Добірка наукової літератури з теми "Β-strand"
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Статті в журналах з теми "Β-strand"
Zhang, Ning, Shan Gao, Lei Zhang, Jishou Ruan та Tao Zhang. "Statistical Analysis of Terminal Extensions of Protein β-Strand Pairs". Advances in Bioinformatics 2013 (28 січня 2013): 1–7. http://dx.doi.org/10.1155/2013/909436.
Повний текст джерелаKEDARISETTI, KANAKA DURGA, MARCIN J. MIZIANTY, SCOTT DICK, and LUKASZ KURGAN. "IMPROVED SEQUENCE-BASED PREDICTION OF STRAND RESIDUES." Journal of Bioinformatics and Computational Biology 09, no. 01 (February 2011): 67–89. http://dx.doi.org/10.1142/s0219720011005355.
Повний текст джерелаTerwilliger, Thomas C. "Rapid model building of β-sheets in electron-density maps". Acta Crystallographica Section D Biological Crystallography 66, № 3 (12 лютого 2010): 276–84. http://dx.doi.org/10.1107/s0907444910000302.
Повний текст джерелаVischer, Henry F., Joke C. M. Granneman, and Jan Bogerd. "Opposite Contribution of Two Ligand-Selective Determinants in the N-Terminal Hormone-Binding Exodomain of Human Gonadotropin Receptors." Molecular Endocrinology 17, no. 10 (October 1, 2003): 1972–81. http://dx.doi.org/10.1210/me.2003-0172.
Повний текст джерелаGao, Yang, Yanxiang Cui, Tara Fox, Shiqiang Lin, Huaibin Wang, Natalia de Val, Z. Hong Zhou, and Wei Yang. "Structures and operating principles of the replisome." Science 363, no. 6429 (January 24, 2019): eaav7003. http://dx.doi.org/10.1126/science.aav7003.
Повний текст джерелаHaworth, Naomi L., та Merridee A. Wouters. "Between-strand disulfides: forbidden disulfides linking adjacent β-strands". RSC Advances 3, № 46 (2013): 24680. http://dx.doi.org/10.1039/c3ra42486c.
Повний текст джерелаHAWORTH, NAOMI L., LINA L. FENG, and MERRIDEE A. WOUTERS. "HIGH TORSIONAL ENERGY DISULFIDES: RELATIONSHIP BETWEEN CROSS-STRAND DISULFIDES AND RIGHT-HANDED STAPLES." Journal of Bioinformatics and Computational Biology 04, no. 01 (February 2006): 155–68. http://dx.doi.org/10.1142/s0219720006001734.
Повний текст джерелаVischer, Henry F., Joke C. M. Granneman та Jan Bogerd. "Identification of Follicle-Stimulating Hormone-Selective β-Strands in the N-Terminal Hormone-Binding Exodomain of Human Gonadotropin Receptors". Molecular Endocrinology 20, № 8 (1 серпня 2006): 1880–93. http://dx.doi.org/10.1210/me.2005-0202.
Повний текст джерелаChandrasekhar, Srivari, Ambadi Sudhakar, Marelli Udaya Kiran, Bathini Nagendra Babu та Bharatam Jagadeesh. "β-Strand mimetics: formation of bend-strands in oligomers of enantiomeric β-amino acids". Tetrahedron Letters 49, № 52 (грудень 2008): 7368–71. http://dx.doi.org/10.1016/j.tetlet.2008.10.031.
Повний текст джерелаTsai, James H., Amy Sue Waldman та James S. Nowick. "Two New β-strand Mimics". Bioorganic & Medicinal Chemistry 7, № 1 (січень 1999): 29–38. http://dx.doi.org/10.1016/s0968-0896(98)00225-9.
Повний текст джерелаДисертації з теми "Β-strand"
Chen, Hongyuan. "Development of macrocyclic β-strand calpain cysteine protease inhibitors". Thesis, University of Canterbury. Chemistry, 2011. http://hdl.handle.net/10092/5582.
Повний текст джерелаAitken, Steven Geoffrey. "Design, synthesis and testing of β-strand mimics as protease inhibitors". Thesis, University of Canterbury. Chemistry, 2006. http://hdl.handle.net/10092/1984.
Повний текст джерелаLutz, Henrik [Verfasser], Bodo [Akademischer Betreuer] Laube та Gerhard [Akademischer Betreuer] Thiel. "Identification and impact of Topoisomerase II β induced DNA double-strand breaks in Glioblastoma multiforme: NMDA-receptor signaling pathway as target structure / Henrik Lutz ; Bodo Laube, Gerhard Thiel". Darmstadt : Universitäts- und Landesbibliothek Darmstadt, 2019. http://d-nb.info/1193177863/34.
