122 Publikationen
-
-
2021 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2955530M. Boschanski, et al., “Site-Specific Conjugation Strategy for Dual Antibody-Drug Conjugates Using Aerobic Formylglycine-Generating Enzymes”, Bioconjugate chemistry, 2021.PUB | DOI | WoS | PubMed | Europe PMC
-
2021 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2956816B. Kowalewski, et al., “Decoding the consecutive lysosomal degradation of 3-O-sulfate containing heparan sulfate by Arylsulfatase G (ARSG)”, Biochemical Journal, 2021.PUB | DOI | WoS | PubMed | Europe PMC
-
-
2020 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2945876C. Trabszo, et al., “Arylsulfatase K inactivation causes mucopolysaccharidosis due to deficient glucuronate desulfation of heparan and chondroitin sulfate”, Biochemical Journal, 2020.PUB | DOI | WoS | PubMed | Europe PMC
-
2020 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2945204L.A. Adang, et al., “Natural history of multiple sulfatase deficiency: retrospective phenotyping and functional variant analysis to characterize an ultra-rare disease.”, Journal of inherited metabolic disease, 2020.PUB | DOI | WoS | PubMed | Europe PMC
-
2020 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2941491O. Staretz-Chacham, et al., “A homozygous missense variant of SUMF1 in the Bedouin population extends the clinical spectrum in ultrarare neonatal multiple sulfatase deficiency.”, Molecular genetics & genomic medicine, vol. 8, 2020, : e1167.PUB | PDF | DOI | WoS | PubMed | Europe PMC
-
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2934113T. Krüger, T. Dierks, and N. Sewald, “Formylglycine-generating enzymes for site-specific bioconjugation”, BIOLOGICAL CHEMISTRY, vol. 400, 2019, pp. 289-297.PUB | DOI | WoS | PubMed | Europe PMC
-
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2936936T. Krüger, et al., “Conversion of Serine-Type Aldehyde Tags by the Radical SAM Protein AtsB from Methanosarcina mazei”, ChemBioChem, vol. 20, 2019, pp. 2074-2078.PUB | DOI | WoS | PubMed | Europe PMC
-
2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2937586L. Schlotawa, et al., “Severe neonatal multiple sulfatase deficiency presenting with hydrops fetalis in a preterm birth patient”, JIMD reports, vol. 49, 2019, pp. 48-52.PUB | PDF | DOI | PubMed | Europe PMC
-
2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2937243M. Korf-Klingebiel, et al., “Heparan Sulfate-Editing Extracellular Sulfatases Enhance Vascular Endothelial Growth Factor Bioavailability for Ischemic Heart Repair”, Circulation research, vol. 125, 2019, pp. 787-801.PUB | DOI | WoS | PubMed | Europe PMC
-
2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2933342S. Bloess, et al., “Expression, characterization, and site-specific covalent immobilization of an L-amino acid oxidase from the fungus Hebeloma cylindrosporum”, Applied microbiology and biotechnology, vol. 103, 2019, pp. 2229-2241.PUB | DOI | WoS | PubMed | Europe PMC
-
-
2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2933913L. Schlotawa, et al., “Protein disulfide isomerase is a possible target for disease modification in multiple sulfatase deficiency”, MOLECULAR GENETICS AND METABOLISM, MOLECULAR GENETICS AND METABOLISM, vol. 126, San Diego: ACADEMIC PRESS INC ELSEVIER SCIENCE, 2019, pp.S131-S132.PUB | DOI | WoS
-
2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2933914T.O. Silva, et al., “Attenuated multiple sulfatase deficiency: Description of two Brazilian patients showing interesting clinical and genetic findings”, MOLECULAR GENETICS AND METABOLISM, MOLECULAR GENETICS AND METABOLISM, vol. 126, ACADEMIC PRESS INC ELSEVIER SCIENCE, 2019, pp.S135-S136.PUB | DOI | WoS
-
-
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920942T. Krüger, et al., “Two-fold Bioorthogonal Derivatization by Different Formylglycine-Generating Enzymes”, Angewandte Chemie International Edition, vol. 57, 2018, pp. 7245-7249.PUB | DOI | WoS | PubMed | Europe PMC
-
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2933928D. Maynard, et al., “The function of the oxylipin 12-oxophytodienoic acid in cell signaling, stress acclimation, and development”, Journal of Experimental Botany , vol. 69, 2018, pp. 5341-5354.PUB | DOI | WoS | PubMed | Europe PMC
