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F14M4.28 | 3-oxo-5-alpha-steroid 4-dehydrogenase (DUF1295). (322 aa) | ||||
DAPB1 | 4-hydroxy-tetrahydrodipicolinate reductase 1, chloroplastic; Catalyzes the conversion of 4-hydroxy-tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate. (347 aa) | ||||
PLR3 | Probable pinoresinol-lariciresinol reductase 3; Probable reductase that might be involved in the reduction of lariciresinol into secoisolariciresinol. In most plant species, a single enzyme is able to reduce both pinoresinol and lariciresinol efficiently while in Arabidopsis, PRR1 and PRR2 show a strict substrate selectivity for pinoresinol; Belongs to the NmrA-type oxidoreductase family. Isoflavone reductase subfamily. (306 aa) | ||||
ACX1 | Peroxisomal acyl-coenzyme A oxidase 1; Catalyzes the desaturation of both long- and medium-chain acyl-CoAs to 2-trans-enoyl-CoAs. Most active with C14-CoA. Activity on long-chain mono-unsaturated substrates is 40% higher than with the corresponding saturated substrates. Seems to be an important factor in the general metabolism of root tips. May be involved in the biosynthesis of jasmonic acid. (664 aa) | ||||
ACX2 | Acyl-coenzyme A oxidase 2, peroxisomal; Catalyzes the desaturation of long-chain acyl-CoAs to 2- trans-enoyl-CoAs. Active on substrates longer than C14 and mostly with C18-CoA. Activity on long-chain mono-unsaturated substrates is double than with the corresponding saturated substrates. (692 aa) | ||||
PORC | Protochlorophyllide reductase C, chloroplastic; Phototransformation of protochlorophyllide (Pchlide) to chlorophyllide (Chlide). (401 aa) | ||||
F2K13.130 | Zinc-binding dehydrogenase family protein. (305 aa) | ||||
K18L3.120 | GroES-like family protein. (108 aa) | ||||
F4IY04_ARATH | Aldolase-type TIM barrel family protein. (329 aa) | ||||
F5I14.9 | Zinc-binding dehydrogenase family protein. (350 aa) | ||||
T10F20.18 | 3-oxo-5-alpha-steroid 4-dehydrogenase (DUF1295). (305 aa) | ||||
K18L3.100 | Allyl alcohol dehydrogenase; NADP-dependent oxidoreductase-like protein. (353 aa) | ||||
K18L3.140 | Allyl alcohol dehydrogenase; NADP-dependent oxidoreductase-like protein. (353 aa) | ||||
SDH2-3 | Succinate dehydrogenase [ubiquinone] iron-sulfur subunit 3, mitochondrial; Iron-sulfur protein (IP) subunit of succinate dehydrogenase (SDH) that is involved in complex II of the mitochondrial electron transport chain and is responsible for transferring electrons from succinate to ubiquinone (coenzyme Q). (309 aa) | ||||
DAPB3 | Dihydrodipicolinate reductase-like protein CRR1, chloroplastic; Dihydrodipicolinate reductase (DHPR)-like protein that may not function as DHPR in lysine biosynthesis. Required for both formation and activity of the chloroplast NAD(P)H dehydrogenase (NDH) complex of the photosynthetic electron transport chain. May function in assembly or stabilization of the NDH complex. (298 aa) | ||||
K16F13.5 | tRNA-dihydrouridine synthase; Catalyzes the synthesis of dihydrouridine, a modified base found in the D-loop of most tRNAs; Belongs to the dus family. (387 aa) | ||||
CYP705A5 | Cytochrome P450 705A5; Converts thalian-diol to a desaturated thalian-diol. Belongs to the cytochrome P450 family. (511 aa) | ||||
K21H1.18 | FMN-linked oxidoreductases superfamily protein. (423 aa) | ||||
PPRD1 | Polyprenol reductase 1; Plays a key role in early steps of protein N-linked glycosylation by being required for the conversion of polyprenol into dolichol. Dolichols are required for the synthesis of dolichol-linked monosaccharides and the oligosaccharide precursor used for N- glycosylation. Acts as a polyprenol reductase that promotes the reduction of the alpha-isoprene unit of polyprenols into dolichols in a NADP-dependent mechanism. Involved in the regulation of plant growth and reproductive processes. (320 aa) | ||||
