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You searched for subject:(Protein ligand). Showing records 1 – 30 of 261 total matches.

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University of Texas – Austin

1. Farley, Christopher Alexander. Design, synthesis, and thermodynamic evaluation of peptidomimetic ligands binding to the Src SH2 domain.

Degree: MA, Chemistry, 2018, University of Texas – Austin

 The ability to predict protein-ligand binding affinities is a difficult and elusive goal in the field of molecular recognition. Models exist to predict binding energetics;… (more)

Subjects/Keywords: Protein-ligand interactions; Protein-ligand binding; Ligand preorganization

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

APA (6th Edition):

Farley, C. A. (2018). Design, synthesis, and thermodynamic evaluation of peptidomimetic ligands binding to the Src SH2 domain. (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68037

Chicago Manual of Style (16th Edition):

Farley, Christopher Alexander. “Design, synthesis, and thermodynamic evaluation of peptidomimetic ligands binding to the Src SH2 domain.” 2018. Masters Thesis, University of Texas – Austin. Accessed December 09, 2019. http://hdl.handle.net/2152/68037.

MLA Handbook (7th Edition):

Farley, Christopher Alexander. “Design, synthesis, and thermodynamic evaluation of peptidomimetic ligands binding to the Src SH2 domain.” 2018. Web. 09 Dec 2019.

Vancouver:

Farley CA. Design, synthesis, and thermodynamic evaluation of peptidomimetic ligands binding to the Src SH2 domain. [Internet] [Masters thesis]. University of Texas – Austin; 2018. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/2152/68037.

Council of Science Editors:

Farley CA. Design, synthesis, and thermodynamic evaluation of peptidomimetic ligands binding to the Src SH2 domain. [Masters Thesis]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/68037


University of Hong Kong

2. Lo, Ka-ching. Case studies on protein-interaction of LSD1 SWIRM-ARDED and Afmp4p/Mp1p : pro-inflammatory mediators.

Degree: PhD, 2012, University of Hong Kong

Protein-ligand and protein-protein interactions play important roles in almost all cellular processes therefore it is a general belief that understanding protein-ligand/protein interaction is essential for… (more)

Subjects/Keywords: Protein binding; Ligand binding (Biochemistry)

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APA (6th Edition):

Lo, K. (2012). Case studies on protein-interaction of LSD1 SWIRM-ARDED and Afmp4p/Mp1p : pro-inflammatory mediators. (Doctoral Dissertation). University of Hong Kong. Retrieved from Lo, K. [羅嘉澄]. (2012). Case studies on protein-interaction of LSD1 SWIRM-ARDED and Afmp4p/Mp1p : pro-inflammatory mediators. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4961748 ; http://dx.doi.org/10.5353/th_b4961748 ; http://hdl.handle.net/10722/221525

Chicago Manual of Style (16th Edition):

Lo, Ka-ching. “Case studies on protein-interaction of LSD1 SWIRM-ARDED and Afmp4p/Mp1p : pro-inflammatory mediators.” 2012. Doctoral Dissertation, University of Hong Kong. Accessed December 09, 2019. Lo, K. [羅嘉澄]. (2012). Case studies on protein-interaction of LSD1 SWIRM-ARDED and Afmp4p/Mp1p : pro-inflammatory mediators. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4961748 ; http://dx.doi.org/10.5353/th_b4961748 ; http://hdl.handle.net/10722/221525.

MLA Handbook (7th Edition):

Lo, Ka-ching. “Case studies on protein-interaction of LSD1 SWIRM-ARDED and Afmp4p/Mp1p : pro-inflammatory mediators.” 2012. Web. 09 Dec 2019.

Vancouver:

Lo K. Case studies on protein-interaction of LSD1 SWIRM-ARDED and Afmp4p/Mp1p : pro-inflammatory mediators. [Internet] [Doctoral dissertation]. University of Hong Kong; 2012. [cited 2019 Dec 09]. Available from: Lo, K. [羅嘉澄]. (2012). Case studies on protein-interaction of LSD1 SWIRM-ARDED and Afmp4p/Mp1p : pro-inflammatory mediators. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4961748 ; http://dx.doi.org/10.5353/th_b4961748 ; http://hdl.handle.net/10722/221525.

Council of Science Editors:

Lo K. Case studies on protein-interaction of LSD1 SWIRM-ARDED and Afmp4p/Mp1p : pro-inflammatory mediators. [Doctoral Dissertation]. University of Hong Kong; 2012. Available from: Lo, K. [羅嘉澄]. (2012). Case studies on protein-interaction of LSD1 SWIRM-ARDED and Afmp4p/Mp1p : pro-inflammatory mediators. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4961748 ; http://dx.doi.org/10.5353/th_b4961748 ; http://hdl.handle.net/10722/221525


KTH

3. Ranganathan, Anirudh. ProteinLigand Binding: Estimation of Binding Free Energies.

Degree: Chemical Science and Engineering (CHE), 2012, KTH

  Accurate prediction of binding free energies of protein-ligand system has long been a focus area for theoretical and computational studies; with important implications in… (more)

Subjects/Keywords: Protein+ligand+binding+free+energy

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APA (6th Edition):

Ranganathan, A. (2012). Protein – Ligand Binding: Estimation of Binding Free Energies. (Thesis). KTH. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-147527

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):

Ranganathan, Anirudh. “Protein – Ligand Binding: Estimation of Binding Free Energies.” 2012. Thesis, KTH. Accessed December 09, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-147527.

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

MLA Handbook (7th Edition):

Ranganathan, Anirudh. “Protein – Ligand Binding: Estimation of Binding Free Energies.” 2012. Web. 09 Dec 2019.

Vancouver:

Ranganathan A. Protein – Ligand Binding: Estimation of Binding Free Energies. [Internet] [Thesis]. KTH; 2012. [cited 2019 Dec 09]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-147527.

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

Council of Science Editors:

Ranganathan A. Protein – Ligand Binding: Estimation of Binding Free Energies. [Thesis]. KTH; 2012. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-147527

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


University of Edinburgh

4. Hsin, Kun-Yi. Development and use of databases for ligand-protein interaction studies.

Degree: 2010, University of Edinburgh

 This project applies structure-activity relationship (SAR), structure-based and database mining approaches to study ligand-protein interactions. To support these studies, we have developed a relational database… (more)

Subjects/Keywords: 572.8; ligand-protein interaction; drug discovery; metalloprotein

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APA (6th Edition):

Hsin, K. (2010). Development and use of databases for ligand-protein interaction studies. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/3974

Chicago Manual of Style (16th Edition):

Hsin, Kun-Yi. “Development and use of databases for ligand-protein interaction studies.” 2010. Doctoral Dissertation, University of Edinburgh. Accessed December 09, 2019. http://hdl.handle.net/1842/3974.

