نتائج البحث - "Marcos V.A.S. Navarro"

1

Membrane fluidity adjusts the insertion of the transacylase PlsX to regulate phospholipid biosynthesis in Gram-positive bacteria

المؤلفون: Diego de Mendoza, Beatriz Trastoy, Javier O. Cifuente, Frederico J. Gueiros-Filho, Marcos V.A.S. Navarro, Luis G.M. Basso, Xabier Contreras, Diego E. Sastre, Marcelo E. Guerin

المصدر: J Biol Chem
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70c1b9d6e30b1a5b672186c1af785018
https://doi.org/10.1074/jbc.ra119.011122

2

The phosphatidic acid pathway enzyme PlsX plays both catalytic and channeling roles in bacterial phospholipid synthesis

المؤلفون: Frederico J. Gueiros-Filho, Caterina G. C. M. Netto, Diego E. Sastre, Diego de Mendoza, Marcos V.A.S. Navarro, Luis G.M. Basso, Jhonathan S. Benites Pariente, Daniela Albanesi, André A. Pulschen, Federico Machinandiarena

المصدر: J Biol Chem
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6585af2c5badec3e7ae599a4bd8f59b4
https://pubmed.ncbi.nlm.nih.gov/31919098

3

Filaments and fingers: Novel structural aspects of the single septin from Chlamydomonas reinhardtii

المؤلفون: Andressa Patrícia Alves Pinto, Marcos V.A.S. Navarro, Frederico Moraes Ferreira, Ricardo DeMarco, Cristina Risi, Ana Paula Ulian de Araújo, Heloisa Ciol, Richard Charles Garratt, José Brandão-Neto, Ana Eliza Zeraik, Humberto M. Pereira, Vitold E. Galkin

المصدر: Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64ba5229787c33a4b8bc734f0e3ec847
https://doi.org/10.1074/jbc.m116.762229

4

Identification of Anti-Inflammatory and Anti-Hypertensive Drugs as Inhibitors of Bacterial Diguanylate Cyclases

المؤلفون: Marcos V.A.S. Navarro, Éverton E. D. Silva, H.J. Wiggers, N. U. Torres, Juliana Cheleski, Edson Crusca

المصدر: Journal of the Brazilian Chemical Society v.29 n.2 2018
Journal of the Brazilian Chemical Society
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP

وصف الملف: text/html

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fadb86e7e96cf3834ce7a4a529369b38
https://doi.org/10.21577/0103-5053.20170141

5

Isothermal Titration Calorimetry to Determine Apparent Dissociation Constants (K d) and Stoichiometry of Interaction (n) of C-di-GMP Binding Proteins

المؤلفون: Bruno Y. Matsuyama, Marcos V.A.S. Navarro, Petya V. Krasteva

المصدر: c-di-GMP Signaling ISBN: 9781493972395

مصطلحات موضوعية: 0301 basic medicine, Chemistry, Intermolecular force, Enthalpy, Isothermal titration calorimetry, 3. Good health, Gibbs free energy, Dissociation constant, 03 medical and health sciences, symbols.namesake, 030104 developmental biology, 0302 clinical medicine, symbols, Physical chemistry, Molecule, Titration, 030217 neurology & neurosurgery, Stoichiometry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::cbfc603a581280adca0caa1590063871
https://doi.org/10.1007/978-1-4939-7240-1_30

6

Mechanistic insights into c-di-GMP-dependent control of the biofilm regulator FleQ from Pseudomonas aeruginosa

المؤلفون: Petya V. Krasteva, Claudine Baraquet, Marcos V.A.S. Navarro, Bruno Y. Matsuyama, Holger Sondermann, Caroline S. Harwood

المساهمون: Instituto de Física de São Carlos (IFSC-USP), Universidade de São Paulo (USP), Biologie Structurale de la Sécrétion Bactérienne, Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS), Cornell University [New York], University of Washington [Seattle], Universidade de São Paulo = University of São Paulo (USP), Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS), Part of this work is based upon research conducted at the Cornell High Energy Synchrotron Source (CHESS), which is supported by the National Science Foundation (NSF) under award DMR-1332208, using the Macromolecular Diffraction at CHESS (MacCHESS) facility, which is supported by award GM-103485 from the National Institute of General Medical Sciences, National Institutes of Health (NIH). The Northeastern Collaborative Access Team beamlines are funded by National Institute of General Medical Sciences/NIH under Award P41-GM103403. This research used resources of the Brazilian National Synchrotron Light Source (LNLS) and the Advanced Photon Source, a US Department of Energy Office of Science User Facility operated for the Department of Energy Office of Science by Argonne National Laboratory under Contract DE-AC02-06CH11357. P.V.K. is currently supported by the European Research Council. Our work was supported by Fundaçao de Amparo à Pesquisa do Estado de Sao Paulo under Grant 2009/13238-0 (to M.V.A.S.N.) and Fundaçao de Amparo à Pesquisa do Estado de Sao Paulo Fellowship 2011/24168-2 (to B.Y.M.), and by the NIH under Grants R01-AI097307 (to H.S.) and R01-GM56665 (to C.S.H.)., We thank Rémi Fronzes for providing access to electron microscopy data collection and analysis software, and João Muniz and Raj Rajashankar for collecting diffraction data

المصدر: Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2015, 113, pp.E209-E218. ⟨10.1073/pnas.1523148113⟩
Proceedings of the National Academy of Sciences of the United States of America, 2015, 113 (2), pp.E209-E218. ⟨10.1073/pnas.1523148113⟩

مصطلحات موضوعية: Models, Molecular, 0301 basic medicine, MESH: Protein Structure, Quaternary, Transcription, Genetic, [SDV]Life Sciences [q-bio], ATPase, Amino Acid Motifs, MESH: Amino Acid Sequence, MESH: Base Sequence, Crystallography, X-Ray, Conserved sequence, MESH: Amino Acid Motifs, MESH: Mutant Proteins, MESH: Protein Structure, Tertiary, MESH: Cyclic GMP, flagella structure, Promoter Regions, Genetic, MESH: Bacterial Proteins, Cyclic GMP, Conserved Sequence, ComputingMilieux_MISCELLANEOUS, MESH: Gene Expression Regulation, Bacterial, MESH: Conserved Sequence, Multidisciplinary, MESH: Protein Multimerization, Protein Stability, Effector, Temperature, MESH: Temperature, Cell biology, Solutions, MESH: Mutagenesis, Site-Directed, Cross-Linking Reagents, PNAS Plus, Biochemistry, MESH: Pseudomonas aeruginosa, Pseudomonas aeruginosa, flagella, MESH: Models, Molecular, Intracellular, DNA, Bacterial, MESH: Trans-Activators, MESH: Cross-Linking Reagents, Molecular Sequence Data, MESH: Sequence Alignment, enhancer binding protein, Sequence alignment, MESH: Biofilms, MESH: Solutions, Calorimetry, Biology, 03 medical and health sciences, Bacterial Proteins, MESH: Protein Stability, MESH: Promoter Regions, Genetic, structure, Amino Acid Sequence, Binding site, MESH: Calorimetry, Protein Structure, Quaternary, MESH: Molecular Sequence Data, Binding Sites, Base Sequence, MESH: Transcription, Genetic, Biofilm, Gene Expression Regulation, Bacterial, MESH: Crystallography, X-Ray, PROTEÍNAS, MESH: DNA, Bacterial, Protein Structure, Tertiary, A-site, 030104 developmental biology, MESH: Binding Sites, Biofilms, gene expression, Mutagenesis, Site-Directed, Trans-Activators, biology.protein, Mutant Proteins, Protein Multimerization, Sequence Alignment