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| | PAL1 | Phenylalanine ammonia-lyase 1; This is a key enzyme of plant metabolism catalyzing the first reaction in the biosynthesis from L-phenylalanine of a wide variety of natural products based on the phenylpropane skeleton; Belongs to the PAL/histidase family. (725 aa) |
| | TPPA | Trehalose-phosphate phosphatase A; Removes the phosphate from trehalose 6-phosphate to produce free trehalose. Trehalose accumulation in plant may improve abiotic stress tolerance. (385 aa) |
| | IRX12 | Laccase-4; Lignin degradation and detoxification of lignin-derived products (By similarity). Required for secondary xylem cell wall lignification; Belongs to the multicopper oxidase family. (558 aa) |
| | LAC2 | Laccase-2; Lignin degradation and detoxification of lignin-derived products (By similarity). Required for root elongation in dehydration conditions; Belongs to the multicopper oxidase family. (573 aa) |
| | F24G24.60 | Probable fructokinase-5; May play an important role in maintaining the flux of carbon towards starch formation. (324 aa) |
| | FD2 | Ferredoxin-2, chloroplastic; Ferredoxins are iron-sulfur proteins that transfer electrons in a wide variety of metabolic reactions; Belongs to the 2Fe2S plant-type ferredoxin family. (148 aa) |
| | CYCD2-1 | Cyclin-D2-1; Acts on the G1 phase of the cell cycle to control cell division rate in both shoot and root meristems. The complex formed with CDKA-1 phosphorylates plant retinoblastoma protein. (361 aa) |
| | CYCD3-1 | Cyclin-D3-1; Involved in the control of the cell cycle at the G1/S (start) transition. Activates the G1/S phase transition in response to cytokinin hormone signal, but declines in response to sucrose starvation leading to G1 arrest. Involved in the induction of mitotic cell division. Plays an important role in the switch from cell proliferation to the final stages of differentiation during plant development. May not be involved in the activation of cell cycle in the root apical meristem (RAM) in the early phase of seed germination. Promotes divisions in the guard cells (GCs) after the [...] (376 aa) |
| | PAL2 | Phenylalanine ammonia-lyase 2; This is a key enzyme of plant metabolism catalyzing the first reaction in the biosynthesis from L-phenylalanine of a wide variety of natural products based on the phenylpropane skeleton; Belongs to the PAL/histidase family. (717 aa) |
| | PAL3 | Phenylalanine ammonia-lyase 3; This is a key enzyme of plant metabolism catalyzing the first reaction in the biosynthesis from L-phenylalanine of a wide variety of natural products based on the phenylpropane skeleton. (694 aa) |
| | AP2 | Floral homeotic protein APETALA 2; Probable transcriptional activator that promotes early floral meristem identity. Is required subsequently for the transition of an inflorescence meristem into a floral meristem. Plays a central role in the specification of floral identity, particularly for the normal development of sepals and petals in the wild-type flower, by spatially controlling the expression domains of multiple floral organ identity genes. Acts as A class cadastral protein by repressing the C class floral homeotic gene AGAMOUS in association with other repressors like LEUNIG and [...] (432 aa) |
| | SUS1 | Sucrose synthase 1; Sucrose-cleaving enzyme that provides UDP-glucose and fructose for various metabolic pathways; Belongs to the glycosyltransferase 1 family. Plant sucrose synthase subfamily. (808 aa) |
| | SUS2 | Sucrose synthase 2; Sucrose-cleaving enzyme that provides UDP-glucose and fructose for various metabolic pathways. Modulates metabolic homeostasis and directs carbon towards starch synthesis in developing seeds. (807 aa) |
| | LAC16 | Laccase-16; Lignin degradation and detoxification of lignin-derived products. (566 aa) |