Повний текст джерелаGanai, Rais Ahmad. "Structural and biochemical basis for the high fidelity and processivity of DNA polymerase ε". Doctoral thesis, Umeå universitet, Institutionen för medicinsk kemi och biofysik, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-97689.
Повний текст джерелаBlomberg, David. "Synthesis of β-turn and pyridine based peptidomimetics". Doctoral thesis, Umeå universitet, Kemi, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-1104.
Повний текст джерелаBose, Anindita. "Modulation of glycogen synthase kinase 3β (GSK3 β) activation and tau phosphorylation by double stranded RNA dependent protein kinase (PKR]". Paris 7, 2010. http://www.theses.fr/2010PA077049.
Повний текст джерелаPKR or double-stranded RNA dependent kinase is a pro-apoptotic kinase that controls protein translation. Previous studies revealed that activated PKR is increased in AD brains. Glycogen Synthase Kinase Aβ(CS K3β) is responsible for tau phosphorylation and PKR can indirectly activate GSK3β in cell cultures. The goal of this work was to détermine if PKR could simultaneously trigger GSK3J5 activation and tau phosphorylation and apoptosis. In AD brains, both activated kinases co-localized with phosphorylated tau in neurons. In SH-SY5Y cell cultures, tunicamycin and Api_42 activate PKR, GSK3β and induce tau phosphorylation which are both attenuated by PKR inhibitors or PKR siRNA. Our results demonstrate that PKR is able to modulate GSK3β activation, tau phosphorylation and apoptosis in neuroblastoma cells exposed to tunicamycin or Aβ PKR could represent a potent pharmacological target to attenuate neurodegeneration and tau phosphorylation
Gholami, Sara [Verfasser]. "Association of neighboring β-Strands to form the β-barrel structure of the voltage-dependent anion channel, human isoform 1 (hVDAC1) precedes membrane insertion and is largely driven by polar interactions between basic and acidic amino acid side-chains / Sara Gholami". Kassel : Universitätsbibliothek Kassel, 2020. http://d-nb.info/1232431893/34.
Повний текст джерелаPehere, Ashok D. "New peptide-based templates constrained into a β-strand by Huisgen cycloaddition". Thesis, 2012. http://hdl.handle.net/2440/87372.
Повний текст джерелаThesis (Ph.D.) -- University of Adelaide, School of Chemistry and Physics, 2012
Jones, Seth Adam. "β-strand mimicry as the basis for a universal approach to protease inhibition". Thesis, 2011. http://hdl.handle.net/2440/72156.
Повний текст джерелаThesis (Ph.D.) -- University of Adelaide, School of Chemistry and Physics, 2011
Lord, Rianne M., A. J. Hebden, C. M. Pask, I. R. Henderson, Simon J. Allison, S. L. Shepherd, Roger M. Phillips та P. C. McGowan. "Hypoxia-Sensitive Metal β‑Ketoiminato Complexes Showing Induced Single-Strand DNA Breaks and Cancer Cell Death by Apoptosis". 2015. http://hdl.handle.net/10454/9491.
Повний текст джерелаA series of ruthenium and iridium complexes have been synthesized and characterized with 20 novel crystal structures discussed. The library of β-ketoiminato complexes has been shown to be active against MCF-7 (human breast carcinoma), HT-29 (human colon carcinoma), A2780 (human ovarian carcinoma), and A2780cis (cisplatin-resistant human ovarian carcinoma) cell lines, with selected complexes’ being more than three times as active as cisplatin against the A2780cis cell line. Selected complexes were also tested against the noncancerous ARPE-19 (retinal pigment epithelial cells) cell line, in order to evaluate the complexes selectivity for cancer cells. Complexes have also been shown to be highly active under hypoxic conditions, with the activities of some complexes increasing with a decrease in O2 concentration. The enzyme thioredoxin reductase is overexpressed in cancer cells, and complexes reported herein have the advantage of inhibiting this enzyme, with IC50 values measured in the nanomolar range. The anticancer activity of these complexes was further investigated to determine whether activity is due to effects on cellular growth or cell survival. The complexes were found to induce significant levels of cancer cell death by apoptosis with levels induced correlating closely with activity in chemosensitivity studies. As a possible cause of cell death, the ability of the complexes to induce damage to cellular DNA was also assessed. The complexes failed to induce double-strand DNA breaks or DNA cross-linking but induced significant levels of single-strand DNA breaks, indicating a mechanism of action different from that of cisplatin.