MLA Handbook (7th Edition):

Hsin, Kun-Yi. “Development and use of databases for ligand-protein interaction studies.” 2010. Web. 09 Dec 2019.

Vancouver:

Hsin K. Development and use of databases for ligand-protein interaction studies. [Internet] [Doctoral dissertation]. University of Edinburgh; 2010. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/1842/3974.

Council of Science Editors:

Hsin K. Development and use of databases for ligand-protein interaction studies. [Doctoral Dissertation]. University of Edinburgh; 2010. Available from: http://hdl.handle.net/1842/3974


Mississippi State University

5. West, Savannah J. Thermodynamic Studies of the Binding of RPC2, ([Ru(Ph2phen)3]2+), to Purified Tubulin and Microtubules.

Degree: MS, Chemistry, 2019, Mississippi State University

 Tubulin and elastin-like polypeptides (ELPs) both form large protein structures which can be thermodynamically evaluated using isothermal titration calorimetry and differential scanning calorimetry. ELPs are… (more)

Subjects/Keywords: protein purification; ligand binding; tubulin; thermodynamics; calorimetry

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APA (6th Edition):

West, S. J. (2019). Thermodynamic Studies of the Binding of RPC2, ([Ru(Ph2phen)3]2+), to Purified Tubulin and Microtubules. (Masters Thesis). Mississippi State University. Retrieved from http://sun.library.msstate.edu/ETD-db/theses/available/etd-03222019-131702/ ;

Chicago Manual of Style (16th Edition):

West, Savannah J. “Thermodynamic Studies of the Binding of RPC2, ([Ru(Ph2phen)3]2+), to Purified Tubulin and Microtubules.” 2019. Masters Thesis, Mississippi State University. Accessed December 09, 2019. http://sun.library.msstate.edu/ETD-db/theses/available/etd-03222019-131702/ ;.

MLA Handbook (7th Edition):

West, Savannah J. “Thermodynamic Studies of the Binding of RPC2, ([Ru(Ph2phen)3]2+), to Purified Tubulin and Microtubules.” 2019. Web. 09 Dec 2019.

Vancouver:

West SJ. Thermodynamic Studies of the Binding of RPC2, ([Ru(Ph2phen)3]2+), to Purified Tubulin and Microtubules. [Internet] [Masters thesis]. Mississippi State University; 2019. [cited 2019 Dec 09]. Available from: http://sun.library.msstate.edu/ETD-db/theses/available/etd-03222019-131702/ ;.

Council of Science Editors:

West SJ. Thermodynamic Studies of the Binding of RPC2, ([Ru(Ph2phen)3]2+), to Purified Tubulin and Microtubules. [Masters Thesis]. Mississippi State University; 2019. Available from: http://sun.library.msstate.edu/ETD-db/theses/available/etd-03222019-131702/ ;


Vanderbilt University

6. Morin, Andrew. The computational design of protein-ligand interfaces.

Degree: PhD, Chemical and Physical Biology, 2011, Vanderbilt University

 ANDREW MORIN Dissertation under the direction of Professor Jens Meiler. Interaction between protein and ligand is a fundamental mechanism in biology. The goal of my… (more)

Subjects/Keywords: computational protein design; Rosetta; ligand interface

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APA (6th Edition):

Morin, A. (2011). The computational design of protein-ligand interfaces. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-05182011-125917/ ;

Chicago Manual of Style (16th Edition):

Morin, Andrew. “The computational design of protein-ligand interfaces.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed December 09, 2019. http://etd.library.vanderbilt.edu/available/etd-05182011-125917/ ;.

MLA Handbook (7th Edition):

Morin, Andrew. “The computational design of protein-ligand interfaces.” 2011. Web. 09 Dec 2019.

Vancouver:

Morin A. The computational design of protein-ligand interfaces. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2019 Dec 09]. Available from: http://etd.library.vanderbilt.edu/available/etd-05182011-125917/ ;.

Council of Science Editors:

Morin A. The computational design of protein-ligand interfaces. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://etd.library.vanderbilt.edu/available/etd-05182011-125917/ ;


University of Missouri – Columbia

7. Replogle, Amy. Molecular characterization of CLE peptide mimicry during cyst nematode pathogenesis.

Degree: 2011, University of Missouri – Columbia

 [ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT AUTHOR'S REQUEST.] Plant-parasitic cyst nematodes establish intimate parasitic relationships with their hosts by penetrating the root as… (more)

Subjects/Keywords: nematode; soybean; arabidopsis; ligand; effector protein

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APA (6th Edition):

Replogle, A. (2011). Molecular characterization of CLE peptide mimicry during cyst nematode pathogenesis. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/14306

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):

Replogle, Amy. “Molecular characterization of CLE peptide mimicry during cyst nematode pathogenesis.” 2011. Thesis, University of Missouri – Columbia. Accessed December 09, 2019. http://hdl.handle.net/10355/14306.

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

MLA Handbook (7th Edition):

Replogle, Amy. “Molecular characterization of CLE peptide mimicry during cyst nematode pathogenesis.” 2011. Web. 09 Dec 2019.

Vancouver:

Replogle A. Molecular characterization of CLE peptide mimicry during cyst nematode pathogenesis. [Internet] [Thesis]. University of Missouri – Columbia; 2011. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/10355/14306.

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

Council of Science Editors:

Replogle A. Molecular characterization of CLE peptide mimicry during cyst nematode pathogenesis. [Thesis]. University of Missouri – Columbia; 2011. Available from: http://hdl.handle.net/10355/14306

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


University of Missouri – Columbia

8. Replogle, Amy. Molecular characterization of CLE peptide mimicry during cyst nematode pathogenesis.

Degree: 2011, University of Missouri – Columbia

 [ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT AUTHOR'S REQUEST.] Plant-parasitic cyst nematodes establish intimate parasitic relationships with their hosts by penetrating the root as… (more)

Subjects/Keywords: nematode; soybean; arabidopsis; ligand; effector protein

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APA (6th Edition):

Replogle, A. (2011). Molecular characterization of CLE peptide mimicry during cyst nematode pathogenesis. (Thesis). University of Missouri – Columbia. Retrieved from https://doi.org/10.32469/10355/14306

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):

Replogle, Amy. “Molecular characterization of CLE peptide mimicry during cyst nematode pathogenesis.” 2011. Thesis, University of Missouri – Columbia. Accessed December 09, 2019. https://doi.org/10.32469/10355/14306.

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

MLA Handbook (7th Edition):

Replogle, Amy. “Molecular characterization of CLE peptide mimicry during cyst nematode pathogenesis.” 2011. Web. 09 Dec 2019.

Vancouver:

Replogle A. Molecular characterization of CLE peptide mimicry during cyst nematode pathogenesis. [Internet] [Thesis]. University of Missouri – Columbia; 2011. [cited 2019 Dec 09]. Available from: https://doi.org/10.32469/10355/14306.

