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METACYC ID Description A0AR23 GO:0004842 (Ubiquitin-Protein Ligase
Electronic Supplementary Material (ESI) for Integrative Biology This journal is © The Royal Society of Chemistry 2012 Heat Stress Responsive Zostera marina Genes, Southern Population (α=0. -
Systems and Chemical Biology Approaches to Study Cell Function and Response to Toxins
Dissertation submitted to the Combined Faculties for the Natural Sciences and for Mathematics of the Ruperto-Carola University of Heidelberg, Germany for the degree of Doctor of Natural Sciences Presented by MSc. Yingying Jiang born in Shandong, China Oral-examination: Systems and chemical biology approaches to study cell function and response to toxins Referees: Prof. Dr. Rob Russell Prof. Dr. Stefan Wölfl CONTRIBUTIONS The chapter III of this thesis was submitted for publishing under the title “Drug mechanism predominates over toxicity mechanisms in drug induced gene expression” by Yingying Jiang, Tobias C. Fuchs, Kristina Erdeljan, Bojana Lazerevic, Philip Hewitt, Gordana Apic & Robert B. Russell. For chapter III, text phrases, selected tables, figures are based on this submitted manuscript that has been originally written by myself. i ABSTRACT Toxicity is one of the main causes of failure during drug discovery, and of withdrawal once drugs reached the market. Prediction of potential toxicities in the early stage of drug development has thus become of great interest to reduce such costly failures. Since toxicity results from chemical perturbation of biological systems, we combined biological and chemical strategies to help understand and ultimately predict drug toxicities. First, we proposed a systematic strategy to predict and understand the mechanistic interpretation of drug toxicities based on chemical fragments. Fragments frequently found in chemicals with certain toxicities were defined as structural alerts for use in prediction. Some of the predictions were supported with mechanistic interpretation by integrating fragment- chemical, chemical-protein, protein-protein interactions and gene expression data. Next, we systematically deciphered the mechanisms of drug actions and toxicities by analyzing the associations of drugs’ chemical features, biological features and their gene expression profiles from the TG-GATEs database. -
The Genome of Nanoarchaeum Equitans: Insights Into Early Archaeal Evolution and Derived Parasitism
The genome of Nanoarchaeum equitans: Insights into early archaeal evolution and derived parasitism Elizabeth Waters†‡, Michael J. Hohn§, Ivan Ahel¶, David E. Graham††, Mark D. Adams‡‡, Mary Barnstead‡‡, Karen Y. Beeson‡‡, Lisa Bibbs†, Randall Bolanos‡‡, Martin Keller†, Keith Kretz†, Xiaoying Lin‡‡, Eric Mathur†, Jingwei Ni‡‡, Mircea Podar†, Toby Richardson†, Granger G. Sutton‡‡, Melvin Simon†, Dieter So¨ ll¶§§¶¶, Karl O. Stetter†§¶¶, Jay M. Short†, and Michiel Noordewier†¶¶ †Diversa Corporation, 4955 Directors Place, San Diego, CA 92121; ‡Department of Biology, San Diego State University, 5500 Campanile Drive, San Diego, CA 92182; §Lehrstuhl fu¨r Mikrobiologie und Archaeenzentrum, Universita¨t Regensburg, Universita¨tsstrasse 31, D-93053 Regensburg, Germany; ‡‡Celera Genomics Rockville, 45 West Gude Drive, Rockville, MD 20850; Departments of ¶Molecular Biophysics and Biochemistry and §§Chemistry, Yale University, New Haven, CT 06520-8114; and ʈDepartment of Biochemistry, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061 Communicated by Carl R. Woese, University of Illinois at Urbana–Champaign, Urbana, IL, August 21, 2003 (received for review July 22, 2003) The hyperthermophile Nanoarchaeum equitans is an obligate sym- (6–8). Genomic DNA was either digested with restriction en- biont growing in coculture with the crenarchaeon Ignicoccus. zymes or sheared to provide clonable fragments. Two plasmid Ribosomal protein and rRNA-based phylogenies place its branching libraries were made by subcloning randomly sheared fragments point early in the archaeal lineage, representing the new archaeal of this DNA into a high-copy number vector (Ϸ2.8 kbp library) kingdom Nanoarchaeota. The N. equitans genome (490,885 base or low-copy number vector (Ϸ6.3 kbp library). DNA sequence pairs) encodes the machinery for information processing and was obtained from both ends of plasmid inserts to create repair, but lacks genes for lipid, cofactor, amino acid, or nucleotide ‘‘mate-pairs,’’ pairs of reads from single clones that should be biosyntheses. -
