Insight into a natural Diels-Alder reaction from the structure of macrophomate synthase - Test2 - elhamkhani - TriplyDB

Insight into a natural Diels-Alder reaction from the structure of macrophomate synthase

Insight into a natural Diels-Alder reaction from the structure of macrophomate synthase

http://www.wikidata.org/entity/Q27640693

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Evolution of Enzymatic Activities in the Enolase Superfamily: l -Rhamnonate Dehydratase † ‡Computational Design of an Enzyme Catalyst for a Stereoselective Bimolecular Diels-Alder Reaction Impact of scaffold rigidity on the design and evolution of an artificial Diels-Alderase Selection of ribozymes that catalyse multiple-turnover Diels-Alder cycloadditions by using in vitro compartmentalization.Biosynthesis of rhizocticins, antifungal phosphonate oligopeptides produced by Bacillus subtilis ATCC6633 Dearomatization strategies in the synthesis of complex natural products Advances in quantum and molecular mechanical (QM/MM) simulations for organic and enzymatic reactions.Ter-dependent stress response systems: novel pathways related to metal sensing, production of a nucleoside-like metabolite, and DNA-processing.Engineering of biocatalysts - from evolution to creation.Recent advances in the field of bioactive tetronates.Biosynthesis of versipelostatin: identification of an enzyme-catalyzed [4+2]-cycloaddition required for macrocyclization of spirotetronate-containing polyketides Active site mutagenesis of the putative Diels-Alderase macrophomate synthase.SbnG, a citrate synthase in Staphylococcus aureus: a new fold on an old enzyme.Hirsutellones and beyond: figuring out the biological and synthetic logics toward chemical complexity in fungal PKS-NRPS compounds.Enzyme-catalysed [4+2] cycloaddition is a key step in the biosynthesis of spinosyn A.Genomic and transcriptomic analysis of the endophytic fungus Pestalotiopsis fici reveals its lifestyle and high potential for synthesis of natural products.The structure of SpnF, a standalone enzyme that catalyzes [4 + 2] cycloaddition Current developments and challenges in the search for a naturally selected Diels-Alderase.Structural basis for Diels-Alder ribozyme-catalyzed carbon-carbon bond formation Natural Diels-Alderases: Elusive and Irresistable.The biosynthesis of spinosyn in Saccharopolyspora spinosa: synthesis of the cross-bridging precursor and identification of the function of SpnJ.Elucidation of the kijanimicin gene cluster: insights into the biosynthesis of spirotetronate antibiotics and nitrosugars.Synthesis of (-)-longithorone A: using organic synthesis to probe a proposed biosynthesis.Asymmetric Cu(II) catalyses for cycloaddition reactions based on π-cation or n-cation interactions.Artificial metalloenzymes as catalysts in stereoselective Diels-Alder reactions.Cyclization of polyketides and non-ribosomal peptides on and off their assembly lines.Mechanisms and Specificity of Phenazine Biosynthesis Protein PhzF.The Enzymology of Organic Transformations: A Survey of Name Reactions in Biological Systems.Natural [4 + 2]-Cyclases.Control of stereoselectivity in an enzymatic reaction by backdoor access.Computational design of a Diels-Alderase from a thermophilic esterase: the importance of dynamics.Computational Insights into an Enzyme-Catalyzed [4+2] Cycloaddition.Graphene Oxide as a Carbocatalyst for a Diels-Alder Reaction in an Aqueous Medium.Cucurbit[7]uril as a Supramolecular Artificial Enzyme for Diels-Alder Reactions.Stereopermutation on the Putative Structure of the Marine Natural Product Mucosin.An enzymatic [4+2] cyclization cascade creates the pentacyclic core of pyrroindomycins.Computational design of a lipase for catalysis of the Diels-Alder reaction De novo chemoenzymatic synthesis of sialic acid Chemoenzymatic synthesis of differentially protected 3-deoxysugars

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Insight into a natural Diels-Alder reaction from the structure of macrophomate synthase

http://www.wikidata.org/entity/Q27640693

description

2003 nî lūn-bûn

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2003 թուականի Մարտին հրատարակուած գիտական յօդուած

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2003 թվականի մարտին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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name

Insight into a natural Diels-Alder reaction from the structure of macrophomate synthase

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Insight into a natural Diels-Alder reaction from the structure of macrophomate synthase

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Insight into a natural Diels-Alder reaction from the structure of macrophomate synthase

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Insight into a natural Diels-Alder reaction from the structure of macrophomate synthase

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Insight into a natural Diels-Alder reaction from the structure of macrophomate synthase

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Insight into a natural Diels-Alder reaction from the structure of macrophomate synthase

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Insight into a natural Diels-Alder reaction from the structure of macrophomate synthase

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Insight into a natural Diels-Alder reaction from the structure of macrophomate synthase

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Insight into a natural Diels-Alder reaction from the structure of macrophomate synthase

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Insight into a natural Diels-Alder reaction from the structure of macrophomate synthase

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Hiromi Watanabe

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Isao Tanaka

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Mamoru Honma

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Min Yao

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Takashi Mie

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Toyoyuki Ose

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

Evolution of shape complementarity and catalytic efficiency from a primordial antibody template

Crystal structures of the metal-dependent 2-dehydro-3-deoxy-galactarate aldolase suggest a novel reaction mechanism

Immunological origins of binding and catalysis in a Diels-Alderase antibody

An antibody exo Diels-Alderase inhibitor complex at 1.95 angstrom resolution

The CCP4 suite: programs for protein crystallography

Macrophomate synthase: characterization, sequence, and expression in Escherichia coli of the novel enzyme catalyzing unusual multistep transformation of 2-pyrones to benzoates

Detailed reaction mechanism of macrophomate synthase. Extraordinary enzyme catalyzing five-step transformation from 2-pyrones to benzoates.

Enzymatic activity and partial purification of solanapyrone synthase: first enzyme catalyzing Diels-Alder reaction.

Lovastatin Nonaketide Synthase Catalyzes an Intramolecular Diels−Alder Reaction of a Substrate Analogue

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10.1038/NATURE01454

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6928

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1035657885

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12634789

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