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

Council of Science Editors:

Replogle A. Molecular characterization of CLE peptide mimicry during cyst nematode pathogenesis. [Thesis]. University of Missouri – Columbia; 2011. Available from: https://doi.org/10.32469/10355/14306

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


Rutgers University

9. Sheleg, Michal, 1983-. Regulation of mouse behavior by ephrin-a5.

Degree: PhD, Toxicology, 2015, Rutgers University

Social behaviors in mammals are regulated by core neural circuits that respond to stimuli from the environment. These circuits are formed by guidance molecules and… (more)

Subjects/Keywords: Receptor-ligand complexes; Protein-tyrosine kinase

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APA (6th Edition):

Sheleg, Michal, 1. (2015). Regulation of mouse behavior by ephrin-a5. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/46436/

Chicago Manual of Style (16th Edition):

Sheleg, Michal, 1983-. “Regulation of mouse behavior by ephrin-a5.” 2015. Doctoral Dissertation, Rutgers University. Accessed December 09, 2019. https://rucore.libraries.rutgers.edu/rutgers-lib/46436/.

MLA Handbook (7th Edition):

Sheleg, Michal, 1983-. “Regulation of mouse behavior by ephrin-a5.” 2015. Web. 09 Dec 2019.

Vancouver:

Sheleg, Michal 1. Regulation of mouse behavior by ephrin-a5. [Internet] [Doctoral dissertation]. Rutgers University; 2015. [cited 2019 Dec 09]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/46436/.

Council of Science Editors:

Sheleg, Michal 1. Regulation of mouse behavior by ephrin-a5. [Doctoral Dissertation]. Rutgers University; 2015. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/46436/


University of Michigan

10. Clark, Jordan. Structural Investigation of Binding Events in Proteins.

Degree: PhD, Medicinal Chemistry, 2018, University of Michigan

 Understanding the biophysical properties that describe protein binding events has allowed for the advancement of drug discovery through structure-based drug design and in silico methodology.… (more)

Subjects/Keywords: Protein flexibility; Protein structure database; Protein-ligand binding; Protein-protein interaction (PPI); Biological Chemistry; Science

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APA (6th Edition):

Clark, J. (2018). Structural Investigation of Binding Events in Proteins. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/145943

Chicago Manual of Style (16th Edition):

Clark, Jordan. “Structural Investigation of Binding Events in Proteins.” 2018. Doctoral Dissertation, University of Michigan. Accessed December 09, 2019. http://hdl.handle.net/2027.42/145943.

MLA Handbook (7th Edition):

Clark, Jordan. “Structural Investigation of Binding Events in Proteins.” 2018. Web. 09 Dec 2019.

Vancouver:

Clark J. Structural Investigation of Binding Events in Proteins. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/2027.42/145943.

Council of Science Editors:

Clark J. Structural Investigation of Binding Events in Proteins. [Doctoral Dissertation]. University of Michigan; 2018. Available from: http://hdl.handle.net/2027.42/145943


University of Alberta

11. Chen, Ke. In-silico characterization and prediction of protein-small ligand interactions.

Degree: PhD, Department of Electrical and Computer Engineering, 2011, University of Alberta

 Proteins, which participate in virtually every process within cells, implement many of their functions through interactions with various ligands. Although a substantial effort in characterization… (more)

Subjects/Keywords: interaction; ligand; protein function annotation; binding site; protein; prediction

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APA (6th Edition):

Chen, K. (2011). In-silico characterization and prediction of protein-small ligand interactions. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/cc08hg940

Chicago Manual of Style (16th Edition):

Chen, Ke. “In-silico characterization and prediction of protein-small ligand interactions.” 2011. Doctoral Dissertation, University of Alberta. Accessed December 09, 2019. https://era.library.ualberta.ca/files/cc08hg940.

MLA Handbook (7th Edition):

Chen, Ke. “In-silico characterization and prediction of protein-small ligand interactions.” 2011. Web. 09 Dec 2019.

Vancouver:

Chen K. In-silico characterization and prediction of protein-small ligand interactions. [Internet] [Doctoral dissertation]. University of Alberta; 2011. [cited 2019 Dec 09]. Available from: https://era.library.ualberta.ca/files/cc08hg940.

Council of Science Editors:

Chen K. In-silico characterization and prediction of protein-small ligand interactions. [Doctoral Dissertation]. University of Alberta; 2011. Available from: https://era.library.ualberta.ca/files/cc08hg940


Georgia State University

12. Zhuo, You. Modulating Calcium Signaling by Protein Design and Analysis of Calcium Binding Proteins.

Degree: PhD, Chemistry, 2013, Georgia State University

  Transient change of cytosolic calcium level leads to physiological actions, which are modulated by the intracellular calcium stores, and gated by membrane calcium channels/pumps.… (more)

Subjects/Keywords: Protein design; Calcium binding; Kinetics; Fluorescence; NMR spectroscopy; Ligand-protein interaction

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APA (6th Edition):

Zhuo, Y. (2013). Modulating Calcium Signaling by Protein Design and Analysis of Calcium Binding Proteins. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_diss/84

Chicago Manual of Style (16th Edition):

Zhuo, You. “Modulating Calcium Signaling by Protein Design and Analysis of Calcium Binding Proteins.” 2013. Doctoral Dissertation, Georgia State University. Accessed December 09, 2019. https://scholarworks.gsu.edu/chemistry_diss/84.

MLA Handbook (7th Edition):

Zhuo, You. “Modulating Calcium Signaling by Protein Design and Analysis of Calcium Binding Proteins.” 2013. Web. 09 Dec 2019.

Vancouver:

Zhuo Y. Modulating Calcium Signaling by Protein Design and Analysis of Calcium Binding Proteins. [Internet] [Doctoral dissertation]. Georgia State University; 2013. [cited 2019 Dec 09]. Available from: https://scholarworks.gsu.edu/chemistry_diss/84.

Council of Science Editors:

Zhuo Y. Modulating Calcium Signaling by Protein Design and Analysis of Calcium Binding Proteins. [Doctoral Dissertation]. Georgia State University; 2013. Available from: https://scholarworks.gsu.edu/chemistry_diss/84


Hong Kong University of Science and Technology

13. Gu, Shuo. Computational exploration of protein ligand interaction and its applications in drug discovery.

Degree: 2015, Hong Kong University of Science and Technology

 My PhD research can be summarized as two major directions. One direction is the theoretical investigation of protein conformational dynamics. In particular, we have developed… (more)

Subjects/Keywords: Protein-protein interactions; Computer simulation; Ligand binding (Biochemistry); Drugs; Design

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APA (6th Edition):

Gu, S. (2015). Computational exploration of protein ligand interaction and its applications in drug discovery. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1514980 ; http://repository.ust.hk/ir/bitstream/1783.1-80261/1/th_redirect.html

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):

Gu, Shuo. “Computational exploration of protein ligand interaction and its applications in drug discovery.” 2015. Thesis, Hong Kong University of Science and Technology. Accessed December 09, 2019. https://doi.org/10.14711/thesis-b1514980 ; http://repository.ust.hk/ir/bitstream/1783.1-80261/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Gu, Shuo. “Computational exploration of protein ligand interaction and its applications in drug discovery.” 2015. Web. 09 Dec 2019.

