Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(allostery). Showing records 1 – 30 of 116 total matches.

[1] [2] [3] [4]

Search Limiters

Last 2 Years | English Only

Country

▼ Search Limiters


Wake Forest University

1. Xiao, Jiajie. UNDERSTANDING GENERALIZED ALLOSTERY IN THROMBIN.

Degree: 2018, Wake Forest University

 Thrombin is a critical drug target for chemotherapeutic and antithrombotic therapy development. Although many experiments have demonstrated that thrombin is a multifunctional allosteric enzyme, the… (more)

Subjects/Keywords: Allostery

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Xiao, J. (2018). UNDERSTANDING GENERALIZED ALLOSTERY IN THROMBIN. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/92371

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

Chicago Manual of Style (16th Edition):

Xiao, Jiajie. “UNDERSTANDING GENERALIZED ALLOSTERY IN THROMBIN.” 2018. Thesis, Wake Forest University. Accessed December 08, 2019. http://hdl.handle.net/10339/92371.

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

MLA Handbook (7th Edition):

Xiao, Jiajie. “UNDERSTANDING GENERALIZED ALLOSTERY IN THROMBIN.” 2018. Web. 08 Dec 2019.

Vancouver:

Xiao J. UNDERSTANDING GENERALIZED ALLOSTERY IN THROMBIN. [Internet] [Thesis]. Wake Forest University; 2018. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/10339/92371.

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

Council of Science Editors:

Xiao J. UNDERSTANDING GENERALIZED ALLOSTERY IN THROMBIN. [Thesis]. Wake Forest University; 2018. Available from: http://hdl.handle.net/10339/92371

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


Texas A&M University

2. Whitaker, Amy Michelle. Exploration of Thermodynamic and Structural Changes Relevant to the Allosteric Inhibition in Phosphofructokinase from Bacillus Stearothermophilus.

Degree: 2015, Texas A&M University

 Phosphofructokinase from Bacillus stearothermophilus (BsPFK) and Escherichia coli (EcPFK) are allosterically inhibited by downstream glycolytic pathway intermediate phosphoenol-pyruvate (PEP). The coupling free energy, ?Gay, describes… (more)

Subjects/Keywords: allostery; phosphofructokinase

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Whitaker, A. M. (2015). Exploration of Thermodynamic and Structural Changes Relevant to the Allosteric Inhibition in Phosphofructokinase from Bacillus Stearothermophilus. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/158914

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

Chicago Manual of Style (16th Edition):

Whitaker, Amy Michelle. “Exploration of Thermodynamic and Structural Changes Relevant to the Allosteric Inhibition in Phosphofructokinase from Bacillus Stearothermophilus.” 2015. Thesis, Texas A&M University. Accessed December 08, 2019. http://hdl.handle.net/1969.1/158914.

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

MLA Handbook (7th Edition):

Whitaker, Amy Michelle. “Exploration of Thermodynamic and Structural Changes Relevant to the Allosteric Inhibition in Phosphofructokinase from Bacillus Stearothermophilus.” 2015. Web. 08 Dec 2019.

Vancouver:

Whitaker AM. Exploration of Thermodynamic and Structural Changes Relevant to the Allosteric Inhibition in Phosphofructokinase from Bacillus Stearothermophilus. [Internet] [Thesis]. Texas A&M University; 2015. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1969.1/158914.

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

Council of Science Editors:

Whitaker AM. Exploration of Thermodynamic and Structural Changes Relevant to the Allosteric Inhibition in Phosphofructokinase from Bacillus Stearothermophilus. [Thesis]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/158914

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


McMaster University

3. AKIMOTO, MADOKA. ALLOSTERIC MECHANISMS FOR THE cAMP-DEPENDENT CONTROL OF FUNCTIONAL INTER-DOMAIN LINKERS.

Degree: PhD, 2015, McMaster University

The activation of Protein Kinase A (PKA) and of Hyperpolarization-activated and Cyclic Nucleotide-modulated channels (HCN) is controlled by cAMP through cAMP binding domains (CBDs), which… (more)

Subjects/Keywords: Allostery; protein; linker

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

AKIMOTO, M. (2015). ALLOSTERIC MECHANISMS FOR THE cAMP-DEPENDENT CONTROL OF FUNCTIONAL INTER-DOMAIN LINKERS. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/18033

Chicago Manual of Style (16th Edition):

AKIMOTO, MADOKA. “ALLOSTERIC MECHANISMS FOR THE cAMP-DEPENDENT CONTROL OF FUNCTIONAL INTER-DOMAIN LINKERS.” 2015. Doctoral Dissertation, McMaster University. Accessed December 08, 2019. http://hdl.handle.net/11375/18033.

MLA Handbook (7th Edition):

AKIMOTO, MADOKA. “ALLOSTERIC MECHANISMS FOR THE cAMP-DEPENDENT CONTROL OF FUNCTIONAL INTER-DOMAIN LINKERS.” 2015. Web. 08 Dec 2019.

Vancouver:

AKIMOTO M. ALLOSTERIC MECHANISMS FOR THE cAMP-DEPENDENT CONTROL OF FUNCTIONAL INTER-DOMAIN LINKERS. [Internet] [Doctoral dissertation]. McMaster University; 2015. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/11375/18033.

Council of Science Editors:

AKIMOTO M. ALLOSTERIC MECHANISMS FOR THE cAMP-DEPENDENT CONTROL OF FUNCTIONAL INTER-DOMAIN LINKERS. [Doctoral Dissertation]. McMaster University; 2015. Available from: http://hdl.handle.net/11375/18033


University of Notre Dame

4. Brendan J. Mahoney. Understanding Response Mechanisms of Post-Translational Phosphorylation in Signaling Proteins</h1>.

Degree: PhD, Chemistry and Biochemistry, 2018, University of Notre Dame

  Proper maintenance of the cell cycle relies on regulation via pathways of signaling proteins. The function of these cell signaling proteins is often modulated… (more)

Subjects/Keywords: allostery; Pin1; phosphorylation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Mahoney, B. J. (2018). Understanding Response Mechanisms of Post-Translational Phosphorylation in Signaling Proteins</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/v118rb7241t

Chicago Manual of Style (16th Edition):

Mahoney, Brendan J.. “Understanding Response Mechanisms of Post-Translational Phosphorylation in Signaling Proteins</h1>.” 2018. Doctoral Dissertation, University of Notre Dame. Accessed December 08, 2019. https://curate.nd.edu/show/v118rb7241t.

