ライフサイエンスコーパス: glycoside hydrolase

1 nd the type I dockerin module from the Cel9D glycoside hydrolase.

2 ses, glycosyltransferases, and one family 16 glycoside hydrolase.

3 /Trp chains appear almost exclusively in the glycoside hydrolases.

4 ycans, S. pneumoniae deploys a wide array of glycoside hydrolases.

5 hose found in both family 127 and 129 of the glycoside hydrolases.

6 or for the detection and characterization of glycoside hydrolases.

7 gically and industrially important family of glycoside hydrolases.

8 (CE4s) and a domain structurally similar to glycoside hydrolases.

9 harides, thereby enhancing the efficiency of glycoside hydrolases.

10 etylated to be protected from degradation by glycoside hydrolases.

11 de that the GH61 proteins are unlikely to be glycoside hydrolases.

12 uding an unusual repertoire of extracellular glycoside hydrolases.

13 arrel structure, which is common to family 1 glycoside hydrolases.

14 ide hydrolases (GH), including 32 family GH2 glycoside hydrolases.

15 volved in binding and import of glycans, and glycoside hydrolases.

16 like system to control production of several glycoside hydrolases.

17 t indicates that it is a member of family 64 glycoside hydrolases.

18 talytic motif of families 16 and 7 retaining glycoside hydrolases.

19 omologous and functionally diverse family of glycoside hydrolases.

20 was proposed that these enzymes function as glycoside hydrolases.

21 substrate, we identified and characterized a glycoside hydrolase 109 (GH109) that is active on blood

22 Glycoside hydrolase 12 (GH12) proteins act as virulence

23 ve proteomics study in which we identify two glycoside hydrolase 13 family enzymes, and three ABC tra

24 BT0997 as a new CAZyme family, classified as glycoside hydrolase 138 (GH138).

25 glycanases are part of the large and diverse glycoside hydrolase 16 (GH16) family and are often lipop

26 ns (ZgAgaC) that is distantly related to the glycoside hydrolase 16 (GH16) family beta-agarases and b

27 315 is an inactive beta-1,3-glucanase of the glycoside hydrolase 16 (GH16) family.

28 beta-Mannanases from the glycoside hydrolase 26 (GH26) family are retaining hydro

29 in beta-glucosidase that belongs to the GH3 (glycoside hydrolase 3) family.

30 ype A-antigen, along with a new subfamily of glycoside hydrolase 31 (GH31) that specifically cleaves

31 62 family enzyme was very similar to that of glycoside hydrolase 43 family enzymes, and the catalytic

32 tive sugar-binding pockets characteristic of glycoside hydrolase 70 (GH70) glucansucrases that are kn

33 terization of small-molecule activators of a glycoside hydrolase (a bacterial O-GlcNAc hydrolase).

34 activity in vivo, and could also be used for glycoside hydrolase activation in many industrial proces

35 This biosensor allowed detection of glycoside hydrolase activities at the picomolar level us

36 est performance to date for the detection of glycoside hydrolase activities.

37 alyzing an MSI data set of a high-throughput glycoside hydrolase activity screen comprising 384 sampl

38 his array for detecting exo- and endo-acting glycoside hydrolase activity using commercial enzymes, a

39 the GhCTL group are assigned to family GH19 glycoside hydrolases along with numerous authentic chiti

40 These linkages are primarily cleaved by glycoside hydrolases, although recently, a family of gly

41 e (NCOAT) is a bifunctional enzyme with both glycoside hydrolase and alkyltransferase activity.

