Thioesterase domains of fungal nonreducing polyketide synthases act as decision gates during combinatorial biosynthesis. - Wikidata - wikimedia - TriplyDB

Thioesterase domains of fungal nonreducing polyketide synthases act as decision gates during combinatorial biosynthesis.

Thioesterase domains of fungal nonreducing polyketide synthases act as decision gates during combinatorial biosynthesis.

http://www.wikidata.org/entity/Q37191237

about

Insights into the biosynthesis of 12-membered resorcylic acid lactones from heterologous production in Saccharomyces cerevisiae.Engineering of New Pneumocandin Side-Chain Analogues from Glarea lozoyensis by Mutasynthesis and Evaluation of Their Antifungal Activity.Diversity-oriented combinatorial biosynthesis of benzenediol lactone scaffolds by subunit shuffling of fungal polyketide synthases.Fungal polyketide engineering comes of age.Diversity-Oriented Combinatorial Biosynthesis of Hybrid Polyketide Scaffolds from Azaphilone and Benzenediol Lactone Biosynthons.Steps towards the synthetic biology of polyketide biosynthesis.Polyketide synthase and non-ribosomal peptide synthetase thioesterase selectivity: logic gate or a victim of fate?Recent advances in combinatorial biosynthesis for drug discovery Saccharomyces cerevisiae as a tool for mining, studying and engineering fungal polyketide synthases.Identification of a type III polyketide synthase involved in the biosynthesis of spirolaxine.Systematic domain swaps of iterative, nonreducing polyketide synthases provide a mechanistic understanding and rationale for catalytic reprogramming.Analysis of the Sequences, Structures, and Functions of Product-Releasing Enzyme Domains in Fungal Polyketide Synthases.Macrodiolide Formation by the Thioesterase of a Modular Polyketide Synthase.Structure, absolute configuration, and conformational study of resorcylic acid derivatives and related congeners from the fungus Penicillium brocae Macrodiolide formation by the thioesterase of a modular polyketide synthase.Hot off the Press

P2860

Q33662361-7210DEB6-8C11-4769-BE11-AEAE06710027 Q33886641-98AAA832-3719-41D7-8E5E-2C6C17D27869 Q34120045-E1EC0CDE-5A2C-45C7-82E5-54C6498CD3CF Q34120221-2E7B5AA5-5C0D-4172-A413-1D07F636871F Q37674660-0D4EF37B-1DF2-4804-954B-F545F7DD711A Q38174180-B1C0194E-E6AD-41A6-AF47-DEE011CFB2D8 Q38340794-BB012CF8-22FB-4DCC-B14B-2EB7C52F1049 Q38364681-09FCB0C3-E2A4-4049-8427-A0A40150CD7D Q38724403-A540CC6C-27F7-4F97-ABE6-538308122463 Q39881647-136257BC-FBAB-4401-A825-4B4AC391F6C0 Q40351270-6DD2684A-20F8-401A-A24E-9F9083AA92F3 Q41473688-D1441DE3-6D98-45C9-8386-7B0B3C768280 Q42075638-11B37C5A-376D-4A6E-B053-5E40C5856553 Q53606057-5EE6574D-7944-4987-AD61-2E3F2CE23EFE Q54960461-8FB29046-DC02-48AC-ADE0-73BFA8BFB2F1 Q58856815-8ED0E946-7F51-4270-AE88-5BDB5BE8BAB9

P2860

Thioesterase domains of fungal nonreducing polyketide synthases act as decision gates during combinatorial biosynthesis.

http://www.wikidata.org/entity/Q37191237

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 12 July 2013

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Thioesterase domains of fungal ...... ng combinatorial biosynthesis.

@en

Thioesterase domains of fungal ...... ng combinatorial biosynthesis.

@nl

type

label

Thioesterase domains of fungal ...... ng combinatorial biosynthesis.

@en

Thioesterase domains of fungal ...... ng combinatorial biosynthesis.

@nl

prefLabel

Thioesterase domains of fungal ...... ng combinatorial biosynthesis.

@en

Thioesterase domains of fungal ...... ng combinatorial biosynthesis.

