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| | JMJ32 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein. (345 aa) |
| | PCO3 | Plant cysteine oxidase 3; Oxidizes N-terminal cysteine residues, thus preparing the protein for N-end rule pathway-mediated proteasomal degradation. Belongs to the cysteine dioxygenase family. (282 aa) |
| | P4H5 | Prolyl 4-hydroxylase 5; Catalyzes the post-translational formation of 4- hydroxyproline in -Xaa-Pro-Gly- sequences in proline-rich peptide sequences of plant glycoproteins and other proteins. Hydroxyprolines are important constituent of many plant cell wall glycoproteins such as extensins, hydroxyproline-rich glycoproteins, lectins and arabinogalactan proteins. Possesses high affinity for leucine-rich repeat and proline-rich extensins of root cell walls that are essential for root hair development. Hydroxyprolines define the subsequent O- glycosylation sites by arabinosyltransferases w [...] (291 aa) |
| | GA3OX1 | Gibberellin 3-beta-dioxygenase 1; Converts the inactive gibberellin (GA) precursors GA9 and GA20 in the bioactives gibberellins GA4 and GA1. Involved in the production of bioactive GA for vegetative growth and development. Belongs to the iron/ascorbate-dependent oxidoreductase family. GA3OX subfamily. (358 aa) |
| | GA20OX1 | Gibberellin 20 oxidase 1; Key oxidase enzyme in the biosynthesis of gibberellin that catalyzes the conversion of GA12 and GA53 to GA9 and GA20 respectively, via a three-step oxidation at C-20 of the GA skeleton. GA53 is less effectively oxidized than GA12, and GA25 is also formed as a minor product. Involved in the promotion of the floral transition, fertility and silique elongation, but plays only a minor role in elongation of seedling organs. Acts redundantly with GA20OX2. Belongs to the iron/ascorbate-dependent oxidoreductase family. GA20OX subfamily. (377 aa) |
| | GA20OX2 | Gibberellin 20 oxidase 2; Key oxidase enzyme in the biosynthesis of gibberellin that catalyzes the conversion of GA12 and GA53 to GA9 and GA20 respectively, via a three-step oxidation at C-20 of the GA skeleton. GA53 is less effectively oxidized than GA12, and GA25 is also formed as a minor product. Involved in the promotion of the floral transition, fertility and silique elongation, but plays only a minor role in elongation of seedling organs. Acts redundantly with GA20OX1. (378 aa) |
| | GA20OX3 | Gibberellin 20 oxidase 3; Key oxidase enzyme in the biosynthesis of gibberellin that catalyzes the conversion of GA12 and GA53 to GA9 and GA20 respectively, via a three-step oxidation at C-20 of the GA skeleton. GA53 is less effectively oxidized than GA12, and GA25 is also formed as a minor product; Belongs to the iron/ascorbate-dependent oxidoreductase family. GA20OX subfamily. (380 aa) |
| | F19G10.24 | Uncharacterized PKHD-type hydroxylase At1g22950. (397 aa) |
| | ACO2 | 1-aminocyclopropane-1-carboxylate oxidase 2; Enzyme involved in the ethylene biosynthesis. Required to mediate the 1-aminocyclopropane-1-carboxylic acid (ACC)-mediated reversion of the ABA-induced inhibition of seed germination via endosperm rupture. May promote stem elongation by maximizing the extensibility cells, possibly by activating ethylene biosynthesis, in response to very-long-chain fatty acids (VLCFAs C20:0 to C30:0). (320 aa) |
| | GA20OX5 | Gibberellin 20 oxidase 5; Key oxidase enzyme in the biosynthesis of gibberellin that catalyzes the conversion of GA12 and GA53 to GA9 and GA20 respectively, via a three-step oxidation at C-20 of the GA skeleton. (385 aa) |
| | T23K23.7 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein. (389 aa) |
| | MDC12.4 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein. (462 aa) |
| | ELF6 | Probable lysine-specific demethylase ELF6; Acts probably as a histone 'Lys-4' (H3K4me) demethylase. Involved in transcriptional gene regulation. Acts as a repressor of the photoperiodic flowering pathway and of FT. Binds around the transcription start site of the FT locus. (1340 aa) |
| | CCD7 | Carotenoid cleavage dioxygenase 7, chloroplastic; Involved in strigolactones biosynthesis by cleaving asymmetrically a variety of linear and cyclic carotenoids at the 9-10 double bond. Produces one C(13) beta-ionone and the C(27) 10'-apo-beta- carotenal. Strigolactones are hormones that inhibit tillering and shoot branching through the MAX-dependent pathway, contribute to the regulation of shoot architectural response to phosphate-limiting conditions and function as rhizosphere signal that stimulates hyphal branching of arbuscular mycorrhizal fungi and trigger seed germination of root [...] (618 aa) |
| | F5O24.290 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein; Belongs to the iron/ascorbate-dependent oxidoreductase family. (348 aa) |
| | F11C1.50 | Probable 2-oxoglutarate-dependent dioxygenase At3g50210; Belongs to the iron/ascorbate-dependent oxidoreductase family. (332 aa) |
