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Probable esterase

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Probable esterase; part of the gene cluster that mediates the biosynthesis of asperfuranone, a probable antitumor agent .

Below are the list of possible Probable esterase products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

Probable esterase afoC

 Probable esterase afoC ELISA Kit
 Probable esterase afoC Recombinant
 Probable esterase afoC Antibody
Also known as Probable esterase afoC (Asperfuranone biosynthesis protein B).
Probable esterase; part of the gene cluster that mediates the biosynthesis of asperfuranone, a probable antitumor agent (PubMed:19199437). The polyketide synthase afoG is responsible for producing the 3,5-dimethyloctadienone moiety from acetyl-CoA, three malonyl-CoA, and two S-adenosyl methionines (SAM) (PubMed:1919943
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7). The 3,5-dimethyloctadienone moiety is then loaded onto the SAT domain of afoE and extended with four malonyl-CoA and one SAM, which leads to the formation of 2,4-dihydroxy-6-(5,7-dimethyl-2-oxo-trans-3-trans-5-nonadienyl)-3-methylbenzaldehyde (compound 2) after reductive release and aldol condensation (PubMed:19199437). AfoD is the next enzyme in the biosynthesis sequence and hydroxylates the side chain at the benzylic position of compound 2 (PubMed:19199437). After benzylic hydroxylation, a furan ring is formed after five-member ring hemiacetal formation and water elimination (PubMed:19199437). AfoF and afoC are proposed to oxidize the R-diketone proton and to reduce the unconjugated carbonyl group, respectively, to generate asperfuranone (PubMed:19199437). Since no intermediates could be isolated from afoF and afoC deletants, the sequence of these two enzymes is not fully understood (PubMed:19199437). Moreover, since afoC deletant still produces a small amount of asperfuranone, other endogenous oxidoreductases might catalyze the same reaction with much less efficiency (PubMed:19199437).
 afoC ELISA Kit
 afoC Recombinant
 afoC Antibody
 AN1032 ELISA Kit
 AN1032 Recombinant
 AN1032 Antibody
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Probable esterase azaC

 Probable esterase azaC ELISA Kit
 Probable esterase azaC Recombinant
 Probable esterase azaC Antibody
Also known as Probable esterase azaC (Azaphilone biosynthesis cluster protein azaC).
Probable esterase; part of the gene cluster that mediates the biosynthesis of azaphilones, a class of fungal metabolites characterized by a highly oxygenated pyrano-quinone bicyclic core and exhibiting a broad range of bioactivities (PubMed:22921072). In the first step, the non-reducing polyketide synthase azaA
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forms the hexaketide precursor from successive condensations of five malonyl-CoA units, presumably with a simple acetyl-CoA starter unit (PubMed:22921072). The reactive polyketide chain then undergoes a PT-mediated C2-C7 cyclization to afford the aromatic ring and is eventually released as an aldehyde through the R-domain (PubMed:22921072). The putative ketoreductase azaE is proposed to catalyze the reduction of the terminal ketone resulting in the early culture product FK17-P2a (PubMed:22921072). The monooxygenase azaH was demonstrated to be the only enzyme required to convert FK17-P2a to azanigerone E (PubMed:22921072). AzaH first hydroxylates the benzaldehyde intermediate FK17-P2a at C4, which triggers the formation of the pyran-ring to afford azanigerone E (PubMed:22921072). In parallel, the 2,4-dimethylhexanoyl chain is synthesized by the HR-PKS azaB and is proposed to be transferred to the C4-hydroxyl of azanigerone E by the acyltransferase azaD directly from the ACP domain of azaB (PubMed:22921072). Alternatively, the 2,4-dimethyl-hexanoyl chain may be offloaded from the HR-PKS as a carboxylic acid and converted to an acyl-CoA by azaF (PubMed:22921072). The resulting acyl-CoA molecule could then be taken up as a substrate by AzaD to form azanigerone B (PubMed:22921072). To yield the carboxylic acid substituent in azanigerone A, the hydroxypropyl side chain of azanigerone B would need to undergo a C-C oxidative cleavage catalyzed by cytochrome P450 AzaI (PubMed:22921072). AzaI is proposed to act on a vicinal diol that leads to a C-C bond scission either through an alkoxyradical intermediate or a peroxy complex (PubMed:22921072). In the biosynthesis of azanigerone A, azanigerone B first undergoes hydroxylation at C10, possibly catalyzed by one of the two FAD-dependent monooxygenases encoded in the cluster, azaG or azaL, resulting in the vicinal diol azanigerone C (PubMed:22921072). Oxidative cleavage of azanigerone C by azaI would yield the corresponding aldehyde derivative of azanigerone A (PubMed:22921072). Finally, the dehydrogenase azaJ is proposed to convert the aldehyde functional group into the carboxylic acid, completing the conversion from azanigerone B to azanigerone A (PubMed:22921072). Alternatively, the oxidation of aldehyde to carboxylic acid may be catalyzed by the same P450 enzyme azaI via consecutive oxidation or by endogenous alcohol dehydrogenase (PubMed:22921072).
 azaC ELISA Kit
 azaC Recombinant
 azaC Antibody
 ASPNIDRAFT_50208 ELISA Kit
 ASPNIDRAFT_50208 Recombinant
 ASPNIDRAFT_50208 Antibody
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Probable esterase D14L