42 paradigm of protein complex assembly beyond glycoside hydrolase and carbohydrate active enzymes, and

43 A comparison of the glycoside hydrolase and cellulosome functional genes rev

44 12 protein, PF13204 and PF12904, as putative glycoside hydrolase and glycoside hydrolase-associated C

45 Here, using glycoside hydrolase and kinase assays and immunoprecipit

46 reveal the first instance of an FMN-binding glycoside hydrolase and suggest a potential link between

47 s are also present in several other R. albus glycoside hydrolases and are phylogentically distinct fr

48 drate-binding modules (CBMs) are appended to glycoside hydrolases and can contribute to the degradati

49 New secreted glycoside hydrolases and carbohydrate esterases were ide

50 ption, biochemical analysis of all predicted glycoside hydrolases and carbohydrate-binding proteins,

51 ure of GTase closely resembles the family 13 glycoside hydrolases and conservation of key catalytic r

52 ferent types of carbohydrate-active enzymes, glycoside hydrolases and glycosyltransferases, have conv

53 lasmic reticulum (ER) and Golgi apparatus by glycoside hydrolases and glycosyltransferases.

54 Globally, 9,003 sequences for glycoside hydrolases and lytic polysaccharide mono-oxyge

55 e-degrading and -modifying enzymes including glycoside hydrolases and lytic polysaccharide monooxygen

56 s interaction with cohesin modules, and only glycoside hydrolases and other carbohydrate active enzym

57 Glycoside hydrolases and phosphorylases are two major cl

58 nisms have evolved elaborate sets of modular glycoside hydrolases and similar enzymes aimed at the de

59 accharide utilization loci encoding numerous glycoside hydrolases, and by signaling the host to produ

60 n proteins such as polysaccharide synthases, glycoside hydrolases, and carbohydrate-binding modules.

61 c of the B(2) (or theme D) group of family 9 glycoside hydrolases, and Cel48A is structurally similar

62 Glycoside hydrolases are clustered into families based o

63 ces, the biochemical properties of these GH2 glycoside hydrolases are currently unclear.

64 These producer-derived glycoside hydrolases are public goods transported extrac

65 Processive glycoside hydrolases are the key components of enzymatic

66 nge of carbohydrate-active enzymes, of which glycoside hydrolases are the main components.

67 lex called a cellulosome, which co-ordinates glycoside hydrolase assembly, bacterial adhesion to subs

68 PF12904, as putative glycoside hydrolase and glycoside hydrolase-associated C-terminal domain respect

69 By contrast, glycoside hydrolases attacking celluloses and nitrogen f

70 -binding modules (CBMs) derived from modular glycoside hydrolases belonging to families 2a, 6, and 29

71 Here we study a family 117 glycoside hydrolase (BpGH117) encoded within a recently

72 ereal type family inhibitors (CTIs) bound to glycoside hydrolases but is structurally analogous to bi

73 metagenomics provide access to libraries of glycoside hydrolases but the biochemical characterizatio

74 s to show that among the dozens of different glycoside hydrolases C. phytofermentans secretes on cell

75 These findings suggest that glycoside hydrolases can exhibit activity against divers

76 ay, the alpha-galactosidase Aga (a family 36 glycoside hydrolase), can cleave alpha-(1->3)-linked gal

77 D is a modular enzyme containing a family 30 glycoside hydrolase catalytic domain and an attached car

78 glucanase comprising an N-terminal family 81 glycoside hydrolase catalytic module, an internal family

79 s of specific gene families belonging to the glycoside hydrolase category reflected contrasting ecolo

80 e-enhancing factors," such as those from the glycoside hydrolase (CAZy) GH61 family.

81 rolase (Cel9B), and the other is a family 48 glycoside hydrolase (Cel48A).

82 One of the polypeptides is a family 9 glycoside hydrolase (Cel9B), and the other is a family 4

83 n, and loop flexibility between the family 7 glycoside hydrolase cellobiohydrolases from H. irregular

84 me, there are fundamental differences in the glycoside hydrolase content that appear to be diet drive

85 We therefore hypothesized that these glycoside hydrolases could exhibit antibiofilm activity

86 Glycoside hydrolases displaying multiple catalytic funct

87 structural data reveal that PlyCA contains a glycoside hydrolase domain in addition to the previously

88 known multicatalytic enzymes contain several glycoside hydrolase domains and one or more carbohydrate

89 Proteins containing glycoside hydrolase domains have recently been identifie

90 activity, suggesting that T6S peptidoglycan glycoside hydrolase effector families may comprise signi

91 e define novel families of T6S peptidoglycan glycoside hydrolase effectors.