| | JMJ14 | Probable lysine-specific demethylase JMJ14; Transcriptional repressor. Histone demethylase that demethylates 'Lys-4' (H3K4me) of histone H3 with a higher activity for H3K4me3 and H3K4me2 than H3K4me1. No activity on H3K9me3/2, H3K36me3/2 and H3K27me3/2. Represses FT and TSF expression to inhibit the floral transition. Binds around the transcription start site of the FT locus. Involved in the DRM2-mediated maintenance of DNA methylation, but not required for the de novo DNA methylation. Required for demethylating histone H3K4me3 at the target of RNA silencing. Together with NAC051/NAC05 [...] (954 aa) |
| | ARD2 | 1,2-dihydroxy-3-keto-5-methylthiopentene dioxygenase 2; Catalyzes the formation of formate and 2-keto-4- methylthiobutyrate (KMTB) from 1,2-dihydroxy-3-keto-5-methylthiopentene (DHK-MTPene). (192 aa) |
| | P4H12 | Probable prolyl 4-hydroxylase 12; Catalyzes the post-translational formation of 4- hydroxyproline in -Xaa-Pro-Gly- sequences in proline-rich peptide sequences of plant glycoproteins and other proteins. Hydroxyprolines are important constituent of many plant cell wall glycoproteins such as extensins, hydroxyproline-rich glycoproteins, lectins and arabinogalactan proteins. (291 aa) |
| | DIN11 | Probable 2-oxoglutarate-dependent dioxygenase DIN11. (357 aa) |
| | ARD4 | 1,2-dihydroxy-3-keto-5-methylthiopentene dioxygenase 4; Catalyzes the formation of formate and 2-keto-4- methylthiobutyrate (KMTB) from 1,2-dihydroxy-3-keto-5-methylthiopentene (DHK-MTPene). (187 aa) |
| | JMJ19 | Probable inactive lysine-specific demethylase JMJ19. (708 aa) |
| | P4H7 | Probable prolyl 4-hydroxylase 7; Catalyzes the post-translational formation of 4- hydroxyproline in -Xaa-Pro-Gly- sequences in proline-rich peptide sequences of plant glycoproteins and other proteins. Hydroxyprolines are important constituent of many plant cell wall glycoproteins such as extensins, hydroxyproline-rich glycoproteins, lectins and arabinogalactan proteins; Belongs to the P4HA family. (316 aa) |
| | P4H4 | Probable prolyl 4-hydroxylase 4; Catalyzes the post-translational formation of 4- hydroxyproline in -Xaa-Pro-Gly- sequences in proline-rich peptide sequences of plant glycoproteins and other proteins. Hydroxyprolines are important constituent of many plant cell wall glycoproteins such as extensins, hydroxyproline-rich glycoproteins, lectins and arabinogalactan proteins. (298 aa) |
| | GA2OX1 | Gibberellin 2-beta-dioxygenase 1; Catalyzes the 2-beta-hydroxylation of several biologically active gibberellins, leading to the homeostatic regulation of their endogenous level. Catabolism of gibberellins (GAs) plays a central role in plant development. Converts GA9/GA20 to GA51/GA29 and GA4/GA1 to GA34/GA8; Belongs to the iron/ascorbate-dependent oxidoreductase family. GA2OX subfamily. (329 aa) |
| | F7C8.140 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein; Belongs to the iron/ascorbate-dependent oxidoreductase family. (349 aa) |
| | PCO2 | Plant cysteine oxidase 2; Oxidizes N-terminal cysteine residues, thus preparing the protein for N-end rule pathway-mediated proteasomal degradation. Controls the preparation of ERF-VII proteins for degradation via the 26S proteasome. Not active on Cys located inside or at the C-terminus of a peptide. Represses the anaerobic response. (276 aa) |
| | JMJ30 | Lysine-specific demethylase JMJ30; Histone demethylase that demethylates 'Lys-36' (H3K36me) of histone H3 with a specific activity for H3K36me3 and H3K36me2. No activity on H3K36me1. Involved in the control of flowering time by demethylating H3K36me2 at the FT locus and repressing its expression. Acts within the central clock. Works in concert with TOC1 to promote the morning-phased clock genes CCA1 and LHY which function as components of the central oscillator. (429 aa) |
| | ALKBH8 | Alkylated DNA repair protein ALKBH8 homolog; Binds tRNA and catalyzes the iron and alpha-ketoglutarate dependent hydroxylation of 5-methylcarboxymethyl uridine at the wobble position of the anticodon loop in tRNA via its dioxygenase domain, giving rise to 5-(S)-methoxycarbonylhydroxymethyluridine. Belongs to the alkB family. (346 aa) |
| | CCD8 | Carotenoid cleavage dioxygenase 8, chloroplastic; Involved in strigolactones biosynthesis by cleaving the C(27) 9-cis-10'-apo-beta-carotenal produced by CCD7. Produces the C(19) carlactone and a C(8) hydroxyaldehyde. Also shows lower activity with all-trans-10'-apo-beta-carotenal producing a C(9) dialdehyde and the C(18) 13-apo-beta-carotenone. Strigolactones are hormones that inhibit tillering and shoot branching through the MAX-dependent pathway, contribute to the regulation of shoot architectural response to phosphate-limiting conditions and function as rhizosphere signal that stimu [...] (570 aa) |
| | Q8VYB9_ARATH | Transcription factor jumonji (JmjC) domain-containing protein. (840 aa) |
| | P4H9 | Probable prolyl 4-hydroxylase 9; Catalyzes the post-translational formation of 4- hydroxyproline in -Xaa-Pro-Gly- sequences in proline-rich peptide sequences of plant glycoproteins and other proteins. Hydroxyprolines are important constituent of many plant cell wall glycoproteins such as extensins, hydroxyproline-rich glycoproteins, lectins and arabinogalactan proteins. (288 aa) |
