Biosynthesis of the salinosporamide A polyketide synthase substrate chloroethylmalonyl-coenzyme A from S-adenosyl-L-methionine.
about
The discovery of salinosporamide K from the marine bacterium "Salinispora pacifica" by genome mining gives insight into pathway evolutionFunction-oriented biosynthesis of beta-lactone proteasome inhibitors in Salinispora tropicaLessons from the past and charting the future of marine natural products drug discovery and chemical biologyComplexity generation during natural product biosynthesis using redox enzymesUnusual carbon fixation gives rise to diverse polyketide extender unitsStructural and Stereochemical Analysis of a Modular Polyketide Synthase Ketoreductase Domain Required for the Generation of a cis-AlkeneRational Control of Polyketide Extender Units by Structure-Based Engineering of a Crotonyl-CoA Carboxylase/Reductase in Antimycin BiosynthesisPrephenate decarboxylases: a new prephenate-utilizing enzyme family that performs nonaromatizing decarboxylation en route to diverse secondary metabolites.Natural products version 2.0: connecting genes to molecules.Salinosporamide natural products: Potent 20 S proteasome inhibitors as promising cancer chemotherapeutics.Identification of a bioactive 51-membered macrolide complex by activation of a silent polyketide synthase in Streptomyces ambofaciens.The natural product domain seeker NaPDoS: a phylogeny based bioinformatic tool to classify secondary metabolite gene diversityCharacterization of 5-chloro-5-deoxy-D-ribose 1-dehydrogenase in chloroethylmalonyl coenzyme A biosynthesis: substrate and reaction profiling.Insights from the sea: structural biology of marine polyketide synthasesThe enzymes of β-lactam biosynthesis.The marine actinomycete genus Salinispora: a model organism for secondary metabolite discoveryBiosynthesis of the allylmalonyl-CoA extender unit for the FK506 polyketide synthase proceeds through a dedicated polyketide synthase and facilitates the mutasynthesis of analogues.Classification of the adenylation and acyl-transferase activity of NRPS and PKS systems using ensembles of substrate specific hidden Markov modelsGenomic basis for natural product biosynthetic diversity in the actinomycetesA sea of biosynthesis: marine natural products meet the molecular age.Biosynthesis of akaeolide and lorneic acids and annotation of type I polyketide synthase gene clusters in the genome of Streptomyces sp. NPS554.Identification and characterization of the biosynthetic gene cluster of polyoxypeptin A, a potent apoptosis inducer.Evolution of secondary metabolite genes in three closely related marine actinomycete speciesMolecular networking and pattern-based genome mining improves discovery of biosynthetic gene clusters and their products from Salinispora species.Selective overproduction of the proteasome inhibitor salinosporamide A via precursor pathway regulation.Screening and Engineering the Synthetic Potential of Carboxylating Reductases from Central Metabolism and Polyketide Biosynthesis.Chemoenzymatic Synthesis of Acyl Coenzyme A Substrates Enables in Situ Labeling of Small Molecules and Proteins.Reinvigorating natural product combinatorial biosynthesis with synthetic biologyUsing Molecular Networking for Microbial Secondary Metabolite Bioprospecting.Marizomib, a proteasome inhibitor for all seasons: preclinical profile and a framework for clinical trialsDesigned biosynthesis of 36-methyl-FK506 by polyketide precursor pathway engineering.Biosynthesis of salinosporamides from alpha,beta-unsaturated fatty acids: implications for extending polyketide synthase diversity.A crotonyl-CoA reductase-carboxylase independent pathway for assembly of unusual alkylmalonyl-CoA polyketide synthase extender units.Challenges and triumphs to genomics-based natural product discoveryDiversity and evolution of secondary metabolism in the marine actinomycete genus Salinispora.Carboxylases in natural and synthetic microbial pathwaysBeyond ethylmalonyl-CoA: the functional role of crotonyl-CoA carboxylase/reductase homologs in expanding polyketide diversity.Antagonistic interactions mediated by marine bacteria: the role of small molecules.Functional diversity of organic molecule enzyme cofactors.Bioinformatics tools for genome mining of polyketide and non-ribosomal peptides.
