CAZypedia needs your help!
We have many unassigned pages in need of Authors and Responsible Curators. See a page that's out-of-date and just needs a touch-up? - You are also welcome to become a CAZypedian. Here's how.
Scientists at all career stages, including students, are welcome to contribute.
Learn more about CAZypedia's misson here and in this article.
Totally new to the CAZy classification? Read this first.

Difference between revisions of "Syn/anti lateral protonation"

From CAZypedia
Jump to navigation Jump to search
(Added GH186 syn protonator)
 
(124 intermediate revisions by 3 users not shown)
Line 1: Line 1:
<!-- CURATORS: Please delete the {{UnderConstruction}} tag below when the page is ready for wider public consumption -->
+
{{CuratorApproved}}
{{UnderConstruction}}
+
* [[Author]]: [[User:Wim Nerinckx|Wim Nerinckx]]
* [[Author]]: ^^^Wim Nerinckx^^^
+
* [[Responsible Curator]]:  [[User:Spencer Williams|Spencer Williams]]
* [[Responsible Curator]]:  ^^^Spencer Williams^^^
 
  
 
----
 
----
Line 8: Line 7:
 
== Overview ==
 
== Overview ==
  
This page provides a table (and eventually a full lexicon article) on the spatial positioning of the catalytic general acid residue in the active sites of glycoside hydrolases. The table below updates those found in the seminal paper on this concept by Heightman and Vasella <cite>HeightmanVasella1999</cite>, and the more recent summary by Nerinckx ''et al.'' <cite>Nerinckx2005</cite>.
+
This page provides a table that summarizes the spatial positioning of the catalytic [[general acid]] residue in the active sites of [[glycoside hydrolase]]s, relative to the substrate. The table below updates those found in the seminal paper on this concept by Heightman and Vasella <cite>HeightmanVasella1999</cite>, and a following paper by Nerinckx ''et al.'' <cite>Nerinckx2005</cite>.
  
== Table of syn/anti protonation examples ==
+
== Background ==
=== Note ===
 
This table contains only one example per GH-family of a ligand-complexed protein structure where the ''syn'' positioning'' (close to the ring-oxygen of the sugar moiety at subsite -1)'' or ''anti'' positioning ''(at the opposite side of the ring-oxygen, close to C-2)'' of the proton donor can be clearly observed.  Where available, the selected examples are Michaelis-type complexes with the ligand spanning the -1/+1 subsites, since these have an intact glycosidic or thioglycosidic bond or are ''N''-analogs of the substrate (''e.g.'' acarbose).  In some examples, the proton donor has been mutated (''e.g.'', to the corresponding amide or to an alanine), and in those cases one may wish to look at a superposition of the given PDB example with the structure of the native enzyme. If a Michaelis-type complex is not yet available, the second and third example choices, respectively, are trapped glycosyl-enzyme intermediates or product complexes with subsite -1 correctly occupied.
 
  
''Please also be aware that this is a large table with many data, so some (hopefully few) errors may have sneaked in.''
+
The ''"not from above, but from the side"'' concept of semi-lateral glycosidic oxygen [[General_acid/base|protonation]] by [[glycoside hydrolase]]s was introduced by Heightman and Vasella <cite>HeightmanVasella1999</cite>. It was originally only described for [[Anomeric centre (alpha and beta)|beta]]-equatorial [[glycoside hydrolase]]s, but appears to be equally applicable to enzymes acting on an [[Anomeric centre (alpha and beta)|alpha]]-axial glycosidic bond <cite>Nerinckx2005</cite>. When dividing [[Sub-site nomenclature|subsite -1]] into half-spaces by a plane defined by the glycosidic oxygen and C1' and H1' of the –1 glycoside, many ligand-complexed structures reveal that the [[General_acid/base|proton donor]] is positioned either in the ''syn'' half-space (near the ring-oxygen of the –1 glycoside), or in the ''anti'' half-space (on the opposite side of the ring-oxygen). Members of the same GH [[Families|family]] appear to share a common ''syn'' or ''anti'' [[General_acid/base|protonator]] arrangement and further, this specificity appears to be preserved within [[Clans|Clans]] of [[Families|families]]. This page's compilation of [[Sub-site nomenclature|subsite -1]] occupied complexes shows that about 70% of all GH [[Families|families]] are ''anti'' [[General_acid/base|protonators]].
 +
 
 +
Closer inspection of crystal structures of [[Sub-site nomenclature|–1/+1 subsite]]-spanning substrates, or substrate-analogue ligands, in complex with enzymes reveals a further intriguing corollary <cite>Nerinckx2005 Wu2012</cite>. In substrate-bound complexes with ''anti'' [[General_acid/base|protonating]] GH enzymes, the scissile [[Anomeric centre (alpha and beta)|anomeric bond]] (often studied using the thio-analogue) shows a dihedral angle φ (O5'-C1'-[O,S]x-Cx) that is in the lowest-energy synclinal (gauche) conformation. The rationale for this is that a minus synclinal dihedral angle φ for an equatorial glycosidic bond, or plus synclinal for an axial glycosidic bond <cite>Perez1978</cite>, allows for hyperconjugative overlap of the C1'-O5' antibonding orbital with an antiperiplanar-oriented lone pair orbital lobe of the glycosidic oxygen, thereby creating partial double bond character and stabilization of the glycosidic bond by 4–5 kcal/mol; this ground-state stabilizing phenomenon is known as the ‘exo-anomeric effect’ <cite>Cramer1997 Johnson2009 Alonso2016</cite>. ''Anti'' [[General_acid/base|protonation]] occurs on the glycosidic oxygen’s antiperiplanar lone pair, thereby removing the stabilizing exo-anomeric effect. This suggests that ''anti'' [[General_acid/base|protonation]] is an enzymic approach for lowering the activation barrier leading to the [[Transition state|transition state]] (Figure 1 centre).
 +
 
 +
''Syn'' [[General_acid/base|protonating]] [[glycoside hydrolase]]s apparently make use of a different approach <cite>Nerinckx2005 Wu2012</cite>. In many [[Sub-site nomenclature|–1/+1 subsite]]-spanning ligand complexes, the dihedral angle φ of the scissile anomeric bond has been rotated away from its lowest-energy synclinal position: clockwise to minus-anticlinal or antiperiplanar for beta-equatorial; counterclockwise to plus-anticlinal or antiperiplanar for alpha-axial [[Anomeric centre (alpha and beta)|anomeric bonds]]. This removes the hyperconjugative overlap and thus also the stabilizing exo-anomeric effect. And because of this rotation, a lone pair of the glycosidic oxygen is directed into the ''syn'' half-space, allowing it to be protonated by the ''syn''-positioned [[General_acid/base|proton donor]] (Figure 1 right).
 +
 
 +
[[File:Syn_anti.jpg|800px|thumb|center|Figure 1. Newman projections, with the glycosidic oxygen as proximal atom and the anomeric carbon as distal atom, showing ''anti'' (centre) versus ''syn'' (right) semi-lateral [[General_acid/base|protonation]] in beta-equatorial (top) and alpha-axial (bottom) [[glycoside hydrolase]]s. The indicated φ is the dihedral angle for O5'-C1'-O4-C4.]]
 +
 
 +
== Table of ''syn/anti'' protonation examples ==
 +
 
 +
This table contains only one example per GH [[Families|family]] of a ligand-complexed protein structure where the ''syn'' or ''anti'' positioning of the [[General_acid/base|proton donor]] can be clearly observed; other examples may be available on a [[Families|family-by-family]] basis. The reader is thus advised to consult the [http://www.cazy.org/fam/acc_GH.html#table CAZy database] for a current, comprehensive list of CAZyme structures. Where available, the selected examples are Michaelis-type complexes with the ligand spanning the [[Sub-site nomenclature|-1/+1 subsites]], since these have an intact glycosidic or thioglycosidic bond, or are ''N''-analogs of the substrate (''e.g.'' acarbose). In some examples, the [[General_acid/base|proton donor]] has been mutated (''e.g.'', to the corresponding amide or to an alanine), and in those cases one may wish to look at a superposition of the given PDB example with the structure of the native enzyme. If a Michaelis-type complex is not yet available, the second and third example choices, respectively, are trapped glycosyl-enzyme [[intermediate]]s and product complexes where [[Sub-site nomenclature|subsite -1]] is occupied.
 +
 
 +
''Please also be aware that this is a large table with many data. Please contact the page Author or Responsible Curator with corrections.''
  
 
=== Table ===
 
=== Table ===
This table can be re-sorted by clicking on the icons in the header (''javascript must be turned on in your browser'').  To reset the page to be sorted by GH family, click the ''page'' tab above the page title.
+
This table can be re-sorted by clicking on the icons in the header (''javascript must be turned on in your browser'').  To reset the page to be sorted by GH family, click the ''View'' tab at the very top of the page.
  
 
{| {{Prettytable}} class="sortable"
 
{| {{Prettytable}} class="sortable"
Line 38: Line 47:
 
| A
 
| A
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}2cer 2cer]
 
| [{{PDBlink}}2cer 2cer]
 
| β-glycosidase S
 
| β-glycosidase S
 
| ''Sulfolobus solfataricus'' P2
 
| ''Sulfolobus solfataricus'' P2
| phenethyl glucoimidazol
+
| phenethyl glucoimidazole
| Glu206
+
| '''Glu206'''
 
| Glu387
 
| Glu387
 
| <cite>Gloster2006</cite>
 
| <cite>Gloster2006</cite>
Line 52: Line 61:
 
| A
 
| A
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}} / alpha-{{Smallcaps|l}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}2vzu 2vzu]
 
| [{{PDBlink}}2vzu 2vzu]
 
| exo-β-glucosaminidase
 
| exo-β-glucosaminidase
 
| ''Amicolatopsis orientalis''
 
| ''Amicolatopsis orientalis''
 
| PNP-β-{{Smallcaps|d}}-glucosamine
 
| PNP-β-{{Smallcaps|d}}-glucosamine
| Glu469
+
| '''Glu469'''
 
| Glu541
 
| Glu541
 
| <cite>van_Bueren2009</cite>
 
| <cite>van_Bueren2009</cite>
Line 66: Line 75:
 
| none
 
| none
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}} / alpha-{{Smallcaps|l}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}1iex 1iex]
 
| [{{PDBlink}}1iex 1iex]
 
| exo-1,3-1,4-glucanase
 
| exo-1,3-1,4-glucanase
 
| ''Hordeum vulgare''
 
| ''Hordeum vulgare''
 
| thiocellobiose
 
| thiocellobiose
| Glu491
+
| '''Glu491'''
 
| Asp285
 
| Asp285
 
| <cite>Hrmova2001</cite>
 
| <cite>Hrmova2001</cite>
 +
|-
 +
| [[GH4]]
 +
| none
 +
| Rossmann + α6/β3 + β3/α4
 +
| beta-{{Smallcaps|d}}
 +
| retaining
 +
| '''''anti'''''
 +
| [{{PDBlink}}1u8x 1u8x]
 +
| 6-P-α-glucosidase
 +
| ''Bacillus subtilis''
 +
| alpha-{{Smallcaps|d}}-glucose-6-phosphate
 +
| '''Asp172'''
 +
| not applicable
 +
| <cite>Rajan2004</cite>
 
|-
 
|-
 
| [[GH5]]
 
| [[GH5]]
 
| A
 
| A
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}1h2j 1h2j]
 
| [{{PDBlink}}1h2j 1h2j]
 
| endo-β-1,4-glucanase
 
| endo-β-1,4-glucanase
 
| ''Bacillus agaradhaerens''
 
| ''Bacillus agaradhaerens''
 
| 2',4'-DNP-2-F-cellobioside
 
| 2',4'-DNP-2-F-cellobioside
| Glu129
+
| '''Glu129'''
 
| Glu228
 
| Glu228
 
| <cite>Varrot2003</cite>
 
| <cite>Varrot2003</cite>
Line 94: Line 117:
 
| none
 
| none
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| inverting
 
| inverting
| ''syn''
+
| '''''syn'''''
 
| [{{PDBlink}}1qjw 1qjw]
 
| [{{PDBlink}}1qjw 1qjw]
 
| cellobiohydrolase 2
 
| cellobiohydrolase 2
 
| ''Hypocrea jecorina''
 
| ''Hypocrea jecorina''
 
| (Glc)<sub>2</sub>-S-(Glc)<sub>2</sub>
 
| (Glc)<sub>2</sub>-S-(Glc)<sub>2</sub>
| Asp221
+
| '''Asp221'''
 
| debated
 
| debated
 
| <cite>Zhou1999</cite>
 
| <cite>Zhou1999</cite>
Line 108: Line 131:
 
| B
 
| B
 
| β-jelly roll
 
| β-jelly roll
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''syn''
+
| '''''syn'''''
 
| [{{PDBlink}}1ovw 1ovw]
 
| [{{PDBlink}}1ovw 1ovw]
 
| endo-1,4-glucanase
 
| endo-1,4-glucanase
 
| ''Fusarium oxysporum''
 
| ''Fusarium oxysporum''
 
| thio-(Glc)<sub>5</sub>
 
| thio-(Glc)<sub>5</sub>
| Glu202
+
| '''Glu202'''
 
| Glu197
 
| Glu197
 
| <cite>Sulzenbacher1999</cite>
 
| <cite>Sulzenbacher1999</cite>
Line 122: Line 145:
 
| M
 
| M
 
| (α/α)<sub>6</sub>
 
| (α/α)<sub>6</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| inverting
 
| inverting
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}1kwf 1kwf]
 
| [{{PDBlink}}1kwf 1kwf]
 
| endo-1,4-glucanase
 
| endo-1,4-glucanase
 
| ''Clostridium thermocellum''
 
| ''Clostridium thermocellum''
 
| cellopentaose
 
| cellopentaose
| Glu95
+
| '''Glu95'''
 
| Asp278
 
| Asp278
 
| <cite>Guerin2002</cite>
 
| <cite>Guerin2002</cite>
Line 136: Line 159:
 
| none
 
| none
 
| (α/α)<sub>6</sub>
 
| (α/α)<sub>6</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| inverting
 
| inverting
| ''syn''
+
| '''''syn'''''
 
| [{{PDBlink}}1rq5 1rq5]
 
| [{{PDBlink}}1rq5 1rq5]
 
| cellobiohydrolase
 
| cellobiohydrolase
 
| ''Clostridium thermocellum''
 
| ''Clostridium thermocellum''
 
| cellotetraose
 
| cellotetraose
| Glu795
+
| '''Glu795'''
 
| Asp383
 
| Asp383
 
| <cite>Schubot2004</cite>
 
| <cite>Schubot2004</cite>
Line 150: Line 173:
 
| A
 
| A
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}2d24 2d24]
 
| [{{PDBlink}}2d24 2d24]
 
| β-1,4-xylanase
 
| β-1,4-xylanase
 
| ''Streptomyces olivaceoviridis'' E-86
 
| ''Streptomyces olivaceoviridis'' E-86
 
| xylopentaose
 
| xylopentaose
| Glu128
+
| '''Glu128'''
 
| Glu236
 
| Glu236
 
| <cite>Suzuki2009</cite>
 
| <cite>Suzuki2009</cite>
Line 164: Line 187:
 
| C
 
| C
 
| β-jelly roll
 
| β-jelly roll
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''syn''
+
| '''''syn'''''
| [{{PDBlink}}1bvv 1bvv]
+
| [{{PDBlink}}4hk8 4hk8]
| xylanase
+
| endo-β-1,4-xylanase
| ''Bacillus circulans''
+
| ''Hypocrea jecorina''
| Xyl-2-F-xylosyl
+
| xylohexaose
| Glu172
+
| '''Glu177'''
| Glu78
+
| Glu86
| <cite>Sidhu1999</cite>
+
| <cite>Wan2014</cite>
 
|-
 
|-
 
| [[GH12]]
 
| [[GH12]]
 
| C
 
| C
 
| β-jelly roll
 
| β-jelly roll
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''syn''
+
| '''''syn'''''
 
| [{{PDBlink}}1w2u 1w2u]
 
| [{{PDBlink}}1w2u 1w2u]
 
| endoglucanase
 
| endoglucanase
 
| ''Humicola grisea''
 
| ''Humicola grisea''
 
| thiocellotetraose
 
| thiocellotetraose
| Glu205
+
| '''Glu205'''
 
| Glu120
 
| Glu120
 
| <cite>Sandgren2004</cite>
 
| <cite>Sandgren2004</cite>
Line 192: Line 215:
 
| H
 
| H
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| alpha
+
| alpha-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}1cxk 1cxk]
 
| [{{PDBlink}}1cxk 1cxk]
 
| β-cyclodextrin glucanotransferase
 
| β-cyclodextrin glucanotransferase
 
| ''Bacillus circulans''
 
| ''Bacillus circulans''
 
| maltononaose
 
| maltononaose
| Glu257
+
| '''Glu257'''
 
| Asp229
 
| Asp229
 
| <cite>Uitdehaag1999</cite>
 
| <cite>Uitdehaag1999</cite>
Line 206: Line 229:
 
| none
 
| none
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| alpha
+
| alpha-{{Smallcaps|d}}
 
| inverting
 
| inverting
| ''syn''
+
| '''''syn'''''
 
| [{{PDBlink}}1itc 1itc]
 
| [{{PDBlink}}1itc 1itc]
 
| β-amylase
 
| β-amylase
 
| ''Bacillus cereus''
 
| ''Bacillus cereus''
 
| maltopentaose
 
| maltopentaose
| Glu172
+
| '''Glu172'''
 
| Glu367
 
| Glu367
 
| <cite>Miyake2003</cite>
 
| <cite>Miyake2003</cite>
Line 220: Line 243:
 
| L
 
| L
 
| (α/α)<sub>6</sub>
 
| (α/α)<sub>6</sub>
| alpha
+
| alpha-{{Smallcaps|d}}
 
| inverting
 
| inverting
| ''syn''
+
| '''''anti'''''
| [{{PDBlink}}1gah 1gah]
+
| [{{PDBlink}}1dog 1dog]
 
| glucoamylase
 
| glucoamylase
 
| ''Aspergillus awamori''
 
| ''Aspergillus awamori''
| acarbose
+
| 1-deoxynojirimycin
| Glu179
+
| '''Glu179'''
 
| Glu400
 
| Glu400
| <cite>Aleshin1996</cite>
+
| <cite>Harris1993</cite>
 
|-
 
|-
 
| [[GH16]]
 
| [[GH16]]
 
| B
 
| B
 
| β-jelly roll
 
| β-jelly roll
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''syn''
+
| '''''syn'''''
 
| [{{PDBlink}}1urx 1urx]
 
| [{{PDBlink}}1urx 1urx]
 
| β-agarase A
 
| β-agarase A
 
| ''Zobellia galactanivorans''
 
| ''Zobellia galactanivorans''
 
| oligoagarose
 
| oligoagarose
| Glu152
+
| '''Glu152'''
 
| Glu147
 
| Glu147
 
| <cite>Allouch2004</cite>
 
| <cite>Allouch2004</cite>
Line 248: Line 271:
 
| A
 
| A
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''predicted anti by clan''
+
| '''''anti'''''
| ''see e.g. at GH1''
+
| [{{PDBlink}}4gzj 4gzj]
|  
+
| endo-β-1,3-glucanase
|  
+
| ''Solanum tuberosum''
|  
+
| laminaratriose + laminarabiose
|  
+
| '''Glu118'''
|  
+
| Glu259
|  
+
| <cite>Wojtkowiak2013</cite>
 
|-
 
|-
 
| [[GH18]]
 
| [[GH18]]
 
| K
 
| K
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}1ffr 1ffr]
 