| | ARD3 | 1,2-dihydroxy-3-keto-5-methylthiopentene dioxygenase 3; Catalyzes the formation of formate and 2-keto-4- methylthiobutyrate (KMTB) from 1,2-dihydroxy-3-keto-5-methylthiopentene (DHK-MTPene); Belongs to the acireductone dioxygenase (ARD) family. (199 aa) |
| | LIGB | Extradiol ring-cleavage dioxygenase; Opens the cyclic ring of caffealdehyde between carbons 2 and 3 or between carbons 4 and 5. Involved in the biosynthesis of arabidopyrones. (269 aa) |
| | LDOX | Leucoanthocyanidin dioxygenase; Involved in anthocyanin and protoanthocyanidin biosynthesis by catalyzing the oxidation of leucoanthocyanidins into anthocyanidins. Possesses low flavonol synthase activity in vitro towards dihydrokaempferol and dihydroquercetin producing kaempferol and quercitin, respectively. Belongs to the iron/ascorbate-dependent oxidoreductase family. (356 aa) |
| | FLS1 | Flavonol synthase/flavanone 3-hydroxylase; Catalyzes the formation of flavonols from dihydroflavonols. It can act on dihydrokaempferol to produce kaempferol, on dihydroquercetin to produce quercitin and on dihydromyricetin to produce myricetin. In vitro catalyzes the oxidation of both enantiomers of naringenin to give both cis- and trans-dihydrokaempferol. Belongs to the iron/ascorbate-dependent oxidoreductase family. (336 aa) |
| | T32G9.27 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein; Belongs to the iron/ascorbate-dependent oxidoreductase family. (329 aa) |
| | GA2OX7 | Gibberellin 2-beta-dioxygenase 7; Catalyzes the 2-beta-hydroxylation of gibberellins (GA) precursors, rendering them unable to be converted to active GAs. Hydroxylates the C20-GA GA12 and GA53, but is not active on C19-GAs, like GA1, GA4, GA9 and GA20. (336 aa) |
| | NCED5 | Probable 9-cis-epoxycarotenoid dioxygenase NCED5, chloroplastic; Has a 11,12(11',12') 9-cis epoxycarotenoid cleavage activity. Catalyzes the first step of abscisic-acid biosynthesis from carotenoids (By similarity); Belongs to the carotenoid oxygenase family. (589 aa) |
| | F13K9.13 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein; Belongs to the iron/ascorbate-dependent oxidoreductase family. (322 aa) |
| | GA2OX4 | Gibberellin 2-beta-dioxygenase 4; Catalyzes the 2-beta-hydroxylation of several biologically active gibberellins, leading to the homeostatic regulation of their endogenous level. Catabolism of gibberellins (GAs) plays a central role in plant development. Converts GA9/GA20 to GA51/GA29 and GA4/GA1 to GA34/GA8; Belongs to the iron/ascorbate-dependent oxidoreductase family. GA2OX subfamily. (321 aa) |
| | F6'H2 | Feruloyl CoA ortho-hydroxylase 2; 2-oxoglutarate (OG)- and Fe(II)-dependent dioxygenase (2OGD)involved in scopoletin biosynthesis. Converts feruloyl CoA into 6'-hydroxyferuloyl CoA but has no activity with ferulic acid, feruloylquinic acid, caffeic acid, caffeoyl CoA, p-coumaric acid, cinnamic acid, cinnamoyl CoA or benzoyl CoA. (361 aa) |
| | GLY3 | Persulfide dioxygenase ETHE1 homolog, mitochondrial; Sulfur dioxygenase that plays an essential role in hydrogen sulfide catabolism in the mitochondrial matrix. Hydrogen sulfide (H(2)S) gives rise to cysteine persulfide residues. ETHE1 consumes molecular oxygen to catalyze the oxidation of the persulfide, once it has been transferred to a thiophilic acceptor, such as glutathione (R- SSH). Plays an important role in metabolic homeostasis in mitochondria by metabolizing hydrogen sulfide and preventing the accumulation of supraphysiological H(2)S levels that have toxic effects, due to the [...] (294 aa) |
| | F14G24.9 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein; Belongs to the iron/ascorbate-dependent oxidoreductase family. (317 aa) |
| | F14G24.8 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein. (289 aa) |
| | P4H6 | Probable prolyl 4-hydroxylase 6; Catalyzes the post-translational formation of 4- hydroxyproline in -Xaa-Pro-Gly- sequences in proline-rich peptide sequences of plant glycoproteins and other proteins. Hydroxyprolines are important constituent of many plant cell wall glycoproteins such as extensins, hydroxyproline-rich glycoproteins, lectins and arabinogalactan proteins. (288 aa) |
| | T9C5.220 | Probable 2-oxoglutarate-dependent dioxygenase At3g49630. (332 aa) |
| | F13K3.9 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein; Belongs to the iron/ascorbate-dependent oxidoreductase family. (366 aa) |
| | P4H13 | Prolyl 4-hydroxylase 13; Catalyzes the post-translational formation of 4- hydroxyproline in -Xaa-Pro-Gly- sequences in proline-rich peptide sequences of plant glycoproteins and other proteins. Hydroxyprolines are important constituent of many plant cell wall glycoproteins such as extensins, hydroxyproline-rich glycoproteins, lectins and arabinogalactan proteins. Possesses high affinity for leucine-rich repeat and proline-rich extensins of root cell walls that are essential for root hair development. Hydroxyprolines define the subsequent O- glycosylation sites by arabinosyltransferases [...] (274 aa) |
