| Species | Dysgonomonas sp900556485 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Lineage | Bacteria; Bacteroidota; Bacteroidia; Bacteroidales; Dysgonomonadaceae; Dysgonomonas; Dysgonomonas sp900556485 | |||||||||||
| CAZyme ID | MGYG000003132_02263 | |||||||||||
| CAZy Family | CBM35 | |||||||||||
| CAZyme Description | hypothetical protein | |||||||||||
| CAZyme Property |
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| Genome Property |
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| Gene Location | Start: 21746; End: 23842 Strand: - | |||||||||||
| Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
|---|---|---|---|---|---|---|---|
| cd14791 | GH36 | 3.80e-09 | 292 | 571 | 3 | 278 | glycosyl hydrolase family 36 (GH36). GH36 enzymes occur in prokaryotes, eukaryotes, and archaea with a wide range of hydrolytic activities, including alpha-galactosidase, alpha-N-acetylgalactosaminidase, stachyose synthase, and raffinose synthase. All GH36 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. GH36 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. |
| Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
|---|---|---|---|---|---|
| EIY66649.1 | 9.06e-202 | 20 | 698 | 75 | 749 |
| QUT74114.1 | 7.26e-201 | 20 | 698 | 75 | 749 |
| QQY38591.1 | 2.89e-192 | 44 | 695 | 50 | 673 |
| ABR38452.1 | 2.89e-192 | 44 | 695 | 50 | 673 |
| BCI61924.1 | 3.44e-192 | 29 | 695 | 26 | 688 |
| Other | SP_Sec_SPI | LIPO_Sec_SPII | TAT_Tat_SPI | TATLIP_Sec_SPII | PILIN_Sec_SPIII |
|---|---|---|---|---|---|
| 0.000454 | 0.996450 | 0.002487 | 0.000199 | 0.000189 | 0.000180 |
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