MLA Handbook (7th Edition):

Mahoney, Brendan J.. “Understanding Response Mechanisms of Post-Translational Phosphorylation in Signaling Proteins</h1>.” 2018. Web. 08 Dec 2019.

Vancouver:

Mahoney BJ. Understanding Response Mechanisms of Post-Translational Phosphorylation in Signaling Proteins</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2018. [cited 2019 Dec 08]. Available from: https://curate.nd.edu/show/v118rb7241t.

Council of Science Editors:

Mahoney BJ. Understanding Response Mechanisms of Post-Translational Phosphorylation in Signaling Proteins</h1>. [Doctoral Dissertation]. University of Notre Dame; 2018. Available from: https://curate.nd.edu/show/v118rb7241t


Texas A&M University

5. Tindall, Amanda Jean. Expression, Purification, and Kinetic Characterization of Human Liver Phosphofructokinase.

Degree: MS, Biochemistry, 2016, Texas A&M University

 Phosphofructokinase (PFK) catalyzes the phosphorylation of fructose 6-phosphate (F6P) to fructose 1,6-bisphosphate (F16BP) in a MgATP dependent reaction. This reaction represents the first committed step… (more)

Subjects/Keywords: phosphofructokinase; glycolysis; allostery; human liver

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Tindall, A. J. (2016). Expression, Purification, and Kinetic Characterization of Human Liver Phosphofructokinase. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/156932

Chicago Manual of Style (16th Edition):

Tindall, Amanda Jean. “Expression, Purification, and Kinetic Characterization of Human Liver Phosphofructokinase.” 2016. Masters Thesis, Texas A&M University. Accessed December 08, 2019. http://hdl.handle.net/1969.1/156932.

MLA Handbook (7th Edition):

Tindall, Amanda Jean. “Expression, Purification, and Kinetic Characterization of Human Liver Phosphofructokinase.” 2016. Web. 08 Dec 2019.

Vancouver:

Tindall AJ. Expression, Purification, and Kinetic Characterization of Human Liver Phosphofructokinase. [Internet] [Masters thesis]. Texas A&M University; 2016. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1969.1/156932.

Council of Science Editors:

Tindall AJ. Expression, Purification, and Kinetic Characterization of Human Liver Phosphofructokinase. [Masters Thesis]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/156932


Texas A&M University

6. Bigley, Andrew N. Investigations on the Mechanism of Allosteric Activtion of Rabbit Muscle Glycogen Phosphorylase b by AMP.

Degree: 2010, Texas A&M University

 Much work has been carried out on glycogen phosphorylase over the last seventy years. Interest has persisted due not only to the usefulness of phosphorylase… (more)

Subjects/Keywords: Allostery; Regulation; Glycogen Phosphorylase; AMP

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bigley, A. N. (2010). Investigations on the Mechanism of Allosteric Activtion of Rabbit Muscle Glycogen Phosphorylase b by AMP. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-483

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

Chicago Manual of Style (16th Edition):

Bigley, Andrew N. “Investigations on the Mechanism of Allosteric Activtion of Rabbit Muscle Glycogen Phosphorylase b by AMP.” 2010. Thesis, Texas A&M University. Accessed December 08, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-483.

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

MLA Handbook (7th Edition):

Bigley, Andrew N. “Investigations on the Mechanism of Allosteric Activtion of Rabbit Muscle Glycogen Phosphorylase b by AMP.” 2010. Web. 08 Dec 2019.

Vancouver:

Bigley AN. Investigations on the Mechanism of Allosteric Activtion of Rabbit Muscle Glycogen Phosphorylase b by AMP. [Internet] [Thesis]. Texas A&M University; 2010. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-483.

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

Council of Science Editors:

Bigley AN. Investigations on the Mechanism of Allosteric Activtion of Rabbit Muscle Glycogen Phosphorylase b by AMP. [Thesis]. Texas A&M University; 2010. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-483

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


Texas A&M University

7. Shubina-McGresham, Maria. Characterization of the Allosteric Properties of Thermus thermophilus Phosphofructokinase and the Sources of Strong Inhibitor Binding Affinity and Weak Inhibitory Response.

Degree: 2012, Texas A&M University

 Characterization of allosteric properties of phosphofructokinase from the extreme thermophile Thermus thermophilus (TtPFK) using thermodynamic linkage analysis revealed several peculiarities. Inhibition and activation of Fru-6-P… (more)

Subjects/Keywords: allostery; thermophile; Thermus thermophilus

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Shubina-McGresham, M. (2012). Characterization of the Allosteric Properties of Thermus thermophilus Phosphofructokinase and the Sources of Strong Inhibitor Binding Affinity and Weak Inhibitory Response. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11750

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

Chicago Manual of Style (16th Edition):

Shubina-McGresham, Maria. “Characterization of the Allosteric Properties of Thermus thermophilus Phosphofructokinase and the Sources of Strong Inhibitor Binding Affinity and Weak Inhibitory Response.” 2012. Thesis, Texas A&M University. Accessed December 08, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11750.

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

MLA Handbook (7th Edition):

Shubina-McGresham, Maria. “Characterization of the Allosteric Properties of Thermus thermophilus Phosphofructokinase and the Sources of Strong Inhibitor Binding Affinity and Weak Inhibitory Response.” 2012. Web. 08 Dec 2019.

Vancouver:

Shubina-McGresham M. Characterization of the Allosteric Properties of Thermus thermophilus Phosphofructokinase and the Sources of Strong Inhibitor Binding Affinity and Weak Inhibitory Response. [Internet] [Thesis]. Texas A&M University; 2012. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11750.

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

Council of Science Editors:

Shubina-McGresham M. Characterization of the Allosteric Properties of Thermus thermophilus Phosphofructokinase and the Sources of Strong Inhibitor Binding Affinity and Weak Inhibitory Response. [Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11750

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


Texas A&M University

8. Perez, Stephanie. Illuminating the Heterotropic Communication of the Pair-wise Interactions in Phosphofructokinase from Bacillus stearothermophilus.

