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You searched for +publisher:"University of Illinois – Urbana-Champaign" +contributor:("Nair, Satish K."). Showing records 1 – 30 of 51 total matches.

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University of Illinois – Urbana-Champaign

1. Chekan, Jonathan Rodi. Biochemical and structural studies on proteins involved in the production of natural products and degradation of polysaccharides.

Degree: PhD, Biochemistry, 2016, University of Illinois – Urbana-Champaign

 One of the major limitations of traditional organic chemical synthesis is the challenge of modifying a starting material with both stereoselectivity and regioselectivity to produce… (more)

Subjects/Keywords: Natural products; Crystallography; Biochemistry; Ribosomally synthesized and post-translationally modified peptides (RiPPs)

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APA (6th Edition):

Chekan, J. R. (2016). Biochemical and structural studies on proteins involved in the production of natural products and degradation of polysaccharides. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95559

Chicago Manual of Style (16th Edition):

Chekan, Jonathan Rodi. “Biochemical and structural studies on proteins involved in the production of natural products and degradation of polysaccharides.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/95559.

MLA Handbook (7th Edition):

Chekan, Jonathan Rodi. “Biochemical and structural studies on proteins involved in the production of natural products and degradation of polysaccharides.” 2016. Web. 17 Jul 2019.

Vancouver:

Chekan JR. Biochemical and structural studies on proteins involved in the production of natural products and degradation of polysaccharides. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/95559.

Council of Science Editors:

Chekan JR. Biochemical and structural studies on proteins involved in the production of natural products and degradation of polysaccharides. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95559


University of Illinois – Urbana-Champaign

2. Hao, Yue. Structural and biochemical studies on tailoring enzymes involved in ribosomal peptides biosynthesis.

Degree: PhD, Biochemistry, 2015, University of Illinois – Urbana-Champaign

 Human history is also a history of the ceaseless fight against various diseases, especially those caused by pathogenic infections. Both scientists and pharmaceutical companies have… (more)

Subjects/Keywords: ribosomally synthesized and post-translationally modified peptides (RiPPs); lantibiotic dehydratases; plantazolicin N-methyltransferases; cyanobactin prenyltransferases

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APA (6th Edition):

Hao, Y. (2015). Structural and biochemical studies on tailoring enzymes involved in ribosomal peptides biosynthesis. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89199

Chicago Manual of Style (16th Edition):

Hao, Yue. “Structural and biochemical studies on tailoring enzymes involved in ribosomal peptides biosynthesis.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/89199.

MLA Handbook (7th Edition):

Hao, Yue. “Structural and biochemical studies on tailoring enzymes involved in ribosomal peptides biosynthesis.” 2015. Web. 17 Jul 2019.

Vancouver:

Hao Y. Structural and biochemical studies on tailoring enzymes involved in ribosomal peptides biosynthesis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/89199.

Council of Science Editors:

Hao Y. Structural and biochemical studies on tailoring enzymes involved in ribosomal peptides biosynthesis. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89199


University of Illinois – Urbana-Champaign

3. 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 (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 July 17, 2019. 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. 17 Jul 2019.

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 2019 Jul 17]. 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 Illinois – Urbana-Champaign

4. Nguyen, Kim-Phung. Structural studies of Butirosin D and FrbG.

Degree: PhD, 0318, 2014, University of Illinois – Urbana-Champaign

 A structural homology model of Butirosin D is presented. This enzyme has been previously re-characterized as a deacetylase, releasing a free acetate molecule when acting… (more)

Subjects/Keywords: Butirosin D; FrbG; structural studies

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APA (6th Edition):

Nguyen, K. (2014). Structural studies of Butirosin D and FrbG. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/50357

Chicago Manual of Style (16th Edition):

Nguyen, Kim-Phung. “Structural studies of Butirosin D and FrbG.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/50357.

MLA Handbook (7th Edition):

Nguyen, Kim-Phung. “Structural studies of Butirosin D and FrbG.” 2014. Web. 17 Jul 2019.

Vancouver:

Nguyen K. Structural studies of Butirosin D and FrbG. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/50357.

Council of Science Editors:

Nguyen K. Structural studies of Butirosin D and FrbG. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/50357


University of Illinois – Urbana-Champaign

5. Garg, Neha. Exploring and understanding lantibiotic biosynthesis.

Degree: PhD, 0318, 2014, University of Illinois – Urbana-Champaign

 The ribosome translates genomic information into structural and catalytic protein molecules. In addition to its role in protein synthesis, the ribosome also produces small non-catalytic… (more)

Subjects/Keywords: Antibiotic resistance; Lantibiotic; Biosynthesis; Stereochemistry

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APA (6th Edition):

Garg, N. (2014). Exploring and understanding lantibiotic biosynthesis. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/46883

Chicago Manual of Style (16th Edition):

Garg, Neha. “Exploring and understanding lantibiotic biosynthesis.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/46883.

MLA Handbook (7th Edition):

Garg, Neha. “Exploring and understanding lantibiotic biosynthesis.” 2014. Web. 17 Jul 2019.

Vancouver:

Garg N. Exploring and understanding lantibiotic biosynthesis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/46883.