| | CWINV2 | Beta-fructofuranosidase, insoluble isoenzyme CWINV2. (590 aa) |
| | BFRUCT4 | Acid beta-fructofuranosidase 4, vacuolar; Possible role in the continued mobilization of sucrose to sink organs. Regulates root elongation. (664 aa) |
| | CYP84A1 | Cytochrome P450 84A1. (520 aa) |
| | BFRUCT3 | Acid beta-fructofuranosidase 3, vacuolar; Possible role in the continued mobilization of sucrose to sink organs. (648 aa) |
| | CWINV1 | Beta-fructofuranosidase, insoluble isoenzyme CWINV1; Beta-fructofuranosidase that can use sucrose and 1-kestose, and, to a lower extent, neokestose and levan, as substrates, but not inuline; Belongs to the glycosyl hydrolase 32 family. (584 aa) |
| | LAC3 | Laccase-3; Lignin degradation and detoxification of lignin-derived products. (570 aa) |
| | TPPJ | Probable trehalose-phosphate phosphatase J; Removes the phosphate from trehalose 6-phosphate to produce free trehalose. Trehalose accumulation in plant may improve abiotic stress tolerance (By similarity). (370 aa) |
| | TPPE | Probable trehalose-phosphate phosphatase E; Removes the phosphate from trehalose 6-phosphate to produce free trehalose. Trehalose accumulation in plant may improve abiotic stress tolerance (By similarity). (354 aa) |
| | TPPD | Probable trehalose-phosphate phosphatase D; Removes the phosphate from trehalose 6-phosphate to produce free trehalose. Trehalose accumulation in plant may improve abiotic stress tolerance (By similarity). (369 aa) |
| | CWINV3 | Beta-fructofuranosidase, insoluble isoenzyme CWINV3; 6-fructan exohydrolase that can use phlein, levan, neokestose, levanbiose, 6-kestose, and 1-kestose as substrates. (594 aa) |
| | LAC10 | Laccase-10; Lignin degradation and detoxification of lignin-derived products. (558 aa) |
| | TT10 | Laccase-15; Lignin degradation and detoxification of lignin-derived products (By similarity). Involved in lignin synthesis in seed coats, in seed coat permeability, in seed germination, and in root elongation. Required for the seed coat (testa) brown pigmentation by mediating the polymerization of proanthocyanidin (tannin) from its monomer precursor epicatechin. Slightly promotes seed dormancy. Belongs to the multicopper oxidase family. (565 aa) |
| | TPPH | Probable trehalose-phosphate phosphatase H; Removes the phosphate from trehalose 6-phosphate to produce free trehalose. Trehalose accumulation in plant may improve abiotic stress tolerance (By similarity). (349 aa) |
| | RGL2 | DELLA protein RGL2; Probable transcriptional regulator that acts as a repressor of the gibberellin (GA) signaling pathway. No effect of the BOI proteins on its stability. Probably acts by participating in large multiprotein complexes that repress transcription of GA-inducible genes. Upon GA application, it is degraded by the proteasome, allowing the GA signaling pathway. Acts as a major GA-response repressor of seed germination, including seed thermoinhibition. Promotes the biosynthesis of abscisic acid (ABA), especially in seed coats to maintain seed dormancy. Delays flowering and adu [...] (547 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) |
| | AMY2 | Probable alpha-amylase 2; Probable alpha-amylase that does not seem to be required for breakdown of transitory starch in leaves. (413 aa) |
| | AMY1 | Alpha-amylase 1; Possesses alpha-amylase activity in vitro, but seems not required for breakdown of transitory starch in leaves. (423 aa) |
| | LAC11 | Laccase-11; Lignin degradation and detoxification of lignin-derived products. (557 aa) |
| | CWINV4 | Beta-fructofuranosidase, insoluble isoenzyme CWINV4. (591 aa) |
| | CWINV6 | Beta-fructofuranosidase, insoluble isoenzyme CWINV6; 6 and 1-fructan exohydrolase that can degrade both inulin and levan-type fructans, such as phlein, levan, neokestose, levanbiose, 6- kestose, 1-kestose, inulin, and 1,1-nystose. (550 aa) |