Degree: 2012, Texas A&M University

 The number of allosteric sites and active sites in phosphofructokinase from Bacillus stearothermophilus create an intricate network of communication within the enzyme. With thermodynamic linkage… (more)

Subjects/Keywords: fluoresence; dynamics; phosphofructokinase; allostery

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Perez, S. (2012). Illuminating the Heterotropic Communication of the Pair-wise Interactions in Phosphofructokinase from Bacillus stearothermophilus. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/148105

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

Chicago Manual of Style (16th Edition):

Perez, Stephanie. “Illuminating the Heterotropic Communication of the Pair-wise Interactions in Phosphofructokinase from Bacillus stearothermophilus.” 2012. Thesis, Texas A&M University. Accessed December 08, 2019. http://hdl.handle.net/1969.1/148105.

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

MLA Handbook (7th Edition):

Perez, Stephanie. “Illuminating the Heterotropic Communication of the Pair-wise Interactions in Phosphofructokinase from Bacillus stearothermophilus.” 2012. Web. 08 Dec 2019.

Vancouver:

Perez S. Illuminating the Heterotropic Communication of the Pair-wise Interactions in Phosphofructokinase from Bacillus stearothermophilus. [Internet] [Thesis]. Texas A&M University; 2012. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1969.1/148105.

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

Council of Science Editors:

Perez S. Illuminating the Heterotropic Communication of the Pair-wise Interactions in Phosphofructokinase from Bacillus stearothermophilus. [Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/148105

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


University of Edinburgh

9. Wawrzynów, Bartosz. Allosteric regulation of MDM2 protein.

Degree: 2010, University of Edinburgh

 The diverse functions of the MDM2 oncoprotein in growth control and tumourigenesis are managed through coordinated regulation of its discrete domains induced by both extrinsic… (more)

Subjects/Keywords: 616.994; MDM2; P53; allostery

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wawrzynów, B. (2010). Allosteric regulation of MDM2 protein. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/4507

Chicago Manual of Style (16th Edition):

Wawrzynów, Bartosz. “Allosteric regulation of MDM2 protein.” 2010. Doctoral Dissertation, University of Edinburgh. Accessed December 08, 2019. http://hdl.handle.net/1842/4507.

MLA Handbook (7th Edition):

Wawrzynów, Bartosz. “Allosteric regulation of MDM2 protein.” 2010. Web. 08 Dec 2019.

Vancouver:

Wawrzynów B. Allosteric regulation of MDM2 protein. [Internet] [Doctoral dissertation]. University of Edinburgh; 2010. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1842/4507.

Council of Science Editors:

Wawrzynów B. Allosteric regulation of MDM2 protein. [Doctoral Dissertation]. University of Edinburgh; 2010. Available from: http://hdl.handle.net/1842/4507


Georgia Tech

10. Smith, McKenzie L. Systematic investigation of protein-metabolite regulatory interactions: methodologies and context.

Degree: PhD, Chemical and Biomolecular Engineering, 2016, Georgia Tech

 A systems-level understanding of metabolism will have far-reaching benefits from medicine to ecology to industry, as it will facilitate the comprehensive profiling and prediction of… (more)

Subjects/Keywords: Allostery; Metabolomics; Systems biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Smith, M. L. (2016). Systematic investigation of protein-metabolite regulatory interactions: methodologies and context. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/56353

Chicago Manual of Style (16th Edition):

Smith, McKenzie L. “Systematic investigation of protein-metabolite regulatory interactions: methodologies and context.” 2016. Doctoral Dissertation, Georgia Tech. Accessed December 08, 2019. http://hdl.handle.net/1853/56353.

MLA Handbook (7th Edition):

Smith, McKenzie L. “Systematic investigation of protein-metabolite regulatory interactions: methodologies and context.” 2016. Web. 08 Dec 2019.

Vancouver:

Smith ML. Systematic investigation of protein-metabolite regulatory interactions: methodologies and context. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1853/56353.

Council of Science Editors:

Smith ML. Systematic investigation of protein-metabolite regulatory interactions: methodologies and context. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/56353


University of Sydney

11. Collett, Michael. An allosteric network within dynamin .

Degree: 2016, University of Sydney

 Dynamins are large enzymes that catalyse the hydrolysis of GTP (GTPase activity). They assemble through oligomerisation into helical polymers during endocytosis to facilitate membrane scission… (more)

Subjects/Keywords: Dynamin; Allostery; Endocytosis; Enzyme; Kinetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Collett, M. (2016). An allosteric network within dynamin . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/15871

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

Chicago Manual of Style (16th Edition):

Collett, Michael. “An allosteric network within dynamin .” 2016. Thesis, University of Sydney. Accessed December 08, 2019. http://hdl.handle.net/2123/15871.

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

MLA Handbook (7th Edition):

Collett, Michael. “An allosteric network within dynamin .” 2016. Web. 08 Dec 2019.

Vancouver:

Collett M. An allosteric network within dynamin . [Internet] [Thesis]. University of Sydney; 2016. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/2123/15871.

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

Council of Science Editors:

Collett M. An allosteric network within dynamin . [Thesis]. University of Sydney; 2016. Available from: http://hdl.handle.net/2123/15871

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

12. Williams, Sandra Gisela. The U1A/U2B"/SNF Family of RNA Binding Proteins: Evolution of RNA Binding Specificity and Contributions of Heterotropic Linkage to snRNP Protein Partitioning.

Degree: PhD, Biology & Biomedical Sciences (Biochemistry), 2015, Washington University in St. Louis

  The U1A/U2B"/SNF is a family of RNA binding proteins that is a highly conserved throughout eukaryotes. These proteins are found in the U1 and/or… (more)

Subjects/Keywords: allostery, evolution, proteins, RNA; Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Williams, S. G. (2015). The U1A/U2B"/SNF Family of RNA Binding Proteins: Evolution of RNA Binding Specificity and Contributions of Heterotropic Linkage to snRNP Protein Partitioning. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/art_sci_etds/482

Chicago Manual of Style (16th Edition):

Williams, Sandra Gisela. “The U1A/U2B"/SNF Family of RNA Binding Proteins: Evolution of RNA Binding Specificity and Contributions of Heterotropic Linkage to snRNP Protein Partitioning.” 2015. Doctoral Dissertation, Washington University in St. Louis. Accessed December 08, 2019. https://openscholarship.wustl.edu/art_sci_etds/482.

