Relevant bibliographies by topics / Cys-34

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  2. Dissertations / Theses
  3. Conference papers

Academic literature on the topic 'Cys-34'

Author: Grafiati
Published: 4 June 2021
Last updated: 10 March 2023

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Journal articles on the topic "Cys-34"

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Snijder, Eric J., Jessika C. Dobbe, and Willy J. M. Spaan. "Heterodimerization of the Two Major Envelope Proteins Is Essential for Arterivirus Infectivity." Journal of Virology 77, no. 1 (2003): 97–104. http://dx.doi.org/10.1128/jvi.77.1.97-104.2003.

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ABSTRACT The two major envelope proteins of arteriviruses, the membrane protein (M) and the major glycoprotein (GP5), associate into a disulfide-linked heterodimer that is incorporated into the virion and has been assumed to be a prerequisite for virus assembly. Using an equine arteritis virus (EAV) infectious cDNA clone, we have analyzed the requirement for GP5-M heterodimerization and have identified the Cys residues involved in the formation of the GP5-M disulfide bond. The single Cys residue (Cys-8) in the M ectodomain was crucial for heterodimerization and virus infectivity. Mutagenesis o
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Chubarov, Alexey, Anna Spitsyna, Olesya Krumkacheva, et al. "Reversible Dimerization of Human Serum Albumin." Molecules 26, no. 1 (2020): 108. http://dx.doi.org/10.3390/molecules26010108.

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Pulsed Dipolar Spectroscopy (PDS) methods of Electron Paramagnetic Resonance (EPR) were used to detect and characterize reversible non-covalent dimers of Human Serum Albumin (HSA), the most abundant protein in human plasma. The spin labels, MTSL and OX063, were attached to Cys-34 and these chemical modifications of Cys-34 did affect the dimerization of HSA, indicating that other post-translational modifications can modulate dimer formation. At physiologically relevant concentrations, HSA does form weak, non-covalent dimers with a well-defined structure. Dimer formation is readily reversible in
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Witte, M. M., and R. C. Dickson. "The C6 zinc finger and adjacent amino acids determine DNA-binding specificity and affinity in the yeast activator proteins LAC9 and PPR1." Molecular and Cellular Biology 10, no. 10 (1990): 5128–37. http://dx.doi.org/10.1128/mcb.10.10.5128-5137.1990.

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LAC9 is a DNA-binding protein that regulates transcription of the lactose-galactose regulon in Kluyveromyces lactis. The DNA-binding domain is composed of a zinc finger and nearby amino acids (M. M. Witte and R. C. Dickson, Mol. Cell. Biol. 8:3726-3733, 1988). The single zinc finger appears to be structurally related to the zinc finger of many other fungal transcription activator proteins that contain positively charged residues and six conserved cysteines with the general form Cys-Xaa2-Cys-Xaa6-Cys-Xaa6-9-Cys-Xaa2-Cys-Xaa 6-Cys, where Xaan indicates a stretch of the indicated number of any am
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Witte, M. M., and R. C. Dickson. "The C6 zinc finger and adjacent amino acids determine DNA-binding specificity and affinity in the yeast activator proteins LAC9 and PPR1." Molecular and Cellular Biology 10, no. 10 (1990): 5128–37. http://dx.doi.org/10.1128/mcb.10.10.5128.

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LAC9 is a DNA-binding protein that regulates transcription of the lactose-galactose regulon in Kluyveromyces lactis. The DNA-binding domain is composed of a zinc finger and nearby amino acids (M. M. Witte and R. C. Dickson, Mol. Cell. Biol. 8:3726-3733, 1988). The single zinc finger appears to be structurally related to the zinc finger of many other fungal transcription activator proteins that contain positively charged residues and six conserved cysteines with the general form Cys-Xaa2-Cys-Xaa6-Cys-Xaa6-9-Cys-Xaa2-Cys-Xaa 6-Cys, where Xaan indicates a stretch of the indicated number of any am
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Katayama, M., T. Cantley, A. Rieke, and B. Day. "316 SUPPLEMENTAL CYSTEINE PRESENCE DURING THE DECONDENSATION OF SPERM CHROMATIN IMPROVES FERTILIZATION AND BLASTOCYST FORMATION AFTER INTRACYTOPLASMIC SPERM INJECTION IN PIGS." Reproduction, Fertility and Development 17, no. 2 (2005): 308. http://dx.doi.org/10.1071/rdv17n2ab316.