| [{{PDBlink}}1ffr 1ffr]
 
| chitinase A
 
| chitinase A
 
| ''Serratia marcescens''
 
| ''Serratia marcescens''
 
| (NAG)<sub>6</sub>
 
| (NAG)<sub>6</sub>
| Glu315
+
| '''Glu315'''
 
| internal
 
| internal
 
| <cite>Papanikolau2001</cite>
 
| <cite>Papanikolau2001</cite>
 +
|-
 +
| [[GH19]]
 +
| none
 +
| lysozyme type
 +
| beta-{{Smallcaps|d}}
 +
| inverting
 +
| '''''syn'''''
 +
| [{{PDBlink}}3wh1 3wh1]
 +
| chitinase
 +
| ''Bryum coronatum''
 +
| (GlcNAc)<sub>4</sub>
 +
| '''Glu61'''
 +
| Glu70
 +
| <cite>Ohnuma2014</cite>
 
|-
 
|-
 
| [[GH20]]
 
| [[GH20]]
 
| K
 
| K
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}1c7s 1c7s]
 
| [{{PDBlink}}1c7s 1c7s]
 
| chitobiase
 
| chitobiase
 
| ''Serratia marcescens''
 
| ''Serratia marcescens''
 
| chitobiose
 
| chitobiose
| Glu540
+
| '''Glu540'''
 
| internal
 
| internal
 
| <cite>Prag2000</cite>
 
| <cite>Prag2000</cite>
Line 290: Line 327:
 
| none
 
| none
 
| lysozyme type
 
| lysozyme type
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''syn''
+
| '''''syn'''''
 
| [{{PDBlink}}1h6m 1h6m]
 
| [{{PDBlink}}1h6m 1h6m]
 
| lysozyme C
 
| lysozyme C
 
| ''Gallus gallus''
 
| ''Gallus gallus''
 
| Chit-2-F-chitosyl
 
| Chit-2-F-chitosyl
| Glu35
+
| '''Glu35'''
 
| Asp52
 
| Asp52
 
| <cite>Vocadlo2001</cite>
 
| <cite>Vocadlo2001</cite>
Line 304: Line 341:
 
| none
 
| none
 
| lysozyme type
 
| lysozyme type
| beta
+
| beta-{{Smallcaps|d}}
 
| inverting
 
| inverting
| ''syn''
+
| '''''syn'''''
 
| [{{PDBlink}}1lsp 1lsp]
 
| [{{PDBlink}}1lsp 1lsp]
 
| lysozyme G
 
| lysozyme G
 
| ''Cygnus atratus''
 
| ''Cygnus atratus''
 
| Bulgecin A
 
| Bulgecin A
| Glu73
+
| '''Glu73'''
 
| internal
 
| internal
 
| <cite>Karlsen1996</cite>
 
| <cite>Karlsen1996</cite>
Line 318: Line 355:
 
| I
 
| I
 
| α + β
 
| α + β
| beta
+
| beta-{{Smallcaps|d}}
 
| inverting
 
| inverting
| ''syn''
+
| '''''syn'''''
 
| [{{PDBlink}}148l 148l]
 
| [{{PDBlink}}148l 148l]
 
| lysozyme E
 
| lysozyme E
 
| Bacteriophage T4
 
| Bacteriophage T4
 
| chitobiosyl
 
| chitobiosyl
| Glu11
+
| '''Glu11'''
 
| Glu26
 
| Glu26
 
| <cite>Baldwin1993</cite>
 
| <cite>Baldwin1993</cite>
Line 332: Line 369:
 
| A
 
| A
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
| [{{PDBlink}}1gw1 1gw1]
+
| [{{PDBlink}}2vx6 2vx6]
| mannanase A
+
| exo-β-mannanase
| ''Cellvibrio japonicus''
+
| ''Cellvibrio japonicus'' Ueda107
| 2',4'-DNP-2-F-cellotrioside
+
| Gal1Man4
| Glu212
+
| '''Glu221'''
| Glu320
+
| Glu338
| <cite>Ducros2002</cite>
+
| <cite>Cartmell2008</cite>
 
|-
 
|-
 
| [[GH27]]
 
| [[GH27]]
 
| D
 
| D
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| alpha
+
| alpha-{{Smallcaps|d}} / beta-{{Smallcaps|l}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
| [{{PDBlink}}1ktc 1ktc]
+
| [{{PDBlink}}3lrm 3lrm]
| α-''N''-acetyl galactosaminidase
+
| α-galactosidase
| ''Gallus gallus''
+
| ''Saccharomyces cerevisiae''
| NAGal
+
| raffinose
| Asp201
+
| '''Asp209'''
| Asp410
+
| Asp141
| <cite>Garman2002</cite>
+
| <cite>Fernandez-Leiro2010</cite>
 
|-
 
|-
 
| [[GH28]]
 
| [[GH28]]
 
| N
 
| N
 
| β-helix
 
| β-helix
| alpha
+
| alpha-{{Smallcaps|d}} (and α-{{Smallcaps|l}}-rham)
 
| inverting
 
| inverting
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}2uvf 2uvf]
 
| [{{PDBlink}}2uvf 2uvf]
 
| exo-polygalacturonosidase
 
| exo-polygalacturonosidase
 
| ''Yersinia enterocolitica'' ATCC9610D
 
| ''Yersinia enterocolitica'' ATCC9610D
 
| digalacturonic acid
 
| digalacturonic acid
| Asp402
+
| '''Asp402'''
 
| Asp381 Asp403
 
| Asp381 Asp403
 
| <cite>Abbott2007</cite>
 
| <cite>Abbott2007</cite>
 
|-
 
|-
 
| [[GH29]]
 
| [[GH29]]
| none
+
| R
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| alpha
+
| alpha-{{Smallcaps|l}}
 
| retaining
 
| retaining
| ''syn''
+
| '''''syn'''''
| [{{PDBlink}}1hl9 1hl9]
+
| [{{PDBlink}}3uet 3uet]
| α-{{Smallcaps|l}}-fucosidase
+
| α-1,3/4-fucosidase
| ''Thermotoga maritima''
+
| ''Bifidobacterium longum'' subsp. infantis
| 2-F-fuco- pyranosyl
+
| lacto-''N''-fucopentaose II
| Glu266
+
| '''Glu217'''
| Asp224
+
| Asp172
| <cite>Sulzenbacher2004</cite>
+
| <cite>Sakurama2012</cite>
 
|-
 
|-
 
| [[GH30]]
 
| [[GH30]]
 
| A
 
| A
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
| [{{PDBlink}}2v3d 2v3d]
+
| [{{PDBlink}}2y24 2y24]
| glucocerebrosidase 1
+
| glucurono-xylanase
| ''Homo sapiens''
+
| ''Dickea chrysanthemi'' D1
| ''N''-butyl-deoxynojirimycin
+
| glucuronoxylan tetrasaccharide
| Glu235
+
| '''Glu163'''
| Glu340
+
| Glu253
| <cite>Brumshtein2007</cite>
+
| <cite>Urbanikova2011</cite>
 
|-
 
|-
 
| [[GH31]]
 
| [[GH31]]
 
| D
 
| D
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| alpha
+
| alpha-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}2qmj 2qmj]
 
| [{{PDBlink}}2qmj 2qmj]
 
| maltase-glucoamylase
 
| maltase-glucoamylase
 
| ''Homo sapiens''
 
| ''Homo sapiens''
 
| acarbose
 
| acarbose
| Asp542
+
| '''Asp542'''
 
| Asp443
 
| Asp443
 
| <cite>Sim2008</cite>
 
| <cite>Sim2008</cite>
Line 416: Line 453:
 
| J
 
| J
 
| 5-fold β-propeller
 
| 5-fold β-propeller
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}2add 2add]
 
| [{{PDBlink}}2add 2add]
 
| fructan β-(2,1)-fructosidase  
 
| fructan β-(2,1)-fructosidase  
 
| ''Cichorium intybus''
 
| ''Cichorium intybus''
 
| sucrose
 
| sucrose
| Glu201
+
| '''Glu201'''
 
| Asp22
 
| Asp22
 
| <cite>Verhaest2007</cite>
 
| <cite>Verhaest2007</cite>
Line 430: Line 467:
 
| E
 
| E
 
| 6-fold β-propeller
 
| 6-fold β-propeller
| alpha
+
| alpha-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}1s0i 1s0i]
 
| [{{PDBlink}}1s0i 1s0i]
| trans-sialidase
+
| transsialidase
 
| ''Trypanosoma cruzi''
 
| ''Trypanosoma cruzi''
| sialyl-lactose
+
| sialyllactose
| Asp59
+
| '''Asp59'''
 
| Tyr342
 
| Tyr342
 
| <cite>Amaya2004</cite>
 
| <cite>Amaya2004</cite>
Line 444: Line 481:
 
| E
 
| E
 
| 6-fold β-propeller
 
| 6-fold β-propeller
| alpha
+
| alpha-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
| [{{PDBlink}}2bat 2bat]
+
| [{{PDBlink}}4gzw 4gzw]
| neuraminidase
+
| N2 neuraminidase
| ''Influenza'' A virus
+
| ''Influenza'' A Tanzania/205/2010 H3N2
| sialic acid
+
| α-{{Smallcaps|d}}-Neup5Ac-(2,3)-β-{{Smallcaps|d}}-Galp-(1,4)-β-{{Smallcaps|d}}-GlcpNAc
| Asp151
+
| '''Asp151'''
 
| Tyr406
 
| Tyr406
| <cite>Varghese1992</cite>
+
| <cite>Zhu2012</cite>
 
|-
 
|-
 
| [[GH35]]
 
| [[GH35]]
 
| A
 
| A
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
| [{{PDBlink}}1xc6 1xc6]
+
| [{{PDBlink}}3ogv 3ogv]
 
| β-galactosidase
 
| β-galactosidase
| ''Penicillium sp.''
+
| ''Hypocrea jecorina''
| {{Smallcaps|d}}-galactose
+
| 2-phenylethyl 1-thio-β-{{Smallcaps|d}}-galactopyranoside
| Glu200
+
| '''Glu200'''
| Glu299
+
| Glu298
| <cite>Rojas2004</cite>
+
| <cite>Maksimainen2011</cite>
 +
|-
 +
| [[GH36]]
 +
| D
 +
| (β/α)<sub>8</sub>
 +
| alpha-{{Smallcaps|d}}
 +
| retaining
 +
| '''''anti'''''
 +
| [{{PDBlink}}4fnu 4fnu]
 +
| β-galactosidase
 +
| ''Geobacillus stearothermophilus''
 +
| stachyose
 +
| '''Asp584'''
 +
| Asp478
 +
| <cite>Merceron2012</cite>
 
|-
 
|-
 
| [[GH37]]
 
| [[GH37]]
 
| G
 
| G
 
| (α/α)<sub>6</sub>
 
| (α/α)<sub>6</sub>
| alpha
+
| alpha-{{Smallcaps|d}}
 
| inverting
 
| inverting
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}2jf4 2jf4]
 
| [{{PDBlink}}2jf4 2jf4]
 
| trehalase
 
| trehalase
| ''Escherechia coli''
+
| ''Escherichia coli''
 
| validoxylamine
 
| validoxylamine
| Asp312
+
| '''Asp312'''
 
| Glu496
 
| Glu496
 
| <cite>Gibson2007</cite>
 
| <cite>Gibson2007</cite>
Line 486: Line 537:
 
| none
 
| none
 
| (β/α)<sub>7</sub>
 
| (β/α)<sub>7</sub>
| alpha
+
| alpha-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
| [{{PDBlink}}1qwn 1qwn]
+
| [{{PDBlink}}3czn 3czn]
| α-mannosidase II
+
| Golgi α-mannosidase II
 
| ''Drosophila melanogaster''
 
| ''Drosophila melanogaster''
| 5-F-β-{{Smallcaps|l}}-gulosyl
+
| GlcNAcMan(5)GlcNAc(2)
| Asp341
+
| '''Asp341'''
 
| Asp204
 
| Asp204
| <cite>Numao2003</cite>
+
| <cite>Shah2008</cite>
 
|-
 
|-
 
| [[GH39]]
 
| [[GH39]]
 
| A
 
| A
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}} / alpha-{{Smallcaps|l}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
| [{{PDBlink}}1uhv 1uhv]
+
| [{{PDBlink}}2bfg 2bfg]
 
| β-xylosidase
 
| β-xylosidase
| ''Thermoanaerobacterium saccharolyticum''
+
| ''Geobacillus stearothermophilus''
| 2-F-xylosyl
+
| 2,5-dinitrophenyl-β-{{Smallcaps|d}}-xyloside
| Glu160
+
| '''Glu160'''
| Glu277
+
| Glu278
| <cite>Yang2004</cite>
+
| <cite>Czjzek2005</cite>
 
|-
 
|-
 
| [[GH42]]
 
| [[GH42]]
 
| A
 
| A
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}} / alpha-{{Smallcaps|l}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
| [{{PDBlink}}1kwk 1kwk]
+
| [{{PDBlink}}4ucf 4ucf]
 
| β-galactosidase
 
| β-galactosidase
| ''Thermus thermophylus'' A4
+
| ''Bifidobacterium bifidum''
 
| {{Smallcaps|d}}-galactose
 
| {{Smallcaps|d}}-galactose
| Glu141
+
| '''Glu161'''
| Glu312
+
| Glu320
| <cite>Hidaka2002</cite>
+
| <cite>Godoy2016</cite>
 +
|-
 +
| [[GH43]]
 +
| F
 +
| 5-fold β-propeller
 +
| beta-{{Smallcaps|d}} / alpha-{{Smallcaps|l}}
 +
| inverting
 +
| '''''anti'''''
 +
| [{{PDBlink}}3akh 3akh]
 +
| exo-1,5-α-{{Smallcaps|l}}-arabinofuranosidase
 +
| ''Streptomyces avermitilis''
 +
| α-1,5-arabinofuranotriose
 +
| '''Glu196'''
 +
| Asp220
 +
| <cite>Fujimoto2010</cite>
 
|-
 
|-
 
| [[GH44]]
 
| [[GH44]]
 
| none
 
| none
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}2eqd 2eqd]
 
| [{{PDBlink}}2eqd 2eqd]
 
| endoglucanase
 
| endoglucanase
 
| ''Clostridium thermocellum''
 
| ''Clostridium thermocellum''
 
| cellooctaose
 
| cellooctaose
| Glu186
+
| '''Glu186'''
 
| Glu359
 
| Glu359
 
| <cite>Kitago2007</cite>
 
| <cite>Kitago2007</cite>
Line 541: Line 606:
 
| [[GH45]]
 
| [[GH45]]
 
| none
 
| none
| 6-strand. β-barrel
+
| 6-stranded β-barrel
| beta
+
| beta-{{Smallcaps|d}}
 
| inverting
 
| inverting
| ''syn''
+
| '''''syn'''''
 
| [{{PDBlink}}4eng 4eng]
 
| [{{PDBlink}}4eng 4eng]
 
| endo-1,4-glucanase
 
| endo-1,4-glucanase
 
| ''Humicola insolens''
 
| ''Humicola insolens''
 
| cellohexaose
 
| cellohexaose
| Asp121
+
| '''Asp121'''
 
| Asp10
 
| Asp10
 
| <cite>Davies1996</cite>
 
| <cite>Davies1996</cite>
Line 555: Line 620:
 
| [[GH46]]
 
| [[GH46]]
 
| I
 
| I
| α + β
+
| lysozyme type
| beta
+
| beta-{{Smallcaps|d}}
 
| inverting
 
| inverting
| ''predicted syn by clan''
+
| '''''syn'''''
| ''see at GH24''
+
| [{{PDBlink}}4olt 4olt]
|  
+
| chitosanase
|  
+
| ''Microbacterium sp.'' OU01
|  
+
| hexa-glucosamine
|  
+
| '''Glu25'''
|  
+
| Asp43
|  
+
| <cite>Lyu2014</cite>
 
|-
 
|-
 
| [[GH47]]
 
| [[GH47]]
 
| none
 
| none
 
| (α/α)<sub>7</sub>
 
| (α/α)<sub>7</sub>
| alpha
+
| alpha-{{Smallcaps|d}}
 
| inverting
 
| inverting
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}1x9d 1x9d]
 
| [{{PDBlink}}1x9d 1x9d]
 
| α-mannosidase I
 
| α-mannosidase I
 
| ''Homo sapiens''
 
| ''Homo sapiens''
 
| Me-2-S-(α-Man)-2-thio-α-Man
 
| Me-2-S-(α-Man)-2-thio-α-Man
| Asp463
+
| '''Asp463'''
 
| Glu599
 
| Glu599
 
| <cite>Karaveg2005</cite>, <cite>Nerinckx2008</cite>
 
| <cite>Karaveg2005</cite>, <cite>Nerinckx2008</cite>
Line 584: Line 649:
 
| M
 
| M
 
| (α/α)<sub>6</sub>
 
| (α/α)<sub>6</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| inverting
 
| inverting
 
| ''predicted anti by clan''
 
| ''predicted anti by clan''
Line 598: Line 663:
 
| N
 
| N
 
| β-helix
 
| β-helix
| alpha
+
| alpha-{{Smallcaps|d}}
 
| inverting
 
| inverting
 
| ''predicted anti by clan''
 
| ''predicted anti by clan''
Line 612: Line 677:
 
| A
 
| A
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''predicted anti by clan''
+
| '''''anti'''''
| ''see e.g. at GH1''
+
| [{{PDBlink}}4bq5 4bq5]
|  
+
| exo-β-agarase
|  
+
| ''Saccharophagus degradans''
|  
+
| neoagarotetraose
|  
+
| '''Glu535'''
|  
+
| Glu695
|  
+
| <cite>Pluvinage2013</cite>
 
|-
 
|-
 
| [[GH51]]
 
| [[GH51]]
 
| A
 
| A
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| alpha
+
| beta-{{Smallcaps|d}} / alpha-{{Smallcaps|l}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}1qw9 1qw9]
 
| [{{PDBlink}}1qw9 1qw9]
| α-{{Smallcaps|l}}-arabino- furanosidase
+
| α-{{Smallcaps|l}}-arabinofuranosidase
 
| ''Geobacillus stearothermophilus''
 
| ''Geobacillus stearothermophilus''
| PNP-{{Smallcaps|l}}-arabino-furanoside
+
| PNP-{{Smallcaps|l}}-arabinofuranoside
| Glu175
+
| '''Glu175'''
 
| Glu294
 
| Glu294
 
| <cite>Hoevel2003</cite>
 
| <cite>Hoevel2003</cite>
 +
|-
 +
| [[GH52]]
 +
| O
 +
| (α/α)<sub>6</sub>
 +
| beta-{{Smallcaps|d}}
 +
| retaining
 +
| '''''anti'''''
 +
| [{{PDBlink}}4c1p 4c1p]
 +
| β-xylosidase
 +
| ''Geobacillus thermoglucosidasius''
 +
| xylobiose
 +
| '''Asp517'''
 +
| Glu537
 +
| <cite>Espina2014</cite>
 
|-
 
|-
 
| [[GH53]]
 
| [[GH53]]
 
| A
 
| A
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''predicted anti by clan''
+
| '''''anti'''''
| ''see e.g. at GH1''
+
| [{{PDBlink}}2ccr 2ccr]
|  
+
| β-1,4-galactanase
|  
+
| ''Bacillus licheniformis''
|  
+
| galactotriose
|  
+
| '''Glu165'''
|  
+
| Glu263
|  
+
| <cite>Le_Nours2009</cite>
 
|-
 
|-
 
| [[GH54]]
 
| [[GH54]]
 