Council of Science Editors:

Garg N. Exploring and understanding lantibiotic biosynthesis. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/46883


University of Illinois – Urbana-Champaign

6. Agarwal, Vinayak. Structural studies of enzymes involved in antibiotic resistance and phosphonate degradation.

Degree: PhD, 0319, 2013, University of Illinois – Urbana-Champaign

 Biological chemistry revolves around the abiogenetic interplay of high energy labile chemical linkages which shuttle energy and chemical potential, and stable and degradation resistant bonds… (more)

Subjects/Keywords: Antibiotic; Phosphonate; X-ray crystallography; enzymology

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APA (6th Edition):

Agarwal, V. (2013). Structural studies of enzymes involved in antibiotic resistance and phosphonate degradation. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/42440

Chicago Manual of Style (16th Edition):

Agarwal, Vinayak. “Structural studies of enzymes involved in antibiotic resistance and phosphonate degradation.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/42440.

MLA Handbook (7th Edition):

Agarwal, Vinayak. “Structural studies of enzymes involved in antibiotic resistance and phosphonate degradation.” 2013. Web. 17 Jul 2019.

Vancouver:

Agarwal V. Structural studies of enzymes involved in antibiotic resistance and phosphonate degradation. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/42440.

Council of Science Editors:

Agarwal V. Structural studies of enzymes involved in antibiotic resistance and phosphonate degradation. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/42440


University of Illinois – Urbana-Champaign

7. Li, Zhi. Structural studies on the biosynthesis and biological functions of natural products.

Degree: PhD, 0318, 2013, University of Illinois – Urbana-Champaign

 Natural products are chemical compounds that are synthesized by living organisms and have biological and pharmacological functions. Many natural products or their derivatives have been… (more)

Subjects/Keywords: natural products; crystal structure

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APA (6th Edition):

Li, Z. (2013). Structural studies on the biosynthesis and biological functions of natural products. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/44791

Chicago Manual of Style (16th Edition):

Li, Zhi. “Structural studies on the biosynthesis and biological functions of natural products.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/44791.

MLA Handbook (7th Edition):

Li, Zhi. “Structural studies on the biosynthesis and biological functions of natural products.” 2013. Web. 17 Jul 2019.

Vancouver:

Li Z. Structural studies on the biosynthesis and biological functions of natural products. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/44791.

Council of Science Editors:

Li Z. Structural studies on the biosynthesis and biological functions of natural products. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/44791


University of Illinois – Urbana-Champaign

8. Cao, Xinyun. Studies of lipoic acid and biotin metabolism in bacteria and higher eukaryotes.

Degree: PhD, Biochemistry, 2018, University of Illinois – Urbana-Champaign

 My PhD research focus has been the study of lipoic acid and biotin metabolism in several bacteria. Lipoic acid and biotin are essential enzyme cofactors… (more)

Subjects/Keywords: lipoic acid; biotin; lipoate protein ligase; methyl esterase; octanoyl transferase; circular permutation; LplA; BioH; LipM; glycine cleavage; enzyme moonlighting; aerobic metabolism; C1 metabolism

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APA (6th Edition):

Cao, X. (2018). Studies of lipoic acid and biotin metabolism in bacteria and higher eukaryotes. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/101113

Chicago Manual of Style (16th Edition):

Cao, Xinyun. “Studies of lipoic acid and biotin metabolism in bacteria and higher eukaryotes.” 2018. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/101113.

MLA Handbook (7th Edition):

Cao, Xinyun. “Studies of lipoic acid and biotin metabolism in bacteria and higher eukaryotes.” 2018. Web. 17 Jul 2019.

Vancouver:

Cao X. Studies of lipoic acid and biotin metabolism in bacteria and higher eukaryotes. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2018. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/101113.

Council of Science Editors:

Cao X. Studies of lipoic acid and biotin metabolism in bacteria and higher eukaryotes. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2018. Available from: http://hdl.handle.net/2142/101113


University of Illinois – Urbana-Champaign

9. Madabhusi Ragunathan, Kaushik. Single molecule fret study on the mechanism of RecA mediated strand exchange.

Degree: PhD, 0319, 2012, University of Illinois – Urbana-Champaign

 RecA plays a critical role during double strand break repair via homologous recombination. During the strand exchange reaction, RecA forms a helical filament on single… (more)

Subjects/Keywords: DNA repair; recombination; single molecule; Fluorescence resonance energy transfer (FRET); fluorescence; Deoxyribonucleic acid (DNA)

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APA (6th Edition):

Madabhusi Ragunathan, K. (2012). Single molecule fret study on the mechanism of RecA mediated strand exchange. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/32044

Chicago Manual of Style (16th Edition):

Madabhusi Ragunathan, Kaushik. “Single molecule fret study on the mechanism of RecA mediated strand exchange.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/32044.

MLA Handbook (7th Edition):

Madabhusi Ragunathan, Kaushik. “Single molecule fret study on the mechanism of RecA mediated strand exchange.” 2012. Web. 17 Jul 2019.