@nl

P1433

Q37191237-B6C72A98-E604-4398-8EF5-90F3659E1EF2

P1476

Q37191237-20BAAB1D-8D83-4256-BFBE-1967CA817E8B

P2093

Q37191237-2C09AC9E-084E-4DB0-8E73-740CA8A5FEF7

Q37191237-608136CA-B1B7-4CAB-ADDA-6FD8AF727136

Q37191237-673EF656-769E-4234-B3BB-129D90893940

Q37191237-D4119A87-6245-4562-AFEC-35303314C225

Q37191237-DD230C8D-EBC9-4368-BB22-2BD96DDADFFB

Q37191237-F598006F-C5F4-4957-B3C4-2848B409A736

P2860

Q37191237-0FF281E4-E81B-47AD-B409-06E9E104ED6D

Q37191237-1073A3C7-7B9F-4055-9360-188101AB0BBD

Q37191237-11667297-71D7-4891-B3BA-B9E72BD3C852

Q37191237-1CFE5111-B1DF-4C8B-B026-99652DB719B3

Q37191237-214DF9E8-6DA5-4406-8CB2-C05612C66636

Q37191237-22A5F876-BDC7-4545-98B2-2ECB12ECEBF9

Q37191237-27B69F02-6F16-48DF-B9AE-8A754323CC0E

Q37191237-29918335-C343-4C8E-9E30-615E93AE7AC5

Q37191237-31C22D88-9FDD-4A0E-9216-9B088A940261

Q37191237-3B143368-8025-4AEE-8309-CBAA4964CDC9

P304

Q37191237-BB4DC19E-632D-4079-8A62-A73DA5DACA3A

P31

Q37191237-4F9C8546-3A51-4BC8-B900-4B706205AC08

P356

Q37191237-DD379AA0-8FD4-4D5B-BB90-F8258D7C4CE4

P407

Q37191237-44ADE196-2014-4110-94C4-E31AA551847F

P433

Q37191237-A46B4E63-CC9C-43D4-8141-2D823DD7C451

P478

Q37191237-C8732198-68B7-45D0-AB5E-8ABF6E6616D6

P577

Q37191237-B682978D-B7AB-4F3E-B2AA-CC8D2E44D7C5

P5875

Q37191237-1DE07D2E-D741-41BF-996C-5D9BE1249EA0

P698

Q37191237-BD64AF6E-E2AA-4E6A-B8F0-ED8861F1FB42

P932

Q37191237-56709B6E-6575-427C-8A20-D450F2F9A634

P356

P1433

Journal of the American Chemical Society

P1476

Thioesterase domains of fungal ...... ng combinatorial biosynthesis.

@en

P2093

István Molnár

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

Jixun Zhan

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

Li-Jiang Xuan

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

Shuwei Zhang

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

Tong Zhou

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

Yuquan Xu

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

P2860

Structural basis for biosynthetic programming of fungal aromatic polyketide cyclization

Structure and function of an iterative polyketide synthase thioesterase domain catalyzing Claisen cyclization in aflatoxin biosynthesis

Biomimetic synthesis and optimization of cyclic peptide antibiotics

Drugging the cancer chaperone HSP90: combinatorial therapeutic exploitation of oncogene addiction and tumor stress

Characterization of the biosynthetic genes for 10,11-dehydrocurvularin, a heat shock response-modulating anticancer fungal polyketide from Aspergillus terreus

Functional Characterization of the Biosynthesis of Radicicol, an Hsp90 Inhibitor Resorcylic Acid Lactone from Chaetomium chiversii

Chemistry and biology of resorcylic acid lactones

Genes for the biosynthesis of the fungal polyketides hypothemycin from Hypomyces subiculosus and radicicol from Pochonia chlamydosporia.

Classification, prediction, and verification of the regioselectivity of fungal polyketide synthase product template domains.

Insights into radicicol biosynthesis via heterologous synthesis of intermediates and analogs

P304

10783-10791

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

P31

scholarly article

P356

10.1021/JA4041362

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

P407

P433

29

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

P478

135

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

P577

2013-07-12T00:00:00Z

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

P5875

245027256

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

P698

23822773

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

P932

3780601

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