Gotowa bibliografia na temat „Amas hydrophobes”
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Artykuły w czasopismach na temat "Amas hydrophobes"
Lim, San Sui, Cael O. Debono, Christopher A. MacRaild, Indu R. Chandrashekaran, Olan Dolezal, Robin F. Anders, Jamie S. Simpson i in. "Development of Inhibitors of Plasmodium falciparum Apical Membrane Antigen 1 Based on Fragment Screening". Australian Journal of Chemistry 66, nr 12 (2013): 1530. http://dx.doi.org/10.1071/ch13266.
Pełny tekst źródłaAlam, Asrar. "Bioinformatic Identification of Peptidomimetic-Based Inhibitors against Plasmodium falciparum Antigen AMA1". Malaria Research and Treatment 2014 (18.12.2014): 1–8. http://dx.doi.org/10.1155/2014/642391.
Pełny tekst źródłaHenderson, Kylie A., Victor A. Streltsov, Andrew M. Coley, Olan Dolezal, Peter J. Hudson, Adrian H. Batchelor, Aditi Gupta i in. "Structure of an IgNAR-AMA1 Complex: Targeting a Conserved Hydrophobic Cleft Broadens Malarial Strain Recognition". Structure 15, nr 11 (listopad 2007): 1452–66. http://dx.doi.org/10.1016/j.str.2007.09.011.
Pełny tekst źródłaHarris, Karen S., Joanne L. Casey, Andrew M. Coley, Rosella Masciantonio, Jennifer K. Sabo, David W. Keizer, Erinna F. Lee i in. "Binding Hot Spot for Invasion Inhibitory Molecules on Plasmodium falciparum Apical Membrane Antigen 1". Infection and Immunity 73, nr 10 (październik 2005): 6981–89. http://dx.doi.org/10.1128/iai.73.10.6981-6989.2005.
Pełny tekst źródłaBai, T., M. Becker, A. Gupta, P. Strike, V. J. Murphy, R. F. Anders i A. H. Batchelor. "Structure of AMA1 from Plasmodium falciparum reveals a clustering of polymorphisms that surround a conserved hydrophobic pocket". Proceedings of the National Academy of Sciences 102, nr 36 (29.08.2005): 12736–41. http://dx.doi.org/10.1073/pnas.0501808102.
Pełny tekst źródłaKatsarou, Erasmia, Costas Charalambopoulos i Nick Hadjiliadis. "Ternary Complexes of cis-(NH3)2PtCl2 (cis-DDP) With Guanosine (guo), Cytidine (cyd) and the Aminoacids Glycine (gly), L-Alanine (ala), L-2-Aminobutyric Acid (2-aba), L-Norvaline (nval) and L-Norleucine (nleu)". Metal-Based Drugs 4, nr 2 (1.01.1997): 57–63. http://dx.doi.org/10.1155/mbd.1997.57.
Pełny tekst źródłaVetrivel, Umashankar, Shalini Muralikumar, B. Mahalakshmi, K. Lily Therese, HN Madhavan, Mohamed Alameen i Indhuja Thirumudi. "Multilevel Precision-Based Rational Design of Chemical Inhibitors Targeting the Hydrophobic Cleft ofToxoplasma gondiiApical Membrane Antigen 1 (AMA1)". Genomics & Informatics 14, nr 2 (2016): 53. http://dx.doi.org/10.5808/gi.2016.14.2.53.
Pełny tekst źródłaHariyanti, Hariyanti, Kusmadi Kurmardi, Arry Yanuar i Hayun Hayun. "Ligand Based Pharmacophore Modeling, Virtual Screening, and Molecular Docking Studies of Asymmetrical Hexahydro-2H-Indazole Analogs of Curcumin (AIACs) to Discover Novel Estrogen Receptors Alpha (ERα) Inhibitor". Indonesian Journal of Chemistry 21, nr 1 (26.11.2020): 137. http://dx.doi.org/10.22146/ijc.54745.