Vancouver:

Madabhusi Ragunathan K. Single molecule fret study on the mechanism of RecA mediated strand exchange. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/32044.

Council of Science Editors:

Madabhusi Ragunathan K. Single molecule fret study on the mechanism of RecA mediated strand exchange. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/32044


University of Illinois – Urbana-Champaign

10. Guerra, Francisco. Investigating pathogen 4Fe-4S protein targets and cancer chemotherapies with bisphosphonate/diphosphate inhibitors.

Degree: PhD, 0319, 2015, University of Illinois – Urbana-Champaign

 The broad, long-term objective of this research is to develop drug leads for new antibiotics, antiparasitics, and cancer chemotherapeutics. Two main areas of focus are… (more)

Subjects/Keywords: isoprenoid; iron-sulfur proteins; 4Fe-4S; bisphosphonate; diphosphate

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APA (6th Edition):

Guerra, F. (2015). Investigating pathogen 4Fe-4S protein targets and cancer chemotherapies with bisphosphonate/diphosphate inhibitors. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/72983

Chicago Manual of Style (16th Edition):

Guerra, Francisco. “Investigating pathogen 4Fe-4S protein targets and cancer chemotherapies with bisphosphonate/diphosphate inhibitors.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/72983.

MLA Handbook (7th Edition):

Guerra, Francisco. “Investigating pathogen 4Fe-4S protein targets and cancer chemotherapies with bisphosphonate/diphosphate inhibitors.” 2015. Web. 17 Jul 2019.

Vancouver:

Guerra F. Investigating pathogen 4Fe-4S protein targets and cancer chemotherapies with bisphosphonate/diphosphate inhibitors. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/72983.

Council of Science Editors:

Guerra F. Investigating pathogen 4Fe-4S protein targets and cancer chemotherapies with bisphosphonate/diphosphate inhibitors. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/72983


University of Illinois – Urbana-Champaign

11. Ahn, Young O. Biochemical characterization of C-family heme copper oxygen reductase.

Degree: PhD, Biochemistry, 2015, University of Illinois – Urbana-Champaign

 Heme copper oxygen reductases (HCOs) are key enzymes for aerobic respiration. As a terminal electron acceptor, HCO catalyzes the sequential transfer of four electrons from… (more)

Subjects/Keywords: cbb3; heme copper oxygen reductase; bioenergetics; vibrio cholerae

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APA (6th Edition):

Ahn, Y. O. (2015). Biochemical characterization of C-family heme copper oxygen reductase. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/78726

Chicago Manual of Style (16th Edition):

Ahn, Young O. “Biochemical characterization of C-family heme copper oxygen reductase.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/78726.

MLA Handbook (7th Edition):

Ahn, Young O. “Biochemical characterization of C-family heme copper oxygen reductase.” 2015. Web. 17 Jul 2019.

Vancouver:

Ahn YO. Biochemical characterization of C-family heme copper oxygen reductase. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/78726.

Council of Science Editors:

Ahn YO. Biochemical characterization of C-family heme copper oxygen reductase. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/78726


University of Illinois – Urbana-Champaign

12. Choi, Sylvia K. The interactions of cytochrome bo3 from Escherichia coli with its substrates - ubiquinone and oxygen.

Degree: PhD, Biophysics & Computional Biology, 2015, University of Illinois – Urbana-Champaign

 Heme-copper respiratory oxygen reductases reduce O2 to water and use the redox free energy to generate the proton motive force. Among the heme-copper oxygen reductases… (more)

Subjects/Keywords: cytochrome bo3; terminal oxidase; respiratory chain; heme copper oxygen reductase; cytochrome c oxidase; quinol oxidase; cytochrome aa3; E. coli; Escherichia coli; Rhodobacter sphaeroides; oxygen channel; oxygen binding; second order rate; flow-flash; site-directed mutagenesis; quinone binding; ubiquinone; ubiquinol; UQ8; UQ1; UQ2; high affinity site; low affinity site; QH; QL; KM; Ki; HQNO; High-performance liquid chromatography (HPLC); oxygen activity; cyt bo3; bo3; quinone extraction; Liposomes; vesicles; NDH2; UQ10; MK7; semiquinone; Electron Paramagnetic Resonance (EPR); methyl hyperfine coupling

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APA (6th Edition):

Choi, S. K. (2015). The interactions of cytochrome bo3 from Escherichia coli with its substrates - ubiquinone and oxygen. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89181

Chicago Manual of Style (16th Edition):

Choi, Sylvia K. “The interactions of cytochrome bo3 from Escherichia coli with its substrates - ubiquinone and oxygen.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/89181.

MLA Handbook (7th Edition):

Choi, Sylvia K. “The interactions of cytochrome bo3 from Escherichia coli with its substrates - ubiquinone and oxygen.” 2015. Web. 17 Jul 2019.

Vancouver:

Choi SK. The interactions of cytochrome bo3 from Escherichia coli with its substrates - ubiquinone and oxygen. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/89181.

