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CYP77A4 | Cytochrome P450 77A4; Catalyzes the epoxidation of physiological unsaturated fatty acids in vitro. Can use laurate, oleate, linoleate, linolenate and vernolate as substrate. (512 aa) | ||||
CYP71B9 | Cytochrome P450 71B9; Belongs to the cytochrome P450 family. (500 aa) | ||||
SQE6 | Squalene epoxidase 6; Catalyzes the stereospecific oxidation of squalene to (S)- 2,3-epoxysqualene, and is considered to be a rate-limiting enzyme in steroid biosynthesis. (517 aa) | ||||
SQE4 | Squalene epoxidase 4; Catalyzes the stereospecific oxidation of squalene to (S)- 2,3-epoxysqualene, and is considered to be a rate-limiting enzyme in steroid biosynthesis. (516 aa) | ||||
SQE5 | Squalene epoxidase 5; Catalyzes the stereospecific oxidation of squalene to (S)- 2,3-epoxysqualene, and is considered to be a rate-limiting enzyme in steroid biosynthesis. (516 aa) | ||||
CYP83B1 | Cytochrome P450 83B1; Involved in the metabolism of aromatic oximes. Catalyzes the oxime metabolizing step in indole glucosinolate biosynthesis by converting indole-3-acetaldoxime into indole-3-S-alkyl-thiohydroximate. Probably required for glucosinolate activation in response to pathogens. Functions in auxin homeostasis because indole-3-acetaldoxime also serves as a precursor for auxin biosynthesis. Specifically metabolizes (E)-p-hydroxyphenylacetaldoxime into an S-alkyl- thiohydroximate. (499 aa) | ||||
CYP71B6 | Cytochrome P450 71B6; Belongs to the cytochrome P450 family. (503 aa) | ||||
CYP81F1 | Cytochrome P450 81F1; Involved in indole glucosinolate biosynthesis. Catalyzes hydroxylation reactions of the glucosinolate indole ring. Converts indol-3-yl-methylglucosinolate (I3M) to 4-hydroxy-indol-3-yl- methylglucosinolate (4OH-I3M) and/or 1-hydroxy-indol-3-yl- methylglucosinolate (1OH-I3M) intermediates. These hydroxy intermediates are converted to 4-methoxy-indol-3-yl-methylglucosinolate (4MO-I3M) and 1-methoxy-indol-3-yl-methylglucosinolate (1MO-I3M) by indole glucosinolate methyltransferase 1 and 2 (IGMT1 and IGMT2). Belongs to the cytochrome P450 family. (500 aa) | ||||
SQE2 | Squalene epoxidase 2, mitochondrial; Catalyzes the stereospecific oxidation of squalene to (S)- 2,3-epoxysqualene, and is considered to be a rate-limiting enzyme in steroid biosynthesis. Produces primarily oxidosqualene. (585 aa) | ||||
CYP707A2 | Abscisic acid 8'-hydroxylase 2; Involved in the oxidative degradation of abscisic acid, but not in the isomerization of the produced 8'-hydroxyabscisic acid (8'- OH-ABA) to (-)-phaseic acid (PA). Involved in the control of seed dormancy and germination. (482 aa) | ||||
CYP79B2 | Tryptophan N-monooxygenase 1; Converts tryptophan to indole-3-acetaldoxime, a precursor for tryptophan-derived glucosinolates and indole-3-acetic acid (IAA). Involved in the biosynthetic pathway to 4-hydroxyindole-3-carbonyl nitrile (4-OH-ICN), a cyanogenic metabolite required for inducible pathogen defense. Belongs to the cytochrome P450 family. (541 aa) | ||||
CYP83A1 | Cytochrome P450 83A1; Involved in the metabolism of aliphatic and aromatic oximes. Involved in the biosynthesis of both short-chain and long-chain aliphatic glucosinolates. Belongs to the cytochrome P450 family. (502 aa) | ||||
CYP73A5 | Trans-cinnamate 4-monooxygenase; Controls carbon flux to pigments essential for pollination or UV protection, to numerous pytoalexins synthesized by plants when challenged by pathogens, and to lignins. (505 aa) | ||||