92 propose a scheme of sequential action by the glycoside hydrolases encoded by the beta-mannan PUL and

93 This work shows that Sph3 is a glycoside hydrolase essential for GAG production and def

94 hat they are beta-porphyranases belonging to glycoside hydrolase families 16 and 86, respectively.

95 d a (beta/alpha)8 fold, with similarities to glycoside hydrolase families 18, 27, and 84.

96 of processive and nonprocessive enzymes from glycoside hydrolase families 6 and 7.

97 Cellulases comprise many glycoside hydrolase families and exist as processive or

98 The glycoside hydrolase families GH5 (PaMan5A) and GH26 (PaM

99 homologous sequences are present in various glycoside hydrolase families.

100 cruiting enzymes from two previously unknown glycoside hydrolase families.

101 Glycoside hydrolase family (GH) 16 comprises a large and

102 identified beetle myrosinase belongs to the glycoside hydrolase family 1 and has up to 76% sequence

103 % to 92% amino acid identity with members of glycoside hydrolase family 1, including their catalytic

104 ucture of a xylanase not belonging to either glycoside hydrolase family 10 or family 11.

105 ted uronyl hydrolases classified in the CAZy glycoside hydrolase family 105.

106 Although xylanases from glycoside hydrolase family 11 (GH11) have been extensive

107 The catalytic domain of XynCDBFV, a glycoside hydrolase family 11 (GH11) xylanase from rumin

108 ive alpha-1,4-galactosaminidase belonging to glycoside hydrolase family 114 (GH114).

109 ndo-1,4-beta-glucanase (Cel12A) belonging to glycoside hydrolase family 12.

110 The enzyme has been classified into glycoside hydrolase family 12; this is the first structu

111 In particular, transglycosylases from glycoside hydrolase family 13 (GH13) and GH77 play well

112 The XTH gene products compose a subfamily of glycoside hydrolase family 16 (GH16), which also compris

113 two distant bacterial phyla, which belong to glycoside hydrolase family 16 and cleave the beta-1,4 li

114 ive beta-porphyranases, all belonging to the glycoside hydrolase family 16.

115 3-1,4-beta-glucan 4-glucanohydrolases of the glycoside hydrolase family 16.

116 lar protein that is predicted to contain two glycoside hydrolase family 18 (GH18) catalytic domains,

117 oh_4555 (ChiA), a 168.9-kDa protein with two glycoside hydrolase family 18 (GH18) domains, was target

118 gnificant similarity to other members of the glycoside hydrolase family 23 (GH23), such as the g-type

119 It encodes two glycoside hydrolase family 26 (GH26) beta-mannanases, Bo

120 d drug design efforts on alpha-GAL and other glycoside hydrolase family 27 enzymes by developing liga

121 The secreted glycoside hydrolase family 29 (GH29) alpha-L-fucosidase

122 physiological roles of the four C. japonicus glycoside hydrolase family 3 (GH3) members on diverse be

123 rchitecture as observed previously for other glycoside hydrolase family 3 beta-glucosidases.

124 Arabidopsis thaliana) beta-glucosidases from glycoside hydrolase family 3.

125 rase and isomaltase) that both belong to the glycoside hydrolase family 31 (GH31) and differ in subst

126 The enzyme belongs to glycoside hydrolase family 31 (GH31) but degrades starch

127 lgi alpha-mannosidase II (GMII), a member of glycoside hydrolase family 38, cleaves two mannosyl resi

128 Here we test the hypothesis that glycoside hydrolase family 43 (GH43) provides a suitable

129 n be differentially modulated in vitro using glycoside hydrolase family 43 and family 51 arabinofuran

130 characterization, and kinetic analysis of a glycoside hydrolase family 43 beta-xylosidase (Xyl43A) f

131 Multiple glycoside hydrolase family 47 (GH47) alpha-mannosidases,

132 Enzymes from glycoside hydrolase family 48 (GH48) are a critical comp

133 To gain insights into how the two glycoside hydrolase family 5 (GH5) enzymes may aid the b

134 microbial expansin (exlx) gene adjacent to a glycoside hydrolase family 5 (gh5) gene.

