Species | Bacteroides xylanisolvens | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Lineage | Bacteria; Bacteroidota; Bacteroidia; Bacteroidales; Bacteroidaceae; Bacteroides; Bacteroides xylanisolvens | |||||||||||
CAZyme ID | MGYG000001345_02105 | |||||||||||
CAZy Family | GT32 | |||||||||||
CAZyme Description | hypothetical protein | |||||||||||
CAZyme Property |
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Genome Property |
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Gene Location | Start: 557994; End: 558773 Strand: + |
Family | Start | End | Evalue | family coverage |
---|---|---|---|---|
GT32 | 10 | 85 | 3.2e-20 | 0.9333333333333333 |
Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
---|---|---|---|---|---|---|---|
COG3774 | OCH1 | 1.03e-12 | 2 | 82 | 91 | 175 | Mannosyltransferase OCH1 or related enzyme [Cell wall/membrane/envelope biogenesis]. |
pfam04488 | Gly_transf_sug | 1.45e-12 | 7 | 82 | 1 | 84 | Glycosyltransferase sugar-binding region containing DXD motif. The DXD motif is a short conserved motif found in many families of glycosyltransferases, which add a range of different sugars to other sugars, phosphates and proteins. DXD-containing glycosyltransferases all use nucleoside diphosphate sugars as donors and require divalent cations, usually manganese. The DXD motif is expected to play a carbohydrate binding role in sugar-nucleoside diphosphate and manganese dependent glycosyltransferases. |
pfam05704 | Caps_synth | 2.35e-07 | 4 | 157 | 59 | 200 | Capsular polysaccharide synthesis protein. This family consists of several capsular polysaccharide proteins. Capsular polysaccharide (CPS) is a major virulence factor in Streptococcus pneumoniae. |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
---|---|---|---|---|---|
QUT23013.1 | 6.20e-197 | 1 | 259 | 1 | 259 |
QDH55390.1 | 2.57e-196 | 1 | 259 | 11 | 269 |
QUT28802.1 | 1.03e-195 | 1 | 259 | 1 | 259 |
QJR76539.1 | 4.50e-75 | 1 | 221 | 11 | 231 |
CBK68805.1 | 6.86e-74 | 1 | 221 | 11 | 231 |
Other | SP_Sec_SPI | LIPO_Sec_SPII | TAT_Tat_SPI | TATLIP_Sec_SPII | PILIN_Sec_SPIII |
---|---|---|---|---|---|
1.000089 | 0.000000 | 0.000000 | 0.000000 | 0.000000 | 0.000000 |
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