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index medicus (239) 239
myxococcales - metabolism (214) 214
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bacterial proteins - genetics (59) 59
myxococcus-xanthus (58) 58
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myxococcales - classification (42) 42
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physiological aspects (40) 40
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models, molecular (39) 39
sequence analysis, dna (39) 39
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myxococcales - physiology (38) 38
research (38) 38
research article (38) 38
biochemistry (37) 37
multigene family (37) 37
chemistry, organic (36) 36
metabolites (35) 35
sorangium cellulosum (35) 35
mutation (34) 34
oxidation-reduction (34) 34
structure elucidation (34) 34
structure-activity relationship (34) 34
chemistry (33) 33
gene-cluster (33) 33
anti-bacterial agents - chemistry (32) 32
drug discovery (32) 32
mice (32) 32
molecular weight (32) 32
myxococcales - isolation & purification (32) 32
dna, bacterial - chemistry (30) 30
enzymes (30) 30
proteins (30) 30
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escherichia coli - genetics (29) 29
myxococcales - drug effects (29) 29
soil microbiology (29) 29
biotechnology (28) 28
multidisciplinary sciences (28) 28
antineoplastic agents - chemistry (27) 27
antineoplastic agents - pharmacology (27) 27
biosynthetic gene-cluster (27) 27
chemical phenomena (27) 27
immunology (27) 27
mass spectrometry (27) 27
sequence alignment (27) 27
polyketide synthases - metabolism (26) 26
rna, ribosomal, 16s - genetics (26) 26
signal transduction (26) 26
substrate specificity (26) 26
fermentation (25) 25
microtubule-stabilizing agents (25) 25
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plant sciences (24) 24
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1. Full Text Structural characterization of the heme‐based oxygen sensor, AfGcHK, its interactions with the cognate response regulator, and their combined mechanism of action in a bacterial two‐component signaling system
by Stranava, Martin and Martínek, Václav and Man, Petr and Fojtikova, Veronika and Kavan, Daniel and Vaněk, Ondřej and Shimizu, Toru and Martinkova, Marketa
Proteins: Structure, Function, and Bioinformatics, ISSN 0887-3585, 10/2016, Volume 84, Issue 10, pp. 1375 - 1389
ABSTRACT The oxygen sensor histidine kinase AfGcHK from the bacterium Anaeromyxobacter sp. Fw 109‐5 forms a two‐component signal transduction system together... 
heme‐based oxygen sensor | analytical ultracentrifugation | homology modeling | two‐component signal transduction system | protein–protein interaction | hydrogen‐deuterium exchange | histidine kinase | protein–protein docking | hydrogen-deuterium exchange | two-component signal transduction system | heme-based oxygen sensor | COMPLEX | protein-protein docking | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSDUCTION | MASS-SPECTROMETRY | COUPLED HISTIDINE KINASE | PROTEIN INTERACTIONS | BIOPHYSICS | protein-protein interaction | SEDIMENTATION-VELOCITY | EXCHANGE | BINDING | AUTOPHOSPHORYLATION | Histidine Kinase - chemistry | Histidine Kinase - metabolism | Phosphorylation | Heme - metabolism | Bacterial Proteins - chemistry | Histidine - metabolism | Oxygen - metabolism | Deuterium Exchange Measurement | Heme - chemistry | Cloning, Molecular | Escherichia coli - metabolism | Oxygen - chemistry | Protein Domains | Aeromonas salmonicida - metabolism | Recombinant Proteins - metabolism | Protein Structure, Secondary | Signal Transduction | Iron - chemistry | Bacterial Proteins - genetics | Recombinant Proteins - chemistry | Recombinant Proteins - genetics | Iron - metabolism | Myxococcales - chemistry | Escherichia coli - genetics | Histidine Kinase - genetics | Myxococcales - enzymology | Aspartic Acid - metabolism | Bacterial Proteins - metabolism | Structural Homology, Protein | Aspartic Acid - chemistry | Histidine - chemistry | Aeromonas salmonicida - genetics | Proteins | Phosphates | Hydrogen | Analysis | Heme | Cellular signal transduction | Mass spectrometry | Protein-protein interactions
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2. Full Text On the potential of natural products in the discovery of pharma leads: A case for reassessment
by Danishefsky, Samuel
Natural Product Reports, ISSN 0265-0568, 08/2010, Volume 27, Issue 8, pp. 1114 - 1116
The central proposition advanced herein is that complex target oriented synthesis, enabled by historic advances in methodology, has enormously expanded the... 
