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Glycosyltransferase Family 47
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Glycosyltransferase Family GT47 | |
Fold | GT-B |
Mechanism | Inverting |
Active site residues | Known/unknown |
CAZy DB link | |
http://www.cazy.org/GT47.html |
Substrate specificities
Glycosyltransferases in GT47 catalyze the transfer of a wide variety of monosaccharides from activated donor sugar nucleotides onto a diversity of acceptor substrates found in plants, animals, insects, and bacteria [1]. Donor sugar nucleotides for discrete clades of GT47 enzymes include UDP-Arabinofuranose (UDP-Araf, i.e. ARAD1), UDP-Arabinopyranose (UDP-Arap), UDP-Xylose (UDP-Xyl, i.e. IRX-10), UDP-Galactose (UDP-Gal , i.e. MUR3), UDP-Galacturonic acid (UDP-GalA, i.e. XUT1), and UDP-Glucuronic acid (UDP-GlcA, i.e. EXT1) [1, 2, 3, 4, 5, 6, 7]. Acceptor substrates for the GT47 enzymes include a diverse collection of plant cell wall polysaccharides in various linkages and heparan sulfate backbone synthesis in mammals [1, 7].
Plants The GT47 family is highly diversified in plants, having an association with the biosynthesis of almost every class of plant cell wall polysaccharide [1]. Although the enzymatic functions for the vast majority of plant GT47s are currently unknown, identified members have been reported to use UDP-GalA, UDP-Gal, UDP-Arap, UDP-Araf, and UDP-Xyl as activated sugar donors. Known acceptor polysaccharide substrates include xyloglucan, xylan, galacto-glucomannan, xylo-galacturonan, and rhamnogalacturonan I.
Xyloglucan
Xyloglucan is a hemicellulose and a major component of the plant primary cell wall [8]. Xyloglucan forms polymer-polymer interactions with cellulose, creating a network through cross-linking cellulose microfibrils. These interactions are influenced by the diversity of sidechains found on xyloglucan which can vary depending on plant species, tissue, and stage of growth [9]. Various members of the GT47 family have been reported to contribute to the synthesis of the numerous sidechains found on xyloglucan, with the two most notable xyloglucan-modifying GT47s being MUR3 and XLT2. These two enzymes catalyze the regiospecific addition of β-D-Gal forming the Gal-β1,2-Xyl-α- (‘L) sidechains of xyloglucan [5, 10]. The GT47s XST1 and XDT are reported to transfer UDP-Araf and UDP-Arap respectively to the 3rd xylose of xyloglucan, forming the Araf-α1,2-Xyl-α- (‘S) and Arap-α1,2- Xyl-α- (‘D) sidechain motifs [11, 12]. XUT1 is reported to transfer UDP-GalA, forming the GalA-β1,2-Xyl-α- (‘Y) sidechain [6]. More recently, the GT47 xyloglucan beta-xylopyranosyltransferase (XBT) has been identified to transfer UDP-Xyl to form the Xyl-β1,2-Xyl-α-(‘U) sidechain [13]. The quantity of GT47s reported to act on xyloglucan is indicative of the important role this family has in contributing to the diversity of this polymer.
Xylan
Unlike the previously mentioned sidechain modifications of xyloglucan, GT47s can additionally contribute to the synthesis of polymer backbones as observed with xylan. Xylan is a hemicellulosic polysaccharide and a major component of the plant secondary cell wall. This polysaccharide is composed of a β1,4-Xyl backbone, synthesized through the actions of multiple GTs. The GT47 IRX10 is one such GT which functions in a complex with two other GTs, IRX9 (GT43) and IRX14 (GT43), using UDP-Xyl as a donor substrate [1, 14, 15]. This xylan synthase complex (XSC) contributes to the synthesis of the xylan backbone, although IRX10 is the only enzyme in the complex which displays an enzymatic function in extending xylan in vivo. Mutations in either IRX9 or IRX14 have been observed to contribute to xylan deficiencies in plants indicating that both proteins have an essential yet currently unknown role in the complex [15]. Loss of function mutations have additionally identified IRX7 as another potential xylan modifying GT47 participating in the synthesis of the xylan reducing end tetrasaccharide β-D-Xyl-1,4-[β-D-Xyl-1,3-α-l-Rha-1,2-α-D-GalA-1,4-D-Xyl] although more evidence is required to elucidate this function [14, 15].
Mannan
Mannan is a hemicellulosic polysaccharide prominently found in the plant primary cell wall. Galactoglucomannan is a classification of mannan with a backbone interspersed with β1,4-Glc which can be further substituted with α1,6-Gal residues. Recently, it was shown that the α1,6-Gal residues of this polymer can additionally be substituted with β1,2-Gal. Loss of function mutations in Arabidopsis have identified the GT47 MBGT1 as a likely candidate in synthesizing the Galβ-1,2-Galα-1,6- sidechains by adding the terminal galactose to the structure [16].
Pectin
Pectin encompasses a diverse group of polymers which include homogalacturonan, rhamnogalacturonan I, rhamnogalacturonan II, and xylogalacturonan. Pectic polysaccharides play many crucial roles in plants such as intercellular adhesion, stress response, seed germination, morphogenesis, and cell communication [1, 17]. Members of the GT47 family have been reported to synthesize sidechain additions on xylogalacturonan and rhamnogalacturonan I. Loss of function mutations in Arabidopsis have identified the GT47 XGD1 as a xylosyltransferase, synthesizing the addition of β1,4-Xyl residues on the GalA backbone of xylogalacturonan [18]. The GT47 ARAD1 has been identified to contribute to the synthesis of arabinose sidechains on rhamnogalacturonan I, identified via the analysis of isolated RG-I from arad1 Arabidopsis mutants [3].
