Your Input: | |||||
F4K6Z5_ARATH | Plant L-ascorbate oxidase; Belongs to the multicopper oxidase family. (588 aa) | ||||
GPX6 | Probable phospholipid hydroperoxide glutathione peroxidase 6, mitochondrial; Protects cells and enzymes from oxidative damage, by catalyzing the reduction of hydrogen peroxide, lipid peroxides and organic hydroperoxide, by glutathione. (232 aa) | ||||
GULLO5 | L-gulonolactone oxidase 5; Catalyzes the oxidation of L-gulono-1,4-lactone to ascorbic acid. L-gulono-1,4-lactone is oxidized to hydrogen peroxide and L-xylo-hexulonolactone which spontaneously isomerizes to L-ascorbate (By similarity); Belongs to the oxygen-dependent FAD-linked oxidoreductase family. (590 aa) | ||||
LGALDH | L-galactose dehydrogenase; Catalyzes the oxidation of L-galactose to L-galactono-1,4- lactone in the presence of NAD(+). Uses NAD(+) as a hydrogen acceptor much more efficiently than NADP(+); Belongs to the aldo/keto reductase family. (319 aa) | ||||
EMB2360 | Glutathione reductase, chloroplastic; Maintains high levels of reduced glutathione in the chloroplast. (565 aa) | ||||
GPX1 | Phospholipid hydroperoxide glutathione peroxidase 1, chloroplastic; Protects cells and enzymes from oxidative damage, by catalyzing the reduction of hydrogen peroxide, lipid peroxides and organic hydroperoxide, by glutathione. (236 aa) | ||||
TL29 | Thylakoid lumenal 29 kDa protein, chloroplastic. (349 aa) | ||||
MDAR5 | Monodehydroascorbate reductase, chloroplastic/mitochondrial; Catalyzes the conversion of monodehydroascorbate (MDA) to ascorbate, oxidizing NADH in the process. Can also use 2,4,6- trinitrotoluene (TNT) and 1-chloro-2,4-dinitrobenzene (CDNB) as substrates, but not 1-chloro-4-nitrobenzene (CNB). Belongs to the FAD-dependent oxidoreductase family. (493 aa) | ||||
F19P19.22 | 1-aminocyclopropane-1-carboxylate oxidase homolog 6; Belongs to the iron/ascorbate-dependent oxidoreductase family. (360 aa) | ||||
APX1 | L-ascorbate peroxidase 1, cytosolic; Plays a key role in hydrogen peroxide removal. Constitutes a central component of the reactive oxygen gene network. (250 aa) | ||||
APX3 | L-ascorbate peroxidase 3; Plays a key role in hydrogen peroxide removal. (287 aa) | ||||
APXS | L-ascorbate peroxidase S, chloroplastic/mitochondrial; Plays a key role in hydrogen peroxide removal; Belongs to the peroxidase family. Ascorbate peroxidase subfamily. (372 aa) | ||||
APXT | L-ascorbate peroxidase T, chloroplastic; Plays a key role in hydrogen peroxide removal; Belongs to the peroxidase family. Ascorbate peroxidase subfamily. (426 aa) | ||||
HISN7 | Bifunctional phosphatase IMPL2, chloroplastic; Phosphatase required for histidine production. Acts also on L-galactose 1-phosphate (L-Gal 1-P), D-myoinositol 3-phosphate (D-Ins 3-P) and D-myoinositol 1-phosphate (D-Ins 1-P). Belongs to the inositol monophosphatase superfamily. (346 aa) | ||||
GULLO2 | L-gulonolactone oxidase 2; Catalyzes the oxidation of L-gulono-1,4-lactone to ascorbic acid. L-gulono-1,4-lactone is oxidized to hydrogen peroxide and L-xylo-hexulonolactone which spontaneously isomerizes to L-ascorbate (By similarity). (591 aa) | ||||
APX5 | L-ascorbate peroxidase 5, peroxisomal; Plays a key role in hydrogen peroxide removal; Belongs to the peroxidase family. Ascorbate peroxidase subfamily. (279 aa) | ||||
APX6 | Putative L-ascorbate peroxidase 6; Plays a key role in hydrogen peroxide removal. (329 aa) | ||||
MIOX4 | Inositol oxygenase 4; Involved in the biosynthesis of UDP-glucuronic acid (UDP- GlcA), providing nucleotide sugars for cell-wall polymers. May be also involved in plant ascorbate biosynthesis. (317 aa) | ||||
MIOX1 | Inositol oxygenase 1; Involved in the biosynthesis of UDP-glucuronic acid (UDP- GlcA), providing nucleotide sugars for cell-wall polymers. May be also involved in plant ascorbate biosynthesis. (311 aa) | ||||
DHAR3 | Glutathione S-transferase DHAR3, chloroplastic; Displays a dual function. As a soluble protein, exhibits glutathione-dependent thiol transferase and dehydroascorbate (DHA) reductase activities. Key component of the ascorbate recycling system. Involved in the redox homeostasis, especially in scavenging of ROS under oxidative stresses (By similarity). (258 aa) | ||||
T10F18.130 | Ascorbate oxidase-like protein; Belongs to the multicopper oxidase family. (573 aa) | ||||
VTC2 | GDP-L-galactose phosphorylase 1; Catalyzes a reaction of the Smirnoff-Wheeler pathway, the major route to ascorbate biosynthesis in plants. Acts as a phosphorylase rather than as a transferase. Uses preferentially GDP-L- galactose and GDP-D-glucose as substrates. Lower activity with GDP-L- fucose, very low activity with GDP-D-mannose, and no activity with UDP- D-glucose, UDP-D-galactose or ADP-D-glucose. Highly specific for inorganic phosphate as the guanylyl acceptor. (442 aa) | ||||
