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You searched for subject:(allostery). Showing records 1 – 30 of 139 total matches.

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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

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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 March 04, 2021. 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. 04 Mar 2021.

Vancouver:

Xiao J. UNDERSTANDING GENERALIZED ALLOSTERY IN THROMBIN. [Internet] [Thesis]. Wake Forest University; 2018. [cited 2021 Mar 04]. 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: PhD, Biochemistry, 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

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APA (6th Edition):

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

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. Doctoral Dissertation, Texas A&M University. Accessed March 04, 2021. http://hdl.handle.net/1969.1/158914.

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. 04 Mar 2021.

Vancouver:

Whitaker AM. Exploration of Thermodynamic and Structural Changes Relevant to the Allosteric Inhibition in Phosphofructokinase from Bacillus Stearothermophilus. [Internet] [Doctoral dissertation]. Texas A&M University; 2015. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/1969.1/158914.

Council of Science Editors:

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


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

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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 March 04, 2021. 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. 04 Mar 2021.

Vancouver:

AKIMOTO M. ALLOSTERIC MECHANISMS FOR THE cAMP-DEPENDENT CONTROL OF FUNCTIONAL INTER-DOMAIN LINKERS. [Internet] [Doctoral dissertation]. McMaster University; 2015. [cited 2021 Mar 04]. 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


Delft University of Technology

4. Saraswat, Yug (author). Colloidal Allostery: Exploring the pathway to innovative separation technologies.

Degree: 2018, Delft University of Technology

Colloidal allostery is a regulatory mechanism where specific metabolites regulate the protein activity by binding to them and changing their energy landscape. The first steps… (more)

Subjects/Keywords: Allostery; Microfluidicsl; Hydrogel

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APA (6th Edition):

Saraswat, Y. (. (2018). Colloidal Allostery: Exploring the pathway to innovative separation technologies. (Masters Thesis). Delft University of Technology. Retrieved from http://resolver.tudelft.nl/uuid:439fc285-ac90-4d38-a7b7-280756cf3ad9

Chicago Manual of Style (16th Edition):

Saraswat, Yug (author). “Colloidal Allostery: Exploring the pathway to innovative separation technologies.” 2018. Masters Thesis, Delft University of Technology. Accessed March 04, 2021. http://resolver.tudelft.nl/uuid:439fc285-ac90-4d38-a7b7-280756cf3ad9.

MLA Handbook (7th Edition):

Saraswat, Yug (author). “Colloidal Allostery: Exploring the pathway to innovative separation technologies.” 2018. Web. 04 Mar 2021.

Vancouver:

Saraswat Y(. Colloidal Allostery: Exploring the pathway to innovative separation technologies. [Internet] [Masters thesis]. Delft University of Technology; 2018. [cited 2021 Mar 04]. Available from: http://resolver.tudelft.nl/uuid:439fc285-ac90-4d38-a7b7-280756cf3ad9.

Council of Science Editors:

Saraswat Y(. Colloidal Allostery: Exploring the pathway to innovative separation technologies. [Masters Thesis]. Delft University of Technology; 2018. Available from: http://resolver.tudelft.nl/uuid:439fc285-ac90-4d38-a7b7-280756cf3ad9


University of Notre Dame

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

Degree: 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

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APA (6th Edition):

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

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):

Mahoney, Brendan J.. “Understanding Response Mechanisms of Post-Translational Phosphorylation in Signaling Proteins</h1>.” 2018. Thesis, University of Notre Dame. Accessed March 04, 2021. https://curate.nd.edu/show/v118rb7241t.

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

MLA Handbook (7th Edition):

Mahoney, Brendan J.. “Understanding Response Mechanisms of Post-Translational Phosphorylation in Signaling Proteins</h1>.” 2018. Web. 04 Mar 2021.

Vancouver:

Mahoney BJ. Understanding Response Mechanisms of Post-Translational Phosphorylation in Signaling Proteins</h1>. [Internet] [Thesis]. University of Notre Dame; 2018. [cited 2021 Mar 04]. Available from: https://curate.nd.edu/show/v118rb7241t.

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

Council of Science Editors:

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

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


Texas A&M University

6. 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

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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 March 04, 2021. 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. 04 Mar 2021.

