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Syn/anti lateral protonation
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- Author: ^^^Wim Nerinckx^^^
- Responsible Curator: ^^^Spencer Williams^^^
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]. 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).
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 page 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 | retaining | anti | 2cer | β-glycosidase S | Sulfolobus solfataricus P2 | phenethyl glucoimidazole | Glu206 | Glu387 | [7] | |
| GH2 | A | (β/α)8 | beta | retaining | anti | 2vzu | exo-β-glucosaminidase | Amicolatopsis orientalis | PNP-β-d-glucosamine | Glu469 | Glu541 | [8] | |
| GH3 | none | (β/α)8 | beta | retaining | anti | 1iex | exo-1,3-1,4-glucanase | Hordeum vulgare | thiocellobiose | Glu491 | Asp285 | [9] | |
| GH5 | A | (β/α)8 | beta | retaining | anti | 1h2j | endo-β-1,4-glucanase | Bacillus agaradhaerens | 2',4'-DNP-2-F-cellobioside | Glu129 | Glu228 | [10] | |
| GH6 | none | (β/α)8 | beta | inverting | syn | 1qjw | cellobiohydrolase 2 | Hypocrea jecorina | (Glc)2-S-(Glc)2 | Asp221 | debated | [11] | |
| GH7 | B | β-jelly roll | beta | retaining | syn | 1ovw | endo-1,4-glucanase | Fusarium oxysporum | thio-(Glc)5 | Glu202 | Glu197 | [12] | |
| GH8 | M | (α/α)6 | beta | inverting | anti | 1kwf | endo-1,4-glucanase | Clostridium thermocellum | cellopentaose | Glu95 | Asp278 | [13] | |
| GH9 | none | (α/α)6 | beta | inverting | syn | 1rq5 | cellobiohydrolase | Clostridium thermocellum | cellotetraose | Glu795 | Asp383 | [14] | |
| GH10 | A | (β/α)8 | beta | retaining | anti | 2d24 | β-1,4-xylanase | Streptomyces olivaceoviridis E-86 | xylopentaose | Glu128 | Glu236 | [15] | |
| GH11 | C | β-jelly roll | beta | retaining | syn | 1bvv | xylanase | Bacillus circulans | Xyl-2-F-xylosyl | Glu172 | Glu78 | [16] | |
| GH12 | C | β-jelly roll | beta | retaining | syn | 1w2u | endoglucanase | Humicola grisea | thiocellotetraose | Glu205 | Glu120 | [17] | |
| GH13 | H | (β/α)8 | alpha | retaining | anti | 1cxk | β-cyclodextrin glucanotransferase | Bacillus circulans | maltononaose | Glu257 | Asp229 | [18] | |
| GH14 | none | (β/α)8 | alpha | inverting | syn | 1itc | β-amylase | Bacillus cereus | maltopentaose | Glu172 | Glu367 | [19] | |
| GH15 | L | (α/α)6 | alpha | inverting | anti | 1dog | glucoamylase | Aspergillus awamori | 1-deoxynojirimycin | Glu179 | Glu400 | [20] | |
| GH16 | B | β-jelly roll | beta | retaining | syn | 1urx | β-agarase A | Zobellia galactanivorans | oligoagarose | Glu152 | Glu147 | [21] | |
| GH17 | A | (β/α)8 | beta | retaining | predicted anti by clan | see e.g. at GH1 | |||||||
| GH18 | K | (β/α)8 | beta | retaining | anti | 1ffr | chitinase A | Serratia marcescens | (NAG)6 | Glu315 | internal | [22] | |
| GH19 | none | lysozyme type | beta | inverting | syn | 3wh1 | chitinase | Bryum coronatum | (GlcNAc)4 | Glu61 | Glu70 | [23] | |
| GH20 | K | (β/α)8 | beta | retaining | anti | 1c7s | chitobiase | Serratia marcescens | chitobiose | Glu540 | internal | [24] | |