Genome of Phaeocystis Globosa Virus Pgv-16T Highlights the Common Ancestry of the Largest Known DNA Viruses Infecting Eukaryotes
Genome of Phaeocystis globosa virus PgV-16T highlights the common ancestry of the largest known DNA viruses infecting eukaryotes Sebastien Santinia, Sandra Jeudya, Julia Bartolia, Olivier Poirota, Magali Lescota, Chantal Abergela, Valérie Barbeb, K. Eric Wommackc, Anna A. M. Noordeloosd, Corina P. D. Brussaardd,e,1, and Jean-Michel Claveriea,f,1 aStructural and Genomic Information Laboratory, Unité Mixte de Recherche 7256, Centre National de la Recherche Scientifique, Aix-Marseille Université, 13288 Marseille Cedex 9, France; bCommissariat à l’Energie Atomique–Institut de Génomique, 91057 Evry Cedex, France; cDepartment of Plant and Soil Sciences, University of Delaware, Newark, DE 19711; dDepartment of Biological Oceanography, Royal Netherlands Institute for Sea Research, NL-1790 AB Den Burg (Texel), The Netherlands; eAquatic Microbiology, Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Amsterdam, The Netherlands; and fService de Santé Publique et d’Information Médicale, Hôpital de la Timone, Assistance Publique–Hôpitaux de Marseille, FR-13385 Marseille, France Edited by James L. Van Etten, University of Nebraska, Lincoln, NE, and approved May 1, 2013 (received for review February 22, 2013) Large dsDNA viruses are involved in the population control of many viruses: 730 kb and 1.28 Mb for CroV and Megavirus chilensis, globally distributed species of eukaryotic phytoplankton and have respectively. Other studies, targeting virus-specific genes [e.g., a prominent role in bloom termination. The genus Phaeocystis (Hap- DNA polymerase B (8) or capsid proteins (9)] have suggested tophyta, Prymnesiophyceae) includes several high-biomass-forming a close phylogenetic relationship between Mimivirus and several phytoplankton species, such as Phaeocystis globosa, the blooms of giant dsDNA viruses infecting various unicellular algae such as which occur mostly in the coastal zone of the North Atlantic and the Pyramimonas orientalis (Chlorophyta, Prasinophyceae), Phaeocys- North Sea. -
Preclinical Evaluation of Protein Disulfide Isomerase Inhibitors for the Treatment of Glioblastoma by Andrea Shergalis
Preclinical Evaluation of Protein Disulfide Isomerase Inhibitors for the Treatment of Glioblastoma By Andrea Shergalis A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy (Medicinal Chemistry) in the University of Michigan 2020 Doctoral Committee: Professor Nouri Neamati, Chair Professor George A. Garcia Professor Peter J. H. Scott Professor Shaomeng Wang Andrea G. Shergalis [email protected] ORCID 0000-0002-1155-1583 © Andrea Shergalis 2020 All Rights Reserved ACKNOWLEDGEMENTS So many people have been involved in bringing this project to life and making this dissertation possible. First, I want to thank my advisor, Prof. Nouri Neamati, for his guidance, encouragement, and patience. Prof. Neamati instilled an enthusiasm in me for science and drug discovery, while allowing me the space to independently explore complex biochemical problems, and I am grateful for his kind and patient mentorship. I also thank my committee members, Profs. George Garcia, Peter Scott, and Shaomeng Wang, for their patience, guidance, and support throughout my graduate career. I am thankful to them for taking time to meet with me and have thoughtful conversations about medicinal chemistry and science in general. From the Neamati lab, I would like to thank so many. First and foremost, I have to thank Shuzo Tamara for being an incredible, kind, and patient teacher and mentor. Shuzo is one of the hardest workers I know. In addition to a strong work ethic, he taught me pretty much everything I know and laid the foundation for the article published as Chapter 3 of this dissertation. The work published in this dissertation really began with the initial identification of PDI as a target by Shili Xu, and I am grateful for his advice and guidance (from afar!). -