Extensin
Unlike the previously mentioned polysaccharides, extensins are rod-like glycoproteins which form crosslinked networks in the plant cell wall. These networks are reported to play a crucial role in regulating cell wall growth and development [19]. A unique member of the GT47 family, ExAD, is reported to synthesize the addition of the fourth arabinofuranose (Araf) on Araf substituted C4-hydroxyprolines (Hyps) creating Hyp-Araf4, a unique feature found on extensins [19, 20].
=== Animals === The abundance of GT47 family enzymes in mammals is more restricted and includes only members of the Exostosin (EXT) and Exostoslin-Like (EXTL) family of enzymes involved in heparan sulfate biosynthesis. Heparan sulfate is comprised of a repeat disaccharide polymer of ( GlcAβ1,4GlcNAcα1,4-)n that is further elaborated with extensive sulfation along the polymer chain. The disaccharide backbone repeat is elongated by the co-polymerase activity of the heterodimeric EXT1-EXT2 complex [7]. EXT1 and EXT2 are homologous two domain enzymes, and each protein chain contains a GT47 β1,4-GlcA transferase-like and a GT64 α1,4GlcNAc transferase-like domain. Surprisingly, only the GT47 domain of EXT1 and GT64 domain of EXT2 exhibit catalytic activity, while the other domains in each subunit are nonfunctional [7]. Additional EXT homologs include the EXTL proteins, EXTL1-3. EXTL1 and EXTL3 are two domain proteins, each harboring a GT47 and GT64 domain like EXT1 and EXT2. However, only the GT64 domains exhibit α1,4GlcNAc transferase activity, while their corresponding GT47 domains are inactive. In contrast, EXTL2 is a single GT64 domain enzyme with a α1,4GlcNAc transferase activity, while the corresponding GT47 domain present in other EXTs is missing. Thus, among the five mammalian EXT or EXTL homologs, only EXT1 contains a functional GT47 domain exhibiting β1,4-GlcA transferase activity.
Kinetics and Mechanism
GT47 enzymes employ an inverting catalytic mechanism where the hydroxyl group of an acceptor substrate presumably acts as a nucleophile in a SN2 single displacement reaction. The result is an inversion of the anomeric configuration of the transferred sugar from an α-linked sugar nucleotide donor to form a β-linked extended glycan product. While an SN2 mechanism would predict the deprotonation of the acceptor nucleophile by an enzyme associated catalytic base, the structure of the EXT1 active site did not appear to contain an appropriately positioned ionizable group to act as catalytic base [7]. Similar structural studies on the inverting GT-B fold glycosyltransferases, POFUT1 [21, 22, 23] and AtFUT1 [24], also indicated the lack of an appropriately positioned catalytic base for deprotonation. In these latter cases a non-canonical SN1-like mechanism was proposed. A similar SN1-like mechanism may also occur for the GT47 enzymes [1, 25].
![](/images/thumb/6/60/GT47_mechanism_V4.jpg/1600px-GT47_mechanism_V4.jpg)
Catalytic Residues
Unlike GT-A fold enzymes, GT-B fold enzymes like GT47s lack the predictable catalytic features, such as a DxD motif, G-loop, xED, and C-term His, that are involved in sugar nucleotide and divalent cation interactions [26]. In place of the bridging interactions between the nucleotide sugar donor diphosphate residues and an enzyme bound divalent cation as found in GT-A fold enzymes, GT-B fold glycosyltransferases employ basic Lys and Arg side chains for interaction with the diphosphate [1, 25, 27]. Mutation of the active site Lys and Arg residues in the GT47 domain of EXT1 completely eliminated β1,4-GlcA transferase activity as well as co-polymerase activity for extension of heparan sulfate backbone synthesis [7]. Additional residues involved in donor and acceptor interactions were identified in the EXT1:UDP:acceptor complex during structural studies, but further mutagenesis studies were not performed to test function [7]. Analogous Lys and Arg residues can be identified in the putative donor binding sites in AlphaFold models plant GT47 enzymes, but their roles in catalysis have not been tested.
Three-dimensional structures
GT47 enzymes are characterized by GT-B fold architecture comprised of two linked Rossmann-fold domains with a cleft between the domains containing the active site. GT47 enzymes bind their nucleotide sugar donor through interactions with the C-terminal Rossmann fold domain, while the acceptor substrate generally binds either in the cleft between the two domains or exclusively with the N-terminal Rossmann fold domain. The binding sites for donor and acceptor residues are generally comprised of loop regions extending from the respective Rossmann fold domains facing toward the cleft between the two domains [1, 25, 27].
![](/images/thumb/f/f8/EXT1EXT2_GT47_structure_rendering_figure_2_V3.jpg/800px-EXT1EXT2_GT47_structure_rendering_figure_2_V3.jpg)
Family Firsts
The first structure of a CAZy family GT47 was the cryo-EM structure of the human EXT1-2 heterocomplex containing a GT47 β1,4-GlcA transferase domain and an inactive GT64 α1,4GlcNAc transferase-like domain of EXT1, while EXT2 contains an inactive GT47 β1,4-GlcA transferase-like domain along with an active GT64 α1,4GlcNAc transferase domain [7]. Structures of UDP and acceptor co-complexes were determined for each of the enzyme active sites to map substrate interactions. The structures provided insight into the overall enzyme fold (GT-B) and catalytic site structure and mechanism (inverting) as a framework for studies on the other CAZy GT47 enzymes, especially the GT47s in plants that lack empirical structures.
References
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