-
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2932772V. Walhorn, et al., “Exploring the Sulfatase 1 Catch Bond Free Energy Landscape using Jarzynski's Equality”, Scientific Reports, vol. 8, 2018, : 16849.PUB | DOI | WoS | PubMed | Europe PMC
-
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920271S. Stroobants, et al., “Sensorimotor and Neurocognitive Dysfunctions Parallel Early Telencephalic Neuropathology in Fucosidosis Mice”, FRONTIERS IN BEHAVIORAL NEUROSCIENCE, vol. 12, 2018, : 15.PUB | DOI | WoS | PubMed | Europe PMC
-
-
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2931507S. Khateb, et al., “A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans”, GENETICS IN MEDICINE, vol. 20, 2018, pp. 1004-1012.PUB | DOI | WoS | PubMed | Europe PMC
-
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2919061R. Ahrens-Nicklas, et al., “Complex care of individuals with multiple sulfatase deficiency: Clinical cases and consensus statement”, MOLECULAR GENETICS AND METABOLISM, vol. 123, 2018, pp. 337-346.PUB | DOI | WoS | PubMed | Europe PMC
-
-
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909071D. Roy, et al., “Loss of HSulf-1: The Missing Link between Autophagy and Lipid Droplets in Ovarian Cancer”, SCIENTIFIC REPORTS, vol. 7, 2017, : 41977.PUB | DOI | WoS | PubMed | Europe PMC
-
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916520I. Jaszczuk, et al., “Expanding the genetic cause of multiple sulfatase deficiency: A novel SUMF1 variant in a patient displaying a severe late infantile form of the disease”, MOLECULAR GENETICS AND METABOLISM, vol. 121, 2017, pp. 252-258.PUB | DOI | WoS | PubMed | Europe PMC
-
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2908778O.P. Dhamale, et al., “Arylsulfatase K is the Lysosomal 2-Sulfoglucuronate Sulfatase”, ACS Chemical Biology, vol. 12, 2017, pp. 367-373.PUB | DOI | WoS | PubMed | Europe PMC
-
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2904124K. Kruszewski, et al., “Degeneration of Photoreceptor Cells in Arylsulfatase G-Deficient Mice”, INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, vol. 57, 2016, pp. 1120-1131.PUB | DOI | WoS | PubMed | Europe PMC
-
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2905616H. Wolf, et al., “A mouse model for fucosidosis recapitulates storage pathology and neurological features of the milder form of the human disease”, Disease Models & Mechanisms, vol. 9, 2016, pp. 1015-1028.PUB | PDF | DOI | WoS | PubMed | Europe PMC
-
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2784664I. Kalus, et al., “Sulf1 and Sulf2 Differentially Modulate Heparan Sulfate Proteoglycan Sulfation during Postnatal Cerebellum Development: Evidence for Neuroprotective and Neurite Outgrowth Promoting Functions”, PLoS ONE, vol. 10, 2015, : e0139853.PUB | DOI | WoS | PubMed | Europe PMC
-
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2788799S. Mondal, et al., “HSulf-1 deficiency dictates a metabolic reprograming of glycolysis and TCA cycle in ovarian cancer”, ONCOTARGET, vol. 6, 2015, pp. 33705-33719.PUB | DOI | WoS | PubMed | Europe PMC
-
2015 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2908650V. Walhorn, et al., “Single-Molecule Mechanics and Force Spectroscopy”, Functional Soft Matter, J. Dhont, et al., eds., Schlüsseltechnologien - Key Technologies, vol. 94, Jülich: Forschungszentrum Jülich Publisher, 2015, pp.C4.1-C4.17.PUB
-
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2780450J. Peng, et al., “Eukaryotic formylglycine-generating enzyme catalyses a monooxygenase type of reaction”, FEBS Journal, vol. 282, 2015, pp. 3262-3274.PUB | DOI | WoS | PubMed | Europe PMC
-
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2709463B. Kowalewski, et al., “Ataxia is the major neuropathological finding in Arylsulfatase G deficient mice: Similarities and dissimilarities to Sanfilippo disease (Mucopolysaccharidosis type III)”, Human Molecular Genetics, vol. 24, 2015, pp. 1856-1868.PUB | DOI | WoS | PubMed | Europe PMC
-
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2732684A. Harder, et al., “Catch Bond Interaction between Cell-Surface Sulfatase Sulf1 and Glycosaminoglycans”, Biophysical journal, vol. 108, 2015, pp. 1709-1717.PUB | DOI | WoS | PubMed | Europe PMC
