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Artykuły w czasopismach na temat "Hexameric proteins"
Skálová, Tereza, Jan Bláha, Karl Harlos, Jarmila Dušková, Tomáš Koval', Jan Stránský, Jindřich Hašek, Ondřej Vaněk i Jan Dohnálek. "Four crystal structures of human LLT1, a ligand of human NKR-P1, in varied glycosylation and oligomerization states". Acta Crystallographica Section D Biological Crystallography 71, nr 3 (26.02.2015): 578–91. http://dx.doi.org/10.1107/s1399004714027928.
Pełny tekst źródłaJomaa, Ahmad, Jack Iwanczyk, Julie Tran i Joaquin Ortega. "Characterization of the Autocleavage Process of the Escherichia coli HtrA Protein: Implications for its Physiological Role". Journal of Bacteriology 191, nr 6 (19.12.2008): 1924–32. http://dx.doi.org/10.1128/jb.01187-08.
Pełny tekst źródłaMyasoedova, Ksenia N., i Natalia N. Magretova. "Cross-Linking Study of Cytochrome P450 1A2 in Proteoliposomes". Bioscience Reports 21, nr 1 (1.02.2001): 63–72. http://dx.doi.org/10.1023/a:1010486118448.
Pełny tekst źródłaChaudhury, Paushali, Chris van der Does i Sonja-Verena Albers. "Characterization of the ATPase FlaI of the motor complex of the Pyrococcus furiosus archaellum and its interactions between the ATP-binding protein FlaH". PeerJ 6 (18.06.2018): e4984. http://dx.doi.org/10.7717/peerj.4984.
Pełny tekst źródłaJomaa, Ahmad, Daniela Damjanovic, Vivian Leong, Rodolfo Ghirlando, Jack Iwanczyk i Joaquin Ortega. "The Inner Cavity of Escherichia coli DegP Protein Is Not Essentialfor Molecular Chaperone and Proteolytic Activity". Journal of Bacteriology 189, nr 3 (22.11.2006): 706–16. http://dx.doi.org/10.1128/jb.01334-06.
Pełny tekst źródłaMiller, Justin M., i Eric J. Enemark. "Archaeal MCM Proteins as an Analog for the Eukaryotic Mcm2–7 Helicase to Reveal Essential Features of Structure and Function". Archaea 2015 (2015): 1–14. http://dx.doi.org/10.1155/2015/305497.
Pełny tekst źródłaSellin, Mikael E., Sonja Stenmark i Martin Gullberg. "Mammalian SEPT9 isoforms direct microtubule-dependent arrangements of septin core heteromers". Molecular Biology of the Cell 23, nr 21 (listopad 2012): 4242–55. http://dx.doi.org/10.1091/mbc.e12-06-0486.
Pełny tekst źródłaZhao, Li, Shuji Kanamaru, Chatree'chalerm Chaidirek i Fumio Arisaka. "P15 and P3, the Tail Completion Proteins of Bacteriophage T4, Both Form Hexameric Rings". Journal of Bacteriology 185, nr 5 (1.03.2003): 1693–700. http://dx.doi.org/10.1128/jb.185.5.1693-1700.2003.
Pełny tekst źródłaOchoa, Jessica M., Oscar Mijares, Andrea A. Acosta, Xavier Escoto, Nancy Leon-Rivera, Joanna D. Marshall, Michael R. Sawaya i Todd O. Yeates. "Structural characterization of hexameric shell proteins from two types of choline-utilization bacterial microcompartments". Acta Crystallographica Section F Structural Biology Communications 77, nr 9 (24.08.2021): 275–85. http://dx.doi.org/10.1107/s2053230x21007470.
Pełny tekst źródłaHeinemann, Udo, Yvette Roske, Anup Arumughan i Erich Wanker. "Remodeling of the AAA+ ATPase p97 by the UBX Adaptor Protein ASPL". Acta Crystallographica Section A Foundations and Advances 70, a1 (5.08.2014): C430. http://dx.doi.org/10.1107/s2053273314095692.
