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You searched for +publisher:"University of Texas – Austin" +contributor:("Fast, Walter L"). Showing records 1 – 18 of 18 total matches.

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1. Linsky, Thomas W. Studies on the mechanism and inhibition of enzymes in the pentein superfamily.

Degree: PhD, Biochemistry, 2012, University of Texas – Austin

 Dimethylarginine dimethylaminohydrolase (DDAH) indirectly regulates nitric oxide production by hydrolyzing methylated arginines, which are endogenous nitric oxide synthase inhibitors. This enzyme is a member of… (more)

Subjects/Keywords: Dimethylarginine dimethylaminohydrolase; Succinylarginine dihydrolase; Pentein; High-throughput screening

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APA (6th Edition):

Linsky, T. W. (2012). Studies on the mechanism and inhibition of enzymes in the pentein superfamily. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/22148

Chicago Manual of Style (16th Edition):

Linsky, Thomas W. “Studies on the mechanism and inhibition of enzymes in the pentein superfamily.” 2012. Doctoral Dissertation, University of Texas – Austin. Accessed August 08, 2020. http://hdl.handle.net/2152/22148.

MLA Handbook (7th Edition):

Linsky, Thomas W. “Studies on the mechanism and inhibition of enzymes in the pentein superfamily.” 2012. Web. 08 Aug 2020.

Vancouver:

Linsky TW. Studies on the mechanism and inhibition of enzymes in the pentein superfamily. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2012. [cited 2020 Aug 08]. Available from: http://hdl.handle.net/2152/22148.

Council of Science Editors:

Linsky TW. Studies on the mechanism and inhibition of enzymes in the pentein superfamily. [Doctoral Dissertation]. University of Texas – Austin; 2012. Available from: http://hdl.handle.net/2152/22148


University of Texas – Austin

2. Villalba, Brian. Kinetic characterization of the inhibition, excision mechanisms, and fidelity of Hepatitis C Virus RNA-dependent RNA polymerase.

Degree: PhD, Biochemistry, 2020, University of Texas – Austin

 NS5B is the RNA-dependent RNA polymerase that catalyzes the replication of the Hepatitis C Virus genome. It is a major target for antiviral drugs including… (more)

Subjects/Keywords: Hepatitis C Virus; RNA polymerase; Enzyme kinetics; Nucleoside analogs

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APA (6th Edition):

Villalba, B. (2020). Kinetic characterization of the inhibition, excision mechanisms, and fidelity of Hepatitis C Virus RNA-dependent RNA polymerase. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/8952

Chicago Manual of Style (16th Edition):

Villalba, Brian. “Kinetic characterization of the inhibition, excision mechanisms, and fidelity of Hepatitis C Virus RNA-dependent RNA polymerase.” 2020. Doctoral Dissertation, University of Texas – Austin. Accessed August 08, 2020. http://dx.doi.org/10.26153/tsw/8952.

MLA Handbook (7th Edition):

Villalba, Brian. “Kinetic characterization of the inhibition, excision mechanisms, and fidelity of Hepatitis C Virus RNA-dependent RNA polymerase.” 2020. Web. 08 Aug 2020.

Vancouver:

Villalba B. Kinetic characterization of the inhibition, excision mechanisms, and fidelity of Hepatitis C Virus RNA-dependent RNA polymerase. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2020. [cited 2020 Aug 08]. Available from: http://dx.doi.org/10.26153/tsw/8952.

Council of Science Editors:

Villalba B. Kinetic characterization of the inhibition, excision mechanisms, and fidelity of Hepatitis C Virus RNA-dependent RNA polymerase. [Doctoral Dissertation]. University of Texas – Austin; 2020. Available from: http://dx.doi.org/10.26153/tsw/8952


University of Texas – Austin

3. -8299-3023. Formylated dipyrromethane based phosphate derivatives receptors.