| GH22 | none | lysozyme type | beta | retaining | syn | 1h6m | lysozyme C | Gallus gallus | Chit-2-F-chitosyl | Glu35 | Asp52 | [25] | |
| GH23 | none | lysozyme type | beta | inverting | syn | 1lsp | lysozyme G | Cygnus atratus | Bulgecin A | Glu73 | internal | [26] | |
| GH24 | I | α + β | beta | inverting | syn | 148l | lysozyme E | Bacteriophage T4 | chitobiosyl | Glu11 | Glu26 | [27] | |
| GH26 | A | (β/α)8 | beta | retaining | anti | 1gw1 | mannanase A | Cellvibrio japonicus | 2',4'-DNP-2-F-cellotrioside | Glu212 | Glu320 | [28] | |
| GH27 | D | (β/α)8 | alpha | retaining | anti | 1ktc | α-N-acetyl galactosaminidase | Gallus gallus | NAGal | Asp201 | Asp410 | [29] | |
| GH28 | N | β-helix | alpha | inverting | anti | 2uvf | exo-polygalacturonosidase | Yersinia enterocolitica ATCC9610D | digalacturonic acid | Asp402 | Asp381 Asp403 | [30] | |
| GH29 | none | (β/α)8 | alpha | retaining | syn | 1hl9 | α-l-fucosidase | Thermotoga maritima | 2-F-fuco- pyranosyl | Glu266 | Asp224 | [31] | |
| GH30 | A | (β/α)8 | beta | retaining | anti | 2v3d | glucocerebrosidase 1 | Homo sapiens | N-butyl-deoxynojirimycin | Glu235 | Glu340 | [32] | |
| GH31 | D | (β/α)8 | alpha | retaining | anti | 2qmj | maltase-glucoamylase | Homo sapiens | acarbose | Asp542 | Asp443 | [33] | |
| GH32 | J | 5-fold β-propeller | beta | retaining | anti | 2add | fructan β-(2,1)-fructosidase | Cichorium intybus | sucrose | Glu201 | Asp22 | [34] | |
| GH33 | E | 6-fold β-propeller | alpha | retaining | anti | 1s0i | trans-sialidase | Trypanosoma cruzi | sialyl-lactose | Asp59 | Tyr342 | [35] | |
| GH34 | E | 6-fold β-propeller | alpha | retaining | anti | 2bat | neuraminidase | Influenza A virus | sialic acid | Asp151 | Tyr406 | [36] | |
| GH35 | A | (β/α)8 | beta | retaining | anti | 1xc6 | β-galactosidase | Penicillium sp. | d-galactose | Glu200 | Glu299 | [37] | |
| GH36 | D | (β/α)8 | alpha | retaining | anti | 4fns | β-galactosidase | Geobacillus stearothermophilus | 1-deoxy galactonojirimycin | Asp584 | Asp478 | [38] | |
| GH37 | G | (α/α)6 | alpha | inverting | anti | 2jf4 | trehalase | Escherechia coli | validoxylamine | Asp312 | Glu496 | [39] | |
| GH38 | none | (β/α)7 | alpha | retaining | anti | 1qwn | α-mannosidase II | Drosophila melanogaster | 5-F-β-l-gulosyl | Asp341 | Asp204 | [40] | |
| GH39 | A | (β/α)8 | beta | retaining | anti | 1uhv | β-xylosidase | Thermoanaerobacterium saccharolyticum | 2-F-xylosyl | Glu160 | Glu277 | [41] | |
| GH42 | A | (β/α)8 | beta | retaining | anti | 4ucf | β-galactosidase | Bifidobacterium bifidum | d-galactose | Glu161 | Glu320 | [42] | |
| GH44 | none | (β/α)8 | beta | retaining | anti | 2eqd | endoglucanase | Clostridium thermocellum | cellooctaose | Glu186 | Glu359 | [43] | |
| GH45 | none | 6-strand. β-barrel | beta | inverting | syn | 4eng | endo-1,4-glucanase | Humicola insolens | cellohexaose | Asp121 | Asp10 | [44] | |
| GH46 | I | lysozyme type | beta | inverting | syn | 4olt | chitosanase | Pseudomonas sp. LL2(2010) | d-glucosamine | Glu25 | Asp43 | [45] | |
