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Difference between revisions of "User:Alex Anderson"
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| − | + | Dr. Anderson recieved his BSc (2017) and MSc (2019) from Wilfrid Laurier University (Canada) in the lab of Dr. [[User:Joel Weadge|Joel Weadge]], alongside [[User:Michael Suits|Michael Suits]], at WLU where he studied the structure and function of the cellulose phosphoethanolamine transferase BcsG in ''E. coli''. Dr. Anderson received his Ph.D. from the University of Guelph in 2024 under the supervision of Dr. [[User:Anthony Clarke|Anthony Clarke]] where he worked on the mechanism of peptidoglycan ''O''-acetyltransferases. Dr. Anderson is presently a postdoctoral fellow at McMaster University in the lab of Dr. John Whitney where he studies Type VI-secreted polymorphic toxins that target carbohydrate structures. | |
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| − | + | Dr. Anderson and colleagues have demonstrated the structures of: | |
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| − | '' | + | CAZy-unclassified ''Escherichia coli'' phosphoethanolamine transferase BcsG (6PCZ/6PD0) <cite>Anderson2020</cite> |
| + | [[GH5]] ''Clostridioides difficile'' endo-β-glucanase CcsZ (6UJE/6UJF) <cite>Scott2020</cite> | ||
| + | CAZy-unclassified ''Campylobacter jejuni'' peptidoglycan O-acetyltransferase PatB (8TLB) | ||
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<biblio> | <biblio> | ||
| − | # | + | #Anderson2020 pmid=32152228 |
| + | #Scott2020 pmid=33264329 | ||
| + | </biblio> | ||
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[[Category:Contributors|Anderson,Alex]] | [[Category:Contributors|Anderson,Alex]] | ||
Latest revision as of 13:18, 23 April 2024
Dr. Anderson recieved his BSc (2017) and MSc (2019) from Wilfrid Laurier University (Canada) in the lab of Dr. Joel Weadge, alongside Michael Suits, at WLU where he studied the structure and function of the cellulose phosphoethanolamine transferase BcsG in E. coli. Dr. Anderson received his Ph.D. from the University of Guelph in 2024 under the supervision of Dr. Anthony Clarke where he worked on the mechanism of peptidoglycan O-acetyltransferases. Dr. Anderson is presently a postdoctoral fellow at McMaster University in the lab of Dr. John Whitney where he studies Type VI-secreted polymorphic toxins that target carbohydrate structures.
Dr. Anderson and colleagues have demonstrated the structures of:
CAZy-unclassified Escherichia coli phosphoethanolamine transferase BcsG (6PCZ/6PD0) [1]
GH5 Clostridioides difficile endo-β-glucanase CcsZ (6UJE/6UJF) [2]
CAZy-unclassified Campylobacter jejuni peptidoglycan O-acetyltransferase PatB (8TLB)
- Anderson AC, Burnett AJN, Hiscock L, Maly KE, and Weadge JT. (2020). The Escherichia coli cellulose synthase subunit G (BcsG) is a Zn(2+)-dependent phosphoethanolamine transferase. J Biol Chem. 2020;295(18):6225-6235. DOI:10.1074/jbc.RA119.011668 |
- Scott W, Lowrance B, Anderson AC, and Weadge JT. (2020). Identification of the Clostridial cellulose synthase and characterization of the cognate glycosyl hydrolase, CcsZ. PLoS One. 2020;15(12):e0242686. DOI:10.1371/journal.pone.0242686 |