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Difference between revisions of "Template:News"
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| + | '''14 May 2014:''' ''Two new CBM pages:'' We are pleased to report that '''[[User:Shinya Fushinobu|Shinya Fushinobu]]''' has produced and given [[Curator Approved]] status to two new [[CBM]] pages. '''[[Carbohydrate Binding Module Family 28]]''' contains Type B CBMs that target non-crystalline beta-glucan chains, while '''[[Carbohydrate Binding Module Family 42]]''' members are Type C CBMs that bind terminal, non-reducing-end L-arabinofuranosyl residues, as found in xylans. Both families are likely to play key role in potentiating biomass degradation by their host organisms, and are therefore relevant to related biotechnological applications. | ||
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'''6 February 2014:''' ''Our second LPMO page:'' '''[[User:Glyn Hemsworth|Glyn Hemsworth]]''' and '''[[User:Gideon Davies|Gideon Davies]]''' have just completed the '''[[Auxiliary Activity Family 11]]''' page. '''[[AA11]]''' is a very recently discovered family of copper-dependent, lytic polysaccharide mono-oxygenases (LPMO), whose defining member catalyzes the oxidative cleavage of chitin. The LPMO field is particularly exciting and rapidly evolving, and we are proud to present the '''[[AA11]]''' page in ''CAZypedia'' so closely after the initial report on this family. | '''6 February 2014:''' ''Our second LPMO page:'' '''[[User:Glyn Hemsworth|Glyn Hemsworth]]''' and '''[[User:Gideon Davies|Gideon Davies]]''' have just completed the '''[[Auxiliary Activity Family 11]]''' page. '''[[AA11]]''' is a very recently discovered family of copper-dependent, lytic polysaccharide mono-oxygenases (LPMO), whose defining member catalyzes the oxidative cleavage of chitin. The LPMO field is particularly exciting and rapidly evolving, and we are proud to present the '''[[AA11]]''' page in ''CAZypedia'' so closely after the initial report on this family. | ||
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Revision as of 13:56, 14 May 2014
14 May 2014: Two new CBM pages: We are pleased to report that Shinya Fushinobu has produced and given Curator Approved status to two new CBM pages. Carbohydrate Binding Module Family 28 contains Type B CBMs that target non-crystalline beta-glucan chains, while Carbohydrate Binding Module Family 42 members are Type C CBMs that bind terminal, non-reducing-end L-arabinofuranosyl residues, as found in xylans. Both families are likely to play key role in potentiating biomass degradation by their host organisms, and are therefore relevant to related biotechnological applications.
6 February 2014: Our second LPMO page: Glyn Hemsworth and Gideon Davies have just completed the Auxiliary Activity Family 11 page. AA11 is a very recently discovered family of copper-dependent, lytic polysaccharide mono-oxygenases (LPMO), whose defining member catalyzes the oxidative cleavage of chitin. The LPMO field is particularly exciting and rapidly evolving, and we are proud to present the AA11 page in CAZypedia so closely after the initial report on this family.
17 January 2014: More on CBMs: The Carbohydrate Binding Module Family 41 page was upgraded to Curator Approved status today by Alicia Lammerts van Bueren and Al Boraston. CBM41 is a family of alpha-glucan-binding modules, which are primarily associated with the pullulanases and debranching enzymes of Glycoside Hydrolase Family 13. Find out more here...!
6 January 2014: A new year, a new CBM page! The Carbohydrate Binding Module Family 6 page was completed and given Curator Approved status today by Author and Curator Mirjam Czjzek. CBM6 was originally defined based on the observation of xylan binding, however the diversity of substrate specificities in this family has now grown to include diverse beta-glucans, chitin, and even the marine polysaccharide agarose; remarkably, some CBM6 members also contain two distinct binding sites. The CBM6 page is CAZypedia's second Carbohydrate Binding Module Family page, and we look forward to the further expansion of this section in the new year!
18 December 2013: A new mannanase page: Today, Rohan Williams and Spencer Williams completed the Glycoside Hydrolase Family 113 page. GH113 is currently a very small family (120 members) with only one characterized member, the Alicyclobacillus acidocaldarius beta(1-4)-mannanase. The seminal crystal structure of this enzyme revealed GH113 to be a member of Clan GH-A. A recent publication from the Williams team and collaborators illuminated further details of the GH113 and GH26 transition states using designed inhibitor-enzyme complexes. Read more about this emerging family here!
New for fall 2013: The CAZy database now presents enzyme ligands! See any family's "Structure" page for examples.