Council of Science Editors:

Choi SK. The interactions of cytochrome bo3 from Escherichia coli with its substrates - ubiquinone and oxygen. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89181


University of Illinois – Urbana-Champaign

13. Zhu, Wei. Targeting isoprenoid biosynthesis for drug discovery.

Degree: PhD, 0319, 2013, University of Illinois – Urbana-Champaign

 Cancer and infectious diseases are huge threats to human beings. With the rapid rise in drug resistance, there is a need for new drugs, and… (more)

Subjects/Keywords: drug discovery; in silico high-throughput screening; peptidoglycan; protein structure; undecaprenyl diphosphate synthase (UPPS); farnesyl diphosphate synthase (FPPS); Deoxyribonucleic acid (DNA)

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APA (6th Edition):

Zhu, W. (2013). Targeting isoprenoid biosynthesis for drug discovery. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/45658

Chicago Manual of Style (16th Edition):

Zhu, Wei. “Targeting isoprenoid biosynthesis for drug discovery.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/45658.

MLA Handbook (7th Edition):

Zhu, Wei. “Targeting isoprenoid biosynthesis for drug discovery.” 2013. Web. 17 Jul 2019.

Vancouver:

Zhu W. Targeting isoprenoid biosynthesis for drug discovery. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/45658.

Council of Science Editors:

Zhu W. Targeting isoprenoid biosynthesis for drug discovery. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/45658


University of Illinois – Urbana-Champaign

14. Enkavi, Giray. Mechanism and energetics of membrane transporters and channels.

Degree: PhD, 0319, 2014, University of Illinois – Urbana-Champaign

 Living cells have evolved specialized transport proteins called membrane transporters and channels that catalyze exchange of materials across the cell membrane. Membrane trans- porters couple… (more)

Subjects/Keywords: membrane transporters; membrane channels; major facilitator superfamily; antiporter; urea; aquaporin

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APA (6th Edition):

Enkavi, G. (2014). Mechanism and energetics of membrane transporters and channels. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/46912

Chicago Manual of Style (16th Edition):

Enkavi, Giray. “Mechanism and energetics of membrane transporters and channels.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/46912.

MLA Handbook (7th Edition):

Enkavi, Giray. “Mechanism and energetics of membrane transporters and channels.” 2014. Web. 17 Jul 2019.

Vancouver:

Enkavi G. Mechanism and energetics of membrane transporters and channels. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/46912.

Council of Science Editors:

Enkavi G. Mechanism and energetics of membrane transporters and channels. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/46912


University of Illinois – Urbana-Champaign

15. Syed, Salman. Single molecule fluorescence studies of replicative helicases.

Degree: PhD, 0319, 2014, University of Illinois – Urbana-Champaign

 DNA helicases are motor enzymes that convert the chemical energy of nucleotide triphosphate hydrolysis into mechanical energy for translocation on single stranded (ss) DNA and… (more)

Subjects/Keywords: Single Molecule Fluorescence T7 Helicase

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APA (6th Edition):

Syed, S. (2014). Single molecule fluorescence studies of replicative helicases. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/46948

Chicago Manual of Style (16th Edition):

Syed, Salman. “Single molecule fluorescence studies of replicative helicases.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/46948.

MLA Handbook (7th Edition):

Syed, Salman. “Single molecule fluorescence studies of replicative helicases.” 2014. Web. 17 Jul 2019.

Vancouver:

Syed S. Single molecule fluorescence studies of replicative helicases. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/46948.

Council of Science Editors:

Syed S. Single molecule fluorescence studies of replicative helicases. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/46948


University of Illinois – Urbana-Champaign

16. Lee, Hyun Ju. The study of aa3-type cytochrome c oxidase in Rhodobacter sphaeroides.

Degree: PhD, 0318, 2010, University of Illinois – Urbana-Champaign

 Cytochrome c oxidase is the final electron acceptor in the respiratory chain and catalyzes the highly exergonic oxygen reduction reaction to water and forms a… (more)

Subjects/Keywords: Cytochrome c oxidase; adenosine triphosphate (ATP); proton pump

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APA (6th Edition):

Lee, H. J. (2010). The study of aa3-type cytochrome c oxidase in Rhodobacter sphaeroides. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/14593

Chicago Manual of Style (16th Edition):

Lee, Hyun Ju. “The study of aa3-type cytochrome c oxidase in Rhodobacter sphaeroides.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/14593.

MLA Handbook (7th Edition):

Lee, Hyun Ju. “The study of aa3-type cytochrome c oxidase in Rhodobacter sphaeroides.” 2010. Web. 17 Jul 2019.

Vancouver:

Lee HJ. The study of aa3-type cytochrome c oxidase in Rhodobacter sphaeroides. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/14593.

Council of Science Editors:

Lee HJ. The study of aa3-type cytochrome c oxidase in Rhodobacter sphaeroides. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/14593


University of Illinois – Urbana-Champaign

17. Ganesan, Krithika. Studies on critical proton-pathway residues in the aa3-type cytochrome c oxidase from Rhodobacter sphaeroides.