CHEMISTRY, ORGANIC | CHEMISTRY, MEDICINAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | Piperidones - chemical synthesis | Epothilones - chemistry | Streptomyces - chemistry | Epothilones - pharmacology | Biological Products - pharmacology | Epothilones - chemical synthesis | Piperidones - pharmacology | Drug Discovery | Myxococcales - chemistry | Biological Products - chemical synthesis | Piperidones - chemistry | Biological Products - chemistry | Animals | Macrolides - chemistry | Macrolides - chemical synthesis | Macrolides - pharmacology | Mice | Molecular Structure
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3. Full Text Characterization of an Unusual Glycerate Esterification Process in Vioprolide Biosynthesis
by Auerbach, David and Yan, Fu and Zhang, Youming and Müller, Rolf
ACS Chemical Biology, ISSN 1554-8929, 11/2018, Volume 13, Issue 11, pp. 3123 - 3130
Bacteria produce a large number of secondary metabolites with extraordinary chemical structures and bioactivities. Vioprolides are promising anticancer and... 
MYXOCOCCUS-XANTHUS | GENE-CLUSTER | SPECIFICITY | POLYKETIDE SYNTHASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | VIRULENCE FACTOR | SECONDARY METABOLITE | ADENYLATION DOMAIN | FATTY-ACIDS | STRUCTURE ELUCIDATION | PEPTIDE | Antifungal Agents - pharmacology | Myxococcales - genetics | HCT116 Cells | Humans | Ligases - genetics | Bacterial Proteins - chemistry | Bacterial Proteins - genetics | Glyceric Acids - chemistry | Antifungal Agents - chemistry | Depsipeptides - pharmacology | Ligases - chemistry | Antineoplastic Agents - chemistry | Esterification | Mycobacterium - genetics | Myxococcales - chemistry | Escherichia coli - genetics | Protein Domains | Antineoplastic Agents - pharmacology | Palmitic Acid - chemistry | Depsipeptides - chemistry
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4. Full Text Salimabromide: Unexpected chemistry from the obligate marine myxobacterium enhygromxya salina
by Felder, Stephan and Dreisigacker, Sandra and Kehraus, Stefan and Neu, Edith and Bierbaum, Gabriele and Wright, Patrick R and Menche, Dirk and Schäberle, Till F and König, Gabriele M
Chemistry - A European Journal, ISSN 0947-6539, 07/2013, Volume 19, Issue 28, pp. 9319 - 9324
Marine myxobacteria (Enhygromyxa, Plesiocystis, Pseudoenhygromyxa, Haliangium) are phylogenetically distant from their terrestrial counterparts. Salimabromide... 
enhygromyxa | natural products | NMR spectroscopy | polyketides | myxobacteria | Myxococcales - chemistry | Myxococcales - genetics | Animals | Arthrobacter - drug effects | Anti-Bacterial Agents - pharmacology | Anti-Bacterial Agents - isolation & purification | Phylogeny | Heterocyclic Compounds, 4 or More Rings - pharmacology | Aquatic Organisms | Heterocyclic Compounds, 4 or More Rings - isolation & purification
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5. Full Text Structural characterization of CYP260A1 from Sorangium cellulosum to investigate the 1α‐hydroxylation of a mineralocorticoid
by Khatri, Yogan and Carius, Yvonne and Ringle, Michael and Lancaster, C. Roy D and Bernhardt, Rita
FEBS Letters, ISSN 0014-5793, 12/2016, Volume 590, Issue 24, pp. 4638 - 4648
In this study, we report the crystal structure of the cytochrome P450 CYP260A1 (PDB 5LIV) from the myxobacterium Sorangium cellulosum So ce56. In addition, we... 