Pełny tekst źródłaRozprawy doktorskie na temat "Hexameric proteins"
Barthe, Lucie. "Les microcompartiments bactériens : étude de l'assemblage des protéines hexamériques des coques et développement d'outils pour les nanotechnologies". Electronic Thesis or Diss., Université de Toulouse (2023-....), 2024. http://www.theses.fr/2024TLSEI002.
Pełny tekst źródłaBacterial microcompartments (BMC) are protein structures, naturally found in some bacteria in which they act as bioreactor and process specific substrates. For instance, depending on the BMC type, the enzymatic set they encapsulate can fixate atmospheric CO2 or catabolize the ethanolamine, 1,2-propanediol or the choline. The BMC shell is polyhedral and is composed of 3 different subunits, including the BMC-H, a protomer associating as an hexamer which are the main and the most diverse shell subunits, in terms of number of homologs within a single BMC operon. Indeed, genomic surveys indicate an average of 3,5 BMC-H homologs per operon, with some organisms like Clostridium saccharolyticum WM1 coding for up to 15 BMC-H split between 3 BMC types.Although it has long been thought that only homo-hexamers existed, it was recently evidenced that hetero-hexamer formation occurred between BMC-H homologs in 2 different β-carboxysome-expressing bacteria. Indeed, numerous BMC-H homologs share a high sequence identity, notably at the intra-hexamer interfaces. Besides paving the way for possible hetero-hexamer formation beyond the β-carboxysome, inside organisms equipped with one BMC type, these recent studies raise the question of possible cross-interactions between BMC-H coming from multiple BMC types.One objective during my PhD thesis was to examine the occurrence of hetero-hexamers in nature. To this end, the tripartite GFP was adapted to study protein-protein interactions among BMC-H and implemented on the case study of Klebsiella pneumonia 342 BMC-H. Of note, this organism is very interesting because it has in its genome 3 BMC loci, comprising a total of 11 BMC-H homologs. Then, besides allowing to determine whether hetero-hexamers do form aside from the β-CBX, in 3 other BMC types, their study would also bring some answer elements to the question of the cross-interactions between BMC-H arising from different BMC types.A novel method to enhance a pathway catalytic efficiency (other than by classical enzymatic engineering) is gaining more and more interests nowadays: enzyme spatial organization. The idea is that, by putting in close proximity or in an arranged fashion the enzymes from a metabolic pathway, one could increase the efficiency of the pathway, through substrate channelling between the different enzymes, for instance, or enzyme clusterisation.The majority of hexamers formed by the BMC-H have the intrinsic property to self-assemble and form higher-ordered macrostructures (nanotubes, Swiss-rolls, 2D sheets) when recombinantly expressed alone in E. coli. This peculiarity has already been exploited in multiple studies to create a protein scaffold for the immobilization of enzymes. In these proof-of-concepts, a sole BMC-H was used to build the scaffold, which would only permit to immobilized different enzymes in a random fashion.Here, we propose to go further with the idea of spatial organization and aimed to elaborate a protein platform starting from an hetero-hexamer. This hetero-hexamer would be composed by 2 up to 6 different BMC-H with each BMC-H constituting an anchoring point for a future enzymatic domain. With such platform, the spatial organization of the enzymes would be more finely controlled which would further enhance the catalysis efficiency of a metabolic pathway.To meet this goal, de novo designed BMC-H were created by 2 collaborator teams of computational design. I studied them and searched for BMC-H couples that would depict orthogonal intra-hexamer interfaces. Indeed, to be able to control precisely the organization onto the platform, this would require to ensure a specific BMC-H order within the hetero-hexamer and thus, tightly control which BMC-H is adjacent to which one and prevent any other association
Valentová, Lucie. "Izolace a stanovení struktur proteinů: hexamerin potemníka Tribolium Castaneum a TmpH fága phi812". Master's thesis, Vysoké učení technické v Brně. Fakulta chemická, 2019. http://www.nusl.cz/ntk/nusl-401898.
