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You searched for subject:(Enzyme Design). Showing records 1 – 30 of 79 total matches.

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University of Adelaide

1. Soares da Costa, Tatiana Pereira. Exploring the structure-function relationship of Biotin Protein Ligase from Staphylococcus aureus : implications for selective inhibitor design.

Degree: 2013, University of Adelaide

 There is a well-documented need to replenish the antibiotic pipeline with new products to combat the rise of drug resistant bacteria, such as the superbug… (more)

Subjects/Keywords: enzyme; inhibitor design; biotin protein ligase

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APA (6th Edition):

Soares da Costa, T. P. (2013). Exploring the structure-function relationship of Biotin Protein Ligase from Staphylococcus aureus : implications for selective inhibitor design. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/90757

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Soares da Costa, Tatiana Pereira. “Exploring the structure-function relationship of Biotin Protein Ligase from Staphylococcus aureus : implications for selective inhibitor design.” 2013. Thesis, University of Adelaide. Accessed June 06, 2020. http://hdl.handle.net/2440/90757.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Soares da Costa, Tatiana Pereira. “Exploring the structure-function relationship of Biotin Protein Ligase from Staphylococcus aureus : implications for selective inhibitor design.” 2013. Web. 06 Jun 2020.

Vancouver:

Soares da Costa TP. Exploring the structure-function relationship of Biotin Protein Ligase from Staphylococcus aureus : implications for selective inhibitor design. [Internet] [Thesis]. University of Adelaide; 2013. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/2440/90757.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Soares da Costa TP. Exploring the structure-function relationship of Biotin Protein Ligase from Staphylococcus aureus : implications for selective inhibitor design. [Thesis]. University of Adelaide; 2013. Available from: http://hdl.handle.net/2440/90757

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

2. Jenkins, Jonathan. Computational design, construction, and characterisation of artificial peroxidases.

Degree: PhD, 2019, University of Bristol

 One of the ambitious goals of synthetic biology is to produce biologically compatible catalysts that are cheap, robust, and sustainable. Tailor-made synthetic proteins that can… (more)

Subjects/Keywords: de novo; enzyme; design; maquette; peroxidase

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APA (6th Edition):

Jenkins, J. (2019). Computational design, construction, and characterisation of artificial peroxidases. (Doctoral Dissertation). University of Bristol. Retrieved from http://hdl.handle.net/1983/f7f37854-66fc-414d-ad50-040c5fc901c4

Chicago Manual of Style (16th Edition):

Jenkins, Jonathan. “Computational design, construction, and characterisation of artificial peroxidases.” 2019. Doctoral Dissertation, University of Bristol. Accessed June 06, 2020. http://hdl.handle.net/1983/f7f37854-66fc-414d-ad50-040c5fc901c4.

MLA Handbook (7th Edition):

Jenkins, Jonathan. “Computational design, construction, and characterisation of artificial peroxidases.” 2019. Web. 06 Jun 2020.

Vancouver:

Jenkins J. Computational design, construction, and characterisation of artificial peroxidases. [Internet] [Doctoral dissertation]. University of Bristol; 2019. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/1983/f7f37854-66fc-414d-ad50-040c5fc901c4.

Council of Science Editors:

Jenkins J. Computational design, construction, and characterisation of artificial peroxidases. [Doctoral Dissertation]. University of Bristol; 2019. Available from: http://hdl.handle.net/1983/f7f37854-66fc-414d-ad50-040c5fc901c4


University of Illinois – Urbana-Champaign

3. Miner, Kyle D. Rational design of functional heme copper oxidases in myoglobin.

Degree: PhD, 0318, 2012, University of Illinois – Urbana-Champaign

 Proteins are involved in nearly every process that occurs in living systems, either as a main participant in the process or preforming a supporting role.… (more)

Subjects/Keywords: Protein Design; Heme Copper Oxidases; Enzyme modeling

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APA (6th Edition):

Miner, K. D. (2012). Rational design of functional heme copper oxidases in myoglobin. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/29570

Chicago Manual of Style (16th Edition):

Miner, Kyle D. “Rational design of functional heme copper oxidases in myoglobin.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed June 06, 2020. http://hdl.handle.net/2142/29570.

MLA Handbook (7th Edition):

Miner, Kyle D. “Rational design of functional heme copper oxidases in myoglobin.” 2012. Web. 06 Jun 2020.

Vancouver:

Miner KD. Rational design of functional heme copper oxidases in myoglobin. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/2142/29570.

Council of Science Editors:

Miner KD. Rational design of functional heme copper oxidases in myoglobin. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/29570


McMaster University

4. Balachandran, Naresh. DAHP Oxime: A Transition State Mimic Inhibitor Of DAHP Synthase.

Degree: PhD, 2014, McMaster University

The rise of bacterial infections and increase of antibiotic resistant bacteria has become a major problem in the treatment of bacterial infections. The use… (more)

Subjects/Keywords: enzyme kinetics; mechanism; drug design; x-ray crystallography; enzyme dynamics; Biochemistry; Biochemistry

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APA (6th Edition):

Balachandran, N. (2014). DAHP Oxime: A Transition State Mimic Inhibitor Of DAHP Synthase. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/14139

Chicago Manual of Style (16th Edition):

Balachandran, Naresh. “DAHP Oxime: A Transition State Mimic Inhibitor Of DAHP Synthase.” 2014. Doctoral Dissertation, McMaster University. Accessed June 06, 2020. http://hdl.handle.net/11375/14139.

MLA Handbook (7th Edition):

Balachandran, Naresh. “DAHP Oxime: A Transition State Mimic Inhibitor Of DAHP Synthase.” 2014. Web. 06 Jun 2020.

Vancouver:

Balachandran N. DAHP Oxime: A Transition State Mimic Inhibitor Of DAHP Synthase. [Internet] [Doctoral dissertation]. McMaster University; 2014. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/11375/14139.

Council of Science Editors:

Balachandran N. DAHP Oxime: A Transition State Mimic Inhibitor Of DAHP Synthase. [Doctoral Dissertation]. McMaster University; 2014. Available from: http://hdl.handle.net/11375/14139


Vanderbilt University

5. Nannemann, David Patrick. Directed Biosynthesis of the Nucleoside Analog Drug Didanosine.

Degree: PhD, Chemistry, 2011, Vanderbilt University

 Nucleoside analogs comprise a large therapeutic class applied to the treatment of HIV, hepatitis, and other diseases. Their broad use and applicability are in contrast… (more)

Subjects/Keywords: Enzyme Engineering; Bioretrosynthesis; Computational Enzyme Design; Directed Evolution; Purine Nucleoside Phosphorylase; Phosphopentomutase

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APA (6th Edition):

Nannemann, D. P. (2011). Directed Biosynthesis of the Nucleoside Analog Drug Didanosine. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-04042011-165321/ ;

Chicago Manual of Style (16th Edition):

Nannemann, David Patrick. “Directed Biosynthesis of the Nucleoside Analog Drug Didanosine.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed June 06, 2020. http://etd.library.vanderbilt.edu//available/etd-04042011-165321/ ;.