135 Carbohydrate-Active Enzyme (CAZy) database, glycoside hydrolase family 5 (GH5) is a large family wit

136 The recent classification of glycoside hydrolase family 5 (GH5) members into subfamil

137 The diversity of activities across glycoside hydrolase family 5 (GH5) suggests that this fa

138 An arabinose specific xylanase from glycoside hydrolase family 5 (GH5) was used to hydrolyse

139 nases revealed three distinct subfamilies of glycoside hydrolase family 5 (GH5).

140 45 kDa, 413-amino acid protein belonging to glycoside hydrolase family 5, has been determined by mul

141 ng forces underlying specificity patterns in glycoside hydrolase family 5, we quantitatively screened

142 lanase activity and subsequently assigned to glycoside hydrolase family 5.

143 Here we present the crystal structure of a glycoside hydrolase family 50 exo-beta-agarase, Aga50D,

144 Glycoside hydrolase Family 6 (GH6) CBHs act from nonredu

145 hydrate binding module family 33 (CBM33) and glycoside hydrolase family 61 (GH61) are likely to play

146 Glycoside hydrolase family 62 (GH62) is currently a smal

147 -L-arabinofuranosidase, which belongs to the glycoside hydrolase family 62 (GH62), hydrolyzes arabino

148 saccharide glucanotransferase belongs to the glycoside hydrolase family 66 and catalyzes an intramole

149 Glycoside hydrolase family 7 (GH7) cellulases are some o

150 and O-glycosylation on a model, multimodular glycoside hydrolase family 7 cellobiohydrolase (Cel7A),

151 haride unit during the processive cycle of a glycoside hydrolase family 7 cellobiohydrolase.

152 H. jecorina Cel7A, cellobiohydrolase I, from glycoside hydrolase family 7, is the workhorse enzyme of

153 3-GBD-CD2 is a transglucosylase belonging to glycoside hydrolase family 70 (GH70) that catalyzes the

154 Highly conserved glycoside hydrolase family 70 glucansucrases are able to

155 Microbial alpha-glucans produced by GH70 (glycoside hydrolase family 70) glucansucrases are gainin

156 n GTF180-DeltaN and GTF-SI glucansucrases of glycoside hydrolase family 70.

157 Glycoside hydrolase family 74 (GH74) is a historically i

158 Glycoside hydrolase family 8 (GH8) includes endoglucanas

159 32 carbohydrate binding module (CBM32) of a glycoside hydrolase family 8 chitosanase from Paenibacil

160 fringens unsaturated glucuronyl hydrolase of glycoside hydrolase family 88 in the CAZy classification

161 The insert carried a glycoside hydrolase family 9 (GH9) catalytic domain with

162 One of these, CelA, comprises a glycoside hydrolase family 9 and a family 48 catalytic d

163 es and endo-alpha-1,2-mannanases, members of glycoside hydrolase family 99 (GH99), are interesting ta

164 s highest overall structural similarity to a glycoside hydrolase family associated with peptidoglycan

165 Rice (Oryza sativa) Os9BGlu31 is a glycoside hydrolase family GH1 transglycosidase that act

166 We identified genes from Glycoside Hydrolase family GH131 as commonly expressed d

167 gracilis, leading to their classification in glycoside hydrolase family GH149.

168 snapshots along the reaction coordinate of a glycoside hydrolase family GH29 alpha-L-fucosidase unvei

169 CAZy glycoside hydrolase family GH3 consists primarily of ste

170 quently hydrolyzed by members of the unusual glycoside hydrolase family GH4.

171 Glycoside hydrolase family GH85 is a family of endo-beta

172 GYxYP-containing proteins constitute a novel glycoside hydrolase family of as yet unknown specificity

173 g the structural feature of this family as a glycoside hydrolase family of enzymes.