-
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2690696J. Poppe, et al., “Structural diversity of polyoxomolybdate clusters along the three-fold axis of the molybdenum storage protein”, Journal of Inorganic Biochemistry, vol. 138, 2014, pp. 122-128.PUB | DOI | WoS | PubMed | Europe PMC
-
-
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2699273B. Kowalewski, et al., “Molecular Characterization of Arylsulfatase G: EXPRESSION, PROCESSING, GLYCOSYLATION, TRANSPORT, AND ACTIVITY”, The Journal of biological chemistry, vol. 289, 2014, pp. 27992-28005.PUB | DOI | WoS | PubMed | Europe PMC
-
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2607389M. Yoo, et al., “Arylsulfatase B Improves Locomotor Function after Mouse Spinal Cord Injury”, Plos One, vol. 8, 2013, : e57415.PUB | DOI | WoS | PubMed | Europe PMC
-
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2625696L. Schlotawa, et al., “Rapid degradation of an active formylglycine generating enzyme variant leads to a late infantile severe form of multiple sulfatase deficiency”, European Journal Of Human Genetics, vol. 21, 2013, pp. 1020-1023.PUB | DOI | WoS | PubMed | Europe PMC
-
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2623550E. Wiegmann, et al., “Arylsulfatase K, a Novel Lysosomal Sulfatase”, Journal of Biological Chemistry, vol. 288, 2013, pp. 30019-30028.PUB | DOI | WoS | PubMed | Europe PMC
-
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2623281I. Maltseva, et al., “The SULFs, Extracellular Sulfatases for Heparan Sulfate, Promote the Migration of Corneal Epithelial Cells during Wound Repair”, PloS one, vol. 8, 2013, : e69642.PUB | DOI | WoS | PubMed | Europe PMC
-
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2565333E. Ennemann, et al., “Proprotein Convertases Process and Thereby Inactivate Formylglycine-generating Enzyme”, Journal of Biological Chemistry, vol. 288, 2013, pp. 5828-5839.PUB | DOI | WoS | PubMed | Europe PMC
-
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2623253J.H. Kim, et al., “Endosulfatases SULF1 and SULF2 limit Chlamydia muridarum infection”, Cellular Microbiology, vol. 15, 2013, pp. 1560-1571.PUB | DOI | WoS | PubMed | Europe PMC
-
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2623533F. Milz, et al., “Cooperation of binding sites at the hydrophilic domain of cell-surface sulfatase Sulf1 allows for dynamic interaction of the enzyme with its substrate heparan sulfate”, Biochim Biophys Acta, vol. 1830, 2013, pp. 5287-5298.PUB | DOI | WoS | PubMed | Europe PMC
-
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2612942A. Seffouh, et al., “HSulf sulfatases catalyze processive and oriented 6-O-desulfation of heparan sulfate that differentially regulates fibroblast growth factor activity”, The Faseb Journal, vol. 27, 2013, pp. 2431-2439.PUB | DOI | WoS | PubMed | Europe PMC
-
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2351519J. Lenger, et al., “Evaluation of sulfatase-directed quinone methide traps for proteomics”, Bioorganic & Medicinal Chemistry, vol. 20, 2012, pp. 622-627.PUB | DOI | WoS | PubMed | Europe PMC
-
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2474206S. Hayano, et al., “Roles of heparan sulfate sulfation in dentinogenesis”, J. Biol. Chem., vol. 287, 2012, pp. 12217-12229.PUB | DOI | WoS | PubMed | Europe PMC
-
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2517966B. Kowalewski, et al., “Nature's Polyoxometalate Chemistry: X-ray Structure of the Mo Storage Protein Loaded with Discrete Polynuclear Mo-O Clusters”, Journal of the American Chemical Society, vol. 134, 2012, pp. 9768-9774.PUB | DOI | WoS | PubMed | Europe PMC
-
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2494022B. Kowalewski, et al., “Arylsulfatase G Inactivation Causes Loss of Heparan Sulfate 3-O-Sulfatase Activity and Mucopolysaccharidosis in Mice”, Proc. Natl. Acad. Sci. USA, vol. 109, 2012, pp. 10310-10315.PUB | DOI | WoS | PubMed | Europe PMC
-
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2003211L. Schlotawa, et al., “SUMF1 mutations affecting stability and activity of formylglycine generating enzyme predict clinical outcome in multiple sulfatase deficiency”, European Journal of Human Genetics, vol. 19, 2011, pp. 253-261.PUB | DOI | WoS | PubMed | Europe PMC