Vancouver:

Gu S. Computational exploration of protein ligand interaction and its applications in drug discovery. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2015. [cited 2019 Dec 09]. Available from: https://doi.org/10.14711/thesis-b1514980 ; http://repository.ust.hk/ir/bitstream/1783.1-80261/1/th_redirect.html.

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

Council of Science Editors:

Gu S. Computational exploration of protein ligand interaction and its applications in drug discovery. [Thesis]. Hong Kong University of Science and Technology; 2015. Available from: https://doi.org/10.14711/thesis-b1514980 ; http://repository.ust.hk/ir/bitstream/1783.1-80261/1/th_redirect.html

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


Vanderbilt University

14. DeLuca, Samuel Louis. Development of Novel Methods for Computational Protein Design and Protein-Ligand Docking.

Degree: PhD, Chemical and Physical Biology, 2015, Vanderbilt University

 The ability to make rapid predictions of macro-molecular structures will enable researchers to carry out effective protein design, virtual High Throughput Screening (vHTS) and rational… (more)

Subjects/Keywords: RosettaScripts; RosettaDesign; protein design; machine learning; Docking; Protein-Ligand Docking; Rosetta

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APA (6th Edition):

DeLuca, S. L. (2015). Development of Novel Methods for Computational Protein Design and Protein-Ligand Docking. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-07022015-151149/ ;

Chicago Manual of Style (16th Edition):

DeLuca, Samuel Louis. “Development of Novel Methods for Computational Protein Design and Protein-Ligand Docking.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed December 09, 2019. http://etd.library.vanderbilt.edu/available/etd-07022015-151149/ ;.

MLA Handbook (7th Edition):

DeLuca, Samuel Louis. “Development of Novel Methods for Computational Protein Design and Protein-Ligand Docking.” 2015. Web. 09 Dec 2019.

Vancouver:

DeLuca SL. Development of Novel Methods for Computational Protein Design and Protein-Ligand Docking. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2019 Dec 09]. Available from: http://etd.library.vanderbilt.edu/available/etd-07022015-151149/ ;.

Council of Science Editors:

DeLuca SL. Development of Novel Methods for Computational Protein Design and Protein-Ligand Docking. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://etd.library.vanderbilt.edu/available/etd-07022015-151149/ ;


Vanderbilt University

15. Bender, Brian Joseph. Knowledge-Based Modeling of G-Protein Coupled Receptors and their Binding Partners.

Degree: PhD, Pharmacology, 2019, Vanderbilt University

 G-protein coupled receptors (GPCRs) represent the largest family of membrane proteins and the most heavily targeted classes of proteins for therapeutic intervention. Relatively little is… (more)

Subjects/Keywords: protein modeling; rosetta; peptide docking; g-protein coupled receptors; ligand docking

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APA (6th Edition):

Bender, B. J. (2019). Knowledge-Based Modeling of G-Protein Coupled Receptors and their Binding Partners. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-01172019-103123/ ;

Chicago Manual of Style (16th Edition):

Bender, Brian Joseph. “Knowledge-Based Modeling of G-Protein Coupled Receptors and their Binding Partners.” 2019. Doctoral Dissertation, Vanderbilt University. Accessed December 09, 2019. http://etd.library.vanderbilt.edu/available/etd-01172019-103123/ ;.

MLA Handbook (7th Edition):

Bender, Brian Joseph. “Knowledge-Based Modeling of G-Protein Coupled Receptors and their Binding Partners.” 2019. Web. 09 Dec 2019.

Vancouver:

Bender BJ. Knowledge-Based Modeling of G-Protein Coupled Receptors and their Binding Partners. [Internet] [Doctoral dissertation]. Vanderbilt University; 2019. [cited 2019 Dec 09]. Available from: http://etd.library.vanderbilt.edu/available/etd-01172019-103123/ ;.

Council of Science Editors:

Bender BJ. Knowledge-Based Modeling of G-Protein Coupled Receptors and their Binding Partners. [Doctoral Dissertation]. Vanderbilt University; 2019. Available from: http://etd.library.vanderbilt.edu/available/etd-01172019-103123/ ;


University of Pennsylvania

16. Harpole, Kyle William. Protein Dynamics and Entropy: Implications for Protein-Ligand Binding.

Degree: 2015, University of Pennsylvania

 The nature of macromolecular interactions has been an area of deep interest for understanding many facets of biology. While a great deal of insight has… (more)

Subjects/Keywords: Drug Design; Entropy; Protein Dynamics; Protein-Ligand Binding; Biochemistry; Biophysics

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APA (6th Edition):

Harpole, K. W. (2015). Protein Dynamics and Entropy: Implications for Protein-Ligand Binding. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1756

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):

Harpole, Kyle William. “Protein Dynamics and Entropy: Implications for Protein-Ligand Binding.” 2015. Thesis, University of Pennsylvania. Accessed December 09, 2019. https://repository.upenn.edu/edissertations/1756.

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

MLA Handbook (7th Edition):

Harpole, Kyle William. “Protein Dynamics and Entropy: Implications for Protein-Ligand Binding.” 2015. Web. 09 Dec 2019.

Vancouver:

Harpole KW. Protein Dynamics and Entropy: Implications for Protein-Ligand Binding. [Internet] [Thesis]. University of Pennsylvania; 2015. [cited 2019 Dec 09]. Available from: https://repository.upenn.edu/edissertations/1756.

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

Council of Science Editors:

Harpole KW. Protein Dynamics and Entropy: Implications for Protein-Ligand Binding. [Thesis]. University of Pennsylvania; 2015. Available from: https://repository.upenn.edu/edissertations/1756

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


University of California – San Francisco

17. Cruz, Leslie Ann. Studies in Structure, Chemistry & Biology Of Receptor-Ligand Interactions for the AMPA & Androgen Receptors.

Degree: Chemistry and Chemical Biology, 2011, University of California – San Francisco

 Numerous small molecules serve to coordinate many biological activities within cells of multicelluar organisms. These ligand-receptor interactions are vital to the control of cellular processes… (more)

Subjects/Keywords: Chemistry; Biophysics; Biochemistry; chemical biology; protein engineering; protein-ligand interactions

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APA (6th Edition):

Cruz, L. A. (2011). Studies in Structure, Chemistry & Biology Of Receptor-Ligand Interactions for the AMPA & Androgen Receptors. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/267353tc

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):

Cruz, Leslie Ann. “Studies in Structure, Chemistry & Biology Of Receptor-Ligand Interactions for the AMPA & Androgen Receptors.” 2011. Thesis, University of California – San Francisco. Accessed December 09, 2019. http://www.escholarship.org/uc/item/267353tc.