Degree: PhD, Chemistry, 2016, University of Texas – Austin

 Anions are key components in many biological and industrial processes. They play crucial roles in both health and the environment. In many cases, it is… (more)

Subjects/Keywords: Dipyrromethane; Phosphate

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APA (6th Edition):

-8299-3023. (2016). Formylated dipyrromethane based phosphate derivatives receptors. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68388

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-8299-3023. “Formylated dipyrromethane based phosphate derivatives receptors.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed August 08, 2020. http://hdl.handle.net/2152/68388.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-8299-3023. “Formylated dipyrromethane based phosphate derivatives receptors.” 2016. Web. 08 Aug 2020.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-8299-3023. Formylated dipyrromethane based phosphate derivatives receptors. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2020 Aug 08]. Available from: http://hdl.handle.net/2152/68388.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-8299-3023. Formylated dipyrromethane based phosphate derivatives receptors. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/68388

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


University of Texas – Austin

4. -8962-3030. Regulation of elongation factor 2 kinase (eEF-2K) by acidity.

Degree: PhD, Cell and Molecular Biology, 2019, University of Texas – Austin

 Eukaryotic elongation factor 2 kinase (eEF-2K) is a calmodulin (CaM)/calcium regulated kinase whose activity disrupts translation elongation resulting in the global decrease of protein synthesis¹.… (more)

Subjects/Keywords: eEF-2K; Acidity; Elongation factor 2 kinase

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APA (6th Edition):

-8962-3030. (2019). Regulation of elongation factor 2 kinase (eEF-2K) by acidity. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/72809

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

-8962-3030. “Regulation of elongation factor 2 kinase (eEF-2K) by acidity.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed August 08, 2020. http://hdl.handle.net/2152/72809.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-8962-3030. “Regulation of elongation factor 2 kinase (eEF-2K) by acidity.” 2019. Web. 08 Aug 2020.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-8962-3030. Regulation of elongation factor 2 kinase (eEF-2K) by acidity. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2020 Aug 08]. Available from: http://hdl.handle.net/2152/72809.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-8962-3030. Regulation of elongation factor 2 kinase (eEF-2K) by acidity. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://hdl.handle.net/2152/72809

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


University of Texas – Austin

5. Stewart, Alesha. An investigation of New Delhi metallo-[beta]-lactamase : clinical variants, lipid modification & inhibition: Investigation of New Delhi metallo-[beta]-lactamase : clinical variants, lipid modification [and] inhibition.

Degree: PhD, Pharmaceutical Sciences, 2017, University of Texas – Austin

 Many β-lactam drugs, including penicillins, monobactams cephalosporins, and carbapenems, are used in clinical treatment of bacterial infections. However, resistant bacterial strains have surfaced, in part… (more)

Subjects/Keywords: NDM-1; Antibiotic resistance; Metallo-β-lactamase; NDM-1 variants; NDM-1 inhibition

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APA (6th Edition):

Stewart, A. (2017). An investigation of New Delhi metallo-[beta]-lactamase : clinical variants, lipid modification & inhibition: Investigation of New Delhi metallo-[beta]-lactamase : clinical variants, lipid modification [and] inhibition. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/3392

Chicago Manual of Style (16th Edition):

Stewart, Alesha. “An investigation of New Delhi metallo-[beta]-lactamase : clinical variants, lipid modification & inhibition: Investigation of New Delhi metallo-[beta]-lactamase : clinical variants, lipid modification [and] inhibition.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed August 08, 2020. http://dx.doi.org/10.26153/tsw/3392.

MLA Handbook (7th Edition):

Stewart, Alesha. “An investigation of New Delhi metallo-[beta]-lactamase : clinical variants, lipid modification & inhibition: Investigation of New Delhi metallo-[beta]-lactamase : clinical variants, lipid modification [and] inhibition.” 2017. Web. 08 Aug 2020.

Vancouver:

Stewart A. An investigation of New Delhi metallo-[beta]-lactamase : clinical variants, lipid modification & inhibition: Investigation of New Delhi metallo-[beta]-lactamase : clinical variants, lipid modification [and] inhibition. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2020 Aug 08]. Available from: http://dx.doi.org/10.26153/tsw/3392.