| none
 
| none
 
| β-sandwich
 
| β-sandwich
| alpha
+
| beta-{{Smallcaps|d}} / alpha-{{Smallcaps|l}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}1wd4 1wd4]
 
| [{{PDBlink}}1wd4 1wd4]
| α-{{Smallcaps|l}}-arabino- furanosidase B
+
| α-{{Smallcaps|l}}-arabinofuranosidase B
 
| ''Aspergillus kawachii''
 
| ''Aspergillus kawachii''
 
| {{Smallcaps|l}}-arabinofuranose
 
| {{Smallcaps|l}}-arabinofuranose
| Asp297
+
| '''Asp297'''
 
| Glu221
 
| Glu221
 
| <cite>Miyanaga2004</cite>
 
| <cite>Miyanaga2004</cite>
Line 668: Line 747:
 
| none
 
| none
 
| β-helix
 
| β-helix
| beta
+
| beta-{{Smallcaps|d}}
 
| inverting
 
| inverting
| ''anti''
+
| '''''syn'''''
| [{{PDBlink}}3eqo 3eqo]
+
| [{{PDBlink}}4tz5 4tz5]
| β-1,3-glucanase
+
| exo-β-1,3-glucanase
| ''Phanerochaete chrysosporium'' K-3
+
| ''Streptomyces sp.'' SirexAA-E
| {{Smallcaps|d}}-gluconolacton
+
| laminarihexaose
| Glu633
+
| '''Glu502'''
 
| unknown
 
| unknown
| <cite>Ishida2009</cite>
+
| <cite>Bianchetti2015</cite>
 
|-
 
|-
 
| [[GH56]]
 
| [[GH56]]
 
| none
 
| none
 
| (β/α)<sub>7</sub>
 
| (β/α)<sub>7</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}1fcv 1fcv]
 
| [{{PDBlink}}1fcv 1fcv]
 
| hyaluronidase
 
| hyaluronidase
 
| ''Apis mellifera''
 
| ''Apis mellifera''
 
| (hyaluron.)<sub>4</sub>
 
| (hyaluron.)<sub>4</sub>
| Glu113
+
| '''Glu113'''
 
| internal
 
| internal
 
| <cite>Markovic-Housley2000</cite>
 
| <cite>Markovic-Housley2000</cite>
Line 696: Line 775:
 
| none
 
| none
 
| (β/α)<sub>7</sub>
 
| (β/α)<sub>7</sub>
| alpha
+
| alpha-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
| [{{PDBlink}}1kly 1kly]
+
| [{{PDBlink}}1k1y 1k1y]
 
| glucanotransferase
 
| glucanotransferase
 
| ''Thermococcus litoralis''
 
| ''Thermococcus litoralis''
 
| acarbose
 
| acarbose
| Asp214
+
| '''Asp214'''
 
| Glu123
 
| Glu123
 
| <cite>Imamura2003</cite>
 
| <cite>Imamura2003</cite>
Line 710: Line 789:
 
| A
 
| A
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''predicted anti by clan''
+
| '''''anti'''''
| ''see e.g. at GH1''
+
| [{{PDBlink}}4ccc 4ccc]
|  
+
| β-galactocerebrosidase
|  
+
| ''Mus musculus''
|  
+
| PNP-β-{{Smallcaps|d}}-galactoside
|  
+
| '''Glu182'''
|  
+
| Glu258
|  
+
| <cite>Hill2013</cite>
 +
|-
 +
| [[GH62]]
 +
| F
 +
| 5-fold β-propeller
 +
| alpha-{{Smallcaps|l}}
 +
| inverting
 +
| '''''anti'''''
 +
| [{{PDBlink}}3wn0 3wn0]
 +
| α-{{Smallcaps|l}}-arabinofuranosidase
 +
| ''Streptomyces coelicolor''
 +
| β-{{Smallcaps|l}}-Arabinofuranose
 +
| '''Glu361'''
 +
| Asp202
 +
| <cite>Maehara2014</cite>
 
|-
 
|-
 
| [[GH63]]
 
| [[GH63]]
 
| G
 
| G
 
| (α/α)<sub>6</sub>
 
| (α/α)<sub>6</sub>
| alpha
+
| alpha-{{Smallcaps|d}}
 
| inverting
 
| inverting
| ''predicted anti by clan''
+
| '''''anti'''''
| ''see at GH37''
+
| [{{PDBlink}}5ca3 5ca3]
|  
+
| α-glucosidase
|  
+
| ''Escherichia coli''
|  
+
| glucose and lactose
|  
+
| '''Asp501'''
|  
+
| Glu727
|  
+
| <cite>Miyazaki2016</cite>
 
|-
 
|-
 
| [[GH65]]
 
| [[GH65]]
 
| L
 
| L
 
| (α/α)<sub>6</sub>
 
| (α/α)<sub>6</sub>
| alpha
+
| alpha-{{Smallcaps|d}} (and α-{{Smallcaps|l}}-rham)
 
| inverting
 
| inverting
| ''predicted syn by clan''
+
| '''''anti'''''
| ''see at GH15''
+
| [{{PDBlink}}4ktr 4ktr]
|  
+
| 2-O-α-glucosylglycerol phosphorylase
|  
+
| ''Bacillus selenitireducens''
|  
+
| isofagomine
|  
+
| '''Glu475'''
|  
+
| phosphate
|  
+
| <cite>Touhara2014</cite>
 +
|-
 +
| [[GH66]]
 +
| none
 +
| (β/α)<sub>8</sub>
 +
| alpha-{{Smallcaps|d}}
 +
| retaining
 +
| '''''anti'''''
 +
| [{{PDBlink}}5axh 5axh]
 +
| dextranase
 +
| ''Thermoanaerobacter pseudethanolicus''
 +
| isomaltohexaose
 +
| '''Glu374'''
 +
| Asp312
 +
| <cite>Suzuki2016</cite>
 
|-
 
|-
 
| [[GH67]]
 
| [[GH67]]
 
| none
 
| none
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| alpha
+
| alpha-{{Smallcaps|d}}
 
| inverting
 
| inverting
| ''syn''
+
| '''''syn'''''
| [{{PDBlink}}1gql 1gql]
+
| [{{PDBlink}}1l8n 1l8n]
 
| α-glucuronidase
 
| α-glucuronidase
| ''Cellvibrio japonicus'' Ueda107
+
| ''Geobacillus stearothermophilus''
| {{Smallcaps|d}}-glucuronic acid
+
| 4-O-methyl-{{Smallcaps|d}}-glucuronic acid and xylotriose
| Glu292
+
| '''Glu286'''
| unknown
+
| Asp364 Glu392
| <cite>Nurizzo2002</cite>
+
| <cite>Golan2004</cite>
 
|-
 
|-
 
| [[GH68]]
 
| [[GH68]]
 
| J
 
| J
 
| 5-fold β-propeller
 
| 5-fold β-propeller
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}1pt2 1pt2]
 
| [{{PDBlink}}1pt2 1pt2]
 
| levansucrase
 
| levansucrase
 
| ''Bacillus subtilis''
 
| ''Bacillus subtilis''
 
| sucrose
 
| sucrose
| Glu342
+
| '''Glu342'''
 
| Asp86
 
| Asp86
 
| <cite>Meng2003</cite>
 
| <cite>Meng2003</cite>
Line 780: Line 887:
 
| H
 
| H
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| alpha
+
| alpha-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''predicted anti by clan''
+
| '''''anti'''''
| ''see e.g. at GH13''
+
| [{{PDBlink}}3aic 3aic]
|  
+
| glucansucrase
|  
+
| ''Streptococcus mutans''
|  
+
| α-acarbose
|  
+
| '''Glu515'''
|  
+
| Asp477
|  
+
| <cite>Ito2011</cite>
 
|-
 
|-
 
| [[GH72]]
 
| [[GH72]]
 
| A
 
| A
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}2w62 2w62]
 
| [{{PDBlink}}2w62 2w62]
| β-1,3-glucano- transferase
+
| β-1,3-glucanotransferase
 
| ''Saccharomyces cerevisiae'' S288C
 
| ''Saccharomyces cerevisiae'' S288C
 
| laminaripentaose
 
| laminaripentaose
| Glu176
+
| '''Glu176'''
 
| Glu275
 
| Glu275
 
| <cite>Hurtado-Gerrero2009</cite>
 
| <cite>Hurtado-Gerrero2009</cite>
Line 808: Line 915:
 
| none
 
| none
 
| 7-fold β-propeller
 
| 7-fold β-propeller
| beta
+
| beta-{{Smallcaps|d}}
 
| inverting
 
| inverting
| ''syn''
+
| '''''syn'''''
 
| [{{PDBlink}}2ebs 2ebs]
 
| [{{PDBlink}}2ebs 2ebs]
 
| cellobiohydrolase (OXG-RCBH)
 
| cellobiohydrolase (OXG-RCBH)
 
| ''Geotrichum sp.'' m128
 
| ''Geotrichum sp.'' m128
 
| xyloglucan heptasaccharide
 
| xyloglucan heptasaccharide
| Asp465
+
| '''Asp465'''
 
| Asp35
 
| Asp35
 
| <cite>Yaoi2007</cite>
 
| <cite>Yaoi2007</cite>
 +
|-
 +
| [[GH76]]
 +
| none
 +
| (α/α)<sub>6</sub>
 +
| alpha-{{Smallcaps|d}}
 +
| retaining
 +
| '''''anti'''''
 +
| [{{PDBlink}}5agd 5agd]
 +
| endo-α-1,6-mannanase
 +
| ''Bacillus circulans''
 +
| α-1,6-mannopentaose
 +
| '''Asp125'''
 +
| Asp124
 +
| <cite>Thompson2015</cite>
 
|-
 
|-
 
| [[GH77]]
 
| [[GH77]]
 
| H
 
| H
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| alpha
+
| alpha-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
| [{{PDBlink}}1esw 1esw]
+
| [{{PDBlink}}2oww 2oww]
| amylomaltase
+
| 4-α-glucanotransferase
| ''Thermus aquaticus''
+
| ''Thermus thermofilus''
| acarbose
+
| acarbose + 4-deoxy-α-{{Smallcaps|d}}-glucose
| Asp395
+
| '''Glu340'''
 
| Asp293
 
| Asp293
| <cite>Przylas2000</cite>
+
| <cite>Barends2007</cite>
 +
|-
 +
| [[GH78]]
 +
| H
 +
| (α/α)<sub>6</sub>
 +
| alpha-{{Smallcaps|l}}
 +
| inverting
 +
| '''''anti'''''
 +
| [{{PDBlink}}3w5n 3w5n]
 +
| α-{{Smallcaps|l}}-rhamnosidase
 +
| ''Streptomyces avermitilis''
 +
| {{Smallcaps|l}}-rhamnose
 +
| '''Glu636'''
 +
| Glu895
 +
| <cite>Fujimoto2013</cite>
 
|-
 
|-
 
| [[GH79]]
 
| [[GH79]]
 
| A
 
| A
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''predicted anti by clan''
+
| '''''anti'''''
| ''see e.g. at GH1''
+
| [{{PDBlink}}5e9c 5e9c]
|  
+
|  heparanase
|  
+
| ''Homo sapiens''
|  
+
| heparin tetrasaccharide
|  
+
| '''Glu225'''
|  
+
| Glu343
|  
+
| <cite>Wu2015</cite>
 
|-
 
|-
 
| [[GH80]]
 
| [[GH80]]
 
| I
 
| I
 
| α + β
 
| α + β
| beta
+
| beta-{{Smallcaps|d}}
 
| inverting
 
| inverting
 
| ''predicted syn by clan''
 
| ''predicted syn by clan''
Line 859: Line 994:
 
|  
 
|  
 
|  
 
|  
|  
+
|
 +
|-
 +
| [[GH81]]
 +
| none
 +
| β-sandwich
 +
| beta-{{Smallcaps|d}}
 +
| inverting
 +
| '''''syn'''''
 +
| [{{PDBlink}}5t4g 5t4g]
 +
| endo-β-1,3-glucanase
 +
| ''Bacillus halodurans'' C-125
 +
| laminarin
 +
| '''Asp466'''
 +
| Glu542
 +
| <cite>Pluvinage2017</cite>
 
|-
 
|-
 
| [[GH83]]
 
| [[GH83]]
 
| E
 
| E
 
| 6-fold β-propeller
 
| 6-fold β-propeller
| alpha
+
| alpha-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''predicted anti by clan''
+
| '''''anti'''''
| ''see e.g. at GH33''
+
| [{{PDBlink}}1z4x 1z4x]
|  
+
| hemagglutinin-neuraminidase
|  
+
| Simian virus 5
|  
+
| α-2,3-sialyllactose
|  
+
| '''Glu247''' relay
|  
+
| Tyr523
|  
+
| <cite>Yuan2005</cite>
 
|-
 
|-
 
| [[GH84]]
 
| [[GH84]]
 
| none
 
| none
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}2chn 2chn]
 
| [{{PDBlink}}2chn 2chn]
| β-''N''-acetyl- glucosaminidase
+
| β-''N''-acetyl-glucosaminidase
| ''Bacteroides thetaiota- omicron'' VPI-5482
+
| ''Bacteroides thetaiotaomicron'' VPI-5482
 
| NAG-thiazoline
 
| NAG-thiazoline
| Glu242
+
| '''Glu242'''
 
| internal
 
| internal
 
| <cite>Dennis2006</cite>
 
| <cite>Dennis2006</cite>
Line 892: Line 1,041:
 
| K
 
| K
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}2w92 2w92]
 
| [{{PDBlink}}2w92 2w92]
| endo-β-''N''-acetyl- glucosaminidase D
+
| endo-β-''N''-acetyl-glucosaminidase D
 
| ''Streptococcus pneumoniae'' TIGR4
 
| ''Streptococcus pneumoniae'' TIGR4
 
| NAG-thiazoline
 
| NAG-thiazoline
| Glu337
+
| '''Glu337'''
 
| internal
 
| internal
 
| <cite>Abbott2009</cite>
 
| <cite>Abbott2009</cite>
Line 906: Line 1,055:
 
| A
 
| A
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''predicted anti by clan''
+
| '''''anti'''''
| ''see e.g. at GH1''
+
| [{{PDBlink}}4aw7 4aw7]
|  
+
| β-porphyranase
|  
+
| ''Bacteroides plebeius''
|  
+
| porphyran fragment
|  
+
| '''Glu152'''
|  
+
| Glu279
|  
+
| <cite>Hehemann_1_2012</cite>
 
|-
 
|-
 
| [[GH89]]
 
| [[GH89]]
 
| none
 
| none
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| alpha
+
| alpha-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}2vcb 2vcb]
 
| [{{PDBlink}}2vcb 2vcb]
| α-''N''-acetyl- glucosaminidase
+
| α-''N''-acetyl-glucosaminidase
 
| ''Clostridium perfringens''
 
| ''Clostridium perfringens''
 
| PUGNAc
 
| PUGNAc
| Glu483
+
| '''Glu483'''
 
| Glu601
 
| Glu601
 
| <cite>Ficko-Blean2008</cite>
 
| <cite>Ficko-Blean2008</cite>
Line 933: Line 1,082:
 
| [[GH92]]
 
| [[GH92]]
 
| none
 
| none
| (α/α)<sub>6</sub> + β-sandw.
+
| (α/α)<sub>6</sub> and β-sandwich
| alpha
+
| alpha-{{Smallcaps|d}}
 
| inverting
 
| inverting
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}2ww1 2ww1]
 
| [{{PDBlink}}2ww1 2ww1]
 
| α-1,2-mannosidase
 
| α-1,2-mannosidase
| ''Bacteroides thetaiota- omicron'' VPI-5482
+
| ''Bacteroides thetaiotaomicron'' VPI-5482
 
| thiomannobioside
 
| thiomannobioside
| Glu533
+
| '''Glu533'''
 
| Asp644 Asp642
 
| Asp644 Asp642
 
| <cite>Zhu2009</cite>
 
| <cite>Zhu2009</cite>
Line 948: Line 1,097:
 
| E
 
| E
 
| 6-fold β-propeller
 
| 6-fold β-propeller
| alpha
+
| alpha-{{Smallcaps|l}}
 
| retaining
 
| retaining
| ''predicted anti by clan''
+
| '''''anti'''''
| ''see e.g. at GH33''
+
| [{{PDBlink}}3a72 3a72]
|  
+
| exo-arabinanase
|  
+
| ''Penicillium chrysogenum''
|  
+
| arabinobiose
|  
+
| '''Glu246'''
|  
+
| Glu174
|  
+
| <cite>Sogabe2011</cite>
 
|-
 
|-
 
| [[GH94]]
 
| [[GH94]]
| none
+
| Q
 
| (α/α)<sub>6</sub>
 
| (α/α)<sub>6</sub>
| beta
+
| beta-{{Smallcaps|d}}
 
| inverting
 
| inverting
| ''syn''
+
| '''''syn'''''
| [{{PDBlink}}1v7x 1v7x]
+
| [{{PDBlink}}4zli 4zli]
| chitobiose phosphorylase
+
| cellobionic acid phosphorylase
| ''Vibrio proteolyticus''
+
| ''Saccharophagus degradans''
| GlcNAc
+
| 3-O-β-{{Smallcaps|d}}-glucopyranosyl-α-{{Smallcaps|d}}-glucopyranuronic acid
| Asp492
+
| '''Asp472'''
 
| phosphate
 
| phosphate
| <cite>Hidaka2004</cite>
+
| <cite>Nam2015</cite>
 
|-
 
|-
 
| [[GH95]]
 
| [[GH95]]
 
| none
 
| none
 
| (α/α)<sub>6</sub>
 
| (α/α)<sub>6</sub>
| alpha
+
| alpha-{{Smallcaps|l}}
 
| inverting
 
| inverting
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}2ead 2ead]
 
| [{{PDBlink}}2ead 2ead]
 
| α-1,2-{{Smallcaps|l}}-fucosidase
 
| α-1,2-{{Smallcaps|l}}-fucosidase
 
| ''Bifidobacterium bifidum''
 
| ''Bifidobacterium bifidum''
 
| Fuc-α-1,2-Gal
 
| Fuc-α-1,2-Gal
| Glu566
+
| '''Glu566'''
 
| Asn423 Asp766
 
| Asn423 Asp766
 
| <cite>Nagae2007</cite>
 
| <cite>Nagae2007</cite>
Line 990: Line 1,139:
 
| none
 
| none
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| alpha
+
| alpha-{{Smallcaps|d}}
 
| retaining + inverting
 
| retaining + inverting
| ''anti''
+
| '''''anti'''''
 
| [{{PDBlink}}2zq0 2zq0]
 
| [{{PDBlink}}2zq0 2zq0]
 
| α-glucosidase
 
| α-glucosidase
| ''Bacteroides thetaiota- omicron'' VPI-5482
+
| ''Bacteroides thetaiotaomicron'' VPI-5482
 
| acarbose
 
| acarbose
| Glu532
+
| '''Glu532'''
 