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

MLA Handbook (7th Edition):

Cruz, Leslie Ann. “Studies in Structure, Chemistry & Biology Of Receptor-Ligand Interactions for the AMPA & Androgen Receptors.” 2011. Web. 09 Dec 2019.

Vancouver:

Cruz LA. Studies in Structure, Chemistry & Biology Of Receptor-Ligand Interactions for the AMPA & Androgen Receptors. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2019 Dec 09]. Available from: http://www.escholarship.org/uc/item/267353tc.

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

Council of Science Editors:

Cruz LA. Studies in Structure, Chemistry & Biology Of Receptor-Ligand Interactions for the AMPA & Androgen Receptors. [Thesis]. University of California – San Francisco; 2011. Available from: http://www.escholarship.org/uc/item/267353tc

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


Hong Kong University of Science and Technology

18. Chan, King Hang LIFS. The molecular basis of ligand selectivity and functional specificity of melatonin receptor subtypes.

Degree: 2015, Hong Kong University of Science and Technology

 MT1 and MT2 melatonin receptors are expressed throughout the body and regulate an immense diversity of physiological processes. While the melatonin receptor subtypes may work… (more)

Subjects/Keywords: Melatonin; Receptors; Ligand binding (Biochemistry); Protein-protein interactions

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APA (6th Edition):

Chan, K. H. L. (2015). The molecular basis of ligand selectivity and functional specificity of melatonin receptor subtypes. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1585311 ; http://repository.ust.hk/ir/bitstream/1783.1-97093/1/th_redirect.html

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):

Chan, King Hang LIFS. “The molecular basis of ligand selectivity and functional specificity of melatonin receptor subtypes.” 2015. Thesis, Hong Kong University of Science and Technology. Accessed December 09, 2019. https://doi.org/10.14711/thesis-b1585311 ; http://repository.ust.hk/ir/bitstream/1783.1-97093/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Chan, King Hang LIFS. “The molecular basis of ligand selectivity and functional specificity of melatonin receptor subtypes.” 2015. Web. 09 Dec 2019.

Vancouver:

Chan KHL. The molecular basis of ligand selectivity and functional specificity of melatonin receptor subtypes. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2015. [cited 2019 Dec 09]. Available from: https://doi.org/10.14711/thesis-b1585311 ; http://repository.ust.hk/ir/bitstream/1783.1-97093/1/th_redirect.html.

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

Council of Science Editors:

Chan KHL. The molecular basis of ligand selectivity and functional specificity of melatonin receptor subtypes. [Thesis]. Hong Kong University of Science and Technology; 2015. Available from: https://doi.org/10.14711/thesis-b1585311 ; http://repository.ust.hk/ir/bitstream/1783.1-97093/1/th_redirect.html

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


University of Oxford

19. Holmes, Peter. Structure and mode of action of the TolA-TolB complex from Pseudomonas aeruginosa.

Degree: PhD, 2016, University of Oxford

Protein-protein interactions (PPIs) across the cell envelope of Gram-negative bacteria are critical for mediating signal transduction pathways that underpin cellular homeostasis. The Ton and Tol… (more)

Subjects/Keywords: 572; Ligand binding; NMR; Protein-Protein Interaction; Tol-Pal; TolA; TolB

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APA (6th Edition):

Holmes, P. (2016). Structure and mode of action of the TolA-TolB complex from Pseudomonas aeruginosa. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:cccb0c88-5c89-4d21-81eb-70ebf513c7ab ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.730263

Chicago Manual of Style (16th Edition):

Holmes, Peter. “Structure and mode of action of the TolA-TolB complex from Pseudomonas aeruginosa.” 2016. Doctoral Dissertation, University of Oxford. Accessed December 09, 2019. http://ora.ox.ac.uk/objects/uuid:cccb0c88-5c89-4d21-81eb-70ebf513c7ab ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.730263.

MLA Handbook (7th Edition):

Holmes, Peter. “Structure and mode of action of the TolA-TolB complex from Pseudomonas aeruginosa.” 2016. Web. 09 Dec 2019.

Vancouver:

Holmes P. Structure and mode of action of the TolA-TolB complex from Pseudomonas aeruginosa. [Internet] [Doctoral dissertation]. University of Oxford; 2016. [cited 2019 Dec 09]. Available from: http://ora.ox.ac.uk/objects/uuid:cccb0c88-5c89-4d21-81eb-70ebf513c7ab ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.730263.

Council of Science Editors:

Holmes P. Structure and mode of action of the TolA-TolB complex from Pseudomonas aeruginosa. [Doctoral Dissertation]. University of Oxford; 2016. Available from: http://ora.ox.ac.uk/objects/uuid:cccb0c88-5c89-4d21-81eb-70ebf513c7ab ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.730263

20. Jaquillard, Lucie. Spectrométrie de masse supramoléculaire : caractérisation de l'intéraction non-covalente entre PEBP1/RKIP humaine et des analogues de nucléotides : Supramolecular mass spectrometry : characterization of the noncovalent interaction between human PEBP1/RKIP and nucleotide analogs.

Degree: Docteur es, Chimie analytique, 2012, Université d'Orléans

L'étude des interactions non-covalentes et des relations structure-fonction est à la base de la compréhension des systèmes biologiques. La MS supramoléculaire est une technique de… (more)

Subjects/Keywords: Interaction protéine-ligand; Molécules anti-métastases; HPEBP1; RKIP; Protein-ligand interaction; Antimetastatic molecules; Phosphatidylethanolamine Binding Protein; Raf kinase Inhibitory protein

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APA (6th Edition):

Jaquillard, L. (2012). Spectrométrie de masse supramoléculaire : caractérisation de l'intéraction non-covalente entre PEBP1/RKIP humaine et des analogues de nucléotides : Supramolecular mass spectrometry : characterization of the noncovalent interaction between human PEBP1/RKIP and nucleotide analogs. (Doctoral Dissertation). Université d'Orléans. Retrieved from http://www.theses.fr/2012ORLE2020

Chicago Manual of Style (16th Edition):

Jaquillard, Lucie. “Spectrométrie de masse supramoléculaire : caractérisation de l'intéraction non-covalente entre PEBP1/RKIP humaine et des analogues de nucléotides : Supramolecular mass spectrometry : characterization of the noncovalent interaction between human PEBP1/RKIP and nucleotide analogs.” 2012. Doctoral Dissertation, Université d'Orléans. Accessed December 09, 2019. http://www.theses.fr/2012ORLE2020.