Council of Science Editors:

Stewart A. An investigation of New Delhi metallo-[beta]-lactamase : clinical variants, lipid modification & inhibition: Investigation of New Delhi metallo-[beta]-lactamase : clinical variants, lipid modification [and] inhibition. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://dx.doi.org/10.26153/tsw/3392


University of Texas – Austin

6. Tavares, Clint Damian Jaxon. Regulation of elongation factor 2 kinase (eEF-2K) by phosphorylation.

Degree: PhD, Cell and Molecular Biology, 2014, University of Texas – Austin

 Eukaryotic elongation factor 2 kinase (eEF-2K) is an atypical calcium/calmodulin-dependent protein kinase (CaMK-III). The kinase provides a mechanism by which cells can globally control the… (more)

Subjects/Keywords: Elongation factor 2 kinase (eEF-2K); Calmodulin; Kinase; Protein synthesis; Calcium; eEF-2, Autophosphorylation; Thr-348; Ser-500

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APA (6th Edition):

Tavares, C. D. J. (2014). Regulation of elongation factor 2 kinase (eEF-2K) by phosphorylation. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/47184

Chicago Manual of Style (16th Edition):

Tavares, Clint Damian Jaxon. “Regulation of elongation factor 2 kinase (eEF-2K) by phosphorylation.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed August 08, 2020. http://hdl.handle.net/2152/47184.

MLA Handbook (7th Edition):

Tavares, Clint Damian Jaxon. “Regulation of elongation factor 2 kinase (eEF-2K) by phosphorylation.” 2014. Web. 08 Aug 2020.

Vancouver:

Tavares CDJ. Regulation of elongation factor 2 kinase (eEF-2K) by phosphorylation. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Aug 08]. Available from: http://hdl.handle.net/2152/47184.

Council of Science Editors:

Tavares CDJ. Regulation of elongation factor 2 kinase (eEF-2K) by phosphorylation. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/47184


University of Texas – Austin

7. Clevenger, Kenneth David. Investigation and engineering of PvdQ, a Pseudomonas aeruginosa enzyme at the nexus of quorum sensing and iron uptake pathways.

Degree: PhD, Biochemistry, 2014, University of Texas – Austin

 The gram-negative human pathogen Pseudomonas aeruginosa is a widespread global health concern. Two key pathways of P. aeruginosa that are involved in its infection and/or… (more)

Subjects/Keywords: NTN-hydrolase; PvdQ; Siderophore; Pyoverdine; NRPS; Quorum-sensing; Quorum-quenching; Alkylboronic acid; Boronic acid; Iron limited growth; Pseudomonas aeruginosa

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APA (6th Edition):

Clevenger, K. D. (2014). Investigation and engineering of PvdQ, a Pseudomonas aeruginosa enzyme at the nexus of quorum sensing and iron uptake pathways. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/32902

Chicago Manual of Style (16th Edition):

Clevenger, Kenneth David. “Investigation and engineering of PvdQ, a Pseudomonas aeruginosa enzyme at the nexus of quorum sensing and iron uptake pathways.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed August 08, 2020. http://hdl.handle.net/2152/32902.

MLA Handbook (7th Edition):

Clevenger, Kenneth David. “Investigation and engineering of PvdQ, a Pseudomonas aeruginosa enzyme at the nexus of quorum sensing and iron uptake pathways.” 2014. Web. 08 Aug 2020.

Vancouver:

Clevenger KD. Investigation and engineering of PvdQ, a Pseudomonas aeruginosa enzyme at the nexus of quorum sensing and iron uptake pathways. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Aug 08]. Available from: http://hdl.handle.net/2152/32902.

Council of Science Editors:

Clevenger KD. Investigation and engineering of PvdQ, a Pseudomonas aeruginosa enzyme at the nexus of quorum sensing and iron uptake pathways. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/32902


University of Texas – Austin

8. -9758-983X. The design of halopyridine-based activity-based probes and mechanistic studies of succinylarginine dihydrolase.

