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F6N18.16 | Alcohol dehydrogenase-like 3. (394 aa) | ||||
ACS | Acetyl-coenzyme A synthetase, chloroplastic/glyoxysomal; Catalyzes the production of acetyl-CoA, an activated form of acetate that can be used for lipid synthesis or for energy generation. May play a limited role in the biosynthesis of lipids. Belongs to the ATP-dependent AMP-binding enzyme family. (743 aa) | ||||
F27M3.11 | Amine oxidase. (677 aa) | ||||
F27M3.9 | Amine oxidase. (681 aa) | ||||
LDL3 | Lysine-specific histone demethylase 1 homolog 3; Probable histone demethylase that reduces the levels of histone H3 'Lys-4' methylation in chromatin. (1628 aa) | ||||
AO1 | Primary amine oxidase 1; Oxidizes preferentially the aliphatic diamine putrescine with production of the corresponding aldehyde, ammonia and hydrogen peroxide. May be involved in the regulation of developmental programmed cell death (PCD) in both vascular tissue and the root cap. Required for jasmonic acid-(MeJA) mediated early protoxylem differentiation associated with putrescine levels reduction and H(2)O(2) accumulation in roots. (650 aa) | ||||
F27M3.13 | Primary amine oxidase 2; Belongs to the copper/topaquinone oxidase family. (662 aa) | ||||
MAF5 | Protein MADS AFFECTING FLOWERING 5; Transcription factor involved in the negative regulation of flowering time in short days, probably through the photoperiodic and vernalization pathways. Prevents premature flowering, particularly in the cv. Landsberg erecta background. In non-inductive photoperiods (e.g. short days), required for flowering through VIL2-mediated maintenance of the epigenetically repressed state of MAF5 via H3K9me2 and plant homeodomain / polycomb repressive complex 2 (PHD-PRC2)- dependent H3K27me3. (198 aa) | ||||
ALDH3H1 | Aldehyde dehydrogenase family 3 member H1; Involved in oxidative stress tolerance by detoxifying reactive aldehydes derived from lipid peroxidation. Medium- to long- chain saturated aldehydes are preferred substrates, while the short- chain aldehyde propanal is a weak substrate. Is strictely NAD(+) specific. (484 aa) | ||||
ALDH3F1 | Aldehyde dehydrogenase family 3 member F1; Belongs to the aldehyde dehydrogenase family. (484 aa) | ||||
PAO4 | Probable polyamine oxidase 4; Flavoenzyme involved in polyamine back-conversion. Catalyzes the oxidation of the secondary amino group of polyamines, such as spermine and spermidine. Substrate preference is spermine > spermidine. No activity detected when putrescine or N(1)-acetylspermine are used as substrates. Plays an important role in the regulation of polyamine intracellular concentration (Probable). (497 aa) | ||||
CuAO1 | Primary amine oxidase; Belongs to the copper/topaquinone oxidase family. (712 aa) | ||||
T4C9.130 | Amine oxidase. (741 aa) | ||||
MHK10.21 | Amine oxidase. (776 aa) | ||||
T4C12_30 | Alcohol dehydrogenase-like 6. (381 aa) | ||||
ALDH2B7 | Aldehyde dehydrogenase family 2 member B7, mitochondrial; Possesses activity on acetaldehyde and glycolaldehyde in vitro; Belongs to the aldehyde dehydrogenase family. (534 aa) | ||||
LDL1 | Lysine-specific histone demethylase 1 homolog 1; Probable histone demethylase that reduces the levels of histone H3 'Lys-4' methylation in chromatin of the floral repressor FLOWERING LOCUS C (FLC) and the sporophytically silenced floral repressor FWA. Seems to act in partial redundancy with FLOWERING LOCUS D (FLD) to repress FLC expression. Required for cytosine methylation of FWA. Controls primary seed dormancy by regulating DOG1 and abscisic acid signaling-related genes. In association with OTU6/OTLD1, involved in transcriptional gene repression via histone deubiquitination and demet [...] (844 aa) | ||||
F13O11.3 | Alcohol dehydrogenase-like 4; Belongs to the zinc-containing alcohol dehydrogenase family. Class-III subfamily. (380 aa) | ||||