MLA Handbook (7th Edition):

Williams, Sandra Gisela. “The U1A/U2B"/SNF Family of RNA Binding Proteins: Evolution of RNA Binding Specificity and Contributions of Heterotropic Linkage to snRNP Protein Partitioning.” 2015. Web. 08 Dec 2019.

Vancouver:

Williams SG. The U1A/U2B"/SNF Family of RNA Binding Proteins: Evolution of RNA Binding Specificity and Contributions of Heterotropic Linkage to snRNP Protein Partitioning. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2015. [cited 2019 Dec 08]. Available from: https://openscholarship.wustl.edu/art_sci_etds/482.

Council of Science Editors:

Williams SG. The U1A/U2B"/SNF Family of RNA Binding Proteins: Evolution of RNA Binding Specificity and Contributions of Heterotropic Linkage to snRNP Protein Partitioning. [Doctoral Dissertation]. Washington University in St. Louis; 2015. Available from: https://openscholarship.wustl.edu/art_sci_etds/482


Victoria University of Wellington

13. Bai, Yu. Structural and Functional Studies of 3-Deoxy-D-arabino- Heptulosonate 7-Phosphate Synthase from Prevotella nigrescens.

Degree: 2019, Victoria University of Wellington

 Multifunctional enzymes, bearing two or more catalytic activities, provide exceptional contributions to the efficient and coherent function of metabolic pathways. Two main benefits of multifunctional… (more)

Subjects/Keywords: Bifunctional enzyme; Allostery; Heterodomain interaction

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bai, Y. (2019). Structural and Functional Studies of 3-Deoxy-D-arabino- Heptulosonate 7-Phosphate Synthase from Prevotella nigrescens. (Doctoral Dissertation). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/8083

Chicago Manual of Style (16th Edition):

Bai, Yu. “Structural and Functional Studies of 3-Deoxy-D-arabino- Heptulosonate 7-Phosphate Synthase from Prevotella nigrescens.” 2019. Doctoral Dissertation, Victoria University of Wellington. Accessed December 08, 2019. http://hdl.handle.net/10063/8083.

MLA Handbook (7th Edition):

Bai, Yu. “Structural and Functional Studies of 3-Deoxy-D-arabino- Heptulosonate 7-Phosphate Synthase from Prevotella nigrescens.” 2019. Web. 08 Dec 2019.

Vancouver:

Bai Y. Structural and Functional Studies of 3-Deoxy-D-arabino- Heptulosonate 7-Phosphate Synthase from Prevotella nigrescens. [Internet] [Doctoral dissertation]. Victoria University of Wellington; 2019. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/10063/8083.

Council of Science Editors:

Bai Y. Structural and Functional Studies of 3-Deoxy-D-arabino- Heptulosonate 7-Phosphate Synthase from Prevotella nigrescens. [Doctoral Dissertation]. Victoria University of Wellington; 2019. Available from: http://hdl.handle.net/10063/8083


University of Edinburgh

14. Worrall, Erin G. Novel concepts in MDM2 protein regulation.

Degree: 2009, University of Edinburgh

 The tumour suppressor p53 has evolved a MDM2-dependent feedback loop that has a dual role as either a stimulator of p53 protein translation through mRNA… (more)

Subjects/Keywords: 616.994; cancer; p53; allostery; tumor suppressor; MDM2

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Worrall, E. G. (2009). Novel concepts in MDM2 protein regulation. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/3889

Chicago Manual of Style (16th Edition):

Worrall, Erin G. “Novel concepts in MDM2 protein regulation.” 2009. Doctoral Dissertation, University of Edinburgh. Accessed December 08, 2019. http://hdl.handle.net/1842/3889.

MLA Handbook (7th Edition):

Worrall, Erin G. “Novel concepts in MDM2 protein regulation.” 2009. Web. 08 Dec 2019.

Vancouver:

Worrall EG. Novel concepts in MDM2 protein regulation. [Internet] [Doctoral dissertation]. University of Edinburgh; 2009. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1842/3889.

Council of Science Editors:

Worrall EG. Novel concepts in MDM2 protein regulation. [Doctoral Dissertation]. University of Edinburgh; 2009. Available from: http://hdl.handle.net/1842/3889


University of Edinburgh

15. Naithani, Ankita. Molecular dynamics study of the allosteric control mechanisms of the glycolytic pathway.

Degree: PhD, 2015, University of Edinburgh

 There is a growing body of interest to understand the regulation of allosteric proteins. Allostery is a phenomenon of protein regulation whereby binding of an… (more)

Subjects/Keywords: 572; allostery; molecular dynamics simulations; pyruvate kinase

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Naithani, A. (2015). Molecular dynamics study of the allosteric control mechanisms of the glycolytic pathway. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/16201

Chicago Manual of Style (16th Edition):

Naithani, Ankita. “Molecular dynamics study of the allosteric control mechanisms of the glycolytic pathway.” 2015. Doctoral Dissertation, University of Edinburgh. Accessed December 08, 2019. http://hdl.handle.net/1842/16201.

MLA Handbook (7th Edition):

Naithani, Ankita. “Molecular dynamics study of the allosteric control mechanisms of the glycolytic pathway.” 2015. Web. 08 Dec 2019.

Vancouver:

Naithani A. Molecular dynamics study of the allosteric control mechanisms of the glycolytic pathway. [Internet] [Doctoral dissertation]. University of Edinburgh; 2015. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1842/16201.