Vancouver:

Tindall AJ. Expression, Purification, and Kinetic Characterization of Human Liver Phosphofructokinase. [Internet] [Masters thesis]. Texas A&M University; 2016. [cited 2021 Mar 04]. 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

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: PhD, Biochemistry, 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

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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. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11750

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. Doctoral Dissertation, Texas A&M University. Accessed March 04, 2021. http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11750.

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. 04 Mar 2021.

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] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11750.

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. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11750


Texas A&M University

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

Degree: PhD, Biochemistry, 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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Perez, Stephanie. “Illuminating the Heterotropic Communication of the Pair-wise Interactions in Phosphofructokinase from Bacillus stearothermophilus.” 2012. Doctoral Dissertation, Texas A&M University. Accessed March 04, 2021. http://hdl.handle.net/1969.1/148105.

MLA Handbook (7th Edition):

Perez, Stephanie. “Illuminating the Heterotropic Communication of the Pair-wise Interactions in Phosphofructokinase from Bacillus stearothermophilus.” 2012. Web. 04 Mar 2021.

Vancouver:

Perez S. Illuminating the Heterotropic Communication of the Pair-wise Interactions in Phosphofructokinase from Bacillus stearothermophilus. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/1969.1/148105.

Council of Science Editors:

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

9. 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

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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 March 04, 2021. 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. 04 Mar 2021.

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 2021 Mar 04]. 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

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

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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 March 04, 2021. 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. 04 Mar 2021.

Vancouver:

Smith ML. Systematic investigation of protein-metabolite regulatory interactions: methodologies and context. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2021 Mar 04]. 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

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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 March 04, 2021. 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. 04 Mar 2021.

Vancouver:

Collett M. An allosteric network within dynamin . [Internet] [Thesis]. University of Sydney; 2016. [cited 2021 Mar 04]. 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


University of California – Berkeley

12. 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

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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 March 04, 2021. 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. 04 Mar 2021.

Vancouver:

Bandaru P. Evolutionary constraints on the sequence of Ras. [Internet] [Thesis]. University of California – Berkeley; 2017. [cited 2021 Mar 04]. 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 Michigan

13. 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

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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 March 04, 2021. http://hdl.handle.net/2027.42/120895.

MLA Handbook (7th Edition):

Livingston, Kathryn Elsa. “Allosteric Modulation of the Mu Opioid Receptor.” 2016. Web. 04 Mar 2021.

Vancouver:

Livingston KE. Allosteric Modulation of the Mu Opioid Receptor. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2021 Mar 04]. 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 North Texas

14. 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.

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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 March 04, 2021. 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. 04 Mar 2021.

Vancouver:

Ingle BL. The Mechanisms of Human Glutathione Synthetase and Related Non-Enyzmatic Catalysis. [Internet] [Thesis]. University of North Texas; 2015. [cited 2021 Mar 04]. 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


Texas Tech University

15. 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

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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 March 04, 2021. http://hdl.handle.net/2346/72384.

MLA Handbook (7th Edition):

Patkar, Presheet P. “Sterol methyltransferase: Probing its drug-target and allosteric properties.” 2016. Web. 04 Mar 2021.

Vancouver:

Patkar PP. Sterol methyltransferase: Probing its drug-target and allosteric properties. [Internet] [Doctoral dissertation]. Texas Tech University; 2016. [cited 2021 Mar 04]. 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 Guelph

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

Degree: PhD, Department of Molecular and Cellular Biology, 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

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APA (6th Edition):

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

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. Doctoral Dissertation, University of Guelph. Accessed March 04, 2021. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/6623.

MLA Handbook (7th Edition):

Carere, Jason. “An Investigation of the Molecular Determinants of Substrate Channeling and Allosteric Activation in Aldolase-Dehydrogenase Complexes.” 2013. Web. 04 Mar 2021.

Vancouver:

Carere J. An Investigation of the Molecular Determinants of Substrate Channeling and Allosteric Activation in Aldolase-Dehydrogenase Complexes. [Internet] [Doctoral dissertation]. University of Guelph; 2013. [cited 2021 Mar 04]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/6623.

