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You searched for subject:(phosphatase substrate). Showing records 1 – 8 of 8 total matches.

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University of California – Berkeley

1. Baguley, Tyler Daniel. Fragment Based Identification of Phosphatase Inhibitors.

Degree: Chemistry, 2014, University of California – Berkeley

 Phosphatases are broadly introduced as an enzyme class with therapeutic implications in a variety of disease areas. A substrate-based fragment approach is used to identify… (more)

Subjects/Keywords: Chemistry; Organic chemistry; Inhibitor; Phosphatase; Substrate Activity Screening

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

APA (6th Edition):

Baguley, T. D. (2014). Fragment Based Identification of Phosphatase Inhibitors. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/252497k3

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):

Baguley, Tyler Daniel. “Fragment Based Identification of Phosphatase Inhibitors.” 2014. Thesis, University of California – Berkeley. Accessed November 21, 2019. http://www.escholarship.org/uc/item/252497k3.

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

MLA Handbook (7th Edition):

Baguley, Tyler Daniel. “Fragment Based Identification of Phosphatase Inhibitors.” 2014. Web. 21 Nov 2019.

Vancouver:

Baguley TD. Fragment Based Identification of Phosphatase Inhibitors. [Internet] [Thesis]. University of California – Berkeley; 2014. [cited 2019 Nov 21]. Available from: http://www.escholarship.org/uc/item/252497k3.

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

Council of Science Editors:

Baguley TD. Fragment Based Identification of Phosphatase Inhibitors. [Thesis]. University of California – Berkeley; 2014. Available from: http://www.escholarship.org/uc/item/252497k3

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


University of Missouri – Columbia

2. Singh, Harkewal. Structural basis of substrate recognition and inactivation in phosphatases.

Degree: 2011, University of Missouri – Columbia

 Phosphatases are ubiquitous enzymes that catalyze the transfer of phosphoryl group to water. In addition to being one of the most important and fundamental reactions… (more)

Subjects/Keywords: x-ray crystallography; substrate recognition; haloacid dehalogenase; class C acid phosphatase

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

APA (6th Edition):

Singh, H. (2011). Structural basis of substrate recognition and inactivation in phosphatases. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/14453

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):

Singh, Harkewal. “Structural basis of substrate recognition and inactivation in phosphatases.” 2011. Thesis, University of Missouri – Columbia. Accessed November 21, 2019. http://hdl.handle.net/10355/14453.

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

MLA Handbook (7th Edition):

Singh, Harkewal. “Structural basis of substrate recognition and inactivation in phosphatases.” 2011. Web. 21 Nov 2019.

Vancouver:

Singh H. Structural basis of substrate recognition and inactivation in phosphatases. [Internet] [Thesis]. University of Missouri – Columbia; 2011. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/10355/14453.

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

Council of Science Editors:

Singh H. Structural basis of substrate recognition and inactivation in phosphatases. [Thesis]. University of Missouri – Columbia; 2011. Available from: http://hdl.handle.net/10355/14453

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


The Ohio State University

3. Selner, Nicholas. PROFILING THE INTRINSIC SEQUENCE SPECIFICITY OF PROTEIN TYROSINE PHOSPHATASES.

Degree: PhD, Chemistry, 2013, The Ohio State University

 Many signaling pathways are mediated by protein tyrosine phosphorylation. Regulation of protein tyrosine phosphorylation is balanced between protein tyrosine kinases (PTKs) and protein tyrosine phosphatases… (more)

Subjects/Keywords: Chemistry; Biochemistry; Combinatorial library, catalytic activity, kinetics, phosphotyrosine, phosphatase, PTP, substrate specificity

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APA (6th Edition):

Selner, N. (2013). PROFILING THE INTRINSIC SEQUENCE SPECIFICITY OF PROTEIN TYROSINE PHOSPHATASES. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1384269733

Chicago Manual of Style (16th Edition):

Selner, Nicholas. “PROFILING THE INTRINSIC SEQUENCE SPECIFICITY OF PROTEIN TYROSINE PHOSPHATASES.” 2013. Doctoral Dissertation, The Ohio State University. Accessed November 21, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1384269733.

MLA Handbook (7th Edition):

Selner, Nicholas. “PROFILING THE INTRINSIC SEQUENCE SPECIFICITY OF PROTEIN TYROSINE PHOSPHATASES.” 2013. Web. 21 Nov 2019.

