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Difference between revisions of "Syn/anti lateral protonation"
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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 (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>. | ||
| − | == Table == | + | == Table of syn/anti protonation examples == |
| + | === 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.'' | |
| − | |||
| − | |||
| + | === 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 ''page'' tab above the page title. | ||
Revision as of 23:41, 11 January 2010
This page is currently under construction. This means that the Responsible Curator has deemed that the page's content is not quite up to CAZypedia's standards for full public consumption. All information should be considered to be under revision and may be subject to major changes.
- Author: ^^^Wim Nerinckx^^^
- Responsible Curator: ^^^Spencer Williams^^^
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 [1], and the more recent summary by Nerinckx et al. [2].
Table of syn/anti protonation examples
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.
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.
| 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 glucoimidazol | Glu206 | Glu387 | [3] |
| GH2 | A | (β/α)8 | beta | retaining | anti | 2vzu | exo-β-glucosaminidase | Amicolatopsis orientalis | PNP-β-d-glucosamine | Glu469 | Glu541 | [4] |
| GH3 | none | (β/α)8 | beta | retaining | anti | 1iex | exo-1,3-1,4-glucanase | Hordeum vulgare | thiocellobiose | Glu491 | Asp285 | [5] |
| GH5 | A | (β/α)8 | beta | retaining | anti | 1h2j | endo-β-1,4-glucanase | Bacillus agaradhaerens | 2',4'-DNP-2-F-cellobioside | Glu129 | Glu228 | [6] |
| GH6 | none | (β/α)8 | beta | inverting | syn | 1qjw | cellobiohydrolase 2 | Hypocrea jecorina | (Glc)2-S-(Glc)2 | Asp221 | debated | [7] |
| GH7 | B | β-jelly roll | beta | retaining | syn | 1ovw | endo-1,4-glucanase | Fusarium oxysporum | thio-(Glc)5 | Glu202 | Glu197 | [8] |
| GH8 | M | (α/α)6 | beta | inverting | anti | 1kwf | endo-1,4-glucanase | Clostridium thermocellum | cellopentaose | Glu95 | Asp278 | [9] |
| GH9 | none | (α/α)6 | beta | inverting | syn | 1rq5 | cellobiohydrolase | Clostridium thermocellum | cellotetraose | Glu795 | Asp383 | [10] |
| GH10 | A | (β/α)8 | beta | retaining | anti | 2d24 | β-1,4-xylanase | Streptomyces olivaceoviridis E-86 | xylopentaose | Glu128 | Glu236 | [11] |
| GH11 | C | β-jelly roll | beta | retaining | syn | 1bvv | xylanase | Bacillus circulans | Xyl-2-F-xylosyl | Glu172 | Glu78 | [12] |
| GH12 | C | β-jelly roll | beta | retaining | syn | 1w2u | endoglucanase | Humicola grisea | thiocellotetraose | Glu205 | Glu120 | [13] |
| GH13 | H | (β/α)8 | alpha | retaining | anti | 1cxk | β-cyclodextrin glucanotransferase | Bacillus circulans | maltononaose | Glu257 | Asp229 | [14] |
| GH14 | none | (β/α)8 | alpha | inverting | syn | 1itc | β-amylase | Bacillus cereus | maltopentaose | Glu172 | Glu367 | [15] |
| GH15 | L | (α/α)6 | alpha | inverting | syn | 1gah | glucoamylase | Aspergillus awamori | acarbose | Glu179 | Glu400 | [16] |
| GH16 | B | β-jelly roll | beta | retaining | syn | 1urx | β-agarase A | Zobellia galactanivorans | oligoagarose | Glu152 | Glu147 | [17] |
| 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 | [18] |