AAE7 | Acetate/butyrate--CoA ligase AAE7, peroxisomal; Peroxisomal acetate/butyrate--CoA ligase that is probably involved in the activation of exogenous acetate for entry into the glyoxylate cycle. May play a role to prevent carbon loss from peroxisomes during lipid mobilization. In vitro, is active with both acetate and butyrate. Belongs to the ATP-dependent AMP-binding enzyme family. (569 aa) | ||||
ALDH3I1 | Aldehyde dehydrogenase family 3 member I1, chloroplastic; Involved in oxidative stress tolerance by detoxifying reactive aldehydes derived from lipid peroxidation. Medium- to long- chain saturated aldehydes are preferred substrates, while the short- chain aldehyde propanal is a weak substrate. Can use both NAD(+) and NADP(+), but the coenzyme preference is substrate dependent. (550 aa) | ||||
PDC2 | Pyruvate decarboxylase 2; Belongs to the TPP enzyme family. (607 aa) | ||||
K5J14.5 | Alcohol dehydrogenase-like 7. (390 aa) | ||||
TAT7 | Probable aminotransferase TAT2; Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family. (414 aa) | ||||
PAO1 | Polyamine oxidase 1; Flavoenzyme involved in polyamine back-conversion. Catalyzes the oxidation of the secondary amino group of polyamines, such as spermine and its acetyl derivatives. Substrate preference is thermospermine > norspermine > spermine > N(1)-acetylspermine. No activity detected when putrescine, spermidine or N(1)-acetylspermidine are used as substrates. Plays an important role in the regulation of polyamine intracellular concentration (Probable). Involved in the production of hydrogen peroxide in response to salt and cold stresses. (472 aa) | ||||
PAO3 | Polyamine oxidase 3; Flavoenzyme involved in polyamine back-conversion. Catalyzes the oxidation of the secondary amino group of polyamines, such as spermine, spermidine and their acetyl derivatives. Substrate preference is spermidine > spermine > N(1)-acetylspermidine > N(1)-acetylspermine. Plays an important role in the regulation of polyamine intracellular concentration (Probable). Involved in the production of hydrogen peroxide during pollen tube growth. Hydrogen peroxide triggers the opening of the hyperpolarization-activated calcium permeable channels in pollen, and thus regulates [...] (488 aa) | ||||
F12E4.110 | Acylphosphatase. (171 aa) | ||||
PDC3 | Pyruvate decarboxylase 3; Belongs to the TPP enzyme family. (592 aa) | ||||
PDC4 | Pyruvate decarboxylase 4; Belongs to the TPP enzyme family. (603 aa) | ||||
TYRDC | Probable tyrosine decarboxylase 2; Belongs to the group II decarboxylase family. (545 aa) | ||||
F23N14_50 | Amine oxidase. (687 aa) | ||||
PAO2 | Polyamine oxidase 2; Flavoenzyme involved in polyamine back-conversion. Catalyzes the oxidation of the secondary amino group of polyamines, such as spermine, spermidine and their acetyl derivatives. Substrate preference is N(1)-acetylspermine > spermine > spermidine. Plays an important role in the regulation of polyamine intracellular concentration (Probable). Involved in abscisic acid-mediated developmental processes. May contribute to nitric oxide-mediated effects on root growth. (490 aa) | ||||
T4C9.120 | Amine oxidase. (300 aa) | ||||
T4C9.110 | Amine oxidase; Belongs to the copper/topaquinone oxidase family. (460 aa) | ||||
ALDH2B4 | Aldehyde dehydrogenase family 2 member B4, mitochondrial; Possesses activity on acetaldehyde and glycolaldehyde in vitro; Belongs to the aldehyde dehydrogenase family. (538 aa) | ||||
PAO5 | Probable polyamine oxidase 5; Flavoenzyme involved in polyamine back-conversion. Catalyzes the oxidation of the secondary amino group of polyamines, such as spermine and its acetyl derivatives. Substrate preference is spermine > N(1)-acetylspermine > thermospermine > norspermine. Plays an important role in the regulation of polyamine intracellular concentration. Involved in xylem differentiation by controlling thermospermine homeostasis, and participating in the tightly controlled interplay between auxin and cytokinin that is necessary for proper xylem differentiation. Involved in the [...] (533 aa) | ||||
ALDH7B4 | Aldehyde dehydrogenase family 7 member B4. (508 aa) | ||||
T22F8.220 | Microtubule-associated protein-like protein. (166 aa) |