Council of Science Editors:

Naithani A. Molecular dynamics study of the allosteric control mechanisms of the glycolytic pathway. [Doctoral Dissertation]. University of Edinburgh; 2015. Available from: http://hdl.handle.net/1842/16201


University of California – Berkeley

16. Bandaru, Pradeep. Evolutionary constraints on the sequence of Ras.

Degree: Molecular & Cell Biology, 2017, University of California – Berkeley

 AbstractEvolutionary constraints on the sequence of RasbyPradeep BandaruDoctor of Philosophy in Molecular and Cellular BiologyUniversity of California, BerkeleyProfessor John Kuriyan, ChairRas proteins are highly conserved… (more)

Subjects/Keywords: Biophysics; Biochemistry; Allostery; Biophysics; Evolution; Systems Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bandaru, P. (2017). Evolutionary constraints on the sequence of Ras. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/0sc6g33x

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

Chicago Manual of Style (16th Edition):

Bandaru, Pradeep. “Evolutionary constraints on the sequence of Ras.” 2017. Thesis, University of California – Berkeley. Accessed December 08, 2019. http://www.escholarship.org/uc/item/0sc6g33x.

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

MLA Handbook (7th Edition):

Bandaru, Pradeep. “Evolutionary constraints on the sequence of Ras.” 2017. Web. 08 Dec 2019.

Vancouver:

Bandaru P. Evolutionary constraints on the sequence of Ras. [Internet] [Thesis]. University of California – Berkeley; 2017. [cited 2019 Dec 08]. Available from: http://www.escholarship.org/uc/item/0sc6g33x.

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

Council of Science Editors:

Bandaru P. Evolutionary constraints on the sequence of Ras. [Thesis]. University of California – Berkeley; 2017. Available from: http://www.escholarship.org/uc/item/0sc6g33x

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


University of Edinburgh

17. Landré, Vivien. Regulation and effects of IRF-1 and p53 ubiquitination.

Degree: PhD, 2013, University of Edinburgh

 Protein ubiquitination is a key regulator of both protein stability and activity, and is involved in the regulation of a vast variety of cellular pathways.… (more)

Subjects/Keywords: 612; ubiquitination; transcription; E3 ligases; allostery

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Landré, V. (2013). Regulation and effects of IRF-1 and p53 ubiquitination. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/10639

Chicago Manual of Style (16th Edition):

Landré, Vivien. “Regulation and effects of IRF-1 and p53 ubiquitination.” 2013. Doctoral Dissertation, University of Edinburgh. Accessed December 08, 2019. http://hdl.handle.net/1842/10639.

MLA Handbook (7th Edition):

Landré, Vivien. “Regulation and effects of IRF-1 and p53 ubiquitination.” 2013. Web. 08 Dec 2019.

Vancouver:

Landré V. Regulation and effects of IRF-1 and p53 ubiquitination. [Internet] [Doctoral dissertation]. University of Edinburgh; 2013. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1842/10639.

Council of Science Editors:

Landré V. Regulation and effects of IRF-1 and p53 ubiquitination. [Doctoral Dissertation]. University of Edinburgh; 2013. Available from: http://hdl.handle.net/1842/10639


University of Edinburgh

18. Yuan, Meng. A study of regulatory mechanisms of glycolytic and gluconeogenic enzymes.

Degree: PhD, 2016, University of Edinburgh

 Many diseases correlate with abnormal glucose metabolism in cells and organisms. For instance, the human M2 isoform of the glycolytic enzyme pyruvate kinase (M2PYK) plays… (more)

Subjects/Keywords: pyruvate kinase; allostery; Fructose-1,6-bisphosphatase

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Yuan, M. (2016). A study of regulatory mechanisms of glycolytic and gluconeogenic enzymes. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/25725

Chicago Manual of Style (16th Edition):

Yuan, Meng. “A study of regulatory mechanisms of glycolytic and gluconeogenic enzymes.” 2016. Doctoral Dissertation, University of Edinburgh. Accessed December 08, 2019. http://hdl.handle.net/1842/25725.

MLA Handbook (7th Edition):

Yuan, Meng. “A study of regulatory mechanisms of glycolytic and gluconeogenic enzymes.” 2016. Web. 08 Dec 2019.

Vancouver:

Yuan M. A study of regulatory mechanisms of glycolytic and gluconeogenic enzymes. [Internet] [Doctoral dissertation]. University of Edinburgh; 2016. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1842/25725.

Council of Science Editors:

Yuan M. A study of regulatory mechanisms of glycolytic and gluconeogenic enzymes. [Doctoral Dissertation]. University of Edinburgh; 2016. Available from: http://hdl.handle.net/1842/25725


University of Minnesota

19. Li, Geoffrey. On the Role of Conformational Dynamics in Allostery and Cooperativity in Protein Kinase A.

Degree: PhD, Chemistry, 2017, University of Minnesota

 Protein kinases are a large class of enzymes that regulate a wide array of vital cellular processes. Their dysregulation has been associated with fatal diseases… (more)

Subjects/Keywords: allostery; conformational dynamics; cooperativity; NMR; protein kinase

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Li, G. (2017). On the Role of Conformational Dynamics in Allostery and Cooperativity in Protein Kinase A. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/195388

Chicago Manual of Style (16th Edition):

Li, Geoffrey. “On the Role of Conformational Dynamics in Allostery and Cooperativity in Protein Kinase A.” 2017. Doctoral Dissertation, University of Minnesota. Accessed December 08, 2019. http://hdl.handle.net/11299/195388.

MLA Handbook (7th Edition):

Li, Geoffrey. “On the Role of Conformational Dynamics in Allostery and Cooperativity in Protein Kinase A.” 2017. Web. 08 Dec 2019.

Vancouver:

Li G. On the Role of Conformational Dynamics in Allostery and Cooperativity in Protein Kinase A. [Internet] [Doctoral dissertation]. University of Minnesota; 2017. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/11299/195388.

