User:Zachary Armstrong - Revision history

Zachary Armstrong at 15:58, 2 April 2020

2020-04-02T15:58:05Z

Zachary Armstrong at 14:20, 2 April 2020

2020-04-02T14:20:00Z

Zachary Armstrong at 14:13, 2 April 2020

2020-04-02T14:13:30Z

Zachary Armstrong at 14:00, 2 April 2020

2020-04-02T14:00:55Z

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2020-01-17T16:39:17Z

Created page with "200px|right '''This is an empty template to help you get started with composing your User page.''' You should begin by opening this page for ed..."

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'''This is an empty template to help you get started with composing your User page.'''

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<biblio>
#Gilbert2008 pmid=18430603

</biblio>


[[Category:Contributors|Armstrong,Zachary]]

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 [[Image:Z_Armstrong.png|200px|right]]
-Dr. Zachary Armstrong, a native of Iqaluit, Nunavut, obtained his B.Sc. — majoring in chemistry and biochemistry — from the [https://www.ubc.ca/ University of British Columbia]. His final year project, performed under the guidance of Professor [[User:Steve Withers|Steve Withers]], focused on the creation of a [[GH11]] thioglycoligase <cite>Armstrong2010</cite>. He completed his PhD at the University of British Columbia, co-supervised by Professors Steven Withers and [http://hallam.microbiology.ubc.ca/ Stephen J. Hallam]. This work focused on the identification of glycoside hydrolases from metagenomic sources — including the beaver gut<cite>Armstrong2018</cite>,a mining bioreactor<cite>Armstrong2013</cite> and soils<cite>Armstrong2019mSys</cite>— and the engineering of glycosynthases from a metagenomes and synthetic gene libraries<cite>Armstrong2019Acs</cite>. In 2018 he joined the group of [[User:Gideon Davies|Gideon Davies]] in the [https://www.york.ac.uk/chemistry/research/ysbl/ York Structural Biology Laboratories] at the [https://www.york.ac.uk/ University of York] as a postdoctoral research associate. His current work focuses on mechanism-based inhibitors and activity-based protein profiling of human carbohydrate processing enzymes.
+Dr. Zachary Armstrong, a native of Iqaluit, Nunavut, obtained his B.Sc. — majoring in chemistry and biochemistry — from the [https://www.ubc.ca/ University of British Columbia]. His final year project, performed under the guidance of Professor [[User:Steve Withers|Steve Withers]], focused on the creation of a [[GH11]] thioglycoligase <cite>Armstrong2010</cite>. He completed his PhD at the University of British Columbia, co-supervised by Professors Steve Withers and [http://hallam.microbiology.ubc.ca/ Steven J. Hallam]. This work focused on the identification of glycoside hydrolases from metagenomic sources — including the beaver gut<cite>Armstrong2018</cite>,a mining bioreactor<cite>Armstrong2013</cite> and soils<cite>Armstrong2019mSys</cite>— and the engineering of glycosynthases from metagenomes and synthetic gene libraries<cite>Armstrong2019Acs</cite>. In 2018 he joined the group of [[User:Gideon Davies|Gideon Davies]] in the [https://www.york.ac.uk/chemistry/research/ysbl/ York Structural Biology Laboratories] at the [https://www.york.ac.uk/ University of York] as a postdoctoral research associate. His current work focuses on mechanism-based inhibitors and activity-based protein profiling of human carbohydrate processing enzymes.
 He has determined the crystal structure of :
 * [[GH164]] ''Bacteroides salyersiae'' beta-mannosidase <cite>Armstrong2019JBC</cite>
-−
 ----
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 #Armstrong2010 pmid=20112321
 #Armstrong2018 pmid=30013164
 #Armstrong2019mSys pmid=31164449
 #Armstrong2013 pmid=23906845
+#Armstrong2019Acs Armstrong Z, Liu F, Chen H-M, Hallam SJ, Withers SG. (2019) Systematic Screening of Synthetic Gene-Encoded Enzymes for Synthesis of Modified Glycosides. ''ACS Catal''. 53, 689-98. | [https://doi.org/10.1021/acscatal.8b05179 DOI: 10.1021/acscatal.8b05179]
 #Armstrong2019JBC pmid=31871050