CYP705A1 | Cytochrome P450 705A1; Cleaves the arabidiol side chain at C15 to form 14-apo- arabidiol and a side-chain fragment. Involved in the biosynthesis of the volatile homoterpene (E)-4,8- dimethyl-1,3,7-nonatriene (DMNT) in roots. Involved in the production of DMNT by degrading the triterpene arabidiol. May be involved in the defense again the fungal root pathogen Pythium irregulare by producing DMNT. (513 aa) | ||||
CYP81F3 | Cytochrome P450 81F3; Involved in indole glucosinolate biosynthesis. Catalyzes hydroxylation reactions of the glucosinolate indole ring. Converts indol-3-yl-methylglucosinolate (I3M) to 4-hydroxy-indol-3-yl- methylglucosinolate (4OH-I3M) and/or 1-hydroxy-indol-3-yl- methylglucosinolate (1OH-I3M) intermediates. These hydroxy intermediates are converted to 4-methoxy-indol-3-yl-methylglucosinolate (4MO-I3M) and 1-methoxy-indol-3-yl-methylglucosinolate (1MO-I3M) by indole glucosinolate methyltransferase 1 and 2 (IGMT1 and IGMT2). Belongs to the cytochrome P450 family. (501 aa) | ||||
CYP89A2 | Cytochrome P450 89A2; Belongs to the cytochrome P450 family. (506 aa) | ||||
CYP79B3 | Tryptophan N-monooxygenase 2; Converts tryptophan to indole-3-acetaldoxime, a precursor for tryptophan derived glucosinolates and indole-3-acetic acid (IAA). Belongs to the cytochrome P450 family. (543 aa) | ||||
Q6ID26_ARATH | FAD/NAD(P)-binding oxidoreductase family protein. (121 aa) | ||||
EMB2421 | FAD/NAD(P)-binding oxidoreductase family protein. (709 aa) | ||||
CYP81G1 | Cytochrome P450, family 81, subfamily G, polypeptide 1; Belongs to the cytochrome P450 family. (507 aa) | ||||
CYP705A4 | Cytochrome P450, family 705, subfamily A, polypeptide 4; Belongs to the cytochrome P450 family. (517 aa) | ||||
SQE3 | Squalene epoxidase 3; Catalyzes the stereospecific oxidation of squalene to (S)- 2,3-epoxysqualene, and is considered to be a rate-limiting enzyme in steroid biosynthesis. Can produce not only oxidosqualene, but also 2,3:22,23-dioxidosqualene. (525 aa) | ||||
YUC6 | Indole-3-pyruvate monooxygenase YUCCA6; Involved in auxin biosynthesis via the indole-3-pyruvic acid (IPA) pathway. Also able to convert in vitro phenyl pyruvate (PPA) to phenyl acetic acid (PAA). 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. (417 aa) | ||||
FMOGS-OX4 | Flavin-containing monooxygenase FMO GS-OX4; Catalyzes the conversion of methylthioalkyl glucosinolates of any chain length into methylsulfinylalkyl glucosinolates. Belongs to the FMO family. (461 aa) | ||||
KO | Ent-kaurene oxidase, chloroplastic; Catalyzes three successive oxidations of the 4-methyl group of ent-kaurene giving kaurenoic acid, a key step in gibberellins (GAs) biosynthesis. GAs, which are involved many processes, including stem elongation, play a central role in plant development. (509 aa) | ||||
CYP85A2 | Cytochrome P450 85A2; Catalyzes the C6-oxidation step in brassinosteroids biosynthesis. Converts 6-deoxocastasterone to castasterone, and castasterone to brassinolide. May also convert 6-deoxoteasterone to teasterone, 3-dehydro-6-deoxoteasterone to 3-dehydroteasterone, and 6- deoxotyphasterol to typhasterol; Belongs to the cytochrome P450 family. (465 aa) | ||||
CYP707A1 | Abscisic acid 8'-hydroxylase 1; Involved in the oxidative degradation of abscisic acid. Plays an important role in determining abscisic acid levels in dry seeds and in the control of postgermination growth; Belongs to the cytochrome P450 family. (467 aa) | ||||
CYP79F1 | Dihomomethionine N-hydroxylase; Catalyzes the conversion of the short chain elongated methionines di-, tri-, and tetrahomomethionine to their respective aldoximes 5-methylthiopentanaldoxime, 6-methylthiohexanaldoxime, and 7- methylheptanaldoxime. (538 aa) | ||||
