Synthesis of unnatural alkaloid scaffolds by exploiting plant polyketide synthase - Test2 - elhamkhani - TriplyDB

Synthesis of unnatural alkaloid scaffolds by exploiting plant polyketide synthase

Synthesis of unnatural alkaloid scaffolds by exploiting plant polyketide synthase

http://www.wikidata.org/entity/Q27671626

about

Biochemical and structural characterization of germicidin synthase: analysis of a type III polyketide synthase that employs acyl-ACP as a starter unit donor Exploiting the Biosynthetic Potential of Type III Polyketide Synthases Desorption Electrospray Ionization (DESI) Mass Spectrometric Imaging of the Distribution of Rohitukine in the Seedling of Dysoxylum binectariferum Hook. F Activation of a plasmid-situated type III PKS gene cluster by deletion of a wbl gene in deepsea-derived Streptomyces somaliensis SCSIO ZH66 Engineering polyketide synthases and nonribosomal peptide synthetases.Identification and characterization of a type III polyketide synthase involved in quinolone alkaloid biosynthesis from Aegle marmelos Correa.Type III polyketide synthases in natural product biosynthesis.Recent advances in combinatorial biosynthesis for drug discovery Type III Polyketide Synthases: Functional Classification and Phylogenomics.Tools of pathway reconstruction and production of economically relevant plant secondary metabolites in recombinant microorganisms.Engineering microbial cell factories for the production of plant natural products: from design principles to industrial-scale production.De novo biosynthesis of terminal alkyne-labeled natural products.Cloning and structure-function analyses of quinolone- and acridone-producing novel type III polyketide synthases from Citrus microcarpa.Structural basis for the formation of acylalkylpyrones from two β-ketoacyl units by the fungal type III polyketide synthase CsyB.Benzalacetone synthase.Enzymatic formation of a resorcylic acid by creating a structure-guided single-point mutation in stilbene synthase.Production of Stealthin C Involves an S-N-Type Smiles Rearrangement.Two polyketide synthases are necessary for 4-hydroxy-5-methylcoumarin biosynthesis in Gerbera hybrida.Gaining Insight Into Reactivity Differences Between Malonic Acid Half Thioesters (MAHT) and Malonic Acid Half Oxyesters (MAHO).Rewriting the Metabolic Blueprint: Advances in Pathway Diversification in Microorganisms.Overexpression of a type III PKS gene affording novel violapyrones with enhanced anti-influenza A virus activity.The International Conference of Natural Product Biosynthesis (ICNPB, 8th US-Japan seminar on the Biosynthesis of Natural Products).

P2860

Q24629843-E1DA9EA0-308A-4DC7-84AB-09278FC06633 Q26747526-EE2F69C8-1FB2-4D50-9E97-9B9F36380913 Q28552285-1C396185-AF0A-48EA-8114-B332CA12BD11 Q28828652-9CD333F9-CD08-4931-B82B-AB6B19BD7F91 Q34739957-FF05DE20-F74F-4041-87F3-A0DB9B1DD5D9 Q36666259-C81BE7E8-32D7-4082-BACD-E4926AAE52C0 Q37987874-A4851405-0468-4931-8594-D80F3ADA8DD8 Q38364681-CF580AEC-9B64-4E43-82A3-7CDFB02F83A8 Q39013122-BA0748D8-245C-46E3-A44F-C16122A1B0C5 Q39051370-6B3F902E-35B9-4131-B0B0-F406DA4B022B Q39445763-79FFC705-7C77-48FA-8D30-C0F615BCC02B Q41659409-CB704DCC-B897-4056-8ECD-0B999F652C7D Q41958701-D2A7DDDC-A213-42AE-8919-08C28F9048FA Q42055975-21ADE0E6-90E9-4630-9CF4-96E89BE826F1 Q42174782-956F408B-A2A7-4B4F-A587-F21733434C7C Q42555100-56DE89D9-B043-425E-B49E-9781D18F649B Q46418759-40034116-22E8-4ABE-8355-53E51D0C5C6A Q46542177-CD9C3B26-70FE-410B-9383-8473E6BAA5FC Q48158135-9413F204-340C-4A12-836F-F4DCE007AE6A Q50281299-8344731C-4498-4EEB-B3B5-1A28561DA63C Q52591403-DB619814-982C-49D1-930C-3C2F8D9F03E4 Q53123518-86F33219-07E5-4CF7-BCB8-207277BDD012

P2860

Synthesis of unnatural alkaloid scaffolds by exploiting plant polyketide synthase

http://www.wikidata.org/entity/Q27671626

description

2011 nî lūn-bûn

@nan

2011 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2011年の論文

@ja

2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

name

Synthesis of unnatural alkaloid scaffolds by exploiting plant polyketide synthase

@ast

Synthesis of unnatural alkaloid scaffolds by exploiting plant polyketide synthase

@en

Synthesis of unnatural alkaloid scaffolds by exploiting plant polyketide synthase