| | JMJ18 | Lysine-specific demethylase JMJ18; Histone demethylase that demethylates 'Lys-4' (H3K4me) of histone H3 with a specific activity for H3K4me3 and H3K4me2. No activity on H3K9me3/2, H3K27me3/2 and H3K36me3/2. Involved in the control of flowering time by demethylating H3K4me3 at the FLC locus and repressing its expression. The repression of FLC level and reduction in H3K4me3 at the FLC locus results in induction of the flowering activator FT, which is a downstream target of FLC. (819 aa) |
| | JMJ16 | Putative lysine-specific demethylase JMJ16; May function as histone H3 lysine demethylase and be involved in regulation of gene expression. (1209 aa) |
| | FLS2 | Putative inactive flavonol synthase 2; Belongs to the iron/ascorbate-dependent oxidoreductase family. (250 aa) |
| | T16N11.5 | 2-oxoglutarate-dependent dioxygenase-like protein; Belongs to the iron/ascorbate-dependent oxidoreductase family. (327 aa) |
| | F11I4.12 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein. (316 aa) |
| | F2K11.14 | Transcription factor jumonji (JmjC) domain-containing protein. (1462 aa) |
| | F2P24.4 | 1-aminocyclopropane-1-carboxylate oxidase 5; Enzyme involved in the ethylene biosynthesis; Belongs to the iron/ascorbate-dependent oxidoreductase family. (307 aa) |
| | F11I4.9 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein. (411 aa) |
| | ACO4 | 1-aminocyclopropane-1-carboxylate oxidase 4; Enzyme involved in the ethylene biosynthesis. May promote stem elongation by maximizing the extensibility cells, possibly by activating ethylene biosynthesis, in response to very-long-chain fatty acids (VLCFAs C20:0 to C30:0); Belongs to the iron/ascorbate-dependent oxidoreductase family. (323 aa) |
| | LOX1 | Linoleate 9S-lipoxygenase 1; 9S-lipoxygenase that can use linoleic acid or linolenic acid as substrates. Plant lipoxygenases may be involved in a number of diverse aspects of plant physiology including growth and development, pest resistance, and senescence or responses to wounding. Catalyzes the hydroperoxidation of lipids containing a cis,cis-1,4-pentadiene structure. Function as regulators of root development by controlling the emergence of lateral roots. (859 aa) |
| | HPD | 4-hydroxyphenylpyruvate dioxygenase; Belongs to the 4HPPD family. (445 aa) |
| | LOX2 | Lipoxygenase 2, chloroplastic; 13S-lipoxygenase that can use linolenic acid as substrates. Plant lipoxygenases may be involved in a number of diverse aspects of plant physiology including growth and development, pest resistance, and senescence or responses to wounding. Catalyzes the hydroperoxidation of lipids containing a cis,cis-1,4-pentadiene structure. Required for the wound-induced synthesis of jasmonic acid (JA) in leaves. (896 aa) |
| | F7F1.5 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein; Belongs to the iron/ascorbate-dependent oxidoreductase family. (362 aa) |
| | F7F1.4 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein; Belongs to the iron/ascorbate-dependent oxidoreductase family. (358 aa) |
| | ANS | Probable 2-oxoglutarate-dependent dioxygenase ANS; Involved in anthocyanin and protoanthocyanidin biosynthesis by catalyzing the oxidation of leucoanthocyanidins into anthocyanidins. (353 aa) |
| | CCD1 | Carotenoid 9,10(9',10')-cleavage dioxygenase 1; Cleaves a variety of carotenoids symmetrically at both the 9- 10 and 9'-10' double bonds. Active on beta,beta-carotene, lutein, zeaxanthin, all-trans-violaxanthin, 9-cis-violaxanthin and 9'-cis- neoxanthin. With most substrates, the carotenoid is symmetrically cleaved. Probably not involved in abscisic acid biosynthesis. Belongs to the carotenoid oxygenase family. (538 aa) |
| | GLX1 | Lactoylglutathione lyase GLX1; Catalyzes the conversion of hemimercaptal, formed from methylglyoxal and glutathione, to S-lactoylglutathione. (283 aa) |
| | F12F1.12 | 1-aminocyclopropane-1-carboxylate oxidase 3; Enzyme involved in the ethylene biosynthesis. May promote stem elongation by maximizing the extensibility cells, possibly by activating ethylene biosynthesis, in response to very-long-chain fatty acids (VLCFAs C20:0 to C30:0); Belongs to the iron/ascorbate-dependent oxidoreductase family. (320 aa) |
| | JMJ15 | Lysine-specific demethylase JMJ15; Histone demethylase that demethylates 'Lys-4' (H3K4me) of histone H3 with a specific activity for H3K4me3. No activity on H3K4me2, H3K4me1, H3K9me3/2, H3K27me3/2 and H3K36me3/2. Involved in the control of flowering time by demethylating H3K4me3 at the FLC locus and repressing its expression. The repression of FLC level and reduction in H3K4me3 at the FLC locus results in induction of the flowering activator FT, which is a downstream target of FLC. (806 aa) |
| | GA2OX3 | Gibberellin 2-beta-dioxygenase 3; Catalyzes the 2-beta-hydroxylation of several biologically active gibberellins, leading to the homeostatic regulation of their endogenous level. Catabolism of gibberellins (GAs) plays a central role in plant development. Converts GA9/GA20 to GA51/GA29 and GA4/GA1 to GA34/GA8; Belongs to the iron/ascorbate-dependent oxidoreductase family. GA2OX subfamily. (335 aa) |
| | CCD4 | Probable carotenoid cleavage dioxygenase 4, chloroplastic; May be involved in carotenoid cleavage; Belongs to the carotenoid oxygenase family. (595 aa) |