T3P18.16 | Flavin-containing monooxygenase FMO GS-OX-like 4; Catalyzes the conversion of methylthioalkyl glucosinolates of any chain length into methylsulfinylalkyl glucosinolates. Belongs to the FMO family. (452 aa) | ||||
CYP90D1 | 3-epi-6-deoxocathasterone 23-monooxygenase CYP90D1; Involved in brassinosteroid (BR) biosynthesis. May convert teasterone to 3- dehydroteasterone, or 6-deoxoteasterone to 3-dehydro-6-deoxoteasterone. C-23 hydroxylase that converts directly (22S,24R)- 22-hydroxy-5-alpha-ergostan-3-one and 3-epi-6-deoxocathasterone to 3- dehydro-6-deoxoteasterone and 6-deoxotyphasterol, respectively. These C-23 hydroxylation shortcuts bypass campestanol, 6-deoxocathasterone, and 6-deoxoteasterone. (491 aa) | ||||
FMOGS-OX2 | Flavin-containing monooxygenase FMO GS-OX2; Catalyzes the conversion of methylthioalkyl glucosinolates of any chain length into methylsulfinylalkyl glucosinolates. (457 aa) | ||||
KAO2 | Ent-kaurenoic acid oxidase 2; Catalyzes three successive oxidations of ent-kaurenoic acid giving gibberellin 12 (GA12), a key step in gibberellins (GAs) biosynthesis. GAs, which are involved many processes, including stem elongation, play a central role in plant development. Belongs to the cytochrome P450 family. (489 aa) | ||||
F9N12.4 | Putative flavin-containing monooxygenase FMO GS-OX-like 10; Catalyzes the conversion of methylthioalkyl glucosinolates of any chain length into methylsulfinylalkyl glucosinolates. Belongs to the FMO family. (448 aa) | ||||
F2K11.25 | Flavin-containing monooxygenase FMO GS-OX-like 5; Catalyzes the conversion of methylthioalkyl glucosinolates of any chain length into methylsulfinylalkyl glucosinolates. Belongs to the FMO family. (450 aa) | ||||
CYP98A9 | Cytochrome P450 98A9; Acts redundantly with CYP98A8 as tricoumaroylspermidine meta- hydroxylase. Involved in phenolamide synthesis, but a recombinant CYP98A9 is unable to hydroxylate triferuloylspermidine. Unable to use 5-O-(4-coumaroyl) D-quinate or 5-O-(4-coumaroyl) shikimate as substrates; Belongs to the cytochrome P450 family. (487 aa) | ||||
CYP98A8 | Cytochrome P450 98A8; Acts redundantly with CYP98A9 as tricoumaroylspermidine meta- hydroxylase. Catalyzes also the meta-hydroxylation of the three triferuloylspermidine phenolic rings. Unable to use 5-O-(4-coumaroyl) D-quinate or 5-O-(4-coumaroyl) shikimate as substrates. (497 aa) | ||||
MXM12.4 | Flavin-containing monooxygenase FMO GS-OX-like 9; Catalyzes the conversion of methylthioalkyl glucosinolates of any chain length into methylsulfinylalkyl glucosinolates. Belongs to the FMO family. (460 aa) | ||||
CYP81D1 | Cytochrome P450 81D1; Belongs to the cytochrome P450 family. (502 aa) | ||||
CYP705A12 | Cytochrome P450 705A12; May be involved in hydroxylation of the triterpene marneral. (499 aa) | ||||
CYP707A3 | Abscisic acid 8'-hydroxylase 3; Involved in the oxidative degradation of abscisic acid, but not in the isomerization of the produced 8'-hydroxyabscisic acid (8'- OH-ABA) to (-)-phaseic acid (PA). Involved in the control of postgermination growth. (463 aa) | ||||
CYP705A5 | Cytochrome P450 705A5; Converts thalian-diol to a desaturated thalian-diol. Belongs to the cytochrome P450 family. (511 aa) | ||||
FMO2 | Putative flavin-containing monooxygenase 2. (459 aa) | ||||
CYP93D1 | Cytochrome P450, family 93, subfamily D, polypeptide 1; Belongs to the cytochrome P450 family. (507 aa) | ||||
CYP79A2 | Phenylalanine N-monooxygenase; Converts L-phenylalanine into phenylacetaldoxime, the precursor of benzylglucosinolate (glucotropeolin). Belongs to the cytochrome P450 family. (529 aa) | ||||
MFB13.9 | Flavin-containing monooxygenase FMO GS-OX-like 8; Catalyzes the conversion of methylthioalkyl glucosinolates of any chain length into methylsulfinylalkyl glucosinolates. (461 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) | ||||