crystal structure of CYP260A1 | steroid hydroxylation | P450 | S326N | mineralocorticoid | MOLECULAR REPLACEMENT | CRYSTAL-STRUCTURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | ESCHERICHIA-COLI | HYDROXYLATION | IDENTIFICATION | CELL BIOLOGY | BIOPHYSICS | INTEGRATION | CYTOCHROME-P450 ENZYMES | CE56 | PROTON DELIVERY | Ferredoxin-NADP Reductase - metabolism | Bacterial Proteins - chemistry | Adrenodoxin - metabolism | Cytochrome P-450 Enzyme System - metabolism | Substrate Specificity | Crystallography, X-Ray | Structure-Activity Relationship | Mineralocorticoids - chemistry | Ferredoxin-NADP Reductase - genetics | Protein Domains | Recombinant Proteins - metabolism | Gene Expression | Hydroxylation | Mineralocorticoids - metabolism | Oxidation-Reduction | Protein Structure, Secondary | Bacterial Proteins - genetics | Recombinant Proteins - chemistry | Recombinant Proteins - genetics | Myxococcales - chemistry | Cytochrome P-450 Enzyme System - chemistry | Myxococcales - enzymology | Desoxycorticosterone - chemistry | Desoxycorticosterone - metabolism | Cytochrome P-450 Enzyme System - genetics | Adrenodoxin - chemistry | Bacterial Proteins - metabolism | Molecular Docking Simulation | Kinetics | Mutation
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6. Full Text Six heterocyclic metabolites from the myxobacterium labilithrix luteola
by Mulwa, Lucky S and Jansen, Rolf and Praditya, Dimas F and Mohr, Kathrin I and Wink, Joachim and Steinmann, Eike and Stadler, Marc
Molecules, ISSN 1420-3049, 2018, Volume 23, Issue 3, p. 542
Two new secondary metabolites, labindole A [2-methyl-3-(2-nitroethyl)-3H-indole] (1) and labindole B [2-methyl-3-(2-nitrovinyl)-3H-indole] (2), were isolated... 
Antimicrobial activity | HCV | Fermentation | Nitroindole | Natural products | Antiviral activity | natural products | CARBAZOLE | nitroindole | BIOCHEMISTRY & MOLECULAR BIOLOGY | fermentation | antiviral activity | antimicrobial activity | DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY | ALKALOIDS | Hepacivirus - drug effects | Antiviral Agents - pharmacology | Magnetic Resonance Spectroscopy | Anti-Infective Agents - pharmacology | Heterocyclic Compounds - pharmacology | Biological Products - pharmacology | Myxococcales - metabolism | Secondary Metabolism | Microbial Sensitivity Tests | Myxococcales - chemistry | Biological Products - chemistry | Heterocyclic Compounds - chemistry | Antiviral Agents - chemistry | Anti-Infective Agents - chemistry | Molecular Structure | Nuclear magnetic resonance--NMR | Fungicides | Indole | Overhauser effect | Viruses | Mass spectroscopy | Carbazole | Coupling (molecular) | Hepatitis | Secondary metabolites | Carbazoles | Metabolites | Ionization | Quinoline | Hepatitis C virus | Hepatitis C | Mass spectrometry
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7. Full Text Acid mediated formation of an N-acyliminium ion from tubulysins: A new methodology for the synthesis of natural tubulysins and their analogs
by Vlahov, Iontcho R and Wang, Yu and Vetzel, Marilynn and Hahn, Spencer and Kleindl, Paul J and Reddy, Joseph A and Leamon, Christopher P
Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, 2011, Volume 21, Issue 22, pp. 6778 - 6781
Tubuylsins are extremely potent cytotoxic agents which inhibit tubulin polymerization and lead to cell cycle arrest and apoptosis. Tubulysins have been... 