Pełny tekst źródłaReddy, Gangadasu E. C. V. Sagar. "Storage and utilization of hexamerin proteins in the pitcher plant mosquito, Wyomyia smithii by Gangadasu E.C.V. Sagar Reddy". Click here to access thesis, 2008. http://www.georgiasouthern.edu/etd/archive/fall2008/gangadasu_s_reddy/reddy_gangadasu_e_200808_ms.pdf.
Pełny tekst źródła"A thesis submitted to the Graduate Faculty of Georgia Southern University in partial fulfillment of the requirements for the degree Master of Science." Directed by William S. Irby. ETD. Includes bibliographical references (p. 42-47) and appendices.
PIROVANO, LAURA. "NUMA:LGN HETERO-HEXAMERS PROMOTE THE ASSEMBLY OF CORTICAL PROTEIN NETWORK TO CONTROL PLANAR CELL DIVISIONS". Doctoral thesis, Università degli Studi di Milano, 2020. http://hdl.handle.net/2434/697169.
Pełny tekst źródłaChakraborti, Srinjoy. "Therapeutic Antibody Against Neisseria gonorrhoeae Lipooligosaccharide, a Phase-variable Virulence Factor". eScholarship@UMMS, 2017. https://escholarship.umassmed.edu/gsbs_diss/905.
Pełny tekst źródłaChakraborti, Srinjoy. "Therapeutic Antibody Against Neisseria gonorrhoeae Lipooligosaccharide, a Phase-variable Virulence Factor". eScholarship@UMMS, 2005. http://escholarship.umassmed.edu/gsbs_diss/905.
Pełny tekst źródłaXue, Yu Lord Susan T. "Study protein-protein interaction in methyl-directed DNA mismatch repair in E. coli exonuclease I Exo I and DNA helicas II UvrD; A minimal exonuclease domain of WRN forms a hexamer on DNA and possesses both 3'-5' exonuclease and 5'-protruding strand endonuclease activities; Solving the structure of the ligand-binding domain of the pregnane-xenobiotic-receptor with 17[beta] estradiol and T1317 /". Chapel Hill, N.C. : University of North Carolina at Chapel Hill, 2008. http://dc.lib.unc.edu/u?/etd,2015.
Pełny tekst źródłaTitle from electronic title page (viewed Feb. 17, 2009). "... in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Department of Chemistry." Discipline: Chemistry; Department/School: Chemistry.
Nagamanju, P. "Hexamerins, their gene and binding protein in rice moth, corcyra cephalonica". Thesis, 2003. http://hdl.handle.net/2009/883.
Pełny tekst źródłaPantakani, Dasaradha Venkata Krishna. "Functional Characterization of Hereditary Spastic Paraplegia Proteins Spastin and ZFYVE27". Doctoral thesis, 2009. http://hdl.handle.net/11858/00-1735-0000-0006-B685-A.
Pełny tekst źródłaPalivec, Vladimír. "Počítačové modelování interakcí iont ů s proteiny: Allosterický efekt iont ů a fenolických ligand ů na strukturu insulinového hexameru". Master's thesis, 2016. http://www.nusl.cz/ntk/nusl-344126.
Pełny tekst źródłaCzęści książek na temat "Hexameric proteins"
Cooke, Roger. "Muscle myosin, skeletal". W Guidebook to the Cytoskeletal and Motor Proteins, 421–24. Oxford University PressOxford, 1999. http://dx.doi.org/10.1093/oso/9780198599579.003.00127.