| | AMY3 | Alpha-amylase 3, chloroplastic; Possesses endoamylolytic activity in vitro, but seems not required for breakdown of transitory starch in leaves. May be involved in the determination of the final structure of glucans by shortening long linear phospho-oligosaccharides in the chloroplast stroma. Can act on both soluble and insoluble glucan substrates to release small linear and branched malto-oligosaccharides. Works synergistically with beta-amylase toward efficient starch degradation. Has activity against p-nitrophenyl maltoheptaoside (BPNP-G7), amylopectin and beta-limit dextrin. Involv [...] (887 aa) |
| | AUX1 | Auxin transporter protein 1; Carrier protein involved in proton-driven auxin influx. Mediates the formation of auxin gradient from developing leaves (site of auxin biosynthesis) to tips by contributing to the loading of auxin in vascular tissues and facilitating acropetal (base to tip) auxin transport within inner tissues of the root apex, and basipetal (tip to base) auxin transport within outer tissues of the root apex. Unloads auxin from the mature phloem to deliver the hormone to the root meristem via the protophloem cell files. Coordinated subcellular localization of AUX1 is regula [...] (485 aa) |
| | F28G11.11 | Probable fructokinase-6, chloroplastic; May play an important role in maintaining the flux of carbon towards starch formation; Belongs to the carbohydrate kinase PfkB family. (384 aa) |
| | T25K17.30 | Probable caffeoyl-CoA O-methyltransferase At4g26220; Methylates caffeoyl-CoA to feruloyl-CoA and 5- hydroxyferuloyl-CoA to sinapoyl-CoA. Plays a role in the synthesis of feruloylated polysaccharides. Involved in the reinforcement of the plant cell wall. Also involved in the responding to wounding or pathogen challenge by the increased formation of cell wall-bound ferulic acid polymers (By similarity); Belongs to the class I-like SAM-binding methyltransferase superfamily. Cation-dependent O-methyltransferase family. CCoAMT subfamily. (232 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) |
| | 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) |
| | RGL1 | DELLA protein RGL1; Probable transcriptional regulator that acts as a repressor of the gibberellin (GA) signaling pathway. No effect of the BOI proteins on its stability. Probably acts by participating in large multiprotein complexes that repress transcription of GA-inducible genes. Has overlapping but distinct roles in GA signaling compared to RGA and GAI. Regulates the floral development. May also participate in seed germination and in ovule and anther development. Its activity is probably regulated by other phytohormones such as auxin and ethylene. (511 aa) |
| | TPPB | Trehalose-phosphate phosphatase B; Removes the phosphate from trehalose 6-phosphate to produce free trehalose. Trehalose accumulation in plant may improve abiotic stress tolerance. (374 aa) |
| | CCOAMT | Putative caffeoyl-CoA O-methyltransferase At1g67980; Methylates caffeoyl-CoA to feruloyl-CoA and 5- hydroxyferuloyl-CoA to sinapoyl-CoA. Plays a role in the synthesis of feruloylated polysaccharides. Involved in the reinforcement of the plant cell wall. Also involved in the responding to wounding or pathogen challenge by the increased formation of cell wall-bound ferulic acid polymers (By similarity). (232 aa) |
| | BZIP8 | Basic leucine zipper 8; Belongs to the bZIP family. (138 aa) |
| | RLK | Leucine-rich repeat receptor-like protein kinase. (751 aa) |
| | HST-2 | Shikimate O-hydroxycinnamoyltransferase; Acyltransferase involved in the biosynthesis of lignin. Accepts caffeoyl-CoA and p- coumaroyl-CoA as substrates and transfers the acyl group on both shikimate and quinate acceptors. (433 aa) |
| | LAC17 | Laccase-17; Lignin degradation and detoxification of lignin-derived products. (577 aa) |
