| Species | Eubacterium_R sp900542875 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Lineage | Bacteria; Firmicutes_A; Clostridia; Oscillospirales; Acutalibacteraceae; Eubacterium_R; Eubacterium_R sp900542875 | |||||||||||
| CAZyme ID | MGYG000001230_00946 | |||||||||||
| CAZy Family | GH27 | |||||||||||
| CAZyme Description | hypothetical protein | |||||||||||
| CAZyme Property |
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| Genome Property |
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| Gene Location | Start: 63458; End: 65185 Strand: + | |||||||||||
| Family | Start | End | Evalue | family coverage |
|---|---|---|---|---|
| GH27 | 328 | 546 | 2.6e-62 | 0.8253275109170306 |
| Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
|---|---|---|---|---|---|---|---|
| cd14792 | GH27 | 1.99e-106 | 61 | 476 | 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 | 5.09e-89 | 61 | 566 | 32 | 381 | alpha-galactosidase |
| PLN02692 | PLN02692 | 1.79e-85 | 61 | 566 | 56 | 406 | alpha-galactosidase |
| PLN02229 | PLN02229 | 2.48e-79 | 61 | 566 | 63 | 415 | alpha-galactosidase |
| pfam16499 | Melibiase_2 | 4.03e-60 | 61 | 476 | 2 | 284 | Alpha galactosidase A. |
| Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
|---|---|---|---|---|---|
| AQS55991.1 | 1.39e-106 | 59 | 568 | 44 | 532 |
| QOR76597.1 | 5.46e-80 | 61 | 568 | 43 | 392 |
| ABK25009.1 | 5.79e-80 | 56 | 573 | 38 | 399 |
| QUH05375.1 | 1.06e-77 | 61 | 568 | 36 | 386 |
| AHM60881.1 | 1.13e-76 | 42 | 569 | 22 | 408 |
| Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
|---|---|---|---|---|---|---|
| 6F4C_B | 2.84e-67 | 59 | 566 | 7 | 358 | Nicotianabenthamiana alpha-galactosidase [Nicotiana benthamiana] |
| 1UAS_A | 3.87e-67 | 59 | 571 | 7 | 362 | ChainA, alpha-galactosidase [Oryza sativa] |
| 3A5V_A | 9.17e-62 | 61 | 567 | 9 | 389 | Crystalstructure of alpha-galactosidase I from Mortierella vinacea [Umbelopsis vinacea] |
| 4OGZ_A | 3.30e-54 | 55 | 518 | 92 | 428 | 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 | 2.57e-53 | 55 | 540 | 92 | 459 | Crystalstructure of a putative alpha-galactosidase (BF1418) from Bacteroides fragilis NCTC 9343 at 1.57 A resolution [Bacteroides fragilis NCTC 9343] |
| Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
|---|---|---|---|---|---|---|
| Q8RX86 | 3.31e-74 | 61 | 569 | 40 | 392 | Alpha-galactosidase 2 OS=Arabidopsis thaliana OX=3702 GN=AGAL2 PE=1 SV=1 |
| Q9FT97 | 2.17e-71 | 61 | 566 | 54 | 404 | Alpha-galactosidase 1 OS=Arabidopsis thaliana OX=3702 GN=AGAL1 PE=2 SV=1 |
| P14749 | 3.53e-69 | 59 | 572 | 54 | 411 | Alpha-galactosidase OS=Cyamopsis tetragonoloba OX=3832 PE=1 SV=1 |
| B3PGJ1 | 4.08e-69 | 59 | 569 | 31 | 402 | Alpha-galactosidase A OS=Cellvibrio japonicus (strain Ueda107) OX=498211 GN=agaA PE=1 SV=1 |
| Q9FXT4 | 9.54e-66 | 59 | 571 | 62 | 417 | Alpha-galactosidase OS=Oryza sativa subsp. japonica OX=39947 GN=Os10g0493600 PE=1 SV=1 |
| Other | SP_Sec_SPI | LIPO_Sec_SPII | TAT_Tat_SPI | TATLIP_Sec_SPII | PILIN_Sec_SPIII |
|---|---|---|---|---|---|
| 1.000065 | 0.000000 | 0.000000 | 0.000000 | 0.000000 | 0.000000 |
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