MLA Handbook (7th Edition):

Jaquillard, Lucie. “Spectrométrie de masse supramoléculaire : caractérisation de l'intéraction non-covalente entre PEBP1/RKIP humaine et des analogues de nucléotides : Supramolecular mass spectrometry : characterization of the noncovalent interaction between human PEBP1/RKIP and nucleotide analogs.” 2012. Web. 09 Dec 2019.

Vancouver:

Jaquillard L. Spectrométrie de masse supramoléculaire : caractérisation de l'intéraction non-covalente entre PEBP1/RKIP humaine et des analogues de nucléotides : Supramolecular mass spectrometry : characterization of the noncovalent interaction between human PEBP1/RKIP and nucleotide analogs. [Internet] [Doctoral dissertation]. Université d'Orléans; 2012. [cited 2019 Dec 09]. Available from: http://www.theses.fr/2012ORLE2020.

Council of Science Editors:

Jaquillard L. Spectrométrie de masse supramoléculaire : caractérisation de l'intéraction non-covalente entre PEBP1/RKIP humaine et des analogues de nucléotides : Supramolecular mass spectrometry : characterization of the noncovalent interaction between human PEBP1/RKIP and nucleotide analogs. [Doctoral Dissertation]. Université d'Orléans; 2012. Available from: http://www.theses.fr/2012ORLE2020


Vanderbilt University

21. Allison, Brittany Ann. Computational Design of Protein-Ligand Interfaces Using RosettaLigand.

Degree: PhD, Chemistry, 2016, Vanderbilt University

 Computational design of protein-ligand interfaces expands understanding of the basic forces involved in molecular recognition, and also contributes to the development of protein therapeutics. My… (more)

Subjects/Keywords: protein engineering; protein ligand binding; RosettaLigand; Rosetta; protein small molecule interactions; interface design; computational design; ligand macromolecule recognition; NMR; binding affinity

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APA (6th Edition):

Allison, B. A. (2016). Computational Design of Protein-Ligand Interfaces Using RosettaLigand. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-03282016-022145/ ;

Chicago Manual of Style (16th Edition):

Allison, Brittany Ann. “Computational Design of Protein-Ligand Interfaces Using RosettaLigand.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed December 09, 2019. http://etd.library.vanderbilt.edu/available/etd-03282016-022145/ ;.

MLA Handbook (7th Edition):

Allison, Brittany Ann. “Computational Design of Protein-Ligand Interfaces Using RosettaLigand.” 2016. Web. 09 Dec 2019.

Vancouver:

Allison BA. Computational Design of Protein-Ligand Interfaces Using RosettaLigand. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2019 Dec 09]. Available from: http://etd.library.vanderbilt.edu/available/etd-03282016-022145/ ;.

Council of Science Editors:

Allison BA. Computational Design of Protein-Ligand Interfaces Using RosettaLigand. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://etd.library.vanderbilt.edu/available/etd-03282016-022145/ ;


Ryerson University

22. Judge, Gurjeet Singh. Clathrin and TOM1L1 regulate epidermal growth factor receptor signaling at the plasma membrane.

Degree: 2015, Ryerson University

 Epidermal growth factor (EGF) receptor (EGFR) controls many aspects of cell physiology via the activation of intracellular signaling pathways. Aberrant EGFR signaling and overexpression of… (more)

Subjects/Keywords: Epidermal growth factor; Cell receptors; Receptor-ligand complexes; Ligand binding (Biochemistry); Protein-tyrosine kinase

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APA (6th Edition):

Judge, G. S. (2015). Clathrin and TOM1L1 regulate epidermal growth factor receptor signaling at the plasma membrane. (Thesis). Ryerson University. Retrieved from https://digital.library.ryerson.ca/islandora/object/RULA%3A4678

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):

Judge, Gurjeet Singh. “Clathrin and TOM1L1 regulate epidermal growth factor receptor signaling at the plasma membrane.” 2015. Thesis, Ryerson University. Accessed December 09, 2019. https://digital.library.ryerson.ca/islandora/object/RULA%3A4678.

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

MLA Handbook (7th Edition):

Judge, Gurjeet Singh. “Clathrin and TOM1L1 regulate epidermal growth factor receptor signaling at the plasma membrane.” 2015. Web. 09 Dec 2019.

Vancouver:

Judge GS. Clathrin and TOM1L1 regulate epidermal growth factor receptor signaling at the plasma membrane. [Internet] [Thesis]. Ryerson University; 2015. [cited 2019 Dec 09]. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A4678.

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

Council of Science Editors:

Judge GS. Clathrin and TOM1L1 regulate epidermal growth factor receptor signaling at the plasma membrane. [Thesis]. Ryerson University; 2015. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A4678

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

23. Graña, Adolfo Orro. Examination of the role of binding site water molecules in molecular recognition.

Degree: 2012, SciLifeLab Stockholm

  A set of algorithms were designed, implemented and evaluated in order to, first, identifyclusters of conserved waters in binding pockets, i.e. hydration sites. Then,… (more)

Subjects/Keywords: Free energy of binding; enthalpy; entropy; ligand; hydration site; ligand-protein binding.

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APA (6th Edition):

Graña, A. O. (2012). Examination of the role of binding site water molecules in molecular recognition. (Thesis). SciLifeLab Stockholm. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-200164

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):

Graña, Adolfo Orro. “Examination of the role of binding site water molecules in molecular recognition.” 2012. Thesis, SciLifeLab Stockholm. Accessed December 09, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-200164.

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

MLA Handbook (7th Edition):

Graña, Adolfo Orro. “Examination of the role of binding site water molecules in molecular recognition.” 2012. Web. 09 Dec 2019.

Vancouver:

Graña AO. Examination of the role of binding site water molecules in molecular recognition. [Internet] [Thesis]. SciLifeLab Stockholm; 2012. [cited 2019 Dec 09]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-200164.

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

Council of Science Editors:

Graña AO. Examination of the role of binding site water molecules in molecular recognition. [Thesis]. SciLifeLab Stockholm; 2012. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-200164

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


Université Paris-Sud – Paris XI

24. Nogaret, Sophie. Etude par RMN de macromolécules biologiques : étude structurale de la protéine CGC-19 impliquée dans la biosynthèse d’un métabolite secondaire, la congocidine chez Streptomyces Ambofaciens. Développement d’inhibiteurs des Bcl-2, protéines modulatrices de l’apoptose : NMR study of biological macromolecules : structural study of CGC-19, a single domain protein involved in the biosynthesis of congocidine, a secondary metabolite from Streptomyces Ambofaciens, NMR contribution to anti-apoptotic protein ligand development.

