Minimum set of cytochromes P450 for reconstituting the biosynthesis of camalexin, a major Arabidopsis antibiotic - Wikidata - awgldk - TriplyDB

Minimum set of cytochromes P450 for reconstituting the biosynthesis of camalexin, a major Arabidopsis antibiotic

Minimum set of cytochromes P450 for reconstituting the biosynthesis of camalexin, a major Arabidopsis antibiotic

http://www.wikidata.org/entity/Q41934305

about

The Biosynthetic Pathway of Indole-3-Carbaldehyde and Indole-3-Carboxylic Acid Derivatives in Arabidopsis.In Vitro Reconstitution of Metabolic Pathways: Insights into Nature's Chemical Logic.Two cytochromes P450 catalyze S-heterocyclizations in cabbage phytoalexin biosynthesis.Computational genomic identification and functional reconstitution of plant natural product biosynthetic pathways.Biosynthesis of polyketides by trans-AT polyketide synthases.Mini-review: In vitro Metabolic Engineering for Biomanufacturing of High-value Products Involvement of SgvP in carbon-sulfur bond formation during Griseoviridin biosynthesis.TRANSCRIPTION ACTIVATOR-LIKE EFFECTOR NUCLEASE-Mediated Generation and Metabolic Analysis of Camalexin-Deficient cyp71a12 cyp71a13 Double Knockout Lines.Herbivore-induced poplar cytochrome P450 enzymes of the CYP71 family convert aldoximes to nitriles which repel a generalist caterpillar.Biosynthesis of cabbage phytoalexins from indole glucosinolate Identification and functional analysis of two P450 enzymes of Gossypium hirsutum involved in DMNT and TMTT biosynthesis.A chemocentric view of the natural product inventory.Expansion of chemical space for natural products by uncommon P450 reactions.The bifurcation of the cyanogenic glucoside and glucosinolate biosynthetic pathways

P2860

Q30317469-B2872B5E-5FFD-44F9-AC78-2B3CC7591F7F Q35866989-04B0E222-B707-44F3-B8F0-B6CCD9C91F22 Q36514858-9F95B954-0062-4189-B4C8-B8CAD7EBC634 Q37181634-636C21D5-686E-4B1A-AA94-370C6B906483 Q38675125-528B73CA-C345-4541-84D5-58FFBBB4617B Q39127430-8FD622E7-3FAD-4A51-ACBB-4AB89C11D204 Q39607858-A213EC67-5582-47A7-9D2E-8E2F9E35CC89 Q40963185-D7132B9A-BA88-40A8-AE4D-861E786A5385 Q42001092-B6293AFD-206A-4EF9-90B3-7CB687959B0F Q42181600-7A1BA30D-9F48-4C9E-A7EA-8CE6E069E58B Q46335567-9A96BCD3-33C6-42C8-BB51-77290D181B42 Q46965285-2982C068-7269-4896-B0C5-4B7386C4BA08 Q47996749-D9150A19-69EC-4DF0-8CFB-171D9FA25FC6 Q55113012-206FFBF5-A409-43D5-943A-EB2E0531B499

P2860

Minimum set of cytochromes P450 for reconstituting the biosynthesis of camalexin, a major Arabidopsis antibiotic