Council of Science Editors:

Li G. On the Role of Conformational Dynamics in Allostery and Cooperativity in Protein Kinase A. [Doctoral Dissertation]. University of Minnesota; 2017. Available from: http://hdl.handle.net/11299/195388


Texas Tech University

20. Patkar, Presheet P. Sterol methyltransferase: Probing its drug-target and allosteric properties.

Degree: PhD, Chemistry, 2016, Texas Tech University

 The methylation of cycloartenol by plant 24-SMT (Glycine max) leads to formation of a single product – 24(28)-methylenecycloartenol. This is in stark contrast to the… (more)

Subjects/Keywords: Sterol methyltransferase; SMT; rational drug design; Allostery

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Patkar, P. P. (2016). Sterol methyltransferase: Probing its drug-target and allosteric properties. (Doctoral Dissertation). Texas Tech University. Retrieved from http://hdl.handle.net/2346/72384

Chicago Manual of Style (16th Edition):

Patkar, Presheet P. “Sterol methyltransferase: Probing its drug-target and allosteric properties.” 2016. Doctoral Dissertation, Texas Tech University. Accessed December 08, 2019. http://hdl.handle.net/2346/72384.

MLA Handbook (7th Edition):

Patkar, Presheet P. “Sterol methyltransferase: Probing its drug-target and allosteric properties.” 2016. Web. 08 Dec 2019.

Vancouver:

Patkar PP. Sterol methyltransferase: Probing its drug-target and allosteric properties. [Internet] [Doctoral dissertation]. Texas Tech University; 2016. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/2346/72384.

Council of Science Editors:

Patkar PP. Sterol methyltransferase: Probing its drug-target and allosteric properties. [Doctoral Dissertation]. Texas Tech University; 2016. Available from: http://hdl.handle.net/2346/72384


University of North Texas

21. Ingle, Brandall L. The Mechanisms of Human Glutathione Synthetase and Related Non-Enyzmatic Catalysis.

Degree: 2015, University of North Texas

 Human glutathione synthetase (hGS) is a homodimeric enzymes that catalyzes the second step in the biological synthesis of glutathione, a critical cellular antioxidant. The enzyme… (more)

Subjects/Keywords: allostery; glutathione; enzyme; catalysis; Glutathione.; Ligases.; Catalysis.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ingle, B. L. (2015). The Mechanisms of Human Glutathione Synthetase and Related Non-Enyzmatic Catalysis. (Thesis). University of North Texas. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc801927/

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

Chicago Manual of Style (16th Edition):

Ingle, Brandall L. “The Mechanisms of Human Glutathione Synthetase and Related Non-Enyzmatic Catalysis.” 2015. Thesis, University of North Texas. Accessed December 08, 2019. https://digital.library.unt.edu/ark:/67531/metadc801927/.

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

MLA Handbook (7th Edition):

Ingle, Brandall L. “The Mechanisms of Human Glutathione Synthetase and Related Non-Enyzmatic Catalysis.” 2015. Web. 08 Dec 2019.

Vancouver:

Ingle BL. The Mechanisms of Human Glutathione Synthetase and Related Non-Enyzmatic Catalysis. [Internet] [Thesis]. University of North Texas; 2015. [cited 2019 Dec 08]. Available from: https://digital.library.unt.edu/ark:/67531/metadc801927/.

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

Council of Science Editors:

Ingle BL. The Mechanisms of Human Glutathione Synthetase and Related Non-Enyzmatic Catalysis. [Thesis]. University of North Texas; 2015. Available from: https://digital.library.unt.edu/ark:/67531/metadc801927/

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


University of Michigan

22. Livingston, Kathryn Elsa. Allosteric Modulation of the Mu Opioid Receptor.

Degree: PhD, Pharmacology, 2016, University of Michigan

 The mu opioid receptor (MOPr), a G protein-coupled receptor (GPCR), is the pharmacological site of action of morphine and related opioid narcotic agonists that bind… (more)

Subjects/Keywords: GPCR; Opioid Pharmacology; Allostery; Efficacy; Science

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Livingston, K. E. (2016). Allosteric Modulation of the Mu Opioid Receptor. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/120895

Chicago Manual of Style (16th Edition):

Livingston, Kathryn Elsa. “Allosteric Modulation of the Mu Opioid Receptor.” 2016. Doctoral Dissertation, University of Michigan. Accessed December 08, 2019. http://hdl.handle.net/2027.42/120895.

MLA Handbook (7th Edition):

Livingston, Kathryn Elsa. “Allosteric Modulation of the Mu Opioid Receptor.” 2016. Web. 08 Dec 2019.

Vancouver:

Livingston KE. Allosteric Modulation of the Mu Opioid Receptor. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/2027.42/120895.

Council of Science Editors:

Livingston KE. Allosteric Modulation of the Mu Opioid Receptor. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/120895


University of Guelph

23. Carere, Jason. An Investigation of the Molecular Determinants of Substrate Channeling and Allosteric Activation in Aldolase-Dehydrogenase Complexes .

Degree: 2013, University of Guelph

 The aldolase-dehydrogenase complex catalyzes the last two steps in the microbial meta-cleavage pathway of various aromatic compounds including polychlorinated biphenyls (bph pathway) and cholesterol (hsa… (more)

Subjects/Keywords: Aldolase; Dehydrogenase; Channeling; Crystallography; Allostery; Cholesterol; PCBs

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Carere, J. (2013). An Investigation of the Molecular Determinants of Substrate Channeling and Allosteric Activation in Aldolase-Dehydrogenase Complexes . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/6623

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

Chicago Manual of Style (16th Edition):

Carere, Jason. “An Investigation of the Molecular Determinants of Substrate Channeling and Allosteric Activation in Aldolase-Dehydrogenase Complexes .” 2013. Thesis, University of Guelph. Accessed December 08, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/6623.

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

MLA Handbook (7th Edition):

Carere, Jason. “An Investigation of the Molecular Determinants of Substrate Channeling and Allosteric Activation in Aldolase-Dehydrogenase Complexes .” 2013. Web. 08 Dec 2019.

Vancouver:

Carere J. An Investigation of the Molecular Determinants of Substrate Channeling and Allosteric Activation in Aldolase-Dehydrogenase Complexes . [Internet] [Thesis]. University of Guelph; 2013. [cited 2019 Dec 08]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/6623.

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

Council of Science Editors:

Carere J. An Investigation of the Molecular Determinants of Substrate Channeling and Allosteric Activation in Aldolase-Dehydrogenase Complexes . [Thesis]. University of Guelph; 2013. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/6623

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


University of Canterbury

24. Cross, Penelope Jane. Unravelling the Evolution of Allosteric Regulation in 3-Deoxy-D-arabino-heptulosonate 7-phosphate Synthase.