@nl

type

label

Synthesis of unnatural alkaloid scaffolds by exploiting plant polyketide synthase

@ast

Synthesis of unnatural alkaloid scaffolds by exploiting plant polyketide synthase

@en

Synthesis of unnatural alkaloid scaffolds by exploiting plant polyketide synthase

@nl

prefLabel

Synthesis of unnatural alkaloid scaffolds by exploiting plant polyketide synthase

@ast

Synthesis of unnatural alkaloid scaffolds by exploiting plant polyketide synthase

@en

Synthesis of unnatural alkaloid scaffolds by exploiting plant polyketide synthase

@nl

P1433

Q27671626-7CED365B-ED27-4269-97A3-F113BCF4F9AE

P1476

Q27671626-558D966E-C783-4F33-81CD-E5149E2492D0

P2093

Q27671626-463818A5-BAAD-4039-B78F-874DCD3CF58B

Q27671626-499F80DE-7465-4662-9A41-859A1954C14D

Q27671626-6848DFDA-F910-4BDF-964A-D5901C74B7C1

Q27671626-77338899-C875-4E2D-A48C-DB08E700E856

Q27671626-AC1EBD35-F574-4995-96E7-D4475A1C5AB4

Q27671626-B4E6B3A9-7115-4AAA-AD23-797503B23F7B

Q27671626-B50013A4-49FD-4ED8-B98D-97D85D2656AD

Q27671626-B82CB3A9-D6ED-4AF0-9FDF-7B9A00597FB1

Q27671626-E243FDC6-C0B4-4C49-B9B7-67D6A71782D2

P2860

Q27671626-021D0489-3C54-4C88-932B-7B9CCAD569A9

Q27671626-0BE3F9D9-9297-4327-95EB-A14D5F7F3E09

Q27671626-1110E929-86D4-445E-A8FB-C017D8213B89

Q27671626-1B7DF3D7-C4DC-4044-A8B7-23D3B6D56EE4

Q27671626-2F2C44FF-246F-4657-AFC6-90DD6732D92E

Q27671626-3438ABF1-F6CC-45D1-B0B7-0D617B66525C

Q27671626-39757909-1A31-4188-8418-3C2A00314074

Q27671626-42F243C1-DE3C-4178-9DED-34AF9E9CFD9A

Q27671626-59884B08-C763-4648-A5FD-E8351705CD71

Q27671626-606768CA-846E-4F8C-A1C8-8446D63A38F0

P304

Q27671626-95FB7779-7339-4282-9DA0-09936F949292

P31

Q27671626-952FA7BE-3DB7-4A86-8B4D-E4B126D01EFE

P3181

Q27671626-92A49956-B88F-412D-A4FC-EE46C6C672CF

P356

Q27671626-66A3FB14-3AB5-4C6C-94DB-2DB483CFEA6D

P407

Q27671626-D77392B1-E988-413C-AFEF-31E696B6F31B

P433

Q27671626-5480CFD7-6A47-4AA4-AC67-68A715DE77C7

P478

Q27671626-A076BB36-4C09-4DDF-B382-B2F419264EC1

P577

Q27671626-58B5F07A-9B68-4931-AF3C-CA6BCBFD5F03

P5875

Q27671626-709E5397-697A-4838-B137-4235D24B9757

P698

Q27671626-AD9B271D-59A8-436F-9D27-9F125E943548

P932

Q27671626-6D798ED5-CEA4-4DCD-8C7E-272DCF30AFDA

P3181

P356

PNAS.1107782108

P1433

Proceedings of the National Academy of Sciences of the United States of America

P1476

Synthesis of unnatural alkaloid scaffolds by exploiting plant polyketide synthase

@en

P2093

Hiroyuki Morita

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

Ikuro Abe

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

Makoto Yamashita

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

Ryohei Kato

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

She-Po Shi

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

Shigetoshi Sugio

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

Shin Kondo

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

Toshiyuki Kohno

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

Toshiyuki Wakimoto

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

P2860

Microbial biofilms

Crystallography & NMR System: A New Software Suite for Macromolecular Structure Determination

PROCHECK: a program to check the stereochemical quality of protein structures

Processing of X-ray diffraction data collected in oscillation mode

Structure of chalcone synthase and the molecular basis of plant polyketide biosynthesis

Expanding the biosynthetic repertoire of plant type III polyketide synthases by altering starter molecule specificity

Structural insight into chain-length control and product specificity of pentaketide chromone synthase from Aloe arborescens

Structural basis for the one-pot formation of the diarylheptanoid scaffold by curcuminoid synthase from Oryza sativa

Dali: a network tool for protein structure comparison

XtalView/Xfit--A versatile program for manipulating atomic coordinates and electron density

P304

13504-9

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

P31

scholarly article

P3181

361579

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

P356

10.1073/PNAS.1107782108

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

P407

P433

33

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

P478

108

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

P577

2011-08-16T00:00:00Z

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

P5875

51555563

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

P698

21825160

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

P932

3158201

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