MLA Handbook (7th Edition):

Nannemann, David Patrick. “Directed Biosynthesis of the Nucleoside Analog Drug Didanosine.” 2011. Web. 06 Jun 2020.

Vancouver:

Nannemann DP. Directed Biosynthesis of the Nucleoside Analog Drug Didanosine. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2020 Jun 06]. Available from: http://etd.library.vanderbilt.edu//available/etd-04042011-165321/ ;.

Council of Science Editors:

Nannemann DP. Directed Biosynthesis of the Nucleoside Analog Drug Didanosine. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://etd.library.vanderbilt.edu//available/etd-04042011-165321/ ;


UCLA

6. Nechay, Michael. Multiscale Modeling of Metalloenzymes: Design and Evolution.

Degree: Chemistry, 2017, UCLA

 With just a simple alphabet of natural amino acids and common metals, enzymes perform a spectacular number of reactions necessary for life on earth with… (more)

Subjects/Keywords: Computational chemistry; catalysis design; enzyme design; metal substitution; multiscale modeling; protein design

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APA (6th Edition):

Nechay, M. (2017). Multiscale Modeling of Metalloenzymes: Design and Evolution. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/6c0848pm

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Nechay, Michael. “Multiscale Modeling of Metalloenzymes: Design and Evolution.” 2017. Thesis, UCLA. Accessed June 06, 2020. http://www.escholarship.org/uc/item/6c0848pm.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Nechay, Michael. “Multiscale Modeling of Metalloenzymes: Design and Evolution.” 2017. Web. 06 Jun 2020.

Vancouver:

Nechay M. Multiscale Modeling of Metalloenzymes: Design and Evolution. [Internet] [Thesis]. UCLA; 2017. [cited 2020 Jun 06]. Available from: http://www.escholarship.org/uc/item/6c0848pm.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Nechay M. Multiscale Modeling of Metalloenzymes: Design and Evolution. [Thesis]. UCLA; 2017. Available from: http://www.escholarship.org/uc/item/6c0848pm

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Penn State University

7. Fazelinia, Hossein. COMPUTATIONAL DESIGN AND EXPERIMENTAL CHARACTERIZATION OF PROTEINS WITH NOVEL FUNCTIONS.

Degree: PhD, Chemical Engineering, 2009, Penn State University

 Protein engineering involves the design of known protein structures to introduce an improved or completely novel function. This is accomplished by either modifying the existing… (more)

Subjects/Keywords: OptGraft; Protein engineering; Computational protein design; Enzyme cofactor alteration; IPRO

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APA (6th Edition):

Fazelinia, H. (2009). COMPUTATIONAL DESIGN AND EXPERIMENTAL CHARACTERIZATION OF PROTEINS WITH NOVEL FUNCTIONS. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/9001

Chicago Manual of Style (16th Edition):

Fazelinia, Hossein. “COMPUTATIONAL DESIGN AND EXPERIMENTAL CHARACTERIZATION OF PROTEINS WITH NOVEL FUNCTIONS.” 2009. Doctoral Dissertation, Penn State University. Accessed June 06, 2020. https://etda.libraries.psu.edu/catalog/9001.

MLA Handbook (7th Edition):

Fazelinia, Hossein. “COMPUTATIONAL DESIGN AND EXPERIMENTAL CHARACTERIZATION OF PROTEINS WITH NOVEL FUNCTIONS.” 2009. Web. 06 Jun 2020.

Vancouver:

Fazelinia H. COMPUTATIONAL DESIGN AND EXPERIMENTAL CHARACTERIZATION OF PROTEINS WITH NOVEL FUNCTIONS. [Internet] [Doctoral dissertation]. Penn State University; 2009. [cited 2020 Jun 06]. Available from: https://etda.libraries.psu.edu/catalog/9001.

Council of Science Editors:

Fazelinia H. COMPUTATIONAL DESIGN AND EXPERIMENTAL CHARACTERIZATION OF PROTEINS WITH NOVEL FUNCTIONS. [Doctoral Dissertation]. Penn State University; 2009. Available from: https://etda.libraries.psu.edu/catalog/9001


Texas A&M University

8. Uzuner, Ugur. Structure Dynamics Guided Enzyme Improvement of ENDO-BETA-1, 4-XYLANASE I.

Degree: 2013, Texas A&M University

Enzyme structure dynamics has recently been revealed to be essential for structure-function relationship. Among various structure dynamics analysis platforms, hydrogen deuterium exchange mass spectrometry stands… (more)

Subjects/Keywords: Xylanase 1; enzyme; structure dynamics; Trichoderma longibrachiatum; HDX-MS; rational design

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APA (6th Edition):

Uzuner, U. (2013). Structure Dynamics Guided Enzyme Improvement of ENDO-BETA-1, 4-XYLANASE I. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/150988

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Uzuner, Ugur. “Structure Dynamics Guided Enzyme Improvement of ENDO-BETA-1, 4-XYLANASE I.” 2013. Thesis, Texas A&M University. Accessed June 06, 2020. http://hdl.handle.net/1969.1/150988.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Uzuner, Ugur. “Structure Dynamics Guided Enzyme Improvement of ENDO-BETA-1, 4-XYLANASE I.” 2013. Web. 06 Jun 2020.