-
2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1968383A. Harder, et al., “Single-Molecule Force Spectroscopy of Cartilage Aggrecan Self-Adhesion”, Biophysical Journal, vol. 99, 2010, pp. 3498-3504.PUB | DOI | WoS | PubMed | Europe PMC
-
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1590897S.E. Guimond, et al., “Rapid Purification and High Sensitivity Analysis of Heparan Sulfate from Cells and Tissues TOWARD GLYCOMICS PROFILING”, JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 284, 2009, pp. 25714-25722.PUB | DOI | WoS | PubMed | Europe PMC
-
2009 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2352302K. von Figura, T. Dierks, and B. Schmidt, “Multiple Sulfatase Deficiency”, Encyclopedia of Molecular Mechanisms of Disease, F. Lang, ed., Berlin Heidelberg: Springer, 2009, pp.1374-1375.PUB
-
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1634198T. Dierks, et al., “Molecular basis of multiple sulfatase deficiency, mucolipidosis II/III and Niemann-Pick C1 disease - Lysosomal storage disorders caused by defects of non-lysosomal proteins”, BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, vol. 1793, 2009, pp. 710-725.PUB | DOI | WoS | PubMed | Europe PMC
-
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1796606I. Kalus, et al., “Differential involvement of the extracellular 6-O-endosulfatases Sulf1 and Sulf2 in brain development and neuronal and behavioural plasticity”, JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, vol. 13, 2009, pp. 4505-4521.PUB | DOI | WoS | PubMed | Europe PMC
-
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1590564M.-A. Frese, et al., “Characterization of the Human Sulfatase Sulf1 and Its High Affinity Heparin/Heparan Sulfate Interaction Domain”, JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 284, 2009, pp. 28033-28044.PUB | DOI | WoS | PubMed | Europe PMC
-
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1635473M.-A. Frese and T. Dierks, “Formylglycine Aldehyde Tag-Protein Engineering through a Novel Post-translational Modification”, CHEMBIOCHEM, vol. 10, 2009, pp. 425-427.PUB | DOI | WoS | PubMed | Europe PMC
-
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1633371A. Busche, et al., “Neonatal manifestation of multiple sulfatase deficiency”, EUROPEAN JOURNAL OF PEDIATRICS, vol. 168, 2009, pp. 969-973.PUB | DOI | WoS | PubMed | Europe PMC
-
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2351244L. Schlotawa, et al., “Molecular analysis of SUMF1 mutations: stability and residual activity of mutant formylglycine-generating enzyme determine disease severity in multiple sulfatase deficiency”, Human Mutation, vol. 29, 2008, pp. 205.PUB | DOI
-
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1592682A. Ratzka, et al., “Redundant function of the heparan sulfate 6-O-endosulfatases Sulf1 and Sulf2 during skeletal development”, DEVELOPMENTAL DYNAMICS, vol. 237, 2008, pp. 339-353.PUB | DOI | WoS | PubMed | Europe PMC
-
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1592488S.L. Gande, et al., “Paralog of the formylglycine-generating enzyme - retention in the endoplasmic reticulum by canonical and noncanonical signals”, FEBS JOURNAL, vol. 275, 2008, pp. 1118-1130.PUB | DOI | WoS | PubMed | Europe PMC
-
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1592481M. Mariappan, et al., “ERp44 mediates a thiol-independent retention of formylglycine-generating enzyme in the endoplasmic reticulum”, JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 283, 2008, pp. 6375-6383.PUB | DOI | WoS | PubMed | Europe PMC
-
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1588435M.-A. Frese, S. Schulz, and T. Dierks, “Arylsulfatase G, a novel lysosomal sulfatase”, JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 283, 2008, pp. 11388-11395.PUB | DOI | WoS | PubMed | Europe PMC
-
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1588440M. Mariappan, et al., “The non-catalytic N-terminal extension of formylglycine-generating enzyme is required for its biological activity and retention in the endoplasmic reticulum”, JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 283, 2008, pp. 11556-11564.PUB | DOI | WoS | PubMed | Europe PMC