Lord RM, Hebden AJ, Pask CM, Henderson IR, Allison SJ, Shepherd SL, Phillips RM, McGowan PC
Книги з теми "Β-strand"
Herwig, Sascha. β-Strang-Ausbildung eines Faltungsintermediates von BamA. Wiesbaden: Springer Fachmedien Wiesbaden, 2020. http://dx.doi.org/10.1007/978-3-658-29029-0.
Повний текст джерелаHerwig, Sascha. β-Strang-Ausbildung eines Faltungsintermediates von BamA: Adsorption an Lipidmembranen induziert lokale Sekundärstruktur in β-Strang 9. Springer Spektrum, 2020.
Знайти повний текст джерелаЧастини книг з теми "Β-strand"
Loughlin, Wendy A., and David P. Fairlie. "Recent Advances in β-Strand Mimetics." In Amino Acids, Peptides and Proteins in Organic Chemistry, 129–47. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527631827.ch3.
Повний текст джерелаDel Valle, Juan R. "Heterocyclic Extended Peptide Surrogates for β-Strand Stabilization." In Topics in Heterocyclic Chemistry, 25–49. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/7081_2015_163.
Повний текст джерелаPehere, Ashok D., and Andrew D. Abell. "Macrocyclic Protease Inhibitors Constrained into a β-Strand Geometry." In Proteases in Health and Disease, 181–92. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-9233-7_11.
Повний текст джерелаChoi, Yoonjoo. "Computational Identification and Design of Complementary β-Strand Sequences." In Methods in Molecular Biology, 83–94. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-1855-4_4.
Повний текст джерелаBionda, Nina, and Rudi Fasan. "Peptidomimetics of α-Helical and β-Strand Protein Binding Epitopes." In Small Molecule Medicinal Chemistry, 431–64. Hoboken, NJ: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118771723.ch15.
Повний текст джерелаHuggins, Kelly N., and Niels H. Andersen. "Quantitating Amino Acid β-Strand Preferences, Turn Propensities and Cross-Strand Interactions in a Designed Hairpin Peptide." In Advances in Experimental Medicine and Biology, 71–72. New York, NY: Springer New York, 2009. http://dx.doi.org/10.1007/978-0-387-73657-0_31.
Повний текст джерелаUrban, Jan, Hiroshi Nakanishi, Cyprian O. Ogbu, Geoffrey Kozu, Kenneth Farber, Polina Kazavchinskaya, and Min S. Lee. "Bicyclic β-Strand Templates: Epimerization and Biological Activity of Non-Electrophilic Serine Protease Inhibitors." In Peptides: The Wave of the Future, 634–35. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-0464-0_295.
Повний текст джерелаHerwig, Sascha. "Einleitung". У β-Strang-Ausbildung eines Faltungsintermediates von BamA, 1–18. Wiesbaden: Springer Fachmedien Wiesbaden, 2020. http://dx.doi.org/10.1007/978-3-658-29029-0_1.
Повний текст джерелаHerwig, Sascha. "Material und Methoden". У β-Strang-Ausbildung eines Faltungsintermediates von BamA, 19–28. Wiesbaden: Springer Fachmedien Wiesbaden, 2020. http://dx.doi.org/10.1007/978-3-658-29029-0_2.
Повний текст джерелаHerwig, Sascha. "Ergebnisse". У β-Strang-Ausbildung eines Faltungsintermediates von BamA, 29–43. Wiesbaden: Springer Fachmedien Wiesbaden, 2020. http://dx.doi.org/10.1007/978-3-658-29029-0_3.
Повний текст джерелаТези доповідей конференцій з теми "Β-strand"
Seo, Yuji, Keita Yoshizaki, Keisuke Tamari, Yutaka Takahashi, Keisuke Otani, Masahiko Koizumi та Kazuhiko Ogawa. "Abstract 5205: Poly(ADP-ribose) polymerase inhibitors induce β-radiosensitization through an altered selection of DNA double-strand break repair pathways". У Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-5205.
Повний текст джерелаHwang, Wonmuk, and Matthew J. Lang. "Mechanism of Force Generation in Kinesin Motility." In ASME 2007 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2007. http://dx.doi.org/10.1115/sbc2007-175543.
Повний текст джерелаREVA, BORIS, та SID TOPIOL. "RECOGNITION OF PROTEIN STRUCTURE: DETERMINING THE RELATIVE ENERGETIC CONTRIBUTIONS OF β-STRANDS, α-HELICES AND LOOPS". У Proceedings of the Pacific Symposium. WORLD SCIENTIFIC, 1999. http://dx.doi.org/10.1142/9789814447331_0016.
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