CHLP | Geranylgeranyl diphosphate reductase, chloroplastic; Catalyzes the reduction of geranylgeranyl diphosphate to phytyl diphosphate, providing phytol for both tocopherol and chlorophyll synthesis; Belongs to the geranylgeranyl reductase family. ChlP subfamily. (467 aa) | ||||
F28B23.3 | Zinc-binding dehydrogenase family protein. (351 aa) | ||||
ACX4 | Acyl-coenzyme A oxidase 4, peroxisomal; Catalyzes the desaturation of short-chain acyl-CoAs to 2- trans-enoyl-CoAs. Active on butyryl-CoA (C4), hexanoyl-CoA (C6), and octanoyl-CoA (C8). Has no activity as acyl-CoA dehydrogenase or on crotonyl-CoA (an unsaturated C4:1 carbocyclic ester) or glutaryl-CoA (a dicarboxylic ester). (436 aa) | ||||
TYRAAT1 | Arogenate dehydrogenase 1, chloroplastic; Involved in the biosynthesis of tyrosine. Has no prephenate dehydrogenase activity; Belongs to the prephenate/arogenate dehydrogenase family. (640 aa) | ||||
SDH4 | Succinate dehydrogenase subunit 4, mitochondrial; Membrane-anchoring subunit of succinate dehydrogenase (SDH). (151 aa) | ||||
CPX2 | Coproporphyrinogen-III oxidase 2, chloroplastic; Key enzyme in heme biosynthesis. Catalyzes the oxidative decarboxylation of propionic acid side chains of rings A and B of coproporphyrinogen III (By similarity). (233 aa) | ||||
F2K13.150 | Zinc-binding dehydrogenase family protein. (345 aa) | ||||
PPOX2 | Protoporphyrinogen oxidase 2, chloroplastic/mitochondrial; Catalyzes the 6-electron oxidation of protoporphyrinogen-IX to form protoporphyrin-IX. (508 aa) | ||||
IBR3 | Probable acyl-CoA dehydrogenase IBR3; Involved with IBR1 and IBR10 in the peroxisomal beta- oxidation of indole-3-butyric acid (IBA) to form indole-3-acetic acid (IAA), a biologically active auxin. May be responsible for catalyzing the first step in IBA-CoA beta-oxidation. May play a role in defense response to pathogenic bacteria. (824 aa) | ||||
Q8LPM0_ARATH | Zinc-binding dehydrogenase family protein. (346 aa) | ||||
RCCR | Red chlorophyll catabolite reductase, chloroplastic; Catalyzes the key reaction of chlorophyll catabolism, porphyrin macrocycle cleavage of pheophorbide a (pheide a) to a primary fluorescent catabolite (pFCC). Works in a two-step reaction with pheophorbide a oxygenase (PaO) by reducing the C20/C1 double bond of the intermediate, RCC. Belongs to the chlorophyll catabolic enzymes (CCEs). (319 aa) | ||||
T6D9.100 | Enoyl-[acyl-carrier-protein] reductase, mitochondrial; Catalyzes the NADPH-dependent reduction of trans-2-enoyl thioesters in mitochondrial fatty acid synthesis (fatty acid synthesis type II). Fatty acid chain elongation in mitochondria uses acyl carrier protein (ACP) as an acyl group carrier, but the enzyme accepts both ACP and CoA thioesters as substrates in vitro. (375 aa) | ||||
SDH2-1 | Succinate dehydrogenase [ubiquinone] iron-sulfur subunit 1, mitochondrial; Iron-sulfur protein (IP) subunit of succinate dehydrogenase (SDH) that is involved in complex II of the mitochondrial electron transport chain and is responsible for transferring electrons from succinate to ubiquinone (coenzyme Q). (279 aa) | ||||
SDH2-2 | Succinate dehydrogenase [ubiquinone] iron-sulfur subunit 2, mitochondrial; Iron-sulfur protein (IP) subunit of succinate dehydrogenase (SDH) that is involved in complex II of the mitochondrial electron transport chain and is responsible for transferring electrons from succinate to ubiquinone (coenzyme Q). (280 aa) | ||||
DAPB2 | 4-hydroxy-tetrahydrodipicolinate reductase 2, chloroplastic; Catalyzes the conversion of 4-hydroxy-tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate; Belongs to the DapB family. (349 aa) | ||||
OPR1 | 12-oxophytodienoate reductase 1; Specifically cleaves olefinic bonds in alpha,beta-unsaturated carbonyls and may be involved in detoxification or modification of these reactive compounds. May be involved in the biosynthesis or metabolism of oxylipin signaling molecules (Probable). In vitro, reduces 9R,13R-12-oxophytodienoic acid (9R,13R-OPDA) to 9R,13R-OPC-8:0, but only poorly 9S,13S-OPDA, the natural precursor of jasmonic acid. Can detoxify the explosive 2,4,6-trinitrotoluene (TNT) in vitro and in vivo by catalyzing its nitroreduction to form hydroxylamino-dinitrotoluene (HADNT). (372 aa) | ||||