Pełny tekst źródłaMoentamaria, Dwina, Zakijah Irfin, Achmad Chumaidi i Heri Septya Kusuma. "Hydrophobic Support: A Phenomenon of Interface Lipase Activation in Polyurethane Foam as a Heterogeneous Biocatalyst in Synthesis of Natural Flavor Ester". Jurnal Teknik Kimia dan Lingkungan 6, nr 1 (30.04.2022): 27. http://dx.doi.org/10.33795/jtkl.v6i1.253.
Pełny tekst źródłaFathanah, Umi, Fachrul Razi, Mirna Rahmah Lubis, Mukramah Yusuf, Yanna Syamsuddin, Hesti Meilina, Syawaliah Muchtar, Suraiya Kamaruzzaman i Aula Khairunnisa. "Modifikasi Membran Polyethersulfone dengan Penambahan Nanopartikel Mg(OH)2 dalam Pelarut Dimethyl Sulfoxide". ALCHEMY Jurnal Penelitian Kimia 18, nr 2 (4.09.2022): 165. http://dx.doi.org/10.20961/alchemy.18.2.58248.165-173.
Pełny tekst źródłaRozprawy doktorskie na temat "Amas hydrophobes"
CANARD, LUC. "Analyse statistique des amas hydrophobes hca contenus dans les banques de sequences de proteines". Paris 6, 1997. http://www.theses.fr/1997PA066627.
Pełny tekst źródłaDulin, Fabienne. "Exploration des caractéristiques tridimensionnelles des amas protéiques hydrophobes issus du formalisme "Hydrophobic Cluster Analysis" (HCA) : modélisation de formes oligomériques solubles du peptide Aβ impliqué dans la maladie d'Alzheimer, et identification d'un 'point chaud" commun à différentes protéines amyloïdes". Paris 6, 2006. http://www.theses.fr/2006PA066465.
Pełny tekst źródłaBruley, Apolline. "Exploitation de signatures des repliements protéiques pour décrire le continuum ordre/désordre au sein des protéomes". Electronic Thesis or Diss., Sorbonne université, 2022. http://www.theses.fr/2022SORUS474.
Pełny tekst źródłaA significant fraction of the proteomes remains unannotated, leaving inaccessible a part of the functional repertoire of life, including molecular innovations with therapeutic or environmental value. Lack of functional annotation is partly due to the limitations of the current approaches in detecting hidden relationships, or to specific features such as disorder. The aim of my PhD thesis was to develop methodological approaches based on the structural signatures of folded domains, in order to further characterize the protein sequences with unknown function even in absence of evolutionary information. First, I developed a scoring system in order to estimate the foldability potential of an amino acid sequence, based on its density in hydrophobic clusters, which mainly correspond to regular secondary structures. I disentangled the continuum between order and disorder, covering various states from extended conformations (random coils) to molten globules and characterize cases of conditional order. Next, I combined this scoring system with the AlphaFold2 (AF2) 3D structure predictions available for 21 reference proteomes. A large fraction of the amino acids with very low AF2 model confidence are included in non-foldable segments, supporting the quality of AF2 as a predictor of disorder. However, within each proteome, long segments with very low AF2 model confidence also exhibit characteristics of soluble, folded domains. This suggests hidden order (conditional or unconditional), which is undetected by AF2 due to lack of evolutionary information, or unrecorded folding patterns. Finally, using these tools, I made a preliminary exploration of unannotated proteins or regions, identified through the development and application of a new annotation workflow. Even though these sequences are enriched in disorder, an important part of them showcases soluble globular-like characteristics. These would make good candidates for further experimental validation and characterization. Moreover, the analysis of experimentally validated de novo genes allowed me to contribute to the still-open debate on the structural features of proteins encoded by these genes, enriched in disorder and displaying a great diversity of structura
Części książek na temat "Amas hydrophobes"
Dey Sarkar, Sovik, i Chirantan Kar. "Cationic Amphiphiles as Antimicrobial Agents". W Recent Trends and The Future of Antimicrobial Agents - Part 2, 54–75. BENTHAM SCIENCE PUBLISHERS, 2023. http://dx.doi.org/10.2174/9789815123975123010006.
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