Vancouver:

Uzuner U. Structure Dynamics Guided Enzyme Improvement of ENDO-BETA-1, 4-XYLANASE I. [Internet] [Thesis]. Texas A&M University; 2013. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/1969.1/150988.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Uzuner U. Structure Dynamics Guided Enzyme Improvement of ENDO-BETA-1, 4-XYLANASE I. [Thesis]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/150988

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


KTH

9. Hermansson, Anders. Calculating Ligand-Protein Binding Energies from Molecular Dynamics Simulations.

Degree: Chemical Science and Engineering (CHE), 2015, KTH

  Indications that existing parameter sets of extended Linear Interaction Energy (LIE) models are transferable between lipases from Rhizomucor Miehei and Thermomyces Lanigunosus in complex… (more)

Subjects/Keywords: Molecular Dynamics; Linear Interaction Energy; Enzyme Design; Lipase; Binding Energy

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APA (6th Edition):

Hermansson, A. (2015). Calculating Ligand-Protein Binding Energies from Molecular Dynamics Simulations. (Thesis). KTH. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-170722

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Hermansson, Anders. “Calculating Ligand-Protein Binding Energies from Molecular Dynamics Simulations.” 2015. Thesis, KTH. Accessed June 06, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-170722.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Hermansson, Anders. “Calculating Ligand-Protein Binding Energies from Molecular Dynamics Simulations.” 2015. Web. 06 Jun 2020.

Vancouver:

Hermansson A. Calculating Ligand-Protein Binding Energies from Molecular Dynamics Simulations. [Internet] [Thesis]. KTH; 2015. [cited 2020 Jun 06]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-170722.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Hermansson A. Calculating Ligand-Protein Binding Energies from Molecular Dynamics Simulations. [Thesis]. KTH; 2015. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-170722

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

10. Rahnel, Hedi. ARC-inhibitors: from reliable biochemical assays to regulators of physiology of cells .

Degree: 2018, Tartu University

 Inimrakk on keeruline süsteem, mis koosneb paljudest molekulidest ning rangelt reguleeritud molekulidevahelisest kommunikatsioonist. Proteiinkinaasid on valgud, mis rakus olulisi protsesse kontrollivad. Häireid proteiinkinaaside töös on… (more)

Subjects/Keywords: protein kinases; inhibitors; ligands; enzyme activity; substrate; afinity; drug design

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APA (6th Edition):

Rahnel, H. (2018). ARC-inhibitors: from reliable biochemical assays to regulators of physiology of cells . (Thesis). Tartu University. Retrieved from http://hdl.handle.net/10062/59834

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Rahnel, Hedi. “ARC-inhibitors: from reliable biochemical assays to regulators of physiology of cells .” 2018. Thesis, Tartu University. Accessed June 06, 2020. http://hdl.handle.net/10062/59834.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Rahnel, Hedi. “ARC-inhibitors: from reliable biochemical assays to regulators of physiology of cells .” 2018. Web. 06 Jun 2020.

Vancouver:

Rahnel H. ARC-inhibitors: from reliable biochemical assays to regulators of physiology of cells . [Internet] [Thesis]. Tartu University; 2018. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/10062/59834.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Rahnel H. ARC-inhibitors: from reliable biochemical assays to regulators of physiology of cells . [Thesis]. Tartu University; 2018. Available from: http://hdl.handle.net/10062/59834

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Southern California

11. Cao, Jie. In silico enzyme modeling: A study of entropic contributions to enzyme catalysis and the design of artificial kemp eliminase.

Degree: PhD, Chemistry, 2011, University of Southern California

 Naturally occurring enzymes are exceptional catalysts. One of the most fundamental challenges in biotechnology, and in some respects in biochemistry, is the ability to design(more)

Subjects/Keywords: computer-aided enzyme design; entropy; QM/MM; kemp eliminase; reorginization; EVB

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APA (6th Edition):

Cao, J. (2011). In silico enzyme modeling: A study of entropic contributions to enzyme catalysis and the design of artificial kemp eliminase. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/472094/rec/3432

Chicago Manual of Style (16th Edition):

Cao, Jie. “In silico enzyme modeling: A study of entropic contributions to enzyme catalysis and the design of artificial kemp eliminase.” 2011. Doctoral Dissertation, University of Southern California. Accessed June 06, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/472094/rec/3432.

MLA Handbook (7th Edition):

Cao, Jie. “In silico enzyme modeling: A study of entropic contributions to enzyme catalysis and the design of artificial kemp eliminase.” 2011. Web. 06 Jun 2020.

Vancouver:

Cao J. In silico enzyme modeling: A study of entropic contributions to enzyme catalysis and the design of artificial kemp eliminase. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2020 Jun 06]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/472094/rec/3432.

Council of Science Editors:

Cao J. In silico enzyme modeling: A study of entropic contributions to enzyme catalysis and the design of artificial kemp eliminase. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/472094/rec/3432


University of Washington

12. Richter, Florian. Computational de-novo design of ester hydrolases.

Degree: PhD, 2013, University of Washington

 Computational protein design is a relatively new technique used to devise amino acid sequences to fold into proteins having novel structures or functions. Here, we… (more)

Subjects/Keywords: catalysis; computational protein design; enzyme design; hydrolysis; synthetic biology; Biochemistry; Chemistry; Biological chemistry

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APA (6th Edition):

Richter, F. (2013). Computational de-novo design of ester hydrolases. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/21829

Chicago Manual of Style (16th Edition):

Richter, Florian. “Computational de-novo design of ester hydrolases.” 2013. Doctoral Dissertation, University of Washington. Accessed June 06, 2020. http://hdl.handle.net/1773/21829.

MLA Handbook (7th Edition):

Richter, Florian. “Computational de-novo design of ester hydrolases.” 2013. Web. 06 Jun 2020.

Vancouver:

Richter F. Computational de-novo design of ester hydrolases. [Internet] [Doctoral dissertation]. University of Washington; 2013. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/1773/21829.

Council of Science Editors:

Richter F. Computational de-novo design of ester hydrolases. [Doctoral Dissertation]. University of Washington; 2013. Available from: http://hdl.handle.net/1773/21829


University of Manchester

13. Ashworth, Mark. Structure-based engineering of CYP105AS1 for the production of high-value molecules.

Degree: PhD, 2018, University of Manchester

 Biocatalysis represents an attractive route to the production of various compounds which are difficult or impossible to synthesise and isolate using traditional chemical synthesis. In… (more)

Subjects/Keywords: 540; Statins; Pravastatin; Biocatalysis; CYP105AS1; Cytochrome P450; Biotechnology; Enzyme engineering; Computational enzyme design; Protein engineering; Synthetic biology; Enantioselectivity

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APA (6th Edition):

Ashworth, M. (2018). Structure-based engineering of CYP105AS1 for the production of high-value molecules. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/structurebased-engineering-of-cyp105as1-for-the-production-of-highvalue-molecules(2e7a9ade-a21e-4138-a692-e84541b517ce).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740368

Chicago Manual of Style (16th Edition):

Ashworth, Mark. “Structure-based engineering of CYP105AS1 for the production of high-value molecules.” 2018. Doctoral Dissertation, University of Manchester. Accessed June 06, 2020. https://www.research.manchester.ac.uk/portal/en/theses/structurebased-engineering-of-cyp105as1-for-the-production-of-highvalue-molecules(2e7a9ade-a21e-4138-a692-e84541b517ce).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740368.