Q8H128_ARATH | FMN-linked oxidoreductases superfamily protein. (419 aa) | ||||
OPR2 | 12-oxophytodienoate reductase 2; Specifically cleaves olefinic bonds in alpha,beta-unsaturated carbonyls and may be involved in detoxification or modification of these reactive compounds (Probable). May be involved in the biosynthesis or metabolism of oxylipin signaling molecules (Probable). In vitro, reduces 9R,13R-12- oxophytodienoic acid (9R,13R-OPDA) to 9R,13R-OPC-8:0, but only poorly 9S,13S-OPDA, the natural precursor of jasmonic acid (JA). Can detoxify the explosive 2,4,6-trinitrotoluene (TNT) in vitro and in vivo by catalyzing its nitroreduction to form hydroxylamino-dinitrotol [...] (374 aa) | ||||
PORA | Protochlorophyllide reductase A, chloroplastic; Phototransformation of protochlorophyllide (Pchlide) to chlorophyllide (Chlide). PORA may also function as a photoprotectant during the transitory stage from dark to light. Functions in skotomorphogenesis, photomorphogenesis and throughout the plant life under specific light conditions. (405 aa) | ||||
P2 | NADP-dependent alkenal double bond reductase P2; Catalyzes the reduction of the 7-8 double bond of phenylpropanal substrates, such as p-coumaryl aldehyde and coniferyl aldehyde (in vitro). Has activity towards toxic substrates, such as 4- hydroxy-(2E)-nonenal (in vitro) (By similarity). May play a distinct role in plant antioxidant defense and is possibly involved in NAD(P)/NAD(P)h homeostasis; Belongs to the NADP-dependent oxidoreductase L4BD family. (343 aa) | ||||
AER | NADPH-dependent oxidoreductase 2-alkenal reductase; Involved in the detoxification of reactive carbonyls. Acts on lipid peroxide-derived reactive aldehydes. Specific to a double bond activated by an adjacent carbonyl group. Can use both quinones and diamide as substrates, but not menadione, ferricyanide or phylloquinone. Can use 4-hydroxy- (2E)-nonenal (HNE), 4-hydroxy-(2E)-hexenal (HHE), (2E)-nonenal, (2E)- hexenal, (2E)-pentenal, propenal (acrolein), 3-buten-2-one and 3- penten-2-one, but not (R)-(-)-carvone, n-nonanal, n-hexanal, (3Z)- hexanal, cyclohex-2-en-1-one or 12-oxo phytodie [...] (345 aa) | ||||
DIM | Delta(24)-sterol reductase; Plays a critical role in the general process of plant cell elongation. Involved in the synthesis of campesterol, an early precursor of brassinolide. Required for the conversion of 24- methylenecholesterol to campesterol and for the conversion of isofucosterol to sitosterol. Necessary for both the isomerization and reduction of 24-methylenecholesterol. Regulates indirectly phytochrome- mediated light responses through the modulation of brassinosteroid biosynthesis. (561 aa) | ||||
DET2 | Steroid 5-alpha-reductase DET2; Involved in a reduction step in the biosynthesis of the plant steroid, brassinolide; acts at the second step in brassinolide biosynthesis in the 5alpha-reduction of (24R)- 24-methylcholest-4-en-3- one, which is further modified to form campestanol. Can use progesterone, testosterone, androstenedione and campestenone as substrate. (262 aa) | ||||
ZDS1 | Zeta-carotene desaturase, chloroplastic/chromoplastic; Plays a crucial role in plant growth and development. Is essential for the biosynthesis of carotenoids. Carotenoids are involved in different physiological processes, including coloration, photoprotection, biosynthesis of abscisic acid (ABA) and chloroplast biogenesis. Catalyzes the conversion of zeta-carotene to lycopene via the intermediary of neurosporene. It carries out two consecutive desaturations (introduction of double bonds) at positions C-7 and C-7'. Shows stereoselectivity toward trans C15-C15'zeta-carotene double bond. [...] (558 aa) | ||||