| Glu508
 
| Glu508
 
| <cite>Kitamura2008</cite>
 
| <cite>Kitamura2008</cite>
 +
|-
 +
| [[GH98]]
 +
| none
 +
| (β/α)<sub>8</sub> and β-sandwich
 +
| beta-{{Smallcaps|d}}
 +
| inverting
 +
| '''''anti'''''
 +
| [{{PDBlink}}2wmg 2wmg]
 +
| endo-β-1,4-galactosidase
 +
| ''Streptococcus pneumoniae''
 +
| A-Lewis<sup>Y</sup> pentasaccharide
 +
| '''Glu158'''
 +
| Asp251 Glu301
 +
| <cite>Higgins2009</cite>
 +
|-
 +
| [[GH99]]
 +
| none
 +
| (β/α)<sub>8</sub>
 +
| alpha-{{Smallcaps|d}}
 +
| retaining
 +
| '''''anti'''''
 +
| [{{PDBlink}}4ad4 4ad4]
 +
| endo-α-mannosidase
 +
| ''Bacteroides xylanisolvens''
 +
| glucose-1,3-isofagomine and α-1,2- mannobiose
 +
| '''Glu336'''
 +
| debated
 +
| <cite>Thompson2012</cite>
 +
|-
 +
| [[GH100]]
 +
| none
 +
| (α/α)<sub>6</sub> core
 +
| beta-{{Smallcaps|d}}
 +
| inverting
 +
| '''''anti'''''
 +
| [{{PDBlink}}5gop 5gop]
 +
| invertase
 +
| ''Anabaena (Nostoc) sp.'' pcc7120
 +
| sucrose
 +
| '''Asp188'''
 +
| Glu414
 +
| <cite>Xie2016</cite>
 
|-
 
|-
 
| [[GH102]]
 
| [[GH102]]
 
| none
 
| none
 
| double-ψ β-barrel
 
| double-ψ β-barrel
| beta
+
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
| ''syn''
+
| '''''syn'''''
 
| [{{PDBlink}}2pi8 2pi8]
 
| [{{PDBlink}}2pi8 2pi8]
 
| lytic transglycosylase A
 
| lytic transglycosylase A
| ''Escherechia coli''
+
| ''Escherichia coli''
 
| chitohexaose
 
| chitohexaose
| Asp308
+
| '''Asp308'''
 
| none
 
| none
 
| <cite>van_Straaten2007</cite>
 
| <cite>van_Straaten2007</cite>
 +
|-
 +
| [[GH103]]
 +
| none
 +
| lysozyme type
 +
| beta-{{Smallcaps|d}}
 +
| retaining
 +
| '''''syn'''''
 +
| [{{PDBlink}}1d0k 1d0k]
 +
| lytic transglycosylase SLT35
 +
| ''Escherichia coli''
 +
| murodipeptides
 +
| '''Glu162'''
 +
| internal
 +
| <cite>van_Asselt2000</cite>
 +
|-
 +
| [[GH106]]
 +
| none
 +
| (β/α)<sub>8</sub>
 +
| alpha-{{Smallcaps|l}}
 +
| inverting
 +
| '''''anti'''''
 +
| [{{PDBlink}}5mwk 5mwk]
 +
| α-{{Smallcaps|l}}-rhamnosidase BT_0986
 +
| ''Bacteroides thetaiotaomicron''
 +
| pectin heptasaccharide
 +
| '''Glu461'''
 +
| Glu593 or Glu561
 +
| <cite>Ndeh2017</cite>
 +
|-
 +
| [[GH107]]
 +
| R
 +
| (β/α)<sub>8</sub>
 +
| alpha-{{Smallcaps|l}}
 +
| retaining
 +
| ''predicted syn by clan''
 +
| ''see at GH29''
 +
|
 +
|
 +
|
 +
|
 +
|
 +
|
 +
|-
 +
| [[GH110]]
 +
| none
 +
| parallel β-helix
 +
| alpha-{{Smallcaps|d}}
 +
| inverting
 +
| '''''anti'''''
 +
| [{{PDBlink}}7jwf 7jwf]
 +
| α-1,3-galactosidase
 +
| ''Pseudoalteromonas distincta''
 +
| Gal-α1,3-Gal
 +
| '''Asp344'''
 +
| Asp321 Asp345
 +
| <cite>McGuire2020</cite>
 
|-
 
|-
 
| [[GH113]]
 
| [[GH113]]
 
| A
 
| A
 
| (β/α)<sub>8</sub>
 
| (β/α)<sub>8</sub>
| beta
+
| beta-{{Smallcaps|d}}
 +
| retaining
 +
| '''''anti'''''
 +
| [{{PDBlink}}4cd8 4cd8]
 +
| β-mannanase
 +
| ''Alicyclobacillus acidocaldarius''
 +
| mannobioimidazole
 +
| '''Glu151'''
 +
| Glu231
 +
| <cite>Williams2014</cite>
 +
|-
 +
| [[GH116]]
 +
| O
 +
| (α/α)<sub>6</sub> and β-sandwich
 +
| beta-{{Smallcaps|d}}
 +
| retaining
 +
| ''predicted anti by clan''
 +
| ''see at GH52''
 +
|
 +
|
 +
|
 +
|
 +
|
 +
|
 +
|-
 +
| [[GH117]]
 +
| none
 +
| 5-fold β-propeller
 +
| alpha-{{Smallcaps|l}}
 +
| inverting
 +
| '''''anti'''''
 +
| [{{PDBlink}}4ak7 4ak7]
 +
| α-1,3-3,6-anhydro-{{Smallcaps|l}}-galactosidase
 +
| ''Bacteroides plebeius''
 +
| neoagarobiose
 +
| '''His302''' (relay from Asp320)
 +
| Asp90
 +
| <cite>Hehemann_2_2012</cite>
 +
|-
 +
| [[GH120]]
 +
| none
 +
| parallel β-helix and β-sandwich
 +
| beta-{{Smallcaps|d}}
 +
| retaining
 +
| '''''anti'''''
 +
| [{{PDBlink}}3vsv 3vsv]
 +
| β-xylosidase XylC
 +
| ''Thermoanaerobacterium saccharolyticum'' JW/SL-YS485
 +
| {{Smallcaps|d}}-xylose
 +
| '''Glu405'''
 +
| Asp382
 +
| <cite>Huang2012</cite>
 +
|-
 +
| [[GH123]]
 +
| none
 +
| (β/α)<sub>8</sub> and β-sandwich
 +
| beta-{{Smallcaps|d}}
 +
| retaining
 +
| '''''anti'''''
 +
| [{{PDBlink}}5fr0 5fr0]
 +
| exo-β-N-acetyl-galactosaminidase
 +
| ''Clostridium perfringens''
 +
| ''N''-difluoroacetyl-{{Smallcaps|d}}-galactosamine
 +
| '''Glu345'''
 +
| internal
 +
| <cite>Noach2016</cite>
 +
|-
 +
| [[GH125]]
 +
| L
 +
| (α/α)<sub>6</sub>
 +
| alpha-{{Smallcaps|d}}
 +
| inverting
 +
| '''''anti'''''
 +
| [{{PDBlink}}5m7y 5m7y]
 +
| exo-α-1,6-mannosidase
 +
| ''Clostridium perfringens''
 +
| 1,6-α-mannotriose
 +
| '''Asp220'''
 +
| Glu393
 +
| <cite>Alonso-Gil2016</cite>
 +
|-
 +
| [[GH127]]
 +
| P
 +
| (α/α)<sub>6</sub> and β-sandwich
 +
| beta-{{Smallcaps|l}}
 +
| retaining
 +
| '''''anti'''''
 +
| [{{PDBlink}}3wrg 3wrg]
 +
| β-{{Smallcaps|l}}-arabinofuranosidase
 +
| ''Bifidobacterium longum''
 +
| {{Smallcaps|l}}-arabinose
 +
| '''Glu322'''
 +
| Cys417
 +
| <cite>Huang2014</cite>
 +
|-
 +
| [[GH128]]
 +
| A
 +
| (β/α)<sub>8</sub>
 +
| beta-{{Smallcaps|d}}
 +
| retaining
 +
| '''''anti'''''
 +
| [{{PDBlink}}6ufl 6ufl]
 +
| β-1,3-glucanase
 +
| ''Amycolatopsis mediterranei''
 +
| laminarihexaose
 +
| '''Glu102'''
 +
| Glu199
 +
| <cite>Santos2020</cite>
 +
|-
 +
| [[GH130]]
 +
| none
 +
| 5-fold β-propeller
 +
| beta-{{Smallcaps|d}}
 +
| inverting
 +
| '''''anti'''''
 +
| [{{PDBlink}}5b0s 5b0s]
 +
| β-1,2-mannobiose phosphorylase
 +
| ''Listeria innocua''
 +
| β-1,2-mannotriose
 +
| '''Asp141''' relay
 +
| phosphate
 +
| <cite>Tsuda2015</cite>
 +
|-
 +
|  [[GH134]]
 +
| none
 +
| β + α
 +
| beta-{{Smallcaps|d}}
 +
| inverting
 +
| '''''syn'''''
 +
| [{{PDBlink}}5jug 5jug]
 +
| β-mannanase
 +
| ''Streptomyces sp.''
 +
| mannopentaose
 +
| '''Glu45'''
 +
| Asp57
 +
| <cite>Jin2016</cite>
 +
|-
 +
|  [[GH136]]
 +
| none
 +
| β-helix
 +
| beta-{{Smallcaps|d}}
 +
| retaining
 +
| '''''syn'''''
 +
| [{{PDBlink}}5gqf 5gqf]
 +
| lacto-N-biosidase
 +
| ''Bifidobacterium longum''
 +
| lacto-N-biose
 +
| '''Asp411'''
 +
| Asp418
 +
| <cite>Yamada2017</cite>
 +
|-
 +
|  [[GH137]]
 +
| none
 +
| 5-fold β-propeller
 +
| beta-{{Smallcaps|l}}
 +
| unknown
 +
| '''''anti'''''
 +
| [{{PDBlink}}5mui 5mui]
 +
| β-{{Smallcaps|l}}-arabinofuranosidase BT_0996
 +
| ''Bacteroides thetaiotaomicron''
 +
| pectin oligosaccharide
 +
| '''Glu240'''
 +
| Glu159
 +
| <cite>Ndeh2017</cite>
 +
|-
 +
|  [[GH138]]
 +
| none
 +
| (β/α)<sub>8</sub>
 +
| alpha-{{Smallcaps|d}}
 +
| retaining
 +
| '''''syn'''''
 +
| [{{PDBlink}}6hzg 6hzg]
 +
| α-1,2-{{Smallcaps|d}}-galacturonidase
 +
| ''Bacteroides paurosaccharolyticus''
 +
| alpha-{{Smallcaps|d}}-galactopyranuronic
 +
| '''Glu294'''
 +
| Glu361
 +
| <cite>Labourel2019</cite>
 +
|-
 +
| [[GH146]]
 +
| P
 +
| (α/α)<sub>6</sub> and β-sandwich
 +
| beta-{{Smallcaps|l}}
 +
| retaining
 +
| '''''anti'''''
 +
| [{{PDBlink}}5opj 5opj]
 +
| β-{{Smallcaps|l}}-arabinofuranosidase BT_0349
 +
| ''Bacteroides thetaiotaomicron''
 +
| {{Smallcaps|l}}-arabinose
 +
| '''Glu320'''
 +
| Cys416
 +
| <cite>Luis2018</cite>
 +
|-
 +
| [[GH147]]
 +
| A
 +
| (β/α)<sub>8</sub>
 +
| beta-{{Smallcaps|d}}
 +
| retaining
 +
| ''predicted anti by clan''
 +
| ''see at e.g. GH1''
 +
|
 +
|
 +
|
 +
|
 +
|
 +
|
 +
|-
 +
| [[GH148]]
 +
| A
 +
| (β/α)<sub>8</sub>
 +
| beta-{{Smallcaps|d}}
 +
| retaining
 +
| ''predicted anti by clan''
 +
| ''see at e.g. GH1''
 +
|
 +
|
 +
|
 +
|
 +
|
 +
|
 +
|-
 +
| [[GH149]]
 +
| Q
 +
| (α/α)<sub>6</sub>
 +
| beta-{{Smallcaps|d}}
 +
| inverting
 +
| ''predicted syn by clan''
 +
| ''see at GH94''
 +
|
 +
|
 +
|
 +
|
 +
|
 +
|
 +
|-
 +
| [[GH156]]
 +
| none
 +
| (β/α)<sub>8</sub>
 +
| alpha-{{Smallcaps|d}}
 +
| inverting
 +
| '''''syn'''''
 +
| [{{PDBlink}}6s0e 6s0e]
 +
| exo-α-sialidase
 +
| uncultured bacterium pG7
 +
| N-acetyl-2,3-dehydro-2-deoxyneuraminic acid
 +
| '''His134''' (relay from Asp132)
 +
| Asp14
 +
| <cite>Bule2019</cite>
 +
|-
 +
| [[GH157]]
 +
| A
 +
| (β/α)<sub>8</sub>
 +
| beta-{{Smallcaps|d}}
 +
| retaining
 +
| ''predicted anti by clan''
 +
| ''see at e.g. GH1''
 +
|
 +
|
 +
|
 +
|
 +
|
 +
|
 +
|-
 +
| [[GH158]]
 +
| A
 +
| (β/α)<sub>8</sub>
 +
| beta-{{Smallcaps|d}}
 
| retaining
 
| retaining
 
| ''predicted anti by clan''
 
| ''predicted anti by clan''
| ''see e.g. at GH1''
+
| ''see at e.g. GH1''
 
|  
 
|  
 
|  
 
|  
Line 1,028: Line 1,541:
 
|  
 
|  
 
|  
 
|  
 +
|-
 +
| [[GH161]]
 +
| Q
 +
| (α/α)<sub>6</sub>
 +
| beta-{{Smallcaps|d}}
 +
| retaining
 +
| ''predicted syn by clan''
 +
| ''see at GH94''
 +
|
 +
|
 +
|
 +
|
 +
|
 +
|
 +
|-
 +
| [[GH162]]
 +
| none
 +
| (α/α)<sub>6</sub>
 +
| beta-{{Smallcaps|d}}
 +
| inverting
 +
| '''''syn'''''
 +
| [{{PDBlink}}6imw 6imw]
 +
| endo-β-1,2-glucanase
 +
| ''Talaromyces funiculosus''
 +
| beta-1,2-glucan
 +
| '''Glu262''' via C3-OH of glc at subs. +2
 +
| Asp446
 +
| <cite>Tanaka2019</cite>
 +
|-
 +
| [[GH164]]
 +
| A
 +
| (β/α)<sub>8</sub>
 +
| beta-{{Smallcaps|d}}
 +
| retaining
 +
| '''''anti'''''
 +
| [{{PDBlink}}6t75 6t75]
 +
| β-mannosidase
 +
| ''Bacteroides salyersiae''
 +
| 2-deoxy-2-F-mannosyl
 +
| '''Glu160'''
 +
| Glu297
 +
| <cite>Armstrong2020</cite>
 +
|-
 +
| [[GH172]]
 +
| none
 +
| β-jelly roll
 +
| alpha-{{Smallcaps|d}}
 +
| retaining
 +
| '''''anti'''''
 +
| [{{PDBlink}}7v1w 7v1w]
 +
| difructose-anhydride synthase
 +
| ''Bifidobacterium dentum''
 +
| beta-{{Smallcaps|d}}-arabinofuranose
 +
| '''Glu270'''
 +
| Glu291
 +
| <cite>Kashima2021</cite>
 +
|-
 +
| [[GH181]]
 +
| E
 +
| 6-fold β-propeller
 +
| alpha-{{Smallcaps|d}}
 +
| inverting
 +
| '''''anti'''''
 +
| [{{PDBlink}}8axi 8axi]
 +
| exo-α-sialidase
 +
| ''Akkermansia muciniphila''
 +
| 2-deoxy-2,3-dehydro-''N''-acetyl-neuraminic acid + T-antigen disaccharide
 +
| '''Asp345'''
 +
| Glu218
 +
| <cite>Shuoker2023</cite>
 +
|-
 +
| [[GH183]]
 +
| none
 +
| 5-bladed β-propeller
 +
| alpha-{{Smallcaps|d}}
 +
| retaining
 +
| '''''anti'''''
 +
| [{{PDBlink}}8ic1 8ic1]
 +
| endo-α-1,5-{{Smallcaps|d}}-arabinofuranosidase
 +
| ''Microbacterium arabinogalactanolyticum'' JCM 9171
 +
| α-{{Smallcaps|d}}-Araf-(1,5)-α-{{Smallcaps|d}}-Araf-(1,5)-α-{{Smallcaps|d}}-Araf-(1,5)-α-{{Smallcaps|d}}-Araf
 +
| '''Asp51'''
 +
| Asp33
 +
| <cite>Shimokawa2023</cite>
 +
|-
 +
| [[GH186]]
 +
| none
 +
| β-sandwich
 +
| beta-{{Smallcaps|d}}
 +
| inverting
 +
| '''''syn'''''
 +
| [{{PDBlink}}8ip1 8ip1]
 +
| β-1,2-glucanase
 +
| ''Escherechia coli''
 +
| β-1,2-glucan
 +
| '''Asp388'''
 +
| Asp300 + 2 waters
 +
| <cite>Motouchi2023</cite>
 +
|-
 +
| [http://www.cazy.org/GH0.html n.c.*]
 +
| none
 +
| parallel β-helix
 +
| alpha-{{Smallcaps|d}}
 +
| inverting
 +
| '''''anti'''''
 +
| [{{PDBlink}}2vjj 2vjj]
 +
| endo-α-N-acetylglucosaminidase
 +
| Bacteriophage HK620
 +
| O18A1 O-antigen hexasaccharide
 +
| '''Asp339'''
 +
| Glu372
 +
| <cite>Barbirz2008</cite>
 
|}
 
|}
 +
<nowiki>*</nowiki> n.c.: Found among the collection of [http://www.cazy.org/GH0.html non-classified GH sequences in the CAZy Database].
  
 
== References ==
 
== References ==
  
 
<biblio>
 
<biblio>
# HeightmanVasella1999 Heightman, T.D. and Vasella, A.T. (1999) Recent Insights into Inhibition, Structure, and Mechanism of Configuration-Retaining Glycosidases. Angewandte Chemie-International Edition 38(6), 750-770. [http://www3.interscience.wiley.com/journal/55000581/abstract Article online].
+
# HeightmanVasella1999 Heightman TD and Vasella AT. ''Recent Insights into Inhibition, Structure, and Mechanism of Configuration-Retaining Glycosidases.'' Angew Chem Int Ed. 1999 38(6):750-770. [http://www3.interscience.wiley.com/journal/55000581/abstract Article online].
 