Degree: PhD, 0319, 2010, University of Illinois – Urbana-Champaign

 Aerobic organisms derive energy needed to sustain life from foodstuffs through the process of cellular respiration. Respiration is performed by a series of soluble and… (more)

Subjects/Keywords: cytochrome c oxidase; membrane protein; electron transfer; proton transfer

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APA (6th Edition):

Ganesan, K. (2010). Studies on critical proton-pathway residues in the aa3-type cytochrome c oxidase from Rhodobacter sphaeroides. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/14698

Chicago Manual of Style (16th Edition):

Ganesan, Krithika. “Studies on critical proton-pathway residues in the aa3-type cytochrome c oxidase from Rhodobacter sphaeroides.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/14698.

MLA Handbook (7th Edition):

Ganesan, Krithika. “Studies on critical proton-pathway residues in the aa3-type cytochrome c oxidase from Rhodobacter sphaeroides.” 2010. Web. 17 Jul 2019.

Vancouver:

Ganesan K. Studies on critical proton-pathway residues in the aa3-type cytochrome c oxidase from Rhodobacter sphaeroides. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/14698.

Council of Science Editors:

Ganesan K. Studies on critical proton-pathway residues in the aa3-type cytochrome c oxidase from Rhodobacter sphaeroides. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/14698


University of Illinois – Urbana-Champaign

18. Lin, Myat T. EPR and solid-state NMR studies on the mechanism of cytochrome bo3 ubiquinol oxidase from escherichia coli.

Degree: PhD, 0319, 2010, University of Illinois – Urbana-Champaign

 Cytochrome bo3 ubiquinol oxidase from E. coli is a member of heme-copper oxidase superfamily. This trans-membrane enzyme complex catalyzes two-electron oxidation of ubiquinol and reduction… (more)

Subjects/Keywords: cytochrome bo3; ubiquinol oxidase; Electron paramagnetic resonance (EPR); Solid-state NMR; selective isotope labeling; auxotrophs; quinone binding site; Nuclear magnetic resonance (NMR)

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APA (6th Edition):

Lin, M. T. (2010). EPR and solid-state NMR studies on the mechanism of cytochrome bo3 ubiquinol oxidase from escherichia coli. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/15565

Chicago Manual of Style (16th Edition):

Lin, Myat T. “EPR and solid-state NMR studies on the mechanism of cytochrome bo3 ubiquinol oxidase from escherichia coli.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/15565.

MLA Handbook (7th Edition):

Lin, Myat T. “EPR and solid-state NMR studies on the mechanism of cytochrome bo3 ubiquinol oxidase from escherichia coli.” 2010. Web. 17 Jul 2019.

Vancouver:

Lin MT. EPR and solid-state NMR studies on the mechanism of cytochrome bo3 ubiquinol oxidase from escherichia coli. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/15565.

Council of Science Editors:

Lin MT. EPR and solid-state NMR studies on the mechanism of cytochrome bo3 ubiquinol oxidase from escherichia coli. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/15565


University of Illinois – Urbana-Champaign

19. Victoria, Doreen C. Electron gating and mechanism of proton exit in quinol oxidation in cyt bc1 complex from R. sphaeroides.

Degree: PhD, 0318, 2010, University of Illinois – Urbana-Champaign

 The cytochrome bc1 complex of Rhodobacter sphaeroides in wild-type and several strains mutated at the conserved -PEWY- glutamate residue (E272 in chicken, E295 in R.… (more)

Subjects/Keywords: Cytochrome bc1 complex; electron gating mechanism of cytochrome bc1 complex; proton exit mechanism of quinol oxidation of cytochrome bc1 complex; quinol oxidation at the Qo-site; second electron transfer of quinol oxidation of the bc1 complex; inter-monomer electron transfer of cyt bc1 complex; bL hemes inter-monomer electron transfer in cyt bc1 complex; pre-steady state kinetics of quinol oxidation at the Qo-site of cyt bc1 complex from R. sphaeoroides; in situ pre-steady state kinetics of cyt bc1 complex in R. sphaeroides; Modified Q-cycle mechanism of Cytochrome bc1 complex; Glu-295 (Glu-271 in bovine or Glu-272) of PEWY loop mutational studies of Cyt bc1 complex; bypass reaction rates in cyt bc1 complex

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APA (6th Edition):

Victoria, D. C. (2010). Electron gating and mechanism of proton exit in quinol oxidation in cyt bc1 complex from R. sphaeroides. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/16129

Chicago Manual of Style (16th Edition):

Victoria, Doreen C. “Electron gating and mechanism of proton exit in quinol oxidation in cyt bc1 complex from R. sphaeroides.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/16129.

MLA Handbook (7th Edition):

Victoria, Doreen C. “Electron gating and mechanism of proton exit in quinol oxidation in cyt bc1 complex from R. sphaeroides.” 2010. Web. 17 Jul 2019.

Vancouver:

Victoria DC. Electron gating and mechanism of proton exit in quinol oxidation in cyt bc1 complex from R. sphaeroides. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/16129.

Council of Science Editors:

Victoria DC. Electron gating and mechanism of proton exit in quinol oxidation in cyt bc1 complex from R. sphaeroides. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/16129


University of Illinois – Urbana-Champaign

20. Lan, Tian. I. In vitro selection of aptamers for perchlorate and melamine II. Towards crystallization of DNAzymes III. A highly selective lead sensor based on a classic lead DNAzyme.