CYP79F2 | Hexahomomethionine N-hydroxylase; Catalyzes the conversion of the long chain elongated methionines penta- and hexahomomethionine to their corresponding aldoximes 8-methylthiooctanaldoxime and 9-methylthiononanaldoxime. (537 aa) | ||||
YUC10 | Probable indole-3-pyruvate monooxygenase YUCCA10; Involved in auxin biosynthesis. Belongs to the FMO family. (383 aa) | ||||
T28K15.13 | Flavin-containing monooxygenase FMO GS-OX-like 6; Catalyzes the conversion of methylthioalkyl glucosinolates of any chain length into methylsulfinylalkyl glucosinolates. Belongs to the FMO family. (470 aa) | ||||
T28K15.10 | Flavin-containing monooxygenase FMO GS-OX-like 1; Catalyzes the conversion of methylthioalkyl glucosinolates of any chain length into methylsulfinylalkyl glucosinolates. Belongs to the FMO family. (468 aa) | ||||
FMO | Flavin-containing monooxygenase FMO GS-OX-like 2; Catalyzes the conversion of methylthioalkyl glucosinolates of any chain length into methylsulfinylalkyl glucosinolates. Belongs to the FMO family. (465 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) | ||||
T27I15_130 | Cytochrome P450, family 76, subfamily C, polypeptide 7; Belongs to the cytochrome P450 family. (498 aa) | ||||
YUC4 | Probable indole-3-pyruvate monooxygenase YUCCA4; Involved in auxin biosynthesis. Both isoforms are catalitically active. 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. (411 aa) | ||||
CYP81D11 | Cytochrome P450 81D11; May play a role in cis-jasmone-activated defense response to aphids. (509 aa) | ||||
CYP705A33 | Cytochrome P450, family 705, subfamily A, polypeptide 33; Belongs to the cytochrome P450 family. (521 aa) | ||||
CYP705A32 | Cytochrome P450, family 705, subfamily A, polypeptide 32; Belongs to the cytochrome P450 family. (526 aa) | ||||
CYP705A30 | Cytochrome P450, family 705, subfamily A, polypeptide 30; Belongs to the cytochrome P450 family. (523 aa) | ||||
CYP71B37 | Cytochrome P450 71B37; Belongs to the cytochrome P450 family. (500 aa) | ||||
CYP71B36 | Cytochrome P450 71B36; Belongs to the cytochrome P450 family. (500 aa) | ||||
CYP71B35 | Cytochrome P450 71B35; Belongs to the cytochrome P450 family. (500 aa) | ||||
CYP71B34 | Cytochrome P450 71B34; Belongs to the cytochrome P450 family. (500 aa) | ||||
CYP707A4 | Abscisic acid 8'-hydroxylase 4; Involved in the oxidative degradation of abscisic acid, but not in the isomerization of the produced 8'-hydroxyabscisic acid (8'- OH-ABA) to (-)-phaseic acid (PA); Belongs to the cytochrome P450 family. (468 aa) | ||||
CYP705A23 | Cytochrome P450, family 705, subfamily A, polypeptide 23; Belongs to the cytochrome P450 family. (510 aa) | ||||
CYP705A22 | Cytochrome P450 705A22; Plays a role in the gravitropic response of the inflorescence stems and roots. May affect the synthesis of flavonols that have a role in regulating auxin transport; Belongs to the cytochrome P450 family. (515 aa) | ||||
CYP705A21 | Cytochrome P450, family 705, subfamily A, polypeptide 21; Belongs to the cytochrome P450 family. (514 aa) | ||||
CYP705A20 | Cytochrome P450 705A20; Belongs to the cytochrome P450 family. (510 aa) | ||||
CYP705A19 | Cytochrome P450, family 705, subfamily A, polypeptide 19; Belongs to the cytochrome P450 family. (513 aa) | ||||
CYP705A18 | Cytochrome P450, family 705, subfamily A, polypeptide 18; Belongs to the cytochrome P450 family. (524 aa) | ||||
CYP705A15 | Cytochrome P450, family 705, subfamily A, polypeptide 15; Belongs to the cytochrome P450 family. (523 aa) | ||||
