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Fig. 54 in The scope of flavin-dependent reactions and processes in the model plant Arabidopsis thaliana

Fig. 54. Mechanism of Erv and Ero as partners for protein disulfide isomerase. In contrast to quiescin sulfhydryl oxidase, Erv and Ero do not interact directly with client proteins but serve to keep protein disulfide isomerase in an active oxidized state in order to allow for the proper generation of disulfide bonds in client proteins. Reduced Erv and Ero are reoxidized by dioxygen giving rise to the production of hydrogen peroxide.

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Fig. 52 in The scope of flavin-dependent reactions and processes in the model plant Arabidopsis thaliana

Fig. 52. Reaction of glutathione reductase with its cognate substrate glutathione. Glutathione reductase is primed by reduction at the expense of NADPH generating the reduced FAD, which subsequently reduces the internal disulfide bond. Next, oxidized glutathione (GSSG) is cleaved to two molecules of (reduced) glutathione (GSH) by a dithiol-disulfide exchange reaction. For a detailed mechanistic discussion see Miller (2013).

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Fig. 51 in The scope of flavin-dependent reactions and processes in the model plant Arabidopsis thaliana

Fig. 51. Proposed reaction mechanism of lysine-specific histone demethylase. The oxidation of a methylated lysine residue (typically in position 4 of histone 3) is shown. Initially, oxidation of the substrate generates reduced FAD, which is re-oxidized by dioxygen leading to the production of hydrogen peroxide. The intermediate imine is hydrolyzed by water to produce the final products, the demethylated lysine side chain and formaldehyde (see also reaction of sarcosine oxidase).

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Fig. 50 in The scope of flavin-dependent reactions and processes in the model plant Arabidopsis thaliana

Fig. 50. Reaction catalyzed by TYW1. N1-methylguanosine (m1G) in position 37 of the tRNA is converted to 4-demethylwyosine (imG-14). The two carbon atoms required to set up the tricyclic system are derived from pyruvate (Lombard and Hamdane, 2017).

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Fig. 45 in The scope of flavin-dependent reactions and processes in the model plant Arabidopsis thaliana

Fig. 45. Reaction catalalyzed by quinone reductases. As an example, the reduction of benzoquinone is shown. However, quinone reductases generally have a broad substrate spectrum with regard to modifications at the aromatic ring. The source of electrons is typically NAD(P)H.

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Fig. 41 in The scope of flavin-dependent reactions and processes in the model plant Arabidopsis thaliana

Fig. 41. Reaction catalyzed by cellodextrin oxidase (AtBBE22/CELLOX). This enzyme oxidizes the reducing end of oligosaccharides with a preference to chains with n = 1–4 (Locci et al., 2019). Based on the analysis of the oxygen reactivity motif, all reduced cellodextrin oxidases are predicted to react with dioxygen to yield hydrogen peroxide (Zafred et al., 2015) (see also discussion below).

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Fig. 49 in The scope of flavin-dependent reactions and processes in the model plant Arabidopsis thaliana

Fig. 49. Reactions catalyzed by tRNA-dihydrouridine synthase (DUS) and the MnmE/MnmG (GidA) complex. (Top) Reduction of tRNA-uridine by tRNA-dihydrouridine synthase. The reduced FMN is generated at the expense of NADH. (Bottom) The modification of tRNA-uridine by the MmnEG complex requires GTP and methylenetetrahydrofolate (MTHF). The latter provides the carbon atom that is directly transferred to the 5′-position of the pryrimidine ring. Depending on whether ammonia or glycine is used as a co-substrate either nm5U or cmnm5U are generated. For more details on the reaction mechanism see text and Moukadiri et al. (2009).

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Fig. 46 in The scope of flavin-dependent reactions and processes in the model plant Arabidopsis thaliana

Fig. 46). The ten genes encoding RBOHs in A. thaliana exhibit distinct expression patterns and exert special roles in various processes ranging from immune responses to plant development (for a review see Smirnoff and Arnaud, 2019). For example, RBOHD was shown to participate in wound response and systemic signaling (Miller et al., 2009) and RBOHD/F is involved in stomatal function and pathogen defense

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Fig. 40 in The scope of flavin-dependent reactions and processes in the model plant Arabidopsis thaliana

Fig. 40. Reaction catalyzed by oligogalacturonide oxidase (AtBBE20). This enzyme specifically oxidizes oligogalacturonides with similar activities found for a chain length of n = 2 to n = 12 (Benedetti et al., 2018). Based on the analysis of the oxygen reactivity motif, all reduced oligogalacturonide oxidases are predicted to react with dioxygen to yield hydrogen peroxide (Zafred et al., 2015).

