Species | Prevotella sp900762125 | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Lineage | Bacteria; Bacteroidota; Bacteroidia; Bacteroidales; Bacteroidaceae; Prevotella; Prevotella sp900762125 | |||||||||||
CAZyme ID | MGYG000003268_00886 | |||||||||||
CAZy Family | GH27 | |||||||||||
CAZyme Description | hypothetical protein | |||||||||||
CAZyme Property |
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Genome Property |
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Gene Location | Start: 3248; End: 3724 Strand: - |
Family | Start | End | Evalue | family coverage |
---|---|---|---|---|
GH27 | 1 | 91 | 2.8e-25 | 0.38427947598253276 |
Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
---|---|---|---|---|---|---|---|
cd14792 | GH27 | 6.56e-24 | 1 | 55 | 215 | 271 | glycosyl hydrolase family 27 (GH27). GH27 enzymes occur in eukaryotes, prokaryotes, and archaea with a wide range of hydrolytic activities, including alpha-glucosidase (glucoamylase and sucrase-isomaltase), alpha-N-acetylgalactosaminidase, and 3-alpha-isomalto-dextranase. All GH27 enzymes cleave a terminal carbohydrate moiety from a substrate that varies considerably in size, depending on the enzyme, and may be either a starch or a glycoprotein. GH27 members are retaining enzymes that cleave their substrates via an acid/base-catalyzed, double-displacement mechanism involving a covalent glycosyl-enzyme intermediate. Two aspartic acid residues have been identified as the catalytic nucleophile and the acid/base, respectively. |
PLN02229 | PLN02229 | 1.80e-17 | 1 | 60 | 270 | 330 | alpha-galactosidase |
PLN02692 | PLN02692 | 5.84e-16 | 1 | 61 | 264 | 325 | alpha-galactosidase |
PLN02808 | PLN02808 | 5.08e-15 | 1 | 86 | 240 | 325 | alpha-galactosidase |
pfam16499 | Melibiase_2 | 2.81e-08 | 1 | 55 | 229 | 284 | Alpha galactosidase A. |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
---|---|---|---|---|---|
QRO26425.1 | 1.26e-22 | 1 | 65 | 236 | 300 |
ALK82782.1 | 2.15e-21 | 1 | 65 | 247 | 311 |
QJR69910.1 | 2.15e-21 | 1 | 65 | 247 | 311 |
QJR74242.1 | 2.15e-21 | 1 | 65 | 247 | 311 |
QJR61495.1 | 2.15e-21 | 1 | 65 | 247 | 311 |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
4OGZ_A | 8.04e-12 | 7 | 77 | 338 | 407 | Crystalstructure of a putative alpha-galactosidase/melibiase (BF4189) from Bacteroides fragilis NCTC 9343 at 2.00 A resolution [Bacteroides fragilis NCTC 9343],4OGZ_B Crystal structure of a putative alpha-galactosidase/melibiase (BF4189) from Bacteroides fragilis NCTC 9343 at 2.00 A resolution [Bacteroides fragilis NCTC 9343] |
6F4C_B | 1.80e-11 | 1 | 92 | 217 | 320 | Nicotianabenthamiana alpha-galactosidase [Nicotiana benthamiana] |
1UAS_A | 2.92e-10 | 1 | 60 | 217 | 277 | ChainA, alpha-galactosidase [Oryza sativa] |
4NZJ_A | 3.22e-10 | 7 | 77 | 338 | 407 | Crystalstructure of a putative alpha-galactosidase (BF1418) from Bacteroides fragilis NCTC 9343 at 1.57 A resolution [Bacteroides fragilis NCTC 9343] |
3LRM_A | 9.42e-09 | 2 | 94 | 264 | 344 | ChainA, Alpha-galactosidase 1 [Saccharomyces cerevisiae],3LRM_B Chain B, Alpha-galactosidase 1 [Saccharomyces cerevisiae],3LRM_C Chain C, Alpha-galactosidase 1 [Saccharomyces cerevisiae],3LRM_D Chain D, Alpha-galactosidase 1 [Saccharomyces cerevisiae] |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
Q8VXZ7 | 2.58e-14 | 1 | 60 | 280 | 340 | Alpha-galactosidase 3 OS=Arabidopsis thaliana OX=3702 GN=AGAL3 PE=1 SV=1 |
Q9FT97 | 1.02e-12 | 1 | 61 | 262 | 323 | Alpha-galactosidase 1 OS=Arabidopsis thaliana OX=3702 GN=AGAL1 PE=2 SV=1 |
Q8RX86 | 4.72e-12 | 1 | 91 | 248 | 338 | Alpha-galactosidase 2 OS=Arabidopsis thaliana OX=3702 GN=AGAL2 PE=1 SV=1 |
Q55B10 | 6.32e-12 | 1 | 65 | 234 | 299 | Probable alpha-galactosidase OS=Dictyostelium discoideum OX=44689 GN=melA PE=3 SV=1 |
B3PGJ1 | 3.06e-11 | 1 | 61 | 250 | 310 | Alpha-galactosidase A OS=Cellvibrio japonicus (strain Ueda107) OX=498211 GN=agaA PE=1 SV=1 |
Other | SP_Sec_SPI | LIPO_Sec_SPII | TAT_Tat_SPI | TATLIP_Sec_SPII | PILIN_Sec_SPIII |
---|---|---|---|---|---|
1.000053 | 0.000000 | 0.000000 | 0.000000 | 0.000000 | 0.000000 |
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