YUC5 | Probable indole-3-pyruvate monooxygenase YUCCA5; Involved in auxin biosynthesis. Belongs to the set of redundant YUCCA genes probably responsible for auxin biosynthesis in roots. (424 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) | ||||
CYP703A2 | Cytochrome P450 703A2; Involved in pollen wall development. Catalyzes the conversion of medium-chain saturated fatty acids to the corresponding monohydroxylated fatty acids, with a preferential hydroxylation of lauric acid at the C-7 position. In-chain hydroxylated fatty acids, together with omega-hydroxylated fatty acids, are key monomeric aliphatic building blocks for sporopollenin synthesis during exine formation; Belongs to the cytochrome P450 family. (510 aa) | ||||
YUC11 | Probable indole-3-pyruvate monooxygenase YUCCA11; Involved in auxin biosynthesis. Belongs to the FMO family. (391 aa) | ||||
CYP705A25 | Cytochrome P450, family 705, subfamily A, polypeptide 25; Belongs to the cytochrome P450 family. (519 aa) | ||||
CYP79C2 | Cytochrome P450, putative; Belongs to the cytochrome P450 family. (530 aa) | ||||
CYP82G1 | Dimethylnonatriene synthase; Involved in the biosynthesis of homoterpenes, attractants of herbivores parasitoids and predators (e.g. predatory mites and parasitoid wasps). Catalyzes the conversion of the C20 (E,E)-geranyllinalool to C16-homoterpene 4,8,12-trimethyltrideca- 1,3,7,11-tetraene (TMTT) of the C15 (E)-nerolidol to C11-homoterpene (E)-4,8-dimethyl-1,3,7-nonatriene (DMNT); these volatile compounds are produced upon insect herbivore attack and emitted from flowers and vegetative tissues during herbivore feeding. Required during resistance responses to the fungus Alternaria bras [...] (515 aa) | ||||
CYP71B26 | Cytochrome P450 71B26; Belongs to the cytochrome P450 family. (500 aa) | ||||
CYP71B10 | Cytochrome P450 71B10; Belongs to the cytochrome P450 family. (502 aa) | ||||
CYP81F2 | Cytochrome P450 81F2; Involved in indole glucosinolate biosynthesis. Catalyzes hydroxylation reactions of the glucosinolate indole ring. Converts indol-3-yl-methylglucosinolate (I3M) to 4-hydroxy-indol-3-yl- methylglucosinolate (4OH-I3M) and/or 1-hydroxy-indol-3-yl- methylglucosinolate (1OH-I3M) intermediates. These hydroxy intermediates are converted to 4-methoxy-indol-3-yl-methylglucosinolate (4MO-I3M) and 1-methoxy-indol-3-yl-methylglucosinolate (1MO-I3M) by indole glucosinolate methyltransferase 1 and 2 (IGMT1 and IGMT2). Contributes to defense against the green peach aphid (Myzus [...] (491 aa) | ||||
EMB3143 | YCF54. (211 aa) | ||||
CYP716A1 | Cytochrome P450 716A1; Possesses triterpene oxidizing activity. Catalyzes the C28 hydroxylation of alpha-amyrin, beta-amyrin, and lupeol, producing uvaol, erythrodiol, and betulin, respectively. Catalyzes the C28 carboxylation of alpha- and beta-amyrin. (477 aa) | ||||
CYP76C3 | Cytochrome P450 76C3; Belongs to the cytochrome P450 family. (515 aa) | ||||
T32M21_230 | Cytochrome P450, family 77, subfamily A, polypeptide 9; Belongs to the cytochrome P450 family. (509 aa) | ||||
CYP90C1 | 3-epi-6-deoxocathasterone 23-monooxygenase CYP90C1; Involved in brassinosteroid (BR) biosynthesis. Converts typhasterol to castasterone and 6-deoxotyphasterol to 6-deoxocastasterone. C-23 hydroxylase that converts directly (22S,24R)- 22-hydroxy-5-alpha-ergostan-3-one and 3-epi-6-deoxocathasterone to 3- dehydro-6-deoxoteasterone and 6-deoxotyphasterol, respectively. These C-23 hydroxylation shortcuts bypass campestanol, 6-deoxocathasterone, and 6-deoxoteasterone. Required for the regulation of polar elongation of leaf cells. Required for the longitudinal elongation of floral organs. (524 aa) | ||||