Degree: PhD, Pharmaceutical Sciences, 2015, University of Texas – Austin

 An important design aspect of covalent inactivators is the balance between reactivity, or reversibility of reaction, with nucleophiles in solution and reactivity with nucleophiles at… (more)

Subjects/Keywords: Dimethylarginine dimethylaminohydrolase; Halopyridine; Activity-based probes; Succinylarginine dihydrolase

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APA (6th Edition):

-9758-983X. (2015). The design of halopyridine-based activity-based probes and mechanistic studies of succinylarginine dihydrolase. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46556

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

-9758-983X. “The design of halopyridine-based activity-based probes and mechanistic studies of succinylarginine dihydrolase.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed August 08, 2020. http://hdl.handle.net/2152/46556.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-9758-983X. “The design of halopyridine-based activity-based probes and mechanistic studies of succinylarginine dihydrolase.” 2015. Web. 08 Aug 2020.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-9758-983X. The design of halopyridine-based activity-based probes and mechanistic studies of succinylarginine dihydrolase. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2020 Aug 08]. Available from: http://hdl.handle.net/2152/46556.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-9758-983X. The design of halopyridine-based activity-based probes and mechanistic studies of succinylarginine dihydrolase. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46556

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Author name may be incomplete


University of Texas – Austin

9. Sun, He, Ph. D. Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways.

Degree: PhD, Pharmaceutical Sciences, 2013, University of Texas – Austin

 The diverse reactions that enzymes catalyze have fascinated enzymologists for decades. Continuing investigations in the biosynthesis of both primary and secondary metabolites have led to… (more)

Subjects/Keywords: Unusual; Catalysis; Enzyme; Biosynthesis; Mechanism; Characterization; UDP-galactopyranose mutase; Sulfur carrier protein activating enzyme; Cobalamin-dependent radical S-adenosyl-L-methionine enzymes

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APA (6th Edition):

Sun, He, P. D. (2013). Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63875

Chicago Manual of Style (16th Edition):

Sun, He, Ph D. “Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways.” 2013. Doctoral Dissertation, University of Texas – Austin. Accessed August 08, 2020. http://hdl.handle.net/2152/63875.

MLA Handbook (7th Edition):

Sun, He, Ph D. “Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways.” 2013. Web. 08 Aug 2020.

Vancouver:

Sun, He PD. Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2020 Aug 08]. Available from: http://hdl.handle.net/2152/63875.

Council of Science Editors:

Sun, He PD. Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways. [Doctoral Dissertation]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/63875


University of Texas – Austin

10. Lin, Chia-I. Biosynthetic studies of lincomycin A, a thiosugar-containing natural product.

Degree: PhD, Chemistry, 2019, University of Texas – Austin

 The dissertation describes biosynthetic studies of lincomycin A, a thiosugarcontaining natural product. Lincomycin A was isolated from Streptomyces lincolnensis and has been used clinically as… (more)

Subjects/Keywords: Biosynthesis; Lincomycin; Thiosugar

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APA (6th Edition):

Lin, C. (2019). Biosynthetic studies of lincomycin A, a thiosugar-containing natural product. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2237

Chicago Manual of Style (16th Edition):

Lin, Chia-I. “Biosynthetic studies of lincomycin A, a thiosugar-containing natural product.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed August 08, 2020. http://dx.doi.org/10.26153/tsw/2237.

MLA Handbook (7th Edition):

Lin, Chia-I. “Biosynthetic studies of lincomycin A, a thiosugar-containing natural product.” 2019. Web. 08 Aug 2020.

Vancouver:

Lin C. Biosynthetic studies of lincomycin A, a thiosugar-containing natural product. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2020 Aug 08]. Available from: http://dx.doi.org/10.26153/tsw/2237.

