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| − | '''13 June 2020:''' ''A GH family with lots of unknowns.'' '''[[Glycoside Hydrolase Family 151]]''' is a fairly old family of alpha-L-fucosidases in the CAZy classification, yet a number of key mechanistic and structure-function questions remain to be explored, as we learn in the '''[[GH151]]''' page completed today by '''[[User:Casper Wilkens|Casper Wilkens]]''', '''[[User:David Teze|David Teze]]''', and '''[[User:Birgitte Zeuner|Birgitte Zeuner]]'''. ''See a current example of how information on [[Glycoside Hydrolase Families]] is constantly evolving [[Glycoside Hydrolase Family 151|here]].'' | + | '''31 October 2025:''' ''A spooktacular addition to the CAZypedia family!'' Come and say 'Boo!' to the frighteningly well written '''[[CBM13]]''' ''CAZypedia'' page. The '''[[CBM13]]''' family is a '''[[Carbohydrate-binding_modules#Blurred Lines: CBMs, Lectins and Outliers|lectin-like CBM family]]'''. Its first characterized members were lectins, including the B chain from the highly toxic [https://en.wikipedia.org/wiki/Ricin ricin] toxin from ''Ricinus communis''. This spine tingling read was authored by '''[[User:Scott Mazurkewich|Scott Mazurkewich]]''' and '''[[User:Lauren McKee|Lauren McKee]]''' who also acted as responsible curator. ''Come and visit the scariest of ''CAZypedia'' CBM pages, '''[[CBM13|here!]]'''... if you dare...'' |
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| − | '''10 June 2020:''' ''A new Senior Curator.'' Today we welcome '''[[User:Elizabeth Ficko-Blean|Elizabeth Ficko-Blean]]''' as a '''[[Board of Curators|Senior Curator]]''' in ''CAZypedia''. Over the past ca. 3 years, [[User:Elizabeth Ficko-Blean|Liz]] has been the major force driving the production of the [[Carbohydrate Binding Module Families|many new Carbohydrate Binding Module Family pages now in ''CAZypedia'']] through the active recruitment of [[Author]]s and [[Responsible Curator]]s, as well as a lot of subsequent editorial work. | + | '''29 July 2025:''' ''[[CBM91]] is in the news!'' The xylan binding '''[[CBM91]]''' family ''CAZypedia'' page is up and running. Appended to mainly [[GH43]] xylanases this [[CBM91]] family drives interaction with substrate. The [[CBM91]] page was authored by '''[[User:Daichi Ito|Daichi Ito]]''' who also discovered the initial xylan-binding function which resulted in the creation of the [[CBM91]] CAZy family. ''Read up on this industrially interesting '''[[CBM91]]''' family '''[[CBM91|here]]'''.'' |
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| − | '''10 June 2020:''' ''Back to the origins of CAZy.'' A page on a [[Carbohydrate-binding modules|Carbohydrate Binding Module]] family that was first classified as Cellulose-Binding Domain Family V (CBD V), and has since been renamed in CAZy as '''[[Carbohydrate Binding Module Family 5]]''', is now on-line in ''CAZypedia''. While originally considered to be cellulose-binding domains, there are now several examples of the [[Carbohydrate-binding_modules#Types|type A]] [[CBM5]] members interacting with chitin. Thank you to '''[[User:Manjeet Kaur|Manjeet Kaur]]''' for [[author]]ing the page and to '''[[User:Appa Rao Podile|Appa Rao Podile]]''' for acting as [[Responsible Curator]]. ''Read up on this old school family of CBMs '''[[CBM5|here]]'''.''
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| − | '''10 June 2020:''' ''Continued growth among the esterases.'' The '''[[Carbohydrate Esterase Family 3]]''' page, [[Author]]ed by grad student '''[[User:Stefen Stangherlin|Stefen Stangherlin]]''', was finalized and [[Curator Approved]] by '''[[User:Joel Weadge|Joel Weadge]]''' and '''[[User:Michael Suits|Michael Suits]]''' today. '''[[CE3]]''' comprises a group of specific acetyl-xylan esterases with a rich history of initial discovery, mechanistic analysis, and structural characterization. ''We thank '''[[User:Stefen Stangherlin|Stefen]]''', '''[[User:Joel Weadge|Joel]]''', and '''[[User:Michael Suits|Mike]]''' for contributing yet another page to the growing [[Carbohydrate Esterase Families|CE family section]] in CAZypedia - read more on CE3 '''[[Carbohydrate Esterase Family 3|here]]'''.''
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| − | '''15 May 2020:''' ''CBM20 for 2020!'' The multifunctional starch-disrupting, starch-binding and enzyme targeting [[CBM20]] family is now up and running in ''CAZypedia''. These pervasive CBMs have been identified in CAZy families including [[glycoside hydrolases]] and [[Auxiliary Activity Families|lytic polysaccharide monooxygenases]] but also in non-CAZy enzymes. The page was authored by '''[[User:Marie Sofie Moeller|Marie Sofie Møller]]''' with '''[[User:Birte Svensson|Birte Svensson]]''' and '''[[User:Stefan Janecek|Stefan Janecek]]''' acting as responsible curators. ''Find out more on this starch-interacting family '''[[CBM20|here]]'''.''