Degree: Docteur es, Ingénierie des protéines, 2011, Université Paris-Sud – Paris XI

 Ma thèse comporte deux volets: d’une part, le développement de ligands ciblant les protéines antiapoptotiques et d’autre part, l’étude par RMN des protéines CGC impliquées… (more)

Subjects/Keywords: Biologie structurale; Métabolisme secondaire; Interaction protéine ligand; Structural biology; Secondary metabolism; Protein ligand interaction

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

APA (6th Edition):

Nogaret, S. (2011). Etude par RMN de macromolécules biologiques : étude structurale de la protéine CGC-19 impliquée dans la biosynthèse d’un métabolite secondaire, la congocidine chez Streptomyces Ambofaciens. Développement d’inhibiteurs des Bcl-2, protéines modulatrices de l’apoptose : NMR study of biological macromolecules : structural study of CGC-19, a single domain protein involved in the biosynthesis of congocidine, a secondary metabolite from Streptomyces Ambofaciens, NMR contribution to anti-apoptotic protein ligand development. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2011PA114848

Chicago Manual of Style (16th Edition):

Nogaret, Sophie. “Etude par RMN de macromolécules biologiques : étude structurale de la protéine CGC-19 impliquée dans la biosynthèse d’un métabolite secondaire, la congocidine chez Streptomyces Ambofaciens. Développement d’inhibiteurs des Bcl-2, protéines modulatrices de l’apoptose : NMR study of biological macromolecules : structural study of CGC-19, a single domain protein involved in the biosynthesis of congocidine, a secondary metabolite from Streptomyces Ambofaciens, NMR contribution to anti-apoptotic protein ligand development.” 2011. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed December 09, 2019. http://www.theses.fr/2011PA114848.

MLA Handbook (7th Edition):

Nogaret, Sophie. “Etude par RMN de macromolécules biologiques : étude structurale de la protéine CGC-19 impliquée dans la biosynthèse d’un métabolite secondaire, la congocidine chez Streptomyces Ambofaciens. Développement d’inhibiteurs des Bcl-2, protéines modulatrices de l’apoptose : NMR study of biological macromolecules : structural study of CGC-19, a single domain protein involved in the biosynthesis of congocidine, a secondary metabolite from Streptomyces Ambofaciens, NMR contribution to anti-apoptotic protein ligand development.” 2011. Web. 09 Dec 2019.

Vancouver:

Nogaret S. Etude par RMN de macromolécules biologiques : étude structurale de la protéine CGC-19 impliquée dans la biosynthèse d’un métabolite secondaire, la congocidine chez Streptomyces Ambofaciens. Développement d’inhibiteurs des Bcl-2, protéines modulatrices de l’apoptose : NMR study of biological macromolecules : structural study of CGC-19, a single domain protein involved in the biosynthesis of congocidine, a secondary metabolite from Streptomyces Ambofaciens, NMR contribution to anti-apoptotic protein ligand development. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2011. [cited 2019 Dec 09]. Available from: http://www.theses.fr/2011PA114848.

Council of Science Editors:

Nogaret S. Etude par RMN de macromolécules biologiques : étude structurale de la protéine CGC-19 impliquée dans la biosynthèse d’un métabolite secondaire, la congocidine chez Streptomyces Ambofaciens. Développement d’inhibiteurs des Bcl-2, protéines modulatrices de l’apoptose : NMR study of biological macromolecules : structural study of CGC-19, a single domain protein involved in the biosynthesis of congocidine, a secondary metabolite from Streptomyces Ambofaciens, NMR contribution to anti-apoptotic protein ligand development. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2011. Available from: http://www.theses.fr/2011PA114848


University of Kansas

25. Roy, Ambrish. Protein structure prediction and structure-based protein function annotation.

Degree: PhD, Biochemistry & Molecular Biology, 2011, University of Kansas

 Nature tends to modify rather than invent function of protein molecules, and the log of the modifications is encrypted in the gene sequence. Analysis of… (more)

Subjects/Keywords: Bioinformatics; Biophysics; Biochemistry; Local structure comparison; Protein function annotation; Protein-ligand binding; Protein structure prediction

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

APA (6th Edition):

Roy, A. (2011). Protein structure prediction and structure-based protein function annotation. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/10695

Chicago Manual of Style (16th Edition):

Roy, Ambrish. “Protein structure prediction and structure-based protein function annotation.” 2011. Doctoral Dissertation, University of Kansas. Accessed December 09, 2019. http://hdl.handle.net/1808/10695.

MLA Handbook (7th Edition):

Roy, Ambrish. “Protein structure prediction and structure-based protein function annotation.” 2011. Web. 09 Dec 2019.

Vancouver:

Roy A. Protein structure prediction and structure-based protein function annotation. [Internet] [Doctoral dissertation]. University of Kansas; 2011. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/1808/10695.

Council of Science Editors:

Roy A. Protein structure prediction and structure-based protein function annotation. [Doctoral Dissertation]. University of Kansas; 2011. Available from: http://hdl.handle.net/1808/10695


Vanderbilt University

26. Fu, Darwin Yu. Improving Protein-Small Molecule Structure Predictions with Ensemble Methods, or Using Computers to Guess How Tiny Things Fit Together.

Degree: PhD, Chemistry, 2018, Vanderbilt University

Protein-small molecule structure prediction, or protein-ligand docking, is a computational method for modeling how binding partners will interaction on an atomic level. Accurate prediction of… (more)

Subjects/Keywords: Rosetta; Protein-Ligand Docking; Molecular Modeling; Small Molecules; G-Protein Coupled Receptors; Protein Structure Prediction

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APA (6th Edition):

Fu, D. Y. (2018). Improving Protein-Small Molecule Structure Predictions with Ensemble Methods, or Using Computers to Guess How Tiny Things Fit Together. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-08012018-164524/ ;

Chicago Manual of Style (16th Edition):

Fu, Darwin Yu. “Improving Protein-Small Molecule Structure Predictions with Ensemble Methods, or Using Computers to Guess How Tiny Things Fit Together.” 2018. Doctoral Dissertation, Vanderbilt University. Accessed December 09, 2019. http://etd.library.vanderbilt.edu/available/etd-08012018-164524/ ;.

MLA Handbook (7th Edition):

Fu, Darwin Yu. “Improving Protein-Small Molecule Structure Predictions with Ensemble Methods, or Using Computers to Guess How Tiny Things Fit Together.” 2018. Web. 09 Dec 2019.

Vancouver:

Fu DY. Improving Protein-Small Molecule Structure Predictions with Ensemble Methods, or Using Computers to Guess How Tiny Things Fit Together. [Internet] [Doctoral dissertation]. Vanderbilt University; 2018. [cited 2019 Dec 09]. Available from: http://etd.library.vanderbilt.edu/available/etd-08012018-164524/ ;.

