메뉴 건너뛰기




Volumn 75, Issue 2, 2009, Pages 373-386

Ferric uptake regulator protein: Binding free energy calculations and per-residue free energy decomposition

Author keywords

Dimerization; DNA binding; Ferric uptake regulator; Free energy calculations; Iron; Metalloregulatory protein; Molecular dynamics

Indexed keywords

FERRIC UPTAKE REGULATOR; ZINC; BACTERIAL PROTEIN; DNA; IRON; IRON UPTAKE REGULATION PROTEIN, BACTERIA; IRON-UPTAKE REGULATION PROTEIN, BACTERIA; REPRESSOR PROTEIN;

EID: 65949100228     PISSN: 08873585     EISSN: 10970134     Source Type: Journal    
DOI: 10.1002/prot.22247     Document Type: Article
Times cited : (35)

References (63)
  • 1
    • 0344321893 scopus 로고    scopus 로고
    • Architecture of a protein central to iron homeostasis: Crystal structure and spectroscopic analysis of the ferric uptake regulator
    • Pohl E, Haller JC, Mijovilovich A, Meyer-Klaucke W, Garman E, Vasil ML. Architecture of a protein central to iron homeostasis: crystal structure and spectroscopic analysis of the ferric uptake regulator. Mol Microbiol 2003;47:903-915.
    • (2003) Mol Microbiol , vol.47 , pp. 903-915
    • Pohl, E.1    Haller, J.C.2    Mijovilovich, A.3    Meyer-Klaucke, W.4    Garman, E.5    Vasil, M.L.6
  • 2
    • 0033985228 scopus 로고    scopus 로고
    • Iron and oxidative stress in bacteria
    • Touati D. Iron and oxidative stress in bacteria. Arch Biochem Bio-phys 2000;373:1-6.
    • (2000) Arch Biochem Bio-phys , vol.373 , pp. 1-6
    • Touati, D.1
  • 3
    • 0035069457 scopus 로고    scopus 로고
    • Iron and metal regulation in bacteria
    • Hantke K. Iron and metal regulation in bacteria. Curr Opin Micro-biol 2001;4:172-177.
    • (2001) Curr Opin Micro-biol , vol.4 , pp. 172-177
    • Hantke, K.1
  • 4
    • 0025942194 scopus 로고
    • Structural dynamics and functional domains of the Fur protein
    • Coy M, Neilands JB. Structural dynamics and functional domains of the Fur protein. Biochemistry 1991;30:8201-8210.
    • (1991) Biochemistry , vol.30 , pp. 8201-8210
    • Coy, M.1    Neilands, J.B.2
  • 5
    • 0030805985 scopus 로고    scopus 로고
    • Electrospray ionization mass spectrometry analysis of the apo-and metal-substituted forms of the Fur protein
    • Michaud-Soret I, Adrait A, Jaquinod M, Forest E, Touati D, Latour JM. Electrospray ionization mass spectrometry analysis of the apo-and metal-substituted forms of the Fur protein. FEBS Lett 1997; 413:473-476.
    • (1997) FEBS Lett , vol.413 , pp. 473-476
    • Michaud-Soret, I.1    Adrait, A.2    Jaquinod, M.3    Forest, E.4    Touati, D.5    Latour, J.M.6
  • 7
    • 34248669001 scopus 로고    scopus 로고
    • Functional specialization within the Fur family of metalloregulators
    • Lee JW, Helmann JD. Functional specialization within the Fur family of metalloregulators. Biometals 2007;20:485-499.
    • (2007) Biometals , vol.20 , pp. 485-499
    • Lee, J.W.1    Helmann, J.D.2
  • 8
    • 0037168511 scopus 로고    scopus 로고
    • Direct inhibition by nitric oxide of the transcriptional ferric uptake regulation protein via nitrosylation of the iron
    • D'Autreaux B, Touati D, Bersch B, Latour JM, Michaud-Soret I. Direct inhibition by nitric oxide of the transcriptional ferric uptake regulation protein via nitrosylation of the iron. Proc Natl Acad Sci USA 2002;99:16619-16624.