Degree: Chemistry, 2012, University of Canterbury

 The enzyme 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase (DAH7PS) catalyses the first reaction in the shikimate pathway, leading to the biosynthesis of aromatic compounds including the aromatic amino… (more)

Subjects/Keywords: Shkimate pathway; allosteric regulation; DAH7PS; ACT domain; gene fusion; modular allostery; 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase; transferable allostery

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Cross, P. J. (2012). Unravelling the Evolution of Allosteric Regulation in 3-Deoxy-D-arabino-heptulosonate 7-phosphate Synthase. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/6823

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

Chicago Manual of Style (16th Edition):

Cross, Penelope Jane. “Unravelling the Evolution of Allosteric Regulation in 3-Deoxy-D-arabino-heptulosonate 7-phosphate Synthase.” 2012. Thesis, University of Canterbury. Accessed December 08, 2019. http://hdl.handle.net/10092/6823.

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

MLA Handbook (7th Edition):

Cross, Penelope Jane. “Unravelling the Evolution of Allosteric Regulation in 3-Deoxy-D-arabino-heptulosonate 7-phosphate Synthase.” 2012. Web. 08 Dec 2019.

Vancouver:

Cross PJ. Unravelling the Evolution of Allosteric Regulation in 3-Deoxy-D-arabino-heptulosonate 7-phosphate Synthase. [Internet] [Thesis]. University of Canterbury; 2012. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/10092/6823.

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

Council of Science Editors:

Cross PJ. Unravelling the Evolution of Allosteric Regulation in 3-Deoxy-D-arabino-heptulosonate 7-phosphate Synthase. [Thesis]. University of Canterbury; 2012. Available from: http://hdl.handle.net/10092/6823

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

25. Laird, Bobby Wayne. Distinguishing Allosteric Interactions Using Thermodynamic Analysis and the First Reported Crystal Structure of Phospho(Enol)Pyruvate Bound E. coli Phosphofructokinase.

Degree: 2015, Texas A&M University

 To better understand the relationship between allosteric ligand structure and the resulting allosteric behavior, we investigated the roles that functional groups and structure play in… (more)

Subjects/Keywords: phosphofructokinase; PFK; allostery

…to as A). The knowledge gained about cell surface receptor allostery and its diversity… …necessity of understanding allostery, this chapter will review the major classes of cell surface… …second assumption. The second important aspect is that the effect of allostery on binding… …slowly, close to slowly or close to quickly (33). Since the purpose of allostery is… 

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Laird, B. W. (2015). Distinguishing Allosteric Interactions Using Thermodynamic Analysis and the First Reported Crystal Structure of Phospho(Enol)Pyruvate Bound E. coli Phosphofructokinase. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/155274

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

Chicago Manual of Style (16th Edition):

Laird, Bobby Wayne. “Distinguishing Allosteric Interactions Using Thermodynamic Analysis and the First Reported Crystal Structure of Phospho(Enol)Pyruvate Bound E. coli Phosphofructokinase.” 2015. Thesis, Texas A&M University. Accessed December 08, 2019. http://hdl.handle.net/1969.1/155274.

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

MLA Handbook (7th Edition):

Laird, Bobby Wayne. “Distinguishing Allosteric Interactions Using Thermodynamic Analysis and the First Reported Crystal Structure of Phospho(Enol)Pyruvate Bound E. coli Phosphofructokinase.” 2015. Web. 08 Dec 2019.

Vancouver:

Laird BW. Distinguishing Allosteric Interactions Using Thermodynamic Analysis and the First Reported Crystal Structure of Phospho(Enol)Pyruvate Bound E. coli Phosphofructokinase. [Internet] [Thesis]. Texas A&M University; 2015. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1969.1/155274.

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

Council of Science Editors:

Laird BW. Distinguishing Allosteric Interactions Using Thermodynamic Analysis and the First Reported Crystal Structure of Phospho(Enol)Pyruvate Bound E. coli Phosphofructokinase. [Thesis]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/155274

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


University of Canterbury

26. Blackmore, Nicola Jean. The regulation of 3-deoxy-D-arabino-heptulosonate 7 phosphate synthase from Mycobacterium tuberculosis.

Degree: Chemistry, 2015, University of Canterbury

 Allosteric regulation of important enzymes is a mechanism frequently employed by organisms to exert control over their metabolism. The shikimate pathway is ultimately responsible for… (more)

Subjects/Keywords: DAH7PS; allostery; enzymes; regulation; chromate mutate; shikimate pathway

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Blackmore, N. J. (2015). The regulation of 3-deoxy-D-arabino-heptulosonate 7 phosphate synthase from Mycobacterium tuberculosis. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/10242

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

Chicago Manual of Style (16th Edition):

Blackmore, Nicola Jean. “The regulation of 3-deoxy-D-arabino-heptulosonate 7 phosphate synthase from Mycobacterium tuberculosis.” 2015. Thesis, University of Canterbury. Accessed December 08, 2019. http://hdl.handle.net/10092/10242.

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

MLA Handbook (7th Edition):

Blackmore, Nicola Jean. “The regulation of 3-deoxy-D-arabino-heptulosonate 7 phosphate synthase from Mycobacterium tuberculosis.” 2015. Web. 08 Dec 2019.

Vancouver:

Blackmore NJ. The regulation of 3-deoxy-D-arabino-heptulosonate 7 phosphate synthase from Mycobacterium tuberculosis. [Internet] [Thesis]. University of Canterbury; 2015. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/10092/10242.

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

Council of Science Editors:

Blackmore NJ. The regulation of 3-deoxy-D-arabino-heptulosonate 7 phosphate synthase from Mycobacterium tuberculosis. [Thesis]. University of Canterbury; 2015. Available from: http://hdl.handle.net/10092/10242

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


University of Canterbury

27. Livingstone, Emma Kathrine. Allosteric Regulation of the First Enzyme in Histidine Biosynthesis.

Degree: Chemistry, 2015, University of Canterbury

 The ATP-PRTase enzyme catalyses the first committed step of histidine biosynthesis in archaea, bacteria, fungi and plants.1 As the catalyst of an energetically expensive pathway,… (more)

Subjects/Keywords: Allostery; ATP-PRTase; HisG; HisZ; phosphoribosyltransferase; histidine biosynthesis; allosteric inhibition; enzyme

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Livingstone, E. K. (2015). Allosteric Regulation of the First Enzyme in Histidine Biosynthesis. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/10470

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

Chicago Manual of Style (16th Edition):

Livingstone, Emma Kathrine. “Allosteric Regulation of the First Enzyme in Histidine Biosynthesis.” 2015. Thesis, University of Canterbury. Accessed December 08, 2019. http://hdl.handle.net/10092/10470.

