunistic pathogen.
Imperi F; Ciccosanti F; Perdomo AB; Tiburzi F; Mancone C; Alonzi T; Ascenzi P; Piacentini M; Visca P; Fimia GM
Proteomics; 2009 Apr; 9(7):1901-15. PubMed ID: 19333994
[TBL] [Abstract][Full Text] [Related]
10. Kinetics of copper incorporation into a biosynthetic purple Cu(A) azurin: characterization of red, blue, and a new intermediate species.
Wilson TD; Savelieff MG; Nilges MJ; Marshall NM; Lu Y
J Am Chem Soc; 2011 Dec; 133(51):20778-92. PubMed ID: 21985501
[TBL] [Abstract][Full Text] [Related]
11. Synthesis of the siderophore pyoverdine in Pseudomonas aeruginosa involves a periplasmic maturation.
Yeterian E; Martin LW; Guillon L; Journet L; Lamont IL; Schalk IJ
Amino Acids; 2010 May; 38(5):1447-59. PubMed ID: 19787431
[TBL] [Abstract][Full Text] [Related]
12. Characterization and crystal structure of zinc azurin, a by-product of heterologous expression in Escherichia coli of Pseudomonas aeruginosa copper azurin.
Nar H; Huber R; Messerschmidt A; Filippou AC; Barth M; Jaquinod M; van de Kamp M; Canters GW
Eur J Biochem; 1992 May; 205(3):1123-9. PubMed ID: 1576995
[TBL] [Abstract][Full Text] [Related]
13. Structural basis of electron transfer modulation in the purple CuA center.
Robinson H; Ang MC; Gao YG; Hay MT; Lu Y; Wang AH
Biochemistry; 1999 May; 38(18):5677-83. PubMed ID: 10231517
[TBL] [Abstract][Full Text] [Related]
14. In vivo studies disprove an obligatory role of azurin in denitrification in Pseudomonas aeruginosa and show that azu expression is under control of rpoS and ANR.
Vijgenboom E; Busch JE; Canters GW
Microbiology (Reading); 1997 Sep; 143 ( Pt 9)():2853-2863. PubMed ID: 9308169
[TBL] [Abstract][Full Text] [Related]
15. Cooperation between two periplasmic copper chaperones is required for full activity of the cbb3 -type cytochrome c oxidase and copper homeostasis in Rhodobacter capsulatus.
Trasnea PI; Utz M; Khalfaoui-Hassani B; Lagies S; Daldal F; Koch HG
Mol Microbiol; 2016 Apr; 100(2):345-61. PubMed ID: 26718481
[TBL] [Abstract][Full Text] [Related]
16. The selenocysteine-substituted blue copper center: spectroscopic investigations of Cys112SeCys Pseudomonas aeruginosa azurin.
Ralle M; Berry SM; Nilges MJ; Gieselman MD; van der Donk WA; Lu Y; Blackburn NJ
J Am Chem Soc; 2004 Jun; 126(23):7244-56. PubMed ID: 15186162
[TBL] [Abstract][Full Text] [Related]
17. Pseudoazurin mediates periplasmic electron flow in a mutant strain of Paracoccus denitrificans lacking cytochrome c550.
Koutný M; Kucera I; Tesarík R; Turánek J; Van Spanning RJ
FEBS Lett; 1999 Apr; 448(1):157-9. PubMed ID: 10217431
[TBL] [Abstract][Full Text] [Related]
18. A periplasmic cupredoxin with a green CuT1.5 center is involved in bacterial copper tolerance.
Durand A; Fouesnard M; Bourbon ML; Steunou AS; Lojou E; Dorlet P; Ouchane S
Metallomics; 2021 Dec; 13(12):. PubMed ID: 34791351
[TBL] [Abstract][Full Text] [Related]
19. The CopA2-Type P
Andrei A; Di Renzo MA; Öztürk Y; Meisner A; Daum N; Frank F; Rauch J; Daldal F; Andrade SLA; Koch HG
Front Microbiol; 2021; 12():712465. PubMed ID: 34589071
[TBL] [Abstract][Full Text] [Related]
20. [Properties of a nitrite reductase inhibitor protein from Pseudomonas aeruginosa].
Karapetian AV; Nalbandian RM
Biokhimiia; 1993 Aug; 58(9):1384-8. PubMed ID: 8218561
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]