N-Acyl- N,O-acetals | N,N′-Diacyl-aminals | Tubulysin | N-Acyl- N,S-thioacetals | N-Acyliminium ion | C–C bond formation | N-Acyl-N,O-acetals | C-C bond formation | N-Acyl-N,S-thioacetals | N,N '-Diacyl-aminals | CHEMISTRY, MEDICINAL | ANTICANCER | CHEMISTRY, ORGANIC | INHIBITORS | BIOLOGICAL-PROPERTIES | MYXOBACTERIA | Chemistry Techniques, Synthetic - economics | Oligopeptides - chemical synthesis | Ions - chemistry | Tubulin Modulators - chemistry | Pipecolic Acids - chemical synthesis | Acetic Acid - chemistry | Chemistry Techniques, Synthetic - methods | Myxococcales - chemistry | Tubulin Modulators - chemical synthesis | Biological Products - chemical synthesis | Biological Products - chemistry | Imines - chemistry | Oligopeptides - chemistry | Pipecolic Acids - chemistry
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8. Full Text Scrutiny of electrochemically-driven electrocatalysis of C-19 steroid 1α-hydroxylase (CYP260A1) from Sorangium cellulosum So ce56
by Kuzikov, Alexey V and Masamrekh, Rami A and Khatri, Yogan and Zavialova, Maria G and Bernhardt, Rita and Archakov, Alexander I and Shumyantseva, Victoria V
Analytical Biochemistry, ISSN 0003-2697, 11/2016, Volume 513, pp. 28 - 35
Direct electrochemistry and bioelectrocatalysis of a newly discovered C-19 steroid 1α-hydroxylase (CYP260A1) from the myxobacterium So ce56 were investigated.... 
Enzyme electrodes | Analytical bioelectrochemistry | Electrocatalysis | Direct electron transfer | C-19 steroid 1α-hydroxylase | Sorangium cellulosum So ce56 | GOLD NANOPARTICLES | RAT-LIVER | CHEMISTRY, ANALYTICAL | C-19 steroid 1 alpha-hydroxylase | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMICAL RESEARCH METHODS | BIOELECTROCHEMISTRY | MONOOXYGENASE | CYTOCHROME-P450 2B4 | REDUCTION | ENZYMES | P450 | PEROXYGENASE PROPERTIES | DIRECT ELECTRON-TRANSFER | Gold - chemistry | Enzymes, Immobilized - chemistry | Cytochrome P-450 Enzyme System - chemistry | Electrochemical Techniques | Androsterone - analysis | Metal Nanoparticles - chemistry | Myxococcales - enzymology | Bacterial Proteins - chemistry | Catalysis | Graphite - chemistry
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9. Full Text Kinetic Analysis of a Globin-Coupled Histidine Kinase, AfGcHK: Effects of the Heme Iron Complex, Response Regulator, and Metal Cations on Autophosphorylation Activity
by Fojtikova, Veronika and Stranava, Martin and Vos, Marten H and Liebl, Ursula and Hranicek, Jakub and Kitanishi, Kenichi and Shimizu, Toru and Martinkova, Marketa
Biochemistry, ISSN 0006-2960, 08/2015, Volume 54, Issue 32, pp. 5017 - 5029
The globin-coupled histidine kinase, AfGcHK, is a part of the two-component signal transduction system from the soil bacterium Anaeromyxobacter sp. Fw109-5.... 