 Probable esterase D14L ELISA Kit
 Probable esterase D14L Recombinant
 Probable esterase D14L Antibody
Also known as Probable esterase D14L (Protein DWARF-14-like) (Protein D14-like) (Protein HEBIBA D14L).
May be involved in strigolactone signaling pathway (). Essential for plant responses to karrikins, a class of butenolide compounds, structurally similar to strigolactones, released from burning vegetation that stimulate seed germination and enhance seedling photomorphogenesis. Mediates a specific perception of karrikin. Required for the establishment of symbiosis with the arbuscular mycorrhizal fungi (AMF) Rhizophagus irregularis and Gigaspora rosea (PubMed:26680197). Karrikin binding indu
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ces a conformational change ().
 D14L ELISA Kit
 D14L Recombinant
 D14L Antibody
 Os03g0437600 ELISA Kit
 Os03g0437600 Recombinant
 Os03g0437600 Antibody
 LOC_Os03g32270 ELISA Kit
 LOC_Os03g32270 Recombinant
 LOC_Os03g32270 Antibody
 Os11g0384789 ELISA Kit
 Os11g0384789 Recombinant
 Os11g0384789 Antibody
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Probable esterase KAI2

 Probable esterase KAI2 ELISA Kit
 Probable esterase KAI2 Recombinant
 Probable esterase KAI2 Antibody
Also known as Probable esterase KAI2 (Protein DWARF-14-like) (Protein D14-like) (Protein HYPOSENSITIVE TO LIGHT) (Protein KARRIKIN INSENSITIVE 2).
HTL belonging to the alpha/beta fold hydrolase superfamily. Mutant and over-expression studies indicates its involvement in seedling de-etiolation process.
 KAI2 ELISA Kit
 KAI2 Recombinant
 KAI2 Antibody
 D14L ELISA Kit
 D14L Recombinant
 D14L Antibody
 HTL ELISA Kit
 HTL Recombinant
 HTL Antibody
 At4g37470 ELISA Kit
 At4g37470 Recombinant
 At4g37470 Antibody
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Probable esterase PIR7A

 Probable esterase PIR7A ELISA Kit
 Probable esterase PIR7A Recombinant
 Probable esterase PIR7A Antibody
 PIR7A ELISA Kit
 PIR7A Recombinant
 PIR7A Antibody
 Os01g0934900 ELISA Kit
 Os01g0934900 Recombinant
 Os01g0934900 Antibody
 LOC_Os01g70860 ELISA Kit
 LOC_Os01g70860 Recombinant
 LOC_Os01g70860 Antibody
 P0423A12.27 ELISA Kit
 P0423A12.27 Recombinant
 P0423A12.27 Antibody
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Probable esterase TOX9

 Probable esterase TOX9 ELISA Kit
 Probable esterase TOX9 Recombinant
 Probable esterase TOX9 Antibody
Also known as Probable esterase TOX9 (T-toxin biosynthesis protein TOX9).
Probable esterase; part of the Tox1A locus, one of the 2 loci that mediate the biosynthesis of T-toxin, a family of linear polyketides 37 to 45 carbons in length, of which the major component is 41 carbons, and which leads to high virulence to maize (PubMed:8953776, PubMed:20192833). One of the PKSs (PKS1 or PKS2) could s
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ynthesize a precursor, used subsequently by the other PKS as starter unit, to add additional carbons (PubMed:16529376). Variability in the length of the final carbon backbone C35-47 could be achieved by varying the number of condensation cycles, or use of different starter or extender units or might be due to decarboxylation of the penultimate product, catalyzed by DEC1 (PubMed:12236595). Additional proteins are required for the biosynthesis of T-toxin, including oxidoreductases RED1, RED2, RED3, LAM1 and OXI1, as well as esterase TOX9 (PubMed:20192833).
 TOX9 ELISA Kit
 TOX9 Recombinant
 TOX9 Antibody
 COCC4DRAFT_155492 ELISA Kit
 COCC4DRAFT_155492 Recombinant
 COCC4DRAFT_155492 Antibody
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