http://www.wikidata.org/entity/Q41934305

description

2013 nî lūn-bûn

@nan

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

2013年论文

@zh

2013年论文

@zh-cn

name

Minimum set of cytochromes P45 ...... a major Arabidopsis antibiotic

@en

type

label

Minimum set of cytochromes P45 ...... a major Arabidopsis antibiotic

@en

prefLabel

Minimum set of cytochromes P45 ...... a major Arabidopsis antibiotic

@en

P1433

Q41934305-C60B1C01-66A5-4FA7-88BC-595104AE60FF

P1476

Q41934305-189FD857-4799-4260-9E80-95B0628418AE

P2093

Q41934305-088A4F3B-D94E-4628-9555-E2DFE8F5C40A

Q41934305-9D1CA91C-DDE8-460B-BF18-9BF128E4C098

P2860

Q41934305-1879CEED-9CFC-490F-AFDC-DAF4FFD4FB36

Q41934305-38E01A77-65C0-4801-BF30-28ED20B830BF

Q41934305-3C8FB7E0-9DCC-4CDF-96A3-9167E1FDBFAC

Q41934305-48CDAA9B-0A9A-4114-82FB-48E885F11487

Q41934305-54094076-D07B-44E1-882E-8E9AF524B24C

Q41934305-618DC485-8A57-4321-A846-D5A559EAA3FB

Q41934305-63C88EEA-E241-4300-A1FD-D46162102A1F

Q41934305-70F73B7A-8A03-4AE8-8928-C1386B866417

Q41934305-B3B4C45D-A322-4E2C-B181-04117827A89A

Q41934305-C9156938-CD30-4B8C-BCDD-FDBA043FAB0E

P304

Q41934305-23A24A92-2487-4832-BCBB-21BFD89E2BD5

P31

Q41934305-F8ECB609-7261-4FE6-8961-D462A2B13A96

P356

Q41934305-FB9084A3-6453-4817-918D-9A9540356C19

P407

Q41934305-323ADC80-32A3-4DB5-BBF3-99AF30407C1C

P433

Q41934305-ED995ECB-8A7B-4F21-96F9-4B653768342A

P478

Q41934305-EA9CC00D-00E7-4859-AECA-E5B92AAC844B

P50

Q41934305-2752CDDC-3B54-4796-9EE5-733F5E63280E

P577

Q41934305-F3457468-2D33-4142-AB9E-2223E245AA64

P698

Q41934305-05D2086F-AED6-48AA-9DA2-778D44CD9285

P921

Q41934305-4D54496C-58A5-466A-B59E-25C958798A81

P932

Q41934305-891D8839-E0E0-48FB-A170-0C61F1FB4D2A

P356

P1433

Angewandte Chemie International Edition

P1476

Minimum set of cytochromes P45 ...... a major Arabidopsis antibiotic

@en

P2093

Elizabeth S Sattely

http://www.w3.org/2001/XMLSchema#string

Gülbenk Anarat-Cappillino

http://www.w3.org/2001/XMLSchema#string

P2860

The multifunctional enzyme CYP71B15 (PHYTOALEXIN DEFICIENT3) converts cysteine-indole-3-acetonitrile to camalexin in the indole-3-acetonitrile metabolic network of Arabidopsis thaliana.

Metabolon formation in dhurrin biosynthesis.

Unusual P450 reactions in plant secondary metabolism.

Sulfur-containing secondary metabolites from Arabidopsis thaliana and other Brassicaceae with function in plant immunity.

Synthesis and cytotoxic activity of indolyl thiazoles.

Innate immune responses activated in Arabidopsis roots by microbe-associated molecular patterns.

CYP83b1 is the oxime-metabolizing enzyme in the glucosinolate pathway in Arabidopsis.

A dedicated glutathione S-transferase mediates carbon-sulfur bond formation in gliotoxin biosynthesis.

Arabidopsis cytochrome P450 monooxygenase 71A13 catalyzes the conversion of indole-3-acetaldoxime in camalexin synthesis.

Cloning of three A-type cytochromes P450, CYP71E1, CYP98, and CYP99 from Sorghum bicolor (L.) Moench by a PCR approach and identification by expression in Escherichia coli of CYP71E1 as a multifunctional cytochrome P450 in the biosynthesis of the cy

P304

13625-13628

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1002/ANIE.201307454

http://www.w3.org/2001/XMLSchema#string

P407

P433

51

http://www.w3.org/2001/XMLSchema#string

P478

52

http://www.w3.org/2001/XMLSchema#string

P50

P577

2013-10-21T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

24151049

http://www.w3.org/2001/XMLSchema#string

P921

P932

3867539

http://www.w3.org/2001/XMLSchema#string