SIGNAL-TRANSDUCTION | OXYGEN SENSOR | TRUNCATED HEMOGLOBIN | DISTAL SIDE | RESONANCE RAMAN-SPECTROSCOPY | BIOCHEMISTRY & MOLECULAR BIOLOGY | MYCOBACTERIUM-TUBERCULOSIS DOSS | ESCHERICHIA-COLI | SENSOR DIGUANYLATE CYCLASE | LIGAND-BINDING DYNAMICS | COLI EC DOS | Protein Kinases - metabolism | Phosphorylation | Protein Kinases - genetics | Bacterial Proteins - chemistry | Protein Kinases - chemistry | Globins - metabolism | Carbon Monoxide - metabolism | Oxygen - metabolism | Heme - chemistry | Adenosine Triphosphate - metabolism | Cations, Divalent - chemistry | Protein Structure, Tertiary | Recombinant Proteins - metabolism | Myxococcales - genetics | Mutagenesis, Site-Directed | Oxidation-Reduction | Signal Transduction | Iron - chemistry | Bacterial Proteins - genetics | Models, Molecular | Recombinant Proteins - chemistry | Recombinant Proteins - genetics | Histidine Kinase | Myxococcales - enzymology | Bacterial Proteins - metabolism | Enzyme Activation | Kinetics | Hydrogen-Ion Concentration | Oxidation-reduction reaction | Iron compounds | Research | Chemical properties | Catalysis | Life Sciences | Chemical Physics | Biochemistry, Molecular Biology | Physics
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10. Full Text Molecular Basis for Olefin Rearrangement in the Gephyronic Acid Polyketide Synthase
by Dodge, Greg J and Ronnow, Danialle and Taylor, Richard E and Smith, Janet L and Argonne National Lab. (ANL), Argonne, IL (United States). Advanced Photon Source (APS)
ACS Chemical Biology, ISSN 1554-8929, 09/2018, Volume 13, Issue 9, pp. 2699 - 2707
Polyketide synthases (PKS) are a rich source of natural products of varied chemical composition and biological significance. Here, we report the... 
ELUCIDATION | DOMAIN | FABZ | CARRIER PROTEIN DEHYDRATASE | PSEUDOMONAS-AERUGINOSA | BIOCHEMISTRY & MOLECULAR BIOLOGY | ISOMERASE | BIOSYNTHETIC-PATHWAY | BETA-HYDROXYDECANOYLTHIOESTER DEHYDRASE | STEREOSPECIFICITY | DOUBLE-BOND FORMATION | Catalytic Domain | Models, Molecular | Substrate Specificity | Biosynthetic Pathways | Myxococcales - metabolism | Myxococcales - chemistry | Alkenes - chemistry | Polyketide Synthases - chemistry | Polyketide Synthases - metabolism | Fatty Acids, Monounsaturated - metabolism | Isomerases - chemistry | Myxococcales - enzymology | Protein Domains | Fatty Acids, Monounsaturated - chemistry | Hydro-Lyases - metabolism | Hydro-Lyases - chemistry | Isomerases - metabolism | Alkenes - metabolism | Index Medicus
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11. Full Text Cystobactamids: Myxobacterial Topoisomerase Inhibitors Exhibiting Potent Antibacterial Activity
by Baumann, Sascha and Herrmann, Jennifer and Raju, Ritesh and Steinmetz, Heinrich and Mohr, Kathrin I and Hüttel, Stephan and Harmrolfs, Kirsten and Stadler, Marc and Müller, Rolf
Angewandte Chemie International Edition, ISSN 1433-7851, 12/2014, Volume 53, Issue 52, pp. 14605 - 14609
The development of new antibiotics faces a severe crisis inter alia owing to a lack of innovative chemical scaffolds with activities against Gram‐negative and... 
natural products | NRPS | topoisomerase inhibitors | antibiotics | myxobacteria | Topoisomerase inhibitors | Myxobacteria | Antibiotics | Natural products | QUINOLONE RESISTANCE | ESCHERICHIA-COLI | CHEMISTRY, MULTIDISCIPLINARY | DISCOVERY | IMPACT | BAD BUGS | DRUGS | DNA GYRASE | Asparagine - pharmacology | Bacterial Proteins - antagonists & inhibitors | DNA Topoisomerases, Type I - metabolism | Gram-Positive Bacteria - drug effects | DNA Topoisomerases, Type I - chemistry | Nitro Compounds - chemistry | Nitro Compounds - chemical synthesis | Peptide Synthases - metabolism | Microbial Sensitivity Tests | Topoisomerase Inhibitors - pharmacology | Asparagine - chemical synthesis | Gram-Negative Bacteria - drug effects | Topoisomerase Inhibitors - metabolism | Asparagine - analogs & derivatives | Anti-Bacterial Agents - chemistry | Myxococcales - enzymology | Nitro Compounds - pharmacology | Bacterial Proteins - metabolism | Anti-Bacterial Agents - biosynthesis | Anti-Bacterial Agents - pharmacology | Topoisomerase Inhibitors - chemistry | Asparagine - chemistry | Exhibitions | Antibacterial agents | Analysis | DNA topoisomerase I | Pathogens | Inhibitors | Congeners | Bacteria | Derivatives | Antibacterial materials | Scaffolds | Antiinfectives and antibacterials
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12. Full Text Natural products from myxobacteria: novel metabolites and bioactivities
by Herrmann, J and Fayad, A Abou and Müller, R
Natural product reports, ISSN 0265-0568, 02/2017, Volume 34, Issue 2, pp. 135 - 160
Covering: 2011-July 2016Myxobacteria are a rich source for structurally diverse secondary metabolites with intriguing biological activities. Here we report on... 