    • (2002) Proc Natl Acad Sci USA , vol.99 , pp. 16619-16624
    • D'Autreaux, B.1    Touati, D.2    Bersch, B.3    Latour, J.M.4    Michaud-Soret, I.5
  • 10
    • 0023692463 scopus 로고
    • Metal ion regulation of gene expression. Fur repressor-operator interaction at the promoter region of the aerobactin system of pColV-K30
    • de Lorenzo V, Giovannini F, Herrero M, Neilands JB. Metal ion regulation of gene expression. Fur repressor-operator interaction at the promoter region of the aerobactin system of pColV-K30. J Mol Biol 1988;203:875-884.
    • (1988) J Mol Biol , vol.203 , pp. 875-884
    • de Lorenzo, V.1    Giovannini, F.2    Herrero, M.3    Neilands, J.B.4
  • 11
    • 0031058129 scopus 로고    scopus 로고
    • An operon containing fumC and sodA encoding fumarase C and manganese superoxide dismutase is controlled by the ferric uptake regulator in Pseudomonas aeruginosa: Fur mutants produce elevated alginate levels
    • Hassett DJ, Howell ML, Ochsner UA, Vasil ML, Johnson Z, Dean GE. An operon containing fumC and sodA encoding fumarase C and manganese superoxide dismutase is controlled by the ferric uptake regulator in Pseudomonas aeruginosa: Fur mutants produce elevated alginate levels. J Bacteriol 1997;179:1452-1459.
    • (1997) J Bacteriol , vol.179 , pp. 1452-1459
    • Hassett, D.J.1    Howell, M.L.2    Ochsner, U.A.3    Vasil, M.L.4    Johnson, Z.5    Dean, G.E.6
  • 12
    • 0032536843 scopus 로고    scopus 로고
    • The interaction of the Vibrio cholerae transcription factors, Fur and Irg B, with the overlapping promoters of two virulence genes, irgA and irgB
    • Watnick PI, Butterton JR, Calderwood SB. The interaction of the Vibrio cholerae transcription factors, Fur and Irg B, with the overlapping promoters of two virulence genes, irgA and irgB. Gene 1998;209:65-70.
    • (1998) Gene , vol.209 , pp. 65-70
    • Watnick, P.I.1    Butterton, J.R.2    Calderwood, S.B.3
  • 13
    • 0029966305 scopus 로고    scopus 로고
    • Gene repression by the ferric uptake regulator in Pseudomonas aeruginosa: Cycle selection of iron-regulated genes
    • Ochsner UA, Vasil ML. Gene repression by the ferric uptake regulator in Pseudomonas aeruginosa: cycle selection of iron-regulated genes. Proc Natl Acad Sci USA 1996;93:4409-414.
    • (1996) Proc Natl Acad Sci USA , vol.93 , pp. 4409-4414
    • Ochsner, U.A.1    Vasil, M.L.2
  • 16
    • 0031033529 scopus 로고    scopus 로고
    • Purification of Vibrio cholerae Fur and estimation of its intracellular abundance by antibody sandwich enzyme-linked immunosorbent assay
    • Watnick PI, Eto T, Takahashi H, Calderwood SB. Purification of Vibrio cholerae Fur and estimation of its intracellular abundance by antibody sandwich enzyme-linked immunosorbent assay. J Bacteriol 1997;179:243-247.
    • (1997) J Bacteriol , vol.179 , pp. 243-247
    • Watnick, P.I.1    Eto, T.2    Takahashi, H.3    Calderwood, S.B.4
  • 17
    • 0035982906 scopus 로고    scopus 로고
    • GeneChip expression analysis of the iron starvation response in Pseudomonas aerugi-nosa: Identification of novel pyoverdine biosynthesis genes
    • Ochsner UA, Wilderman PJ, Vasil AI, Vasil ML. GeneChip expression analysis of the iron starvation response in Pseudomonas aerugi-nosa: identification of novel pyoverdine biosynthesis genes. Mol Microbiol 2002;45:1277-1287.