Council of Science Editors:

Lin C. Biosynthetic studies of lincomycin A, a thiosugar-containing natural product. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/2237


University of Texas – Austin

11. -7992-3267. Structure-based mechanism of hydratase-aldolases in the Type I aldolase superfamily and structures of tautomerase superfamily members.

Degree: PhD, Biochemistry, 2017, University of Texas – Austin

 Polycyclic Aromatic Hydrocarbons (PAHs) are composed of multiple benzene-like rings and their bacterial catabolism has potential utility for bioremediation. In the breakdown of each ring,… (more)

Subjects/Keywords: Hydratase-aldolase; Naphthalene; Phenanthrene; Mycobacterium vanbaalenii PYR-1; Pseudomonas putida G7; Type I aldolase; 4-oxalocrotonate tautomerase; Cis-3-chloroacrylic acid dehalogenase; Malonate semialdehyde decarboxylase; Tautomerase superfamily

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APA (6th Edition):

-7992-3267. (2017). Structure-based mechanism of hydratase-aldolases in the Type I aldolase superfamily and structures of tautomerase superfamily members. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2230

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-7992-3267. “Structure-based mechanism of hydratase-aldolases in the Type I aldolase superfamily and structures of tautomerase superfamily members.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed August 08, 2020. http://dx.doi.org/10.26153/tsw/2230.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-7992-3267. “Structure-based mechanism of hydratase-aldolases in the Type I aldolase superfamily and structures of tautomerase superfamily members.” 2017. Web. 08 Aug 2020.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-7992-3267. Structure-based mechanism of hydratase-aldolases in the Type I aldolase superfamily and structures of tautomerase superfamily members. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2020 Aug 08]. Available from: http://dx.doi.org/10.26153/tsw/2230.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-7992-3267. Structure-based mechanism of hydratase-aldolases in the Type I aldolase superfamily and structures of tautomerase superfamily members. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://dx.doi.org/10.26153/tsw/2230

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Author name may be incomplete


University of Texas – Austin

12. Liu, Cheng-Hao. Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues.

Degree: PhD, Chemistry, 2014, University of Texas – Austin

 Enzymes are biological catalysts which greatly accelerate the rate of chemical reactions with remarkable substrate specificity and stereoselectivity. To optimize their catalytic abilities, many enzymes… (more)

Subjects/Keywords: Enzyme mechanism; Chiral substrate; ACC deaminase; PLP; Difluorocyclopropane; Tight-binding inhibitor; IspH; chiral methyl analysis; Iron-sulfur cluster

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APA (6th Edition):

Liu, C. (2014). Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63859

Chicago Manual of Style (16th Edition):

Liu, Cheng-Hao. “Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed August 08, 2020. http://hdl.handle.net/2152/63859.

MLA Handbook (7th Edition):

Liu, Cheng-Hao. “Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues.” 2014. Web. 08 Aug 2020.

Vancouver:

Liu C. Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Aug 08]. Available from: http://hdl.handle.net/2152/63859.

Council of Science Editors:

Liu C. Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/63859


University of Texas – Austin

13. Romo, Anthony James. Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin.

Degree: PhD, Pharmaceutical Sciences, 2019, University of Texas – Austin

 Advancements in our ability to obtain high quality bacterial whole genome sequences have increased the rate natural product biosynthetic gene clusters are identified, but these… (more)

Subjects/Keywords: Next generation sequencing; Peptidyl nucleoside antibiotics; Gene cluster; Streptomyces

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APA (6th Edition):

Romo, A. J. (2019). Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2198

Chicago Manual of Style (16th Edition):

Romo, Anthony James. “Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed August 08, 2020. http://dx.doi.org/10.26153/tsw/2198.

MLA Handbook (7th Edition):

Romo, Anthony James. “Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin.” 2019. Web. 08 Aug 2020.

Vancouver:

Romo AJ. Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2020 Aug 08]. Available from: http://dx.doi.org/10.26153/tsw/2198.