| | SAUR19 | Auxin-responsive protein SAUR19; Functions as positive effectors of cell expansion through modulation of auxin transport; Belongs to the ARG7 family. (90 aa) |
| | MTI20.9 | HXXXD-type acyl-transferase family protein. (443 aa) |
| | OMT1 | Flavone 3'-O-methyltransferase 1; Methylates OH residues of flavonoid compounds. Converts quercetin into isorhamnetin. Dihydroquercetin is not a substrate. Catalyzes the methylation of monolignols, the lignin precursors. Does not contribute to the phenylpropanoid pattern of the pollen tryphine, but is probably confined to isorhamnetin glycoside biosynthesis. Involved in melatonin biosynthesis. Can function as acetylserotonin O- methyltransferase. Catalyzes the transfer of a methyl group onto N- acetylserotonin, producing melatonin (N-acetyl-5-methoxytryptamine). Belongs to the class I- [...] (363 aa) |
| | LAC12 | Laccase-12; Lignin degradation and detoxification of lignin-derived products. (565 aa) |
| | BXL4 | Beta-D-xylosidase 4; Beta-D-xylosidase showing an optimal efficiency with the natural substrate xylobiose; Belongs to the glycosyl hydrolase 3 family. (784 aa) |
| | MIO24.3 | Probable fructokinase-7; May play an important role in maintaining the flux of carbon towards starch formation. (343 aa) |
| | SUS6 | Sucrose synthase 6; Sucrose-cleaving enzyme that provides UDP-glucose and fructose for various metabolic pathways. Functions in callose synthesis at the site of phloem sieve elements. (942 aa) |
| | LAC14 | Laccase-14; Lignin degradation and detoxification of lignin-derived products. (569 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) |
| | RGL3 | DELLA protein RGL3; Probable transcriptional regulator that acts as a repressor of the gibberellin (GA) signaling pathway. No effect of the BOI proteins on its stability. Probably acts by participating in large multiprotein complexes that repress transcription of GA-inducible genes. Its activity may be regulated by phytohormones such as auxin and ethylene (By similarity); Belongs to the GRAS family. DELLA subfamily. (523 aa) |
| | LAC9 | Laccase-9; Lignin degradation and detoxification of lignin-derived products. (586 aa) |
| | LAC8 | Laccase-8; Lignin degradation and detoxification of lignin-derived products (By similarity). Involved in the flowering time inhibition. (584 aa) |
| | CWINV5 | Beta-fructofuranosidase, insoluble isoenzyme CWINV5. (572 aa) |
| | BXL5 | Probable beta-D-xylosidase 5. (781 aa) |
| | LAC1 | Laccase-1; Lignin degradation and detoxification of lignin-derived products. (581 aa) |
| | T21E18.8 | Probable fructokinase-2; May play an important role in maintaining the flux of carbon towards starch formation. (329 aa) |
| | T21E18.7 | Probable fructokinase-3; May play an important role in maintaining the flux of carbon towards starch formation. (345 aa) |
| | GAI | DELLA protein GAI; Transcriptional regulator that acts as a repressor of the gibberellin (GA) signaling pathway. Transcription coactivator of the zinc finger transcription factors GAF1/IDD2 and ENY/IDD1 in regulation of gibberellin homeostasis and signaling. No effect of the BOI proteins on its stability. Probably acts by participating in large multiprotein complexes that repress transcription of GA-inducible genes. Positively regulates XERICO expression. In contrast to RGA, it is less sensitive to GA. Its activity is probably regulated by other phytohormones such as auxin and ethylene [...] (533 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) |
| | BXL3 | Beta-D-xylosidase 3; Involved in the hydrolysis of arabinan. Can hydrolyze (1,3)- alpha-, (1,2)-alpha-linked side group residues and non-reducing terminal L-arabinofuranose residues of debranched (1,5)-alpha-L- arabinan backbone. Acts also as a beta-D-xylosidase, releasing D-xylose from arabinoxylan and xylan; Belongs to the glycosyl hydrolase 3 family. (773 aa) |