| | GA2OX8 | Gibberellin 2-beta-dioxygenase 8; Catalyzes the 2-beta-hydroxylation of gibberellins (GA) precursors, rendering them unable to be converted to active GAs. Hydroxylates the C20-GA GA12 and GA53, but is not active on C19-GAs, like GA1, GA4, GA9 and GA20; Belongs to the iron/ascorbate-dependent oxidoreductase family. GA2OX subfamily. (338 aa) |
| | NCED2 | 9-cis-epoxycarotenoid dioxygenase NCED2, chloroplastic; Has a 11,12(11',12') 9-cis epoxycarotenoid cleavage activity. Catalyzes the first step of abscisic-acid biosynthesis from carotenoids; Belongs to the carotenoid oxygenase family. (583 aa) |
| | ARD1 | 1,2-dihydroxy-3-keto-5-methylthiopentene dioxygenase 1; Catalyzes the formation of formate and 2-keto-4- methylthiobutyrate (KMTB) from 1,2-dihydroxy-3-keto-5-methylthiopentene (DHK-MTPene). (199 aa) |
| | MQD22.4 | Transcription factor jumonji (Jmj) family protein / zinc finger (C5HC2 type) family protein. (787 aa) |
| | MWD22.26 | Gibberellin 20-oxidase-like protein; Negative regulator of root hair growth. (325 aa) |
| | T20L15.50 | 2-oxoglutarate-dependent dioxygenase family protein. (442 aa) |
| | FLS4 | Probable flavonol synthase 4. (279 aa) |
| | FLS6 | Probable flavonol synthase 6. (293 aa) |
| | K9D7.3 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein. (410 aa) |
| | T29J13.260 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein. (549 aa) |
| | F14G24.7 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein; Belongs to the iron/ascorbate-dependent oxidoreductase family. (314 aa) |
| | F14G24.6 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein; Belongs to the iron/ascorbate-dependent oxidoreductase family. (310 aa) |
| | GA20OX4 | Gibberellin 20 oxidase 4; Key oxidase enzyme in the biosynthesis of gibberellin that catalyzes the conversion of GA12 and GA53 to GA9 and GA20 respectively, via a three-step oxidation at C-20 of the GA skeleton. (376 aa) |
| | GA3OX4 | Gibberellin 3-beta-dioxygenase 4; Converts the inactive gibberellin (GA) precursors GA9 and GA20 in the bioactives gibberellins GA4 and GA1. Involved in the production of bioactive GA for reproductive development. (355 aa) |
| | F5I6.7 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein. (320 aa) |
| | DOX2 | Alpha-dioxygenase 2; Alpha-dioxygenase that catalyzes the primary oxygenation of fatty acids into oxylipins. May be involved in the senescence process. Belongs to the peroxidase family. (631 aa) |
| | F1M20.12 | ER membrane protein, putative (DUF962). (208 aa) |
| | LOX6 | Lipoxygenase 6, chloroplastic; Plant lipoxygenases may be involved in a number of diverse aspects of plant physiology including growth and development, pest resistance, and senescence or responses to wounding. Catalyzes the hydroperoxidation of lipids containing a cis,cis-1,4-pentadiene structure (By similarity). 13S-lipoxygenase that can use linolenic acid as substrates. (917 aa) |
| | MOP10.14 | Probable 2-oxoglutarate-dependent dioxygenase At5g05600; Involved in anthocyanin and protoanthocyanidin biosynthesis by catalyzing the oxidation of leucoanthocyanidins into anthocyanidins (By similarity). May be involved in the catabolism of cytotoxic polycyclic aromatic hydrocarbons (PAHs). Belongs to the iron/ascorbate-dependent oxidoreductase family. (371 aa) |
| | FLS5 | Probable flavonol synthase 5; Belongs to the iron/ascorbate-dependent oxidoreductase family. (325 aa) |
| | FLS3 | Flavonol synthase 3; Catalyzes the formation of flavonols from dihydroflavonols. Possesses low activity in vitro towards dihydrokaempferol and dihydroquercetin producing kaempferol and quercitin, respectively. Belongs to the iron/ascorbate-dependent oxidoreductase family. (308 aa) |
| | DMR6 | Protein DOWNY MILDEW RESISTANCE 6; Converts salicylic acid (SA) to 2,3-dihydroxybenzoic acid (2,3-DHBA) (By similarity). Suppressor of immunity. Regulates negatively defense associated genes expression (e.g. PR-1, PR-2, and PR-5). Negative regulator of defense against Hyaloperonospora arabidopsidis. (Microbial infection) Required for susceptibility to Pseudomonas syringae pv. tomato DC3000; Belongs to the iron/ascorbate-dependent oxidoreductase family. (341 aa) |
| | P4H10 | Probable prolyl 4-hydroxylase 10; Catalyzes the post-translational formation of 4- hydroxyproline in -Xaa-Pro-Gly- sequences in proline-rich peptide sequences of plant glycoproteins and other proteins. Hydroxyprolines are important constituent of many plant cell wall glycoproteins such as extensins, hydroxyproline-rich glycoproteins, lectins and arabinogalactan proteins; Belongs to the P4HA family. (289 aa) |
| | P4H8 | Probable prolyl 4-hydroxylase 8; Catalyzes the post-translational formation of 4- hydroxyproline in -Xaa-Pro-Gly- sequences in proline-rich peptide sequences of plant glycoproteins and other proteins. Hydroxyprolines are important constituent of many plant cell wall glycoproteins such as extensins, hydroxyproline-rich glycoproteins, lectins and arabinogalactan proteins. (290 aa) |
| | F16G20.40 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein; Belongs to the iron/ascorbate-dependent oxidoreductase family. (324 aa) |