-
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1586139W.C. Lamanna, et al., “Sulf loss influences N-, 2-O-, and 6-O-sulfation of multiple heparan sulfate proteoglycans and modulates fibroblast growth factor signaling”, JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 283, 2008, pp. 27724-27735.PUB | DOI | WoS | PubMed | Europe PMC
-
2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1593622E. Zito, et al., “Sulfatase modifying factor 1 trafficking through the cells: from endoplasmic reticulum to the endoplasmic reticulum”, EMBO JOURNAL, vol. 26, 2007, pp. 2443-2453.PUB | DOI | WoS | PubMed | Europe PMC
-
2007 | Konferenzbeitrag | Veröffentlicht | PUB-ID: 1594028W.C. Lamanna, et al., “The heparanome - The enigma of encoding and decoding heparan sulfate sulfation”, Journal of Biotechnology, JOURNAL OF BIOTECHNOLOGY, vol. 129, ELSEVIER SCIENCE BV, 2007, pp.290-307.PUB | DOI | WoS | PubMed | Europe PMC
-
2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1597019W.C. Lamanna, et al., “Heparan sulfate 6-O-endosulfatases: discrete in vivo activities and functional co-operativity”, BIOCHEMICAL JOURNAL, vol. 400, 2006, pp. 63-73.PUB | DOI | WoS | PubMed | Europe PMC
-
2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1600859D. Roeser, et al., “A general binding mechanism for all human sulfatases by the formylglycine-generating enzyme”, PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, vol. 103, 2006, pp. 81-86.PUB | DOI | WoS | PubMed | Europe PMC
-
2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350692T. Dierks, et al., “Molecular basis for multiple sulfatase deficiency and mechanism for formylglycine generation of the human formylglycine-generating enzyme”, CELL, vol. 121, 2005, pp. 541-552.PUB | DOI | WoS | PubMed | Europe PMC
-
2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350712M. Mariappan, et al., “Expression, localization, structural, and functional characterization of pFGE, the paralog of the C alpha-formylglycine-generating enzyme”, JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 280, 2005, pp. 15173-15179.PUB | DOI | WoS | PubMed | Europe PMC
-
2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350723A. Dickmanns, et al., “Crystal structure of human pFGE, the paralog of the C alpha-formylglycine-generating enzyme”, JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 280, 2005, pp. 15180-15187.PUB | DOI | WoS | PubMed | Europe PMC
-
2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1603995A. Preusser-Kunze, et al., “Molecular characterization of the human C alpha-formylglycine-generating enzyme”, JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 280, 2005, pp. 14900-14910.PUB | DOI | WoS | PubMed | Europe PMC
-
2004 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350732Q.H. Fang, J.H. Peng, and T. Dierks, “Post-translational formylglycine modification of bacterial sulfatases by the radical S-adenosylmethionine protein AtsB”, JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 279, 2004, pp. 14570-14578.PUB | DOI | WoS | PubMed | Europe PMC
-
2004 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350737I. Muller, et al., “Crystal structure of the alkylsulfatase AtsK: Insights into the catalytic mechanism of the Fe(II) alpha-ketoglutarate-dependent dioxygenase superfamily”, BIOCHEMISTRY, vol. 43, 2004, pp. 3075-3088.PUB | DOI | WoS | PubMed | Europe PMC
-
2004 | Patent | Veröffentlicht | PUB-ID: 2375304K. von Figura, et al., “Diagnosis and treatment of multiple sulfatase deficiency and other sulfatase deficiencies”, 2004.PUB
-
-
2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350768C. Marquordt, et al., “Posttranslational modification of serine to formylglycine in bacterial sulfatases - Recognition of the modification motif by the iron-sulfur protein AtsB”, JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 278, 2003, pp. 2212-2218.PUB | DOI | WoS | PubMed | Europe PMC
-