Myxococcales - chemistry | Biological Products - chemistry | Biological Products - pharmacology | Molecular Structure | Biological Products - isolation & purification
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13. Full Text Biosynthesis and Total Synthesis of Pyrronazol B: a Secondary Metabolite from Nannocystis pusilla
by Witte, Swjatoslaw N. R and Hug, Joachim J and Géraldy, Magalie N. E and Müller, Rolf and Kalesse, Markus
Chemistry – A European Journal, ISSN 0947-6539, 11/2017, Volume 23, Issue 63, pp. 15917 - 15921
The first stereoselective total synthesis of the natural product pyrronazol B, which contains a chlorinated pyrrole–oxazole–pyrone framework, has been... 
deprotection | pyrronazol | biosynthetic gene cluster | total synthesis | DOMAIN | NATURAL-PRODUCTS | POLYKETIDE SYNTHASES | CHEMISTRY, MULTIDISCIPLINARY | STRUCTURE ELUCIDATION | Pyrroles - metabolism | Multigene Family | Myxococcales - genetics | Oxazoles - metabolism | Models, Molecular | Myxococcales - metabolism | Oxazoles - chemistry | Myxococcales - chemistry | Biological Products - chemical synthesis | Biological Products - chemistry | Oxazoles - chemical synthesis | Pyrones - chemistry | Biosynthetic Pathways - genetics | Pyrroles - chemical synthesis | Biological Products - metabolism | Pyrroles - chemistry | Pyrones - metabolism | Pyrones - chemical synthesis | Synthesis | Metabolites | Oxazoles | Genomics | Physiological aspects | Proline | Biosynthesis | Organic compounds | Serine | Stable isotopes | Oxazole | Methionine | L-Serine | Genomes | Isotopes | L-Proline | Gene sequencing
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14. Full Text Highly Efficient CYP167A1 (EpoK) dependent Epothilone B Formation and Production of 7-Ketone Epothilone D as a New Epothilone Derivative
by Kern, Fredy and Dier, Tobias K. F and Khatri, Yogan and Ewen, Kerstin M and Jacquot, Jean-Pierre and Volmer, Dietrich A and Bernhardt, Rita
Scientific Reports, ISSN 2045-2322, 10/2015, Volume 5, Issue 1, p. 14881
Since their discovery in the soil bacterium Sorangium cellulosum, epothilones have emerged as a valuable substance class with promising anti-tumor activity.... 