    • (2002) Mol Microbiol , vol.45 , pp. 1277-1287
    • Ochsner, U.A.1    Wilderman, P.J.2    Vasil, A.I.3    Vasil, M.L.4
  • 18
    • 0032704951 scopus 로고    scopus 로고
    • The response of Pseudomonas aeruginosa to iron: Genetics, biochemistry and virulence
    • Vasil ML, Ochsner UA. The response of Pseudomonas aeruginosa to iron: genetics, biochemistry and virulence. Mol Microbiol 1999;34: 399-413.
    • (1999) Mol Microbiol , vol.34 , pp. 399-413
    • Vasil, M.L.1    Ochsner, U.A.2
  • 21
    • 28444438519 scopus 로고    scopus 로고
    • Iron and Fur regulation in Vibrio cholerae and the role of Fur in virulence
    • Mey AR, Wyckoff EE, Kanukurthy V, Fisher CR, Payne SM. Iron and Fur regulation in Vibrio cholerae and the role of Fur in virulence. Infect Immun 2005;73:8167-8178.
    • (2005) Infect Immun , vol.73 , pp. 8167-8178
    • Mey, A.R.1    Wyckoff, E.E.2    Kanukurthy, V.3    Fisher, C.R.4    Payne, S.M.5
  • 22
    • 33746455962 scopus 로고    scopus 로고
    • Structural changes of Esch-erichia coli ferric uptake regulator during metal-dependent dimeri-zation and activation explored by NMR and X-ray crystallography
    • Pecqueur L, D'Autreaux B, Dupuy J, Nicolet Y, Jacquamet L, Brutscher B, Michaud-Soret I, Bersch B. Structural changes of Esch-erichia coli ferric uptake regulator during metal-dependent dimeri-zation and activation explored by NMR and X-ray crystallography. J Biol Chem 2006;281:21286-21295.
    • (2006) J Biol Chem , vol.281 , pp. 21286-21295
    • Pecqueur, L.1    D'Autreaux, B.2    Dupuy, J.3    Nicolet, Y.4    Jacquamet, L.5    Brutscher, B.6    Michaud-Soret, I.7    Bersch, B.8
  • 23
    • 34248219997 scopus 로고    scopus 로고
    • Crystal structure and function of the zinc uptake regulator FurB from Mycobacterium tuberculosis
    • Lucarelli D, Russo S, Garman E, Milano A, Meyer-Klaucke W, Pohl E. Crystal structure and function of the zinc uptake regulator FurB from Mycobacterium tuberculosis. J Biol Chem 2007;282:9914-9922.
    • (2007) J Biol Chem , vol.282 , pp. 9914-9922
    • Lucarelli, D.1    Russo, S.2    Garman, E.3    Milano, A.4    Meyer-Klaucke, W.5    Pohl, E.6
  • 25
    • 26844508470 scopus 로고    scopus 로고
    • Characterization of the DNA-binding site in the ferric uptake regulator protein from Esche-richia coli by UV crosslinking and mass spectrometry
    • Tiss A, Barre O, Michaud-Soret I, Forest E. Characterization of the DNA-binding site in the ferric uptake regulator protein from Esche-richia coli by UV crosslinking and mass spectrometry. FEBS Lett 2005;579:5454-5460.
    • (2005) FEBS Lett , vol.579 , pp. 5454-5460
    • Tiss, A.1    Barre, O.2    Michaud-Soret, I.3    Forest, E.4
  • 27
    • 0000311380 scopus 로고    scopus 로고
    • Identification of the two zinc-bound cysteines in the ferric uptake regulation protein from Escherichia coli: Chemical modification and mass spectrometry analysis
    • Gonzalez de Peredo A, Saint-Pierre C, Adrait A, Jacquamet L, Latour JM, Michaud-Soret I, Forest E. Identification of the two zinc-bound cysteines in the ferric uptake regulation protein from Escherichia coli: chemical modification and mass spectrometry analysis. Biochemistry 1999;38:8582-8589.