# Nerinckx2005 pmid=15642336
 
# Nerinckx2005 pmid=15642336
 +
# Wu2012 pmid=23137336
 +
# Perez1978 Pérez S and Marchessault RH. ''The exo-anomeric effect: experimental evidence from crystal structures.'' Carbohydr res. 1978 65:114-120. [http://dx.doi.org/10.1016/S0008-6215(00)84218-4 DOI:10.1016/S0008-6215(00)84218-4]
 +
# Cramer1997 Cramer CJ, Truhlar DG, and French AD. ''Exo-anomeric effects on energies and geometries of different conformations of glucose and related systems in the gas phase and aqueous solution.'' Carbohydr res. 1997 298:1-14. [http://dx.doi.org/10.1016/S0008-6215(96)00297-2 DOI:10.1016/S0008-6215(96)00297-2]
 +
# Johnson2009 pmid=19733839
 +
# Alonso2016 pmid=26889578
 
# Gloster2006 pmid=17002288
 
# Gloster2006 pmid=17002288
 
# van_Bueren2009 pmid=18976664
 
# van_Bueren2009 pmid=18976664
 
# Hrmova2001 pmid=11709165
 
# Hrmova2001 pmid=11709165
 +
# Rajan2004 pmid=15341727
 
# Varrot2003 pmid=12595701
 
# Varrot2003 pmid=12595701
 
# Zhou1999 pmid=10508787
 
# Zhou1999 pmid=10508787
 
# Sulzenbacher1999 pmid=10200171
 
# Sulzenbacher1999 pmid=10200171
# Brumshtein2007 pmid=17666401
+
# Urbanikova2011 pmid=21501386
 
# Guerin2002 pmid=11884144
 
# Guerin2002 pmid=11884144
 
# Schubot2004 pmid=14756552
 
# Schubot2004 pmid=14756552
 
# Suzuki2009 pmid=19279191
 
# Suzuki2009 pmid=19279191
# Sidhu1999 pmid=10220321
+
# Wan2014 pmid=24419374
 
# Sandgren2004 pmid=15364577
 
# Sandgren2004 pmid=15364577
 
# Uitdehaag1999 pmid=10331869
 
# Uitdehaag1999 pmid=10331869
 
# Miyake2003 pmid=12741813
 
# Miyake2003 pmid=12741813
# Aleshin1996 pmid=8679589
+
# Harris1993 pmid=8431441
 
# Allouch2004 pmid=15062085
 
# Allouch2004 pmid=15062085
 +
# Wojtkowiak2013 pmid=23275163
 
# Papanikolau2001 pmid=11560481
 
# Papanikolau2001 pmid=11560481
 
# Prag2000 pmid=10884356
 
# Prag2000 pmid=10884356
Line 1,056: Line 1,689:
 
# Karlsen1996 pmid=15299731
 
# Karlsen1996 pmid=15299731
 
# Baldwin1993 pmid=8259514
 
# Baldwin1993 pmid=8259514
# Ducros2002 pmid=12203498
+
# Cartmell2008 pmid=18799462
# Garman2002 pmid=12005440
+
# Fernandez-Leiro2010 pmid=20592022
 
# Abbott2007 pmid=17397864
 
# Abbott2007 pmid=17397864
# Sulzenbacher2004 pmid=14715651
+
# Sakurama2012 pmid=22451675
 
# Sim2008 pmid=18036614
 
# Sim2008 pmid=18036614
 
# Verhaest2007 pmid=17335500
 
# Verhaest2007 pmid=17335500
 
# Amaya2004 pmid=15130470
 
# Amaya2004 pmid=15130470
# Varghese1992 pmid=1438172
+
# Zhu2012 pmid=23015718
# Rojas2004 pmid=15491613
+
# Maksimainen2011 pmid=21130883
 +
# Merceron2012 pmid=23012371
 
# Gibson2007 pmid=17455176
 
# Gibson2007 pmid=17455176
# Numao2003 pmid=12960159
+
# Shah2008 pmid=18599462
# Yang2004 pmid=14659747
+
# Czjzek2005 pmid=16212978
# Hidaka2002 pmid=12215416
+
# Godoy2016 pmid=27685756
 +
# Fujimoto2010 pmid=20739278
 
# Kitago2007 pmid=17905739
 
# Kitago2007 pmid=17905739
 
# Davies1996 pmid=15299721
 
# Davies1996 pmid=15299721
 +
# Lyu2014 pmid=24766439
 
# Karaveg2005 pmid=15713668
 
# Karaveg2005 pmid=15713668
 
# Nerinckx2008 pmid=18619586
 
# Nerinckx2008 pmid=18619586
 +
# Pluvinage2013 pmid=23921382
 +
# Yuan2005 pmid=15893670
 
# Hoevel2003 pmid=14517232
 
# Hoevel2003 pmid=14517232
 +
# Espina2014 pmid=24816105
 +
# Le_Nours2009 pmid=19089956
 
# Miyanaga2004 pmid=15292273
 
# Miyanaga2004 pmid=15292273
# Ishida2009 pmid=19193645
+
# Bianchetti2015 pmid=25752603
 
# Markovic-Housley2000 pmid=11080624
 
# Markovic-Housley2000 pmid=11080624
 
# Imamura2003 pmid=12618437
 
# Imamura2003 pmid=12618437
# Nurizzo2002 pmid=11937059
+
# Hill2013 pmid=24297913
 +
# Maehara2014 pmid=24482228
 +
# Miyazaki2016 pmid=27688023
 +
# Touhara2014 pmid=24828502
 +
# Suzuki2016 pmid=26494689
 +
# Golan2004 pmid=14573597
 
# Meng2003 pmid=14517548
 
# Meng2003 pmid=14517548
 +
# Ito2011 pmid=21354427
 
# Hurtado-Gerrero2009 pmid=19097997
 
# Hurtado-Gerrero2009 pmid=19097997
 
# Yaoi2007 pmid=17498741
 
# Yaoi2007 pmid=17498741
# Przylas2000 pmid=11082203
+
# Thompson2015 pmid=25772148
 +
# Barends2007 pmid=17420245
 +
# Fujimoto2013 pmid=23486481
 +
# Wu2015 pmid=26575439
 +
# Pluvinage2017 pmid=28781080
 
# Dennis2006 pmid=16565725
 
# Dennis2006 pmid=16565725
 
# Abbott2009 pmid=19181667
 
# Abbott2009 pmid=19181667
 +
# Hehemann_1_2012 pmid=23150581
 
# Ficko-Blean2008 pmid=18443291
 
# Ficko-Blean2008 pmid=18443291
# Zhu2009 Zhu et al. (2010) Nature Chemical Biology in the press; [http://dx.doi.org/10.1038/nchembio.278 DOI: 10.1038/nchembio.278] [http://www.nature.com/nchembio/journal/vaop/ncurrent/abs/nchembio.278.html ''direct link''].
+
# Zhu2009 pmid=20081828
# Hidaka2004 pmid=15274915
+
# Sogabe2011 pmid=21543843
 +
# Nam2015 pmid=26041776
 
# Nagae2007 pmid=17459873
 
# Nagae2007 pmid=17459873
 
# Kitamura2008 pmid=18981178
 
# Kitamura2008 pmid=18981178
 +
# Higgins2009 pmid=19608744
 
# van_Straaten2007 pmid=17502382
 
# van_Straaten2007 pmid=17502382
 +
# van_Asselt2000 pmid=10684641
 +
# Ndeh2017 pmid=28329766
 +
# Labourel2019 pmid=30877196
 +
# Luis2018 pmid=29255254
 +
# Bule2019 pmid=31645552
 +
# Jin2016 Jin Y, Petricevic M, John A, Raich L, Jenkins H, Portela De Souza L, Cuskin F, Gilbert HJ, Rovira C, Goddard-Borger ED, Williams SJ, and Davies GJ. ''A β-Mannanase with a Lysozyme-like Fold and a Novel Molecular Catalytic Mechanism.'' ACS Cent Sci. 2016 Nov [http://dx.doi.org/10.1021/acscentsci.6b00232 DOI:10.1021/acscentsci.6b00232]
 +
# Yamada2017 pmid=28392148
 +
# Ohnuma2014 pmid=24582745
 +
# Thompson2012 pmid=22219371
 +
# Xie2016 pmid=27777307
 +
# Williams2014 pmid=24339341
 +
# Hehemann_2_2012 pmid=22393053
 +
# Huang2012 pmid=22992047
 +
# Noach2016 pmid=27038508
 +
# Alonso-Gil2016 pmid=28026180
 +
# Huang2014 Huang CH, Zhu Z, Cheng YS, Chan HC, Ko TP, Chen CC, Wang I, Ho MR, Hsu ST, Zeng YF, Huang YN, Liu JR, Guo RT. ''Structure and Catalytic Mechanism of a Glycoside Hydrolase Family-127 β-L-Arabinofuranosidase (HypBA1).'' J Bioprocess Biotech. 2014 4:171 [http://dx.doi.org/10.4172/2155-9821.1000171 DOI:10.4172/2155-9821.1000171]
 +
# Tsuda2015 pmid=26632508
 +
# Barbirz2008 pmid=18547389
 +
# Tanaka2019 pmid=30926603
 +
# Armstrong2020 pmid=31871050
 +
# Santos2020 pmid=32451508
 +
# Kashima2021 pmid=34688653
 +
# McGuire2020 pmid=33127644
 +
# Shuoker2023 pmid=37005422
 +
# Shimokawa2023 pmid=37726269
 +
# Motouchi2023 pmid=37735577
 +
 
</biblio>
 
</biblio>
 
 
[[Category:Definitions and explanations]]
 
[[Category:Definitions and explanations]]

Latest revision as of 01:46, 29 October 2024

Approve icon-50px.png

This page has been approved by the Responsible Curator as essentially complete. CAZypedia is a living document, so further improvement of this page is still possible. If you would like to suggest an addition or correction, please contact the page's Responsible Curator directly by e-mail.


Overview

This page provides a table that summarizes the spatial positioning of the catalytic general acid residue in the active sites of glycoside hydrolases, relative to the substrate. The table below updates those found in the seminal paper on this concept by Heightman and Vasella [1], and a following paper by Nerinckx et al. [2].

Background

The "not from above, but from the side" concept of semi-lateral glycosidic oxygen protonation by glycoside hydrolases was introduced by Heightman and Vasella [1]. It was originally only described for beta-equatorial glycoside hydrolases, but appears to be equally applicable to enzymes acting on an alpha-axial glycosidic bond [2]. When dividing subsite -1 into half-spaces by a plane defined by the glycosidic oxygen and C1' and H1' of the –1 glycoside, many ligand-complexed structures reveal that the proton donor is positioned either in the syn half-space (near the ring-oxygen of the –1 glycoside), or in the anti half-space (on the opposite side of the ring-oxygen). Members of the same GH family appear to share a common syn or anti protonator arrangement and further, this specificity appears to be preserved within Clans of families. This page's compilation of subsite -1 occupied complexes shows that about 70% of all GH families are anti protonators.

Closer inspection of crystal structures of –1/+1 subsite-spanning substrates, or substrate-analogue ligands, in complex with enzymes reveals a further intriguing corollary [2, 3]. In substrate-bound complexes with anti protonating GH enzymes, the scissile anomeric bond (often studied using the thio-analogue) shows a dihedral angle φ (O5'-C1'-[O,S]x-Cx) that is in the lowest-energy synclinal (gauche) conformation. The rationale for this is that a minus synclinal dihedral angle φ for an equatorial glycosidic bond, or plus synclinal for an axial glycosidic bond [4], allows for hyperconjugative overlap of the C1'-O5' antibonding orbital with an antiperiplanar-oriented lone pair orbital lobe of the glycosidic oxygen, thereby creating partial double bond character and stabilization of the glycosidic bond by 4–5 kcal/mol; this ground-state stabilizing phenomenon is known as the ‘exo-anomeric effect’ [5, 6, 7]. Anti protonation occurs on the glycosidic oxygen’s antiperiplanar lone pair, thereby removing the stabilizing exo-anomeric effect. This suggests that anti protonation is an enzymic approach for lowering the activation barrier leading to the transition state (Figure 1 centre).

Syn protonating glycoside hydrolases apparently make use of a different approach [2, 3]. In many –1/+1 subsite-spanning ligand complexes, the dihedral angle φ of the scissile anomeric bond has been rotated away from its lowest-energy synclinal position: clockwise to minus-anticlinal or antiperiplanar for beta-equatorial; counterclockwise to plus-anticlinal or antiperiplanar for alpha-axial anomeric bonds. This removes the hyperconjugative overlap and thus also the stabilizing exo-anomeric effect. And because of this rotation, a lone pair of the glycosidic oxygen is directed into the syn half-space, allowing it to be protonated by the syn-positioned proton donor (Figure 1 right).

Figure 1. Newman projections, with the glycosidic oxygen as proximal atom and the anomeric carbon as distal atom, showing anti (centre) versus syn (right) semi-lateral protonation in beta-equatorial (top) and alpha-axial (bottom) glycoside hydrolases. The indicated φ is the dihedral angle for O5'-C1'-O4-C4.

Table of syn/anti protonation examples

This table contains only one example per GH family of a ligand-complexed protein structure where the syn or anti positioning of the proton donor can be clearly observed; other examples may be available on a family-by-family basis. The reader is thus advised to consult the CAZy database for a current, comprehensive list of CAZyme structures. Where available, the selected examples are Michaelis-type complexes with the ligand spanning the -1/+1 subsites, since these have an intact glycosidic or thioglycosidic bond, or are N-analogs of the substrate (e.g. acarbose). In some examples, the proton donor has been mutated (e.g., to the corresponding amide or to an alanine), and in those cases one may wish to look at a superposition of the given PDB example with the structure of the native enzyme. If a Michaelis-type complex is not yet available, the second and third example choices, respectively, are trapped glycosyl-enzyme intermediates and product complexes where subsite -1 is occupied.

Please also be aware that this is a large table with many data. Please contact the page Author or Responsible Curator with corrections.

Table

This table can be re-sorted by clicking on the icons in the header (javascript must be turned on in your browser). To reset the page to be sorted by GH family, click the View tab at the very top of the page.