| GH47 | none | (α/α)7 | alpha | inverting | anti | 1x9d | α-mannosidase I | Homo sapiens | Me-2-S-(α-Man)-2-thio-α-Man | Asp463 | Glu599 | [46], [47] | |
| GH48 | M | (α/α)6 | beta | inverting | predicted anti by clan | see at GH8 | |||||||
| GH49 | N | β-helix | alpha | inverting | predicted anti by clan | see at GH28 | |||||||
| GH50 | A | (β/α)8 | beta | retaining | anti | 4bq5 | exo-β-agarase | Saccharophagus degradans | neoagarotetraose | Glu535 | Glu695 | [48] | |
| GH51 | A | (β/α)8 | alpha | retaining | anti | 1qw9 | α-l-arabino- furanosidase | Geobacillus stearothermophilus | PNP-l-arabino-furanoside | Glu175 | Glu294 | [49] | |
| GH52 | O | (α/α)6 | beta | retaining | anti | 4c1p | β-xylosidase | Geobacillus thermoglucosidasius | xylobiose | Asp517 | Glu537 | [50] | |
| GH53 | A | (β/α)8 | beta | retaining | anti | 2ccr | β-1,4-galactanase | Bacillus licheniformis | galactotriose | Glu165 | Glu263 | [51] | |
| GH54 | none | β-sandwich | alpha | retaining | anti | 1wd4 | α-l-arabino- furanosidase B | Aspergillus kawachii | l-arabinofuranose | Asp297 | Glu221 | [52] | |
| GH55 | none | β-helix | beta | inverting | anti | 3eqo | β-1,3-glucanase | Phanerochaete chrysosporium K-3 | d-gluconolacton | Glu633 | unknown | [53] | |
| GH56 | none | (β/α)7 | beta | retaining | anti | 1fcv | hyaluronidase | Apis mellifera | (hyaluron.)4 | Glu113 | internal | [54] | |
| GH57 | none | (β/α)7 | alpha | retaining | anti | 1k1y | glucanotransferase | Thermococcus litoralis | acarbose | Asp214 | Glu123 | [55] | |
| GH59 | A | (β/α)8 | beta | retaining | anti | 4ccc | β-galactocerebrosidase | Mus musculus | PNP-β-d-gal | Glu182 | Glu258 | [56] | |
| GH63 | G | (α/α)6 | alpha | inverting | predicted anti by clan | see at GH37 | |||||||
| GH65 | L | (α/α)6 | alpha | inverting | anti | 4ktr | 2-O-α-glucosylglycerol phosphorylase | Bacillus selenitireducens | isofagomine | Glu475 | phosphate | [57] | |
| GH66 | L | (β/α)8 | alpha | retaining | anti | 5axh | dextranase | Thermoanaerobacter pseudethanolicus | isomaltohexaose | Glu374 | Asp312 | [58] | |
| GH67 | none | (β/α)8 | alpha | inverting | syn | 1gql | α-glucuronidase | Cellvibrio japonicus Ueda107 | d-glucuronic acid | Glu292 | unknown | [59] | |
| GH68 | J | 5-fold β-propeller | beta | retaining | anti | 1pt2 | levansucrase | Bacillus subtilis | sucrose | Glu342 | Asp86 | [60] | |
| GH70 | H | (β/α)8 | alpha | retaining | anti | 3aic | glucansucrase | Streptococcus mutans | α-acarbose | Glu515 | Asp477 | [61] | |
| GH72 | A | (β/α)8 | beta | retaining | anti | 2w62 | β-1,3-glucano- transferase | Saccharomyces cerevisiae S288C | laminaripentaose | Glu176 | Glu275 | [62] | |
| GH74 | none | 7-fold β-propeller | beta | inverting | syn | 2ebs | cellobiohydrolase (OXG-RCBH) | Geotrichum sp. m128 | xyloglucan heptasaccharide | Asp465 | Asp35 | [63] | |
| GH76 | none | (α/α)6 | alpha | retaining | anti | 5agd | endo-α-1,6-mannanase | Bacillus circulans | α-1,6-mannopentaose | Asp125 | Asp124 | [64] | |
| GH77 | H | (β/α)8 | alpha | retaining | anti | 1esw | amylomaltase | Thermus aquaticus | acarbose | Asp395 | Asp293 | [65] | |