Serine Proteases with Altered Sensitivity to Activity-Modulating
(19) & (11) EP 2 045 321 A2 (12) EUROPEAN PATENT APPLICATION (43) Date of publication: (51) Int Cl.: 08.04.2009 Bulletin 2009/15 C12N 9/00 (2006.01) C12N 15/00 (2006.01) C12Q 1/37 (2006.01) (21) Application number: 09150549.5 (22) Date of filing: 26.05.2006 (84) Designated Contracting States: • Haupts, Ulrich AT BE BG CH CY CZ DE DK EE ES FI FR GB GR 51519 Odenthal (DE) HU IE IS IT LI LT LU LV MC NL PL PT RO SE SI • Coco, Wayne SK TR 50737 Köln (DE) •Tebbe, Jan (30) Priority: 27.05.2005 EP 05104543 50733 Köln (DE) • Votsmeier, Christian (62) Document number(s) of the earlier application(s) in 50259 Pulheim (DE) accordance with Art. 76 EPC: • Scheidig, Andreas 06763303.2 / 1 883 696 50823 Köln (DE) (71) Applicant: Direvo Biotech AG (74) Representative: von Kreisler Selting Werner 50829 Köln (DE) Patentanwälte P.O. Box 10 22 41 (72) Inventors: 50462 Köln (DE) • Koltermann, André 82057 Icking (DE) Remarks: • Kettling, Ulrich This application was filed on 14-01-2009 as a 81477 München (DE) divisional application to the application mentioned under INID code 62. (54) Serine proteases with altered sensitivity to activity-modulating substances (57) The present invention provides variants of ser- screening of the library in the presence of one or several ine proteases of the S1 class with altered sensitivity to activity-modulating substances, selection of variants with one or more activity-modulating substances. A method altered sensitivity to one or several activity-modulating for the generation of such proteases is disclosed, com- substances and isolation of those polynucleotide se- prising the provision of a protease library encoding poly- quences that encode for the selected variants. -
Genetic Expression Profile Analysis of the Temporal Inhibition of Quercetin and Naringenin on Lactobacillus Rhamnosus GG
robioti f P cs o & l a H n e r a u l t o h J Liu, et al., J Prob Health 2016, 4:2 Journal of Probiotics & Health DOI: 10.4172/2329-8901.1000139 ISSN: 2329-8901 Research Article Open Access Genetic Expression Profile Analysis of the Temporal Inhibition of Quercetin and Naringenin on Lactobacillus Rhamnosus GG Linshu Liu1*, Jenni Firrman1, Gustavo Arango Argoty2, Peggy Tomasula1, Masuko Kobori3, Liqing Zhang2 and Weidong Xiao4* 1Dairy and Functional Foods Research Unit, Eastern Regional Research Center, Agricultural Research Service, US Department of Agriculture, 600 E Mermaid Lane, Wyndmoor, PA 19038, USA 2Virginia Tech College of Engineering, Department of Computer Science, 1425 S Main St. Blacksburg, VA 24061, USA 3National Food Research Institute, National Agriculture and Food Research Organization, Tsukuba, Ibaraki 305-8642, Japan 4*Department of Microbiology and Immunology, Temple University School of Medicine, 3400 North Broad Street, Philadelphia, USA *Corresponding author: Weidong Xiao, Department of Microbiology and Immunology, Temple University School of Medicine, 3400 North Broad Street, Philadelphia, USA, Tel: 215-707-6392; E-mail: [email protected], LinShu Liu, Dairy and Functional Foods Research Unit, Eastern Regional Research Center, Agricultural Research Service, US Department of Agriculture, 600 E Mermaid Lane, Wyndmoor, PA 19038, USA. E-mail: [email protected] Received date: Jan 29, 2015; Accepted date: Feb 15, 2016; Published date: Feb 22, 2016 Copyright: © 2016 Liu LS, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. -
Effect of Physical Exercise on Lipolysis in White Adipocytes
J Phys Fitness Sports Med, 1(2): 351-356 (2012) JPFSM: Short Review Article Effect of physical exercise on lipolysis in white adipocytes Junetsu Ogasawara1*, Takuya Sakurai1, Takako Kizaki1, Kazuto Takahashi2, Hitoshi Ishida2, Tetsuya Izawa3, Koji Toshinai4, Norihiko Nakano5 and Hideki Ohno1 1 Department of Molecular Predictive Medicine and Sport Science, Kyorin University, School of Medicine,6-20-2 Shinkawa, Mitaka, Tokyo 181-8611, Japan 2 Third Department of Internal Medicine, Kyorin University, School of Medicine,6-20-2 Shinkawa, Mitaka, Tokyo 181-8611, Japan 3 Department of Sports Biochemistry, Faculty of Health and Sports Science, Doshisha University, Tataramiyakodani, Kyotanabe, Kyoto 