Degree: PhD, 0318, 2013, University of Illinois – Urbana-Champaign

 Nature has given nucleic acids irreplaceable roles for all living creatures. It plays important roles in genetic information storage and transfer, as well as regulating… (more)

Subjects/Keywords: systematic evolution of ligands by exponential enrichment (SELEX); aptamer; DNAzyme; deoxyribozyme; biosensor; melamine; Lead II Ion (Pb2+); GR-5 DNAzyme; 8-17 DNAzyme; crystallization

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APA (6th Edition):

Lan, T. (2013). I. In vitro selection of aptamers for perchlorate and melamine II. Towards crystallization of DNAzymes III. A highly selective lead sensor based on a classic lead DNAzyme. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/42441

Chicago Manual of Style (16th Edition):

Lan, Tian. “I. In vitro selection of aptamers for perchlorate and melamine II. Towards crystallization of DNAzymes III. A highly selective lead sensor based on a classic lead DNAzyme.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/42441.

MLA Handbook (7th Edition):

Lan, Tian. “I. In vitro selection of aptamers for perchlorate and melamine II. Towards crystallization of DNAzymes III. A highly selective lead sensor based on a classic lead DNAzyme.” 2013. Web. 17 Jul 2019.

Vancouver:

Lan T. I. In vitro selection of aptamers for perchlorate and melamine II. Towards crystallization of DNAzymes III. A highly selective lead sensor based on a classic lead DNAzyme. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/42441.

Council of Science Editors:

Lan T. I. In vitro selection of aptamers for perchlorate and melamine II. Towards crystallization of DNAzymes III. A highly selective lead sensor based on a classic lead DNAzyme. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/42441


University of Illinois – Urbana-Champaign

21. Liu, Yi-Liang. Structure, function and inhibition of GcpE, FPPS and GGPPS: targeting isoprenoid biosynthesis for drug discovery.

Degree: PhD, 0319, 2013, University of Illinois – Urbana-Champaign

 IspG, farnesyl diphosphate synthase (FPPS) and geranylgeranyl diphosphate synthase (GGPPS) are enzymes involved in isoprenoid biosynthesis. Most bacterial IspGs contain two domains: a TIM barrel… (more)

Subjects/Keywords: X-ray Crystallography; Iron-sulfur protein; Catalysis; Drug Discovery; IspG; GcpE; geranylgeranyl diphosphate synthase (GGPPS); farnesyl diphosphate synthase (FPPS)

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APA (6th Edition):

Liu, Y. (2013). Structure, function and inhibition of GcpE, FPPS and GGPPS: targeting isoprenoid biosynthesis for drug discovery. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/42471

Chicago Manual of Style (16th Edition):

Liu, Yi-Liang. “Structure, function and inhibition of GcpE, FPPS and GGPPS: targeting isoprenoid biosynthesis for drug discovery.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/42471.

MLA Handbook (7th Edition):

Liu, Yi-Liang. “Structure, function and inhibition of GcpE, FPPS and GGPPS: targeting isoprenoid biosynthesis for drug discovery.” 2013. Web. 17 Jul 2019.

Vancouver:

Liu Y. Structure, function and inhibition of GcpE, FPPS and GGPPS: targeting isoprenoid biosynthesis for drug discovery. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/42471.

Council of Science Editors:

Liu Y. Structure, function and inhibition of GcpE, FPPS and GGPPS: targeting isoprenoid biosynthesis for drug discovery. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/42471


University of Illinois – Urbana-Champaign

22. Sperling, Lindsay J. Solid-state NMR studies of membrane proteins and membrane protein complexes.

Degree: PhD, 0335, 2011, University of Illinois – Urbana-Champaign

 Membrane proteins help control nearly every process in the cell, which is why approximately 50% of pharmaceuticals currently on the market target membrane proteins. Knowledge… (more)

Subjects/Keywords: Cytochrome bo3 oxidase; DsbA/DsbB; Magic-angle Spinning; Membrane Proteins; Solid-state nuclear magnetic resonance (NMR)

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APA (6th Edition):

Sperling, L. J. (2011). Solid-state NMR studies of membrane proteins and membrane protein complexes. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/26275

Chicago Manual of Style (16th Edition):

Sperling, Lindsay J. “Solid-state NMR studies of membrane proteins and membrane protein complexes.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/26275.

MLA Handbook (7th Edition):

Sperling, Lindsay J. “Solid-state NMR studies of membrane proteins and membrane protein complexes.” 2011. Web. 17 Jul 2019.

Vancouver:

Sperling LJ. Solid-state NMR studies of membrane proteins and membrane protein complexes. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/26275.

Council of Science Editors:

Sperling LJ. Solid-state NMR studies of membrane proteins and membrane protein complexes. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/26275


University of Illinois – Urbana-Champaign

23. Murali, Ranjani. Studies on the cytochrome bd-type oxygen reductase superfamily and the discovery of a novel nitric oxide reductase.