@@ Line 1: / Line 1: @@
 [[Image:Z_Armstrong.png|200px|right]]
-Dr. Zachary Armstrong, a native of Iqaluit, Nunavut, obtained his B.Sc. — majoring in chemistry and biochemistry — from the [https://www.ubc.ca/ University of British Columbia]. His final year project, performed under the guidance of Professor [[User:Steve Withers|Steve Withers]], focused on the creation of a [[GH11]] thioglycoligase <cite>Armstrong2010</cite>. He completed his PhD at the University of British Columbia, co-supervised by Professors Steven Withers and Stephen J. Hallam. This work focused on the identification of glycoside hydrolases from metagenomic sources — including the beaver gut<cite>Armstrong2018</cite>,a mining bioreactor<cite>Armstrong2013</cite> and soils<cite>Armstrong2019mSys</cite>— and the engineering of glycosynthases from a metagenomes and synthetic gene libraries (ref). In 2018 he joined the group of [[User:Gideon Davies|Gideon Davies]] in the [https://www.york.ac.uk/chemistry/research/ysbl/ York Structural Biology Laboratories] at the [https://www.york.ac.uk/ University of York] as a postdoctoral research associate. His current work focuses on mechanism-based inhibitors and activity-based protein profiling of human carbohydrate processing enzymes.
+Dr. Zachary Armstrong, a native of Iqaluit, Nunavut, obtained his B.Sc. — majoring in chemistry and biochemistry — from the [https://www.ubc.ca/ University of British Columbia]. His final year project, performed under the guidance of Professor [[User:Steve Withers|Steve Withers]], focused on the creation of a [[GH11]] thioglycoligase <cite>Armstrong2010</cite>. He completed his PhD at the University of British Columbia, co-supervised by Professors Steven Withers and [http://hallam.microbiology.ubc.ca/ Stephen J. Hallam]. This work focused on the identification of glycoside hydrolases from metagenomic sources — including the beaver gut<cite>Armstrong2018</cite>,a mining bioreactor<cite>Armstrong2013</cite> and soils<cite>Armstrong2019mSys</cite>— and the engineering of glycosynthases from a metagenomes and synthetic gene libraries<cite>Armstrong2019Acs</cite>. In 2018 he joined the group of [[User:Gideon Davies|Gideon Davies]] in the [https://www.york.ac.uk/chemistry/research/ysbl/ York Structural Biology Laboratories] at the [https://www.york.ac.uk/ University of York] as a postdoctoral research associate. His current work focuses on mechanism-based inhibitors and activity-based protein profiling of human carbohydrate processing enzymes.
 He has determined the crystal structure of :
-* [[GH164]] ''Bacteroides salyersiae'' beta-mannosidase <cite> </cite>
+* [[GH164]] ''Bacteroides salyersiae'' beta-mannosidase <cite>Armstrong2019JBC</cite>
@@ Line 17: / Line 17: @@
 #Armstrong2019mSys pmid=31164449
 #Armstrong2013 pmid=23906845
 </biblio>
 <!-- Do not remove this Category tag -->
 [[Category:Contributors|Armstrong,Zachary]]

@@ Line 1: / Line 1: @@
-[[Image:Blank_user-200px.png|200px|right]]
+[[Image:Z_Armstrong.png|200px|right]]
-Dr. Zachary Armstrong, a native of Iqaluit, Nunavut, obtained his B.Sc. — majoring in chemistry and biochemistry — from the University of British Columbia (https://www.ubc.ca/). His final year project, performed under the guidance of [[User:Steve Withers|Steve Withers]], focused on the creation of a [[GH11]] thioglycoligase <cite>Armstrong2010</cite>. He completed his PhD at the University of British Columbia, co-supervised by Professor Steven Withers and Stephen Hallam. This work focused on the identification of glycoside hydrolases from metagenomic sources — including the beaver gut<cite>Armstrong2018</cite>,a mining bioreactor<cite>Armstrong2013</cite> and soils<cite>Armstrong2019mSys</cite>— and the engineering of glycosynthases from a metagenomes and synthetic gene libraries (ref). In 2018 he joined the group of [[User:Gideon Davies|Gideon Davies]] in the York Structural Biology Laboratories (https://www.york.ac.uk/chemistry/research/ysbl/ ) at the University of York (https://www.york.ac.uk/)  as a postdoctoral research associate. His current work focuses on mechanism-based inhibitors and activity-based protein profiling of human carbohydrate processing enzymes.
+Dr. Zachary Armstrong, a native of Iqaluit, Nunavut, obtained his B.Sc. — majoring in chemistry and biochemistry — from the [https://www.ubc.ca/ University of British Columbia]. His final year project, performed under the guidance of Professor [[User:Steve Withers|Steve Withers]], focused on the creation of a [[GH11]] thioglycoligase <cite>Armstrong2010</cite>. He completed his PhD at the University of British Columbia, co-supervised by Professors Steven Withers and Stephen J. Hallam. This work focused on the identification of glycoside hydrolases from metagenomic sources — including the beaver gut<cite>Armstrong2018</cite>,a mining bioreactor<cite>Armstrong2013</cite> and soils<cite>Armstrong2019mSys</cite>— and the engineering of glycosynthases from a metagenomes and synthetic gene libraries (ref). In 2018 he joined the group of [[User:Gideon Davies|Gideon Davies]] in the [https://www.york.ac.uk/chemistry/research/ysbl/ York Structural Biology Laboratories] at the [https://www.york.ac.uk/ University of York] as a postdoctoral research associate. His current work focuses on mechanism-based inhibitors and activity-based protein profiling of human carbohydrate processing enzymes.
 He has determined the crystal structure of :
 * [[GH164]] ''Bacteroides salyersiae'' beta-mannosidase <cite> </cite>