MLA Handbook (7th Edition):

Ashworth, Mark. “Structure-based engineering of CYP105AS1 for the production of high-value molecules.” 2018. Web. 06 Jun 2020.

Vancouver:

Ashworth M. Structure-based engineering of CYP105AS1 for the production of high-value molecules. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2020 Jun 06]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/structurebased-engineering-of-cyp105as1-for-the-production-of-highvalue-molecules(2e7a9ade-a21e-4138-a692-e84541b517ce).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740368.

Council of Science Editors:

Ashworth M. Structure-based engineering of CYP105AS1 for the production of high-value molecules. [Doctoral Dissertation]. University of Manchester; 2018. Available from: https://www.research.manchester.ac.uk/portal/en/theses/structurebased-engineering-of-cyp105as1-for-the-production-of-highvalue-molecules(2e7a9ade-a21e-4138-a692-e84541b517ce).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740368


Universidade do Rio Grande do Sul

14. Rodrigues, Rafael Costa. Síntese de biodiesel através de transesterificação enzimática de óleos vegetais catalisada por lipase imobilizada por ligação covalente multipontual.

Degree: 2009, Universidade do Rio Grande do Sul

 Biodiesel consiste de ésteres alquílicos de ácidos graxos produzidos pela transesterificação de triglicerídeos com álcoois de cadeia curta. Tradicionalmente, a reação ocorre na presença de… (more)

Subjects/Keywords: Ethanolysis; Biodiesel; Vegetable oils; Óleos vegetais; Experimental design; Lipase; Multipoint immobilization; Enzyme stability

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APA (6th Edition):

Rodrigues, R. C. (2009). Síntese de biodiesel através de transesterificação enzimática de óleos vegetais catalisada por lipase imobilizada por ligação covalente multipontual. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/15447

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Rodrigues, Rafael Costa. “Síntese de biodiesel através de transesterificação enzimática de óleos vegetais catalisada por lipase imobilizada por ligação covalente multipontual.” 2009. Thesis, Universidade do Rio Grande do Sul. Accessed June 06, 2020. http://hdl.handle.net/10183/15447.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Rodrigues, Rafael Costa. “Síntese de biodiesel através de transesterificação enzimática de óleos vegetais catalisada por lipase imobilizada por ligação covalente multipontual.” 2009. Web. 06 Jun 2020.

Vancouver:

Rodrigues RC. Síntese de biodiesel através de transesterificação enzimática de óleos vegetais catalisada por lipase imobilizada por ligação covalente multipontual. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2009. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/10183/15447.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Rodrigues RC. Síntese de biodiesel através de transesterificação enzimática de óleos vegetais catalisada por lipase imobilizada por ligação covalente multipontual. [Thesis]. Universidade do Rio Grande do Sul; 2009. Available from: http://hdl.handle.net/10183/15447

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Kentucky

15. Hou, Shurong. HUMAN BUTYRYLCHOLINESTERASE MUTANTS FOR COCAINE DETOXIFICATION.

Degree: 2014, University of Kentucky

 Cocaine is one of the most reinforcing drugs of abuse and has caused serious medical and social problems. There is no FDA-approved medication specific for… (more)

Subjects/Keywords: Protein drug; enzyme therapy; human butyrylcholinesterase; cocaine; drug abuse treatment; Pharmaceutics and Drug Design

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Hou, S. (2014). HUMAN BUTYRYLCHOLINESTERASE MUTANTS FOR COCAINE DETOXIFICATION. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacy_etds/38

Chicago Manual of Style (16th Edition):

Hou, Shurong. “HUMAN BUTYRYLCHOLINESTERASE MUTANTS FOR COCAINE DETOXIFICATION.” 2014. Doctoral Dissertation, University of Kentucky. Accessed June 06, 2020. https://uknowledge.uky.edu/pharmacy_etds/38.

MLA Handbook (7th Edition):

Hou, Shurong. “HUMAN BUTYRYLCHOLINESTERASE MUTANTS FOR COCAINE DETOXIFICATION.” 2014. Web. 06 Jun 2020.

Vancouver:

Hou S. HUMAN BUTYRYLCHOLINESTERASE MUTANTS FOR COCAINE DETOXIFICATION. [Internet] [Doctoral dissertation]. University of Kentucky; 2014. [cited 2020 Jun 06]. Available from: https://uknowledge.uky.edu/pharmacy_etds/38.

Council of Science Editors:

Hou S. HUMAN BUTYRYLCHOLINESTERASE MUTANTS FOR COCAINE DETOXIFICATION. [Doctoral Dissertation]. University of Kentucky; 2014. Available from: https://uknowledge.uky.edu/pharmacy_etds/38


University of Kentucky

16. Chen, Xiabin. DEVELOPMENT OF COCAINE HYDROLASE FOR THERAPEUTIC TREATMENT OF COCAINE ABUSE.

Degree: 2016, University of Kentucky

 Cocaine abuse is a world-wide public health and social problem without a U.S. Food and Drug Administration (FDA)-approved medication. An ideal anti-cocaine medication would accelerate… (more)

Subjects/Keywords: Cocaine abuse; benzoylecgonine; enzyme therapy; protein engineering; butyrylcholinesterase; LC-MS/MS; Pharmaceutics and Drug Design

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APA (6th Edition):

Chen, X. (2016). DEVELOPMENT OF COCAINE HYDROLASE FOR THERAPEUTIC TREATMENT OF COCAINE ABUSE. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacy_etds/59

Chicago Manual of Style (16th Edition):

Chen, Xiabin. “DEVELOPMENT OF COCAINE HYDROLASE FOR THERAPEUTIC TREATMENT OF COCAINE ABUSE.” 2016. Doctoral Dissertation, University of Kentucky. Accessed June 06, 2020. https://uknowledge.uky.edu/pharmacy_etds/59.

MLA Handbook (7th Edition):

Chen, Xiabin. “DEVELOPMENT OF COCAINE HYDROLASE FOR THERAPEUTIC TREATMENT OF COCAINE ABUSE.” 2016. Web. 06 Jun 2020.

Vancouver:

Chen X. DEVELOPMENT OF COCAINE HYDROLASE FOR THERAPEUTIC TREATMENT OF COCAINE ABUSE. [Internet] [Doctoral dissertation]. University of Kentucky; 2016. [cited 2020 Jun 06]. Available from: https://uknowledge.uky.edu/pharmacy_etds/59.