2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350753A. Yaghootfam, et al., “Recognition of arylsulfatase A and B by the UDP-N-acetylglucosamine : lysosomal enzyme N-acetylglucosamine-phosphotransferase”, JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 278, 2003, pp. 32653-32661.PUB | DOI | WoS | PubMed | Europe PMC
-
2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350747J. Landgrebe, et al., “The human SUMF1 gene, required for posttranslational sulfatase modification, defines a new gene family which is conserved from pro- to eukaryotes”, GENE, vol. 316, 2003, pp. 47-56.PUB | DOI | WoS | PubMed | Europe PMC
-
2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350759T. Dierks, et al., “Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C-alpha-formylglycine generating enzyme”, CELL, vol. 113, 2003, pp. 435-444.PUB | DOI | WoS | PubMed | Europe PMC
-
2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350776J.H. Peng, et al., “Identification of formylglycine in sulfatases by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry”, JOURNAL OF MASS SPECTROMETRY, vol. 38, 2003, pp. 80-86.PUB | DOI | WoS | PubMed | Europe PMC
-
2002 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350782R. Bulow von, et al., “Defective oligomerization of arylsulfatase A as a cause of its instability in lysosomes and metachromatic leukodystrophy”, JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 277, 2002, pp. 9455-9461.PUB | DOI | WoS | PubMed | Europe PMC
-
2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350811R. Bulow von, et al., “Crystal structure of an enzyme-substrate complex provides insight into the interaction between human arylsulfatase A and its substrates during catalysis”, JOURNAL OF MOLECULAR BIOLOGY, vol. 305, 2001, pp. 269-277.PUB | DOI | WoS | PubMed | Europe PMC
-
2001 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2372494T. Dierks, “Sulfatases”, Encyclopedia of Molecular Medicine, T.E. Creighton, ed., New York: J. Wiley, 2001, pp.3042-3046.PUB
-
2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350792J. Fey, et al., “Characterization of posttranslational formylglycine formation by luminal components of the endoplasmic reticulum”, JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 276, 2001, pp. 47021-47028.PUB | DOI | WoS | PubMed | Europe PMC
-
2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350800I. Boltes, et al., “1.3 angstrom structure of arylsulfatase from Pseudomonas aeruginosa establishes the catalytic mechanism of sulfate ester cleavage in the sulfatase family”, STRUCTURE, vol. 9, 2001, pp. 483-491.PUB | DOI | WoS | PubMed | Europe PMC
-
2001 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2372492T. Dierks, “Cysteine-modifying enzyme”, Encyclopedia of Molecular Medicine, T.E. Creighton, ed., New York: J. Wiley, 2001, pp.974-976.PUB
-
2001 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2372496T. Dierks and B. Schmidt, “Arylsulfatases”, Encyclopedia of Molecular Medicine, T.E. Creighton, ed., New York: J. Wiley, 2001, pp.266-268.PUB
-
1999 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350826A. Waldow, et al., “Amino acid residues forming the active site of arylsulfatase A - Role in catalytic activity and substrate binding”, JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 274, 1999, pp. 12284-12288.PUB | DOI | WoS | PubMed | Europe PMC
-
1999 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350833T. Dierks, et al., “Sequence determinants directing conversion of cysteine to formylglycine in eukaryotic sulfatases”, EMBO JOURNAL, vol. 18, 1999, pp. 2084-2091.PUB | DOI | WoS | PubMed | Europe PMC
-
1999 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350818C. Szameit, et al., “The iron sulfur protein AtsB is required for posttranslational formation of formylglycine in the Klebsiella sulfatase”, JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 274, 1999, pp. 15375-15381.PUB | DOI | WoS | PubMed | Europe PMC
-
1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350840A. Knaust, et al., “Residues critical for formylglycine formation and/or catalytic activity of arylsulfatase A”, BIOCHEMISTRY, vol. 37, 1998, pp. 13941-13946.PUB | DOI | WoS | PubMed | Europe PMC
-