    • (1999) Biochemistry , vol.38 , pp. 8582-8589
    • Gonzalez de Peredo, A.1    Saint-Pierre, C.2    Adrait, A.3    Jacquamet, L.4    Latour, J.M.5    Michaud-Soret, I.6    Forest, E.7
  • 28
    • 0035967907 scopus 로고    scopus 로고
    • Conformational changes of the ferric uptake regulation protein upon metal activation and DNA binding; first evidence of structural homologies with the diphtheria toxin repressor
    • Gonzalez de Peredo A, Saint-Pierre C, Latour JM, Michaud-Soret I, Forest E. Conformational changes of the ferric uptake regulation protein upon metal activation and DNA binding; first evidence of structural homologies with the diphtheria toxin repressor. J Mol Biol 2001;310:83-91.
    • (2001) J Mol Biol , vol.310 , pp. 83-91
    • Gonzalez de Peredo, A.1    Saint-Pierre, C.2    Latour, J.M.3    Michaud-Soret, I.4    Forest, E.5
  • 29
    • 0019447069 scopus 로고
    • Regulation of ferric iron transport in Escherichia coli K12: Isolation of a constitutive mutant
    • Hantke K. Regulation of ferric iron transport in Escherichia coli K12: isolation of a constitutive mutant. Mol Gen Genet 1981;182: 288-292.
    • (1981) Mol Gen Genet , vol.182 , pp. 288-292
    • Hantke, K.1
  • 30
    • 0025802603 scopus 로고
    • The binding of the ferric uptake regulation protein to a DNA fragment
    • Saito T, Williams RJ. The binding of the ferric uptake regulation protein to a DNA fragment. Eur J Biochem 1991;197:43-47.
    • (1991) Eur J Biochem , vol.197 , pp. 43-47
    • Saito, T.1    Williams, R.J.2
  • 31
    • 0029041226 scopus 로고
    • Lethal oxi-dative damage and mutagenesis are generated by iron in 8 Fur mutants of Escherichia coli: Protective role of superoxide dismutase
    • Touati D, Jacques M, Tardat B, Bouchard L, Despied S. Lethal oxi-dative damage and mutagenesis are generated by iron in 8 Fur mutants of Escherichia coli: protective role of superoxide dismutase. J Bacteriol 1995;177:2305-2314.
    • (1995) J Bacteriol , vol.177 , pp. 2305-2314
    • Touati, D.1    Jacques, M.2    Tardat, B.3    Bouchard, L.4    Despied, S.5
  • 32
    • 0028151003 scopus 로고
    • Site-directed mutagenesis of the ferric uptake regulation gene of Escherichia-coli
    • Coy M, Doyle C, Besser J, Neilands JB. Site-directed mutagenesis of the ferric uptake regulation gene of Escherichia-coli. Biometals 1994;7:292-298.
    • (1994) Biometals , vol.7 , pp. 292-298
    • Coy, M.1    Doyle, C.2    Besser, J.3    Neilands, J.B.4
  • 33
    • 0027955329 scopus 로고
    • Characterization of the Vibrio anguillarum Fur gene-role in regulation of expression of the fata outer-membrane protein and catechols
    • Tolmasky ME, Wertheimer AM, Actis LA, Crosa JH. Characterization of the Vibrio anguillarum Fur gene-role in regulation of expression of the fata outer-membrane protein and catechols. J Bac-teriol 1994;176:213-220.
    • (1994) J Bac-teriol , vol.176 , pp. 213-220
    • Tolmasky, M.E.1    Wertheimer, A.M.2    Actis, L.A.3    Crosa, J.H.4
  • 34
    • 0033545903 scopus 로고    scopus 로고
    • Spectroscopic and saturation magnetization properties of the manganese-and cobalt-substituted Fur (ferric uptake regulation) protein from Escherichia coli
    • Adrait A, Jacquamet L, Le Pape L, de Peredo AG, Aberdam D, Hazemann JL, Latour JM, Michaud-Soret I. Spectroscopic and saturation magnetization properties of the manganese-and cobalt-substituted Fur (ferric uptake regulation) protein from Escherichia coli. Biochemistry 1999;38:6248-6260.