Pełny tekst źródłaLittlewood, Trevor D., i Gerard I. Evan. "Sequence-specific DNA binding by HLH proteins". W Helix-Loop-Helix Transcription Factors, 36. Oxford University PressOxford, 1998. http://dx.doi.org/10.1093/oso/9780198502487.003.0004.
Pełny tekst źródłaSilva, Jerson L., i Andrea T. Da Poian. "Pressure and Cold Denaturation of Proteins, Protein-DNA Complexes, and Viruses". W High Pressure Effects in Molecular Biophysics and Enzymology. Oxford University Press, 1996. http://dx.doi.org/10.1093/oso/9780195097221.003.0013.
Pełny tekst źródłaRemigante, Alessia, Rossana Morabito, Sara Spinelli, Angela Marino, Silvia Dossena i Michael Pusch. "VRAC Channels and the Cellular Redox Balance". W Human Physiology - Annual Volume 2023 [Working Title]. IntechOpen, 2023. http://dx.doi.org/10.5772/intechopen.109563.
Pełny tekst źródłaCrampton, Donald J., i Charles C. Richardson. "Bacteriophage T7 gene 4 protein: A hexameric DNA helicase". W Energy Coupling and Molecular Motors, 277–302. Elsevier, 2003. http://dx.doi.org/10.1016/s1874-6047(04)80007-6.
Pełny tekst źródłaItsathitphaisarn, Ornchuma, Richard A. Wing, William K. Eliason, Jimin Wang i Thomas A. Steitz. "The Hexameric Helicase DnaB Adopts a Nonplanar Conformation during Translocation". W Structural Insights into Gene Expression and Protein Synthesis, 365–75. WORLD SCIENTIFIC, 2020. http://dx.doi.org/10.1142/9789811215865_0042.
Pełny tekst źródłaDunn, Michael F., Richard Palmieri, Niels C. Kaarsholm, Melinda Roy, Robert W. K. Lee, Zbignew Dauter, Christopher Hill i Guy G. Dodson. "THE 2-ZINC INSULIN HEXAMER IS A CALCIUM-BINDING PROTEIN". W Calcium-Binding Proteins in Health and Disease, 372–83. Elsevier, 1987. http://dx.doi.org/10.1016/b978-0-12-521040-9.50062-0.
Pełny tekst źródłaPapini, E., i J. L. Telford. "Vacuolating cytotoxin (Helicobacter pylori)". W Guidebook to Protein Toxins and Their Use in Cell Biology, 110–11. Oxford University PressOxford, 1997. http://dx.doi.org/10.1093/oso/9780198599555.003.0038.
Pełny tekst źródłaRoy, Melinda, Robert Lee i Michael F. Dunn. "1H FT NMR STUDIES OF THE Co3+-SUBSTITUTED HEXAMER: CHARACTERIZATION OF METAL ION BINDING TO THE GLU(B13) SITE". W Calcium-Binding Proteins in Health and Disease, 424–26. Elsevier, 1987. http://dx.doi.org/10.1016/b978-0-12-521040-9.50076-0.
Pełny tekst źródłaMenestrina, G., i M. Ferreras). "α-Toxin (Staphylococcus aureus)". W Guidebook to Protein Toxins and Their Use in Cell Biology, 10–12. Oxford University PressOxford, 1997. http://dx.doi.org/10.1093/oso/9780198599555.003.0004.
Pełny tekst źródłaStreszczenia konferencji na temat "Hexameric proteins"
Stewart, Ross A., Natalie Tigue, Samantha Ireland, James Hair, Lisa Bamber, Michael Oberst, Rebecca Leyland i in. "Abstract 561: MEDI1873: A novel hexameric GITRL fusion protein with potent agonsitic and immunomodulatory activities in preclinical systems". W Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-561.
Pełny tekst źródłaAndrieux, A., M. H. Charon, G. Hudry-Clergeon i G. Marguerie. "FIBRINOGEN SEQUENCES INTERACTING WITH PLATELET GPIIbIIIa". W XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643519.
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