Degree: PhD, Biochemistry, 2016, University of Illinois – Urbana-Champaign

 Respiration is the process by which an organism utilizes the reducing equivalents (electrons) produced during catabolism to create an electrochemical potential across the cellular membrane,… (more)

Subjects/Keywords: cytochrome bd; denitrification; heme-copper oxidase; caldivirga maquilingensis; nitric oxide reductase

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APA (6th Edition):

Murali, R. (2016). Studies on the cytochrome bd-type oxygen reductase superfamily and the discovery of a novel nitric oxide reductase. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/90911

Chicago Manual of Style (16th Edition):

Murali, Ranjani. “Studies on the cytochrome bd-type oxygen reductase superfamily and the discovery of a novel nitric oxide reductase.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/90911.

MLA Handbook (7th Edition):

Murali, Ranjani. “Studies on the cytochrome bd-type oxygen reductase superfamily and the discovery of a novel nitric oxide reductase.” 2016. Web. 17 Jul 2019.

Vancouver:

Murali R. Studies on the cytochrome bd-type oxygen reductase superfamily and the discovery of a novel nitric oxide reductase. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/90911.

Council of Science Editors:

Murali R. Studies on the cytochrome bd-type oxygen reductase superfamily and the discovery of a novel nitric oxide reductase. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/90911


University of Illinois – Urbana-Champaign

24. Blair, Patricia M. Discovery and characterization of ribosomally synthesized and post-translationally modified peptide natural products.

Degree: PhD, Chemistry, 2016, University of Illinois – Urbana-Champaign

 Bacterial secondary metabolites have historically been a rich source of antibiotic compounds. The genomic era has shown that bacteria harbor the potential to produce even… (more)

Subjects/Keywords: Ribosomally synthesized and post-translationally modified peptide; Natural products; Chemical probes; Mode of action

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APA (6th Edition):

Blair, P. M. (2016). Discovery and characterization of ribosomally synthesized and post-translationally modified peptide natural products. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95476

Chicago Manual of Style (16th Edition):

Blair, Patricia M. “Discovery and characterization of ribosomally synthesized and post-translationally modified peptide natural products.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/95476.

MLA Handbook (7th Edition):

Blair, Patricia M. “Discovery and characterization of ribosomally synthesized and post-translationally modified peptide natural products.” 2016. Web. 17 Jul 2019.

Vancouver:

Blair PM. Discovery and characterization of ribosomally synthesized and post-translationally modified peptide natural products. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/95476.

Council of Science Editors:

Blair PM. Discovery and characterization of ribosomally synthesized and post-translationally modified peptide natural products. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95476


University of Illinois – Urbana-Champaign

25. Tietz, Jonathan I. Genomics as a tool for natural product structure elucidation.

Degree: PhD, Chemistry, 2016, University of Illinois – Urbana-Champaign

 Natural product discovery is in the midst of a transition from a largely serendipity-based effort to an informatics-driven one. For most of the 20th century,… (more)

Subjects/Keywords: natural products; antibiotics; bioinformatics; lasso peptides; structure elucidation; JBIR-100; streptomonomicin; biosynthesis

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APA (6th Edition):

Tietz, J. I. (2016). Genomics as a tool for natural product structure elucidation. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95593

Chicago Manual of Style (16th Edition):

Tietz, Jonathan I. “Genomics as a tool for natural product structure elucidation.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/95593.

MLA Handbook (7th Edition):

Tietz, Jonathan I. “Genomics as a tool for natural product structure elucidation.” 2016. Web. 17 Jul 2019.

Vancouver:

Tietz JI. Genomics as a tool for natural product structure elucidation. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/95593.

Council of Science Editors:

Tietz JI. Genomics as a tool for natural product structure elucidation. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95593


University of Illinois – Urbana-Champaign

26. Dunbar, Kyle. Revealing the molecular details of azoline formation in ribosomal natural product biosynthesis.

Degree: PhD, 0335, 2015, University of Illinois – Urbana-Champaign

 The thiazole/oxazole-modified microcins (TOMMs) are a recently grouped class of ribosomally synthesized and posttranslationally modified peptides. Encoded by many bacteria and archaea, these natural products… (more)

Subjects/Keywords: Azoline Biosynthesis; ribosomally synthesized and post-translationally modified peptide (RiPP) Biosynthesis; thiazole/oxazole-modified microcin (TOMM) Biosynthesis; Cyclodehydratase; YcaO

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APA (6th Edition):

Dunbar, K. (2015). Revealing the molecular details of azoline formation in ribosomal natural product biosynthesis. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/73109

Chicago Manual of Style (16th Edition):

Dunbar, Kyle. “Revealing the molecular details of azoline formation in ribosomal natural product biosynthesis.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/73109.

MLA Handbook (7th Edition):

Dunbar, Kyle. “Revealing the molecular details of azoline formation in ribosomal natural product biosynthesis.” 2015. Web. 17 Jul 2019.

Vancouver:

Dunbar K. Revealing the molecular details of azoline formation in ribosomal natural product biosynthesis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/73109.