    • (1999) Biochemistry , vol.38 , pp. 6248-6260
    • Adrait, A.1    Jacquamet, L.2    Le Pape, L.3    de Peredo, A.G.4    Aberdam, D.5    Hazemann, J.L.6    Latour, J.M.7    Michaud-Soret, I.8
  • 36
    • 51349134974 scopus 로고    scopus 로고
    • Structure-based prediction of transcription factor binding sites using a protein-DNA docking approach
    • Liu Z, Guo JT, Li T, Xu Y. Structure-based prediction of transcription factor binding sites using a protein-DNA docking approach. Proteins 2008;72:1114-1124.
    • (2008) Proteins , vol.72 , pp. 1114-1124
    • Liu, Z.1    Guo, J.T.2    Li, T.3    Xu, Y.4
  • 37
    • 66449095082 scopus 로고    scopus 로고
    • Case DA, Darden TA, Cheatham TE, I, Simmerling CL, Wang J, Duke RE, Luo R, Merz KM, Pearlman DA, Crowley M, Walker RC, Zhang W, Wang B, Hayik S, Roitberg AE, Seabra G, Wong KF, Paesani F, Wu X, Brozell S, Tsui V, Gohlke H, Yang L, Tan C, Mongan J, Hornak V, Cui G, Beroza P, Mathews DH, Schafmeister C, Ross WS, Kollman PA. AMBER9. San Francisco: University of California; 2006.
    • Case DA, Darden TA, Cheatham TE, I, Simmerling CL, Wang J, Duke RE, Luo R, Merz KM, Pearlman DA, Crowley M, Walker RC, Zhang W, Wang B, Hayik S, Roitberg AE, Seabra G, Wong KF, Paesani F, Wu X, Brozell S, Tsui V, Gohlke H, Yang L, Tan C, Mongan J, Hornak V, Cui G, Beroza P, Mathews DH, Schafmeister C, Ross WS, Kollman PA. AMBER9. San Francisco: University of California; 2006.
  • 38
    • 0037174385 scopus 로고    scopus 로고
    • All-atom structure prediction and folding simulations of a stable protein
    • Simmerling C, Strockbine B, Roitberg AE. All-atom structure prediction and folding simulations of a stable protein. J Am Chem Soc 2002;124:11258-11259.
    • (2002) J Am Chem Soc , vol.124 , pp. 11258-11259
    • Simmerling, C.1    Strockbine, B.2    Roitberg, A.E.3
  • 42
    • 4444240014 scopus 로고    scopus 로고
    • Classical force field parameters for the heme prosthetic group of cytochrome c
    • Autenrieth F, Tajkhorshid E, Baudry J, Luthey-Schulten Z. Classical force field parameters for the heme prosthetic group of cytochrome c. J Comput Chem 2004;25:1613-1622.
    • (2004) J Comput Chem , vol.25 , pp. 1613-1622
    • Autenrieth, F.1    Tajkhorshid, E.2    Baudry, J.3    Luthey-Schulten, Z.4
  • 43
    • 34548044247 scopus 로고    scopus 로고
    • Protein environment facilitates O-2 binding in non-heme iron enzyme. An insight from ONIOM calculations on isopenicillin N synthase (IPNS)
    • Lundberg M, Morokuma K. Protein environment facilitates O-2 binding in non-heme iron enzyme. An insight from ONIOM calculations on isopenicillin N synthase (IPNS). J Phys Chem B 2007; 111:9380-9389.
    • (2007) J Phys Chem B , vol.111 , pp. 9380-9389
    • Lundberg, M.1    Morokuma, K.2
  • 44
    • 0033927682 scopus 로고    scopus 로고
    • Structural differences of matrix metalloproteinases. Homology modeling and energy minimization of enzyme-substrate complexes
    • Terp GE, Christensen IT, Jorgensen FS. Structural differences of matrix metalloproteinases. Homology modeling and energy minimization of enzyme-substrate complexes. J Biomol Struct Dyn 2000; 17:933-946.
    • (2000) J Biomol Struct Dyn , vol.17 , pp. 933-946
    • Terp, G.E.1    Christensen, I.T.2    Jorgensen, F.S.3
  • 45
    • 0029115487 scopus 로고
    • Zinc-binding in proteins and solution-a simple but accurate nonbonded representation
    • Stote RH, Karplus M. Zinc-binding in proteins and solution-a simple but accurate nonbonded representation. Proteins: Struct Funct Genet 1995;23:12-31.