| GH20 | K | (β/α)8 | beta | retaining | anti | 1c7s | chitobiase | Serratia marcescens | chitobiose | Glu540 | internal | [19] |
| GH22 | none | lysozyme type | beta | retaining | syn | 1h6m | lysozyme C | Gallus gallus | Chit-2-F-chitosyl | Glu35 | Asp52 | [20] |
| GH23 | none | lysozyme type | beta | inverting | syn | 1lsp | lysozyme G | Cygnus atratus | Bulgecin A | Glu73 | internal | [21] |
| GH24 | I | α + β | beta | inverting | syn | 148l | lysozyme E | Bacteriophage T4 | chitobiosyl | Glu11 | Glu26 | [22] |
| GH26 | A | (β/α)8 | beta | retaining | anti | 1gw1 | mannanase A | Cellvibrio japonicus | 2',4'-DNP-2-F-cellotrioside | Glu212 | Glu320 | [23] |
| GH27 | D | (β/α)8 | alpha | retaining | anti | 1ktc | α-N-acetyl galactosaminidase | Gallus gallus | NAGal | Asp201 | Asp410 | [24] |
| GH28 | N | β-helix | alpha | inverting | anti | 2uvf | exo-polygalacturonosidase | Yersinia enterocolitica ATCC9610D | digalacturonic acid | Asp402 | Asp381 Asp403 | [25] |
| GH29 | none | (β/α)8 | alpha | retaining | syn | 1hl9 | α-l-fucosidase | Thermotoga maritima | 2-F-fuco- pyranosyl | Glu266 | Asp224 | [26] |
| GH30 | A | (β/α)8 | beta | retaining | anti | 2v3d | glucocerebrosidase 1 | Homo sapiens | N-butyl-deoxynojirimycin | Glu235 | Glu340 | [27] |
| GH31 | D | (β/α)8 | alpha | retaining | anti | 2qmj | maltase-glucoamylase | Homo sapiens | acarbose | Asp542 | Asp443 | [28] |
| GH32 | J | 5-fold β-propeller | beta | retaining | anti | 2add | fructan β-(2,1)-fructosidase | Cichorium intybus | sucrose | Glu201 | Asp22 | [29] |
| GH33 | E | 6-fold β-propeller | alpha | retaining | anti | 1s0i | trans-sialidase | Trypanosoma cruzi | sialyl-lactose | Asp59 | Tyr342 | [30] |
| GH34 | E | 6-fold β-propeller | alpha | retaining | anti | 2bat | neuraminidase | Influenza A virus | sialic acid | Asp151 | Tyr406 | [31] |
| GH35 | A | (β/α)8 | beta | retaining | anti | 1xc6 | β-galactosidase | Penicillium sp. | d-galactose | Glu200 | Glu299 | [32] |
| GH37 | G | (α/α)6 | alpha | inverting | anti | 2jf4 | trehalase | Escherechia coli | validoxylamine | Asp312 | Glu496 | [33] |
| GH38 | none | (β/α)7 | alpha | retaining | anti | 1qwn | α-mannosidase II | Drosophila melanogaster | 5-F-β-l-gulosyl | Asp341 | Asp204 | [34] |
| GH39 | A | (β/α)8 | beta | retaining | anti | 1uhv | β-xylosidase | Thermoanaerobacterium saccharolyticum | 2-F-xylosyl | Glu160 | Glu277 | [35] |
| GH42 | A | (β/α)8 | beta | retaining | anti | 1kwk | β-galactosidase | Thermus thermophylus A4 | d-galactose | Glu141 | Glu312 | [36] |
| GH44 | none | (β/α)8 | beta | retaining | anti | 2eqd | endoglucanase | Clostridium thermocellum | cellooctaose | Glu186 | Glu359 | [37] |
| GH45 | none | 6-strand. β-barrel | beta | inverting | syn | 4eng | endo-1,4-glucanase | Humicola insolens | cellohexaose | Asp121 | Asp10 | [38] |
| GH46 | I | α + β | beta | inverting | predicted syn by clan | see at GH24 | ||||||
| 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 | [39], [40] |
| 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 | predicted anti by clan | see e.g. at GH1 | ||||||
| GH51 | A | (β/α)8 | alpha | retaining | anti | 1qw9 | α-l-arabino- furanosidase | Geobacillus stearothermophilus | PNP-l-arabino-furanoside | Glu175 | Glu294 | [41] |
| GH53 | A | (β/α)8 | beta | retaining | predicted anti by clan | see e.g. at GH1 | ||||||