Vancouver:

Selner N. PROFILING THE INTRINSIC SEQUENCE SPECIFICITY OF PROTEIN TYROSINE PHOSPHATASES. [Internet] [Doctoral dissertation]. The Ohio State University; 2013. [cited 2019 Nov 21]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1384269733.

Council of Science Editors:

Selner N. PROFILING THE INTRINSIC SEQUENCE SPECIFICITY OF PROTEIN TYROSINE PHOSPHATASES. [Doctoral Dissertation]. The Ohio State University; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1384269733


University of Lethbridge

4. Van Herk, Peter. Specificity of a novel myo-inositol phosphatase towards less-phosphorylated myo-inositol phosphates .

Degree: 2014, University of Lethbridge

 Protein tyrosine phosphatase-like myo-inositol phosphatases (PTPLPs) remove phosphoryl groups from phosphorylated myo-inositols (IPs) via largely ordered pathways. To understand the substrate specificity of this enzyme… (more)

Subjects/Keywords: Crystallography; Biochemistry; Enzyme; Phosphatase; Myo-Inositol; PTPLP; Fluorescence Spectroscopy; Kinetic; Substrate Specificity; Physical Biochemistry

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APA (6th Edition):

Van Herk, P. (2014). Specificity of a novel myo-inositol phosphatase towards less-phosphorylated myo-inositol phosphates . (Thesis). University of Lethbridge. Retrieved from http://hdl.handle.net/10133/3638

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):

Van Herk, Peter. “Specificity of a novel myo-inositol phosphatase towards less-phosphorylated myo-inositol phosphates .” 2014. Thesis, University of Lethbridge. Accessed November 21, 2019. http://hdl.handle.net/10133/3638.

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

MLA Handbook (7th Edition):

Van Herk, Peter. “Specificity of a novel myo-inositol phosphatase towards less-phosphorylated myo-inositol phosphates .” 2014. Web. 21 Nov 2019.

Vancouver:

Van Herk P. Specificity of a novel myo-inositol phosphatase towards less-phosphorylated myo-inositol phosphates . [Internet] [Thesis]. University of Lethbridge; 2014. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/10133/3638.

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

Council of Science Editors:

Van Herk P. Specificity of a novel myo-inositol phosphatase towards less-phosphorylated myo-inositol phosphates . [Thesis]. University of Lethbridge; 2014. Available from: http://hdl.handle.net/10133/3638

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

5. Varela-Nieto, Isabel. Insulin receptor substrate 2 (IRS2)-deficient mice show sensorineural hearing loss that is delayed by concomitant protein tyrosine phosphatase 1B (PTP1B) loss of function.

Degree: 2018, Feinstein Institute for Medical Research

Subjects/Keywords: Cochlea; Mitogen-Activated Protein Kinases; Protein Tyrosine Phosphatase; Insulin Receptor Substrate Proteins; Medicina

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APA (6th Edition):

Varela-Nieto, I. (2018). Insulin receptor substrate 2 (IRS2)-deficient mice show sensorineural hearing loss that is delayed by concomitant protein tyrosine phosphatase 1B (PTP1B) loss of function. (Thesis). Feinstein Institute for Medical Research. Retrieved from http://hdl.handle.net/10486/663875

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):

Varela-Nieto, Isabel. “Insulin receptor substrate 2 (IRS2)-deficient mice show sensorineural hearing loss that is delayed by concomitant protein tyrosine phosphatase 1B (PTP1B) loss of function.” 2018. Thesis, Feinstein Institute for Medical Research. Accessed November 21, 2019. http://hdl.handle.net/10486/663875.

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

MLA Handbook (7th Edition):

Varela-Nieto, Isabel. “Insulin receptor substrate 2 (IRS2)-deficient mice show sensorineural hearing loss that is delayed by concomitant protein tyrosine phosphatase 1B (PTP1B) loss of function.” 2018. Web. 21 Nov 2019.

Vancouver:

Varela-Nieto I. Insulin receptor substrate 2 (IRS2)-deficient mice show sensorineural hearing loss that is delayed by concomitant protein tyrosine phosphatase 1B (PTP1B) loss of function. [Internet] [Thesis]. Feinstein Institute for Medical Research; 2018. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/10486/663875.