610-0394, Japan 4 Neurology, Respirology, Endocrinology, and Metabolism, Division of Internal Medicine, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki 889-1692, Japan 5 Aino Institute of Regeneration and Rehabilitation, Aino University, 4-5-4 Higashiohara, Ibaraki, Osaka 567-0012, Japan Received: April 27, 2012 / Accepted: June 12, 2012 Abstract Fatty acids are derived from the hydrolysis of triacylglycerol (TG) found in white adipose tissue, muscle tissue and circulating lipoproteins. The mobilization of free fatty acids (FFA) from white adipose tissue contributes to about 50% of the FFA utilized during moderate- intensity exercise. The delivery of FFA from white adipose tissue is improved by hormone- stimulated lipolytic events in white adipocytes (WA). Thus, the lipolysis in WA that provides fuel for metabolism has been a highly conserved function throughout the course of evolution. This short review outlines our current understanding of the molecular regulation of TG lipases via the lipolytic cascade in WA, as well as provides an account of our recent findings concern- ing changes in the lipolytic molecules of WA that result from acute and habitual exercise. -
Optimization of Lipase Production in Burkholderia Glumae
Optimization of lipase production in Burkholderia glumae Dissertation zur Erlangung des Grades eines Doktors der Naturwissenschaften der Fakultät für Biologie an der Internationalen Graduiertenschule Biowissenschaften der Ruhr-Universität Bochum angefertigt am Institut für Molekulare Enzymtechnologie vorgelegt von Anke Beselin aus Frankfurt a. Main Bochum August 2005 Optimierung der Lipaseproduktion in Burkholderia glumae Dissertation zur Erlangung des Grades eines Doktors der Naturwissenschaften der Fakultät für Biologie an der Internationalen Graduiertenschule Biowissenschaften der Ruhr-Universität Bochum angefertigt am Institut für Molekulare Enzymtechnologie vorgelegt von Anke Beselin aus Frankfurt a. Main Bochum August 2005 Die vorliegende Arbeit wurde im Rahmen des Europäischen Graduiertenkollegs der Ruhr- Universität Bochum (EGC 795): Regulatory Circuits in Cellular Systems: Fundamentals and Biotechnological Applications angefertigt. Referent: Prof. Dr. K.-E. Jäger Korreferent: Prof. Dr. W. J. Quax Tag der mündlichen Prüfung: 28.10.2005 ___________________________________________________________________________ Danksagungen Herrn Prof. Dr. K.-E. Jäger danke ich für die Überlassung des interessanten und aktuellen Themas, für das rege Interesse am Fortschritt meiner Arbeit, die konstruktiven Diskussionen und die mir gebotene Möglichkeit, die experimentelle Arbeit frei und selbständig zu gestalten. I would like to thank Prof. Dr. W. J. Quax, Laboratory of Pharmaceutical Biology- Rijksuniversität Groningen (NL) for agreeing to co-supervise -
Biological Phosphorylation of an Unnatural Base Pair (UBP) Using a Drosophila Melanogaster Deoxynucleoside Kinase (Dmdnk) Mutant
RESEARCH ARTICLE Biological phosphorylation of an Unnatural Base Pair (UBP) using a Drosophila melanogaster deoxynucleoside kinase (DmdNK) mutant Fei Chen1,2,3☯*, Yuan Zhang4☯, Ashley B. Daugherty5, Zunyi Yang3, Ryan Shaw3, Mengxing Dong1,2, Stefan Lutz5, Steven A. Benner3* a1111111111 1 CAS Key Laboratory of Genome Sciences & Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China, 2 University of Chinese Academy of Sciences, Beijing, China, 3 Foundation for a1111111111 Applied Molecular Evolution (FfAME), Alachua, Florida, United States of America, 4 College of Chemistry, a1111111111 Beijing Normal University, Beijing, China, 5 Department of Chemistry, Emory University School of Medicine, a1111111111 Atlanta, Georgia, United States of America a1111111111 ☯ These authors contributed equally to this work. * [email protected] (FC); [email protected] (SAB) OPEN ACCESS Abstract Citation: Chen F, Zhang Y, Daugherty AB, Yang Z, Shaw R, Dong M, et al. (2017) Biological One research goal for unnatural base pair (UBP) is to replicate, transcribe and translate phosphorylation of an Unnatural Base Pair (UBP) them in vivo. Accordingly, the corresponding unnatural nucleoside triphosphates must be using a Drosophila melanogaster deoxynucleoside available at sufficient concentrations within the cell. To achieve this goal, the unnatural kinase (DmdNK) mutant. PLoS ONE 12(3): nucleoside analogues must be phosphorylated to the corresponding nucleoside triphos- e0174163. https://doi.org/10.1371/journal. pone.0174163 phates by a cascade of three kinases. The first step is the monophosphorylation of unnatural deoxynucleoside catalyzed by deoxynucleoside kinases (dNK), which is generally consid- Editor: Giovanni Maga, Istituto di Genetica Molecolare, ITALY ered the rate limiting step because of the high specificity of dNKs. -