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Fig. 36 in The scope of flavin-dependent reactions and processes in the model plant Arabidopsis thaliana

Fig. 36. Putative mechanism of isomerization followed by reduction. Isomerization is initiated by hydride transfer resulting in the removal of a deuteride from the (25)-carbon. This deuteride may be accepted by the flavin cofactor in exchange to the hydride provided in the initial step. Since the hydrogens of the reduced FAD cofactor are prone to exchange with solvent-borne hydrogens the reduction of the double bond will occur by transfer of a hydride

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Fig. 38 in The scope of flavin-dependent reactions and processes in the model plant Arabidopsis thaliana

Fig. 38. Reduction of (9S,13S)-12-oxophytodienoic acid by 12-oxophytodienoic acid reductase 3. The preferred electron donor for this reaction is NADH, which is also the case for most old yellow enzyme homologs characterized thus far. Although the exact role of the other homologs in plant biochemistry is currently unknown, we hypothesize that they carry out similar C– –C-bond reductions in as yet unidentified substrates.

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Fig. 32 in The scope of flavin-dependent reactions and processes in the model plant Arabidopsis thaliana

Fig. 32. Last step in abscisic acid biosynthesis catalyzed by abscisic aldehyde oxidase. Note that substrate oxidation occurs at the Moco and electrons are transferred to the FAD cofactor via two iron-sulfur-clusters, i.e. the same reaction mechanism as found in xanthine dehydrogenase. Reoxidation of reduced FAD occurs by dioxygen generating hydrogen peroxide.

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Fig. 31 in The scope of flavin-dependent reactions and processes in the model plant Arabidopsis thaliana

Fig. 31. Reaction of zeaxanthin epoxidase. The enzyme catalyzes the consecutive epoxidation (monooxygenation) of both β-ionone rings in all-trans- zeaxanthin at the expense of reduced NAD(P)H. Dioxygen is cleaved during the reaction with one oxygen atom introduced into the substrate and the other one being released as water.

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Fig. 26 in The scope of flavin-dependent reactions and processes in the model plant Arabidopsis thaliana

Fig. 26. Reaction catalyzed by protoporphyrinogen IX oxidase. The conversion of protoporphyrinogen IX to protoporphyrin IX, the last common step in heme and chlorophyll biosynthesis, requires three consecutive two-electron oxidations. Regeneration of the reduced FAD cofactor occurs by reoxidation with dioxygen leading to the production of hydrogen peroxide.

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Fig. 21 in The scope of flavin-dependent reactions and processes in the model plant Arabidopsis thaliana

Fig. 21. Oxidation of L-aspartate to iminoaspartate initiates NADþ biosynthesis. The reduced FAD cofactor is reoxidized by dioxygen or fumarate leading to the production of either hydrogen peroxide or succinate (not shown).

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Fig. 19 in The scope of flavin-dependent reactions and processes in the model plant Arabidopsis thaliana

Fig. 19. Reaction catalyzed by squalene epoxidase. The reducing equivalents are delivered by NADPH, and therefore, the enzyme was assigned to subclass A of flavin-dependent monooxygenases (Paul et al., 2021). Similar to zeaxanthine epoxidase the enzyme forms an unusual epoxide (see Fig. 31).

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Fig. 18 in The scope of flavin-dependent reactions and processes in the model plant Arabidopsis thaliana

Fig. 18. Reaction catalyzed by dihydrooroate dehydrogenase. In the pyrimidine-half reaction the FMN cofactor is reduced by transfer of a hydride to the N(5)-position of the isoalloxazine ring (highlighted in red) followed by proton abstraction from the 5-position of dihydroorotate. A. thaliana dihydrooroate dehydrogenase belongs to the class 2 enzymes that are localized in the inter membrane space and associated with the inner mitochondrial membrane. Thus, reoxidation occurs by two successive one-electron transfer steps from the reduced FMN to CoQ (shown here as a single step). For a detailed discussion on the reaction mechanism see Palfey (2013). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

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Fig. 35 in The scope of flavin-dependent reactions and processes in the model plant Arabidopsis thaliana

Fig. 35. Reaction catalyzed by 3-β-hydroxysterol Δ24-reductase. The top reaction shows the formal reduction of the side chain double bond in the conversion of 24-methylenecholesterol to campesterol. The middle and bottom reactions depict the reduction of different side chains as present in isofucosterol, dolichosterone and 6-deoxodolichosterone. In the case of the human ortholog, NADPH serves as the reducing agent for the reduction of the FAD (Waterham et al., 2001).

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Fig. 27 in The scope of flavin-dependent reactions and processes in the model plant Arabidopsis thaliana

Fig. 27. Reaction of 7-hydroxymethyl chlorophyll a reductase. Based on the structure of the enzyme, ferredoxin serves as the electron donor for a proton-activated electron transfer pathway (for mechanistic details see Wang and Liu, 2016). The hydroxymethyl-group subjected to reduction is highlighted in red. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

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Fig. 37 in The scope of flavin-dependent reactions and processes in the model plant Arabidopsis thaliana

Fig. 37. Reaction of cytokinin dehydrogenase. Note that the electron acceptor for the reoxidation of the covalently bound FAD cofactor remains unknown. However, quinones efficiently oxidize the reduced FAD, and thus, are likely candidates as electron acceptors, at least for some of the cytokinin dehydrogenases (Fr´ebortov´a et al., 2004).

opennotspecifiedSep 2021View details →

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Allen Brain Atlas

Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.

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behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

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electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

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behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record