Council of Science Editors:

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


University of Waikato

17. Hamill, Carlin James. Understanding allosteric enzyme regulation using macromolecular rate theory .

Degree: 2020, University of Waikato

 Enzyme catalysed reaction rates produce a curved temperature dependence with a temperature optimum, Topt. Traditionally enzyme temperature dependence has been modelled by the Arrhenius and… (more)

Subjects/Keywords: Enzyme; Enzymes; MMRT; Allostery; Allosteric regulation

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APA (6th Edition):

Hamill, C. J. (2020). Understanding allosteric enzyme regulation using macromolecular rate theory . (Masters Thesis). University of Waikato. Retrieved from http://hdl.handle.net/10289/13541

Chicago Manual of Style (16th Edition):

Hamill, Carlin James. “Understanding allosteric enzyme regulation using macromolecular rate theory .” 2020. Masters Thesis, University of Waikato. Accessed March 04, 2021. http://hdl.handle.net/10289/13541.

MLA Handbook (7th Edition):

Hamill, Carlin James. “Understanding allosteric enzyme regulation using macromolecular rate theory .” 2020. Web. 04 Mar 2021.

Vancouver:

Hamill CJ. Understanding allosteric enzyme regulation using macromolecular rate theory . [Internet] [Masters thesis]. University of Waikato; 2020. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/10289/13541.

Council of Science Editors:

Hamill CJ. Understanding allosteric enzyme regulation using macromolecular rate theory . [Masters Thesis]. University of Waikato; 2020. Available from: http://hdl.handle.net/10289/13541


University of Minnesota

18. 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

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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 March 04, 2021. 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. 04 Mar 2021.

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 2021 Mar 04]. 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


University of Edinburgh

19. 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: 572; pyruvate kinase; allostery; Fructose-1,6-bisphosphatase

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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 March 04, 2021. http://hdl.handle.net/1842/25725.

MLA Handbook (7th Edition):

Yuan, Meng. “A study of regulatory mechanisms of glycolytic and gluconeogenic enzymes.” 2016. Web. 04 Mar 2021.

Vancouver:

Yuan M. A study of regulatory mechanisms of glycolytic and gluconeogenic enzymes. [Internet] [Doctoral dissertation]. University of Edinburgh; 2016. [cited 2021 Mar 04]. 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 Edinburgh

20. 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

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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 March 04, 2021. 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. 04 Mar 2021.

Vancouver:

Naithani A. Molecular dynamics study of the allosteric control mechanisms of the glycolytic pathway. [Internet] [Doctoral dissertation]. University of Edinburgh; 2015. [cited 2021 Mar 04]. 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 Edinburgh

21. 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

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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 March 04, 2021. http://hdl.handle.net/1842/10639.

MLA Handbook (7th Edition):

Landré, Vivien. “Regulation and effects of IRF-1 and p53 ubiquitination.” 2013. Web. 04 Mar 2021.

Vancouver:

Landré V. Regulation and effects of IRF-1 and p53 ubiquitination. [Internet] [Doctoral dissertation]. University of Edinburgh; 2013. [cited 2021 Mar 04]. 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 Georgia

22. Maheshwari, Surabhi. Identification of conserved structural motifs associated with phosphorylation sites in kinases.

Degree: 2014, University of Georgia

 Background: Protein phosphorylation plays a crucial role in the regulation of several cellular processes. Protein kinases are enzymes that catalyze the event of phosphorylation and… (more)

Subjects/Keywords: phosphorylation; protein kinase; RD-pocket; regulation; allostery

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APA (6th Edition):

Maheshwari, S. (2014). Identification of conserved structural motifs associated with phosphorylation sites in kinases. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/28340

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):

Maheshwari, Surabhi. “Identification of conserved structural motifs associated with phosphorylation sites in kinases.” 2014. Thesis, University of Georgia. Accessed March 04, 2021. http://hdl.handle.net/10724/28340.

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

MLA Handbook (7th Edition):

Maheshwari, Surabhi. “Identification of conserved structural motifs associated with phosphorylation sites in kinases.” 2014. Web. 04 Mar 2021.

Vancouver:

Maheshwari S. Identification of conserved structural motifs associated with phosphorylation sites in kinases. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/10724/28340.

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

Council of Science Editors:

Maheshwari S. Identification of conserved structural motifs associated with phosphorylation sites in kinases. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/28340

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


San Jose State University

23. Cabreros, Christiane. Using Kinetics and Small Angle X-ray Scattering to Elucidate the Allosteric Regulation of SIRT1.