| | F7H19.50 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein. (153 aa) |
| | Dl4195c | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein; Belongs to the iron/ascorbate-dependent oxidoreductase family. (364 aa) |
| | LOX5 | Linoleate 9S-lipoxygenase 5; 9S-lipoxygenase that can use linoleic acid or linolenic acid as substrates. Plant lipoxygenases may be involved in a number of diverse aspects of plant physiology including growth and development, pest resistance, and senescence or responses to wounding. Catalyzes the hydroperoxidation of lipids containing a cis,cis-1,4-pentadiene structure. Function as regulators of root development by controlling the emergence of lateral roots. (886 aa) |
| | MZN1.11 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein; Belongs to the iron/ascorbate-dependent oxidoreductase family. (352 aa) |
| | MRC8.20 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein. (394 aa) |
| | PCO1 | Plant cysteine oxidase 1; Oxidizes N-terminal cysteine residues, thus preparing the protein for N-end rule pathway-mediated proteasomal degradation. Controls the preparation of ERF-VII proteins for degradation via the 26S proteasome. Not active on Cys located inside or at the C-terminus of a peptide. Represses the anaerobic response. (293 aa) |
| | PCO5 | Plant cysteine oxidase 5; Oxidizes N-terminal cysteine residues, thus preparing the protein for N-end rule pathway-mediated proteasomal degradation. (242 aa) |
| | JRG21 | Probable 2-oxoglutarate-dependent dioxygenase JRG21; Involved in anthocyanin and protoanthocyanidin biosynthesis by catalyzing the oxidation of leucoanthocyanidins into anthocyanidins. (363 aa) |
| | NCED9 | 9-cis-epoxycarotenoid dioxygenase NCED9, chloroplastic; Has a 11,12(11',12') 9-cis epoxycarotenoid cleavage activity. Catalyzes the first step of abscisic-acid biosynthesis from carotenoids. Contributes probably to abscisic acid synthesis for the induction of seed dormancy. (657 aa) |
| | F6A14.17 | ER membrane protein, putative (DUF962). (206 aa) |
| | F3H | Naringenin,2-oxoglutarate 3-dioxygenase; Catalyzes the 3-beta-hydroxylation of 2S-flavanones to 2R,3R- dihydroflavonols which are intermediates in the biosynthesis of flavonols, anthocyanidins, catechins and proanthocyanidins in plants. (358 aa) |
| | F25C20.6 | Alpha-ketoglutarate-dependent dioxygenase alkB; Putative dioxygenase that may repair alkylated DNA or RNA by oxidative demethylation. Requires molecular oxygen, alpha-ketoglutarate and iron (By similarity). (345 aa) |
| | MSJ1.9 | 2-nitropropane dioxygenase-like protein. (333 aa) |
| | K19P17.17 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein; Belongs to the iron/ascorbate-dependent oxidoreductase family. (349 aa) |
| | LOX4 | Lipoxygenase 4, chloroplastic; Plant lipoxygenases may be involved in a number of diverse aspects of plant physiology including growth and development, pest resistance, and senescence or responses to wounding. Catalyzes the hydroperoxidation of lipids containing a cis,cis-1,4-pentadiene structure (By similarity). 13S-lipoxygenase that can use linolenic acid as substrates. (926 aa) |
| | GA2OX6 | Gibberellin 2-beta-dioxygenase 6; Catalyzes the 2-beta-hydroxylation of several biologically active gibberellins, leading to the homeostatic regulation of their endogenous level. Catabolism of gibberellins (GAs) plays a central role in plant development. Converts GA9/GA20 to GA51/GA29 and GA4/GA1 to GA34/GA8. Has no C20-GA 2 oxidase activity against GA12 and GA53. (329 aa) |
| | S8H | Scopoletin 8-hydroxylase; Involved in the pathway of sideretin biosynthesis from feruloyl CoA, a redox-active catecholic metabolite exuded by roots in response to iron deficiency in order to facilitate the uptake of iron; this pathway consists in the successive conversion from feruloyl CoA to scopoletin, from scopoletin to fraxetin and from fraxetin to sideretin. Catalyzes the biosynthesis of fraxetin via scopoletin hydroxylation. Belongs to the iron/ascorbate-dependent oxidoreductase family. (357 aa) |
| | F6'H1 | Feruloyl CoA ortho-hydroxylase 1; 2-oxoglutarate (OG)- and Fe(II)-dependent dioxygenase (2OGD) involved in scopoletin biosynthesis. Converts feruloyl CoA into 6'-hydroxyferuloyl CoA but has no activity with ferulic acid, feruloylquinic acid, caffeic acid, caffeoyl CoA, p- coumaric acid, cinnamic acid, cinnamoyl CoA or benzoyl CoA. Required for the production and secretion of compounds (e.g. fluorescent coumarins) that facilitate the mobilization and uptake of iron from sources with low bioavailability or in high pH- induced iron deficiency conditions. Involved in the pathway of sideret [...] (361 aa) |
| | LBO1 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein; Belongs to the iron/ascorbate-dependent oxidoreductase family. (364 aa) |
| | Q9LJH2_ARATH | 2-oxoglutarate-dependent dioxygenase family protein. (455 aa) |
| | FMO1 | Probable flavin-containing monooxygenase 1; Required for the establishment of systemic acquired resistance (SAR). Not involved in local defense mechanisms. Confers a salicylic acid-dependent (SA) resistance to virulent pathogens such as P.syringae pv tomato and H.parasitica. (530 aa) |