DVR | Divinyl chlorophyllide a 8-vinyl-reductase, chloroplastic; Catalyzes the conversion of divinyl chlorophyllide to monovinyl chlorophyllide. Reduces the 8-vinyl group of the tetrapyrrole to an ethyl group using NADPH as the reductant. The best substrate is (3,8-divinyl)-chlorophyllide a (DV-Chlidea). Very low activity with (3,8-divinyl)-protochlorophyllide a (DV-Pchlidea) and (3,8-divinyl)- magnesium-protoporphyrin IX monomethyl ester (DV-MPE). No activity with (3,8-divinyl)-chlorophyllide b (DV-Chlideb), (3,8-divinyl)-magnesium- protoporphyrin IX (DV-Mg-Proto) and either (3,8-divinyl)-c [...] (417 aa) | ||||
FAR2 | Fatty acyl-CoA reductase 2; Catalyzes the reduction of fatty acyl-CoA to fatty alcohols. Involved in the synthesis of the lipid component in sporopollenin. (616 aa) | ||||
PDS | 15-cis-phytoene desaturase, chloroplastic/chromoplastic; Converts phytoene into zeta-carotene via the intermediary of phytofluene by the symmetrical introduction of two double bonds at the C-11 and C-11' positions of phytoene with a concomitant isomerization of two neighboring double bonds at the C9 and C9' positions from trans to cis; Belongs to the carotenoid/retinoid oxidoreductase family. (566 aa) | ||||
PPOX1 | Protoporphyrinogen oxidase 1, chloroplastic; Catalyzes the 6-electron oxidation of protoporphyrinogen-IX to form protoporphyrin-IX. (537 aa) | ||||
FAD2 | Delta(12)-fatty-acid desaturase; ER (microsomal) omega-6 fatty acid desaturase introduces the second double bond in the biosynthesis of 18:3 fatty acids, important constituents of plant membranes. Delta(12)-desaturase with regioselectivity determined by the double bond (delta(9) position) and carboxyl group of the substrate. Can use both 16:1 and 18:1 fatty acids as substrates. It is thought to use cytochrome b5 as an electron donor and to act on fatty acids esterified to phosphatidylcholine (PC) and, possibly, other phospholipids. Very low constitutive hydroxylation activity. Required [...] (383 aa) | ||||
PYRD | Dihydroorotate dehydrogenase (quinone), mitochondrial; Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor; Belongs to the dihydroorotate dehydrogenase family. Type 2 subfamily. (460 aa) | ||||
PORB | Protochlorophyllide reductase B, chloroplastic; Phototransformation of protochlorophyllide (Pchlide) to chlorophyllide (Chlide); Belongs to the short-chain dehydrogenases/reductases (SDR) family. POR subfamily. (401 aa) | ||||
SDH3-2 | Succinate dehydrogenase subunit 3-2, mitochondrial; Membrane-anchoring subunit of succinate dehydrogenase (SDH). (213 aa) | ||||
MDC12.26 | Oxygen-independent coproporphyrinogen-like protein. (484 aa) | ||||
OPR3 | 12-oxophytodienoate reductase 3, N-terminally processed; Specifically cleaves olefinic bonds in cyclic enones. Involved in the biosynthesis of jasmonic acid (JA) and perhaps in biosynthesis or metabolism of other oxylipin signaling moleclules. Required for the spatial and temporal regulation of JA levels during dehiscence of anthers, promoting the stomium degeneration program. In vitro, reduces 9S,13S-12- oxophytodienoic acid (9S,13S-OPDA) and 9R,13R-OPDA to 9S,13S-OPC-8:0 and 9R,13R-OPC-8:0, respectively. Can detoxify the explosive 2,4,6-trinitrotoluene (TNT) in vitro by catalyzing it [...] (391 aa) | ||||
PRR1 | Pinoresinol reductase 1; Reductase involved in lignan biosynthesis. Unlike conventional pinoresinol reductases that can reduce both pinoresinol and lariciresinol, PRR1 shows a strict substrate preference toward pinoresinol. Active on both (+) and (-)-pinoresinol. Abstracts the 4R- hydride from the NADPH cofactor during catalysis. (317 aa) | ||||
FK | Delta(14)-sterol reductase; Reduces the C14=C15 double bond of 4,4-dimethyl-cholesta- 8,14,24-trienol to produce 4,4-dimethyl-cholesta-8,24-dienol. Required for cell division and expansion and is involved in proper organization of the embryo. (369 aa) | ||||