Council of Science Editors:

Chen X. DEVELOPMENT OF COCAINE HYDROLASE FOR THERAPEUTIC TREATMENT OF COCAINE ABUSE. [Doctoral Dissertation]. University of Kentucky; 2016. Available from: https://uknowledge.uky.edu/pharmacy_etds/59


University of Southern California

17. Frushicheva, Maria P. Quantitative computer-aided studies of artificial and enantioselective enzymes.

Degree: PhD, Chemistry, 2012, University of Southern California

 A fundamental challenge in biotechnology and in biochemistry is an ability to design effective enzymes. Despite a gradual progress on this front, most of the… (more)

Subjects/Keywords: artificial enzymes; catalytic reactions; computational chemistry; computer-aided enzyme design; enantioselectivity; enzymology

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Frushicheva, M. P. (2012). Quantitative computer-aided studies of artificial and enantioselective enzymes. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/115440/rec/5355

Chicago Manual of Style (16th Edition):

Frushicheva, Maria P. “Quantitative computer-aided studies of artificial and enantioselective enzymes.” 2012. Doctoral Dissertation, University of Southern California. Accessed June 06, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/115440/rec/5355.

MLA Handbook (7th Edition):

Frushicheva, Maria P. “Quantitative computer-aided studies of artificial and enantioselective enzymes.” 2012. Web. 06 Jun 2020.

Vancouver:

Frushicheva MP. Quantitative computer-aided studies of artificial and enantioselective enzymes. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2020 Jun 06]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/115440/rec/5355.

Council of Science Editors:

Frushicheva MP. Quantitative computer-aided studies of artificial and enantioselective enzymes. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/115440/rec/5355


University of Kentucky

18. Holbrook, Selina Y. L. DISCOVERY OF NEW ANTIMICROBIAL OPTIONS AND EVALUATION OF AMINOGLYCOSIDE RESISTANCE ENZYME-ASSOCIATED RESISTANCE EPIDEMIC.

Degree: 2018, University of Kentucky

 The extensive and sometimes incorrect and noncompliant use of various types of antimicrobial agents has accelerated the development of antimicrobial resistance (AMR). In fact, AMR… (more)

Subjects/Keywords: aminoglycoside-modifying enzyme (AME); enzyme engineering; substrate promiscuity; enzyme kinetics; minimum inhibitory concentrations (MICs); drug combination; Bacteria; Bacterial Infections and Mycoses; Fungi; Medicinal and Pharmaceutical Chemistry; Microbiology; Pharmaceutics and Drug Design

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APA (6th Edition):

Holbrook, S. Y. L. (2018). DISCOVERY OF NEW ANTIMICROBIAL OPTIONS AND EVALUATION OF AMINOGLYCOSIDE RESISTANCE ENZYME-ASSOCIATED RESISTANCE EPIDEMIC. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacy_etds/89

Chicago Manual of Style (16th Edition):

Holbrook, Selina Y L. “DISCOVERY OF NEW ANTIMICROBIAL OPTIONS AND EVALUATION OF AMINOGLYCOSIDE RESISTANCE ENZYME-ASSOCIATED RESISTANCE EPIDEMIC.” 2018. Doctoral Dissertation, University of Kentucky. Accessed June 06, 2020. https://uknowledge.uky.edu/pharmacy_etds/89.

MLA Handbook (7th Edition):

Holbrook, Selina Y L. “DISCOVERY OF NEW ANTIMICROBIAL OPTIONS AND EVALUATION OF AMINOGLYCOSIDE RESISTANCE ENZYME-ASSOCIATED RESISTANCE EPIDEMIC.” 2018. Web. 06 Jun 2020.

Vancouver:

Holbrook SYL. DISCOVERY OF NEW ANTIMICROBIAL OPTIONS AND EVALUATION OF AMINOGLYCOSIDE RESISTANCE ENZYME-ASSOCIATED RESISTANCE EPIDEMIC. [Internet] [Doctoral dissertation]. University of Kentucky; 2018. [cited 2020 Jun 06]. Available from: https://uknowledge.uky.edu/pharmacy_etds/89.

Council of Science Editors:

Holbrook SYL. DISCOVERY OF NEW ANTIMICROBIAL OPTIONS AND EVALUATION OF AMINOGLYCOSIDE RESISTANCE ENZYME-ASSOCIATED RESISTANCE EPIDEMIC. [Doctoral Dissertation]. University of Kentucky; 2018. Available from: https://uknowledge.uky.edu/pharmacy_etds/89


Universitetet i Tromsø

19. Michetti, Davide. Surface properties tune thermal adaptation of enzymes - Computational studies of endonuclease A .

Degree: 2017, Universitetet i Tromsø

 The endonucleases A from Aliivibrio salmonicida (VsEndA, cold-adapted) and Vibrio cholerae (VcEndA, warm-adapted) have been studied in this work. The goal was to compare these… (more)

Subjects/Keywords: Enzyme cold adaptation; Empirical Valence Bond; Enzyme Design; Enzyme catalysis; VDP::Matematikk og Naturvitenskap: 400::Basale biofag: 470::Biokjemi: 476; VDP::Mathematics and natural science: 400::Basic biosciences: 470::Biochemistry: 476

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APA (6th Edition):

Michetti, D. (2017). Surface properties tune thermal adaptation of enzymes - Computational studies of endonuclease A . (Doctoral Dissertation). Universitetet i Tromsø. Retrieved from http://hdl.handle.net/10037/11153

Chicago Manual of Style (16th Edition):

Michetti, Davide. “Surface properties tune thermal adaptation of enzymes - Computational studies of endonuclease A .” 2017. Doctoral Dissertation, Universitetet i Tromsø. Accessed June 06, 2020. http://hdl.handle.net/10037/11153.

MLA Handbook (7th Edition):

Michetti, Davide. “Surface properties tune thermal adaptation of enzymes - Computational studies of endonuclease A .” 2017. Web. 06 Jun 2020.

Vancouver:

Michetti D. Surface properties tune thermal adaptation of enzymes - Computational studies of endonuclease A . [Internet] [Doctoral dissertation]. Universitetet i Tromsø 2017. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/10037/11153.