174 Recently three members of a glycoside hydrolase family, GH115, were shown to hydroly

175 sential for GAG production and defines a new glycoside hydrolase family, GH135.

176 d function necessitate the creation of a new glycoside hydrolase family, GH166, whose structural and

177 cation is still needed, as is exemplified by glycoside hydrolase family-3 (GH3) proteins.

178 We propose that the increased affinity of glycoside hydrolases for polysaccharides, through the sy

179 ence-quenched substrates for other mammalian glycoside hydrolases for use in live cell imaging.

180 Starting with the family 98 glycoside hydrolase from Streptococcus pneumoniae SP3-BS

181 in nature that is processed by a variety of glycoside hydrolases from different families.

182 A fungal endoxylanase belonging to the glycoside hydrolase gene family 11 (GH11) was obtained f

183 Expression profiles of most endo-acting glycoside hydrolase genes correlated well with their rep

184 biochemical properties, although exo-acting glycoside hydrolase genes displayed less specific expres

185 lucose generally repressed expression of all glycoside hydrolase genes, other sugars induced or repre

186 Remarkably, some beta-glucosidases of the glycoside hydrolase (GH) 1 family are tolerant to or eve

187 By analysis of 513 pyranoside-bound glycoside hydrolase (GH) crystal structures, we determin

188 Many glycoside hydrolase (GH) enzymes act via a processive me

189 Nature uses a diversity of glycoside hydrolase (GH) enzymes to convert polysacchari

190 lobal MS data, revealing ABP selectivity for glycoside hydrolase (GH) enzymes, in addition to a large

191 beta-Mannanases, located in glycoside hydrolase (GH) families 5 and 26, hydrolyze gl

192 Organization of glycoside hydrolase (GH) families into clans expands the

193 ng protein sequence space has revealed a new glycoside hydrolase (GH) family (GH164) of putative mann

194 In plants, Glycoside Hydrolase (GH) Family 1 beta -glycosidases are

195 ed carbohydrate active genes encode a unique glycoside hydrolase (GH) family 10 endoxylanase (BiXyn10

196 antii harbors four genes predicted to encode glycoside hydrolase (GH) family 3 (GH3) enzymes.

197 A putative glycoside hydrolase (GH) family 3 beta-D-glucosidase gen

198 the pK(a) values of titratable residues of a glycoside hydrolase (GH) family 6 cellobiohydrolase (Cel

199 enzymes have 97% identity and belong to the glycoside hydrolase (GH) family GH36 for which few struc

200 e, BT3686, which is the founding member of a glycoside hydrolase (GH) family, GH145.

201 ermite hindgut was observed when we compared glycoside hydrolase (GH) profile of buffalo rumen metage

202 Glycoside hydrolases (GH) are enzymes that mainly hydrol

203 h, produces an extensive array of exo-acting glycoside hydrolases (GH), including 32 family GH2 glyco

204 we identify and characterize a new family 20 glycoside hydrolase, GH20C, from S. pneumoniae.

205 d comprises a cohesin module and a family 25 glycoside hydrolase (GH25).

206 r2455) were identified that encode family 39 glycoside hydrolases (GH39s), and have conserved structu

207 Family 43 glycoside hydrolases (GH43s) are known to exhibit variou

208 f EXPB1 domain 1 resembles that of family-45 glycoside hydrolase (GH45), with conservation of most of

209 Family 45 glycoside hydrolases (GH45) are endoglucanases that are

210 PMOs were incorrectly annotated as family 61 glycoside hydrolases (GH61s) or family 33 carbohydrate-b

211 Family 72 glycoside hydrolases (GH72) are ubiquitous in fungal org

212 hy3367 gene, which encodes the sole family 9 glycoside hydrolase (GH9) in the C. phytofermentans geno