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

Council of Science Editors:

Varela-Nieto I. Insulin receptor substrate 2 (IRS2)-deficient mice show sensorineural hearing loss that is delayed by concomitant protein tyrosine phosphatase 1B (PTP1B) loss of function. [Thesis]. Feinstein Institute for Medical Research; 2018. Available from: http://hdl.handle.net/10486/663875

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

6. Vigbedor, Maa Ohui Shormeh. Structure and regulation of G-substrate in neurodegenerative disease.

Degree: PhD, 2013, University of Edinburgh

 G-substrate is a 23 kDa protein named as a specific substrate of cGMP-dependent protein kinase and found predominantly in cerebellar Purkinje cells. As a component… (more)

Subjects/Keywords: 572; G-substrate; Parkinson's disease; phosphatase inhibition; Alzheimer's disease

…inhibition studies suggest that the G-substrate variants affect phosphatase activity to different… …substrate Phospho-G-substrate is known to effectively inhibit protein phosphatase 1 (PP1)… …PP2Ac to assay the protein phosphatase inhibitory activities of human and rat G-substrate… …Structure and Regulation of G-substrate in Neurodegenerative Disease 1.1.5.2 Protein Phosphatase… …Structure and Regulation of G-substrate in Neurodegenerative Disease Figure 4.8: Activity… 

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

APA (6th Edition):

Vigbedor, M. O. S. (2013). Structure and regulation of G-substrate in neurodegenerative disease. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/8292

Chicago Manual of Style (16th Edition):

Vigbedor, Maa Ohui Shormeh. “Structure and regulation of G-substrate in neurodegenerative disease.” 2013. Doctoral Dissertation, University of Edinburgh. Accessed November 21, 2019. http://hdl.handle.net/1842/8292.

MLA Handbook (7th Edition):

Vigbedor, Maa Ohui Shormeh. “Structure and regulation of G-substrate in neurodegenerative disease.” 2013. Web. 21 Nov 2019.

Vancouver:

Vigbedor MOS. Structure and regulation of G-substrate in neurodegenerative disease. [Internet] [Doctoral dissertation]. University of Edinburgh; 2013. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1842/8292.

Council of Science Editors:

Vigbedor MOS. Structure and regulation of G-substrate in neurodegenerative disease. [Doctoral Dissertation]. University of Edinburgh; 2013. Available from: http://hdl.handle.net/1842/8292


University of Illinois – Urbana-Champaign

7. Hebbard, Carleigh Fredda Frances. Mechanisms of polyphosphate degradation.

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

 The goal of my research has been to investigate the mechanisms by which inorganic polyphosphate (polyP) is degraded in vivo. PolyP is a linear chain… (more)

Subjects/Keywords: polyphosphate; polyP; Nudt2; Nudt3; pNP; p-nitrophenol; 4-nitrophenol; Nudix; phosphoanhydride; phosphoester; chromogenic substrate; fluorogenic substrate; phosphatase substrate; spectrophotometry; DAPI; 4-methylumbeliferone; dinucleotide polyphosphate; diadenosine polyphosphate; phosphate; phosphatase; phosphoanhydrase; phosphodiesterase; alkaline phosphatase; acid phosphatase; endopolyphosphatase; exopolyphosphatase; calcium; acidocalcisome; volutin granule; azurophilic granule; chitin; Chs2; ScChs2; cell wall; polysaccharide; oligosaccharide; calcium phosphate sink; ocean phosphate; serum; GlcNAc; UDP-GlcNAc; platelet; clotting; blood; coagulation; coagulation cascade; processive; polymer; TLC; carbohydrate; primer; TCA-insoluble; YO1531; inositol; inositol phosphate; ApnA; Ap3A; Ap4A; Ap6A; NpnA; diadenosine tetraphosphate; diadenosine pentaphosphate; diadenosine hexaphosphate; phytic acid; metaphosphate; phosphate melt; inositol hexaphosphate; 5-phosphoribosyl 1-pyrophosphate; PNPP; p-nitrophenol phosphate; DIPP; diphosphoinositol polyphosphate phosphohydrolase; Ddp1p; YOR163w; Saccharomyces cerevisiae; GlcN; GalNAc; ManNAc; Glc; GlcNAc2; GlcNAc3; N-propanoylglucosamine; GlcNPr; N-butanoylglucosamine; GlcNBu; N-glycolylglucosamine; GlcNGc

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

APA (6th Edition):

Hebbard, C. F. F. (2016). Mechanisms of polyphosphate degradation. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/91597

Chicago Manual of Style (16th Edition):

Hebbard, Carleigh Fredda Frances. “Mechanisms of polyphosphate degradation.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed November 21, 2019. http://hdl.handle.net/2142/91597.