1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350871R. Recksiek, et al., “Sulfatases, trapping of the sulfated enzyme intermediate by substituting the active site formylglycine”, JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 273, 1998, pp. 6096-6103.PUB
-
1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350847T. Dierks, et al., “Posttranslational formation of formylglycine in prokaryotic sulfatases by modification of either cysteine or serine”, JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 273, 1998, pp. 25560-25564.PUB | DOI | WoS | PubMed | Europe PMC
-
1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350855J. Reiss, et al., “Mutations in a polycistronic nuclear gene associated with molybdenum cofactor deficiency”, NATURE GENETICS, vol. 20, 1998, pp. 51-53.PUB | DOI | WoS | PubMed | Europe PMC
-
1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350865K. Figura von, et al., “A novel protein modification generating an aldehyde group in sulfatases: its role in catalysis and disease”, BIOESSAYS, vol. 20, 1998, pp. 505-510.PUB | DOI | WoS | PubMed | Europe PMC
-
1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350877C. Miech, et al., “Arylsulfatase from Klebsiella pneumoniae carries a formylglycine generated from a serine”, JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 273, 1998, pp. 4835-4837.PUB | DOI | WoS | PubMed | Europe PMC
-
1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350884T. Dierks, et al., “Conversion of cysteine to formylglycine in eukaryotic sulfatases occurs by a common mechanism in the endoplasmic reticulum”, FEBS LETTERS, vol. 423, 1998, pp. 61-65.PUB | DOI | WoS | PubMed | Europe PMC
-
1997 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350890T. Dierks, B. Schmidt, and K. VonFigura, “Conversion of cysteine to formylglycine: A protein modification in the endoplasmic reticulum”, PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, vol. 94, 1997, pp. 11963-11968.PUB | DOI | WoS | PubMed | Europe PMC
-
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350895T. Dierks, et al., “A microsomal ATP-binding protein involved in efficient protein transport into the mammalian endoplasmic reticulum”, EMBO JOURNAL, vol. 15, 1996, pp. 6931-6942.PUB
-
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350906M. Brunke, et al., “Luciferase assembly after transport into mammalian microsomes involves molecular chaperones and peptidyl-prolyl cis/trans-isomerases”, JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 271, 1996, pp. 23487-23494.PUB
-
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350925P. Klappa, T. Dierks, and R. Zimmermann, “Cyclosporin A inhibits the degradation of signal sequences after processing of presecretory proteins by signal peptidase”, EUROPEAN JOURNAL OF BIOCHEMISTRY, vol. 239, 1996, pp. 509-518.PUB | DOI | WoS | PubMed | Europe PMC
-
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350916J. Tyedmers, et al., “Efficient folding of firefly luciferase after transport into mammalian microsomes in the absence of luminal chaperones and folding catalysts”, JOURNAL OF BIOLOGICAL CHEMISTRY, vol. 271, 1996, pp. 19509-19513.PUB
-
1994 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2372523T. Dierks, R. Stappen, and R. Krämer, “Channel properties of mitochondrial carriers”, Molecular Biology of Mitochondrial Transport Systems, M. Forte and M. Colombini, eds., Nato ASI Series, vol. H83, Berlin: Springer, 1994, pp.117-129.PUB
-
1993 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350937F. BISACCIA, et al., “REACTION-MECHANISM OF THE RECONSTITUTED TRICARBOXYLATE CARRIER FROM RAT-LIVER MITOCHONDRIA”, BIOCHIMICA ET BIOPHYSICA ACTA, vol. 1142, 1993, pp. 139-145.PUB | DOI | WoS | PubMed | Europe PMC
-
1993 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350944T. Dierks, et al., “THE ROLE OF MOLECULAR CHAPERONES IN PROTEIN-TRANSPORT INTO THE ENDOPLASMIC-RETICULUM”, PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, vol. 339, 1993, pp. 335-341.PUB | DOI | WoS | PubMed | Europe PMC
-
1993 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2372500P. Klappa, et al., “Components and mechanisms involved in transport of proteins into the endoplasmic reticulum”, Endoplasmic reticulum, N. Borgese and J.R. Harris, eds., Subcellular Biochemistry, vol. 21, Berlin: Springer, 1993, pp.17-40.PUB