Degree: MS, Chemistry, 2020, San Jose State University

  SIRT1 is an NAD+ dependent deacetylase that has been implicated in many important cellular functions such as neurodegeneration and aging. SIRT1 has also been… (more)

Subjects/Keywords: Allostery; Kinetics; Resveratrol; SAXS; SIRT1; Sirtuin

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APA (6th Edition):

Cabreros, C. (2020). Using Kinetics and Small Angle X-ray Scattering to Elucidate the Allosteric Regulation of SIRT1. (Masters Thesis). San Jose State University. Retrieved from https://doi.org/10.31979/etd.64rk-ad2j ; https://scholarworks.sjsu.edu/etd_theses/5120

Chicago Manual of Style (16th Edition):

Cabreros, Christiane. “Using Kinetics and Small Angle X-ray Scattering to Elucidate the Allosteric Regulation of SIRT1.” 2020. Masters Thesis, San Jose State University. Accessed March 04, 2021. https://doi.org/10.31979/etd.64rk-ad2j ; https://scholarworks.sjsu.edu/etd_theses/5120.

MLA Handbook (7th Edition):

Cabreros, Christiane. “Using Kinetics and Small Angle X-ray Scattering to Elucidate the Allosteric Regulation of SIRT1.” 2020. Web. 04 Mar 2021.

Vancouver:

Cabreros C. Using Kinetics and Small Angle X-ray Scattering to Elucidate the Allosteric Regulation of SIRT1. [Internet] [Masters thesis]. San Jose State University; 2020. [cited 2021 Mar 04]. Available from: https://doi.org/10.31979/etd.64rk-ad2j ; https://scholarworks.sjsu.edu/etd_theses/5120.

Council of Science Editors:

Cabreros C. Using Kinetics and Small Angle X-ray Scattering to Elucidate the Allosteric Regulation of SIRT1. [Masters Thesis]. San Jose State University; 2020. Available from: https://doi.org/10.31979/etd.64rk-ad2j ; https://scholarworks.sjsu.edu/etd_theses/5120


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

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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 March 04, 2021. 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. 04 Mar 2021.

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 2021 Mar 04]. 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


University of Canterbury

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

Degree: PhD, Biochemistry, 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

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APA (6th Edition):

Cross, P. J. (2012). Unravelling the Evolution of Allosteric Regulation in 3-Deoxy-D-arabino-heptulosonate 7-phosphate Synthase. (Doctoral Dissertation). University of Canterbury. Retrieved from http://dx.doi.org/10.26021/9052

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. Doctoral Dissertation, University of Canterbury. Accessed March 04, 2021. http://dx.doi.org/10.26021/9052.

MLA Handbook (7th Edition):

Cross, Penelope Jane. “Unravelling the Evolution of Allosteric Regulation in 3-Deoxy-D-arabino-heptulosonate 7-phosphate Synthase.” 2012. Web. 04 Mar 2021.

Vancouver:

Cross PJ. Unravelling the Evolution of Allosteric Regulation in 3-Deoxy-D-arabino-heptulosonate 7-phosphate Synthase. [Internet] [Doctoral dissertation]. University of Canterbury; 2012. [cited 2021 Mar 04]. Available from: http://dx.doi.org/10.26021/9052.

Council of Science Editors:

Cross PJ. Unravelling the Evolution of Allosteric Regulation in 3-Deoxy-D-arabino-heptulosonate 7-phosphate Synthase. [Doctoral Dissertation]. University of Canterbury; 2012. Available from: http://dx.doi.org/10.26021/9052


University of California – Berkeley

26. 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

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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 March 04, 2021. 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. 04 Mar 2021.

Vancouver:

Engel KA. Studies of the Allosteric Activation of the Epidermal Growth Factor Receptor. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2021 Mar 04]. 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 Rochester

27. Leioatts, Nicholas. Allostery and Activation in the G Protein-Coupled Receptor, Rhodopsin.

Degree: PhD, 2014, University of Rochester

 G protein-coupled receptors (GPCRs) are a biomedically important class of membrane proteins that are targeted by many small molecule drugs. These proteins act as molecular… (more)

Subjects/Keywords: G Protein-Coupled Receptors; Rhodopsin; Allostery; Signal Transduction

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APA (6th Edition):

Leioatts, N. (2014). Allostery and Activation in the G Protein-Coupled Receptor, Rhodopsin. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/28968

Chicago Manual of Style (16th Edition):

Leioatts, Nicholas. “Allostery and Activation in the G Protein-Coupled Receptor, Rhodopsin.” 2014. Doctoral Dissertation, University of Rochester. Accessed March 04, 2021. http://hdl.handle.net/1802/28968.