Council of Science Editors:

Dunbar K. Revealing the molecular details of azoline formation in ribosomal natural product biosynthesis. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/73109


University of Illinois – Urbana-Champaign

27. Tang, Weixin. Mechanistic studies of lanthipeptide biosynthesis.

Degree: PhD, Chemistry, 2015, University of Illinois – Urbana-Champaign

 Natural products and natural product derivatives have been the leading source of pharmaceutical compounds since the initial application of modern medicine. To fight the increasing… (more)

Subjects/Keywords: Enzyme mechanism; Lanthipeptide

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APA (6th Edition):

Tang, W. (2015). Mechanistic studies of lanthipeptide biosynthesis. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/78752

Chicago Manual of Style (16th Edition):

Tang, Weixin. “Mechanistic studies of lanthipeptide biosynthesis.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/78752.

MLA Handbook (7th Edition):

Tang, Weixin. “Mechanistic studies of lanthipeptide biosynthesis.” 2015. Web. 17 Jul 2019.

Vancouver:

Tang W. Mechanistic studies of lanthipeptide biosynthesis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/78752.

Council of Science Editors:

Tang W. Mechanistic studies of lanthipeptide biosynthesis. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/78752


University of Illinois – Urbana-Champaign

28. Bouvier, Jason T. Functional discovery in the oxidative D-galacturonate assimilation pathway and development of the enzyme similarity web tool.

Degree: PhD, Biochemistry, 2015, University of Illinois – Urbana-Champaign

 Sequencing technology has improved dramatically over the past few decades. Before the sequencing of complete genomes was possible, the sequencing of a gene was directly… (more)

Subjects/Keywords: Hexuronate degradation; sequence similarity network; Enzyme Function Initiative

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APA (6th Edition):

Bouvier, J. T. (2015). Functional discovery in the oxidative D-galacturonate assimilation pathway and development of the enzyme similarity web tool. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/88275

Chicago Manual of Style (16th Edition):

Bouvier, Jason T. “Functional discovery in the oxidative D-galacturonate assimilation pathway and development of the enzyme similarity web tool.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/88275.

MLA Handbook (7th Edition):

Bouvier, Jason T. “Functional discovery in the oxidative D-galacturonate assimilation pathway and development of the enzyme similarity web tool.” 2015. Web. 17 Jul 2019.

Vancouver:

Bouvier JT. Functional discovery in the oxidative D-galacturonate assimilation pathway and development of the enzyme similarity web tool. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/88275.

Council of Science Editors:

Bouvier JT. Functional discovery in the oxidative D-galacturonate assimilation pathway and development of the enzyme similarity web tool. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/88275


University of Illinois – Urbana-Champaign

29. Garcia De Gonzalo, Chantal V. Studies on the mechanism of action of the antimicrobial S-linked glycopeptide sublancin.

Degree: PhD, Chemistry, 2015, University of Illinois – Urbana-Champaign

 Infectious diseases are a continuing threat to human health. In particular, the rapid development of bacterial antibiotic resistance not only decreases the effectiveness of known… (more)

Subjects/Keywords: Glycocin; Ribosomally synthesized and post-translationally modified peptide (RiPP); Antimicrobial; S-Linked

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APA (6th Edition):

Garcia De Gonzalo, C. V. (2015). Studies on the mechanism of action of the antimicrobial S-linked glycopeptide sublancin. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89179

Chicago Manual of Style (16th Edition):

Garcia De Gonzalo, Chantal V. “Studies on the mechanism of action of the antimicrobial S-linked glycopeptide sublancin.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/89179.

MLA Handbook (7th Edition):

Garcia De Gonzalo, Chantal V. “Studies on the mechanism of action of the antimicrobial S-linked glycopeptide sublancin.” 2015. Web. 17 Jul 2019.

Vancouver:

Garcia De Gonzalo CV. Studies on the mechanism of action of the antimicrobial S-linked glycopeptide sublancin. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/89179.

Council of Science Editors:

Garcia De Gonzalo CV. Studies on the mechanism of action of the antimicrobial S-linked glycopeptide sublancin. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89179


University of Illinois – Urbana-Champaign

30. Yang, Xiao. Biosynthesis and engineering of lanthipeptide natural products for novel applications.

Degree: PhD, Chemistry, 2015, University of Illinois – Urbana-Champaign

 Natural products have played prominent roles in science and medicine due to their diverse chemical scaffolds and biological activities. Ribosomally synthesized and post-translationally modified peptides… (more)

Subjects/Keywords: Lanthipeptide; Lantibiotic; natural product; biosynthesis

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APA (6th Edition):

Yang, X. (2015). Biosynthesis and engineering of lanthipeptide natural products for novel applications. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89185

Chicago Manual of Style (16th Edition):

Yang, Xiao. “Biosynthesis and engineering of lanthipeptide natural products for novel applications.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/89185.

MLA Handbook (7th Edition):

Yang, Xiao. “Biosynthesis and engineering of lanthipeptide natural products for novel applications.” 2015. Web. 17 Jul 2019.

Vancouver:

Yang X. Biosynthesis and engineering of lanthipeptide natural products for novel applications. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/89185.

Council of Science Editors:

Yang X. Biosynthesis and engineering of lanthipeptide natural products for novel applications. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89185

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