Analysis of Benzoate 1,2-Dioxygenase Identifies Shared Electron Transfer Components With DxnA1A2 in Rhizorhabdus wittichii RW1. [PDF]
Ivanovski I, Eleya S, Zylstra GJ.
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Regulating ferredoxin electron transfer using nanobody and antigen interactions
Albert Truong, Jonathan J. Silberg
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Direct coupling of lactate oxidation with butyryl-CoA formation via a canonical electron transfer flavoprotein in Fusobacterium nucleatum. [PDF]
Do LTM, Godin R, Wolthers KR.
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The cryo-EM structure of Photosystem I from Chromera velia with a bound superoxide dismutase heterodimer. [PDF]
Yuan X +11 more
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A widespread hydrogenase supports fermentative growth of gut bacteria in healthy people. [PDF]
Welsh C +29 more
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Computational approaches in chemical space exploration for carbon fixation pathways. [PDF]
Abel AS +5 more
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Predicting Iron-Sulfur Cluster Redox Potentials: A Simple Model Derived from Protein Structures. [PDF]
Min J +4 more
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Ferredoxin and Photosynthetic Phosphorylation
Nature, 1967The iron-bearing protein ferredoxin is present in all photosynthetlc cells. It has now been shown that ferredoxin can catalyse, by two distinct photochemical reactions, the production of ATP in cell-free photosynthetic systems at rates comparable with the maximum rates of photosynthesis in vivo.
D I, Arnon, H Y, Tsujimoto, B D, McSwain
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Immobilized ferredoxins for affinity chromatography of ferredoxin-dependent enzymes
Journal of Chromatography A, 1992An immobilized ferredoxin more stable than the conventional immobilized spinach ferrodoxin was prepared by reacting CNBr-Sepharose with ferredoxins isolated from barley and Synechococcus vulcanus, a thermophilic blue-green alga. The dissociation constants of immobilized ferredoxin from spinach, barley and S.
N, Sakihama +5 more
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Interaction of ferredoxin and ferredoxin-NADP reductase with thylakoids
Archives of Biochemistry and Biophysics, 1983Ferredoxin-NADP reductase accounts for about 50% of the NADPH diaphorase activity of spinach leaf homogenates. The enzyme is bound to thylakoid membranes, but can be slowly extracted by aqueous buffers. Ferredoxin-NADP reductase can be extracted from the membranes by a 1- to 2-min treatment with a low concentration of trypsin. This treatment completely
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