MLA Handbook (7th Edition):

Leioatts, Nicholas. “Allostery and Activation in the G Protein-Coupled Receptor, Rhodopsin.” 2014. Web. 04 Mar 2021.

Vancouver:

Leioatts N. Allostery and Activation in the G Protein-Coupled Receptor, Rhodopsin. [Internet] [Doctoral dissertation]. University of Rochester; 2014. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/1802/28968.

Council of Science Editors:

Leioatts N. Allostery and Activation in the G Protein-Coupled Receptor, Rhodopsin. [Doctoral Dissertation]. University of Rochester; 2014. Available from: http://hdl.handle.net/1802/28968


Vanderbilt University

28. Thaker, Tarjani Mahesh. Investigations into Allosteric Mechanisms of G Protein Activation.

Degree: PhD, Biochemistry, 2013, Vanderbilt University

 The G protein coupled receptor (GPCR) family is comprised of ubiquitous, membrane-bound proteins that are highly conserved in structure, yet varied in their cognate ligand.… (more)

Subjects/Keywords: G proteins; GPCR; Allostery; Bicelles; Acetate Kinase; Kinase

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APA (6th Edition):

Thaker, T. M. (2013). Investigations into Allosteric Mechanisms of G Protein Activation. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14837

Chicago Manual of Style (16th Edition):

Thaker, Tarjani Mahesh. “Investigations into Allosteric Mechanisms of G Protein Activation.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed March 04, 2021. http://hdl.handle.net/1803/14837.

MLA Handbook (7th Edition):

Thaker, Tarjani Mahesh. “Investigations into Allosteric Mechanisms of G Protein Activation.” 2013. Web. 04 Mar 2021.

Vancouver:

Thaker TM. Investigations into Allosteric Mechanisms of G Protein Activation. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/1803/14837.

Council of Science Editors:

Thaker TM. Investigations into Allosteric Mechanisms of G Protein Activation. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://hdl.handle.net/1803/14837


University of Saskatchewan

29. 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

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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 March 04, 2021. 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. 04 Mar 2021.

Vancouver:

Conly C. Determination of the Structural Allosteric Inhibitory Mechanism of Dihydrodipicolinate Synthase. [Internet] [Thesis]. University of Saskatchewan; 2015. [cited 2021 Mar 04]. 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


McMaster University

30. Moleschi, Kody. Dissecting the Determinants of cAMP Affinity in Protein Kinase A.

Degree: MSc, 2015, McMaster University

cAMP receptors contain highly conserved cAMP binding pockets, in part responsible for allosteric activation, yet CBDs exhibit a wide array of cAMP binding affinities. While… (more)

Subjects/Keywords: Allostery; Binding; cAMP; Dynamics; HCN; NMR; PKA; Selectivity; Signalling; STD

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APA (6th Edition):

Moleschi, K. (2015). Dissecting the Determinants of cAMP Affinity in Protein Kinase A. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/18117

Chicago Manual of Style (16th Edition):

Moleschi, Kody. “Dissecting the Determinants of cAMP Affinity in Protein Kinase A.” 2015. Masters Thesis, McMaster University. Accessed March 04, 2021. http://hdl.handle.net/11375/18117.

MLA Handbook (7th Edition):

Moleschi, Kody. “Dissecting the Determinants of cAMP Affinity in Protein Kinase A.” 2015. Web. 04 Mar 2021.

Vancouver:

Moleschi K. Dissecting the Determinants of cAMP Affinity in Protein Kinase A. [Internet] [Masters thesis]. McMaster University; 2015. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/11375/18117.

Council of Science Editors:

Moleschi K. Dissecting the Determinants of cAMP Affinity in Protein Kinase A. [Masters Thesis]. McMaster University; 2015. Available from: http://hdl.handle.net/11375/18117

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