Council of Science Editors:

Michetti D. Surface properties tune thermal adaptation of enzymes - Computational studies of endonuclease A . [Doctoral Dissertation]. Universitetet i Tromsø 2017. Available from: http://hdl.handle.net/10037/11153


University of California – Berkeley

20. Bhowmick, Asmit. Understanding and Improving Designed Enzymes by Computer Simulations.

Degree: Chemical Engineering, 2016, University of California – Berkeley

 AbstractUnderstanding and Improving Designed Enzymes by Computer SimulationsBy Asmit BhowmickDoctor of Philosophy in Chemical EngineeringUniversity of California, BerkeleyProfessor Teresa Head-Gordon, ChairThe ability to control for… (more)

Subjects/Keywords: Chemical engineering; Biophysics; Physical chemistry; Electrostatic Stabilization; Enzyme Design; Molecular Dynamics; Monte Carlo; Mutual Information; Protein Engineering

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APA (6th Edition):

Bhowmick, A. (2016). Understanding and Improving Designed Enzymes by Computer Simulations. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/9t13q8v7

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Bhowmick, Asmit. “Understanding and Improving Designed Enzymes by Computer Simulations.” 2016. Thesis, University of California – Berkeley. Accessed June 06, 2020. http://www.escholarship.org/uc/item/9t13q8v7.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Bhowmick, Asmit. “Understanding and Improving Designed Enzymes by Computer Simulations.” 2016. Web. 06 Jun 2020.

Vancouver:

Bhowmick A. Understanding and Improving Designed Enzymes by Computer Simulations. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2020 Jun 06]. Available from: http://www.escholarship.org/uc/item/9t13q8v7.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Bhowmick A. Understanding and Improving Designed Enzymes by Computer Simulations. [Thesis]. University of California – Berkeley; 2016. Available from: http://www.escholarship.org/uc/item/9t13q8v7

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

21. Braga, Anna Rafaela Cavalcante. Viabilização da utilização de co-produtos da agroindústria na produção de β-Galactosidade.

Degree: 2009, Universidade Federal do Rio Grande

Dissertação(mestrado) - Universidade Federal do Rio Grande, Programa de Pós-Graduação em Engenharia e Ciência de Alimentos, Escola de Química e Alimentos, 2009.

A hidrólise enzimática… (more)

Subjects/Keywords: Água de parboilização de arroz; Kluyveromyces; Planejamento experimental; Soro de leite; Enzyme; Experimental design; Parboiled rice effluents; Whey

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APA (6th Edition):

Braga, A. R. C. (2009). Viabilização da utilização de co-produtos da agroindústria na produção de β-Galactosidade. (Masters Thesis). Universidade Federal do Rio Grande. Retrieved from http://repositorio.furg.br/handle/1/2551

Chicago Manual of Style (16th Edition):

Braga, Anna Rafaela Cavalcante. “Viabilização da utilização de co-produtos da agroindústria na produção de β-Galactosidade.” 2009. Masters Thesis, Universidade Federal do Rio Grande. Accessed June 06, 2020. http://repositorio.furg.br/handle/1/2551.

MLA Handbook (7th Edition):

Braga, Anna Rafaela Cavalcante. “Viabilização da utilização de co-produtos da agroindústria na produção de β-Galactosidade.” 2009. Web. 06 Jun 2020.

Vancouver:

Braga ARC. Viabilização da utilização de co-produtos da agroindústria na produção de β-Galactosidade. [Internet] [Masters thesis]. Universidade Federal do Rio Grande; 2009. [cited 2020 Jun 06]. Available from: http://repositorio.furg.br/handle/1/2551.

Council of Science Editors:

Braga ARC. Viabilização da utilização de co-produtos da agroindústria na produção de β-Galactosidade. [Masters Thesis]. Universidade Federal do Rio Grande; 2009. Available from: http://repositorio.furg.br/handle/1/2551


Freie Universität Berlin

22. Heier, Jason L. De novo self-assembling Peptide mit Esterase Eigenschaften.

Degree: 2016, Freie Universität Berlin

 Die Fähigkeit von Enzymen, Reaktionen unter Erhalt einer exzellenten Substrat- und Produktspezifität zu beschleunigen, interessiert Chemiker seit Jahrzehnten. Bei der Adaption von Enzymen für die… (more)

Subjects/Keywords: De novo design; self-assembly; catalysis; peptide; enzyme; 500 Naturwissenschaften und Mathematik::540 Chemie::547 Organische Chemie

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APA (6th Edition):

Heier, J. L. (2016). De novo self-assembling Peptide mit Esterase Eigenschaften. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-8114

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Heier, Jason L. “De novo self-assembling Peptide mit Esterase Eigenschaften.” 2016. Thesis, Freie Universität Berlin. Accessed June 06, 2020. http://dx.doi.org/10.17169/refubium-8114.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Heier, Jason L. “De novo self-assembling Peptide mit Esterase Eigenschaften.” 2016. Web. 06 Jun 2020.

Vancouver:

Heier JL. De novo self-assembling Peptide mit Esterase Eigenschaften. [Internet] [Thesis]. Freie Universität Berlin; 2016. [cited 2020 Jun 06]. Available from: http://dx.doi.org/10.17169/refubium-8114.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Heier JL. De novo self-assembling Peptide mit Esterase Eigenschaften. [Thesis]. Freie Universität Berlin; 2016. Available from: http://dx.doi.org/10.17169/refubium-8114

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Toronto

23. Li, Buren. Structural Studies of the Klebsiella Pneumoniae Pantothenate Kinase in Complex with Pantothenamide Substrate Analogues.

Degree: 2012, University of Toronto

N-substituted pantothenamides are analogues of pantothenate, the precursor of the essential metabolic cofactor coenzyme A (CoA). These compounds are substrates of pantothenate kinase (PanK) in… (more)

Subjects/Keywords: pantothenate kinase; X-ray crystallography; vitamin B5 analogues; enzyme-substrate complex; antimicrobial drug design; structural biology; 0419

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APA (6th Edition):

Li, B. (2012). Structural Studies of the Klebsiella Pneumoniae Pantothenate Kinase in Complex with Pantothenamide Substrate Analogues. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33287

Chicago Manual of Style (16th Edition):

Li, Buren. “Structural Studies of the Klebsiella Pneumoniae Pantothenate Kinase in Complex with Pantothenamide Substrate Analogues.” 2012. Masters Thesis, University of Toronto. Accessed June 06, 2020. http://hdl.handle.net/1807/33287.

MLA Handbook (7th Edition):

Li, Buren. “Structural Studies of the Klebsiella Pneumoniae Pantothenate Kinase in Complex with Pantothenamide Substrate Analogues.” 2012. Web. 06 Jun 2020.