DWF5 | 7-dehydrocholesterol reductase; Production of cholesterol by reduction of C7-C8 double bond of 7-dehydrocholesterol (7-DHC). Lesions in the gene coding for the enzyme cause dwarfism; Belongs to the ERG4/ERG24 family. (432 aa) | ||||
F2K13.110 | Zinc-binding dehydrogenase family protein. (346 aa) | ||||
F1N13.150 | 3-oxo-5-alpha-steroid 4-dehydrogenase family protein. (268 aa) | ||||
ACX3.2 | Putative acyl-coenzyme A oxidase 3.2, peroxisomal; Catalyzes the desaturation of acyl-CoAs to 2-trans-enoyl- CoAs. (675 aa) | ||||
TYRAAT2 | Arogenate dehydrogenase 2, chloroplastic; Involved in the biosynthesis of tyrosine. Has a weak prephenate dehydrogenase activity; Belongs to the prephenate/arogenate dehydrogenase family. (358 aa) | ||||
CPX1 | Coproporphyrinogen-III oxidase 1, chloroplastic; Key enzyme in heme biosynthesis. Catalyzes the oxidative decarboxylation of propionic acid side chains of rings A and B of coproporphyrinogen III; Belongs to the aerobic coproporphyrinogen-III oxidase family. (386 aa) | ||||
K19A23.1 | Zinc-binding dehydrogenase family protein. (353 aa) | ||||
SDRB | Peroxisomal 2,4-dienoyl-CoA reductase; Auxiliary enzyme of beta-oxidation. Participates in the degradation of unsaturated fatty enoyl-CoA esters having double bonds in both even- and odd-numbered positions in peroxisome. Catalyzes the NADP-dependent reduction of 2,4-dienoyl-CoA to yield trans-3-enoyl-CoA (By similarity). (298 aa) | ||||
PYD1 | Dihydropyrimidine dehydrogenase (NADP(+)), chloroplastic; Involved in pyrimidine base degradation. Catalyzes the reduction of uracil to 5,6-dihydrouracil (DHU) by using NADH as a specific cosubstrate and the reduction of thymine to 5,6-dihydrothymine (DHT). Involved in the recycling of nitrogen from nucleobases to general nitrogen metabolism; Belongs to the dihydropyrimidine dehydrogenase family. (426 aa) | ||||
T28A8_130 | 3-oxo-5-alpha-steroid 4-dehydrogenase family protein. (84 aa) | ||||
ECR | Very-long-chain enoyl-CoA reductase; Catalyzes the last of the four reactions of the long-chain fatty acids elongation cycle. This endoplasmic reticulum-bound enzymatic process, allows the addition of 2 carbons to the chain of long- and very long-chain fatty acids/VLCFAs per cycle. This enzyme reduces the trans-2,3-enoyl-CoA fatty acid intermediate to an acyl-CoA that can be further elongated by entering a new cycle of elongation. Thereby, it participates in the production of VLCFAs of different chain lengths that are involved in multiple biological processes as precursors of membrane [...] (310 aa) | ||||
T17B22.23 | Zinc-binding dehydrogenase family protein. (350 aa) | ||||
BAN | Anthocyanidin reductase; Involved in the biosynthesis of condensed tannins. Converts cyanidin into (-)-epicatechin as the major product. Belongs to the NAD(P)-dependent epimerase/dehydratase family. Dihydroflavonol-4-reductase subfamily. (340 aa) | ||||
PPRD2 | Polyprenol reductase 2; Plays a key role in early steps of protein N-linked glycosylation by being required for the conversion of polyprenol into dolichol. Dolichols are required for the synthesis of dolichol-linked monosaccharides and the oligosaccharide precursor used for N- glycosylation. Acts as a polyprenol reductase that promotes the reduction of the alpha-isoprene unit of polyprenols into dolichols in a NADP-dependent mechanism. Involved in the regulation of plant growth and reproductive processes. (343 aa) | ||||
MOD1 | Enoyl-[acyl-carrier-protein] reductase [NADH], chloroplastic; Catalyzes the NAD-dependent reduction of a carbon-carbon double bond in an enoyl moiety that is covalently linked to an acyl carrier protein (ACP). Catalyzes the last reduction step in the de novo synthesis cycle of fatty acids. Involved in the elongation cycle of fatty acids which are used in lipid metabolism. Required for normal plant growth. (390 aa) | ||||