MLA Handbook (7th Edition):

Hebbard, Carleigh Fredda Frances. “Mechanisms of polyphosphate degradation.” 2016. Web. 21 Nov 2019.

Vancouver:

Hebbard CFF. Mechanisms of polyphosphate degradation. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/2142/91597.

Council of Science Editors:

Hebbard CFF. Mechanisms of polyphosphate degradation. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/91597


Université du Luxembourg

8. Köhler, Christian. Biopharm - the Influence of Macro-substrates & Conditioning on Pharmaceutical Removal Rates by Moving Bed Biofilm Reactors.

Degree: 2015, Université du Luxembourg

 Organic micropollutants with endocrine disruptive properties are present in the aquatic environment. A major part of their emission is caused by municipal wastewater treatment plants… (more)

Subjects/Keywords: pharmaceuticals; xenobiotics; wastewater; wwtp; moving bed biofilm reactor; MBBR; wastewater treatment plant; lab-scale; metabolism; co-metabolism; training; conditioning; 16S rRNA; DNA; RNA; cDNA; enzyme; fingerprinting; consortia; structure; enzyme activity; respirometry; maximum growth rate; SOUR; degradation kinetics; kbiol; macro-substrate; substrate; LC MS/MS; esterase; phosphatase; glucosidase; aminopeptidase; exoenzyme; activity; atenolol; diclofenac; PCA; PCoA; Delftia; Lysobacter; Life sciences :: Biochemistry, biophysics & molecular biology [F05]; Sciences du vivant :: Biochimie, biophysique & biologie moléculaire [F05]; Life sciences :: Biotechnology [F06]; Sciences du vivant :: Biotechnologie [F06]; Life sciences :: Environmental sciences & ecology [F08]; Sciences du vivant :: Sciences de l'environnement & écologie [F08]; Engineering, computing & technology :: Civil engineering [C04]; Ingénierie, informatique & technologie :: Ingénierie civile [C04]; Engineering, computing & technology :: Multidisciplinary, general & others [C99]; Ingénierie, informatique & technologie :: Multidisciplinaire, généralités & autres [C99]

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

APA (6th Edition):

Köhler, C. (2015). Biopharm - the Influence of Macro-substrates & Conditioning on Pharmaceutical Removal Rates by Moving Bed Biofilm Reactors. (Doctoral Dissertation). Université du Luxembourg. Retrieved from http://orbilu.uni.lu/handle/10993/22418

Chicago Manual of Style (16th Edition):

Köhler, Christian. “Biopharm - the Influence of Macro-substrates & Conditioning on Pharmaceutical Removal Rates by Moving Bed Biofilm Reactors.” 2015. Doctoral Dissertation, Université du Luxembourg. Accessed November 21, 2019. http://orbilu.uni.lu/handle/10993/22418.

MLA Handbook (7th Edition):

Köhler, Christian. “Biopharm - the Influence of Macro-substrates & Conditioning on Pharmaceutical Removal Rates by Moving Bed Biofilm Reactors.” 2015. Web. 21 Nov 2019.

Vancouver:

Köhler C. Biopharm - the Influence of Macro-substrates & Conditioning on Pharmaceutical Removal Rates by Moving Bed Biofilm Reactors. [Internet] [Doctoral dissertation]. Université du Luxembourg; 2015. [cited 2019 Nov 21]. Available from: http://orbilu.uni.lu/handle/10993/22418.

Council of Science Editors:

Köhler C. Biopharm - the Influence of Macro-substrates & Conditioning on Pharmaceutical Removal Rates by Moving Bed Biofilm Reactors. [Doctoral Dissertation]. Université du Luxembourg; 2015. Available from: http://orbilu.uni.lu/handle/10993/22418

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