Family Clan Structure fold Anomeric specificity Mechanism Syn/anti protonator Example PDB ID Enzyme Organism Ligand General acid Nucleophile or General base Reference
GH1 A (β/α)8 beta-d retaining anti 2cer β-glycosidase S Sulfolobus solfataricus P2 phenethyl glucoimidazole Glu206 Glu387 [8]
GH2 A (β/α)8 beta-d / alpha-l retaining anti 2vzu exo-β-glucosaminidase Amicolatopsis orientalis PNP-β-d-glucosamine Glu469 Glu541 [9]
GH3 none (β/α)8 beta-d / alpha-l retaining anti 1iex exo-1,3-1,4-glucanase Hordeum vulgare thiocellobiose Glu491 Asp285 [10]
GH4 none Rossmann + α6/β3 + β3/α4 beta-d retaining anti 1u8x 6-P-α-glucosidase Bacillus subtilis alpha-d-glucose-6-phosphate Asp172 not applicable [11]
GH5 A (β/α)8 beta-d retaining anti 1h2j endo-β-1,4-glucanase Bacillus agaradhaerens 2',4'-DNP-2-F-cellobioside Glu129 Glu228 [12]
GH6 none (β/α)8 beta-d inverting syn 1qjw cellobiohydrolase 2 Hypocrea jecorina (Glc)2-S-(Glc)2 Asp221 debated [13]
GH7 B β-jelly roll beta-d retaining syn 1ovw endo-1,4-glucanase Fusarium oxysporum thio-(Glc)5 Glu202 Glu197 [14]
GH8 M (α/α)6 beta-d inverting anti 1kwf endo-1,4-glucanase Clostridium thermocellum cellopentaose Glu95 Asp278 [15]
GH9 none (α/α)6 beta-d inverting syn 1rq5 cellobiohydrolase Clostridium thermocellum cellotetraose Glu795 Asp383 [16]
GH10 A (β/α)8 beta-d retaining anti 2d24 β-1,4-xylanase Streptomyces olivaceoviridis E-86 xylopentaose Glu128 Glu236 [17]
GH11 C β-jelly roll beta-d retaining syn 4hk8 endo-β-1,4-xylanase Hypocrea jecorina xylohexaose Glu177 Glu86 [18]
GH12 C β-jelly roll beta-d retaining syn 1w2u endoglucanase Humicola grisea thiocellotetraose Glu205 Glu120 [19]
GH13 H (β/α)8 alpha-d retaining anti 1cxk β-cyclodextrin glucanotransferase Bacillus circulans maltononaose Glu257 Asp229 [20]
GH14 none (β/α)8 alpha-d inverting syn 1itc β-amylase Bacillus cereus maltopentaose Glu172 Glu367 [21]
GH15 L (α/α)6 alpha-d inverting anti 1dog glucoamylase Aspergillus awamori 1-deoxynojirimycin Glu179 Glu400 [22]
GH16 B β-jelly roll beta-d retaining syn 1urx β-agarase A Zobellia galactanivorans oligoagarose Glu152 Glu147 [23]
GH17 A (β/α)8 beta-d retaining anti 4gzj endo-β-1,3-glucanase Solanum tuberosum laminaratriose + laminarabiose Glu118 Glu259 [24]
GH18 K (β/α)8 beta-d retaining anti 1ffr chitinase A Serratia marcescens (NAG)6 Glu315 internal [25]
GH19 none lysozyme type beta-d inverting syn 3wh1 chitinase Bryum coronatum (GlcNAc)4 Glu61 Glu70 [26]
GH20 K (β/α)8 beta-d retaining anti 1c7s chitobiase Serratia marcescens chitobiose Glu540 internal [27]
GH22 none lysozyme type beta-d retaining syn 1h6m lysozyme C Gallus gallus Chit-2-F-chitosyl Glu35 Asp52 [28]
GH23 none lysozyme type beta-d inverting syn 1lsp lysozyme G Cygnus atratus Bulgecin A Glu73 internal [29]
GH24 I α + β beta-d inverting syn 148l lysozyme E Bacteriophage T4 chitobiosyl Glu11 Glu26 [30]
GH26 A (β/α)8 beta-d retaining anti 2vx6 exo-β-mannanase Cellvibrio japonicus Ueda107 Gal1Man4 Glu221 Glu338 [31]
GH27 D (β/α)8 alpha-d / beta-l retaining anti 3lrm α-galactosidase Saccharomyces cerevisiae raffinose Asp209 Asp141 [32]
GH28 N β-helix alpha-d (and α-l-rham) inverting anti 2uvf exo-polygalacturonosidase Yersinia enterocolitica ATCC9610D digalacturonic acid Asp402 Asp381 Asp403 [33]
GH29 R (β/α)8 alpha-l retaining syn 3uet α-1,3/4-fucosidase Bifidobacterium longum subsp. infantis lacto-N-fucopentaose II Glu217 Asp172 [34]
GH30 A (β/α)8 beta-d retaining anti 2y24 glucurono-xylanase Dickea chrysanthemi D1 glucuronoxylan tetrasaccharide Glu163 Glu253 [35]
GH31 D (β/α)8 alpha-d retaining anti 2qmj maltase-glucoamylase Homo sapiens acarbose Asp542 Asp443 [36]
GH32 J 5-fold β-propeller beta-d retaining anti 2add fructan β-(2,1)-fructosidase Cichorium intybus sucrose Glu201 Asp22 [37]
GH33 E 6-fold β-propeller alpha-d retaining anti 1s0i transsialidase Trypanosoma cruzi sialyllactose Asp59 Tyr342 [38]
GH34 E 6-fold β-propeller alpha-d retaining anti 4gzw N2 neuraminidase Influenza A Tanzania/205/2010 H3N2 α-d-Neup5Ac-(2,3)-β-d-Galp-(1,4)-β-d-GlcpNAc Asp151 Tyr406 [39]
GH35 A (β/α)8 beta-d retaining anti 3ogv β-galactosidase Hypocrea jecorina 2-phenylethyl 1-thio-β-d-galactopyranoside Glu200 Glu298 [40]
GH36 D (β/α)8 alpha-d retaining anti 4fnu β-galactosidase Geobacillus stearothermophilus stachyose Asp584 Asp478 [41]
GH37 G (α/α)6 alpha-d inverting anti 2jf4 trehalase Escherichia coli validoxylamine Asp312 Glu496 [42]
GH38 none (β/α)7 alpha-d retaining anti 3czn Golgi α-mannosidase II Drosophila melanogaster GlcNAcMan(5)GlcNAc(2) Asp341 Asp204 [43]
GH39 A (β/α)8 beta-d / alpha-l retaining anti 2bfg β-xylosidase Geobacillus stearothermophilus 2,5-dinitrophenyl-β-d-xyloside Glu160 Glu278 [44]
GH42 A (β/α)8 beta-d / alpha-l retaining anti 4ucf β-galactosidase Bifidobacterium bifidum d-galactose Glu161 Glu320 [45]
GH43 F 5-fold β-propeller beta-d / alpha-l inverting anti 3akh exo-1,5-α-l-arabinofuranosidase Streptomyces avermitilis α-1,5-arabinofuranotriose Glu196 Asp220 [46]
GH44 none (β/α)8 beta-d retaining anti 2eqd endoglucanase Clostridium thermocellum cellooctaose Glu186 Glu359 [47]
GH45 none 6-stranded β-barrel beta-d inverting syn 4eng endo-1,4-glucanase Humicola insolens cellohexaose Asp121 Asp10 [48]
GH46 I lysozyme type beta-d inverting syn 4olt chitosanase Microbacterium sp. OU01 hexa-glucosamine Glu25 Asp43 [49]
GH47 none (α/α)7 alpha-d inverting anti 1x9d α-mannosidase I Homo sapiens Me-2-S-(α-Man)-2-thio-α-Man Asp463 Glu599 [50], [51]
GH48 M (α/α)6 beta-d inverting predicted anti by clan see at GH8
GH49 N β-helix alpha-d inverting predicted anti by clan see at GH28
GH50 A (β/α)8 beta-d retaining anti 4bq5 exo-β-agarase Saccharophagus degradans neoagarotetraose Glu535 Glu695 [52]
GH51 A (β/α)8 beta-d / alpha-l retaining anti 1qw9 α-l-arabinofuranosidase Geobacillus stearothermophilus PNP-l-arabinofuranoside Glu175 Glu294 [53]
GH52 O (α/α)6 beta-d retaining anti 4c1p β-xylosidase Geobacillus thermoglucosidasius xylobiose Asp517 Glu537 [54]
GH53 A (β/α)8 beta-d retaining anti 2ccr β-1,4-galactanase Bacillus licheniformis galactotriose Glu165 Glu263 [55]
GH54 none β-sandwich beta-d / alpha-l retaining anti 1wd4 α-l-arabinofuranosidase B Aspergillus kawachii l-arabinofuranose Asp297 Glu221 [56]
GH55 none β-helix beta-d inverting syn 4tz5 exo-β-1,3-glucanase Streptomyces sp. SirexAA-E laminarihexaose Glu502 unknown [57]
GH56 none (β/α)7 beta-d retaining anti 1fcv hyaluronidase Apis mellifera (hyaluron.)4 Glu113 internal [58]
GH57 none (β/α)7 alpha-d retaining anti 1k1y glucanotransferase Thermococcus litoralis acarbose Asp214 Glu123 [59]
GH59 A (β/α)8 beta-d retaining anti 4ccc β-galactocerebrosidase Mus musculus PNP-β-d-galactoside Glu182 Glu258 [60]
GH62 F 5-fold β-propeller alpha-l inverting anti 3wn0 α-l-arabinofuranosidase Streptomyces coelicolor β-l-Arabinofuranose Glu361 Asp202 [61]
GH63 G (α/α)6 alpha-d inverting anti 5ca3 α-glucosidase Escherichia coli glucose and lactose Asp501 Glu727 [62]
GH65 L (α/α)6 alpha-d (and α-l-rham) inverting anti 4ktr 2-O-α-glucosylglycerol phosphorylase Bacillus selenitireducens isofagomine Glu475 phosphate [63]
GH66 none (β/α)8 alpha-d retaining anti 5axh dextranase Thermoanaerobacter pseudethanolicus isomaltohexaose Glu374 Asp312 [64]
GH67 none (β/α)8 alpha-d inverting syn 1l8n α-glucuronidase Geobacillus stearothermophilus 4-O-methyl-d-glucuronic acid and xylotriose Glu286 Asp364 Glu392 [65]
GH68 J 5-fold β-propeller beta-d retaining anti 1pt2 levansucrase Bacillus subtilis sucrose Glu342 Asp86 [66]
GH70 H (β/α)8 alpha-d retaining anti 3aic glucansucrase Streptococcus mutans α-acarbose Glu515 Asp477 [67]
GH72 A (β/α)8 beta-d retaining anti 2w62 β-1,3-glucanotransferase Saccharomyces cerevisiae S288C laminaripentaose Glu176 Glu275 [68]
GH74 none 7-fold β-propeller beta-d inverting syn 2ebs cellobiohydrolase (OXG-RCBH) Geotrichum sp. m128 xyloglucan heptasaccharide Asp465 Asp35 [69]
GH76 none (α/α)6 alpha-d retaining anti 5agd endo-α-1,6-mannanase Bacillus circulans α-1,6-mannopentaose Asp125 Asp124 [70]
GH77 H (β/α)8 alpha-d retaining anti 2oww 4-α-glucanotransferase Thermus thermofilus acarbose + 4-deoxy-α-d-glucose Glu340 Asp293 [71]
GH78 H (α/α)6 alpha-l inverting anti 3w5n α-l-rhamnosidase Streptomyces avermitilis l-rhamnose Glu636 Glu895 [72]
GH79 A (β/α)8 beta-d retaining anti 5e9c heparanase Homo sapiens heparin tetrasaccharide Glu225 Glu343 [73]
GH80 I α + β beta-d inverting predicted syn by clan see at GH24
GH81 none β-sandwich beta-d inverting syn 5t4g endo-β-1,3-glucanase Bacillus halodurans C-125 laminarin Asp466 Glu542 [74]
GH83 E 6-fold β-propeller alpha-d retaining anti 1z4x hemagglutinin-neuraminidase Simian virus 5 α-2,3-sialyllactose Glu247 relay Tyr523 [75]
GH84 none (β/α)8 beta-d retaining anti 2chn β-N-acetyl-glucosaminidase Bacteroides thetaiotaomicron VPI-5482 NAG-thiazoline Glu242 internal [76]
GH85 K (β/α)8 beta-d retaining anti 2w92 endo-β-N-acetyl-glucosaminidase D Streptococcus pneumoniae TIGR4 NAG-thiazoline Glu337 internal [77]
GH86 A (β/α)8 beta-d retaining anti 4aw7 β-porphyranase Bacteroides plebeius porphyran fragment Glu152 Glu279 [78]
GH89 none (β/α)8 alpha-d retaining anti 2vcb α-N-acetyl-glucosaminidase Clostridium perfringens PUGNAc Glu483 Glu601 [79]
GH92 none (α/α)6 and β-sandwich alpha-d inverting anti 2ww1 α-1,2-mannosidase Bacteroides thetaiotaomicron VPI-5482 thiomannobioside Glu533 Asp644 Asp642 [80]
GH93 E 6-fold β-propeller alpha-l retaining anti 3a72 exo-arabinanase Penicillium chrysogenum arabinobiose Glu246 Glu174 [81]
GH94 Q (α/α)6 beta-d inverting syn 4zli cellobionic acid phosphorylase Saccharophagus degradans 3-O-β-d-glucopyranosyl-α-d-glucopyranuronic acid Asp472 phosphate [82]
GH95 none (α/α)6 alpha-l inverting anti 2ead α-1,2-l-fucosidase Bifidobacterium bifidum Fuc-α-1,2-Gal Glu566 Asn423 Asp766 [83]
GH97 none (β/α)8 alpha-d retaining + inverting anti 2zq0 α-glucosidase Bacteroides thetaiotaomicron VPI-5482 acarbose Glu532 Glu508 [84]
GH98 none (β/α)8 and β-sandwich beta-d inverting anti 2wmg endo-β-1,4-galactosidase Streptococcus pneumoniae A-LewisY pentasaccharide Glu158 Asp251 Glu301 [85]
GH99 none (β/α)8 alpha-d retaining anti 4ad4 endo-α-mannosidase Bacteroides xylanisolvens glucose-1,3-isofagomine and α-1,2- mannobiose Glu336 debated [86]
GH100 none (α/α)6 core beta-d inverting anti 5gop invertase Anabaena (Nostoc) sp. pcc7120 sucrose Asp188 Glu414 [87]
GH102 none double-ψ β-barrel beta-d retaining syn 2pi8 lytic transglycosylase A Escherichia coli chitohexaose Asp308 none [88]
GH103 none lysozyme type beta-d retaining syn 1d0k lytic transglycosylase SLT35 Escherichia coli murodipeptides Glu162 internal [89]
GH106 none (β/α)8 alpha-l inverting anti 5mwk α-l-rhamnosidase BT_0986 Bacteroides thetaiotaomicron pectin heptasaccharide Glu461 Glu593 or Glu561 [90]
GH107 R (β/α)8 alpha-l retaining predicted syn by clan see at GH29
GH110 none parallel β-helix alpha-d inverting anti 7jwf α-1,3-galactosidase Pseudoalteromonas distincta Gal-α1,3-Gal Asp344 Asp321 Asp345 [91]
GH113 A (β/α)8 beta-d retaining anti 4cd8 β-mannanase Alicyclobacillus acidocaldarius mannobioimidazole Glu151 Glu231 [92]
GH116 O (α/α)6 and β-sandwich beta-d retaining predicted anti by clan see at GH52
GH117 none 5-fold β-propeller alpha-l inverting anti 4ak7 α-1,3-3,6-anhydro-l-galactosidase Bacteroides plebeius neoagarobiose His302 (relay from Asp320) Asp90 [93]
GH120 none parallel β-helix and β-sandwich beta-d retaining anti 3vsv β-xylosidase XylC Thermoanaerobacterium saccharolyticum JW/SL-YS485 d-xylose Glu405 Asp382 [94]
GH123 none (β/α)8 and β-sandwich beta-d retaining anti 5fr0 exo-β-N-acetyl-galactosaminidase Clostridium perfringens N-difluoroacetyl-d-galactosamine Glu345 internal [95]
GH125 L (α/α)6 alpha-d inverting anti 5m7y exo-α-1,6-mannosidase Clostridium perfringens 1,6-α-mannotriose Asp220 Glu393 [96]
GH127 P (α/α)6 and β-sandwich beta-l retaining anti 3wrg β-l-arabinofuranosidase Bifidobacterium longum l-arabinose Glu322 Cys417 [97]
GH128 A (β/α)8 beta-d retaining anti 6ufl β-1,3-glucanase Amycolatopsis mediterranei laminarihexaose Glu102 Glu199 [98]
GH130 none 5-fold β-propeller beta-d inverting anti 5b0s β-1,2-mannobiose phosphorylase Listeria innocua β-1,2-mannotriose Asp141 relay phosphate [99]
GH134 none β + α beta-d inverting syn 5jug β-mannanase Streptomyces sp. mannopentaose Glu45 Asp57 [100]
GH136 none β-helix beta-d retaining syn 5gqf lacto-N-biosidase Bifidobacterium longum lacto-N-biose Asp411 Asp418 [101]
GH137 none 5-fold β-propeller beta-l unknown anti 5mui β-l-arabinofuranosidase BT_0996 Bacteroides thetaiotaomicron pectin oligosaccharide Glu240 Glu159 [90]
GH138 none (β/α)8 alpha-d retaining syn 6hzg α-1,2-d-galacturonidase Bacteroides paurosaccharolyticus alpha-d-galactopyranuronic Glu294 Glu361 [102]
GH146 P (α/α)6 and β-sandwich beta-l retaining anti 5opj β-l-arabinofuranosidase BT_0349 Bacteroides thetaiotaomicron l-arabinose Glu320 Cys416 [103]
GH147 A (β/α)8 beta-d retaining predicted anti by clan see at e.g. GH1
GH148 A (β/α)8 beta-d retaining predicted anti by clan see at e.g. GH1
GH149 Q (α/α)6 beta-d inverting predicted syn by clan see at GH94
GH156 none (β/α)8 alpha-d inverting syn 6s0e exo-α-sialidase uncultured bacterium pG7 N-acetyl-2,3-dehydro-2-deoxyneuraminic acid His134 (relay from Asp132) Asp14 [104]
GH157 A (β/α)8 beta-d retaining predicted anti by clan see at e.g. GH1
GH158 A (β/α)8 beta-d retaining predicted anti by clan see at e.g. GH1
GH161 Q (α/α)6 beta-d retaining predicted syn by clan see at GH94
GH162 none (α/α)6 beta-d inverting syn 6imw endo-β-1,2-glucanase Talaromyces funiculosus beta-1,2-glucan Glu262 via C3-OH of glc at subs. +2 Asp446 [105]
GH164 A (β/α)8 beta-d retaining anti 6t75 β-mannosidase Bacteroides salyersiae 2-deoxy-2-F-mannosyl Glu160 Glu297 [106]
GH172 none β-jelly roll alpha-d retaining anti 7v1w difructose-anhydride synthase Bifidobacterium dentum beta-d-arabinofuranose Glu270 Glu291 [107]
GH181 E 6-fold β-propeller alpha-d inverting anti 8axi exo-α-sialidase Akkermansia muciniphila 2-deoxy-2,3-dehydro-N-acetyl-neuraminic acid + T-antigen disaccharide Asp345 Glu218 [108]
GH183 none 5-bladed β-propeller alpha-d retaining anti 8ic1 endo-α-1,5-d-arabinofuranosidase Microbacterium arabinogalactanolyticum JCM 9171 α-d-Araf-(1,5)-α-d-Araf-(1,5)-α-d-Araf-(1,5)-α-d-Araf Asp51 Asp33 [109]
GH186 none β-sandwich beta-d inverting syn 8ip1 β-1,2-glucanase Escherechia coli β-1,2-glucan Asp388 Asp300 + 2 waters [110]
n.c.* none parallel β-helix alpha-d inverting anti 2vjj endo-α-N-acetylglucosaminidase Bacteriophage HK620 O18A1 O-antigen hexasaccharide Asp339 Glu372 [111]

* n.c.: Found among the collection of non-classified GH sequences in the CAZy Database.

References

  1. Heightman TD and Vasella AT. Recent Insights into Inhibition, Structure, and Mechanism of Configuration-Retaining Glycosidases. Angew Chem Int Ed. 1999 38(6):750-770. Article online.

    [HeightmanVasella1999]
  2. Nerinckx W, Desmet T, Piens K, and Claeyssens M. (2005). An elaboration on the syn-anti proton donor concept of glycoside hydrolases: electrostatic stabilisation of the transition state as a general strategy. FEBS Lett. 2005;579(2):302-12. DOI:10.1016/j.febslet.2004.12.021 | PubMed ID:15642336 [Nerinckx2005]
  3. Wu M, Nerinckx W, Piens K, Ishida T, Hansson H, Sandgren M, and Ståhlberg J. (2013). Rational design, synthesis, evaluation and enzyme-substrate structures of improved fluorogenic substrates for family 6 glycoside hydrolases. FEBS J. 2013;280(1):184-98. DOI:10.1111/febs.12060 | PubMed ID:23137336 [Wu2012]
  4. Pérez S and Marchessault RH. The exo-anomeric effect: experimental evidence from crystal structures. Carbohydr res. 1978 65:114-120. DOI:10.1016/S0008-6215(00)84218-4

    [Perez1978]
  5. Cramer CJ, Truhlar DG, and French AD. Exo-anomeric effects on energies and geometries of different conformations of glucose and related systems in the gas phase and aqueous solution. Carbohydr res. 1997 298:1-14. DOI:10.1016/S0008-6215(96)00297-2