GME | GDP-mannose 3,5-epimerase; Catalyzes a reversible epimerization of GDP-D-mannose that precedes the committed step in the biosynthesis of vitamin C (L- ascorbate), resulting in the hydrolysis of the highly energetic glycosyl-pyrophosphoryl linkage. Able to catalyze 2 distinct epimerization reactions and can release both GDP-L-galactose and GDP-L- gulose from GDP-mannose. (377 aa) | ||||
MDAR2 | Monodehydroascorbate reductase 2; Catalyzes the conversion of monodehydroascorbate to ascorbate, oxidizing NADH in the process. (435 aa) | ||||
F28I16.200 | Probable receptor-like protein kinase At5g20050. (452 aa) | ||||
GULLO1 | Probable L-gulonolactone oxidase 1; May be involved in the biosynthesis of ascorbic acid. Belongs to the oxygen-dependent FAD-linked oxidoreductase family. (595 aa) | ||||
VTC5 | GDP-L-galactose phosphorylase 2; Catalyzes a reaction of the Smirnoff-Wheeler pathway, the major route to ascorbate biosynthesis in plants. Acts as a phosphorylase rather than as a transferase. Uses preferentially GDP-L- galactose and GDP-D-glucose as substrates. Lower activity with GDP-L- fucose, very low activity with GDP-D-mannose, and no activity with UDP- D-glucose, UDP-D-galactose or ADP-D-glucose. Highly specific for inorganic phosphate as the guanylyl acceptor. (431 aa) | ||||
GULLO4 | Probable L-gulonolactone oxidase 4; May be involved in the biosynthesis of ascorbic acid. Belongs to the oxygen-dependent FAD-linked oxidoreductase family. (577 aa) | ||||
GULLO7 | Probable truncated L-gulonolactone oxidase 7, mitochondrial; May be involved in the biosynthesis of ascorbic acid. (252 aa) | ||||
UBP25 | Ubiquitin carboxyl-terminal hydrolase 25; Recognizes and hydrolyzes the peptide bond at the C-terminal Gly of ubiquitin. Involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins (By similarity). Belongs to the peptidase C19 family. (661 aa) | ||||
DHAR2 | Glutathione S-transferase DHAR2; Displays a dual function. As a soluble protein, exhibits glutathione-dependent thiol transferase and dehydroascorbate (DHA) reductase activities. Exhibits glutathione-dependent thiol transferase and dehydroascorbate (DHA) reductase activities. Key component of the ascorbate recycling system. Involved in the redox homeostasis, especially in scavenging of ROS under oxidative stresses. Plays a role in ozone tolerance; Belongs to the GST superfamily. DHAR family. (213 aa) | ||||
DHAR1 | Glutathione S-transferase DHAR1, mitochondrial; Displays a dual function. As a soluble protein, exhibits glutathione-dependent thiol transferase and dehydroascorbate (DHA) reductase activities. Key component of the ascorbate recycling system. Involved in the redox homeostasis, especially in scavenging of ROS under oxidative stresses, subsequently to biotic or abiotic inducers. As a peripheral membrane protein, could also function as voltage-gated ion channel. Belongs to the GST superfamily. DHAR family. (213 aa) | ||||
MDAR1 | Monodehydroascorbate reductase 1, peroxisomal; Catalyzes the conversion of monodehydroascorbate to ascorbate, oxidizing NADH in the process. Belongs to the FAD-dependent oxidoreductase family. (434 aa) | ||||
sks13 | BNH protein pectinesterase-like protein pollen-secific protein-like. (551 aa) | ||||
sks11 | L-ascorbate oxidase pectinesterase-like protein pollen-specific protein-like. (554 aa) | ||||
F18O14.31 | Glutathione S-transferase family protein. (153 aa) | ||||
GULLO3 | L-gulonolactone oxidase 3; Catalyzes the oxidation of L-gulono-1,4-lactone to ascorbic acid. L-gulono-1,4-lactone is oxidized to hydrogen peroxide and L-xylo-hexulonolactone which spontaneously isomerizes to L-ascorbate (By similarity). (585 aa) | ||||
GGP2 | Gamma-glutamyl peptidase 2; Involved in glucosinolate biosynthesis. Hydrolyzes the gamma- glutamyl peptide bond of several glutathione (GSH) conjugates to produce Cys-Gly conjugates related to glucosinolates. The gamma-Glu- Cys-Gly-GSH conjugates are the sulfur-donating molecule in glucosinolate biosynthesis. (248 aa) | ||||
T2E12.5 | Probable leucine-rich repeat receptor-like protein kinase At1g68400; Belongs to the protein kinase superfamily. Ser/Thr protein kinase family. (670 aa) | ||||
AMR1 | Putative F-box protein At1g65770. (360 aa) | ||||
MDAR3 | Monodehydroascorbate reductase 3; Catalyzes the conversion of monodehydroascorbate to ascorbate, oxidizing NADH in the process. Required for producing sufficient ascorbate to maintain the interaction between Piriformospora indica and Arabidopsis in a mutualistic state. (441 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) | ||||
Sks12 | At1g55570/T5A14_1. (555 aa) |