| | SUS4 | Sucrose synthase 4; Sucrose-cleaving enzyme that provides UDP-glucose and fructose for various metabolic pathways; Belongs to the glycosyltransferase 1 family. Plant sucrose synthase subfamily. (808 aa) |
| | LAC13 | Laccase-13; Lignin degradation and detoxification of lignin-derived products. (569 aa) |
| | SUS3 | Sucrose synthase 3; Sucrose-cleaving enzyme that provides UDP-glucose and fructose for various metabolic pathways. Modulates metabolic homeostasis and direct carbon towards starch synthesis in developing seeds. (809 aa) |
| | T16L24.30 | Probable fructokinase-4; May play an important role in maintaining the flux of carbon towards starch formation. (326 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) |
| | CCR1-2 | Cinnamoyl-CoA reductase 1; Involved in the latter stages of lignin biosynthesis. Catalyzes one of the last steps of monolignol biosynthesis, the conversion of cinnamoyl-CoAs into their corresponding cinnamaldehydes. (344 aa) |
| | CCR2-2 | Cinnamoyl-CoA reductase 2; Cinnamoyl-CoA reductase probably involved in the formation of phenolic compounds associated with the hypersensitive response. Seems not to be involved in lignin biosynthesis. Belongs to the NAD(P)-dependent epimerase/dehydratase family. Dihydroflavonol-4-reductase subfamily. (332 aa) |
| | T28P16.12 | Probable fructokinase-1; May play an important role in maintaining the flux of carbon towards starch formation. (325 aa) |
| | LAC5 | Laccase-5; Lignin degradation and detoxification of lignin-derived products. (580 aa) |
| | RGA | DELLA protein RGA; Probable transcriptional regulator that acts as a repressor of the gibberellin (GA) signaling pathway. Probably acts by participating in large multiprotein complexes that repress transcription of GA-inducible genes. Positively regulates XERICO expression in seeds. Upon GA application, it is degraded by the proteasome, allowing the GA signaling pathway. Compared to other DELLA proteins, it is the most sensitive to GA application. No effect of the BOI proteins on its stability. Its activity is probably regulated by other phytohormones such as auxin and ethylene, attenu [...] (587 aa) |
| | LAC7 | Laccase-7; Lignin degradation and detoxification of lignin-derived products. (567 aa) |
| | PAL4 | Phenylalanine ammonia-lyase 4; This is a key enzyme of plant metabolism catalyzing the first reaction in the biosynthesis from L-phenylalanine of a wide variety of natural products based on the phenylpropane skeleton; Belongs to the PAL/histidase family. (707 aa) |
| | GID2 | F-box protein GID2; Essential component of the SCF-type E3 ligase complex, SCF(GID2), a complex that positively regulates the gibberellin signaling pathway. Upon gibberellin treatment, the SCF(GID2) complex mediates the ubiquitination and subsequent degradation of DELLA proteins (GAI, RGA and RGL2), some repressors of the gibberellin pathway, leading to activate the pathway. (151 aa) |
| | TPPF | Probable trehalose-phosphate phosphatase F; Removes the phosphate from trehalose 6-phosphate to produce free trehalose. Trehalose accumulation in plant may improve abiotic stress tolerance (By similarity). (368 aa) |
| | TPPG | Probable trehalose-phosphate phosphatase G; Removes the phosphate from trehalose 6-phosphate to produce free trehalose. Trehalose accumulation in plant may improve abiotic stress tolerance (By similarity). (377 aa) |
| | ENDO1 | Endonuclease 1; Endonuclease that can use RNA, single-stranded and double- stranded DNA as substrates. Hydrolyzes single- stranded DNA and RNA without apparent specificity for bases during senescence. Endonuclease that recognizes and cleaves all types of mismatches with high efficiency, including heteroduplex double-stranded DNA. Maybe involved in programmed cell death (PCD) and senescence. (305 aa) |