213 Carbohydrate-active enzymes such as glycoside hydrolases (GHs) and glycosyltransferases (GTs

214 These SLH proteins include five glycoside hydrolases (GHs) and one polysaccharide lyase,

215 The independent activities of PUL-encoded glycoside hydrolases (GHs) and surface glycan-binding pr

216 Glycoside hydrolases (GHs) catalyze hydrolyses of glycoc

217 Glycoside hydrolases (GHs) cleave glycosidic linkages in

218 Glycoside hydrolases (GHs) distort carbohydrate ring geo

219 The identification of glycoside hydrolases (GHs) for efficient polysaccharide

220 Glycoside hydrolases (GHs) have attracted considerable a

221 The conversion of glycoside hydrolases (GHs) into transglycosylases (TGs),

222 comprised of glycosylated linkers connecting glycoside hydrolases (GHs) to carbohydrate-binding modul

223 Focusing on Glycoside Hydrolases (GHs) we found that, across samples

224 Processive glycoside hydrolases (GHs), like cellobiohydrolase Cel7A

225 by mixtures of processive and nonprocessive glycoside hydrolases (GHs), which exhibit synergistic ac

226 uster of eight genes (nixE to nixL) encoding glycoside hydrolases (GHs).

227 micellulose, facilitated by a diverse set of glycoside hydrolases (GHs).

228 sessed a gene cluster containing multidomain glycoside hydrolases (GHs).

229 Deficiency of the lysosomal glycoside hydrolase glucocerebrosidase (GCase) leads to

230 ed action of a variety of enzymes, including glycoside hydrolases, glycoside phosphorylases, and tran

231 ing is controlled by the equilibrium between glycoside hydrolases, glycosyltransferases, and transgly

232 Some glycoside hydrolases have broad specificity for hydrolys

233 filtrate was identified as the only family 7 glycoside hydrolase in the genome, which consists of a s

234 alysis revealed the existence of 29 putative glycoside hydrolases in addition to the previously ident

235 Glycoside hydrolases in family 101 are presently the onl

236 linear alpha-Gal epitope can be processed by glycoside hydrolases in family GH110, whereas the presen

237 ite more efficiently than mannan-hydrolyzing glycoside hydrolases in related enzyme families.

238 ule to potentiate the activity of a range of glycoside hydrolases including cellulases.

239 ing the activity of endogenous levels of any glycoside hydrolases, including GCase, has proven proble

240 ean, MGIIa_P contained higher proportions of glycoside hydrolases, indicating the ability of MGIIa_P

241 Evaluated as glycoside hydrolase inhibitors, these quinolizidines rev

242 highly conserved, significant differences in glycoside hydrolase inventories and numbers of carbohydr

243 hydrolase domains from Sph3, an A. fumigatus glycoside hydrolase involved in GAG synthesis, and PelA,

244 -mannosidase (MANEA) is the sole endo-acting glycoside hydrolase involved in N-glycan trimming and is

245 enes, in particular a strong upregulation of glycoside hydrolases involved in mannan degradation.

246 The degradation of the plant cell wall by glycoside hydrolases is central to environmentally susta

247 bohydrate-binding modules (CBM) of microbial glycoside hydrolases is central to natural and efficient

248 The function of CBMs appended to exo-acting glycoside hydrolases is unclear because their typical en

249 rrespondence to other family 5 and family 10 glycoside hydrolases, lie inside this cleft on the C-ter

250 urated uronic acid, is removed from AGP by a glycoside hydrolase located in family GH105, producing t

251 C. japonicus possesses an extensive range of glycoside hydrolases, lyases, and esterases.

252 ultifunctional enzyme mixtures consisting of glycoside hydrolases, lytic polysaccharide mono-oxygenas

253 we propose a new variation of the retaining glycoside hydrolase mechanism wherein the intervening wa

254 t A.actinomycetemcomitans produces a soluble glycoside hydrolase named dispersin B, which degrades PG

255 thetaiotaomicron contains a large number of glycoside hydrolases not represented in our own proteome

256 subfamily would rather work in synergy with glycoside hydrolases of the GH92 and GH18 families in th

257 Glycoside hydrolases often contain multiple copies of no

258 drate binding modules (CBMs) of cell surface glycoside hydrolases often drive binding to the target s

