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Significance Diflavin-linked disulfide oxidoreductases (DDORs) are structurally related to the low - molecular-weight type NADP-dependent thioredoxin reductases, although they do not share a common function. The biochemical and structural characterization of DDORs has revealed a previously unreported mechanism for the transfer of reducing equivalents in flavoenzymes. The present work illustrates the extent to which nature has experimented with flavins as enzyme cofactors in the evolution of redox reactions.
Models, Molecular, Protein Conformation, alpha-Helical, Protein Folding, Thioredoxin-Disulfide Reductase, Protein Conformation, Rossmann fold, Gene Expression, Crystallography, X-Ray, Cyanobacteria, Substrate Specificity, Bacterial Proteins, Models, flavoprotein, Protein Interaction Domains and Motifs, Amino Acid Sequence, Disulfides, redox active disulfide, sulfhydryl, Structural Homology, Crystallography, Binding Sites, Protein, alpha-Helical, Cell Membrane, Synechocystis, Molecular, transfer of reducing equivalents, Recombinant Proteins, Flavoprotein, Kinetics, Redox active disulfide, Structural Homology, Protein, Transfer of reducing equivalents, X-Ray, Biocatalysis, Flavin-Adenine Dinucleotide, beta-Strand, Protein Conformation, beta-Strand, Sulfhydry, Oxidoreductases, Sequence Alignment, Protein Binding
Models, Molecular, Protein Conformation, alpha-Helical, Protein Folding, Thioredoxin-Disulfide Reductase, Protein Conformation, Rossmann fold, Gene Expression, Crystallography, X-Ray, Cyanobacteria, Substrate Specificity, Bacterial Proteins, Models, flavoprotein, Protein Interaction Domains and Motifs, Amino Acid Sequence, Disulfides, redox active disulfide, sulfhydryl, Structural Homology, Crystallography, Binding Sites, Protein, alpha-Helical, Cell Membrane, Synechocystis, Molecular, transfer of reducing equivalents, Recombinant Proteins, Flavoprotein, Kinetics, Redox active disulfide, Structural Homology, Protein, Transfer of reducing equivalents, X-Ray, Biocatalysis, Flavin-Adenine Dinucleotide, beta-Strand, Protein Conformation, beta-Strand, Sulfhydry, Oxidoreductases, Sequence Alignment, Protein Binding
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