    • (1995) Proteins: Struct Funct Genet , vol.23 , pp. 12-31
    • Stote, R.H.1    Karplus, M.2
  • 46
    • 0034597622 scopus 로고    scopus 로고
    • Calculation and prediction of binding free energies for the matrix metalloproteinases
    • Donini OA, Kollman PA. Calculation and prediction of binding free energies for the matrix metalloproteinases. J Med Chem 2000;43:4180-4188.
    • (2000) J Med Chem , vol.43 , pp. 4180-4188
    • Donini, O.A.1    Kollman, P.A.2
  • 47
    • 33846823909 scopus 로고
    • Particle mesh Ewald-an N.Log(N) method for Ewald sums in large systems
    • Darden T, York D, Pedersen L. Particle mesh Ewald-an N.Log(N) method for Ewald sums in large systems. J Chem Phys 1993;98: 10089-10092.
    • (1993) J Chem Phys , vol.98 , pp. 10089-10092
    • Darden, T.1    York, D.2    Pedersen, L.3
  • 48
    • 33646940952 scopus 로고
    • Numerical-integration of cartesian equations of motion of a system with constraints-molecular-dynamics of N-alkanes
    • Ryckaert JP, Ciccotti G, Berendsen HJC. Numerical-integration of cartesian equations of motion of a system with constraints-molecular-dynamics of N-alkanes. J Comput Phys 1977;23:327-341.
    • (1977) J Comput Phys , vol.23 , pp. 327-341
    • Ryckaert, J.P.1    Ciccotti, G.2    Berendsen, H.J.C.3
  • 50
    • 0032560959 scopus 로고    scopus 로고
    • Continuum solvent studies of the stability of DNA, RNA, and phos-phoramidate-DNA helices
    • Srinivasan J, Cheatham TE, Cieplak P, Kollman PA, Case DA. Continuum solvent studies of the stability of DNA, RNA, and phos-phoramidate-DNA helices. J Am Chem Soc 1998;120:9401-9409.
    • (1998) J Am Chem Soc , vol.120 , pp. 9401-9409
    • Srinivasan, J.1    Cheatham, T.E.2    Cieplak, P.3    Kollman, P.A.4    Case, D.A.5
  • 51
    • 0036771626 scopus 로고    scopus 로고
    • Accelerated Poisson-Boltzmann calculations for static and dynamic systems
    • LuoR,DavidL,GilsonMK.Accelerated Poisson-Boltzmann calculations for static and dynamic systems. J Comput Chem 2002;23: 1244-1253.
    • (2002) J Comput Chem , vol.23 , pp. 1244-1253
    • Luo, R.1    David, L.2    Gilson, M.K.3
  • 52
    • 0000043930 scopus 로고    scopus 로고
    • Solvation free energy of biomacro-molecules: Parameters for a modified generalized born model consistent with the AMBER force field
    • Jayaram B, Sprous D, Beveridge DL. Solvation free energy of biomacro-molecules: parameters for a modified generalized born model consistent with the AMBER force field. J Phys Chem B 1998;102: 9571-9576.
    • (1998) J Phys Chem B , vol.102 , pp. 9571-9576
    • Jayaram, B.1    Sprous, D.2    Beveridge, D.L.3
  • 53
    • 0000538815 scopus 로고
    • Analytical molecular-surface calculation
    • Connolly ML. Analytical molecular-surface calculation. J Appl Crys-tallogr 1983;16:548-558.
    • (1983) J Appl Crys-tallogr , vol.16 , pp. 548-558
    • Connolly, M.L.1
  • 54
    • 0000408363 scopus 로고    scopus 로고
    • Approximate atomic surfaces from linear combinations of pairwise overlaps (LCPO)
    • Weiser J, Shenkin PS, Still WC. Approximate atomic surfaces from linear combinations of pairwise overlaps (LCPO). J Comput Chem 1999;20:217-230.