    [Cramer1997]
  6. Johnson GP, Petersen L, French AD, and Reilly PJ. (2009). Twisting of glycosidic bonds by hydrolases. Carbohydr Res. 2009;344(16):2157-66. DOI:10.1016/j.carres.2009.08.011 | PubMed ID:19733839 [Johnson2009]
  7. Alonso ER, Peña I, Cabezas C, and Alonso JL. (2016). Structural Expression of Exo-Anomeric Effect. J Phys Chem Lett. 2016;7(5):845-50. DOI:10.1021/acs.jpclett.6b00028 | PubMed ID:26889578 [Alonso2016]
  8. Gloster TM, Roberts S, Perugino G, Rossi M, Moracci M, Panday N, Terinek M, Vasella A, and Davies GJ. (2006). Structural, kinetic, and thermodynamic analysis of glucoimidazole-derived glycosidase inhibitors. Biochemistry. 2006;45(39):11879-84. DOI:10.1021/bi060973x | PubMed ID:17002288 [Gloster2006]
  9. van Bueren AL, Ghinet MG, Gregg K, Fleury A, Brzezinski R, and Boraston AB. (2009). The structural basis of substrate recognition in an exo-beta-D-glucosaminidase involved in chitosan hydrolysis. J Mol Biol. 2009;385(1):131-9. DOI:10.1016/j.jmb.2008.10.031 | PubMed ID:18976664 [van_Bueren2009]
  10. Hrmova M, Varghese JN, De Gori R, Smith BJ, Driguez H, and Fincher GB. (2001). Catalytic mechanisms and reaction intermediates along the hydrolytic pathway of a plant beta-D-glucan glucohydrolase. Structure. 2001;9(11):1005-16. DOI:10.1016/s0969-2126(01)00673-6 | PubMed ID:11709165 [Hrmova2001]
  11. Rajan SS, Yang X, Collart F, Yip VL, Withers SG, Varrot A, Thompson J, Davies GJ, and Anderson WF. (2004). Novel catalytic mechanism of glycoside hydrolysis based on the structure of an NAD+/Mn2+ -dependent phospho-alpha-glucosidase from Bacillus subtilis. Structure. 2004;12(9):1619-29. DOI:10.1016/j.str.2004.06.020 | PubMed ID:15341727 [Rajan2004]
  12. Varrot A and Davies GJ. (2003). Direct experimental observation of the hydrogen-bonding network of a glycosidase along its reaction coordinate revealed by atomic resolution analyses of endoglucanase Cel5A. Acta Crystallogr D Biol Crystallogr. 2003;59(Pt 3):447-52. DOI:10.1107/s0907444902023405 | PubMed ID:12595701 [Varrot2003]
  13. Zou Jy, Kleywegt GJ, Ståhlberg J, Driguez H, Nerinckx W, Claeyssens M, Koivula A, Teeri TT, and Jones TA. (1999). Crystallographic evidence for substrate ring distortion and protein conformational changes during catalysis in cellobiohydrolase Ce16A from trichoderma reesei. Structure. 1999;7(9):1035-45. DOI:10.1016/s0969-2126(99)80171-3 | PubMed ID:10508787 [Zhou1999]
  14. Sulzenbacher G, Mackenzie LF, Wilson KS, Withers SG, Dupont C, and Davies GJ. (1999). The crystal structure of a 2-fluorocellotriosyl complex of the Streptomyces lividans endoglucanase CelB2 at 1.2 A resolution. Biochemistry. 1999;38(15):4826-33. DOI:10.1021/bi982648i | PubMed ID:10200171 [Sulzenbacher1999]
  15. Guérin DM, Lascombe MB, Costabel M, Souchon H, Lamzin V, Béguin P, and Alzari PM. (2002). Atomic (0.94 A) resolution structure of an inverting glycosidase in complex with substrate. J Mol Biol. 2002;316(5):1061-9. DOI:10.1006/jmbi.2001.5404 | PubMed ID:11884144 [Guerin2002]
  16. Schubot FD, Kataeva IA, Chang J, Shah AK, Ljungdahl LG, Rose JP, and Wang BC. (2004). Structural basis for the exocellulase activity of the cellobiohydrolase CbhA from Clostridium thermocellum. Biochemistry. 2004;43(5):1163-70. DOI:10.1021/bi030202i | PubMed ID:14756552 [Schubot2004]
  17. Suzuki R, Fujimoto Z, Ito S, Kawahara S, Kaneko S, Taira K, Hasegawa T, and Kuno A. (2009). Crystallographic snapshots of an entire reaction cycle for a retaining xylanase from Streptomyces olivaceoviridis E-86. J Biochem. 2009;146(1):61-70. DOI:10.1093/jb/mvp047 | PubMed ID:19279191 [Suzuki2009]
  18. Wan Q, Zhang Q, Hamilton-Brehm S, Weiss K, Mustyakimov M, Coates L, Langan P, Graham D, and Kovalevsky A. (2014). X-ray crystallographic studies of family 11 xylanase Michaelis and product complexes: implications for the catalytic mechanism. Acta Crystallogr D Biol Crystallogr. 2014;70(Pt 1):11-23. DOI:10.1107/S1399004713023626 | PubMed ID:24419374 [Wan2014]
  19. Sandgren M, Berglund GI, Shaw A, Ståhlberg J, Kenne L, Desmet T, and Mitchinson C. (2004). Crystal complex structures reveal how substrate is bound in the -4 to the +2 binding sites of Humicola grisea Cel12A. J Mol Biol. 2004;342(5):1505-17. DOI:10.1016/j.jmb.2004.07.098 | PubMed ID:15364577 [Sandgren2004]
  20. Uitdehaag JC, Mosi R, Kalk KH, van der Veen BA, Dijkhuizen L, Withers SG, and Dijkstra BW. (1999). X-ray structures along the reaction pathway of cyclodextrin glycosyltransferase elucidate catalysis in the alpha-amylase family. Nat Struct Biol. 1999;6(5):432-6. DOI:10.1038/8235 | PubMed ID:10331869 [Uitdehaag1999]
  21. Miyake H, Kurisu G, Kusunoki M, Nishimura S, Kitamura S, and Nitta Y. (2003). Crystal structure of a catalytic site mutant of beta-amylase from Bacillus cereus var. mycoides cocrystallized with maltopentaose. Biochemistry. 2003;42(19):5574-81. DOI:10.1021/bi020712x | PubMed ID:12741813 [Miyake2003]
  22. Harris EM, Aleshin AE, Firsov LM, and Honzatko RB. (1993). Refined structure for the complex of 1-deoxynojirimycin with glucoamylase from Aspergillus awamori var. X100 to 2.4-A resolution. Biochemistry. 1993;32(6):1618-26. DOI:10.1021/bi00057a028 | PubMed ID:8431441 [Harris1993]
  23. Allouch J, Helbert W, Henrissat B, and Czjzek M. (2004). Parallel substrate binding sites in a beta-agarase suggest a novel mode of action on double-helical agarose. Structure. 2004;12(4):623-32. DOI:10.1016/j.str.2004.02.020 | PubMed ID:15062085 [Allouch2004]
  24. Wojtkowiak A, Witek K, Hennig J, and Jaskolski M. (2013). Structures of an active-site mutant of a plant 1,3-β-glucanase in complex with oligosaccharide products of hydrolysis. Acta Crystallogr D Biol Crystallogr. 2013;69(Pt 1):52-62. DOI:10.1107/S0907444912042175 | PubMed ID:23275163 [Wojtkowiak2013]
  25. Papanikolau Y, Prag G, Tavlas G, Vorgias CE, Oppenheim AB, and Petratos K. (2001). High resolution structural analyses of mutant chitinase A complexes with substrates provide new insight into the mechanism of catalysis. Biochemistry. 2001;40(38):11338-43. DOI:10.1021/bi010505h | PubMed ID:11560481 [Papanikolau2001]
  26. Ohnuma T, Umemoto N, Nagata T, Shinya S, Numata T, Taira T, and Fukamizo T. (2014). Crystal structure of a "loopless" GH19 chitinase in complex with chitin tetrasaccharide spanning the catalytic center. Biochim Biophys Acta. 2014;1844(4):793-802. DOI:10.1016/j.bbapap.2014.02.013 | PubMed ID:24582745 [Ohnuma2014]
  27. Prag G, Papanikolau Y, Tavlas G, Vorgias CE, Petratos K, and Oppenheim AB. (2000). Structures of chitobiase mutants complexed with the substrate Di-N-acetyl-d-glucosamine: the catalytic role of the conserved acidic pair, aspartate 539 and glutamate 540. J Mol Biol. 2000;300(3):611-7. DOI:10.1006/jmbi.2000.3906 | PubMed ID:10884356 [Prag2000]
  28. Vocadlo DJ, Davies GJ, Laine R, and Withers SG. (2001). Catalysis by hen egg-white lysozyme proceeds via a covalent intermediate. Nature. 2001;412(6849):835-8. DOI:10.1038/35090602 | PubMed ID:11518970 [Vocadlo2001]
  29. Karlsen S, Hough E, Rao ZH, and Isaacs NW. (1996). Structure of a bulgecin-inhibited g-type lysozyme from the egg white of the Australian black swan. A comparison of the binding of bulgecin to three muramidases. Acta Crystallogr D Biol Crystallogr. 1996;52(Pt 1):105-14. DOI:10.1107/S0907444995008468 | PubMed ID:15299731 [Karlsen1996]
  30. Baldwin EP, Hajiseyedjavadi O, Baase WA, and Matthews BW. (1993). The role of backbone flexibility in the accommodation of variants that repack the core of T4 lysozyme. Science. 1993;262(5140):1715-8. DOI:10.1126/science.8259514 | PubMed ID:8259514 [Baldwin1993]
  31. Cartmell A, Topakas E, Ducros VM, Suits MD, Davies GJ, and Gilbert HJ. (2008). The Cellvibrio japonicus mannanase CjMan26C displays a unique exo-mode of action that is conferred by subtle changes to the distal region of the active site. J Biol Chem. 2008;283(49):34403-13. DOI:10.1074/jbc.M804053200 | PubMed ID:18799462 [Cartmell2008]
  32. Fernández-Leiro R, Pereira-Rodríguez A, Cerdán ME, Becerra M, and Sanz-Aparicio J. (2010). Structural analysis of Saccharomyces cerevisiae alpha-galactosidase and its complexes with natural substrates reveals new insights into substrate specificity of GH27 glycosidases. J Biol Chem. 2010;285(36):28020-33. DOI:10.1074/jbc.M110.144584 | PubMed ID:20592022 [Fernandez-Leiro2010]
  33. Abbott DW and Boraston AB. (2007). The structural basis for exopolygalacturonase activity in a family 28 glycoside hydrolase. J Mol Biol. 2007;368(5):1215-22. DOI:10.1016/j.jmb.2007.02.083 | PubMed ID:17397864 [Abbott2007]
  34. Sakurama H, Fushinobu S, Hidaka M, Yoshida E, Honda Y, Ashida H, Kitaoka M, Kumagai H, Yamamoto K, and Katayama T. (2012). 1,3-1,4-α-L-fucosynthase that specifically introduces Lewis a/x antigens into type-1/2 chains. J Biol Chem. 2012;287(20):16709-19. DOI:10.1074/jbc.M111.333781 | PubMed ID:22451675 [Sakurama2012]
  35. Urbániková L, Vršanská M, Mørkeberg Krogh KB, Hoff T, and Biely P. (2011). Structural basis for substrate recognition by Erwinia chrysanthemi GH30 glucuronoxylanase. FEBS J. 2011;278(12):2105-16. DOI:10.1111/j.1742-4658.2011.08127.x | PubMed ID:21501386 [Urbanikova2011]
  36. Sim L, Quezada-Calvillo R, Sterchi EE, Nichols BL, and Rose DR. (2008). Human intestinal maltase-glucoamylase: crystal structure of the N-terminal catalytic subunit and basis of inhibition and substrate specificity. J Mol Biol. 2008;375(3):782-92. DOI:10.1016/j.jmb.2007.10.069 | PubMed ID:18036614 [Sim2008]
  37. Verhaest M, Lammens W, Le Roy K, De Ranter CJ, Van Laere A, Rabijns A, and Van den Ende W. (2007). Insights into the fine architecture of the active site of chicory fructan 1-exohydrolase: 1-kestose as substrate vs sucrose as inhibitor. New Phytol. 2007;174(1):90-100. DOI:10.1111/j.1469-8137.2007.01988.x | PubMed ID:17335500 [Verhaest2007]
  38. Amaya MF, Watts AG, Damager I, Wehenkel A, Nguyen T, Buschiazzo A, Paris G, Frasch AC, Withers SG, and Alzari PM. (2004). Structural insights into the catalytic mechanism of Trypanosoma cruzi trans-sialidase. Structure. 2004;12(5):775-84. DOI:10.1016/j.str.2004.02.036 | PubMed ID:15130470 [Amaya2004]
  39. Zhu X, McBride R, Nycholat CM, Yu W, Paulson JC, and Wilson IA. (2012). Influenza virus neuraminidases with reduced enzymatic activity that avidly bind sialic Acid receptors. J Virol. 2012;86(24):13371-83. DOI:10.1128/JVI.01426-12 | PubMed ID:23015718 [Zhu2012]
  40. Maksimainen M, Hakulinen N, Kallio JM, Timoharju T, Turunen O, and Rouvinen J. (2011). Crystal structures of Trichoderma reesei β-galactosidase reveal conformational changes in the active site. J Struct Biol. 2011;174(1):156-63. DOI:10.1016/j.jsb.2010.11.024 | PubMed ID:21130883 [Maksimainen2011]
  41. Merceron R, Foucault M, Haser R, Mattes R, Watzlawick H, and Gouet P. (2012). The molecular mechanism of thermostable α-galactosidases AgaA and AgaB explained by x-ray crystallography and mutational studies. J Biol Chem. 2012;287(47):39642-52. DOI:10.1074/jbc.M112.394114 | PubMed ID:23012371 [Merceron2012]
  42. Gibson RP, Gloster TM, Roberts S, Warren RA, Storch de Gracia I, García A, Chiara JL, and Davies GJ. (2007). Molecular basis for trehalase inhibition revealed by the structure of trehalase in complex with potent inhibitors. Angew Chem Int Ed Engl. 2007;46(22):4115-9. DOI:10.1002/anie.200604825 | PubMed ID:17455176 [Gibson2007]
  43. Shah N, Kuntz DA, and Rose DR. (2008). Golgi alpha-mannosidase II cleaves two sugars sequentially in the same catalytic site. Proc Natl Acad Sci U S A. 2008;105(28):9570-5. DOI:10.1073/pnas.0802206105 | PubMed ID:18599462 [Shah2008]
  44. Czjzek M, Ben David A, Bravman T, Shoham G, Henrissat B, and Shoham Y. (2005). Enzyme-substrate complex structures of a GH39 beta-xylosidase from Geobacillus stearothermophilus. J Mol Biol. 2005;353(4):838-46. DOI:10.1016/j.jmb.2005.09.003 | PubMed ID:16212978 [Czjzek2005]
  45. Godoy AS, Camilo CM, Kadowaki MA, Muniz HD, Espirito Santo M, Murakami MT, Nascimento AS, and Polikarpov I. (2016). Crystal structure of β1→6-galactosidase from Bifidobacterium bifidum S17: trimeric architecture, molecular determinants of the enzymatic activity and its inhibition by α-galactose. FEBS J. 2016;283(22):4097-4112. DOI:10.1111/febs.13908 | PubMed ID:27685756 [Godoy2016]
  46. Fujimoto Z, Ichinose H, Maehara T, Honda M, Kitaoka M, and Kaneko S. (2010). Crystal structure of an Exo-1,5-{alpha}-L-arabinofuranosidase from Streptomyces avermitilis provides insights into the mechanism of substrate discrimination between exo- and endo-type enzymes in glycoside hydrolase family 43. J Biol Chem. 2010;285(44):34134-43. DOI:10.1074/jbc.M110.164251 | PubMed ID:20739278 [Fujimoto2010]
  47. Kitago Y, Karita S, Watanabe N, Kamiya M, Aizawa T, Sakka K, and Tanaka I. (2007). Crystal structure of Cel44A, a glycoside hydrolase family 44 endoglucanase from Clostridium thermocellum. J Biol Chem. 2007;282(49):35703-11. DOI:10.1074/jbc.M706835200 | PubMed ID:17905739 [Kitago2007]
  48. Davies GJ, Dodson G, Moore MH, Tolley SP, Dauter Z, Wilson KS, Rasmussen G, and Schülein M. (1996). Structure determination and refinement of the Humicola insolens endoglucanase V at 1.5 A resolution. Acta Crystallogr D Biol Crystallogr. 1996;52(Pt 1):7-17. DOI:10.1107/S0907444995009280 | PubMed ID:15299721 [Davies1996]
  49. Lyu Q, Wang S, Xu W, Han B, Liu W, Jones DN, and Liu W. (2014). Structural insights into the substrate-binding mechanism for a novel chitosanase. Biochem J. 2014;461(2):335-45. DOI:10.1042/BJ20140159 | PubMed ID:24766439 [Lyu2014]
  50. Karaveg K, Siriwardena A, Tempel W, Liu ZJ, Glushka J, Wang BC, and Moremen KW. (2005). Mechanism of class 1 (glycosylhydrolase family 47) {alpha}-mannosidases involved in N-glycan processing and endoplasmic reticulum quality control. J Biol Chem. 2005;280(16):16197-207. DOI:10.1074/jbc.M500119200 | PubMed ID:15713668 [Karaveg2005]
  51. Cantú D, Nerinckx W, and Reilly PJ. (2008). Theory and computation show that Asp463 is the catalytic proton donor in human endoplasmic reticulum alpha-(1-->2)-mannosidase I. Carbohydr Res. 2008;343(13):2235-42. DOI:10.1016/j.carres.2008.05.026 | PubMed ID:18619586 [Nerinckx2008]
  52. Pluvinage B, Hehemann JH, and Boraston AB. (2013). Substrate recognition and hydrolysis by a family 50 exo-β-agarase, Aga50D, from the marine bacterium Saccharophagus degradans. J Biol Chem. 2013;288(39):28078-88. DOI:10.1074/jbc.M113.491068 | PubMed ID:23921382 [Pluvinage2013]
  53. Hövel K, Shallom D, Niefind K, Belakhov V, Shoham G, Baasov T, Shoham Y, and Schomburg D. (2003). Crystal structure and snapshots along the reaction pathway of a family 51 alpha-L-arabinofuranosidase. EMBO J. 2003;22(19):4922-32. DOI:10.1093/emboj/cdg494 | PubMed ID:14517232 [Hoevel2003]
  54. Espina G, Eley K, Pompidor G, Schneider TR, Crennell SJ, and Danson MJ. (2014). A novel β-xylosidase structure from Geobacillus thermoglucosidasius: the first crystal structure of a glycoside hydrolase family GH52 enzyme reveals unpredicted similarity to other glycoside hydrolase folds. Acta Crystallogr D Biol Crystallogr. 2014;70(Pt 5):1366-74. DOI:10.1107/S1399004714002788 | PubMed ID:24816105 [Espina2014]
  55. Le Nours J, De Maria L, Welner D, Jørgensen CT, Christensen LL, Borchert TV, Larsen S, and Lo Leggio L. (2009). Investigating the binding of beta-1,4-galactan to Bacillus licheniformis beta-1,4-galactanase by crystallography and computational modeling. Proteins. 2009;75(4):977-89. DOI:10.1002/prot.22310 | PubMed ID:19089956 [Le_Nours2009]
  56. Miyanaga A, Koseki T, Matsuzawa H, Wakagi T, Shoun H, and Fushinobu S. (2004). Crystal structure of a family 54 alpha-L-arabinofuranosidase reveals a novel carbohydrate-binding module that can bind arabinose. J Biol Chem. 2004;279(43):44907-14. DOI:10.1074/jbc.M405390200 | PubMed ID:15292273 [Miyanaga2004]
  57. Bianchetti CM, Takasuka TE, Deutsch S, Udell HS, Yik EJ, Bergeman LF, and Fox BG. (2015). Active site and laminarin binding in glycoside hydrolase family 55. J Biol Chem. 2015;290(19):11819-32. DOI:10.1074/jbc.M114.623579 | PubMed ID:25752603 [Bianchetti2015]
  58. Marković-Housley Z, Miglierini G, Soldatova L, Rizkallah PJ, Müller U, and Schirmer T. (2000). Crystal structure of hyaluronidase, a major allergen of bee venom. Structure. 2000;8(10):1025-35. DOI:10.1016/s0969-2126(00)00511-6 | PubMed ID:11080624 [Markovic-Housley2000]
  59. Imamura H, Fushinobu S, Yamamoto M, Kumasaka T, Jeon BS, Wakagi T, and Matsuzawa H. (2003). Crystal structures of 4-alpha-glucanotransferase from Thermococcus litoralis and its complex with an inhibitor. J Biol Chem. 2003;278(21):19378-86. DOI:10.1074/jbc.M213134200 | PubMed ID:12618437 [Imamura2003]
  60. Hill CH, Graham SC, Read RJ, and Deane JE. (2013). Structural snapshots illustrate the catalytic cycle of β-galactocerebrosidase, the defective enzyme in Krabbe disease. Proc Natl Acad Sci U S A. 2013;110(51):20479-84. DOI:10.1073/pnas.1311990110 | PubMed ID:24297913 [Hill2013]
  61. Maehara T, Fujimoto Z, Ichinose H, Michikawa M, Harazono K, and Kaneko S. (2014). Crystal structure and characterization of the glycoside hydrolase family 62 α-L-arabinofuranosidase from Streptomyces coelicolor. J Biol Chem. 2014;289(11):7962-72. DOI:10.1074/jbc.M113.540542 | PubMed ID:24482228 [Maehara2014]
  62. Miyazaki T, Nishikawa A, and Tonozuka T. (2016). Crystal structure of the enzyme-product complex reveals sugar ring distortion during catalysis by family 63 inverting α-glycosidase. J Struct Biol. 2016;196(3):479-486. DOI:10.1016/j.jsb.2016.09.015 | PubMed ID:27688023 [Miyazaki2016]
  63. Touhara KK, Nihira T, Kitaoka M, Nakai H, and Fushinobu S. (2014). Structural basis for reversible phosphorolysis and hydrolysis reactions of 2-O-α-glucosylglycerol phosphorylase. J Biol Chem. 2014;289(26):18067-75. DOI:10.1074/jbc.M114.573212 | PubMed ID:24828502 [Touhara2014]
  64. Suzuki N, Kishine N, Fujimoto Z, Sakurai M, Momma M, Ko JA, Nam SH, Kimura A, and Kim YM. (2016). Crystal structure of thermophilic dextranase from Thermoanaerobacter pseudethanolicus. J Biochem. 2016;159(3):331-9. DOI:10.1093/jb/mvv104 | PubMed ID:26494689 [Suzuki2016]
  65. Golan G, Shallom D, Teplitsky A, Zaide G, Shulami S, Baasov T, Stojanoff V, Thompson A, Shoham Y, and Shoham G. (2004). Crystal structures of Geobacillus stearothermophilus alpha-glucuronidase complexed with its substrate and products: mechanistic implications. J Biol Chem. 2004;279(4):3014-24. DOI:10.1074/jbc.M310098200 | PubMed ID:14573597 [Golan2004]
  66. Meng G and Fütterer K. (2003). Structural framework of fructosyl transfer in Bacillus subtilis levansucrase. Nat Struct Biol. 2003;10(11):935-41. DOI:10.1038/nsb974 | PubMed ID:14517548 [Meng2003]
  67. Ito K, Ito S, Shimamura T, Weyand S, Kawarasaki Y, Misaka T, Abe K, Kobayashi T, Cameron AD, and Iwata S. (2011). Crystal structure of glucansucrase from the dental caries pathogen Streptococcus mutans. J Mol Biol. 2011;408(2):177-86. DOI:10.1016/j.jmb.2011.02.028 | PubMed ID:21354427 [Ito2011]
  68. Hurtado-Guerrero R, Schüttelkopf AW, Mouyna I, Ibrahim AF, Shepherd S, Fontaine T, Latgé JP, and van Aalten DM. (2009). Molecular mechanisms of yeast cell wall glucan remodeling. J Biol Chem. 2009;284(13):8461-9. DOI:10.1074/jbc.M807990200 | PubMed ID:19097997 [Hurtado-Gerrero2009]
  69. Yaoi K, Kondo H, Hiyoshi A, Noro N, Sugimoto H, Tsuda S, Mitsuishi Y, and Miyazaki K. (2007). The structural basis for the exo-mode of action in GH74 oligoxyloglucan reducing end-specific cellobiohydrolase. J Mol Biol. 2007;370(1):53-62. DOI:10.1016/j.jmb.2007.04.035 | PubMed ID:17498741 [Yaoi2007]
  70. Thompson AJ, Speciale G, Iglesias-Fernández J, Hakki Z, Belz T, Cartmell A, Spears RJ, Chandler E, Temple MJ, Stepper J, Gilbert HJ, Rovira C, Williams SJ, and Davies GJ. (2015). Evidence for a boat conformation at the transition state of GH76 α-1,6-mannanases--key enzymes in bacterial and fungal mannoprotein metabolism. Angew Chem Int Ed Engl. 2015;54(18):5378-82. DOI:10.1002/anie.201410502 | PubMed ID:25772148 [Thompson2015]
  71. Barends TR, Bultema JB, Kaper T, van der Maarel MJ, Dijkhuizen L, and Dijkstra BW. (2007). Three-way stabilization of the covalent intermediate in amylomaltase, an alpha-amylase-like transglycosylase. J Biol Chem. 2007;282(23):17242-9. DOI:10.1074/jbc.M701444200 | PubMed ID:17420245 [Barends2007]
  72. Fujimoto Z, Jackson A, Michikawa M, Maehara T, Momma M, Henrissat B, Gilbert HJ, and Kaneko S. (2013). The structure of a Streptomyces avermitilis α-L-rhamnosidase reveals a novel carbohydrate-binding module CBM67 within the six-domain arrangement. J Biol Chem. 2013;288(17):12376-85. DOI:10.1074/jbc.M113.460097 | PubMed ID:23486481 [Fujimoto2013]
  73. Wu L, Viola CM, Brzozowski AM, and Davies GJ. (2015). Structural characterization of human heparanase reveals insights into substrate recognition. Nat Struct Mol Biol. 2015;22(12):1016-22. DOI:10.1038/nsmb.3136 | PubMed ID:26575439 [Wu2015]
  74. Pluvinage B, Fillo A, Massel P, and Boraston AB. (2017). Structural Analysis of a Family 81 Glycoside Hydrolase Implicates Its Recognition of β-1,3-Glucan Quaternary Structure. Structure. 2017;25(9):1348-1359.e3. DOI:10.1016/j.str.2017.06.019 | PubMed ID:28781080 [Pluvinage2017]
  75. Yuan P, Thompson TB, Wurzburg BA, Paterson RG, Lamb RA, and Jardetzky TS. (2005). Structural studies of the parainfluenza virus 5 hemagglutinin-neuraminidase tetramer in complex with its receptor, sialyllactose. Structure. 2005;13(5):803-15. DOI:10.1016/j.str.2005.02.019 | PubMed ID:15893670 [Yuan2005]
  76. Dennis RJ, Taylor EJ, Macauley MS, Stubbs KA, Turkenburg JP, Hart SJ, Black GN, Vocadlo DJ, and Davies GJ. (2006). Structure and mechanism of a bacterial beta-glucosaminidase having O-GlcNAcase activity. Nat Struct Mol Biol. 2006;13(4):365-71. DOI:10.1038/nsmb1079 | PubMed ID:16565725 [Dennis2006]
  77. Abbott DW, Macauley MS, Vocadlo DJ, and Boraston AB. (2009). Streptococcus pneumoniae endohexosaminidase D, structural and mechanistic insight into substrate-assisted catalysis in family 85 glycoside hydrolases. J Biol Chem. 2009;284(17):11676-89. DOI:10.1074/jbc.M809663200 | PubMed ID:19181667 [Abbott2009]
  78. Hehemann JH, Kelly AG, Pudlo NA, Martens EC, and Boraston AB. (2012). Bacteria of the human gut microbiome catabolize red seaweed glycans with carbohydrate-active enzyme updates from extrinsic microbes. Proc Natl Acad Sci U S A. 2012;109(48):19786-91. DOI:10.1073/pnas.1211002109 | PubMed ID:23150581 [Hehemann_1_2012]
  79. Ficko-Blean E, Stubbs KA, Nemirovsky O, Vocadlo DJ, and Boraston AB. (2008). Structural and mechanistic insight into the basis of mucopolysaccharidosis IIIB. Proc Natl Acad Sci U S A. 2008;105(18):6560-5. DOI:10.1073/pnas.0711491105 | PubMed ID:18443291 [Ficko-Blean2008]
  80. Zhu Y, Suits MD, Thompson AJ, Chavan S, Dinev Z, Dumon C, Smith N, Moremen KW, Xiang Y, Siriwardena A, Williams SJ, Gilbert HJ, and Davies GJ. (2010). Mechanistic insights into a Ca2+-dependent family of alpha-mannosidases in a human gut symbiont. Nat Chem Biol. 2010;6(2):125-32. DOI:10.1038/nchembio.278 | PubMed ID:20081828 [Zhu2009]
  81. Sogabe Y, Kitatani T, Yamaguchi A, Kinoshita T, Adachi H, Takano K, Inoue T, Mori Y, Matsumura H, Sakamoto T, and Tada T. (2011). High-resolution structure of exo-arabinanase from Penicillium chrysogenum. Acta Crystallogr D Biol Crystallogr. 2011;67(Pt 5):415-22. DOI:10.1107/S0907444911006299 | PubMed ID:21543843 [Sogabe2011]
  82. Nam YW, Nihira T, Arakawa T, Saito Y, Kitaoka M, Nakai H, and Fushinobu S. (2015). Crystal Structure and Substrate Recognition of Cellobionic Acid Phosphorylase, Which Plays a Key Role in Oxidative Cellulose Degradation by Microbes. J Biol Chem. 2015;290(30):18281-92. DOI:10.1074/jbc.M115.664664 | PubMed ID:26041776 [Nam2015]
  83. Nagae M, Tsuchiya A, Katayama T, Yamamoto K, Wakatsuki S, and Kato R. (2007). Structural basis of the catalytic reaction mechanism of novel 1,2-alpha-L-fucosidase from Bifidobacterium bifidum. J Biol Chem. 2007;282(25):18497-18509. DOI:10.1074/jbc.M702246200 | PubMed ID:17459873 [Nagae2007]
  84. Kitamura M, Okuyama M, Tanzawa F, Mori H, Kitago Y, Watanabe N, Kimura A, Tanaka I, and Yao M. (2008). Structural and functional analysis of a glycoside hydrolase family 97 enzyme from Bacteroides thetaiotaomicron. J Biol Chem. 2008;283(52):36328-37. DOI:10.1074/jbc.M806115200 | PubMed ID:18981178 [Kitamura2008]
  85. Higgins MA, Whitworth GE, El Warry N, Randriantsoa M, Samain E, Burke RD, Vocadlo DJ, and Boraston AB. (2009). Differential recognition and hydrolysis of host carbohydrate antigens by Streptococcus pneumoniae family 98 glycoside hydrolases. J Biol Chem. 2009;284(38):26161-73. DOI:10.1074/jbc.M109.024067 | PubMed ID:19608744 [Higgins2009]
  86. Thompson AJ, Williams RJ, Hakki Z, Alonzi DS, Wennekes T, Gloster TM, Songsrirote K, Thomas-Oates JE, Wrodnigg TM, Spreitz J, Stütz AE, Butters TD, Williams SJ, and Davies GJ. (2012). Structural and mechanistic insight into N-glycan processing by endo-α-mannosidase. Proc Natl Acad Sci U S A. 2012;109(3):781-6. DOI:10.1073/pnas.1111482109 | PubMed ID:22219371 [Thompson2012]
  87. Xie J, Cai K, Hu HX, Jiang YL, Yang F, Hu PF, Cao DD, Li WF, Chen Y, and Zhou CZ. (2016). Structural Analysis of the Catalytic Mechanism and Substrate Specificity of Anabaena Alkaline Invertase InvA Reveals a Novel Glucosidase. J Biol Chem. 2016;291(49):25667-25677. DOI:10.1074/jbc.M116.759290 | PubMed ID:27777307 [Xie2016]
  88. van Straaten KE, Barends TR, Dijkstra BW, and Thunnissen AM. (2007). Structure of Escherichia coli Lytic transglycosylase MltA with bound chitohexaose: implications for peptidoglycan binding and cleavage. J Biol Chem. 2007;282(29):21197-205. DOI:10.1074/jbc.M701818200 | PubMed ID:17502382 [van_Straaten2007]
  89. van Asselt EJ, Kalk KH, and Dijkstra BW. (2000). Crystallographic studies of the interactions of Escherichia coli lytic transglycosylase Slt35 with peptidoglycan. Biochemistry. 2000;39(8):1924-34. DOI:10.1021/bi992161p | PubMed ID:10684641 [van_Asselt2000]
  90. Ndeh D, Rogowski A, Cartmell A, Luis AS, Baslé A, Gray J, Venditto I, Briggs J, Zhang X, Labourel A, Terrapon N, Buffetto F, Nepogodiev S, Xiao Y, Field RA, Zhu Y, O'Neil MA, Urbanowicz BR, York WS, Davies GJ, Abbott DW, Ralet MC, Martens EC, Henrissat B, and Gilbert HJ. (2017). Complex pectin metabolism by gut bacteria reveals novel catalytic functions. Nature. 2017;544(7648):65-70. DOI:10.1038/nature21725 | PubMed ID:28329766 [Ndeh2017]
  91. McGuire BE, Hettle AG, Vickers C, King DT, Vocadlo DJ, and Boraston AB. (2020). The structure of a family 110 glycoside hydrolase provides insight into the hydrolysis of α-1,3-galactosidic linkages in λ-carrageenan and blood group antigens. J Biol Chem. 2020;295(52):18426-18435. DOI:10.1074/jbc.RA120.015776 | PubMed ID:33127644 [McGuire2020]
  92. Williams RJ, Iglesias-Fernández J, Stepper J, Jackson A, Thompson AJ, Lowe EC, White JM, Gilbert HJ, Rovira C, Davies GJ, and Williams SJ. (2014). Combined inhibitor free-energy landscape and structural analysis reports on the mannosidase conformational coordinate. Angew Chem Int Ed Engl. 2014;53(4):1087-91. DOI:10.1002/anie.201308334 | PubMed ID:24339341 [Williams2014]
  93. Hehemann JH, Smyth L, Yadav A, Vocadlo DJ, and Boraston AB. (2012). Analysis of keystone enzyme in Agar hydrolysis provides insight into the degradation (of a polysaccharide from) red seaweeds. J Biol Chem. 2012;287(17):13985-95. DOI:10.1074/jbc.M112.345645 | PubMed ID:22393053 [Hehemann_2_2012]
  94. Huang CH, Sun Y, Ko TP, Chen CC, Zheng Y, Chan HC, Pang X, Wiegel J, Shao W, and Guo RT. (2012). The substrate/product-binding modes of a novel GH120 β-xylosidase (XylC) from Thermoanaerobacterium saccharolyticum JW/SL-YS485. Biochem J. 2012;448(3):401-7. DOI:10.1042/BJ20121359 | PubMed ID:22992047 [Huang2012]
  95. Noach I, Pluvinage B, Laurie C, Abe KT, Alteen MG, Vocadlo DJ, and Boraston AB. (2016). The Details of Glycolipid Glycan Hydrolysis by the Structural Analysis of a Family 123 Glycoside Hydrolase from Clostridium perfringens. J Mol Biol. 2016;428(16):3253-3265. DOI:10.1016/j.jmb.2016.03.020 | PubMed ID:27038508 [Noach2016]
  96. Alonso-Gil S, Males A, Fernandes PZ, Williams SJ, Davies GJ, and Rovira C. (2017). Computational Design of Experiment Unveils the Conformational Reaction Coordinate of GH125 α-Mannosidases. J Am Chem Soc. 2017;139(3):1085-1088. DOI:10.1021/jacs.6b11247 | PubMed ID:28026180 [Alonso-Gil2016]
  97. Huang CH, Zhu Z, Cheng YS, Chan HC, Ko TP, Chen CC, Wang I, Ho MR, Hsu ST, Zeng YF, Huang YN, Liu JR, Guo RT. Structure and Catalytic Mechanism of a Glycoside Hydrolase Family-127 β-L-Arabinofuranosidase (HypBA1). J Bioprocess Biotech. 2014 4:171 DOI:10.4172/2155-9821.1000171