HY2 | Phytochromobilin:ferredoxin oxidoreductase, chloroplastic; Catalyzes the two-electron reduction of biliverdin IX-alpha to the tetrapyrrole chromophore phytochromobilin (PPhiB); Belongs to the HY2 family. (329 aa) | ||||
VEP1 | 3-oxo-Delta(4,5)-steroid 5-beta-reductase; Involved in vascular strand development. Catalyzes the stereospecific conversion of progesterone to 5-beta-pregnane-3,20- dione. Can use progesterone, testosterone, 21-acetyl cortexone, 2- cyclohexenone, but-1-en-3-one, ethyl acrylate, ethylmethacrylate, cortisone and canarigenone as substrates, lower activity with 3-methyl- 2-cyclohexenone and 3,5,5-trimethyl-2-cyclohexenone as substrate, and no activity with canarigenin, canarigenin digitoxoside and pregnenolone. May be involved in the formation of 5-beta phytoecdysteroids; Belongs to the sh [...] (388 aa) | ||||
GLDH | L-galactono-1,4-lactone dehydrogenase, mitochondrial; Involved in the biosynthesis of ascorbic acid. Required for the accumulation of respiratory complex I. Uses L-galactono-1,4-lactone and L-gulono-1,4-lactone as substrates, but not D-galactono-1,4- lactone, D-gulono-1,4-lactone, L-mannono-1,4-lactone or D-galactonic acid. Also active with phenazine methosulfate and 1,4-benzoquinone as electron acceptors. (610 aa) | ||||
PRR2 | Pinoresinol reductase 2; Reductase involved in lignan biosynthesis. Unlike conventional pinoresinol reductases that can reduce both pinoresinol and lariciresinol, PRR2 shows a strict substrate selectivity for (-)- pinoresinol. No activity with (+)-pinoresinol or lariciresinol. Abstracts the 4R-hydride from the NADPH cofactor during catalysis. Belongs to the NmrA-type oxidoreductase family. Isoflavone reductase subfamily. (317 aa) | ||||
IVD | Isovaleryl-CoA dehydrogenase, mitochondrial; Involved in degradation of the branched-chain amino acids, phytol and lysine for the supply of carbon and electrons to the ETF/ETFQO complex during dark-induced sugar starvation. Belongs to the acyl-CoA dehydrogenase family. (409 aa) | ||||
F19H22.4 | tRNA-dihydrouridine(47) synthase [NAD(P)(+)]-like; Catalyzes the synthesis of dihydrouridine, a modified base found in the D-loop of most tRNAs; Belongs to the Dus family. Dus3 subfamily. (691 aa) | ||||
F28J9.2 | Uncharacterized protein. (195 aa) | ||||
Q9XE46_ARATH | NAD(P)-binding Rossmann-fold superfamily protein. (156 aa) | ||||
SDH1-2 | Succinate dehydrogenase [ubiquinone] flavoprotein subunit 2, mitochondrial; Flavoprotein (FP) subunit of succinate dehydrogenase (SDH) that is involved in complex II of the mitochondrial electron transport chain and is responsible for transferring electrons from succinate to ubiquinone (coenzyme Q). (632 aa) | ||||
ACX1.2 | Putative peroxisomal acyl-coenzyme A oxidase 1.2; Catalyzes the desaturation of acyl-CoAs to 2-trans-enoyl- CoAs. (664 aa) | ||||
AOR | NADPH-dependent alkenal/one oxidoreductase, chloroplastic; Reduces the double bond in short-chain unsaturated carbonyls. Acts preferentially on alpha,beta-unsaturated ketones rather on alpha,beta-unsaturated aldehydes. Has no activity with (E)-2-hexenal and (E)-2-pentenal. Contributes to detoxify stromal reactive carbonyls produced under oxidative stress. Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily. (386 aa) | ||||
SDH3-1 | Succinate dehydrogenase subunit 3-1, mitochondrial; Membrane-anchoring subunit of succinate dehydrogenase (SDH). (213 aa) | ||||
F3E22.17 | Putative acyl-coenzyme A oxidase At3g06690. (187 aa) | ||||
ACX3 | Acyl-coenzyme A oxidase 3, peroxisomal; Catalyzes the desaturation of medium-chain acyl-CoAs to 2- trans-enoyl-CoAs. Active on C8:0- to C14:0-CoA with a maximal activity on C12:0-CoA. (675 aa) | ||||
SDH1-1 | Succinate dehydrogenase [ubiquinone] flavoprotein subunit 1, mitochondrial; Flavoprotein (FP) subunit of succinate dehydrogenase (SDH) that is involved in complex II of the mitochondrial electron transport chain and is responsible for transferring electrons from succinate to ubiquinone (coenzyme Q). (634 aa) |