about
Structure of PatF fromProchloron didemniThe Cyanobactin Heterocyclase Enzyme: A Processive Adenylase That Operates with a Defined Order of ReactionChaxapeptin, a Lasso Peptide from Extremotolerant Streptomyces leeuwenhoekii Strain C58 from the Hyperarid Atacama DesertThe 9th European Conference on Marine Natural ProductsSynthesis of Hybrid Cyclopeptides through Enzymatic MacrocyclizationEnzymatic Macrocyclization of 1,2,3-Triazole Peptide MimeticsAntimicrobial Activity of Monoramnholipids Produced by Bacterial Strains Isolated from the Ross Sea (Antarctica)Dermacozines H-J isolated from a deep-sea strain of Dermacoccus abyssi from Mariana Trench sediments.Increased Biological Activity of Aneurinibacillus migulanus Strains Correlates with the Production of New Gramicidin Secondary Metabolites.Spongionella Secondary Metabolites Regulate Store Operated Calcium Entry Modulating Mitochondrial Functioning in SH-SY5Y Neuroblastoma Cells.Nivetetracyclates A and B: novel compounds isolated from Streptomyces niveus.Structural analysis of leader peptide binding enables leader-free cyanobactin processingDraft Genome Sequence of Streptomyces sp. Strain CT34, Isolated from a Ghanaian Soil Sample.Access to and use of marine genetic resources: understanding the legal framework.Draft Genome Sequence of Aneurinibacillus migulanus Strain Nagano.Draft Genome Sequence of Aneurinibacillus migulanus NCTC 7096.A Unique Tryptophan C-Prenyltransferase from the Kawaguchipeptin Biosynthetic PathwayThe Catalytic Mechanism of the Marine-Derived Macrocyclase PatGmacMitigation of ROS insults by Streptomyces secondary metabolites in primary cortical neurons.Spongionella secondary metabolites protect mitochondrial function in cortical neurons against oxidative stress.The origins of cyanobactin chemistry and biology.Evaluation of the Antioxidant Activity of the Marine Pyrroloiminoquinone Makaluvamines.A Blind Test of Computational Technique for Predicting the Likelihood of Peptide Sequences to Cyclize.Targeted Dereplication of Microbial Natural Products by High-Resolution MS and Predicted LC Retention Time.Gracilins: Spongionella-derived promising compounds for Alzheimer disease.Structure of the cyanobactin oxidase ThcOx from Cyanothece sp. PCC 7425, the first structure to be solved at Diamond Light Source beamline I23 by means of S-SADDual Induction of New Microbial Secondary Metabolites by Fungal Bacterial Co-cultivation.Isolation and anti-HIV-1 integrase activity of lentzeosides A-F from extremotolerant lentzea sp. H45, a strain isolated from a high-altitude Atacama Desert soil.Strain-level diversity of secondary metabolism in the biocontrol species Aneurinibacillus migulanus.Biosynthesis of Neocarazostatin A Reveals the Sequential Carbazole Prenylation and Hydroxylation in the Tailoring Steps.Legonaridin, a new member of linaridin RiPP from a Ghanaian Streptomyces isolate.Spongionella Secondary Metabolites, Promising Modulators of Immune Response through CD147 Receptor Modulation.Butremycin, the 3-hydroxyl derivative of ikarugamycin and a protonated aromatic tautomer of 5'-methylthioinosine from a Ghanaian Micromonospora sp. K310.Microbiology: a talented genus.Bypassing the proline/thiazoline requirement of the macrocyclase PatG.Cyclic peptide production using a macrocyclase with enhanced substrate promiscuity and relaxed recognition determinants.Disruption of a methyltransferase gene in actinomycin G gene cluster in Streptomyces iakyrus increases the production of phenazinomycin.Asenjonamides A-C, antibacterial metabolites isolated from Streptomyces asenjonii strain KNN 42.f from an extreme-hyper arid Atacama Desert soil.Natural product diversity of actinobacteria in the Atacama Desert.Identification of Spongionella compounds as cyclosporine A mimics.
P50
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P50
description
onderzoeker
@nl
researcher, ORCID id # 0000-0002-2426-6028
@en
name
Marcel Jaspars
@ast
Marcel Jaspars
@en
Marcel Jaspars
@es
Marcel Jaspars
@nl
type
label
Marcel Jaspars
@ast
Marcel Jaspars
@en
Marcel Jaspars
@es
Marcel Jaspars
@nl
prefLabel
Marcel Jaspars
@ast
Marcel Jaspars
@en
Marcel Jaspars
@es
Marcel Jaspars
@nl
P108
P106
P31
P496
0000-0002-2426-6028