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| − | '''15 May 2020:''' ''More on beta(1,3)-glucanases.'' The '''[[Glycoside Hydrolase Family 64]]''' page, [[Author]]ed by '''[[User:Julie Grondin|Julie Grondin]]''', was completed and [[Curator Approved]] today. '''[[GH64]]''' comprises a group of β-1,3-glucanases, primarily from bacteria.The archetype of this family was originally cloned from a ''Streptomyces'' species in the late 1990's and was the subject of mechanistic and structural analysis through the first decade of the new millenium. Notably, analysis by a team led by '''[[User:Bernard Henrissat|Bernard Henrissat]]''' defined that this enzyme, and thus family, uses an [[inverting]] mechanism, further disntiguishing it from well-known [[retaining]] beta(1,3)-glucanases of [[GH16]], [[GH17]], and others, including the recently described [[GH158]] beta(1,3)-glucanases reported below. ''Read more about the unique '''[[Glycoside Hydrolase Family 64|Glycoside Hydrolase Family 64 here]]'''.''
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| − | '''11 May 2020:''' ''Three more from the gut.'' '''[[User:Alan Cartmell|Alan Cartmell]]''' completed no less than three new [[Glycoside Hydrolase Families|Glycoside Hydrolase Family]] pages on this day. '''[[Glycoside Hydrolase Family 137]]''', '''[[Glycoside Hydrolase Family 140]]''', and '''[[Glycoside Hydrolase Family 145]]''' were all created from a series of studies of Polysacchardie Utilization Loci from human gut bacteria by '''[[User:Harry Gilbert|Harry Gilbert]]'s''' group, to which '''[[User:Alan Cartmell|Alan]]''' contributed defining crystallography. '''[[User:Alan Cartmell|Alan]]''' has also taken over the duty of [[Responsible Curator]] of these pages following the retirement of the venerable '''[[User:Harry Gilbert|Professor Gilbert]]''', one of ''CAZypedia's'' [[CAZypedia:History|founding Senior Curators]]. ''Read more about the substrate specificity and structural biology of these three diverse families on their corresponding pages.''
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| − | '''6 May 2020:''' ''CE #1!'' The first [[Carbohydrate Esterase Families|Carbohydrate Esterase Family]] page in the series, '''[[CE1]]''', was [[Curator Approved]] today. [[Author]]ed by '''[[User:Casper Wilkens|Casper Wilkens]]''', the '''[[Carbohydrate Esterase Family 1]]''' page describes an old family of carbohydrate-specific and other esterases, members of which were identified through classical biochemistry before the present age of easy gene cloning and sequencing. Carbohydrate-active members of '''[[CE1]]''' include acetyl xylan esterases, cinnamoyl esterases, and feruloyl esterases responsible for hydrolyzing pendant acyl groups from plant cell wall matrix glycans (hemicelluloses). ''Read more about the long history of '''[[Carbohydrate Esterase Family 1]]''' here.''
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| − | '''10 April 2020:''' ''Yet another new one from the gut.'' Today, [[Author]] '''[[User:Kazune Tamura|Kazune Tamura]]''' completed the '''[[Glycoside Hydrolase Family 158]]''' page. '''[[GH158]]''' emerged in 2019 from a high-throughput biochemical survey of sequences identified as distantly related to [[glycoside hydrolases]] by the CAZy team, who first demonstrated ''endo''-beta(1,3)-glucanase activity for the founding member of the family from the human gut bacterium ''Victivallis vadensis''. Contemporaneously, analysis of homolgos from human gut ''Bacteroides'' species by Guillaume Dejean and '''[[User:Kazune Tamura|Kazune Tamura]]''' resolved details of the specificity, mechanism, and tertiary structure of '''[[GH158]]''' members in Polysaccharide Utilization Loci. ''Read about the detailed history and juicy details of this new GH family '''[[Glycoside Hydrolase Family 158|here]]'''.''
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| − | '''8 April 2020:''' ''Another new one from the gut.'' The '''[[Glycoside Hydrolase Family 164]]''' page, which was [[author]]ed by '''[[User:Zachary Armstrong|Zachary Armstrong]]''', was upgraded to [[Curator Approved]] status by [[Responsible Curator]] '''[[User:Gideon Davies|Gideon Davies]]''' today. '''[[Glycoside Hydrolase Family 164]]''' is yet another newly discovered [[Glycoside Hydrolase Families|GH family]] from a human gut bacterium - this time through a large-scale effort by teams at AFMB and CERMAV spearheaded by [[User:Bernard Henrissat|Bernard Henrissat]]. The founding member of '''[[GH164]]''' is a beta-mannosidase from ''Bacteroides salyersiae'', on which '''[[User:Zachary Armstrong|Zach]]''' and '''[[User:Gideon Davies|Gideon]]''' performed a classic mechanistic and structural analysis to define the central aspects of catalysis in this new family. ''Read more about this new - and currently tiny - GH family '''[[Glycoside Hydrolase Family 164|here]]'''.''
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