| | P4H3 | Probable prolyl 4-hydroxylase 3; Catalyzes the post-translational formation of 4- hydroxyproline in -Xaa-Pro-Gly- sequences in proline-rich peptide sequences of plant glycoproteins and other proteins. Hydroxyprolines are important constituent of many plant cell wall glycoproteins such as extensins, hydroxyproline-rich glycoproteins, lectins and arabinogalactan proteins. (287 aa) |
| | LOX3 | Lipoxygenase 3, chloroplastic; 13S-lipoxygenase that can use linolenic acid as substrates. Plant lipoxygenases may be involved in a number of diverse aspects of plant physiology including growth and development, pest resistance, and senescence or responses to wounding. Catalyzes the hydroperoxidation of lipids containing a cis,cis-1,4-pentadiene structure (By similarity). (919 aa) |
| | NCED6 | 9-cis-epoxycarotenoid dioxygenase NCED6, chloroplastic; Has a 11,12(11',12') 9-cis epoxycarotenoid cleavage activity. Catalyzes the first step of abscisic-acid biosynthesis from carotenoids. Contributes probably to abscisic acid synthesis for the induction of seed dormancy. (577 aa) |
| | NCED3 | 9-cis-epoxycarotenoid dioxygenase NCED3, chloroplastic; Has a 11,12(11',12') 9-cis epoxycarotenoid cleavage activity. Catalyzes the first step of abscisic-acid biosynthesis from carotenoids, in response to water stress. (599 aa) |
| | MJM18.3 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein. (250 aa) |
| | DOX1 | Alpha-dioxygenase 1; Alpha-dioxygenase that catalyzes the primary oxygenation of fatty acids into oxylipins. Mediates a protection against oxidative stress and cell death, probably by generating some lipid-derived molecules. Promotes local and systemic plant defense in a salicylic acid (SA)-dependent manner, including the establishment of systemic acquired resistance (SAR) in response to incompatible interaction. Involved in a negative regulation of abscisic acid (ABA)-mediated signaling pathway. (639 aa) |
| | ALKBH2 | DNA oxidative demethylase ALKBH2; Dioxygenase that repairs alkylated DNA containing 1- methyladenine and 1-ethenoadenine by oxidative demethylation. Accepts double-stranded and single-stranded substrates, with a preference for dsDNA over ssDNA. Confers resistance to methylating agents such as methylmethanesulphonate (MMS). (314 aa) |
| | PCO4 | Plant cysteine oxidase 4; Oxidizes N-terminal cysteine residues, thus preparing the protein for N-end rule pathway-mediated proteasomal degradation. Belongs to the cysteine dioxygenase family. (241 aa) |
| | GSL-OH | Probable 2-oxoacid dependent dioxygenase; Necessary for the hydroxylation of but-3-enyl glucosinolate to 2-hydroxybut-3-enyl glucosinolate, which is toxic to insects, bacteria and nematodes, inhibits seed germination and produces bitter flavors; Belongs to the iron/ascorbate-dependent oxidoreductase family. (359 aa) |
| | ALKBH9B | RNA demethylase ALKBH9B; Dioxygenase that demethylates RNA by oxidative demethylation: specifically demethylates N(6)-methyladenosine (m6A) RNA, the most prevalent internal modification of messenger RNA (mRNA) in higher eukaryotes. Modulates viral infection of the alfalfa mosaic virus (AMV) and the m6A abundance in its genomic RNAs. (507 aa) |
| | F11B9.11 | Probable 2-oxoglutarate-dependent dioxygenase At3g111800; Involved in anthocyanin and protoanthocyanidin biosynthesis by catalyzing the oxidation of leucoanthocyanidins into anthocyanidins. Belongs to the iron/ascorbate-dependent oxidoreductase family. (400 aa) |
| | JMJ25 | Lysine-specific demethylase JMJ25; Histone demethylase that demethylates 'Lys-9' (H3K9me) of histone H3 with a specific activity for H3K9me2 and H3K9me1. No activity on H3K9me3, H3K4me3/2/1, H3K27me3/2/1 and H3K36me3/2/1. Involved in the control of several developmental processes by protecting genes from silencing. Demethylates H3K9me2 in the promoter regions of RDR2 and DCL3 and mediates the repression of ectopic non-CpG methylation at RDR2, DCL3 and APC13 loci. Protects also a large number of transcribed genes from non-CpG methylation. May regulate gene expression via a pathway invol [...] (1027 aa) |
| | REF6 | Lysine-specific demethylase REF6; Histone demethylase that demethylates 'Lys-27' (H3K27me) of histone H3. Demethylates both tri- (H3K27me3) and di-methylated (H3K27me2) H3K27me. Demethylates also H3K4me3/2 and H3K36me3/2 in an in vitro assay. Involved in the transcriptional regulation of hundreds of genes regulating developmental patterning and responses to various stimuli. Binds DNA via its four zinc fingers in a sequence- specific manner, 5'-CTCTGYTY-3', to promote the demethylation of H3K27me3 and the regulation of organ boundary formation. Involved in the regulation of flowering ti [...] (1360 aa) |
| | GA3OX3 | Gibberellin 3-beta-dioxygenase 3; Converts the inactive gibberellin (GA) precursors GA9 and GA20 in the bioactives gibberellins GA4 and GA1. Involved in the production of bioactive GA for reproductive development. Belongs to the iron/ascorbate-dependent oxidoreductase family. GA3OX subfamily. (349 aa) |