| | YUC1 | Probable indole-3-pyruvate monooxygenase YUCCA1; Involved in auxin biosynthesis, but not in the tryptamine or the CYP79B2/B3 branches. Catalyzes in vitro the N-oxidation of tryptamine to form N-hydroxyl tryptamine. Involved during embryogenesis and seedling development. Required for the formation of floral organs and vascular tissues. Belongs to the set of redundant YUCCA genes probably responsible for auxin biosynthesis in shoots. (414 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) |
| | LAC6 | Laccase-6; Lignin degradation and detoxification of lignin-derived products; Belongs to the multicopper oxidase family. (569 aa) |
| | CSLA7 | Glucomannan 4-beta-mannosyltransferase 7; Probable mannan synthase which consists of a 4-beta- mannosyltransferase activity on mannan using GDP-mannose. The beta-1,4- mannan product is the backbone for galactomannan synthesis by galactomannan galactosyltransferase. Galactomannan is a noncellulosic polysaccharides of plant cell wall. Required for synthesis of a cell wall polysaccharide essential for pollen tube growth, for cell wall structure, or for signaling during plant embryo development. (556 aa) |
| | F5F19.5 | O-methyltransferase family protein; Belongs to the class I-like SAM-binding methyltransferase superfamily. Cation-independent O-methyltransferase family. (363 aa) |
| | TPPC | Probable trehalose-phosphate phosphatase C; Removes the phosphate from trehalose 6-phosphate to produce free trehalose. Trehalose accumulation in plant may improve abiotic stress tolerance (By similarity). (320 aa) |
| | SAUR63 | Auxin-responsive protein SAUR63; May promote auxin-stimulated organ elongation, such as hypocotyls, stamen filaments and petals; Belongs to the ARG7 family. (141 aa) |
| | F5A9.20 | S-adenosyl-L-methionine-dependent methyltransferases superfamily protein. (291 aa) |
| | SUS5 | Sucrose synthase 5; Sucrose-cleaving enzyme that provides UDP-glucose and fructose for various metabolic pathways. Functions in callose synthesis at the site of phloem sieve elements. (836 aa) |
| | F17I14.110 | Glycosyl hydrolase family protein. (526 aa) |
| | TPPI | Probable trehalose-phosphate phosphatase I; Removes the phosphate from trehalose 6-phosphate to produce free trehalose. Trehalose accumulation in plant may improve abiotic stress tolerance (By similarity). (369 aa) |
| | ERD6 | Sugar transporter ERD6; Sugar transporter; Belongs to the major facilitator superfamily. Sugar transporter (TC 2.A.1.1) family. (496 aa) |
| | CCOAOMT1 | Caffeoyl-CoA O-methyltransferase 1; Methylates caffeoyl-CoA to feruloyl-CoA. Has a very low activity with caffeic acid and esculetin. Involved in scopoletin biosynthesis in roots; Belongs to the class I-like SAM-binding methyltransferase superfamily. Cation-dependent O-methyltransferase family. CCoAMT subfamily. (259 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) |
| | 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) |
| | CCD4 | Probable carotenoid cleavage dioxygenase 4, chloroplastic; May be involved in carotenoid cleavage; Belongs to the carotenoid oxygenase family. (595 aa) |
| | SHT | Spermidine hydroxycinnamoyl transferase; Hydroxycinnamoyl transferase involved in the conjugation of feruloyl CoA to spermidine. Able to perform all three conjugating steps required for the biosynthesis of N1,N5,N10-triferuloyl-spermidine. Spermidine is the only acceptor substrate while feruloyl CoA > caffeoyl CoA > coumaroyl CoA > cinnamoyl CoA >> sinapoyl CoA are efficient acyl donors. No activity with hydroxyferuloyl CoA. (451 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) |
| | TO1 | Thioredoxin O1, mitochondrial; Thiol-disulfide oxidoreductase that may participate in various redox reactions. Possesses insulin disulfide bonds reducing activity. Reduced by thioredoxin reductases NTRA and NTRB. Belongs to the thioredoxin family. Plant O-type subfamily. (194 aa) |