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

MLA Handbook (7th Edition):

Livingstone, Emma Kathrine. “Allosteric Regulation of the First Enzyme in Histidine Biosynthesis.” 2015. Web. 08 Dec 2019.

Vancouver:

Livingstone EK. Allosteric Regulation of the First Enzyme in Histidine Biosynthesis. [Internet] [Thesis]. University of Canterbury; 2015. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/10092/10470.

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

Council of Science Editors:

Livingstone EK. Allosteric Regulation of the First Enzyme in Histidine Biosynthesis. [Thesis]. University of Canterbury; 2015. Available from: http://hdl.handle.net/10092/10470

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


University of Canterbury

28. Davies, Andrew. Investigating the selectivity and mechanism of allosteric regulation in α-IPMS enzymes.

Degree: Department of Chemistry, 2015, University of Canterbury

 Enzymes are nature’s wizards: balanced delicately on the margin of order and entropy, they perform chemical reactions and syntheses at rates and yields human chemists… (more)

Subjects/Keywords: enzyme; allostery; biochemistry; biotechnology; regulation; biosynthesis; metabolism; metabolic pathway

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Davies, A. (2015). Investigating the selectivity and mechanism of allosteric regulation in α-IPMS enzymes. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/10849

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

Chicago Manual of Style (16th Edition):

Davies, Andrew. “Investigating the selectivity and mechanism of allosteric regulation in α-IPMS enzymes.” 2015. Thesis, University of Canterbury. Accessed December 08, 2019. http://hdl.handle.net/10092/10849.

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

MLA Handbook (7th Edition):

Davies, Andrew. “Investigating the selectivity and mechanism of allosteric regulation in α-IPMS enzymes.” 2015. Web. 08 Dec 2019.

Vancouver:

Davies A. Investigating the selectivity and mechanism of allosteric regulation in α-IPMS enzymes. [Internet] [Thesis]. University of Canterbury; 2015. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/10092/10849.

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

Council of Science Editors:

Davies A. Investigating the selectivity and mechanism of allosteric regulation in α-IPMS enzymes. [Thesis]. University of Canterbury; 2015. Available from: http://hdl.handle.net/10092/10849

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


University of California – Berkeley

29. Engel, Katherine Anne. Studies of the Allosteric Activation of the Epidermal Growth Factor Receptor.

Degree: Molecular & Cell Biology, 2013, University of California – Berkeley

 Ligand binding to the extracellular domain of the epidermal growth factor receptor (EGFR) results in receptor dimerization and allosteric activation of the kinase domain through… (more)

Subjects/Keywords: Biochemistry; Molecular biology; activation; allostery; dimerization; Epidermal Growth Factor Receptor; kinase

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Engel, K. A. (2013). Studies of the Allosteric Activation of the Epidermal Growth Factor Receptor. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/6g31k0nr

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

Chicago Manual of Style (16th Edition):

Engel, Katherine Anne. “Studies of the Allosteric Activation of the Epidermal Growth Factor Receptor.” 2013. Thesis, University of California – Berkeley. Accessed December 08, 2019. http://www.escholarship.org/uc/item/6g31k0nr.

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

MLA Handbook (7th Edition):

Engel, Katherine Anne. “Studies of the Allosteric Activation of the Epidermal Growth Factor Receptor.” 2013. Web. 08 Dec 2019.

Vancouver:

Engel KA. Studies of the Allosteric Activation of the Epidermal Growth Factor Receptor. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2019 Dec 08]. Available from: http://www.escholarship.org/uc/item/6g31k0nr.

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

Council of Science Editors:

Engel KA. Studies of the Allosteric Activation of the Epidermal Growth Factor Receptor. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/6g31k0nr

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


University of Saskatchewan

30. Conly, Cuylar. Determination of the Structural Allosteric Inhibitory Mechanism of Dihydrodipicolinate Synthase.

Degree: 2015, University of Saskatchewan

 Dihydrodipicolinate Synthase (EC 4.3.3.7; DHDPS), the product of the dapA gene, is an enzyme that catalyzes the condensation of pyruvate and S-aspartate-β-semialdehyde (ASA) into dihydrodipicolinate… (more)

Subjects/Keywords: protein crystallography; antibiotic drug design; DHDPS; dihydrodipicolinate synthase; Allostery; Campylobacter jejuni

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Conly, C. (2015). Determination of the Structural Allosteric Inhibitory Mechanism of Dihydrodipicolinate Synthase. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2015-11-2317

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

Chicago Manual of Style (16th Edition):

Conly, Cuylar. “Determination of the Structural Allosteric Inhibitory Mechanism of Dihydrodipicolinate Synthase.” 2015. Thesis, University of Saskatchewan. Accessed December 08, 2019. http://hdl.handle.net/10388/ETD-2015-11-2317.

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

MLA Handbook (7th Edition):

Conly, Cuylar. “Determination of the Structural Allosteric Inhibitory Mechanism of Dihydrodipicolinate Synthase.” 2015. Web. 08 Dec 2019.

Vancouver:

Conly C. Determination of the Structural Allosteric Inhibitory Mechanism of Dihydrodipicolinate Synthase. [Internet] [Thesis]. University of Saskatchewan; 2015. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/10388/ETD-2015-11-2317.

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

Council of Science Editors:

Conly C. Determination of the Structural Allosteric Inhibitory Mechanism of Dihydrodipicolinate Synthase. [Thesis]. University of Saskatchewan; 2015. Available from: http://hdl.handle.net/10388/ETD-2015-11-2317

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

[1] [2] [3] [4]

.