259 he nature of such a reaction intermediate in glycoside hydrolases operating via substrate-assisted ca

260 nt processes, such as bioprospecting for new glycoside hydrolases or identifying novel energy sources

261 In nature, many microbes secrete mixtures of glycoside hydrolases, oxidoreductases, and accessory enz

262 endent enzymes (EC 1.14.99.53-56) that, with glycoside hydrolases, participate in the degradation of

263 Microbial glycoside hydrolases play a dominant role in the biochem

264 d to analyze both endo-acting and exo-acting glycoside hydrolases, polysaccharide lyases, carbohydrat

265 Many glycoside hydrolases possess carbohydrate-binding module

266 membrane polysaccharide-binding proteins and glycoside hydrolases, prioritized the consumption of lib

267 genetic studies have shown that the putative glycoside hydrolase PslG is essential for Psl biosynthes

268 residues similar to those of other family 39 glycoside hydrolases, PslG(31-442) exhibits a unique 32-

269 on a polysaccharide if the producer-derived glycoside hydrolase, responsible for PBP generation, is

270 Endoglycosidase S (EndoS) is a glycoside-hydrolase secreted by the bacterium Streptococ

271 at from MvX56, a module found in a family 33 glycoside hydrolase sialidase from Micromonospora viridi

272 It encodes three glycoside-hydrolases specific for xylo-oligosaccharides,

273 case (OGA), representing the first family 84 glycoside hydrolase structure.

274 mulated 284 putative fucoidanases, including glycoside hydrolases, sulfatases and carbohydrate estera

275 Across many environments microbial glycoside hydrolases support the enzymatic processing of

276 c onto proteins and O-GlcNAcase (OGA) is the glycoside hydrolase that acts to remove O-GlcNAc from pr

277 , we show that recombinant Ega3 is an active glycoside hydrolase that disrupts GAG-dependent A. fumig

278 ate binding modules (CBMs) are components of glycoside hydrolases that attack generally inaccessible

279 in the identification of several families of glycoside hydrolases that can degrade mannan.

280 Among the many families of glycoside hydrolases that catalyze cellulose and hemicel

281 the relatively high cost of enzymes such as glycoside hydrolases that catalyze cellulose hydrolysis

282 Hyaluronidases are a family of endolytic glycoside hydrolases that cleave the beta1-4 linkage bet

283 oned, expressed and characterized all of the glycoside hydrolases that contain a dockerin module.

284 indicates that they are members of family 16 glycoside hydrolases that have significant sequence iden

285 alpha-L-arabinofuranosidases are glycoside hydrolases that specifically hydrolyze non-red

286 analysis reveals approximately 130 predicted glycoside hydrolases that target the major structural an

287 This system contains several glycoside hydrolases that trim the remnants of other pec

288 d in this enzyme and those of other family 9 glycoside hydrolases, the active site of GH9_CbhA is blo

289 domain with significant similarity to known glycoside hydrolases, the C-terminal domain has a beta-s

290 ative protein-coding genes, of which 103 are glycoside hydrolases, the highest detected number in clu

291 The inhibition of glycoside hydrolases, through transition-state mimicry,

292 ofermentans has a repertoire of 108 putative glycoside hydrolases to break down cellulose and hemicel

293 ulases, hemicellulases, xylanases, and other glycoside hydrolases to facilitate the degradation of hi

294 idomain extracellular and S-layer-associated glycoside hydrolases to process the carbohydrate content

295 functional transpeptidases and glycosidases (glycoside hydrolases), trimeric peptide crosslinks, cell

296 hypothetical protein with low similarity to glycoside hydrolases was shown to possess endoxylanase a

297 larity to any of the 97 existing families of glycoside hydrolases, we have proposed to assign this un

298 Glycoside hydrolases, which are ubiquitous in nature, ty

299 modules (CBMs) are ubiquitous components of glycoside hydrolases, which degrade polysaccharides in n

300 er feature differs from the vast majority of glycoside hydrolases, which use a carboxylic acid, highl