MICROTUBULE-STABILIZING AGENTS | BIOSYNTHETIC GENE-CLUSTER | ELECTRON-TRANSFER | ADRENODOXIN REDUCTASE | SORANGIUM-CELLULOSUM | MULTIDISCIPLINARY SCIENCES | ESCHERICHIA-COLI | CHLAMYDOMONAS-REINHARDTII FERREDOXIN | HETEROLOGOUS EXPRESSION | CE56 | CYTOTOXIC ACTIVITY | Electron Transport | Ferredoxins - genetics | Epothilones - chemistry | Bacterial Proteins - chemistry | Ferredoxins - chemistry | Cytochrome P-450 Enzyme System - metabolism | Phylogeny | Antineoplastic Agents - metabolism | Cloning, Molecular | Escherichia coli - metabolism | Protein Engineering | Recombinant Proteins - metabolism | Gene Expression | Biocatalysis | Epothilones - biosynthesis | Oxidation-Reduction | Ferredoxins - metabolism | Bacterial Proteins - genetics | Recombinant Proteins - chemistry | Recombinant Proteins - genetics | Antineoplastic Agents - chemistry | Myxococcales - chemistry | Cytochrome P-450 Enzyme System - chemistry | Escherichia coli - genetics | Myxococcales - enzymology | Ketones - chemistry | Cytochrome P-450 Enzyme System - genetics | Bacterial Proteins - metabolism | Ketones - metabolism | Electrons | Protein engineering | Antitumor agents | Soil microorganisms | Neurodegenerative diseases | Ketones | Cytochrome P450 | Epoxidation | Drug development | Cancer | Life Sciences
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15. Full Text Enantioselective Synthesis of (+)-Crocacin C. An Example of a Highly Challenging Mismatched Double Asymmetric δ-Stannylcrotylboration Reaction
by Chen, Ming and Roush, William R
Organic Letters, ISSN 1523-7060, 04/2012, Volume 14, Issue 7, pp. 1880 - 1883
A concise, enantioselective synthesis of (+)-crocacin C is described, featuring a highly diastereoselective mismatched double asymmetric... 
Myxococcales - chemistry | Alkenes - chemistry | Tin - chemistry | Amides - chemical synthesis | Stereoisomerism | Amides - chemistry | Organometallic Compounds - chemistry | Molecular Structure | Alkenes - chemical synthesis | Aldehydes - chemistry
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16. Full Text Synthesis of pretubulysin-derivatives via the TubUgi-approach
by Hoffmann, Judith and Gorges, Jan and Junk, Lukas and Kazmaier, Uli
Organic & biomolecular chemistry, ISSN 1477-0520, 06/2015, Volume 13, Issue 21, pp. 6010 - 6020
The Ugi reaction is found to be a very powerful tool for the synthesis of (pre)tubulysin derivatives, allowing the introduction of various functionalized side... 
Myxococcales - chemistry | Ethers - chemical synthesis | Oligopeptides - chemical synthesis | Alkynes - chemical synthesis | Cyclization | Click Chemistry | Ethers - chemistry | Alkynes - chemistry | Oligopeptides - chemistry
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17. Full Text Isolation of Coralmycins A and B, Potent Anti-Gram Negative Compounds from the Myxobacteria Corallococcus coralloides M23
by Kim, Yu Jin and Kim, Hyun-Ju and Kim, Geon-Woo and Cho, Kyungyun and Takahashi, Shunya and Koshino, Hiroyuki and Kim, Won-Gon
Journal of Natural Products, ISSN 0163-3864, 09/2016, Volume 79, Issue 9, pp. 2223 - 2228
Two new potent anti-Gram negative compounds, coralmycins A (1) and B (2), were isolated from cultures of the myxobacteria Corallococcus coralloides M23,... 
AMERICA | IMPACT | CHEMISTRY, MEDICINAL | NO ESKAPE | PHARMACOLOGY & PHARMACY | UPDATE | BACILLI | INFECTIOUS-DISEASES SOCIETY | PLANT SCIENCES | Klebsiella pneumoniae - drug effects | Escherichia coli - drug effects | Humans | Nitro Compounds - chemistry | Depsipeptides - isolation & purification | Depsipeptides - pharmacology | Structure-Activity Relationship | Anti-Bacterial Agents - isolation & purification | Pseudomonas aeruginosa - drug effects | Hep G2 Cells | Microbial Sensitivity Tests | Myxococcales - chemistry | Asparagine - analogs & derivatives | Anti-Bacterial Agents - chemistry | Nuclear Magnetic Resonance, Biomolecular | Anti-Bacterial Agents - pharmacology | Molecular Structure | Aspartic Acid - analogs & derivatives | Aspartic Acid - chemistry | Depsipeptides - chemistry | Asparagine - chemistry
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