P2860
Q24599741-EFDFAE1D-F2C1-4825-8A0B-67A9695C46E5Q24646019-2A6E3B65-6463-478D-A89C-5B621E9FA7ACQ26863108-3ECF7F53-43E5-443B-A9F1-0ADC8BD82856Q27000500-F97A5B9A-A01A-401A-9821-8CA40CE664D1Q27675936-4DC1EEEA-566E-4B38-BAB5-99DE64360009Q27678720-4380B2F2-A8DA-426F-A1F7-AF41B7B38875Q27702125-989A238F-3855-48DA-8FA0-22169A3FAA01Q33700902-C541EA70-AC3D-4419-B579-992FA5AC056AQ34096062-899C7F4E-1AF5-44BA-B6EC-55E279390B05Q34142223-051D1FF6-3289-406F-A01E-E9F927133C92Q34173936-AF396035-D01C-40CC-B9E5-4E7A882F1F34Q34222047-6BCBEF5A-849C-42DB-8113-7C0C2871DD0CQ34231950-3E553201-8564-4D0D-ACF4-46B61C34AE3DQ34267983-AFDBD544-EA85-4893-9FCE-C26AB8618807Q34310470-AA1BE6A6-0408-4F02-917F-A5574514100AQ34465208-1282749D-0445-4907-BEC1-4FEA489B54D1Q34538163-B991E033-BF28-449E-AF49-B5B90B66C5A0Q34700983-9382121A-A449-45AC-8D8C-129B7D0A3961Q34711979-2C676F9D-9ADF-45CC-A5AC-CBBB75C94776Q35006338-7C355B1B-6AC6-40B0-A535-E221FCAE48FDQ35015405-D2449B82-6B1E-414F-A608-2BFFD966B19CQ35088943-69E6234D-C2B1-4F92-AED4-B24B4D4B3860Q35362075-9C20C92A-4BF4-491C-9F64-49E963065431Q35538609-48253B2A-8C6C-46F2-A23E-26229A8DAD5FQ35634544-D3E85704-C59D-44B5-9564-BC31B7AEA13CQ35780235-16524C8E-46A3-4D8E-B652-0C54F414D2F5Q36482701-56003C08-F7D4-47F9-80D2-A3BCB36053A5Q36590659-078DF8B6-EE92-4658-B7DC-298E6F6DE64DQ36741597-5C13502B-2261-4941-8301-A38E389F4786Q37017342-A6032685-5FCC-47B0-9555-628B5FA53220Q37028302-F08DBE83-6DF1-4898-A1FB-D20EDDF211D8Q37331323-B48226A1-4EF7-4F39-B7F6-01F6B60E1FCFQ37533520-6DC8C33C-535C-46EB-AF08-CB0C35B09DFFQ37625408-119869F4-4A80-405D-9725-B85C058307E0Q37674497-42D0DF0C-5523-4683-9DBC-C8FE6CC8894BQ37946335-5667E9BD-78E3-48CB-B414-E125F1F72235Q37962381-EDF219E1-8828-4302-982A-C7FDC0EA39FDQ38121455-AB8516A8-1B0F-4CBD-9765-E889D3FAAEF8Q38128203-6E0149F7-B5DC-47A2-9D19-15BB8FF00578Q38156708-E8CD5B13-FCAD-4363-8C2B-43C0516562F0
P2860
Biosynthesis of the salinosporamide A polyketide synthase substrate chloroethylmalonyl-coenzyme A from S-adenosyl-L-methionine.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 09 July 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Biosynthesis of the salinospor ...... from S-adenosyl-L-methionine.
@en
Biosynthesis of the salinospor ...... from S-adenosyl-L-methionine.
@nl
type
label
Biosynthesis of the salinospor ...... from S-adenosyl-L-methionine.
@en
Biosynthesis of the salinospor ...... from S-adenosyl-L-methionine.
@nl
prefLabel
Biosynthesis of the salinospor ...... from S-adenosyl-L-methionine.
@en
Biosynthesis of the salinospor ...... from S-adenosyl-L-methionine.
@nl
P2093
P2860
P356
P1476
Biosynthesis of the salinospor ...... from S-adenosyl-L-methionine.
@en
P2093
Alessandra S Eustáquio
Andrew J Kale
Anna Lechner
Bradley S Moore
Christopher Hazzard
Galina Florova
Kevin A Reynolds
Laura L Beer
Mamoun M Alhamadsheh
Ryan P McGlinchey
P2860
P304
12295-12300
P356
10.1073/PNAS.0901237106
P407
P577
2009-07-09T00:00:00Z