| GH78 | H | (α/α)6 | alpha | inverting | anti | 3w5n | α-l-rhamnosidase | Streptomyces avermitilis | l-rhamnose | Glu636 | Glu895 | [66] | |
| GH79 | A | (β/α)8 | beta | retaining | anti | 5e9c | heparanase | Homo sapiens | heparin tetrasaccharide | Glu225 | Glu343 | [67] | |
| GH80 | I | α + β | beta | inverting | predicted syn by clan | see at GH24 | |||||||
| GH83 | E | 6-fold β-propeller | alpha | retaining | predicted anti by clan | see e.g. at GH33 | |||||||
| GH84 | none | (β/α)8 | beta | retaining | anti | 2chn | β-N-acetyl- glucosaminidase | Bacteroides thetaiota- omicron VPI-5482 | NAG-thiazoline | Glu242 | internal | [68] | |
| GH85 | K | (β/α)8 | beta | retaining | anti | 2w92 | endo-β-N-acetyl- glucosaminidase D | Streptococcus pneumoniae TIGR4 | NAG-thiazoline | Glu337 | internal | [69] | |
| GH86 | A | (β/α)8 | beta | retaining | anti | 4aw7 | β-porphyranase | Bacteroides plebeius | porphyran fragment | Glu152 | Glu279 | [70] | |
| GH89 | none | (β/α)8 | alpha | retaining | anti | 2vcb | α-N-acetyl- glucosaminidase | Clostridium perfringens | PUGNAc | Glu483 | Glu601 | [71] | |
| GH92 | none | (α/α)6 + β-sandw. | alpha | inverting | anti | 2ww1 | α-1,2-mannosidase | Bacteroides thetaiota- omicron VPI-5482 | thiomannobioside | Glu533 | Asp644 Asp642 | [72] | |
| GH93 | E | 6-bladed β-propeller | alpha | retaining | anti | 3a72 | exo-arabinanase | Penicillium chrysogenum | arabinobiose | Glu246 | Glu174 | [73] | |
| GH94 | none | (α/α)6 | beta | inverting | syn | 1v7x | chitobiose phosphorylase | Vibrio proteolyticus | GlcNAc | Asp492 | phosphate | [74] | |
| GH95 | none | (α/α)6 | alpha | inverting | anti | 2ead | α-1,2-l-fucosidase | Bifidobacterium bifidum | Fuc-α-1,2-Gal | Glu566 | Asn423 Asp766 | [75] | |
| GH97 | none | (β/α)8 | alpha | retaining + inverting | anti | 2zq0 | α-glucosidase | Bacteroides thetaiota- omicron VPI-5482 | acarbose | Glu532 | Glu508 | [76] | |
| GH99 | none | (β/α)8 | alpha | retaining | anti | 4ad4 | endo-α-mannosidase | Bacteroides xylanisolvens | glucose-1,3-isofagomine and α-1,2- mannobiose | Glu336 | debated | [77] | |
| GH100 | none | (α/α)6 core | beta | inverting | anti | 5gop | invertase | Anabaena (Nostoc) sp. pcc7120 | sucrose | Asp188 | Glu414 | [78] | |
| GH102 | none | double-ψ β-barrel | beta | retaining | syn | 2pi8 | lytic transglycosylase A | Escherichia coli | chitohexaose | Asp308 | none | [79] | |
| GH113 | A | (β/α)8 | beta | retaining | anti | 4cd8 | β-mannanase | Alicyclobacillus acidocaldarius | mannobioimidazole | Glu151 | Glu231 | [80] | |
| GH117 | none | five-bladed β-propeller | alpha | inverting | anti | 4ak7 | α-1,3-3,6-anhydro-l-galactosidase | Bacteroides plebeius | neoagarobiose | His302 | Asp90 | [81] | |
| GH123 | none | (β/α)8 + β-sandwich | beta | retaining | anti | 5fr0 | exo-β-N-acetylgalactosaminidase | Clostridium perfringens | N-difluoroacetyl-d-galactosamine | Glu345 | internal | [82] | |
| GH134 | none | β + α | beta | inverting | anti | 5jug | β-mannanase | Streptomyces sp. | mannopentaose | Glu45 | Asp57 | [83] |
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