Council of Science Editors:

Romo AJ. Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/2198

14. -9681-2721. On the reactions of trans-3-chloroacrylic acid dehalogenase and a cis-3-chloroacrylic acid dehalogenase homologue, Cg10062 : mechanistic and evolutionary implications.

Degree: PhD, Pharmaceutical Sciences, 2015, University of Texas – Austin

 The tautomerase superfamily (TSF) provides an excellent model system to study enzyme specificity, catalysis, and divergent evolution. trans-3-Cholroacrylic acid dehalogenase (CaaD), cis-3-chloroacrylic acid dehalogenase (cis-CaaD),… (more)

Subjects/Keywords: Enzymes; Kinetics; Divergent evolution

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APA (6th Edition):

-9681-2721. (2015). On the reactions of trans-3-chloroacrylic acid dehalogenase and a cis-3-chloroacrylic acid dehalogenase homologue, Cg10062 : mechanistic and evolutionary implications. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30531

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-9681-2721. “On the reactions of trans-3-chloroacrylic acid dehalogenase and a cis-3-chloroacrylic acid dehalogenase homologue, Cg10062 : mechanistic and evolutionary implications.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed August 08, 2020. http://hdl.handle.net/2152/30531.

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MLA Handbook (7th Edition):

-9681-2721. “On the reactions of trans-3-chloroacrylic acid dehalogenase and a cis-3-chloroacrylic acid dehalogenase homologue, Cg10062 : mechanistic and evolutionary implications.” 2015. Web. 08 Aug 2020.

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Author name may be incomplete

Vancouver:

-9681-2721. On the reactions of trans-3-chloroacrylic acid dehalogenase and a cis-3-chloroacrylic acid dehalogenase homologue, Cg10062 : mechanistic and evolutionary implications. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2020 Aug 08]. Available from: http://hdl.handle.net/2152/30531.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-9681-2721. On the reactions of trans-3-chloroacrylic acid dehalogenase and a cis-3-chloroacrylic acid dehalogenase homologue, Cg10062 : mechanistic and evolutionary implications. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/30531

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Author name may be incomplete

15. -3965-1137. Enzyme promiscuity : a review on select tautomerase superfamily members.

Degree: MSin Pharmaceutical Sciences, Pharmaceutical sciences, 2016, University of Texas – Austin

 Enzymes are categorized into families based on sequence similarity and conserved features. Superfamilies are composed of families of enzymes with common folds and conserved features.… (more)

Subjects/Keywords: 4-oxalocrotonate tautomerase; Enzyme superfamilies; Malonate semialdehyde decarboxylase; 3-chloroacrylic dehalogenase

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APA (6th Edition):

-3965-1137. (2016). Enzyme promiscuity : a review on select tautomerase superfamily members. (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/41721

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-3965-1137. “Enzyme promiscuity : a review on select tautomerase superfamily members.” 2016. Masters Thesis, University of Texas – Austin. Accessed August 08, 2020. http://hdl.handle.net/2152/41721.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-3965-1137. “Enzyme promiscuity : a review on select tautomerase superfamily members.” 2016. Web. 08 Aug 2020.

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Author name may be incomplete

Vancouver:

-3965-1137. Enzyme promiscuity : a review on select tautomerase superfamily members. [Internet] [Masters thesis]. University of Texas – Austin; 2016. [cited 2020 Aug 08]. Available from: http://hdl.handle.net/2152/41721.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-3965-1137. Enzyme promiscuity : a review on select tautomerase superfamily members. [Masters Thesis]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/41721

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Author name may be incomplete

16. -6306-7187. Synthesis of isosteric analogues of rooperol.