Vancouver:

Li B. Structural Studies of the Klebsiella Pneumoniae Pantothenate Kinase in Complex with Pantothenamide Substrate Analogues. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/1807/33287.

Council of Science Editors:

Li B. Structural Studies of the Klebsiella Pneumoniae Pantothenate Kinase in Complex with Pantothenamide Substrate Analogues. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33287


KTH

24. Olsson, Philip. Datorbaserad analys av enzymdesign för Diels-Alder  reaktioner.

Degree: Chemical Science and Engineering (CHE), 2011, KTH

  This thesis has been focused around the Diels Alder reaction with the goal to design an enzyme catalyzed reaction pathway. To achieve this goal… (more)

Subjects/Keywords: Diels-Alder; Enzyme Design; Quantum Chemistry; Density Functional Theory (DFT); Protein Docking; Physical chemistry; Fysikalisk kemi

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APA (6th Edition):

Olsson, P. (2011). Datorbaserad analys av enzymdesign för Diels-Alder  reaktioner. (Thesis). KTH. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-34153

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Olsson, Philip. “Datorbaserad analys av enzymdesign för Diels-Alder  reaktioner.” 2011. Thesis, KTH. Accessed June 06, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-34153.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Olsson, Philip. “Datorbaserad analys av enzymdesign för Diels-Alder  reaktioner.” 2011. Web. 06 Jun 2020.

Vancouver:

Olsson P. Datorbaserad analys av enzymdesign för Diels-Alder  reaktioner. [Internet] [Thesis]. KTH; 2011. [cited 2020 Jun 06]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-34153.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Olsson P. Datorbaserad analys av enzymdesign för Diels-Alder  reaktioner. [Thesis]. KTH; 2011. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-34153

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

25. Kumar, Rakesh. Surface modification of electrodes for enzymatic fuel cell application .

Degree: 2016, National University of Ireland – Galway

 The immobilisation chemistry of enzymes and redox complexes capable of shuttling electrons between enzymes and electrode surface can have an impact on the magnitude and… (more)

Subjects/Keywords: Biofuel cell; Mediator; Surface modification; Design of experiment; Osmium complex; Enzyme immobilisation; Redox active layer; Physical chemistry; Chemistry; Ryan Institute

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APA (6th Edition):

Kumar, R. (2016). Surface modification of electrodes for enzymatic fuel cell application . (Thesis). National University of Ireland – Galway. Retrieved from http://hdl.handle.net/10379/5462

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kumar, Rakesh. “Surface modification of electrodes for enzymatic fuel cell application .” 2016. Thesis, National University of Ireland – Galway. Accessed June 06, 2020. http://hdl.handle.net/10379/5462.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kumar, Rakesh. “Surface modification of electrodes for enzymatic fuel cell application .” 2016. Web. 06 Jun 2020.

Vancouver:

Kumar R. Surface modification of electrodes for enzymatic fuel cell application . [Internet] [Thesis]. National University of Ireland – Galway; 2016. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/10379/5462.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kumar R. Surface modification of electrodes for enzymatic fuel cell application . [Thesis]. National University of Ireland – Galway; 2016. Available from: http://hdl.handle.net/10379/5462

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University College Cork

26. Miller, Charlotte M. Design, synthesis and evaluation of novel ellipticine derivatives and analogues as anti-cancer agents.

Degree: 2011, University College Cork

 This thesis describes work carried out on the synthesis of novel 5- and 11-substituted ellipticines and derivatives of the ellipticine analogues, isoellipticine and deazaellipticine, followed… (more)

Subjects/Keywords: Ellipticine; Anti-cancer; Topoisomerase inhibitor; Organic synthesis; Antineoplastic agents – Development; Enzyme inhibitors; Drugs – Design; Cancer – Chemotherapy; Organic compounds – Synthesis

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APA (6th Edition):

Miller, C. M. (2011). Design, synthesis and evaluation of novel ellipticine derivatives and analogues as anti-cancer agents. (Thesis). University College Cork. Retrieved from http://hdl.handle.net/10468/534

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Miller, Charlotte M. “Design, synthesis and evaluation of novel ellipticine derivatives and analogues as anti-cancer agents.” 2011. Thesis, University College Cork. Accessed June 06, 2020. http://hdl.handle.net/10468/534.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Miller, Charlotte M. “Design, synthesis and evaluation of novel ellipticine derivatives and analogues as anti-cancer agents.” 2011. Web. 06 Jun 2020.

Vancouver:

Miller CM. Design, synthesis and evaluation of novel ellipticine derivatives and analogues as anti-cancer agents. [Internet] [Thesis]. University College Cork; 2011. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/10468/534.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Miller CM. Design, synthesis and evaluation of novel ellipticine derivatives and analogues as anti-cancer agents. [Thesis]. University College Cork; 2011. Available from: http://hdl.handle.net/10468/534

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of South Florida

27. Nichols, Derek Allen. Structure-Based Design of Novel Inhibitors and Ultra High Resolution Analysis of CTX-M Beta-Lactamase.

Degree: 2014, University of South Florida

 The emergence of CTX-M class-A extended-spectrum β-lactamases, which confer resistance to second and third-generation cephalosporins, poses a serious health threat to the public. CTX-M β-lactamases… (more)

Subjects/Keywords: antibiotic resistance; beta-lactam antibiotics; beta-lactamase; enzyme mechanism; non-covalent inhibitors; structure-aided design; Biochemistry; Microbiology; Molecular Biology

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APA (6th Edition):

Nichols, D. A. (2014). Structure-Based Design of Novel Inhibitors and Ultra High Resolution Analysis of CTX-M Beta-Lactamase. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/5284

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Nichols, Derek Allen. “Structure-Based Design of Novel Inhibitors and Ultra High Resolution Analysis of CTX-M Beta-Lactamase.” 2014. Thesis, University of South Florida. Accessed June 06, 2020. https://scholarcommons.usf.edu/etd/5284.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Nichols, Derek Allen. “Structure-Based Design of Novel Inhibitors and Ultra High Resolution Analysis of CTX-M Beta-Lactamase.” 2014. Web. 06 Jun 2020.