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The effect of a cysteine supplement in culture media for oocytes matured in vitro after intracytoplasmic sperm injection (ICSI) on fertilization and embryo development were examined. In the first experiment, sperm injected oocytes were cultured in NCSU23 (control) or NCSU23 supplemented with 0.57–3.71 mM cysteine (0.57–3.71 Cys) for 12 h after ICSI, and then fixed to observe pronuclear formation. In the second experiment, to examine the appropriate duration time of cysteine supplement to support fertilization, sperm-injected oocytes were transferred into NCSU23 following culture in NCSU23 supp
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Aslan Abadi, Naser, Roghaiyeh Afsargharehbagh, Aliakbar Nasiri, et al. "Assessment of Coronary Slow Flow, Cystatin C, and Body Mass Index in Female Candidates for Diagnostic Coronary Artery Angiography." International Journal of Basic Science in Medicine 5, no. 1 (2020): 4–8. http://dx.doi.org/10.34172/ijbsm.2020.03.

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Introduction: Evidence indicates that the associations between coronary slow flow (CSF), cystatin C (Cys C), and body mass index (BMI) are unclear. Therefore, the purpose of our study was to determine the association among the above-mentioned parameters in female patients. Methods: This was a descriptive-analytical study and the participants were those who were referred to the Shohada Cardiovascular Center of Urmia in 2015-2016. The participants were measured by a quantitative method under angiography (corrected TIMI frame count, CTFC) for CSF assessment, followed by evaluating physiological i
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DONG, Jiaowang, Jang-Su PARK, and Suk-Hee LEE. "In vitro analysis of the zinc-finger motif in human replication protein A." Biochemical Journal 337, no. 2 (1999): 311–17. http://dx.doi.org/10.1042/bj3370311.

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Human replication protein A (RPA) is composed of 70, 34 and 11 kDa subunits (p70, p34 and p11 respectively) and functions in all three major DNA metabolic processes: replication, repair and recombination. Recent deletion analysis demonstrated that the large subunit of RPA, p70, has multiple functional domains, including a DNA polymerase α-stimulation domain and a single-stranded DNA-binding domain. It also contains a putative metal-binding domain of the 4-cysteine type (Cys-Xaa4-Cys-Xaa13-Cys-Xaa2-Cys) that is highly conserved among eukaryotes. To study the role of this domain in DNA metabolis
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Wang, Run, Shiying Sun, Evan J. Bekos, and Frank V. Bright. "Dynamics Surrounding Cys-34 in Native, Chemically Denatured, and Silica-Adsorbed Bovine Serum Albumin." Analytical Chemistry 67, no. 1 (1995): 149–59. http://dx.doi.org/10.1021/ac00097a024.

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Alharthi, Nahed S., Haroon Khan, Fahad Jibran Siyal, et al. "Glutathione, Cysteine, and D-Penicillamine Role in Exchange of Silver Metal from the Albumin Metal Complex." BioMed Research International 2022 (August 8, 2022): 1–10. http://dx.doi.org/10.1155/2022/3619308.

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The purpose of this study is to investigate the exchange reaction taking place among the bovine serum albumin (BSA), 5,5 ′ -dithiobis-(2-nitrobenzoic acid (ESSE), reduced glutathione, N-acetylcysteine, D-penicillamine (thiolates), and silver metal (AgI). For this purpose, stock solutions of BSA and Ellman’s reagent were prepared by dissolving 264 mg of BSA in 5 ml of reaction buffer (0.1 M KH2PO4 at pH 7.8) and 23.8 mg of ESSE in 1.0 ml of reaction buffer which were mixed together. Mixture of BSA-AgI was prepared in a separate procedure by dissolving 0.17 mg of silver nitrate in 1 ml of reacti
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Rakhshandeh, Anoosh, Cornelis F. M. de Lange, John K. Htoo, Abbasali Gheisari, and Amanda R. Rakhshandeh. "Immune system stimulation increases the plasma cysteine flux and whole-body glutathione synthesis rate in starter pigs1." Journal of Animal Science 97, no. 9 (2019): 3871–81. http://dx.doi.org/10.1093/jas/skz211.