Degree: MSin Pharmaceutical Sciences, Pharmaceutical Sciences, 2017, University of Texas – Austin

 Hypoxoside is a norlignan bisglycoside derived from Hypoxis hemerocallidae (African potato), a medicinal plant used in Africa to treat a variety of disorders, including cancer,… (more)

Subjects/Keywords: Rooperol; Hypoxoside; Catechol; Natural products; Glucosides; Prodrug

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APA (6th Edition):

-6306-7187. (2017). Synthesis of isosteric analogues of rooperol. (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/47298

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-6306-7187. “Synthesis of isosteric analogues of rooperol.” 2017. Masters Thesis, University of Texas – Austin. Accessed August 08, 2020. http://hdl.handle.net/2152/47298.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-6306-7187. “Synthesis of isosteric analogues of rooperol.” 2017. Web. 08 Aug 2020.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-6306-7187. Synthesis of isosteric analogues of rooperol. [Internet] [Masters thesis]. University of Texas – Austin; 2017. [cited 2020 Aug 08]. Available from: http://hdl.handle.net/2152/47298.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-6306-7187. Synthesis of isosteric analogues of rooperol. [Masters Thesis]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/47298

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Author name may be incomplete

17. Burstein, Gayle Diane. An investigation of the irreversible inhibition of human N[superscript ω], N[superscript ω]- dimethylarginine dimethylaminohydrolase (DDAH1).

Degree: PhD, Biochemistry, 2014, University of Texas – Austin

 Nitric oxide synthases (NOS) are responsible for the production of nitric oxide (NO), an essential cell-signaling molecule, in mammals. There are three isoforms of NOS… (more)

Subjects/Keywords: Enzymology; Dimethylarginine; Nitric oxide; Covalent inhibition; Drug design; DDAH1; Nitroxyl; ADMA; Chloroacetamidine

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

APA (6th Edition):

Burstein, G. D. (2014). An investigation of the irreversible inhibition of human N[superscript ω], N[superscript ω]- dimethylarginine dimethylaminohydrolase (DDAH1). (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/31281

Chicago Manual of Style (16th Edition):

Burstein, Gayle Diane. “An investigation of the irreversible inhibition of human N[superscript ω], N[superscript ω]- dimethylarginine dimethylaminohydrolase (DDAH1).” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed August 08, 2020. http://hdl.handle.net/2152/31281.

MLA Handbook (7th Edition):

Burstein, Gayle Diane. “An investigation of the irreversible inhibition of human N[superscript ω], N[superscript ω]- dimethylarginine dimethylaminohydrolase (DDAH1).” 2014. Web. 08 Aug 2020.

Vancouver:

Burstein GD. An investigation of the irreversible inhibition of human N[superscript ω], N[superscript ω]- dimethylarginine dimethylaminohydrolase (DDAH1). [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Aug 08]. Available from: http://hdl.handle.net/2152/31281.

Council of Science Editors:

Burstein GD. An investigation of the irreversible inhibition of human N[superscript ω], N[superscript ω]- dimethylarginine dimethylaminohydrolase (DDAH1). [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/31281

18. -2576-1079. Activation of caspase-9 within the Apaf-1 apoptosome.

Degree: PhD, Cell and Molecular Biology, 2015, University of Texas – Austin

 A family of cysteinyl aspartate-specific proteases (caspases) induces dramatic biochemical and morphological changes during apoptosis. Initiator caspases are thought to be activated through induced homodimerization,… (more)

Subjects/Keywords: Apoptosis; Caspase-9; Apaf-1; Apoptosome; Auto-catalytic cleavage; Molecular timer; Non-cleavable caspase-9 knock-in mouse

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

APA (6th Edition):

-2576-1079. (2015). Activation of caspase-9 within the Apaf-1 apoptosome. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46811

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-2576-1079. “Activation of caspase-9 within the Apaf-1 apoptosome.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed August 08, 2020. http://hdl.handle.net/2152/46811.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-2576-1079. “Activation of caspase-9 within the Apaf-1 apoptosome.” 2015. Web. 08 Aug 2020.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-2576-1079. Activation of caspase-9 within the Apaf-1 apoptosome. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2020 Aug 08]. Available from: http://hdl.handle.net/2152/46811.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-2576-1079. Activation of caspase-9 within the Apaf-1 apoptosome. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46811

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Author name may be incomplete

.