Council of Science Editors:

Fu DY. Improving Protein-Small Molecule Structure Predictions with Ensemble Methods, or Using Computers to Guess How Tiny Things Fit Together. [Doctoral Dissertation]. Vanderbilt University; 2018. Available from: http://etd.library.vanderbilt.edu/available/etd-08012018-164524/ ;


Texas A&M University

27. Liu, Yang. Characterization of Membrane Proteins and Ligand Interactions by Native Ion Mobility Mass Spectrometry.

Degree: PhD, Medical Sciences, 2019, Texas A&M University

 Membrane proteins interact intimately with the lipid bilayer in which they are embedded. Interactions between membrane proteins and ligands such as lipids and other small… (more)

Subjects/Keywords: Membrane Protein Biophysics; Native Mass Spectrometry; Ion-Mobility Spectrometry; Protein Ligand Interactions; Protein Lipid Interactions

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

APA (6th Edition):

Liu, Y. (2019). Characterization of Membrane Proteins and Ligand Interactions by Native Ion Mobility Mass Spectrometry. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/184960

Chicago Manual of Style (16th Edition):

Liu, Yang. “Characterization of Membrane Proteins and Ligand Interactions by Native Ion Mobility Mass Spectrometry.” 2019. Doctoral Dissertation, Texas A&M University. Accessed December 09, 2019. http://hdl.handle.net/1969.1/184960.

MLA Handbook (7th Edition):

Liu, Yang. “Characterization of Membrane Proteins and Ligand Interactions by Native Ion Mobility Mass Spectrometry.” 2019. Web. 09 Dec 2019.

Vancouver:

Liu Y. Characterization of Membrane Proteins and Ligand Interactions by Native Ion Mobility Mass Spectrometry. [Internet] [Doctoral dissertation]. Texas A&M University; 2019. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/1969.1/184960.

Council of Science Editors:

Liu Y. Characterization of Membrane Proteins and Ligand Interactions by Native Ion Mobility Mass Spectrometry. [Doctoral Dissertation]. Texas A&M University; 2019. Available from: http://hdl.handle.net/1969.1/184960


Duke University

28. Xu, Yingrong. Development and Application of Covalent-Labeling Strategies for the Large-Scale Thermodynamic Analysis of Protein Folding and Ligand Binding .

Degree: 2016, Duke University

  Thermodynamic stability measurements on proteins and protein-ligand complexes can offer insights not only into the fundamental properties of protein folding reactions and protein functions,… (more)

Subjects/Keywords: Chemistry; Biochemistry; covalent labeling; ligand binding; mass spectrometry; protein-ligand binding; protein thermodynamic stability; proteome-wide

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APA (6th Edition):

Xu, Y. (2016). Development and Application of Covalent-Labeling Strategies for the Large-Scale Thermodynamic Analysis of Protein Folding and Ligand Binding . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/12204

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):

Xu, Yingrong. “Development and Application of Covalent-Labeling Strategies for the Large-Scale Thermodynamic Analysis of Protein Folding and Ligand Binding .” 2016. Thesis, Duke University. Accessed December 09, 2019. http://hdl.handle.net/10161/12204.

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

MLA Handbook (7th Edition):

Xu, Yingrong. “Development and Application of Covalent-Labeling Strategies for the Large-Scale Thermodynamic Analysis of Protein Folding and Ligand Binding .” 2016. Web. 09 Dec 2019.

Vancouver:

Xu Y. Development and Application of Covalent-Labeling Strategies for the Large-Scale Thermodynamic Analysis of Protein Folding and Ligand Binding . [Internet] [Thesis]. Duke University; 2016. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/10161/12204.

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

Council of Science Editors:

Xu Y. Development and Application of Covalent-Labeling Strategies for the Large-Scale Thermodynamic Analysis of Protein Folding and Ligand Binding . [Thesis]. Duke University; 2016. Available from: http://hdl.handle.net/10161/12204

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


Georgia Tech

29. Enekwa, C. Denise. In silico design of novel binding ligands for biological targets.

Degree: MS, Chemistry and Biochemistry, 2010, Georgia Tech

 An in silico design algorithm has been developed to design binding ligands for protein targets of known three-dimensional structure. In this method, the binding energy… (more)

Subjects/Keywords: De novo binding; In silico design; Protein docking; Computer simulation; Ligand binding (Biochemistry); Protein engineering

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

APA (6th Edition):

Enekwa, C. D. (2010). In silico design of novel binding ligands for biological targets. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/41067

Chicago Manual of Style (16th Edition):

Enekwa, C Denise. “In silico design of novel binding ligands for biological targets.” 2010. Masters Thesis, Georgia Tech. Accessed December 09, 2019. http://hdl.handle.net/1853/41067.

MLA Handbook (7th Edition):

Enekwa, C Denise. “In silico design of novel binding ligands for biological targets.” 2010. Web. 09 Dec 2019.

Vancouver:

Enekwa CD. In silico design of novel binding ligands for biological targets. [Internet] [Masters thesis]. Georgia Tech; 2010. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/1853/41067.

Council of Science Editors:

Enekwa CD. In silico design of novel binding ligands for biological targets. [Masters Thesis]. Georgia Tech; 2010. Available from: http://hdl.handle.net/1853/41067

30. Olson, Andrew Lawrence. NMR-Based and Automated Docking Characterization of Protein Structure, Dynamics, and Ligand Binding.

Degree: 2010, Marquette University

 NMR-based methods used in conjunction with a technique called docking are used to characterize ligand binding to proteins. Standard NMR methods were used to study… (more)

Subjects/Keywords: Ligand binding (Biochemistry); Ligands; Protein binding; Proteins; Chemistry  – Dissertations docking; nmr; protein; Chemistry

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

APA (6th Edition):

Olson, A. L. (2010). NMR-Based and Automated Docking Characterization of Protein Structure, Dynamics, and Ligand Binding. (Thesis). Marquette University. Retrieved from https://epublications.marquette.edu/dissertations_mu/81

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):

Olson, Andrew Lawrence. “NMR-Based and Automated Docking Characterization of Protein Structure, Dynamics, and Ligand Binding.” 2010. Thesis, Marquette University. Accessed December 09, 2019. https://epublications.marquette.edu/dissertations_mu/81.

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

MLA Handbook (7th Edition):

Olson, Andrew Lawrence. “NMR-Based and Automated Docking Characterization of Protein Structure, Dynamics, and Ligand Binding.” 2010. Web. 09 Dec 2019.

Vancouver:

Olson AL. NMR-Based and Automated Docking Characterization of Protein Structure, Dynamics, and Ligand Binding. [Internet] [Thesis]. Marquette University; 2010. [cited 2019 Dec 09]. Available from: https://epublications.marquette.edu/dissertations_mu/81.

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

Council of Science Editors:

Olson AL. NMR-Based and Automated Docking Characterization of Protein Structure, Dynamics, and Ligand Binding. [Thesis]. Marquette University; 2010. Available from: https://epublications.marquette.edu/dissertations_mu/81

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

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