-
1993 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2372529T. Dierks, et al., “The role of molecular chaperones in protein transport into the endoplasmic reticulum”, Molecular Chaperones, R.J. Ellis, R.A. Laskey, and G.H. Lorimer, eds., London: Chapman and Hall, 1993, pp.79-85.PUB
-
1993 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350930C. INDIVERI, et al., “KINETIC CHARACTERIZATION OF THE RECONSTITUTED DICARBOXYLATE CARRIER FROM MITOCHONDRIA - A 4-BINDING-SITE SEQUENTIAL TRANSPORT-SYSTEM”, BIOCHIMICA ET BIOPHYSICA ACTA, vol. 1143, 1993, pp. 310-318.PUB | DOI | WoS | PubMed | Europe PMC
-
1992 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350950C. INDIVERI, et al., “THE MITOCHONDRIAL CARNITINE CARRIER - CHARACTERIZATION OF SH-GROUPS RELEVANT FOR ITS TRANSPORT FUNCTION”, BIOCHIMICA ET BIOPHYSICA ACTA, vol. 1140, 1992, pp. 53-58.PUB | DOI | WoS | PubMed | Europe PMC
-
1992 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350957R. STAPPEN, et al., “PROBING THE ACTIVE-SITE OF THE RECONSTITUTED ASPARTATE GLUTAMATE CARRIER FROM MITOCHONDRIA - STRUCTURE-FUNCTION RELATIONSHIP INVOLVING ONE LYSINE AND 2 CYSTEINE RESIDUES”, EUROPEAN JOURNAL OF BIOCHEMISTRY, vol. 210, 1992, pp. 269-277.PUB | DOI | WoS | PubMed | Europe PMC
-
1992 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350963T. Dierks, et al., “PROBING THE ACTIVE-SITE OF THE RECONSTITUTED ASPARTATE GLUTAMATE CARRIER FROM BOVINE HEART-MITOCHONDRIA - CARBODIIMIDE-CATALYZED ACYLATION OF A FUNCTIONAL LYSINE RESIDUE”, BIOCHIMICA ET BIOPHYSICA ACTA, vol. 1103, 1992, pp. 13-24.PUB | DOI | WoS | PubMed | Europe PMC
-
1991 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350977C. INDIVERI, et al., “REACTION-MECHANISM OF THE RECONSTITUTED OXOGLUTARATE CARRIER FROM BOVINE HEART-MITOCHONDRIA”, EUROPEAN JOURNAL OF BIOCHEMISTRY, vol. 198, 1991, pp. 339-347.PUB | DOI | WoS | PubMed | Europe PMC
-
1991 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350969F.E. SLUSE, et al., “KINETIC-STUDY OF THE ASPARTATE GLUTAMATE CARRIER IN INTACT RAT-HEART MITOCHONDRIA AND COMPARISON WITH A RECONSTITUTED SYSTEM”, BIOCHIMICA ET BIOPHYSICA ACTA, vol. 1058, 1991, pp. 329-338.PUB | DOI | WoS | PubMed | Europe PMC
-
1990 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350989T. Dierks, A. SALENTIN, and R. KRAMER, “PORE-LIKE AND CARRIER-LIKE PROPERTIES OF THE MITOCHONDRIAL ASPARTATE GLUTAMATE CARRIER AFTER MODIFICATION BY SH-REAGENTS - EVIDENCE FOR A PREFORMED CHANNEL AS A STRUCTURAL REQUIREMENT OF CARRIER-MEDIATED TRANSPORT”, BIOCHIMICA ET BIOPHYSICA ACTA, vol. 1028, 1990, pp. 281-288.PUB | DOI | WoS | PubMed | Europe PMC
-
1990 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350983T. Dierks, et al., “THE MITOCHONDRIAL ASPARTATE GLUTAMATE AND ADP/ATP CARRIER SWITCH FROM OBLIGATE COUNTEREXCHANGE TO UNIDIRECTIONAL TRANSPORT AFTER MODIFICATION BY SH-REAGENTS”, BIOCHIMICA ET BIOPHYSICA ACTA, vol. 1028, 1990, pp. 268-280.PUB | DOI | WoS | PubMed | Europe PMC
-
1989 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350994C. INDIVERI, et al., “KINETIC DISCRIMINATION OF 2 SUBSTRATE BINDING-SITES OF THE RECONSTITUTED DICARBOXYLATE CARRIER FROM RAT-LIVER MITOCHONDRIA”, BIOCHIMICA ET BIOPHYSICA ACTA, vol. 977, 1989, pp. 194-199.PUB | DOI | WoS | PubMed | Europe PMC
-
1989 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2372511T. Dierks and R. Krämer, “Reaction mechanism of the reconstituted aspartate / glutamate carrier from mitochondria. Reversible switching to uniport function”, Anion Carriers of Mitochondrial Membranes, A. Azzi, et al., eds., Berlin: Springer, 1989, pp.99-110.PUB
-
1988 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2351000T. Dierks, E. RIEMER, and R. KRAMER, “REACTION-MECHANISM OF THE RECONSTITUTED ASPARTATE GLUTAMATE CARRIER FROM BOVINE HEART-MITOCHONDRIA”, BIOCHIMICA ET BIOPHYSICA ACTA, vol. 943, 1988, pp. 231-244.PUB | DOI | WoS | PubMed | Europe PMC
-
1988 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2351005T. Dierks and R. KRAMER, “ASYMMETRIC ORIENTATION OF THE RECONSTITUTED ASPARTATE GLUTAMATE CARRIER FROM MITOCHONDRIA”, BIOCHIMICA ET BIOPHYSICA ACTA, vol. 937, 1988, pp. 112-126.PUB | DOI | WoS | PubMed | Europe PMC