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Abstract Glutathione (GSH) is the major intracellular thiol that plays a role in numerous detoxification, bio-reduction, and conjugation reactions. The availability of Cys is thought to be the rate-limiting factor for the synthesis of GSH. The effects of immune system stimulation (ISS) on GSH levels and the GSH synthesis rate in various tissues, as well as the plasma flux of Cys, were measured in starter pigs fed a sulfur AA (SAA; Met + Cys) limiting diet. Ten feed-restricted gilts with initial body weight (BW) of 7.0 ± 0.12 kg were injected i.m. twice at 48-h intervals with either sterile sal
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Dissertations / Theses on the topic "Cys-34"

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Tong, Grace C. "Characterization of Cys-34 in serum albumin." Columbus, Ohio : Ohio State University, 2003. http://rave.ohiolink.edu/etdc/view?acc%5fnum=osu1061473878.

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Thesis (Ph. D.)--Ohio State University, 2003.<br>Title from first page of PDF file. Document formatted into pages; contains xxiii, 325 p.; also contains graphics (some col.). Includes abstract and vita. Advisor: Gary E. Means, Dept. of Biochemistry. Includes bibliographical references (p. 206-225).
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Pancotti, A. "PROTEOMIC APPROACHES IN DRUGS AND BIOMARKERS DISCOVERY." Doctoral thesis, Università degli Studi di Milano, 2013. http://hdl.handle.net/2434/217538.

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DOTTORATO DI RICERCA IN CHIMICA DEL FARMACO (XXV CICLO) Proteomic approaches in Drugs and Biomarkers Discovery Dott. Andrea Pancotti Tutor: Prof. Marina Carini Co-tutor: Prof. Sergio Romeo Abstract My thesis project is focused on development and application of proteomic approaches in two fundamental research areas: the drug discovery process and the discovery of disease biomarkers. In particular, new and reliable strategies by mass spectrometry for the fast identification and validation of drug targets, lead compounds and disease biomarkers have been considered. Proteomic Approache
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Unterer, Bea [Verfasser], and Peter [Akademischer Betreuer] Gmeiner. "Domänenarchitektur inhibitorischer Ionenkanäle der Cys-Loop-Rezeptorfamilie / Bea Unterer. Betreuer: Peter Gmeiner." Erlangen : Universitätsbibliothek der Universität Erlangen-Nürnberg, 2013. http://d-nb.info/1033029890/34.

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Guo, Wei [Verfasser]. "Identification and Characterization of Regulators of 2-Cys-Peroxiredoxin A in Arabidopsis thaliana / Wei Guo." Berlin : Freie Universität Berlin, 2013. http://d-nb.info/1043687629/34.

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Hiltscher, Heiko [Verfasser]. "Identifizierung und Charakterisierung von Signaltransduktionselementen der 2‐Cys‐Peroxiredoxin A Regulation in Arabidopsis thaliana / Heiko Hiltscher." Düsseldorf : Universitäts- und Landesbibliothek der Heinrich-Heine-Universität Düsseldorf, 2012. http://d-nb.info/1019397985/34.

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Kurpiers, Thomas [Verfasser]. "Entwicklung einer neuen Methode zur chemo- und regioselektiven Cys-tag-Modifikation von Proteinen mithilfe von gespaltenen Inteinen / vorgelegt von Thomas Kurpiers." 2008. http://d-nb.info/991582683/34.

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Sadtler, Sven [Verfasser]. "Synthesis, assembly, and intracellular trafficking of members of the cys-loop and P2X families of ligand gated ion channels / von Sven Sadtler." 2006. http://d-nb.info/978957911/34.

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Conference papers on the topic "Cys-34"

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Fuhlendorff, J., I. Clemmensen, and S. Magnusson. "PRIMARY STRUCTURE OF TETRANECTIN. SEQUENCE HOMOLOGY WITH ASIALOGLYCOPROTEIN RECEPTORS AND WITH PROTEOGLYCAN CORE PROTEIN FROM CARTILAGE." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644380.

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Tetranectin (Mr = 68,000) is a tetrameric blood plasma protein, which binds to plasminogen and also to the lysine-binding site of the isolated kringle 4 from plasminogen. Its four polypeptide chains, which are non-covalently bound, each consists of 181 amino acid residues. We have determined the complete amino acid sequence and the disulfide bonds. Each position corresponds to a single amino acid residue except 34 which contains Ala and Ser and 37 which contains Val and Met in equimolar amounts. The three disulfide bonds connect Cys-50 to Cys-60, Cys-77 to Cys-176 and Cys-152 to Cys-168. The s
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