| Species | Parabacteroides bouchesdurhonensis | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Lineage | Bacteria; Bacteroidota; Bacteroidia; Bacteroidales; Tannerellaceae; Parabacteroides; Parabacteroides bouchesdurhonensis | |||||||||||
| CAZyme ID | MGYG000000221_00653 | |||||||||||
| CAZy Family | CBM51 | |||||||||||
| CAZyme Description | hypothetical protein | |||||||||||
| CAZyme Property |
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| Genome Property |
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| Gene Location | Start: 44958; End: 46913 Strand: + | |||||||||||
| Family | Start | End | Evalue | family coverage |
|---|---|---|---|---|
| GH27 | 367 | 627 | 3.4e-70 | 0.9781659388646288 |
| CBM51 | 22 | 155 | 2.3e-35 | 0.9925373134328358 |
| Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
|---|---|---|---|---|---|---|---|
| cd14792 | GH27 | 4.22e-122 | 273 | 550 | 1 | 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. |
| PLN02808 | PLN02808 | 2.91e-84 | 252 | 651 | 11 | 386 | alpha-galactosidase |
| PLN02229 | PLN02229 | 7.01e-80 | 262 | 641 | 52 | 410 | alpha-galactosidase |
| PLN02692 | PLN02692 | 7.07e-80 | 250 | 629 | 32 | 388 | alpha-galactosidase |
| pfam16499 | Melibiase_2 | 1.48e-65 | 272 | 550 | 1 | 284 | Alpha galactosidase A. |
| Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
|---|---|---|---|---|---|
| QBJ19564.1 | 3.13e-312 | 20 | 650 | 29 | 662 |
| QMI80969.1 | 3.13e-312 | 20 | 650 | 29 | 662 |
| QUT65548.1 | 2.61e-311 | 20 | 650 | 20 | 653 |
| QUT97956.1 | 3.70e-311 | 20 | 650 | 20 | 653 |
| ALJ57993.1 | 3.42e-309 | 5 | 650 | 6 | 662 |
| Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
|---|---|---|---|---|---|---|
| 4OGZ_A | 3.01e-98 | 183 | 578 | 10 | 415 | 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] |
| 4NZJ_A | 1.98e-92 | 183 | 582 | 10 | 419 | Crystalstructure of a putative alpha-galactosidase (BF1418) from Bacteroides fragilis NCTC 9343 at 1.57 A resolution [Bacteroides fragilis NCTC 9343] |
| 1UAS_A | 3.27e-69 | 267 | 650 | 3 | 361 | ChainA, alpha-galactosidase [Oryza sativa] |
| 3A5V_A | 6.74e-67 | 267 | 649 | 3 | 391 | Crystalstructure of alpha-galactosidase I from Mortierella vinacea [Umbelopsis vinacea] |
| 6F4C_B | 5.66e-64 | 265 | 651 | 1 | 363 | Nicotianabenthamiana alpha-galactosidase [Nicotiana benthamiana] |
| Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
|---|---|---|---|---|---|---|
| P14749 | 1.40e-74 | 267 | 650 | 50 | 409 | Alpha-galactosidase OS=Cyamopsis tetragonoloba OX=3832 PE=1 SV=1 |
| Q8VXZ7 | 1.47e-74 | 225 | 651 | 24 | 430 | Alpha-galactosidase 3 OS=Arabidopsis thaliana OX=3702 GN=AGAL3 PE=1 SV=1 |
| Q8RX86 | 1.89e-73 | 262 | 648 | 29 | 391 | Alpha-galactosidase 2 OS=Arabidopsis thaliana OX=3702 GN=AGAL2 PE=1 SV=1 |
| Q55B10 | 5.31e-73 | 267 | 650 | 22 | 383 | Probable alpha-galactosidase OS=Dictyostelium discoideum OX=44689 GN=melA PE=3 SV=1 |
| B3PGJ1 | 5.58e-69 | 268 | 650 | 28 | 403 | 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 |
|---|---|---|---|---|---|
| 0.000494 | 0.998446 | 0.000353 | 0.000227 | 0.000220 | 0.000203 |
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