    [Huang2014]
  98. Santos CR, Costa PACR, Vieira PS, Gonzalez SET, Correa TLR, Lima EA, Mandelli F, Pirolla RAS, Domingues MN, Cabral L, Martins MP, Cordeiro RL, Junior AT, Souza BP, Prates ÉT, Gozzo FC, Persinoti GF, Skaf MS, and Murakami MT. (2020). Structural insights into β-1,3-glucan cleavage by a glycoside hydrolase family. Nat Chem Biol. 2020;16(8):920-929. DOI:10.1038/s41589-020-0554-5 | PubMed ID:32451508 [Santos2020]
  99. Tsuda T, Nihira T, Chiku K, Suzuki E, Arakawa T, Nishimoto M, Kitaoka M, Nakai H, and Fushinobu S. (2015). Characterization and crystal structure determination of β-1,2-mannobiose phosphorylase from Listeria innocua. FEBS Lett. 2015;589(24 Pt B):3816-21. DOI:10.1016/j.febslet.2015.11.034 | PubMed ID:26632508 [Tsuda2015]
  100. Jin Y, Petricevic M, John A, Raich L, Jenkins H, Portela De Souza L, Cuskin F, Gilbert HJ, Rovira C, Goddard-Borger ED, Williams SJ, and Davies GJ. A β-Mannanase with a Lysozyme-like Fold and a Novel Molecular Catalytic Mechanism. ACS Cent Sci. 2016 Nov DOI:10.1021/acscentsci.6b00232

    [Jin2016]
  101. Yamada C, Gotoh A, Sakanaka M, Hattie M, Stubbs KA, Katayama-Ikegami A, Hirose J, Kurihara S, Arakawa T, Kitaoka M, Okuda S, Katayama T, and Fushinobu S. (2017). Molecular Insight into Evolution of Symbiosis between Breast-Fed Infants and a Member of the Human Gut Microbiome Bifidobacterium longum. Cell Chem Biol. 2017;24(4):515-524.e5. DOI:10.1016/j.chembiol.2017.03.012 | PubMed ID:28392148 [Yamada2017]
  102. Labourel A, Baslé A, Munoz-Munoz J, Ndeh D, Booth S, Nepogodiev SA, Field RA, and Cartmell A. (2019). Structural and functional analyses of glycoside hydrolase 138 enzymes targeting chain A galacturonic acid in the complex pectin rhamnogalacturonan II. J Biol Chem. 2019;294(19):7711-7721. DOI:10.1074/jbc.RA118.006626 | PubMed ID:30877196 [Labourel2019]
  103. Luis AS, Briggs J, Zhang X, Farnell B, Ndeh D, Labourel A, Baslé A, Cartmell A, Terrapon N, Stott K, Lowe EC, McLean R, Shearer K, Schückel J, Venditto I, Ralet MC, Henrissat B, Martens EC, Mosimann SC, Abbott DW, and Gilbert HJ. (2018). Dietary pectic glycans are degraded by coordinated enzyme pathways in human colonic Bacteroides. Nat Microbiol. 2018;3(2):210-219. DOI:10.1038/s41564-017-0079-1 | PubMed ID:29255254 [Luis2018]
  104. Bule P, Chuzel L, Blagova E, Wu L, Gray MA, Henrissat B, Rapp E, Bertozzi CR, Taron CH, and Davies GJ. (2019). Inverting family GH156 sialidases define an unusual catalytic motif for glycosidase action. Nat Commun. 2019;10(1):4816. DOI:10.1038/s41467-019-12684-7 | PubMed ID:31645552 [Bule2019]
  105. Tanaka N, Nakajima M, Narukawa-Nara M, Matsunaga H, Kamisuki S, Aramasa H, Takahashi Y, Sugimoto N, Abe K, Terada T, Miyanaga A, Yamashita T, Sugawara F, Kamakura T, Komba S, Nakai H, and Taguchi H. (2019). Identification, characterization, and structural analyses of a fungal endo-β-1,2-glucanase reveal a new glycoside hydrolase family. J Biol Chem. 2019;294(19):7942-7965. DOI:10.1074/jbc.RA118.007087 | PubMed ID:30926603 [Tanaka2019]
  106. Armstrong Z and Davies GJ. (2020). Structure and function of Bs164 β-mannosidase from Bacteroides salyersiae the founding member of glycoside hydrolase family GH164. J Biol Chem. 2020;295(13):4316-4326. DOI:10.1074/jbc.RA119.011591 | PubMed ID:31871050 [Armstrong2020]
  107. Kashima T, Okumura K, Ishiwata A, Kaieda M, Terada T, Arakawa T, Yamada C, Shimizu K, Tanaka K, Kitaoka M, Ito Y, Fujita K, and Fushinobu S. (2021). Identification of difructose dianhydride I synthase/hydrolase from an oral bacterium establishes a novel glycoside hydrolase family. J Biol Chem. 2021;297(5):101324. DOI:10.1016/j.jbc.2021.101324 | PubMed ID:34688653 [Kashima2021]
  108. Shuoker B, Pichler MJ, Jin C, Sakanaka H, Wu H, Gascueña AM, Liu J, Nielsen TS, Holgersson J, Nordberg Karlsson E, Juge N, Meier S, Morth JP, Karlsson NG, and Abou Hachem M. (2023). Sialidases and fucosidases of Akkermansia muciniphila are crucial for growth on mucin and nutrient sharing with mucus-associated gut bacteria. Nat Commun. 2023;14(1):1833. DOI:10.1038/s41467-023-37533-6 | PubMed ID:37005422 [Shuoker2023]
  109. Shimokawa M, Ishiwata A, Kashima T, Nakashima C, Li J, Fukushima R, Sawai N, Nakamori M, Tanaka Y, Kudo A, Morikami S, Iwanaga N, Akai G, Shimizu N, Arakawa T, Yamada C, Kitahara K, Tanaka K, Ito Y, Fushinobu S, and Fujita K. (2023). Identification and characterization of endo-α-, exo-α-, and exo-β-D-arabinofuranosidases degrading lipoarabinomannan and arabinogalactan of mycobacteria. Nat Commun. 2023;14(1):5803. DOI:10.1038/s41467-023-41431-2 | PubMed ID:37726269 [Shimokawa2023]
  110. Motouchi S, Kobayashi K, Nakai H, and Nakajima M. (2023). Identification of enzymatic functions of osmo-regulated periplasmic glucan biosynthesis proteins from Escherichia coli reveals a novel glycoside hydrolase family. Commun Biol. 2023;6(1):961. DOI:10.1038/s42003-023-05336-6 | PubMed ID:37735577 [Motouchi2023]
  111. Barbirz S, Müller JJ, Uetrecht C, Clark AJ, Heinemann U, and Seckler R. (2008). Crystal structure of Escherichia coli phage HK620 tailspike: podoviral tailspike endoglycosidase modules are evolutionarily related. Mol Microbiol. 2008;69(2):303-16. DOI:10.1111/j.1365-2958.2008.06311.x | PubMed ID:18547389 [Barbirz2008]

All Medline abstracts: PubMed