Thesis for Word XP
Thesis for doctoral degree (Ph.D.) 2010 Thesis for doctoral degree (Ph.D.) 2010 The role of 5’-nucleotidases and Deoxynucleoside Kinases in Responses to Nucleoside Analogues Saeedeh Mirzaee The role of 5’-nucleotidases and Deoxynucleoside Kinases in Responses to Nucleoside Analogues Saeedeh Mirzaee From the Department of Oncology and Pathology, Cancer Centrum Karolinska Karolinska Institutet, Stockholm, Sweden The role of 5’-nucleotidases and deoxynucleoside kinases in responses to nucleoside analogues Saeedeh Mirzaee Stockholm 2010 All previously published papers were reproduced with permission from the publisher. Published by Karolinska Institutet. Printed by Larserics Digital Print. © Saeedeh Mirzaee, 2010 ISBN 978-91-7409-908-9 Some look at things that are, and ask why. I dream of things that never were and ask why not? George Bernard Shaw ABSTRACT The efficacy of nucleoside analogues (NAs) in treating several hematological malignancies, solid tumors and viral infections is limited primarily by side-effects and the development of drug resistance. The aims of the present thesis were to elucidate mechanism(s) involved in tissue-specific toxicity associated with NA therapy, as well as the mechanisms underlying resistance to these drugs. The mRNA levels and activities of different cytosolic and mitochondrial deoxynucleoside kinases (dNKs) and 5'-nucleotidases (5'- NTs) exhibit a distinct pattern for each of a variety of mouse tissues. Heart and skeletal muscle, as well as adipose tissue demonstrate low levels of both the anabolic and catabolic enzymes, which may explain at least some of the adverse side-effects of NA treatment. A novel approach based on high-performance liquid chromatography (HPLC) revealed that each of 14 different mouse and rat tissues exhibits a unique profile of dNK and 5'NT activities, with 2-3-fold species differences for certain of these tissues. -
Deoxynucleoside Kinases Development in Vitro by Inhibition
Restoration of Adenosine Deaminase-Deficient Human Thymocyte Development In Vitro by Inhibition of Deoxynucleoside Kinases This information is current as of September 26, 2021. Michelle L. Joachims, Patrick A. Marble, Aletha B. Laurent, Peter Pastuszko, Marco Paliotta, Michael R. Blackburn and Linda F. Thompson J Immunol 2008; 181:8153-8161; ; doi: 10.4049/jimmunol.181.11.8153 Downloaded from http://www.jimmunol.org/content/181/11/8153 References This article cites 54 articles, 20 of which you can access for free at: http://www.jimmunol.org/ http://www.jimmunol.org/content/181/11/8153.full#ref-list-1 Why The JI? Submit online. • Rapid Reviews! 30 days* from submission to initial decision • No Triage! Every submission reviewed by practicing scientists by guest on September 26, 2021 • Fast Publication! 4 weeks from acceptance to publication *average Subscription Information about subscribing to The Journal of Immunology is online at: http://jimmunol.org/subscription Permissions Submit copyright permission requests at: http://www.aai.org/About/Publications/JI/copyright.html Email Alerts Receive free email-alerts when new articles cite this article. Sign up at: http://jimmunol.org/alerts The Journal of Immunology is published twice each month by The American Association of Immunologists, Inc., 1451 Rockville Pike, Suite 650, Rockville, MD 20852 Copyright © 2008 by The American Association of Immunologists All rights reserved. Print ISSN: 0022-1767 Online ISSN: 1550-6606. The Journal of Immunology Restoration of Adenosine Deaminase-Deficient Human Thymocyte Development In Vitro by Inhibition of Deoxynucleoside Kinases1,2 Michelle L. Joachims,* Patrick A. Marble,* Aletha B. Laurent,* Peter Pastuszko,3† Marco Paliotta,† Michael R.