| | P4H11 | Probable prolyl 4-hydroxylase 11; Catalyzes the post-translational formation of 4- hydroxyproline in -Xaa-Pro-Gly- sequences in proline-rich peptide sequences of plant glycoproteins and other proteins. Hydroxyprolines are important constituent of many plant cell wall glycoproteins such as extensins, hydroxyproline-rich glycoproteins, lectins and arabinogalactan proteins. (272 aa) |
| | GA2OX2 | Gibberellin 2-beta-dioxygenase 2; Catalyzes the 2-beta-hydroxylation of several biologically active gibberellins, leading to the homeostatic regulation of their endogenous level. Catabolism of gibberellins (GAs) plays a central role in plant development. Converts GA9/GA20 to GA51/GA29 and GA4/GA1 to GA34/GA8. (341 aa) |
| | F7A19.21 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein; Belongs to the iron/ascorbate-dependent oxidoreductase family. (308 aa) |
| | F7A19.20 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein; Belongs to the iron/ascorbate-dependent oxidoreductase family. (312 aa) |
| | F13F21.18 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein; Belongs to the iron/ascorbate-dependent oxidoreductase family. (348 aa) |
| | HGO | Homogentisate 1,2-dioxygenase. (461 aa) |
| | DLO2 | Protein DMR6-LIKE OXYGENASE 2; Converts salicylic acid (SA) to 2,3-dihydroxybenzoic acid (2,3-DHBA) (By similarity). Negative regulator of defense against Hyaloperonospora arabidopsidis. Belongs to the iron/ascorbate-dependent oxidoreductase family. (348 aa) |
| | DLO1 | Protein DMR6-LIKE OXYGENASE 1; Converts salicylic acid (SA) to both 2,3-dihydroxybenzoic acid (2,3-DHBA) and 2,5-DHBA in vitro but only 2,3-DHBA in vivo. Component of a negative feedback regulation system of SA levels during senescence. Regulates both onset and progression of leaf senescence. Negative regulator of defense against Hyaloperonospora arabidopsidis. Belongs to the iron/ascorbate-dependent oxidoreductase family. (349 aa) |
| | GA3OX2 | Gibberellin 3-beta-dioxygenase 2; Converts the inactive gibberellin (GA) precursors GA9 and GA20 in the bioactives gibberellins GA4 and GA1. Involved in the production of bioactive GA for vegetative growth and development. Belongs to the iron/ascorbate-dependent oxidoreductase family. GA3OX subfamily. (347 aa) |
| | ALKBH10B | RNA demethylase ALKBH10B; Dioxygenase that demethylates RNA by oxidative demethylation: specifically demethylates N(6)-methyladenosine (m6A) RNA, the most prevalent internal modification of messenger RNA (mRNA) in higher eukaryotes. ALKBH10B-mediated mRNA m6A demethylation stabilizes the mRNA of the key flowering time regulators FT, SPL3 and SPL9, which are involved in the control of floral transition. (569 aa) |
| | AOP3 | 2-oxoglutarate-dependent dioxygenase AOP3; 2-oxoglutarate-dependent dioxygenase involved in glucosinolates biosynthesis. Catalyzes the conversion of methylsulfinylalkyl glucosinolates to hydroxyalkyl glucosinolates (By similarity); Belongs to the iron/ascorbate-dependent oxidoreductase family. (411 aa) |
| | AOP2 | Probable inactive 2-oxoglutarate-dependent dioxygenase AOP2. (399 aa) |
| | AOP1 | Probable 2-oxoglutarate-dependent dioxygenase AOP1; Probable 2-oxoglutarate-dependent dioxygenase that may be involved in glucosinolates biosynthesis. May play a role in the production of aliphatic glucosinolates (By similarity); Belongs to the iron/ascorbate-dependent oxidoreductase family. (322 aa) |
| | PAHX | Phytanoyl-CoA dioxygenase; Converts phytanoyl-CoA to 2-hydroxyphytanoyl-CoA. Belongs to the PhyH family. (283 aa) |
| | T4E14.7 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein. (148 aa) |
| | P4H1 | Prolyl 4-hydroxylase 1; Catalyzes the post-translational formation of 4- hydroxyproline in -Xaa-Pro-Gly- sequences in proline-rich peptide sequences of plant glycoproteins and other proteins. Hydroxylates preferentially prolines in second positions in the -Pro-Pro-Gly- triplets. Hydroxyprolines are important constituent of many plant cell wall glycoproteins such as extensins, hydroxyproline-rich glycoproteins, lectins and arabinogalactan proteins. Can hydroxylate collagen-like peptides and hypoxia-inducible transcription factor peptides; Belongs to the P4HA family. (283 aa) |
| | F4JFR7_ARATH | 2-oxoglutarate-dependent dioxygenase family protein. (473 aa) |
| | P4H2 | Prolyl 4-hydroxylase 2; Catalyzes the post-translational formation of 4- hydroxyproline in -Xaa-Pro-Gly- sequences in proline-rich peptide sequences of plant glycoproteins and other proteins. Hydroxyprolines are important constituent of many plant cell wall glycoproteins such as extensins, hydroxyproline-rich glycoproteins, lectins and arabinogalactan proteins. Possesses high affinity for leucine-rich repeat and proline-rich extensins of root cell walls that are essential for root hair development. Hydroxyprolines define the subsequent O- glycosylation sites by arabinosyltransferases w [...] (299 aa) |
| | F4JAD4_ARATH | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein; Belongs to the iron/ascorbate-dependent oxidoreductase family. (331 aa) |