    • (1999) J Comput Chem , vol.20 , pp. 217-230
    • Weiser, J.1    Shenkin, P.S.2    Still, W.C.3
  • 56
    • 0028331255 scopus 로고
    • Normal-mode analysis of protein dynamics
    • Case DA. Normal-mode analysis of protein dynamics. Curr Opin Struct Biol 1994;4:285-290.
    • (1994) Curr Opin Struct Biol , vol.4 , pp. 285-290
    • Case, D.A.1
  • 57
    • 0036667431 scopus 로고    scopus 로고
    • The ferric uptake regulator of Pseudomonas aeruginosa has no essential cyste-ine residues and does not contain a structural zinc ion
    • Lewin AC, Doughty PA, Flegg L, Moore GR, Spiro S. The ferric uptake regulator of Pseudomonas aeruginosa has no essential cyste-ine residues and does not contain a structural zinc ion. Microbiology 2002;148:2449-2456.
    • (2002) Microbiology , vol.148 , pp. 2449-2456
    • Lewin, A.C.1    Doughty, P.A.2    Flegg, L.3    Moore, G.R.4    Spiro, S.5
  • 58
    • 33747722767 scopus 로고    scopus 로고
    • 21 site in the Bacillus subtilis peroxide sensor PerR
    • 21 site in the Bacillus subtilis peroxide sensor PerR. J Biol Chem 2006;281:23567-23578.
    • (2006) J Biol Chem , vol.281 , pp. 23567-23578
    • Lee, J.W.1    Helmann, J.D.2
  • 59
    • 33645037891 scopus 로고    scopus 로고
    • The PerR transcription factor senses H2O2 by metal-catalysed histidine oxidation
    • Lee JW, Helmann JD. The PerR transcription factor senses H2O2 by metal-catalysed histidine oxidation. Nature 2006;440: 363-367.
    • (2006) Nature , vol.440 , pp. 363-367
    • Lee, J.W.1    Helmann, J.D.2
  • 60
    • 26644471490 scopus 로고    scopus 로고
    • Metal binding characteristics and role of iron oxidation in the ferric uptake regulator from Escherichia coli
    • Mills SA, Marletta MA. Metal binding characteristics and role of iron oxidation in the ferric uptake regulator from Escherichia coli. Biochemistry 2005;44:13553-13559.
    • (2005) Biochemistry , vol.44 , pp. 13553-13559
    • Mills, S.A.1    Marletta, M.A.2
  • 61
    • 0032581662 scopus 로고    scopus 로고
    • Structure of the metal-ion-activated diphtheria toxin repressor tox operator complex
    • White A, Ding XC, vanderSpek JC, Murphy JR, Ringe D. Structure of the metal-ion-activated diphtheria toxin repressor tox operator complex. Nature 1998;394:502-506.
    • (1998) Nature , vol.394 , pp. 502-506
    • White, A.1    Ding, X.C.2    vanderSpek, J.C.3    Murphy, J.R.4    Ringe, D.5
  • 62
    • 0000868851 scopus 로고    scopus 로고
    • Crystal structure of a cobalt-activated diphtheria toxin repressor-DNA complex reveals a metal-binding SH3-like domain
    • Pohl E, Holmes RK, Hol WG. Crystal structure of a cobalt-activated diphtheria toxin repressor-DNA complex reveals a metal-binding SH3-like domain. J Mol Biol 1999;292:653-667.
    • (1999) J Mol Biol , vol.292 , pp. 653-667
    • Pohl, E.1    Holmes, R.K.2    Hol, W.G.3
  • 63
    • 0027936183 scopus 로고
    • Structural and functional analyses of mutant Fur proteins with impaired regulatory function
    • Wertheimer AM, Tolmasky ME, Actis LA, Crosa JH. Structural and functional analyses of mutant Fur proteins with impaired regulatory function. J Bacteriol 1994;176:5116-5122.
    • (1994) J Bacteriol , vol.176 , pp. 5116-5122
    • Wertheimer, A.M.1    Tolmasky, M.E.2    Actis, L.A.3    Crosa, J.H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.