CRD1 | Magnesium-protoporphyrin IX monomethyl ester [oxidative] cyclase, chloroplastic; Catalyzes the formation of the isocyclic ring in chlorophyll biosynthesis. Mediates the cyclase reaction, which results in the formation of divinylprotochlorophyllide (Pchlide) characteristic of all chlorophylls from magnesium-protoporphyrin IX 13-monomethyl ester (MgPMME). (409 aa) | ||||
CYP51G1 | Sterol 14-demethylase; Involved in sterol biosynthesis. Catalyzes the 14-alpha demethylation of obtusifoliol to 4 alpha-methyl-5 alpha-ergosta- 8,14,24(28)-trien-3 beta-ol. (488 aa) | ||||
CYP77B1 | Cytochrome P450, family 77, subfamily B, polypeptide 1; Belongs to the cytochrome P450 family. (510 aa) | ||||
CYP75B1 | Flavonoid 3'-monooxygenase; Catalyzes the 3'-hydroxylation of the flavonoid B-ring to the 3',4'-hydroxylated state. Convert naringenin to eriodictyol and dihydrokaempferol to dihydroquercetin; Belongs to the cytochrome P450 family. (513 aa) | ||||
CYP705A24 | Cytochrome P450, family 705, subfamily A, polypeptide 24; Belongs to the cytochrome P450 family. (521 aa) | ||||
F2K11.23-2 | Putative flavin-containing monooxygenase FMO GS-OX-like 11; Catalyzes the conversion of methylthioalkyl glucosinolates of any chain length into methylsulfinylalkyl glucosinolates. Belongs to the FMO family. (168 aa) | ||||
CYP705A13 | Cytochrome P450, family 705, subfamily A, polypeptide 13; Belongs to the cytochrome P450 family. (518 aa) | ||||
CYP705A6 | Cytochrome P450, family 705, subfamily A, polypeptide 6. (442 aa) | ||||
SQE1 | Squalene epoxidase 1; Catalyzes the stereospecific oxidation of squalene to (S)- 2,3-epoxysqualene, and is considered to be a rate-limiting enzyme in steroid biosynthesis. Can produce not only oxidosqualene, but also 2,3:22,23-dioxidosqualene. Main squalene epoxidase in the root. Sqe1 mutants may show defects in membrane lipid rafts, impairing the correct localization of RHD2 NADPH oxidase and the proper polarized production of ROS. (531 aa) | ||||
F13M14.16 | Putative cytochrome P450; 47418-45874; Belongs to the cytochrome P450 family. (514 aa) | ||||
F13M14.15 | Cytochrome P450, family 77, subfamily A, polypeptide 6; Belongs to the cytochrome P450 family. (513 aa) | ||||
CYP89A9 | Cytochrome P450 89A9; Involved in the chlorophyll breakdown by its action in nonpolar fluorescent chlorophyll catabolite (FCC) decarbonylation. (511 aa) | ||||
FMOGS-OX1 | Flavin-containing monooxygenase FMO GS-OX1; Catalyzes the conversion of methylthioalkyl glucosinolates into methylsulfinylalkyl glucosinolates. Able to S-oxygenate both desulfo- and intact 4-methylthiobutyl glucosinolates, but no activity with methionine, dihomomethionine or 5-methylthiopentaldoxime. (459 aa) | ||||
FAH2 | Dihydroceramide fatty acyl 2-hydroxylase FAH2; Fatty acid 2-hydroxylase involved in the alpha-hydroxylation of the long-chain fatty acid (LCFA) palmitic acid. Probably involved in the resistance response to oxidative stress. (237 aa) | ||||
YUC2 | Indole-3-pyruvate monooxygenase YUCCA2; Involved in auxin biosynthesis. Converts the indole-3-pyruvic acid (IPA) produced by the TAA family to indole-3-acetic acid (IAA). Unable to use tryptamine (TAM) as substrate. 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. (415 aa) | ||||
YUC8 | Probable indole-3-pyruvate monooxygenase YUCCA8; Involved in auxin biosynthesis. Belongs to the set of redundant YUCCA genes probably responsible for auxin biosynthesis in roots. (426 aa) | ||||
C7A10.50 | Cytochrome P450, family 81, subfamily H, polypeptide 1; Belongs to the cytochrome P450 family. (518 aa) | ||||
T3P18.18 | Flavin-containing monooxygenase FMO GS-OX-like 3; Catalyzes the conversion of methylthioalkyl glucosinolates of any chain length into methylsulfinylalkyl glucosinolates. Belongs to the FMO family. (450 aa) | ||||