| GH54 | none | β-sandwich | alpha | retaining | anti | 1wd4 | α-l-arabino- furanosidase B | Aspergillus kawachii | l-arabinofuranose | Asp297 | Glu221 | [42] |
| GH55 | none | β-helix | beta | inverting | anti | 3eqo | β-1,3-glucanase | Phanerochaete chrysosporium K-3 | d-gluconolacton | Glu633 | unknown | [43] |
| GH56 | none | (β/α)7 | beta | retaining | anti | 1fcv | hyaluronidase | Apis mellifera | (hyaluron.)4 | Glu113 | internal | [44] |
| GH57 | none | (β/α)7 | alpha | retaining | anti | 1kly | glucanotransferase | Thermococcus litoralis | acarbose | Asp214 | Glu123 | [45] |
| GH59 | A | (β/α)8 | beta | retaining | predicted anti by clan | see e.g. at GH1 | ||||||
| GH63 | G | (α/α)6 | alpha | inverting | predicted anti by clan | see at GH37 | ||||||
| GH65 | L | (α/α)6 | alpha | inverting | predicted syn by clan | see at GH15 | ||||||
| GH67 | none | (β/α)8 | alpha | inverting | syn | 1gql | α-glucuronidase | Cellvibrio japonicus Ueda107 | d-glucuronic acid | Glu292 | unknown | [46] |
| GH68 | J | 5-fold β-propeller | beta | retaining | anti | 1pt2 | levansucrase | Bacillus subtilis | sucrose | Glu342 | Asp86 | [47] |
| GH70 | H | (β/α)8 | alpha | retaining | predicted anti by clan | see e.g. at GH13 | ||||||
| GH72 | A | (β/α)8 | beta | retaining | anti | 2w62 | β-1,3-glucano- transferase | Saccharomyces cerevisiae S288C | laminaripentaose | Glu176 | Glu275 | [48] |
| GH74 | none | 7-fold β-propeller | beta | inverting | syn | 2ebs | cellobiohydrolase (OXG-RCBH) | Geotrichum sp. m128 | xyloglucan heptasaccharide | Asp465 | Asp35 | [49] |
| GH77 | H | (β/α)8 | alpha | retaining | anti | 1esw | amylomaltase | Thermus aquaticus | acarbose | Asp395 | Asp293 | [50] |
| GH79 | A | (β/α)8 | beta | retaining | predicted anti by clan | see e.g. at GH1 | ||||||
| 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 | [51] |
| GH85 | K | (β/α)8 | beta | retaining | anti | 2w92 | endo-β-N-acetyl- glucosaminidase D | Streptococcus pneumoniae TIGR4 | NAG-thiazoline | Glu337 | internal | [52] |
| GH86 | A | (β/α)8 | beta | retaining | predicted anti by clan | see e.g. at GH1 | ||||||
| GH89 | none | (β/α)8 | alpha | retaining | anti | 2vcb | α-N-acetyl- glucosaminidase | Clostridium perfringens | PUGNAc | Glu483 | Glu601 | [53] |
| GH92 | none | (α/α)6 + β-sandw. | alpha | inverting | anti | 2ww1 | α-1,2-mannosidase | Bacteroides thetaiota- omicron VPI-5482 | thiomannobioside | Glu533 | Asp644 Asp642 | [54] |
| GH93 | E | 6-fold β-propeller | alpha | retaining | predicted anti by clan | see e.g. at GH33 | ||||||
| GH94 | none | (α/α)6 | beta | inverting | syn | 1v7x | chitobiose phosphorylase | Vibrio proteolyticus | GlcNAc | Asp492 | phosphate | [55] |
| GH95 | none | (α/α)6 | alpha | inverting | anti | 2ead | α-1,2-l-fucosidase | Bifidobacterium bifidum | Fuc-α-1,2-Gal | Glu566 | Asn423 Asp766 | [56] |
| GH97 | none | (β/α)8 | alpha | retaining + inverting | anti | 2zq0 | α-glucosidase | Bacteroides thetaiota- omicron VPI-5482 | acarbose | Glu532 | Glu508 | [57] |
| GH102 | none | double-ψ β-barrel | beta | retaining | syn | 2pi8 | lytic transglycosylase A | Escherechia coli | chitohexaose | Asp308 | none | [58] |
| GH113 | A | (β/α)8 | beta | retaining | predicted anti by clan | see e.g. at GH1 |
References
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