Vancouver:

Nichols DA. Structure-Based Design of Novel Inhibitors and Ultra High Resolution Analysis of CTX-M Beta-Lactamase. [Internet] [Thesis]. University of South Florida; 2014. [cited 2020 Jun 06]. Available from: https://scholarcommons.usf.edu/etd/5284.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Nichols DA. Structure-Based Design of Novel Inhibitors and Ultra High Resolution Analysis of CTX-M Beta-Lactamase. [Thesis]. University of South Florida; 2014. Available from: https://scholarcommons.usf.edu/etd/5284

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Université Montpellier II

28. Turtaut, François. Conception, synthèse et activité de nouveaux agents anti-infectieux ciblant l'histidinol deshydrogénase de bactéries à développement intracellulaire : Design, synthesis and activity of new anti-infectious agents targeting histidinol dehydrogenase of intracellular bacteria.

Degree: Docteur es, Ingénérie Moléculaire, 2011, Université Montpellier II

L'accentuation des phénomènes de résistance aux antibiotiques augmente la difficulté d'enrayer les infections bactériennes. Afin de palier ce problème, la mise au point de nouvelles… (more)

Subjects/Keywords: Drug design; Inhibiteurs d'enzyme; Histidinol DesHydrogénase; Brucella suis; Mycobaterium tuberculosis; Dosages enzymatiques; Drug design; Enzyme inhibitors; Histidinol DeHydrogenase; Brucella suis; Mycobaterium tuberculosis; Enzymatic assays

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APA (6th Edition):

Turtaut, F. (2011). Conception, synthèse et activité de nouveaux agents anti-infectieux ciblant l'histidinol deshydrogénase de bactéries à développement intracellulaire : Design, synthesis and activity of new anti-infectious agents targeting histidinol dehydrogenase of intracellular bacteria. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2011MON20094

Chicago Manual of Style (16th Edition):

Turtaut, François. “Conception, synthèse et activité de nouveaux agents anti-infectieux ciblant l'histidinol deshydrogénase de bactéries à développement intracellulaire : Design, synthesis and activity of new anti-infectious agents targeting histidinol dehydrogenase of intracellular bacteria.” 2011. Doctoral Dissertation, Université Montpellier II. Accessed June 06, 2020. http://www.theses.fr/2011MON20094.

MLA Handbook (7th Edition):

Turtaut, François. “Conception, synthèse et activité de nouveaux agents anti-infectieux ciblant l'histidinol deshydrogénase de bactéries à développement intracellulaire : Design, synthesis and activity of new anti-infectious agents targeting histidinol dehydrogenase of intracellular bacteria.” 2011. Web. 06 Jun 2020.

Vancouver:

Turtaut F. Conception, synthèse et activité de nouveaux agents anti-infectieux ciblant l'histidinol deshydrogénase de bactéries à développement intracellulaire : Design, synthesis and activity of new anti-infectious agents targeting histidinol dehydrogenase of intracellular bacteria. [Internet] [Doctoral dissertation]. Université Montpellier II; 2011. [cited 2020 Jun 06]. Available from: http://www.theses.fr/2011MON20094.

Council of Science Editors:

Turtaut F. Conception, synthèse et activité de nouveaux agents anti-infectieux ciblant l'histidinol deshydrogénase de bactéries à développement intracellulaire : Design, synthesis and activity of new anti-infectious agents targeting histidinol dehydrogenase of intracellular bacteria. [Doctoral Dissertation]. Université Montpellier II; 2011. Available from: http://www.theses.fr/2011MON20094


University of Illinois – Urbana-Champaign

29. Park, David S. Structural and biochemical studies on enzymes involved in natural product biosynthesis and cellular respiration.

Degree: PhD, Biophysics & Computnl Biology, 2016, University of Illinois – Urbana-Champaign

 Natural products have recently become an interest in modern research. This is due to their synthesis mainly by living organisms and their natural biosynthesis and… (more)

Subjects/Keywords: X-Ray Crystallography; Natural Products, Protein; Enzyme Structure; Drug Design; Membrane Protein; Protein Purification; Alginate Lyase; Plumbemycin; Rhizocticin; Antibiotic; Antifungal; aa3-Menaquinone Oxidase; Mining Microbial Genomics; Biofuels; Biodiesel; Enzyme Kinetics; Electron Transport Chain

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Park, D. S. (2016). Structural and biochemical studies on enzymes involved in natural product biosynthesis and cellular respiration. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/90469

Chicago Manual of Style (16th Edition):

Park, David S. “Structural and biochemical studies on enzymes involved in natural product biosynthesis and cellular respiration.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed June 06, 2020. http://hdl.handle.net/2142/90469.

MLA Handbook (7th Edition):

Park, David S. “Structural and biochemical studies on enzymes involved in natural product biosynthesis and cellular respiration.” 2016. Web. 06 Jun 2020.

Vancouver:

Park DS. Structural and biochemical studies on enzymes involved in natural product biosynthesis and cellular respiration. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/2142/90469.

Council of Science Editors:

Park DS. Structural and biochemical studies on enzymes involved in natural product biosynthesis and cellular respiration. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/90469


University of Manchester

30. Iorgu, Andreea Iulia. Molecular basis of ene-reductases reactivity and selectivity towards nicotinamide coenzymes.

Degree: 2019, University of Manchester

 Understanding the physical basis of enzyme catalysis is critical for deciphering the physiological function of enzymes, and for driving developments in contemporary areas of research,… (more)

Subjects/Keywords: ene-reductases; coenzyme specificity; kinetic isotope effects; enzyme kinetics; hydride transfer; protein dynamics; protein NMR; protein crystallography; rational enzyme design; pentaerythritol tetranitrate reductase; morphinone reductase; Old Yellow Enzymes; backbone resonance assignments; flavoenzymes

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Iorgu, A. I. (2019). Molecular basis of ene-reductases reactivity and selectivity towards nicotinamide coenzymes. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:318627

Chicago Manual of Style (16th Edition):

Iorgu, Andreea Iulia. “Molecular basis of ene-reductases reactivity and selectivity towards nicotinamide coenzymes.” 2019. Doctoral Dissertation, University of Manchester. Accessed June 06, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:318627.

MLA Handbook (7th Edition):

Iorgu, Andreea Iulia. “Molecular basis of ene-reductases reactivity and selectivity towards nicotinamide coenzymes.” 2019. Web. 06 Jun 2020.

Vancouver:

Iorgu AI. Molecular basis of ene-reductases reactivity and selectivity towards nicotinamide coenzymes. [Internet] [Doctoral dissertation]. University of Manchester; 2019. [cited 2020 Jun 06]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:318627.

Council of Science Editors:

Iorgu AI. Molecular basis of ene-reductases reactivity and selectivity towards nicotinamide coenzymes. [Doctoral Dissertation]. University of Manchester; 2019. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:318627

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