NOGC1 | Flavin-containing monooxygenase FMO GS-OX-like 7; Catalyzes the conversion of methylthioalkyl glucosinolates of any chain length into methylsulfinylalkyl glucosinolates. Belongs to the FMO family. (464 aa) | ||||
FMOGS-OX3 | Flavin-containing monooxygenase FMO GS-OX3; Catalyzes the conversion of methylthioalkyl glucosinolates of any chain length into methylsulfinylalkyl glucosinolates. Prefers probably short-chain methylthioalkyl glucosinolates in cv. Landsberg erecta; Belongs to the FMO family. (462 aa) | ||||
CYP82C4 | Xanthotoxin 5-hydroxylase CYP82C4; Can hydroxylate xanthotoxin (8-methoxypsoralen) to form 5- hydroxyxanthotoxin (5-hydroxy-8-methoxypsoralen) in vivo and in vitro. Involved in the early iron deficiency response, possibly through an IDE1-like mediated pathway. 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 si [...] (524 aa) | ||||
CYP81D2 | Cytochrome P450, family 81, subfamily D, polypeptide 2; Belongs to the cytochrome P450 family. (499 aa) | ||||
CYP81D8 | Cytochrome P450, family 81, subfamily D, polypeptide 8; Belongs to the cytochrome P450 family. (497 aa) | ||||
CYP81F4 | Cytochrome P450 81F4; Involved in indole glucosinolate biosynthesis. Catalyzes hydroxylation reactions of the glucosinolate indole ring. Converts indol-3-yl-methylglucosinolate (I3M) to 1-hydroxy-indol-3-yl- methylglucosinolate (1OH-I3M) intermediate. This hydroxy intermediates is converted to 1-methoxy-indol-3-yl-methylglucosinolate (1MO-I3M) by indole glucosinolate methyltransferase 1 and 2 (IGMT1 and IGMT2). Belongs to the cytochrome P450 family. (501 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) | ||||
CYP89A5 | Cytochrome P450, family 89, subfamily A, polypeptide 5; Belongs to the cytochrome P450 family. (510 aa) | ||||
CYP89A6 | Cytochrome P450, family 87, subfamily A, polypeptide 6; Belongs to the cytochrome P450 family. (511 aa) | ||||
CYP89A7 | Cytochrome P450, family 87, subfamily A, polypeptide 7; Belongs to the cytochrome P450 family. (511 aa) | ||||
F23M2.31 | Cytochrome P450 superfamily protein; Belongs to the cytochrome P450 family. (512 aa) | ||||
CYP705A9 | Cytochrome P450, family 705, subfamily A, polypeptide 9; Belongs to the cytochrome P450 family. (498 aa) | ||||
CYP705A8 | Cytochrome P450, family 705, subfamily A, polypeptide 8; Belongs to the cytochrome P450 family. (514 aa) | ||||
CYP716A2 | Cytochrome P450 716A2; Possesses triterpene oxidizing activity. Catalyzes the C28 hydroxylation of alpha-amyrin, beta-amyrin, and lupeol, producing uvaol, erythrodiol, and betulin, respectively. Catalyzes the C28 carboxylation of alpha- and beta-amyrin. Possesses 22alpha- hydroxylation activity against alpha- and beta-amaryn. (473 aa) | ||||
FMOGS-OX5 | Flavin-containing monooxygenase FMO GS-OX5; Catalyzes the conversion of methylthioalkyl glucosinolates into methylsulfinylalkyl glucosinolates. Specific for 8-methylthiooctyl (8-MTO) glucosinolates; Belongs to the FMO family. (459 aa) | ||||
CYP705A27 | Cytochrome P450, family 705, subfamily A, polypeptide 27; Belongs to the cytochrome P450 family. (533 aa) | ||||
CYP79C1 | Cytochrome P450, family 79, subfamily C, polypeptide 1; Belongs to the cytochrome P450 family. (546 aa) | ||||
CYP705A28 | Cytochrome P450, family 705, subfamily A, polypeptide 28; Belongs to the cytochrome P450 family. (348 aa) | ||||
