| Species | Prevotella lascolaii | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Lineage | Bacteria; Bacteroidota; Bacteroidia; Bacteroidales; Bacteroidaceae; Prevotella; Prevotella lascolaii | |||||||||||
| CAZyme ID | MGYG000001164_00309 | |||||||||||
| CAZy Family | GH27 | |||||||||||
| CAZyme Description | hypothetical protein | |||||||||||
| CAZyme Property |
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| Genome Property |
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| Gene Location | Start: 13777; End: 16002 Strand: + | |||||||||||
| Family | Start | End | Evalue | family coverage |
|---|---|---|---|---|
| GH27 | 467 | 720 | 7.7e-78 | 0.9781659388646288 |
| Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
|---|---|---|---|---|---|---|---|
| cd14792 | GH27 | 5.22e-123 | 372 | 653 | 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 | 6.96e-98 | 345 | 722 | 1 | 364 | alpha-galactosidase |
| PLN02692 | PLN02692 | 1.62e-89 | 368 | 722 | 52 | 388 | alpha-galactosidase |
| PLN02229 | PLN02229 | 6.08e-82 | 362 | 721 | 53 | 396 | alpha-galactosidase |
| pfam16499 | Melibiase_2 | 6.08e-69 | 371 | 653 | 1 | 284 | Alpha galactosidase A. |
| Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
|---|---|---|---|---|---|
| SDS12868.1 | 5.02e-254 | 6 | 739 | 5 | 739 |
| QTE63205.1 | 5.44e-247 | 1 | 739 | 1 | 739 |
| QEM17823.1 | 5.44e-247 | 1 | 739 | 1 | 739 |
| QTE57332.1 | 5.44e-247 | 1 | 739 | 1 | 739 |
| QTE52244.1 | 5.44e-247 | 1 | 739 | 1 | 739 |
| Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
|---|---|---|---|---|---|---|
| 4NZJ_A | 3.51e-113 | 285 | 694 | 13 | 427 | Crystalstructure of a putative alpha-galactosidase (BF1418) from Bacteroides fragilis NCTC 9343 at 1.57 A resolution [Bacteroides fragilis NCTC 9343] |
| 4OGZ_A | 1.58e-109 | 285 | 686 | 13 | 419 | 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] |
| 1UAS_A | 8.87e-79 | 368 | 715 | 5 | 334 | ChainA, alpha-galactosidase [Oryza sativa] |
| 6F4C_B | 2.83e-75 | 368 | 715 | 5 | 334 | Nicotianabenthamiana alpha-galactosidase [Nicotiana benthamiana] |
| 3A5V_A | 9.11e-65 | 368 | 738 | 5 | 389 | Crystalstructure of alpha-galactosidase I from Mortierella vinacea [Umbelopsis vinacea] |
| Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
|---|---|---|---|---|---|---|
| P14749 | 3.62e-86 | 368 | 735 | 52 | 403 | Alpha-galactosidase OS=Cyamopsis tetragonoloba OX=3832 PE=1 SV=1 |
| Q8RX86 | 3.83e-83 | 368 | 721 | 36 | 371 | Alpha-galactosidase 2 OS=Arabidopsis thaliana OX=3702 GN=AGAL2 PE=1 SV=1 |
| B3PGJ1 | 3.84e-81 | 366 | 739 | 27 | 401 | Alpha-galactosidase A OS=Cellvibrio japonicus (strain Ueda107) OX=498211 GN=agaA PE=1 SV=1 |
| Q9FT97 | 1.02e-77 | 368 | 740 | 50 | 407 | Alpha-galactosidase 1 OS=Arabidopsis thaliana OX=3702 GN=AGAL1 PE=2 SV=1 |
| Q55B10 | 1.88e-77 | 368 | 733 | 24 | 375 | Probable alpha-galactosidase OS=Dictyostelium discoideum OX=44689 GN=melA PE=3 SV=1 |
| Other | SP_Sec_SPI | LIPO_Sec_SPII | TAT_Tat_SPI | TATLIP_Sec_SPII | PILIN_Sec_SPIII |
|---|---|---|---|---|---|
| 0.000768 | 0.998463 | 0.000262 | 0.000176 | 0.000164 | 0.000165 |
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