COQ6 | Ubiquinone biosynthesis monooxygenase COQ6, mitochondrial; FAD-dependent monooxygenase required for the C5-ring hydroxylation during ubiquinone biosynthesis. Catalyzes the hydroxylation of 3-polyprenyl-4-hydroxybenzoic acid to 3-polyprenyl- 4,5-dihydroxybenzoic acid. The electrons required for the hydroxylation reaction may be funneled indirectly from NADPH via a ferredoxin/ferredoxin reductase system to COQ6. (507 aa) | ||||
F1M23.15 | Cytochrome P450 superfamily protein; Belongs to the cytochrome P450 family. (502 aa) | ||||
CYP89A3 | Cytochrome P450, family 89, subfamily A, polypeptide 3; Belongs to the cytochrome P450 family. (497 aa) | ||||
CYP712A2 | Cytochrome P450, family 712, subfamily A, polypeptide 2; Belongs to the cytochrome P450 family. (521 aa) | ||||
CYP81D6 | Cytochrome P450, family 81, subfamily D, polypeptide 6; Belongs to the cytochrome P450 family. (515 aa) | ||||
CYP81D7 | Cytochrome P450, family 81, subfamily D, polypeptide 7; Belongs to the cytochrome P450 family. (543 aa) | ||||
CYP98A3 | Cytochrome P450 98A3; Cytochrome P450 which catalyzes 3'-hydroxylation of p- coumaric esters of shikimic/quinic acids to form lignin monomers. Can use p-coumarate, p-coumaraldehyde, p-coumaroyl methyl ester, 5-O-(4- coumaroyl) D-quinate and 5-O-(4-coumaroyl) shikimate as substrates, but not p-coumaryl alcohol, p-coumaroyl CoA, 1-O-p-coumaroyl-beta-D- glucose, p-hydroxy-cinnamyl alcohol, cinnamate, caffeate or ferulate. Has a weak activity on tri(p-coumaroyl)spermidine, but none on triferuloylspermidine. Hydroxylates preferentially the 5-O-isomer, but can also convert the 4-O- and 3-O-i [...] (508 aa) | ||||
YUC3 | Probable indole-3-pyruvate monooxygenase YUCCA3; Involved in auxin biosynthesis. Belongs to the set of redundant YUCCA genes probably responsible for auxin biosynthesis in roots. (437 aa) | ||||
KAO1 | Ent-kaurenoic acid oxidase 1; Catalyzes three successive oxidations of ent-kaurenoic acid giving gibberellin 12 (GA12), a key step in gibberellins (GAs) biosynthesis. GAs, which are involved many processes, including stem elongation, play a central role in plant development. Belongs to the cytochrome P450 family. (490 aa) | ||||
C7A10.20 | Cytochrome P450, family 81, subfamily D, polypeptide 3; Belongs to the cytochrome P450 family. (500 aa) | ||||
C7A10.30 | Cytochrome P450, family 81, subfamily D, polypeptide 4; Belongs to the cytochrome P450 family. (492 aa) | ||||
dl3725w | Cytochrome P450, family 705, subfamily A, polypeptide 3; Belongs to the cytochrome P450 family. (527 aa) | ||||
dl3720w | Cytochrome P450, family 705, subfamily A, polypeptide 2. (509 aa) | ||||
CYP712A1 | Cytochrome P450, family 712, subfamily A, polypeptide 1; Belongs to the cytochrome P450 family. (514 aa) | ||||
FAH1 | Dihydroceramide fatty acyl 2-hydroxylase FAH1; Fatty acid 2-hydroxylase involved in the alpha-hydroxylation of sphingolipid-associated very long-chain fatty acids (VLCFA). Probably involved in the resistance response to oxidative stress. (237 aa) | ||||
YUC7 | Probable indole-3-pyruvate monooxygenase YUCCA7; Involved in auxin biosynthesis. Belongs to the set of redundant YUCCA genes probably responsible for auxin biosynthesis in roots. (431 aa) | ||||
CYP82C2 | Xanthotoxin 5-hydroxylase CYP82C2; Involved in the biosynthetic pathway to 4-hydroxyindole-3- carbonyl nitrile (4-OH-ICN), a cyanogenic metabolite required for inducible pathogen defense. Converts indole-3-carbonyl nitrile (ICN) into 4-OH-ICN. Can hydroxylate xanthotoxin (8- methoxypsoralen) to form 5-hydroxyxanthotoxin (5-hydroxy-8- methoxypsoralen) in vivo and in vitro. Belongs to the cytochrome P450 family. (523 aa) | ||||
YUC9 | Probable indole-3-pyruvate monooxygenase YUCCA9; Involved in auxin biosynthesis. Belongs to the set of redundant YUCCA genes probably responsible for auxin biosynthesis in roots. (421 aa) |